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1.
PURPOSE
BACKGROUND
Risks of vaccination range from common, minor and inconvenient side effects to rare,
severe, and life-threatening conditions.
Recommendations for immunization balance the scientific evidence of benefits, costs, and
risks. The Peace Corps Medical Officer (PCMO) must be fully acquainted with all vaccines
administered and should consult the following publications for additional information:
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3. RECOMMENDED VACCINATIONS
See ATTACHMENT A for recommended vaccines.
4. VACCINE ADMINISTRATION
4.1
Types of Vaccines
There are three main types of immunizations available. Live vaccines and inactivated
vaccines both provide immunity by stimulating the immune system whereas passive
vaccines contain antibodies and provide immediate immunity without stimulating an
immune response.
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Live Vaccines
BCG*
Influenza
Measles, Mumps/Rubella
(MMR)
Oral Polio (OPV) **
Oral Typhoid (Ty21a)
Rotavirus*
Varicella**
Yellow Fever
Inactivated Vaccines
Anthrax*
Cholera*
Diphtheria
Tetanus
Pertussis*
Hemophilus Influenzae
type B**
Hepatitis A
Hepatitis B (recombinant)
Hepatitis A & B
HPV2, HPV4*
Human Papilloma Virus*
Influenza
Japanese Encephalitis***
Lyme Disease*
Meningococcal
Plague*
Pneumococcal
Inactivated Polio Virus
(IPV)
Rabies
Tick-borne encephalitis
(TBE)
Typhoid (ViCPS or
inactivated)
Zoster
Passive Vaccines
Immune Globulin (IG)**
Human Rabies Immune
Globulin (HRIG)
Hepatitis B Immune
Globulin (HBIG)**
Varicella Zoster Immune
Globulin (VZIG)**
*
indicates vaccines which are not indicated for use by Volunteers at this time
** indicates vaccines with very limited use
*** indicates vaccine approved for PC use, not licensed in the US
4.2
Vaccine-Induced Anaphylaxis
4.3
The PCMO should be familiar with the signs, symptoms and management of
anaphylaxis (see TG 615).
Anaphylaxis may occur with any vaccination, even if that vaccine has been given
before.
Wherever vaccinations are given, equipment and medication for emergency
treatment of anaphylaxis must be available for immediate use. The anaphylaxis
treatment protocol must be posted in any area where vaccines are administered.
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Primary Immunization
Many vaccines require more than one dose to provide adequate immunity.
Interval between Doses (primary immunization series)
Increased Time between Doses: Increasing the time between doses does not reduce
the final antibody concentration. If a dose is delayed, it is not necessary to repeat
the entire series or to add extra doses. However, if any dose in a primary series is
delayed, subsequent doses should be rescheduled according to the recommended
interval schedule in the primary series (see example below). PCMOs should make
every effort to administer doses on time and according to the recommended interval
schedule to provide protection at the earliest date.
EXAMPLE: Rabies vaccine is recommended on days 0, 7, and 21 (see
section 10). If the second dose is delayed until day 10, the third dose
would be given no sooner than day 24. The second dose must be given at
least seven days after the first and the third dose must be given at least 14
days after the second. Note that the 21 day schedule has been chosen to
provide pre-exposure immunity as quickly as possible.
Decreased time between doses: Decreasing the time between doses may decrease
the antibody response. If a dose is given before it is due, PCMOs should not count it
as part of the immunization series and should continue the series as if it had not
been given, i.e., repeat the dose at the appropriate time.
Booster Doses
Booster doses are doses given after a completed primary immunization series, e.g.,
tetanus boosters every ten years for Volunteers. Some vaccines do not require
booster doses. For those that do, the booster will be effective if given anytime
within the recommended booster interval (within ten years for tetanus vaccine in the
preceding example). Exceeding the recommended interval could result in a decrease
in protection.
RECAP NOTE:
Vaccine doses for primary immunization must be given no sooner than the
recommended interval.
Booster doses should be given no later than the recommended interval.
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Inactivated vaccines
All inactivated vaccines may be given any time before, with, or after other
inactivated vaccines, live vaccines, or immune globulin. Injections should be given
at separate sites.
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Egg proteins
Egg proteins are found in MMR, influenza, yellow fever, and purified chick embryo
cell rabies vaccines. Persons who can eat eggs or egg-containing foods without
adverse effects can safely receive these vaccines. Persons with urticaria,
angioedema, throat swelling, or other reactions (even if mild) are at risk for severe
allergic reactions. PCMOs should consult OMS when considering vaccination of
persons who may be allergic to egg proteins.
4.5
Neomycin
Only if the Volunteer has had an anaphylactic reaction to neomycin in the past, s/he
should not receive the rabies vaccine, MMR, Varicella, or polio vaccine.
Note: Persons who have already COSed are not eligible to receive vaccines from
the PC Health Unit.
4.6
Minor illnesses such as mild upper respiratory infections are not a reason to delay.
Although a moderate or severe acute illness is sufficient reason to postpone
vaccination, minor illnesses (such as diarrhea, mild upper respiratory infection
with or without low-grade fever, other low-grade febrile illness) are not
contraindications to vaccination (CDC, 2016).
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4.7
People with moderate or severe acute illness, with or without fever, should be
vaccinated as soon as the condition improves. This precaution is to avoid
superimposing adverse effects from the vaccine on underlying illness, or mistakenly
attributing a manifestation of underlying illness to the vaccine.
4.8
4.9
Recording immunizations
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Type of Vaccine
Dosage
Expiration date;
Vaccine manufacturer;
VIS Date;
Education Date.
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For detailed instructions on how to use these PCMEDICS immunization features, refer
to the PCMEDICS user scripts that can be found at:
https://in.peacecorps.gov/HQ/OHS/HIU/_layouts/15/start.aspx#/User%20Scripts
Paper Immunization Rosters/Records
Paper Immunization Roster and Immunization Records are no longer necessary as this
information is placed directly on PCMEDICS.
WHO Cards
Peace Corps no longer provides WHO cards. If a Volunteer presents a WHO Card to
the health unit requesting in-service vaccines be documented on it, the PCMO may
document the immunizations administered during service.
4.10 Special circumstances
Splenectomy: If an Applicant has had a splenectomy, the applicant must have received
the meningococcal, Haemeophilus Influenzae type b, and Pneumococcal vaccines prior to
entry on duty.
4.11 US Department of State Vaccination list
Whenever possible, FDA-licensed vaccines are to be used at Peace Corps Medical Units
overseas. When an FDA-licensed vaccine is either unavailable through normal
procurement channels or unreasonably delayed in shipment, a more readily obtained
equivalent non-FDA licensed vaccine manufactured by well-known reputable multinational pharmaceutical companies may be considered.
ATTACHMENT D is a list of State MED-approved vaccines. The US Department of
State maintains a list of approved vaccines which are for use overseas but not available in
the US. These are acceptable for Peace Corps Medical Officers to stock and administer.
Also listed are vaccines that are not approved by State MED and Peace Corps.
4.12 Immunizations Necessary for PCMOs/ PCMOs on TDY
All PCMOs may be reimbursed for the annual influenza vaccine. See ATTACHMENT
E.
Host Country National (HCN) PCMOs who are traveling on temporary duty status (TDY)
and require immunizations for the TDY country of service will be reimburseed from
OHS for vaccination-incurred costs. Traveling (TDY) PCMOs should save vaccine
related receipts and submit them with the travel voucher after travel. If possible, vaccine
related costs should be added to the TA prior to travel.
5. REPORTING ADVERSE REACTIONS (VAERS)
The Vaccine Adverse Event Reporting System (VAERS) is a system designed for the
collection and analysis of reports of adverse events following use of any vaccine in the U.S.
In the U.S., all providers are required to report all vaccine adverse events using this system.
The VAERS is a passive reporting system.
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Peace Corps works with the CDC to participate in the VAERS system. The VAERS accepts
all vaccine reports, including reports for non-U.S. licensed vaccines that have been
authorized by OMS for use overseas. Reports from Peace Corps are of special significance
due to the inclusion of vaccines that are not routinely used in the U.S. The PCMO should
consult OMS if a Volunteer has a medical contraindication to vaccination, i.e., history of a
significant reaction to a vaccine or vaccine component.
If adverse event suspected, review the VAERS resource and information below:
o Any event which is specifically required to be reported which occurs within the
specified time period or within seven days of vaccination as defined by the
table Reportable Events Following Vaccination found at:
http://vaers.hhs.gov/resources/VAERS_Table_of_Reportable_Events_Foll
owing_Vaccination.pdf
o Any event listed in the manufacturers package insert as a contraindication to
subsequent doses of the vaccine.
o Any clinically significant adverse event occurring after the administration of
any vaccine. Reporting of an adverse event does not necessarily imply that the
vaccine(s) caused the event.
Contact the EPI Unit if you suspect an adverse reaction as it must be reported on a
VAERS form. The EPI unit will assist the PCMO with reporting adverse reactions.
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For maximum reliability of refrigeration, store all vaccines in the interior compartment of
the refrigerator or freezer, never in the doors. Remove only the vaccines necessary for
immediate use and return them to the refrigerator immediately after use.
8. TECHNICAL REFERENCE INFORMATION
This section addresses the most important aspects of individual vaccines included in the
Volunteer immunization program. Some of the vaccines are used on a worldwide basis,
others are used only in certain regions, countries, or areas.
Adverse Reactions
Local symptoms of pain and tenderness were the most commonly reported symptoms in a
safety study with 1,993 adult participants who received 2 doses of Ixiaro. Headache, myalgia,
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fatigue, and an influenza like illness were each reported at a rate of >10%. Because Ixiaro was
licensed after the study in <5,000 recipients, the possibility of rare serious adverse events
cannot be excluded. Post licensure studies and surveillance are ongoing to further evaluate the
safety of Ixiaro in a larger population.
Primary Immunization
Ixiaro: 0.5 ml IM on days 0 and 28
Imojev: 0.5 ml IM single dose
Booster Doses
Ixiaro: If primary series >1 year then 0.5 ml booster may be given. See
http://wwwnc.cdc.gov/travel/yellowbook/2016/infectious-diseases-related-to-travel/japaneseencephalitis for updated guidelines on boosters.
Imojev: no booster is needed for 5 years after receiving the Imojev live vaccine
Storage
Unreconstituted vaccine should be stored between 2-8C (36-46F). DO NOT FREEZE. The
reconstituted vaccine should be stored between 2-8C and used within 8 hours. DO NOT
FREEZE.
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(Microgen, Russia). Immunogenicity studies suggest that the European and Russian vaccines
should provide cross-protection against all 3 TBEV subtypes. For both FSME-IMMUN and
Encepur, the primary vaccination series consists of 3 doses. The specific recommended intervals
between doses vary by country and vaccine. Although no formal efficacy trials of these vaccines
have been conducted, indirect evidence suggests that their efficacy is >95%. Vaccine failures
have been reported, particularly in people aged 50 years.
Indications in Volunteers
Vaccination is recommended for Volunteers residing in rural areas or who work outdoors in
endemic areas.*
All Volunteers should be advised to use insect repellent (DEET) and wear appropriate clothing.
Unpasteurized dairy products should not be consumed.
*Endemic areas are well defined in Central Europe. All forested areas in the former Soviet
Union should be considered to be endemic areas unless specific epidemiologic information is
available.
Contrindications
FSME-Immun (Baxter, Canada)
Persons with systemic allergies to eggs should not be vaccinated.
Adverse Reactions
Mild injection site reactions (>10%) and headache, nausea, myalgia, and fatigue (1-10%) may
occur.
Primary Immunization
0.5 ml intramuscularly in months 0, 1, and 10-12.
Booster Doses
0.5 ml intramuscularly three years after the last dose.
Accelerated Dosing
0.5 ml intramuscularly given on days 0, 7, and 21.
Storage
Store between 2-8C (36-46F). DO NOT FREEZE.
HEPATITIS A (HAV)
Distribution and Transmission
HAV infection is highly endemic throughout the developing world, where it is primarily a
childhood infection. Transmission occurs via person-to-person contact or from the ingestion of
contaminated food or water.
Vaccines
Inactivated vaccines are available in the U.S. from GlaxoSmithKline (Havrix) and Merck
(Vaqta). Havrix (GlaxoSmithKline) contains 1440 ELISA units (EL.U.) per dose and Vaqta
(Merck) contains 50 units (U.) per dose. Both vaccines are authorized for use as described
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below. Less potent pediatric formulations (Havrix 720 EL.U./dose, Vaqta 25 U./dose) should
not be used.
One dose of vaccine produces high levels of antibody within four weeks. Immune Globulin
(IG) (see IG section below) may be given in addition to hepatitis A vaccine to provide
immediate protection. IG should be administered during the first month of service in settings
where Trainees will be at significant risk for acquiring hepatitis A before high antibody levels
are achieved from HAV vaccine. A second dose of vaccine is necessary to maintain protection
beyond one year (see below).
Indications in Volunteers
All Volunteers must be immunized against HAV infection. Hepatitis A vaccine should be
administered upon arrival unless proof of immunity is present, i.e., positive anti-HAV antibody
titer or documentation of prior vaccination with the hepatitis A vaccine (see above).
Contraindications
Persons allergic to vaccine or any of its components (e.g., alum, 2-phenoxyethanol for Havrix)
should not be vaccinated. IG should be used every four months in such persons.
Adverse reactions
Local pain and tenderness at the injection site, occasional mild systemic symptoms.
Primary immunization
1.0 ml intramuscularly in months 0 and 6. Volunteers should receive the second dose at the
first opportunity for vaccination (six to12 months after first dose).
(If IG is used, it is given 14 days after arrival in country to prevent interaction with MMR
vaccine and must be given at a separate injection site).
Booster Doses
The need for booster doses following the primary series has not been determined. Research has
shown the primary dose to be effective for >25 years (ACIP, 2006).
Storage
Store between 2- 8C (36-46F). DO NOT FREEZE.
Immune Globulin
IG, Gamma Globulin IG is a sterile solution of immunoglobulin (antibodies) prepared from
pooled human plasma. IG offers short-term protection against HAV infection for at least four
months. IG is available for intramuscular injection.
Indications in Volunteers
IG may be administered to provide protection during the first month after vaccination and for
person allergic to hepatitis A vaccine. See hepatitis A vaccine information above.
Contraindications
IG should not be given to persons with known immunoglobulin A deficiency. IG should not be
given in patients with a history of prior systemic allergic reactions to IG. IG for intramuscular
use should NEVER BE GIVEN INTRAVENOUSLY..
Adverse reactions
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Local pain and tenderness at the injection site, urticaria, and angioedema may occur following
IG administration. Serious reactions are rare.
How Administered
Short-term protection (less than three months)
2.0 ml intramuscularly is effective for up to 3 months. (0.02 ml/kg)
Long-term protection (more than three months)
5.0 ml intramuscularly is effective for at least four months. (0.06 ml/kg)
Volunteers who cannot receive hepatitis A vaccine should receive IG every four months.
Interactions
IG must be given three months before, or two weeks after, MMR vaccine. IG does not interfere
with yellow fever or polio vaccines.
IG does not produce a clinically significant drop in the response to hepatitis A vaccine and may
be given before, with, or after vaccination.
Storage
IG should be refrigerated at 2- 8C (36-46F). DO NOT FREEZE.
HEPATITIS B (HBV)
Distribution and Transmission
Hepatitis B is a disease caused by hepatitis B virus (HBV), a small, circular, partially doublestranded DNA virus in the Hepadnaviridae family.
HBV is moderately to highly endemic in most countries where Volunteers serve. Endemicity
can be classified based on the prevalence of HBV carriers (HBsAg positive) as:
High endemicity (HBsAg prevalence 8-15%)
SE Asia, Central Asia, China, Tropical Africa, Pacific Islands, Amazon Basin;
Intermediate endemicity (HBsAg prevalence 2-7%)
Central Europe, Mediterranean, Central and Tropical South America, Haiti, the
Dominican Republic, Middle East, India, Russia; Low endemicity (HBsAg prevalence <02%)
North America, Western Europe, Australia, New Zealand, Temperate South America.
HBV transmission occurs via percutaneous or permucosal exposure to infected blood or bloodderived fluid, especially occupational blood exposure, exposure to contaminated needles or
blood, and perinatal and sexual transmission.
Approximately 5% of U.S. residents become infected with HBV during their lives, most often
during young adulthood.
Vaccines
Recombinant hepatitis B vaccines are produced by yeast cultures into which the gene for
hepatitis B surface antigen (HBsAg) has been inserted. Vaccines are available in the U.S. from
Merck (Recombivax HB) and Glaxo SmithKline (Engerix-B). Additionally, a combined
hepatitis A and B vaccine is available from Glaxo SmithKline (Twinrix).
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Protective antibodies are produced in more than 90% of healthy young adults. Vaccine
response rates decrease somewhat with age (see below).
Indications in Volunteers
Universal vaccination of all Volunteers is required. The majority of Volunteers serve in areas
of intermediate to high HBV endemicity*. In addition, sexually active adults benefit from
vaccination. Pre-service is required to document the status of anti-HBs. If it is negative, the
Volunteer should repeat the primary series (of 3 vaccinations) OR the PCMO may repeat the
sAB test one month after vaccination; if negative, continue the two shots to complete the
series.
Contraindications
Hypersensitivity to any component of the vaccine is a contraindication to its use. There is no
apparent risk of adverse events to developing fetuses when hepatitis B vaccine is administered
to pregnant women.
Adverse Reactions
Hepatitis B vaccines have been shown to be safe when administered to both adults and
children. The major side-effects have been soreness and redness at the site of injection.
Primary Immunization
Recombivax HB, Engerix-B
1.0 ml intramuscularly (deltoid only) in months 0, 1, and 6.
Accelerated: 1.0 ml IM months 0, 1, and 2 with a booster at 12 months
Recombivax HB and Engerix-B may be interchanged without affecting vaccine response.
Twinrix
1.0 ml IM in months 0, 1, and 6
Accelerated; 1.0 ml IM on days 0, 7, 21-30, and a booster at 12 months
Serologic testing one to two months after completing all doses to confirm vaccine response
(defined as antibody to hepatitis B surface antibody [anti-HBS] concentration > 10 mIU/mL) is
recommended by OMS for health care workers and others at occupational risk of HBV
infection. Additional doses of vaccine may be necessary. See CDC recommendations for more
information.
Booster Doses
Additional booster doses are not recommended for healthy adults for the standard dosing;
boosters necessary for accelerated dosing.
Storage
Vaccine should be refrigerated at 2- 8C (36-46F). DO NOT FREEZE. Freezing destroys the
potency of the vaccine.
INFLUENZA
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Contraindications
MMR should not be given to pregnant women and pregnancy should be avoided for three
months after vaccination. MMR contains small amounts of neomycin and should not be given
to persons who have had anaphylactic reactions to neomycin. Any person with reduced
immunity should not receive the vaccine. MMR should not be given to persons who have had
anaphylactic reactions to gelatin or gelatin-containing products. Individuals with a severe
hypersensitivity to eggs should not be given vaccine. Persons who can eat eggs or eggcontaining foods without adverse effects can be vaccinated safely.
Interactions
Immune Globulin
Immune Globulin (IG) must be given three months before, or two weeks after, MMR vaccine.
Repeat MMR vaccine if IG administered less than three months before, or less than two weeks
after, MMR vaccination.
Live Vaccines
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MMR and yellow fever vaccines (and other live vaccines except oral typhoid vaccine) must be
given either on the same day or four weeks apart. Oral typhoid vaccine and all inactivated
vaccines may be given anytime before, with, or after MMR vaccine.
Adverse Reactions
Measles vaccine
Fever greater than 39C (103F) is seen in approximately 5-15% of those vaccinated, usually
beginning between the 5th and 12th days after vaccination and lasting for one to two days.
Transient rashes occur in approximately 5% of vaccines.
Up to 55% of persons who were vaccinated with killed measles vaccine during 1963-1967
experience a local or mild systemic reaction after live measles vaccination. Occasionally illness
may be more severe but is much milder than that seen with atypical measles (measles which
occurs in persons who are partially immune).
Mumps vaccine
Parotitis and encephalitis have been reported rarely. Revaccination is not associated with
increased adverse effects.
Rubella vaccine
Adverse events are only seen in persons without previous vaccination or natural infection (i.e.,
no rubella immunity). Up to 40% of susceptible adults experience joint pains in the small
joints, knees, or both. Women are more often affected than are men or children. Symptoms
appear one to three weeks after vaccination and generally persist for one day to three weeks.
Chronic joint complaints following vaccination are generally rare and occur at a rate
considerably less than that following natural infection. Transient peripheral neurologic
complaints are also reported rarely.
Primary Immunization
MMR 0.5 ml subcutaneously, two doses given at least one month apart.
Long lasting protection is obtained in 95% of vaccinated persons after one dose and 100% after
two doses of MMR.
Booster Dose
Immunity following two doses of MMR vaccine is long lasting. Additional doses are not
required.
Vaccine Storage
Store vaccine at 2-8C (36-46F). Protect from light. Store reconstituted vaccine at 2-8C,
protect from light, and use within eight hours.
MENINGOCOCCAL VACCINE
Distribution and Transmission
N. meningitidis is found worldwide. At any time, 5%10% of the population may be carriers of
N. meningitidis. Invasive disease is rare in nonepidemic areas, occurring at a rate of 0.510
cases per 100,000 population per year, but can occur at a rate of up to 1,000 cases per 100,000
population per year in epidemic regions. The incidence of meningococcal disease is several
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times higher in the meningitis belt in Africa (stretching from The Gambia to Ethiopia) than in
the United States, with periodic epidemics during the dry season (DecemberJune). During
nonepidemic periods, the rate of meningococcal disease in this region is roughly 510 cases
per 100,000 population per year. During epidemics, the rate can be as high as 1,000 cases per
100,000 population. Serogroup A predominates in the meningitis belt, although serogroups C,
X, and W-135 are also found. Transmission is by direct person-to-person spread of bacteria
from nasal and pharyngeal secretions (most infected persons remain asymptomatic or have
only a mild respiratory illness).
Vaccine
Two quadrivalent meningococcal polysaccharideprotein conjugate vaccines are licensed for
use in the United States: Menactra (Sanofi Pasteur) and Menveo (Novartis). A 1-dose primary
series of Menactra is licensed for people aged 255 years; a 2-dose primary series of Menactra
is licensed for children aged 923 months. Menveo is licensed for people aged 255 years.
Quadrivalent meningococcal polysaccharide vaccine (Menomune, Sanofi-Pasteur) is licensed
for use among people aged 2 years. These vaccines protect against meningococcal disease
caused by serogroups A, C, Y, and W-135. A vaccine was licensed in the US (Trumenba) for
meningococcus B. Approximately 710 days are required after vaccination for development of
protective antibody levels. Either of the conjugate vaccines is preferred for people aged 255
years; polysaccharide vaccine should be used for people >55 years.
Indications in Volunteers
Volunteers serving in areas experiencing epidemic or highly endemic meningococcal disease in
Africa should be immunized. ACIP recommends that children previously vaccinated at ages 9
months through 6 years who remain at an increased risk for meningococcal disease receive an
additional dose of conjugate vaccine 3 years after their previous meningococcal vaccine and
every 5 years thereafter, if at continued risk. Likewise, people who were previously vaccinated
at ages 755 years and who remain at an increased risk for meningococcal disease should
receive an additional dose of conjugate vaccine 5 years after their previous dose and every
5 years thereafter, if at continued risk. Travelers aged >55 years should be vaccinated or
revaccinated with polysaccharide vaccine if it has been >5 years since their last meningococcal
vaccine. Previously unvaccinated travelers <56 years of age who have a history of complement
component deficiency (C3, properdin, factor D, or late component), functional or anatomic
asplenia, or HIV should receive a 2-dose primary series of conjugate vaccine, 812 weeks
apart. For those aged 56 years with these conditions, a single dose of polysaccharide vaccine
should be given before travel if possible.
Contraindications
People with moderate or severe acute illness should defer vaccination until their condition
improves. Vaccination is contraindicated for people who have severe allergic reaction to any
component of the vaccines. People with dry natural rubber latex allergy should not receive
Menactra. Polysaccharide vaccine is an acceptable alternative for protection against
meningococcal disease in these people. All meningococcal vaccines are inactivated and may be
given to immunosuppressed people.
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Adverse reactions
Local reactions such as pain, tenderness, induration, and erythema may occur.
Primary immunization
0.5 ml subcutaneously (Menomune)/ 0.5 ml intramuscular (Menactra/ Menveo)
Booster Doses
A booster dose after 3 years is indicated if at continued risk.
Storage
Store freeze-dried and reconstituted vaccine between 2-8C (36-46F). Discard reconstituted
vaccine after 24 hours (single dose vial) or after five days (multi-dose vial).
PNEUMOCOCCAL VACCINE
Distribution and Transmission
Pneumococcal pneumonia is the most common post-viral bacterial pneumonia, and is a
significant cause of morbidity in areas where epidemic influenza or a high incidence of
respiratory diseases occurs.
Vaccine
A meta-analysis of 15 randomized controlled trials (RCTs) and seven nonrandomized
observational studies of PPSV23 efficacy and effectiveness suggested an overall efficacy of 74%
against IPD (CI = 56%--85%), based on pooled results of 10 of the RCTs.
Volunteers meeting any of the following criteria are to be vaccinated prior to PC service.
However, if a Volunteer is not able to be immunized prior to service, PC should provide the
vaccine for him/her:
>65 OR will be turning 65 during PC service
Chronic heart disease (excluding hypertension)
Chronic lung disease, including asthma
Diabetes Mellitus
Cochlear implant
Cigarette smoking
Sickle cell disease and other hemoglobinopathies
Congenital or acquired asplenia, splenic dysfunction, or splenectomy
Congenital or acquired immunodeficiencies
HIV infection
Diseases requiring treatment with immunosuppressive drugs, including long-term
systemic corticosteroids or radiation therapy
Contraindications
The safety of pneumococcal polysaccharide vaccine among pregnant women has not been
evaluated. Women at high risk of pneumococcal disease ideally should be vaccinated before
becoming pregnant.
Adverse Reactions
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About half of persons vaccinated experience mild side effects such as erythema and pain at the
site of injection. Fever, myalgias and severe local reactions have been reported by <1% of
recipients. Anaphylactic reactions are rare.
Primary Immunization
0.5 ml subcutaneously or intramuscularly (one dose)
Booster Doses
Revaccination is recommended one time 5 years after the first dose for persons who are
asplenic and for chronic renal failure, nephrotic syndrome, and organ transplant recipients.
Revaccination is also recommended over age 65 if they were vaccinated when they were <65
years of age. An interval of at least five years should be maintained between doses of PPSV23.
Storage
Store between 2-8C (36-46F).
POLIO
Distribution and Transmission
Polio is endemic in some parts of the world. See
http://www.polioeradication.org/Dataandmonitoring/Poliothisweek.aspx for reference.
Transmission is primarily by direct contact via fecal-oral contamination or contact with
pharyngeal secretions.
Vaccines
Completion of a primary series provides >95% immunity to all three polioviruses.
Inactivated Polio Vaccine (IPV)
Inactivated polio vaccine (IPV) should be used for the primary immunization of adults.
Oral polio vaccine (OPV) is an alternative only if IPV is unavailable.
Indications in Volunteers
Volunteers who have completed a primary series should receive one booster dose of IPV after
the age of 18 or provide proof of documented immunity.
Contraindications
Inactivated Polio Vaccine (IPV)
IPV may be given to pregnant women if immediate protection against poliomyelitis is needed.
IPV may be given to persons who are immunocompromised, their household members or other
close contacts.
Oral Polio Vaccine (OPV)
Pregnant women and persons who are immunocompromised should not be vaccinated with
OPV. Household contacts of immunocompromised persons should not be vaccinated with
OPV.
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Adverse Reactions
Inactivated Polio Vaccine (IPV)
IPV has had no serious side effects documented. IPV contains trace amounts of streptomycin
and neomycin and hypersensitivity reactions are possible among persons sensitive to these
antibiotics.
Oral Polio Vaccine (OPV)
There is a small (about two per million) risk of paralytic polio occurring in first-dose vaccine
recipients or their contacts.
Primary series
Volunteers whose primary immunization is in doubt should receive IPV, 0.5 ml
subcutaneously in months 0, 1, and 2.
Booster doses
One booster dose is required after the age of 18.
IPV 0.5 ml subcutaneously
(If OPV must be used, the booster dose is 0.5 ml orally)
Storage
IPV
Store between 2-8C (36-46F). DO NOT FREEZE.
RABIES
Distribution and Transmission
Rabies is endemic in most countries. Virus-infected saliva from a rabid animal may be
introduced through a bite wound, or very rarely through broken skin or through intact mucous
membrane exposure.
Vaccines
Human Diploid Cell Vaccine (HDCV), Rabies Vaccine Adsorbed (RVA), and Purified Chick
Embryo Cell (PCEC) vaccines are approved for use in the U.S. RVA or PCEC are appropriate
for persons allergic to HDCV. Verorab is a vaccine manufactured overseas that is approved for
use in PC. Intradermal vaccines are not approved for use by PC.
Indications in Volunteers
Pre-exposure Prophylaxis
Volunteers in countries where rabies is highly endemic are to receive pre-exposure
immunization (see below) in addition to instructions on cleansing wounds and on the need for
post-exposure prophylaxis with rabies vaccine.
Volunteers in countries with low rabies endemicity where contact with stray animals is
common are also recommended to receive pre-exposure prophylaxis to simplify post-exposure
treatment and to avoid use of potentially hazardous vaccines available locally.
Volunteers in countries with low rabies endemicity and little contact with stray animals and
where access to post-exposure rabies vaccine and rabies immune globulin (human) is reliable
June 2016
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Immunization
do not need to be given pre-exposure vaccine. They must be instructed on cleansing wounds
and on the need for post-exposure prophylaxis (rabies vaccine and rabies immune globulin),
which must be stocked for at least two complete treatment doses (immune globulin + 4 IM
vaccines).
Post-exposure Prophylaxis
All animal bites and scratches should immediately be thoroughly washed with soap and water.
Many species of mammals have been documented to transmit rabies via bites and scratches
including bats, dogs, cats, skunks, foxes, coyotes, raccoons, bobcats, and other carnivores. In
endemic areas, if the animal is suspected to be rabid, the bitten Volunteer should be vaccinated
unless the animal is proven to be rabies negative by rabies testing. Vaccination should also
occur when a bite cannot be reasonably excluded; such as during sleep, when the victim is
intoxicated, or when the victim cannot clearly communicate, e.g., a child. Bites from livestock,
rodents, rabbits, and hares rarely require vaccination.
Contraindications
Persons with a history of hypersensitivity to eggs to PCEC. Persons with a history of
hypersensitivity to HDCV, RVA, or PCEC.
Adverse Reactions
Local reactions such as pain, erythema, and swelling or itching at the injection site are
frequently reported. Mild systemic reactions such as headache, nausea, abdominal pain, muscle
aches and dizziness also occur. Serious anaphylactic, systemic or neuroparalytic reactions are
extremely rare.
Up to 6% of persons receiving booster vaccination with HDCV experience urticaria, pruritus,
and malaise (immune complex-like reaction).
Interactions
Corticosteroids and other immunosuppressive agents can interfere with the development of
active immunity and should not be administered during pre-exposure therapy.
Pre-exposure immunization
HDCV/ PCEC/ RVA: 1.0 ml intramuscularly on days 0, 7, and 21* or days 0, 7, and 28.
Verorab: 0.5 ml intramuscularly on days 0, 7, and 21 or days 0, 7, and 28
*The 21 day schedule is preferred for Volunteers serving in highly rabies endemic areas.
Rabies vaccine is effective if intervals between doses are longer than those listed, however the
onset of an adequate response would be delayed. For this reason, all three doses should be
completed within 21-28 days whenever possible.
Booster Immunization
In general, OMS recommends rabies boosters for Volunteers 3-5 years once the primary series
has been completed. US DoS does not recommend a one year booster with Verorab.
Immunization of PCV animals
PCVs that possess animals should be highly encouraged to vaccinate their pet against rabies.
Post-Exposure Immunization
Completed 3-dose primary series (IM)
1.0 ml intramuscularly on days 0 and 3. Rabies immune globulin (RIG) should not be given.
Office of Health Services
June 2016
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Immunization
June 2016
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Immunization
Adolescents aged 11-18 years who have completed their childhood vaccination series with DT,
DTaP and/or DTwP should receive a single dose of Tdap instead of Td for booster immunization
against tetanus as well as diphtheria and pertussis. Adults aged 19-64 years who have not
previously received Tdap should receive a single dose of Tdap if their last dose of tetanus toxoidcontaining vaccine was administered more than 10 years prior. Tdap is not licensed or
recommended for adults older than 65 years, who should receive Td instead.
Anyone who has received only one or two prior doses of tetanus and diphtheria toxoids should
receive additional does to complete the three-dose series. A single dose of Tdap can be
substituted for any of the Td doses.
Contraindications
An immediate anaphylactic reaction to a prior dose of vaccine or vaccine component is a
contraindication to further vaccination with DTaP, DT, or adult Td or Tdap. Encephalopathy not
due to another identifiable cause within 7 days of vaccination is a contraindication to further
vaccination with a pertussis-containing vaccine. DT or Td may be substituted for DTaP or Tdap,
respectively. Moderate or severe acute illness is a precaution to vaccination. Mild illnesses, such
as otitis media or upper respiratory infection, are not contraindications. Anyone for whom
vaccination is deferred because of moderate or severe acute illness should be vaccinated when
the condition improves.
Adverse Reactions
Local reactions such as local redness, induration, and tenderness are common, particularly
among persons who have received multiple boosters of tetanus toxoid. Systemic reactions such
as malaise and fever are less common. Rarely, neurologic complications following
administration of tetanus toxoid have been reported.
Primary Immunization
Adolescents or adults who have never been immunized against tetanus, or whose immunization
history is uncertain, should receive a three-dose series of vaccinations. The preferred schedule is
a single Tdap dose, followed by a dose of Td 4-8 weeks after the Tdap dose, and a second dose
of Td 6-12 months after the first Td dose; however, a single dose of Tdap can be substituted for
any one of the three doses in the series.
Booster Doses
Anyone who has received only one or two prior doses of tetanus and diphtheria toxoids should
receive additional doses to complete the three-dose series. A single dose of Tdap can be
substituted for any of the Td doses. The Td or Tdap vaccine must be given stateside within the
past seven years prior to departure (will cover volunteer for up to ten years or three in service). ii
NOTE: Volunteers should be instructed during pre-service training never to allow any local
facility to administer any form of tetanus immunization. Several potentially dangerous vaccines
are routinely used abroad.
Storage
Tetanus diphtheria toxoid vaccine (Td) and Tetanus, diphtheria and pertussis (Tdap) should be
stored between 2- 8C (35- 46F). DO NOT FREEZE. Discard if the vaccine has been frozen.
Do not use after expiration date shown on the label.
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TG 300
Immunization
TYPHOID FEVER
Distribution and Transmission
Typhoid fever is caused by infection with Salmonella typhi through exposure to contaminated
food and water. It is endemic throughout Africa, Asia, and Central and South America.
Vaccines
Two newer vaccines that are as effective and better tolerated than the older heat-phenol
inactivated vaccine are now available.
Vi capsular polysaccharide vaccine (ViCPS)
ViCPS vaccine is the preferred vaccine for overseas use because of the single dose
convenience, reasonable cost, and less stringent shipping requirements. Typhim Vi is
manufactured by Pasteur Merieux and distributed in the U.S. by Connaught.
Oral typhoid vaccine (Ty21a)
Ty21a is a live attenuated bacterial vaccine that is well tolerated; however in-country
vaccination is more difficult due to multiple dose issues, shipping requirements, and the need
to defer vaccination during episodes of acute gastrointestinal illness and antibiotic use.
Indications in Volunteers
All Volunteers should be vaccinated except those serving in countries without risk of typhoid
(i.e., most of Northern Europe).
Even after vaccination, food and water should be selected carefully. A large inoculum of
Salmonella typhi may overwhelm the protective effect of the vaccine.
Contraindications
Vi capsular polysaccharide vaccine (ViCPS)
Contraindicated in patients with a history of hypersensitivity to this vaccine.
Oral typhoid vaccine (Ty21a)
Not recommended for children under six years of age or immunocompromised persons
(including those with asymptomatic HIV infection). Vaccination should be deferred in
individuals with an acute febrile or gastrointestinal illness.
Adverse Reactions
Vi capsular polysaccharide vaccine (ViCPS)
Mild local reactions may occur. ViCPS vaccine is most often associated with headache (16%
20%) and injection-site reactions (7%).
Oral typhoid vaccine (Ty21a)
Adverse reactions to Ty21a vaccine are rare and mainly consist of abdominal discomfort, nausea,
vomiting, and rash.
Interactions
Oral typhoid vaccine (Ty21a)
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TG 300
Immunization
June 2016
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TG 300
Immunization
Birth in the United States before 1980 (not a criterion for Global Health Service
Partnership Volunteers and immunocompromised people)
Indications in Volunteers
All Volunteers should be vaccinated or demonstrate immunity to Varicella.
Contraindications
People with contraindications for varicella vaccine should not receive varicella vaccine,
including anyone who
Adverse reactions
The most commonly reported health problems after vaccination were rash, fever, and pain,
redness, and soreness at the injection site
Primary immunization
Varicella vaccine contains live, attenuated varicella-zoster virus. CDC recommends varicella
vaccination for all people aged 12 months without evidence of immunity to varicella who do
not have contraindications to the vaccine: 2 doses for people aged 4 years. The minimum
interval between doses is 4 weeks for people aged 13 years. When evidence of immunity is
uncertain, a possible history of varicella is not a contraindication to varicella vaccination.
Booster Doses
Immunity following two doses of Varicella vaccine is long lasting. Additional doses are not
required.
Storage
For potency to be maintained, the lyophilized varicella vaccines must be stored frozen at an
average temperature of 5F (-15C) or colder. Diluent should be stored separately either at room
temperature or in the refrigerator. Vaccines should be reconstituted according to the directions in
the package insert and only with the diluent supplied with the vaccine, which does not contain
preservative or other antiviral substances that could inactivate the vaccine virus. Once
reconstituted, vaccine should be used immediately to minimize loss of potency. Vaccine should
be discarded if not used within 30 minutes after reconstitution.
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Immunization
YELLOW FEVER
Distribution and Transmission
Yellow fever occurs in sub-Saharan Africa and tropical South America, where it is endemic
and intermittently epidemic. Most yellow fever disease in humans is due to sylvatic (jungle) or
intermediate (savannah) transmission cycles. However, urban yellow fever occurs periodically
in Africa and sporadically in the Americas. In Africa, natural immunity accumulates with age,
and thus, infants and children are at highest risk for disease. In South America, yellow fever
occurs most frequently in unimmunized young men who are exposed to mosquito vectors
through their work in forested areas.
Vaccine
Yellow Fever vaccine is an attenuated live virus vaccine grown in chick embryos. Immunity is
induced by a single subcutaneous (SC) injection of 0.5 ml of reconstituted vaccine and persists
for at least ten years.
Yellow fever vaccines should be administered at an official yellow fever vaccination center
and validated by an official stamp. PCMOs may reimburse currently-serving volunteers who
go to local facilities to get vaccinated for the cost of the vaccine & visit only (not travel to
clinic). If a clinic is not available, the responsibility lies with the Volunteer.
Indications in Volunteers
(1) Volunteers serving in countries with a risk of yellow fever transmission (yellow fever
endemic areas).
(2) Volunteers who are required to have a certificate of vaccination for entry into their country
of service or are planning to travel to a country that requires the vaccine. PCMO should not
store YF vaccine. PCVs should receive the immunization in an approved facility, if available.
As proof of receipt of YF vaccine, all vaccinees should possess a completed International
Certificate of Vaccination or Prophylaxis (ICVP), validated with the provider's signature and
official YF vaccination center stamp. An ICVP must be complete in every detail; if it is
incomplete or inaccurate, it is not valid. Failure to secure validations can cause a traveler to be
quarantined, denied entry, or possibly revaccinated at the point of entry to a country.
Volunteers with either of these indications should be vaccinated unless they have been
vaccinated within the past seven years.
Contraindications
Allergy to vaccine component (eggs, egg products, chicken proteins, or gelatin.) The
stopper used in vials of vaccine also contains dry natural latex rubber, which may
cause an allergic reaction
Thymus disorder associated with abnormal immune function
Primary immunodeficiencies
Malignant neoplasms
Transplantation
Immunosuppressive and immunomodulatory therapies.
Precautions
Office of Health Services
June 2016
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TG 300
Immunization
Age > 60 years: assess Volunteer and give vaccine if healthy; defer if immunecompromised
Pregnancy
Breastfeeding
Interactions
Yellow fever vaccine must be given simultaneously with, or more than four weeks before or
after MMR. It does not interact with OPV or oral typhoid vaccine.
Adverse Reactions
Common adverse reactions
Reactions to yellow fever vaccine are generally mild; 10%30% of vaccinees report mild
systemic adverse events. Reported events typically include low-grade fever, headache, and
myalgias that begin within days after vaccination and last 510 days. Approximately 1% of
vaccinees temporarily curtail their regular activities because of these reactions.
Severe adverse reactions
Hypersensitivity
Immediate hypersensitivity reactions, characterized by rash, urticaria, bronchospasm, or a
combination of these, are uncommon. Anaphylaxis after yellow fever vaccine is reported to
occur at a rate of 1.8 cases per 100,000 doses administered.
Yellow fever vaccineassociated neurologic disease (YEL-AND)
YEL-AND represents a conglomerate of different clinical syndromes, including
meningoencephalitis, Guillain-Barr syndrome, acute disseminated encephalomyelitis, and
rarely, bulbar and Bell palsies. Historically, YEL-AND was seen primarily among infants as
encephalitis, but more recent reports have been among people of all ages.
The onset of illness for documented cases is 328 days after vaccination, and almost all cases
were in first-time vaccine recipients. YEL-AND is rarely fatal. The incidence of YEL-AND in
the United States is 0.8 per 100,000 doses administered. The rate is higher in people aged 60
years, with a rate of 1.6 per 100,000 doses in people aged 6069 years and 2.3 per 100,000 doses
in people aged 70 years.
Yellow fever vaccineassociated viscerotropic disease (YEL-AVD)
YEL-AVD is a severe illness similar to wild-type disease, with vaccine virus proliferating in
multiple organs and often leading to multisystem organ failure and death. Since the initial cases
of YEL-AVD were published in 2001, >60 confirmed and suspected cases have been reported
throughout the world.
YEL-AVD has been reported to occur only after the first dose of yellow fever vaccine; there
have been no reports of YEL-AVD following booster doses. The median time from YF
vaccination until symptom onset for YEL-AVD cases was 4 days (range, 08 days). The caseOffice of Health Services
June 2016
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Immunization
fatality ratio for all reported YEL-AVD cases worldwide is 63%. The incidence of YEL-AVD in
the United States is 0.4 cases per 100,000 doses of vaccine administered. The rate is higher for
people aged 60 years, with a rate of 1.0 per 100,000 doses in people aged 6069 years and 2.3
per 100,000 doses in people aged 70 years.
Primary Immunization
0.5 ml subcutaneously (one dose).
Booster Doses
Some countries consider one dose to be valid for a lifetime. See ATTACHMENT A for list of
countries. Others require a booster every 10 years.
Storage
Yellow Fever Vaccine must be stored frozen and used within 60 minutes of reconstitution.
REFERENCES
Advisory Committee on Immunization Practices (ACIP) website:
http://www.cdc.gov/vaccines/acip/index.html
Centers for Disease Control and Prevention (CDC). Health Information for International Travel,
2016. Available online at: http://wwwnc.cdc.gov/travel/yellowbook/2016/table-of-contents
Centers for Disease Control and Prevention (CDC). Epidemiology and Prevention of VaccinePreventable Diseases. 13th Edition. 2015; Available online at:
http://www.cdc.gov/vaccines/pubs/pinkbook/index.html
World Health Organization; Alert, response, and capacity building under the International Health
Regulations (IHR). Available online at: http://www.who.int/ihr/en/index.html
i
ii
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Hepatitis A Hepatitis B
As of July 2016
Albania
Armenia
Belize
Benin
Botswana
Burma
Burkina Faso
Cambodia
Cameroon
China
Colombia
Comoros
Costa Rica
Dominican Republic
Eastern Caribbean
Ecuador
Ethiopia
Fiji
Georgia
Ghana
Guatemala
Guinea
Guyana
Indonesia
Jamaica
Kenya
Kosovo
Kyrgyz Republic
Lesotho
Liberia
Macedonia
Madagascar
Malawi
Mali
Mexico
Micronesia
Moldova
Mongolia
Morocco
Mozambique
Namibia
Nepal
Nicaragua
Panama
Paraguay
Peru
Philippines
Rwanda
Samoa
Senegal
Sierra Leone
South Africa
Swaziland
Tanzania
Thailand
The Gambia
Timor L'este
Togo
Tonga
Ukraine
Uganda
Vanuatu
Zambia
1 Volunteers going to Africa need
to provide proof of immunity to
polio or childhood series+
booster; Elsewhere presumed
immunity may be adequate (if
attended public school in US/
military)
2 L means a YF vaccine is valid
for a lifetime
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
Measles,
Mumps and
Rubella
Polio
Pneumococcal
Tetanus
Diphtheria
and
Pertussis/
TD
Varicella
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
Yellow
Fever2
L
X
L
X
L
X
L
X
L
X
L
X
X
L
L
X
L
X
X
L
X
L
L
X
L
X
L
Rabies
B
X
X
X
X
X
X
X
X
X
X
X
B
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
B
X
X
X
X
Meningococcal
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
Influenza
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
Japanese
Encephalitis
X
X
X
Typhoid
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
Tickborne
Encephalities
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
TG 300 ATTACHMENT B
IMMUNIZATIONS
Immunizations for Peace Corps Volunteers
Indications and Administration
Vaccine
Encephalitis,
Japanese (JE)
Indications
All Volunteers serving
in endemic areas (see
text)
Primary Series
0.5ml IM days 0,28
Booster
If primary series >1yr
then 0.5 ml booster may
be given
JE-VC
Precautions / comments
Delayed hypersensitivity
may be seen up to 10 days
later
Local or mild systemic
reactions in 20%
Ixiaro
Imojev
Encephalitis,
Tick-Borne
(TBE)
IMMUNO
Hepatitis A
0.5 ml IM x 1
Every 5 years
0.5ml IM months 0, 1,
and 12
Accelerated: 0.5 ml IM
days 0, 7, and 21
Egg anaphylaxis,
thimerosol anaphylaxis
Immuno (Austrian) vaccine
is effective and well
tolerated
All Volunteers
Hepatitis A vaccine
1.0ml IM months 0, 6
GLAXO-SMITH-KLINE (HAVRIX)
MERCK (VAQTA)
5ml (0.06ml/kg) IM
Prefer to complete
Preservice
1.0ml IM (deltoid):
months 0, 1, 6
GLAXO-
SMITHKLINE
MERCK
PASTEUR
Serologic evidence of
immunity (see TG)
Accelerated: 1.0 ml IM
months 0, 1, and 2 with
a booster at 12 months
Hepatitis B
Also: if occupational
risk of blood exposure,
measure antibody level
1-6 months after series
Influenza
All Volunteers
0.5 ml IM annually
(Sept/Oct for Northern
Hemisphere)
repeat annually
TG 300 ATTACHMENT B
Vaccine
Indications
Primary Series
Meningococcal
Meningitis
A, C, Y,
W-135
All Volunteers in
endemic or epidemic
areas.
0.5ml SC (1 dose)
Pneumococcal
Pneumonia
PPSV23
0.5ml IM (1 dose)
PCV13
Age 65
Surgical or functional
asplenia.
At risk for infection or
complication.
Immunocompromised,
cochlear implant,
smoking, heart disease,
pulmonary disease
Precautions / comments
Pregnancy,
immunosuppression,
neomycin anaphylaxis,
gelatin anaphylaxis, egg
anaphylaxis.
Fever 5-12 days later in
15%. rash in 5%;
arthralgias or arthritis some
women
Every 5 years
Pregnancy (consider
risk/benefit)
Local mild reactions seen
Not recommended
Pregnancy (consider
risk/benefit)
Local reactions common,
occasional mild systemic
0.5ml IM (1 dose)
Polio
Rabies
(preexposure)
HDCV
PCEC
VERORAB
REQUIRED:
highly endemic areas
and/or inadequate access
to post-exposure series
HDCV
PCEC
0.5ml SC months 0, 1,
and 2 if prior
vaccination in doubt
0.5ml SC once as an
adult for countries
mentioned in TG
Anaphylaxis to neomycin,
streptomycin, polymyxin
well tolerated
RVA
Booster
HDCV/ PCEC
Preferred: 1.0ml IM
only:
days 0, 7, 21
COMPLETED
PREEXPOSURE:
2 doses 1.0ml IM:
days 0, 3
INCOMPLETE OR NO
PREEXPOSURE:
HRIG plus 4 doses IM:
days 0, 3, 7, 14
TG 300 ATTACHMENT B
Indications
Primary Series
Tetanusdiphtheria (Td)
0.5ml IM every 2
years; optional for
PCVs completing
regular 27 month tour
Hypersensitivity to ViCPS
Delay if experiencing GI
illness or if on antibiotics;
give 24 hrs before or after
mefloquine or Diamox
Tetanusdiphtheriapertussis (Tdap)
Booster
Precautions / comments
Vaccine
Typhoid
Yellow Fever
0.5ml SC days 0, 30
All Volunteers in
0.5ml SC (one dose)
endemic areas, those
requiring vaccination
entry into country of
service, those volunteers
traveling to country
where vaccine required*
every 10 years
Precautions: Do not administer this vaccine if any of the listed conditions are present. Consult OMS to review the
risks and benefits, which may include vaccination after informing the Volunteer of the risks and benefits or transfer
or medical separation to avoid exposure to this disease.
*Countries where YF/ Official certificate vaccine required: Coming from US: Benin, Burkina Faso, Cameroon,
Ghana, Liberia, Mali, Rwanda, Sierra Leone, Togo; Coming from country with transmission risk: Botswana, Cape
Verde, Ethiopia, Gambia, Guinea, Kenya, Lesotho, Madagascar, Malawi, Mozambique, Namibia, Senegal, South
Africa, Swaziland, Tanzania, Uganda, Zambia
TG 300 Attachment D
MMR
IPV
TD
Date:
Date:
Date:
Hep A
#1
Date:
Hep A
#2
Date:
Hep B
#1
Date:
Hep B
#2
Date:
Hep B
#3
Date:
Typhoid
Date:
PC-1562 (4/2014)
TG 300 ATTACHMENT E
Flu shots for staff
1. Presently the Peace Corps provides flu shots to all Volunteers and Washington staff but
not to overseas staff.
2. The Peace Corps has the legal authority to provide flu shots to both US and non-US
citizens and both direct-hire and PSC employees. Flu shots will be voluntary.
3. We propose a variety of options be made available to Posts and Posts be given the
discretion to choose one or more options.
4. OHS has informed State MED of Peace Corps intention to provide flu shots to host
country staff and State MED raised no objections. State MED has no overall policy for
flu shots for local staff. It is the decision of each US Embassy Medical Unit.
Options
1. PCMO gives flu shots to staff. The PCMO will order enough vaccine to cover the staff
members interested in having a flu shot as well as for the PCVs. (Note: the flu shot is
optional for staff but mandatory for PCVs). Therefore, most Posts will be covered by the
option of the PCMO then administering the vaccine. PCMOs will have liability under
local law for host country citizen employees, but the risk is minimal. The Peace Corps
has authority to indemnify PCMO for any damages and to pay attorney costs, but the
decision to do so is done after there is a claim. There may be some reluctance on part of
PCMOs as to increase liability and PCMOs will be permitted to opt out of administering
vaccine to staff at Post.
2. Reimbursement to private doctors in country to give flu shots. Posts set a fixed price and
determine if vaccine is available locally. Posts could contract directly with doctor;
reimburse employee; or reimburse doctor based on employees voucher. If the vaccine
is not available, Peace Corps will provide vaccine and syringes for administration to local
doctor if permitted by local law.
June 2016
WEBSITE: www.vaers.hhs.gov
E-MAIL: info@vaers.org
FAX: 1-877-721-0366
Last
M.I.
Address
State
City
Responsible
Physician
Facility Name/Address
Relation
Vaccine Provider
Patient/Parent
to Patient
Manufacturer
Other
Address (if different from patient or provider)
State
Zip
4. Patient age
mm
dd
yy
9. Patient recovered
YES
NO
5. Sex
M
mm
dd
yy
UNKNOWN
Zip
8.
7. Describe adverse events(s) (symptoms, signs, time course) and treatment, if any
State
City
Date Received
City
Zip
VAERS Number
mm
dd
yy
mm
dd
yy
AM
AM
Time ____________ PM Time ____________ PM
No. Previous
Doses
Route/Site
Lot number
Manufacturer
a.
b.
c.
d.
14. Any other vaccinations within 4 weeks prior to the date listed in no. 10
Vaccine (type)
Manufacturer
Lot number
Date
given
No. Previous
doses
Route/Site
a.
b.
15. Vaccinated at:
Private doctor's office/hospital
Public health clinic/hospital
Military clinic/hospital
Other/unknown
No
To doctor
To health department
To manufacturer
21. Adverse event following prior vaccination (check all applicable, specify)
Onset
Type
Dose no.
Adverse
Age
Vaccine
in series
Event
In patient
In brother
or sister
Yes
No
Initial
Follow-Up
Health care providers and manufacturers are required by law (42 USC 300aa-25) to report reactions to vaccines listed in the Table of Reportable Events Following Immunization.
Reports for reactions to other vaccines are voluntary except when required as a condition of immunization grant awards.
Form VAERS-1(FDA)
320621.qxd5
10/3/02
10:29 PM
Page 2
ROCKVILLE, MD
VAERS
Use a separate form for each patient. Complete the form to the best of your abilities. Items 3, 4, 7, 8, 10, 11, and 13 are considered
essential and should be completed whenever possible. Parents/Guardians may need to consult the facility where the vaccine was
administered for some of the information (such as manufacturer, lot number or laboratory data.)
Refer to the Reportable Events Table (RET) for events mandated for reporting by law. Reporting for other serious events felt to be
related but not on the RET is encouraged.
Health care providers other than the vaccine administrator (VA) treating a patient for a suspected adverse event should notify the
VA and provide the information about the adverse event to allow the VA to complete the form to meet the VA's legal responsibility.
These data will be used to increase understanding of adverse events following vaccination and will become part of CDC Privacy
Act System 09-20-0136, "Epidemiologic Studies and Surveillance of Disease Problems". Information identifying the person who
received the vaccine or that person's legal representative will not be made available to the public, but may be available to the
vaccinee or legal representative.
Postage will be paid by addressee. Forms may be photocopied (must be front & back on same sheet).
SPECIFIC INSTRUCTIONS
Form Completed By: To be used by parents/guardians, vaccine manufacturers/distributors, vaccine administrators, and/or the person
completing the form on behalf of the patient or the health professional who administered the vaccine.
Item 7:
Describe the suspected adverse event. Such things as temperature, local and general signs and symptoms, time course,
duration of symptoms, diagnosis, treatment and recovery should be noted.
Item 9:
Check "YES" if the patient's health condition is the same as it was prior to the vaccine, "NO" if the patient has not returned
to the pre-vaccination state of health, or "UNKNOWN" if the patient's condition is not known.
Item 10: Give dates and times as specifically as you can remember. If you do not know the exact time, please
and 11: indicate "AM" or "PM" when possible if this information is known. If more than one adverse event, give the onset date and
time for the most serious event.
Item 12: Include "negative" or "normal" results of any relevant tests performed as well as abnormal findings.
Item 13: List ONLY those vaccines given on the day listed in Item 10.
Item 14: List any other vaccines that the patient received within 4 weeks prior to the date listed in Item 10.
Item 16: This section refers to how the person who gave the vaccine purchased it, not to the patient's insurance.
Item 17: List any prescription or non-prescription medications the patient was taking when the vaccine(s) was given.
Item 18: List any short term illnesses the patient had on the date the vaccine(s) was given (i.e., cold, flu, ear infection).
Item 19: List any pre-existing physician-diagnosed allergies, birth defects, medical conditions (including developmental and/or
neurologic disorders) for the patient.
Item 21: List any suspected adverse events the patient, or the patient's brothers or sisters, may have had to previous vaccinations.
If more than one brother or sister, or if the patient has reacted to more than one prior vaccine, use additional pages to
explain completely. For the onset age of a patient, provide the age in months if less than two years old.
Item 26: This space is for manufacturers' use only.
TG 300 ATTACHMENT G
April 2014
ATTACHMENT G: US Department of State-MED Approved and Non Approved Non FDA Licensed Vaccines
Approved:
Vaccine
Contents
Manufacturer
Act-HIB
HIB conjugate
Sanofi-Pasteur
Adacel
Tdap
Sanofi-Pasteur
Avaxim
Hep A
Sanofi-Pasteur
Avaxim Ped
Hep A
Sanofi-Pasteur MSD
Covaxis
Tdap
Sanofi-Pasteur MSD
Encepur
TBE
Novartis
Engerix-B
(Erwachsene)
Hep B
GSK
Hep B
Trivalent seasonal
influenza
TBE
LG life Sciences
JEV
Green Cross
Havrix
Hep A
GSK
Havrix Jr. or
Havrix 720 Kinder
Hep A
GSK
Gardasil
HPV quadrivalent
Sanofi-Pasteur MSD
Hexavac
DTaP/HepB/IPV/Hib
Sanofi-Pasteur
Hexaxim
DTaP/IPV/HepB/Hib
Sanofi-Pasteur
IMOJEV
Sanofi-Pasteur
Imovax d.t.
Imovax Polio
Inactivated Influenza
Vaccine (Split Virion)
BP
Td
IPV
Sanofi-Pasteur
Sanofi-Pasteur
Trivalent seasonal
influenza
Sanofi-Pasteur MSD
Infanrix
DTaP
GSK
Infanrix Hexa
DTaP/HepB/IPV/Hib
GSK
GSK/Australia
Infanrix-IPV
DTaP/IPV
GSK
Euvax B
Afluria
FSME-Immune
Green Cross Japanese
Encepahalitis
CSL Biotherapies
Baxter
Comments
Equivalent FDA approved product from
same company.
WHO prequalified.
FDA approved but limited to ages 9+
years
Best alternative; no US vaccine.
Best alternative; for countries where no
US vaccine is available.
Equivalent FDA approved product from
same company.
Equivalent FDA approved product from
same company.
Equivalent FDA approved product from
same company.
Equivalent to approved components from
recognized multinational company.
Equivalent to approved components from
recognized multinational company
(Pentaxim plus Hep B)
Best alternative; for countries where no
US vaccine is available.
WHO prequalified.
WHO prequalified.
Infanrix-IPV+Hib
DTaP/IPV/Hib
GSK
Influvac
Trivalent seasonal
influenza
Abbott
IPV Merioux
Polio
Sanofi-Pasteur
JEEV
JEV
Biological Evans,
Ltd
JESPECT
JEV
Intercell
Mencevax ACW135Y
Mencevax ACWY
Meningitis Polysaccharide
GSK
Merieux (MIRV)
Rabies, inactivated
Sanofi-Pasteur
M-M-R vaxPro
MMR
Mutagrip
Trivalent seasonal
influenza
Sanofi-Pasteur
Nimenrix
Meningococcal TT
conjugate A, C, Y, W-135
GSK
Pentavac
DTaP/IPV/HIB
Sanofi-Pasteur
Pentaxim
DTaP/IPV/HIB
Sanofi-Pasteur
Poliorix
IPV
GSK
Pneumo 23
PPSV-23
Sanofi-Pasteur
Prevenar 13
PCV13
Wyeth, Pfizer
Priorix
MMR
GSK
Priorix-Tetra
MMRV
GSK
Quadracel
DTaP/IPV
Sanofi-Pasteur
Rabigam IM
RIG
National
Bioproducts Institute
Rabipor
Rabies
Chiron Behring
Vaccines Pvt. Ltd
Rabipur
Rouvax
Rabies
Measles
Chiron/Germany
Sanofi-Pasteur
WHO prequalified.
WHO prequalified.
Equivalent product from recognized
multinational company, components of
same strength FDA approved (Adacel)
WHO prequalified.
Equivalent FDA approved product from
same company. (Td and IPOL).
Repevax
dTap/IPV
Sanofi-Pasteur
Stamaril
YF
Sanofi-Pasteur
Td Polio Adsorbed
Td/IPV
Sanofi-Pasteur
Tetavax
TT
Sanofi-Pasteur
Tetravac
DTaP/IPV
Sanofi-Pasteur
Tetraxim
DTaP/IPV
Sanofi-Pasteur
Trimovax
MMR
Sanofi-Pasteur
WHO prequalified.
TwinRix
Hep A and B
GSK
Typhim Vi
Typhoid
Sanofi-Pasteur
Varilrix
Varicella
GSK
Varivax
Varicella
Sanofi-Pasteur MSD
Vaxigrip
TVI seasonal
Sanofi-Pasteur
Verorab
Rabies
Sanofi-Pasteur
CD.JEVAX
JEV
Chengdu Institute
Kuo Kwang
JEV
Adimmune
Okavax
Varicella
BIKEN
Prevenar 7
PCV7
Wyeth
Rabivax
Rabies
SII/India
Synflorix
PCV10
GSK
Tresivac
MMR
SII/India
Non Approved:
Safer options available. Monitoring of
safety and efficacy are not transparent.
Safer FDA approved options available;
different primary series schedule from
approved mouse brain products.
Peace Corps
Technical Guideline 301
INITIAL CLINICAL INTAKE INTERVIEW PROCESS
1.
PURPOSE
To provide guidance on initial clinical intake interview activities for Peace Corps Trainees and
Peace Corps Response Volunteers. Note: For purposes of this TG, Trainee can mean Trainee or
Response Volunteer.
2.
BACKGROUND
The purpose of the initial intake interview is for the PCMO to:
Meet with the Trainee one-on-one
Review information from the Trainee Clinical Intake Questionnaire,
Provide the Trainee with a hard copy of the Continuous Care Document (CCD) to validate
information in the Trainees medical record
Update information in the Trainees medical record
Identify any non-disclosures
Briefly assess current health status of the Trainee
Determine required immunizations while in-country
Determine and dispense malaria prophylaxis (if applicable)
Discuss treatment plans for chronic and/or accommodated health issues
Obtain Volunteer Email Authorization form (TG 210 , Attachment G)
Obtain Volunteer Immunization Consent form (TG 300, Attachment D)
Obtain Volunteer Consent to Disclose to Family/Friends form (TG 301, Attachment B)
Reinforce health promotion and disease prevention activities
The initial clinical intake interview is critical in establishing clinician-patient rapport and
validating the basic clinical care needs of the trainee for his or her service. All Trainees must
undergo an initial clinical intake interview performed by the PCMO within 72 hours upon arrival
to country. The Trainee Clinical Intake Questionnaire (Attachment A) contains two sets of
questions: provider questions that are needed immediately for the PCMO to assume care of the
Trainee and screening questions that are needed for the PCMO to have a more holistic
understanding of the Trainees health, lifestyle, and prevention areas.
Time on the Pre-Service Training (PST) schedule must be provided to the PCMO and Trainees in
order to complete the Trainee Clinical Intake Questionnaire (Attachment A). Time may vary for
this interview depending on the health needs of the Trainee. A minimum of twenty (20) minutes
should be allotted per interview. Depending on the outcome of the initial interview and health
care needs of the Trainee, subsequent discussion(s) may be needed.
December 2015
As outlined by their scope of practice and defined duties, medical assistants may assist the
PCMO in the intake interview process. Please contact OHS if there is a question regarding
PCMEDICS intake duties for medical assistants.
3. CLINICAL INTAKE INTERVIEW PREPARATION
Steps:
1. Print out each Trainees individual Continuous Care Document (CCD) and take to PST site
where clinical intake interviews are taking place.
2. Sync the laptop so that you have a current instance of PCMEDICS to take to the PST site.
3. Ensure that you have the equipment and supplies for the Clinical Intake Interview:
a. Laptop with PCMEDICS
b. Electrical cord and plug
c. Extension cord
d. Handheld scanner (if applicable)
e. Paper copies of blank Clinical Intake Questionnaires (Attachment A)
f. Paper copy of each Trainees CCD
g. General medications and supplies
h. Immunization consent form
i. Email consent form (TG 210 G)
4. COMPONENTS OF THE INITIAL INTAKE INTERVIEW
There are four basic components to an intake interview: Health Record Information and
Validation, Health Assessment, Healthcare Treatment Planning, and Documentation.
Health Record Information and Validation
Steps:
1. Provide each Trainee with a hard copy of the CCD and ask them to review prior to the
interview.
2. Provide the Trainee the Clinical Intake Questionnaire (Attachment A) in paper form for
the Trainee to complete (both provider and screening questions) prior to the intake
interview.
3. Meet with each Trainee individually to discuss the information on Trainee Clinical Intake
Questionnaire.
4. Review with the Trainee his or her electronic medical record (CCD) to ensure data is
correct and to socialize the Trainee to his/her electronic medical record. The PCMO
edits/updates data directly into PCMEDICS based on the Trainee Clinical Intake
Questionnaire and discussion.
5. Discuss any discovered non-disclosed information with the Trainee. If non-disclosure
suspected, PCMO to follow TG 190, Medical Non-Disclosure.
Health Assessment
Steps:
Based on general appearance and basic questioning (e.g. How are you? Any current
health issues that need medical attention?), the PCMO should assess the current health
December 2015
status of the Trainee. Baseline vital signs and weight should be obtained. No
examination is required at this time, but should be at the discretion of the PCMO
according to information provided by the Trainee on his or her current health status.
Healthcare Treatment Planning
Steps:
1. Determine immunizations required for service (TG 300, Immunization) by reviewing any
immunization documentation in the medical record as well as presented by the Trainee
(e.g. WHO card, child immunization record, etc.)
2. Obtain Vaccine Consent Form signed by Trainee (TG 300, Attachment C)
3. Discuss and document malaria prophylaxis plan if applicable (TG 840, Prevention of
Malaria) and obtain consent form signed by Trainee
4. Discuss accommodation treatment/care plans outlined by Pre-Service
5. Discuss communication with the PCMO (Volunteer Email Authorization form) and obtain
signed form indicating Trainees preference (TG 210 Attachment G)
6. Discuss which information the PCV would like shared and with whom in the event of
illness and obtain signed form (TG 301 Attachment B)
7. Provide any preventative education pertinent at this time
Documentation of the Interview
Steps:
At the end of the Clinical Intake interview, the PCMO should:
1. Complete a Patient Encounter Form and e-Sign in PCMEDICS within 72 hours of the
intake interview.
2. Scan the Trainees Clinical Intake Questionnaire and upload to document folder PST
Intake Documents in PCMEDICS.
3. Scan all Consent and Authorization Forms into PCMEDICS in document folder Volunteer
Consents/Waivers.
4. If unable to complete an electronic PEF at PST, the PCMO will need to capture the data
on a blank PEF (TG 210, Health Records, Attachment E) at PST and then enter the PEF
discrete data once the PCMO has access to PCMEDICS or attach to paper record.
Note: The information may be entered directly into PCMEDICS at PST if connectivity exists or in
offline mode to be syncd once back at the medical office.
December 2015
Peace Corps
Technical Guideline 302
VOLUNTEER CONCERNS
1.
PURPOSE
To provide a means for Volunteers to report concerns related to health care.
2.
BACKGROUND
PROCESS
______________________________________________________________________________
Office of Health Services
January 2016
Page 1 of 2
Peace Corps staff may not retaliate against a Volunteer for reporting a concern. This
forum (email) is open to Volunteers only.
4.
POST REPONSIBILITIES
All Posts are required to post the name, title, location, and telephone number of the
individual at Post who is responsible for receiving concerns and conducting
investigations, as well as the headquarters quality improvement email address and
instructions on how to file a concern.
5.
HEADQUARTERS RESPONSIBILITIES
Maintain the email box
Respond timely and appropriately to the Volunteers concerns
Keep post involved in the problem solving process
Provide post with announcements to post in offices (contact QI unit for posters)
Trend Volunteer concerns
______________________________________________________________________________
Office of Health Services
January 2016
Page 2 of 2
TG 302 Attachment A
Peace Corps
Office of Health Services
CONSENT/AUTHORIZATION FORM
Date
Date of birth
Peace Corps
Technical Guideline 304
HEALTH CARE CONSULTANT ON-LINE SATISFACTION SURVEY
1.
PURPOSE
To provide an avenue through which Volunteers and trainees (together,
Volunteers) can give non-urgent feedback to Peace Corps Medical Officers
(PCMOs) or the Office of Health Services (OHS) regarding the health care
provided to them.
If a Volunteer has an urgent or emergent concern related to quality of care that he or
she thinks is not being addressed appropriately by the PCMO, the Volunteer should
access Headquarters staff through the Medical Duty Officer.
2.
BACKGROUND
Peace Corps intent is to promote a medical culture that embraces Volunteer safety,
quality health care, and service satisfaction. As part of that effort, Volunteers are
offered the opportunity to provide input on health services received from outside
consultants and contracted facilities.
Aggregate data obtained from the survey will assist posts and OHS in assessing the
quality of care given by the health providers used by Volunteers. Peace Corps staff
may not retaliate against any Volunteer in relation to any feedback given.
3.
B. For input on any provider, discuss with the PCMO directly about the care
received; and/or
C. For input on any provider, file an email concern with the headquarters Quality
Improvement (QI) department at QualityNurse@peacecorps.gov (Refer to TG
302).
4.
______________________________________________________________________________
Office of Health Services
December 2012
Page 1 of 3
B. For input on any provider, discuss with your Volunteer Support International
Health Coordinator or RMO directly about the care received, and/or
C. For input on any provider, file an email concern with the headquarters Quality
Improvement (QI) department at QualityNurse@peacecorps.gov (Refer to TG
302)
5.
6.
______________________________________________________________________________
Office of Health Services
December 2012
Page 2 of 3
______________________________________________________________________________
Office of Health Services
December 2012
Page 3 of 3
HEALTH CARE
CONSULTANT
SATISFACTION SURVEY
Question
Survey
Good or Bad, We want to know.
/s/surveyonhealthproviders
Thank you for assisting us in assessing and monitoring our clinical care program.
Peace Corps
Technical Guideline 305
PCMO OVERSIGHT OF THE HOSPITALIZED VOLUNTEER
1.
PURPOSE
To provide information regarding Peace Corps Medical Officer (PCMO) oversight
responsibilities of a hospitalized Volunteer.
2.
BACKGROUND
It has always been the responsibility of PCMOs to provide oversight of the
hospitalized Volunteer regardless of severity of illness and/or disease.
3.
______________________________________________________________________________
Office of Health Services
June 2016
Page 1 of 2
If the PCV is able to communicate, the PCMO must make contact with the PCV
at least daily.
Documentation of any contact with the PCV and/or providers caring for the PCV
must be noted in the health record (refer to TG 210).
The PCMO will notify the Country Director when any significant situations, such
as changes in the PCVs condition or need to medevac, arise.
______________________________________________________________________________
Office of Health Services
June 2016
Page 2 of 2
Peace Corps
Technical Guideline 310
1. PURPOSE
To provide Peace Corps Medical Officers (PCMOs) and Peace Corps staff with guidance on
the health and safety training of Volunteers.
March 2015
Page 1
TG 310
Health & Safety Training
The health training program provides health education and prevention concepts and materials
to Trainees as they enter the overseas environment and supports, reinforces, and expands on
their skills at every opportunity throughout Volunteer service. At close of service (COS), the
program ensures that Volunteers are informed of their rights and responsibilities with respect
to post-service benefits, continuing health maintenance and health care.
The PCMOs must remind the PC staff, Peace Corps Trainees, and Peace Corps Volunteers
that V/Ts are not authorized to participate in direct health care activities unless they are
participants in the Global Health Services Partnership (GHSP) and authorized by the Country
Director. These activities include, but are not limited to, participating in immunization
programs, attending or otherwise assisting with childbirths, performing phlebotomy, insertion
of intravenous catheters, and other activities that may place them at risk for exposure to
blood or body fluids.
3. SAFETY TRAINING
The Office of Volunteer Safety and Security (SS) in Washington provides leadership and
guidance that supports Country Directors (CDs), overseas staff and Volunteers in all aspects
of safety and security.
Comprehensive safety training is a component of in-country Volunteer support and is the
responsibility of all Peace Corps staff. Safety training is delivered by Office of Safety and
Security. PCMOs are expected to collaborate with Office of Safety and Security
representatives and other PC post units and their staff to provide safety training during PreService Health Training (PST) and throughout the Volunteers service.
The safety training program is designed to prepare Volunteers for safe, healthy, and
productive service. Based on the unique circumstances under which Volunteers live and
work, the Agency has established the policy that:
Each post must provide Volunteers/Trainees (V/Ts) with a program of ongoing safety and
security training within the framework established by the Office of Safety and Security. The
training will be designed to increase V/Ts awareness of their in-country environment, build
their capacity to cope effectively with the many challenges they will face, and provide the
tools to adopt a safe and appropriate lifestyle. The training must promote a realistic
understanding of the possibility of accident, crime, disaster, injury, psychological trauma,
and loss of property during service. It must help V/Ts recognize factors that contribute to
March 2015
Page 2
TG 310
Health & Safety Training
those risks and encourage compliance with Peace Corps policy. The training must be
designed to instill attitudes consistent with adopting a culturally appropriate lifestyle and
practicing measures expected to reduce risk (Peace Corps Manual Section (MS) 270, 5.0).
5. TRAINING MATERIALS
The Volunteer Health System is responsible for providing consistent and accurate health
education to all Volunteers using prevention strategies based on the best available
information and Volunteer needs. The Office of Health Services (OHS) in collaboration with
the agencys other offices (e.g. Overseas Program and Training Support Office) establishes
training standards for health education (see section 2 above) and provides training materials
for use by in-country health and safety training programs. These materials are available on
the Peace Corps Office of Health Services Trainings website.
Health Training/Sessions
Health/Medical Pre-Service Training (PST) Curriculum is a teaching resource developed by
OHS for use by PCMOs in providing comprehensive health and wellbeing training at PST.
It is recommended for posts to use the new Global Core medical (curriculum) PST sessions
to meet the TLOs. The TLOs are stated on the cover page of each session plan. The session
objectives are designed to facilitate the achievement of the TLOs. The goal of each session
includes meeting the objectives and focusing on competency.
The resource contains eleven (11) Medical Global Core TLOs translated into fourteen (14)
medical sessions. Incorporation of the TLOs into PST is mandatory to the extent applicable
to each post.
The topics are as follows:
Alcohol
March 2015
Page 3
TG 310
Health & Safety Training
Diarrhea
Emergencies
Malaria
Nutrition
In addition or as part of the listed sessions, PCMOs should include the following countryspecific health topics in training:
Orientation to in-country care, e.g., accessing the health unit, contacting the PCMO, incountry medical facilities, and emergency preparedness;
PCMOs may develop and use pre- and post-tests and training evaluations to assess and
improve the effectiveness of the training. The Personal Health Plan is an assessment tool.
The sessions include the recommended time frame to complete the material and optimize
Volunteers success. Posts are, however, at liberty to adapt the training to meet the objectives
in a manner that best fits posts context. Consequently, posts, and medical units in particular,
may adjust the amount of time; and have control of sequence and approach of topics as well
as choices of available training resources such as PC/Washington, post-developed session
plans or other methods of learning.
Personal Health Plan
Volunteers must assume considerable responsibility for their health during Peace Corps
service while working as partners with PCMOs. This Personal Health Plan allows trainers
and trainees to work towards reaching that goal.
March 2015
Page 4
TG 310
Health & Safety Training
The Personal Health Plan is a platform for trainees to demonstrate a synthesis of their
learning and to create personal strategies of how to manage their health and wellbeing in
service. The complete Personal Health document becomes part of the Volunteers medical
records and a tool for discussion when a Volunteer needs/seeks support. It can be referenced
at in-service trainings and during medical appointments.
Posts are responsible for assessing the trainees achievement of the TLOs using the Trainee
Assessment Portfolio (TAP). Medical/health content is evaluated through the development of
the Personal Health Plan (a component of the TAP). The plan is an integral part of the health
training process to ensure that Volunteers take responsibility for their health and well-being.
Each Volunteer must submit a completed plan by the end of PST which a PCMO will review
and subsequently provide feedback shortly after but no later than 45 days upon conclusion of
PST (Health Plan Instructions provide details as on how to accomplish both).
Submission of the Personal Health Plan to the PCMO is required prior to swearing in.
PCMOs must ensure scheduling of sufficient work time to support the development of the
Personal Health Plan. A PCMO will need to review each Volunteers Health Plan
individually and provide complete and timely feedback to trainees/Volunteers in a caring and
coaching manner to provide ample opportunities for achieving mastery of all TLOs. The
completed Personal Health Plan must be signed by the Volunteer and the PCMO.
The Volunteers Personal Health Plan is a living document and should be revaluated during
IST and utilized during medical encounters for updates and adjustments. E.g. the PCMO can
take a copy of the plan and update when performing site visits.
Health Handbook
The PCMO is responsible for updating a country-specific Volunteer health handbook. This
handbook should be distributed to all Volunteers at PST. A basic Volunteer health handbook
contains four elements:
Overview of Peace Corps health policies and any country-specific Volunteer health
support program policies;
Information developed by OHS, including TGs and their attachments, may be used in
revising and updating the Volunteer Health Handbook at posts.
March 2015
Page 5
TG 310 ATTACHMENT A
Training Dates:
Training Site:
Training Director:
Contact Info:
1.
March 2015
Page 1
TG 310 Attachment A
Page 2
TG 310 Attachment A
8. COORDINATION
Make list of accommodations to share with Country Director.
Make list of homestay restrictions for Training Director.
Page 3
Peace Corps
Technical Guideline 320
1. PURPOSE
To provide guidance on Interim Health Evaluations for Peace Corps Volunteers.
2. BACKGROUND
All Volunteers should be seen at least one time 12 to 18 months after entry on duty. The
interim health evaluation can be performed concurrently with a medical visit for an acute
problem or separately with a scheduled visit.
The purpose of the interim health evaluation is to:
Evaluate and document the status of known chronic conditions, unresolved conditions,
and current medical problems including compliance and tolerance of prescribed
treatments by inviting the Volunteer to review the PCMEDICS Summary Page and
confirm/update: Allergies, Medications, Problems
Peace Corps Medical Officers (PCMOs) document the interim health evaluation on the
electronic Peace Corps Interim Health Evaluation form in PCMEDICS, based on a detailed
history provided by the Volunteer and history-guided examination.
All Volunteers
All Volunteers
December 2015
Page 1
TG 320
Interim Health Evaluation
All Volunteers
All Volunteers
3.1
Immunization status
December 2015
Page 2
TG 320
Interim Health Evaluation
5. Scan and upload any related dental, diagnostic, consultation, and/or laboratory
reports and images in the appropriate PCMEDICS document folders according
to TG 214 Attachment B.
3.3
Screening Mammography
Screening mammography is not available at all Peace Corps posts. Current USPSTF
recommendations are that women between the ages of 50 and 74 get screening
mammography every two years. Prior to service, female applicants age 50 and over
with previous normal mammograms are permitted to waive this recommendation.
(Refer to TG 355 Mammography sections 3 and 4)
3.4
Screening Tests
Tuberculosis Skin Testing (TST)/Interferon gamma releasing assay (IGRA)
Tuberculosis (TB) skin testing using the Intradermal (Mantoux) test is required for
Volunteers who have had contact with persons with known infectious TB or who live
or work in high risk settings. Results should read by the PCMO 48-72 hours after
placement. A reminder can be set up in the PCMOs PCMEDICS calendar to follow-up
for this purpose. If a Volunteer has a history of a positive intradermal test and
appropriate treatment at any time in the past, a new intradermal test is not necessary;
the Volunteer should be screened for symptoms of active Tuberculosis disease.
IGRA can be substituted for TST. FDA approved IGRAs include the T-Spot and
QuantiFERON-TB Gold. (Refer to TG 645 Pulmonary Tuberculosis)
Stool for Ova and Parasites
If clinically indicated, stool examination for ova and parasites should be performed.
(Refer to TG 815 Stool Examination for Parasites)
December 2015
Page 3
TG 320
Interim Health Evaluation
Dental Exam
In countries where adequate facilities and expertise exist, annual cleaning and scaling
should be performed. (Refer to TG 180 Dental Policy.)
Medevac is not authorized for the purposes of providing routine preventive dental care.
Volunteers who are returning to the U.S. on home leave may be authorized to have
dental care in the U.S. if adequate care is not available in country.
3.6
3.7
December 2015
Page 4
Peace Corps
Technical Guide line 330
To describe the post-service health benefits infor mation that must be pr ovided to
Volunteers at Close of Service.
To outline the Peace Corps Medical Off icer (PCMO) responsibilities for conducting
Close of Service (COS) health eva luations.
To outline the PCMO respons ibilities for conducting Extens ion of Service (EOS) health
evaluations.
2. B ACKGROUND
Most Returning Peace Corps Volunteers (RPCVs) learn about the ir post-service health
benefits and begin COS hea lth eva luations dur ing COS conferences that occur roughly 60
days pr ior to the Volunteers actual COS.
Not all Volunteers COS with their or igina l tra ining c lass. However, Peace Corps and Cris is
Corps Volunteers must receive health benef its inf or mation and hea lth eva luations when they
leave service, regardless of the reasons or circumstances of COS.
When to Provide Post-Service Health Benefits Information and
Conduct a Close of Service Health Evaluation
Completion of Tour
Early Termination
Resignation
Volunteers may resign their positions at any
time during training or service.
Early COS
Under certain circumstances, Volunteers
are permitted to leave their assignments
up to 90 days before their schedules
COS.
Interrupted Service
Volunteers may close service for reasons
beyond their control, such as country
evacuation or program closure.
Administrative Separation
Volunteers may be separated from service due
to unacceptable conduct or policy violations.
(See Technical Guideline (TG) 155 and Peace
Corps Manual Section (MS) 281.)
Medical Separation
Health problems may cause the Office of
Volunteer Support (VS) to separate a
Volunteer from service (see TG 160).
January 2016
Page 1
TG 330
Post-Service Benefits
Extens ion of Service (EOS) hea lth eva luations are conducted for Volunteers who wish to
extend the ir service for six months or more, or to transfer to another country program.
Show the Post-Service/ Federal Employees Compensation Act (FECA) Benefits Video.
Distribute the Post-Service Health Benefits at Glance information sheet.
Distribute the AfterCorps insurance brochure/extension form.
Collect completed AfterCorps insurance extension forms and give them to the post
Administrative Officer (AO).
Ensure that Volunteers have had the opportunity to ask questions about these benefit
programs.
Note: As circumstances dictate, the AfterCorps program and enrollment procedures may be
provided to Volunteers by the PCMO or AO.
Returning Peace Corps Volunteers are covered by a three-tiered health benefit program.
These benefits are:
127C authorization. 127C author izations are used to authorize evaluation of Peace
Corps service-related hea lth conditions;
FECA be ne fits. FECA covers the cost of treatment for service-related health conditions;
and
Afte rCorps ins urance . Afte rCorps is a comprehe ns ive health insurance policy that
covers non-service-re lated medica l pr oble ms.
The following table is a synopsis of each tier of the benefit program. Detailed information
about each type of benefit appears in subsequent sections.
January 2016
Page 2
TG 330
Post-Service Benefits
Benefit
Mechanism
Time Limit
How Accessed
127C
Authorization
May be issued by
PCMOs or VS staff.
FECA
Benefits
AfterCorps
Insurance
Non-service-related
medical problems.
Specifically:
Pre-existing conditions
not covered by FECA
Conditions that arose
while in the U.S. on
vacation, home leave,
emergency leave, or
medevac
New health problems
after COS
Contact AfterCorps
Customer Service for:
Emergency medical
assistance
Referrals to Network
hospitals, physicians,
and other health
services
Insurance coverage
extensions
January 2016
Page 3
TG 330
Post-Service Benefits
Second, it can be used to author ize presumptive antire lapse therapy (PART) for
malar ia. In these cases the author ization should read as follows :
Primary care consultation for G6PD testing ( if preservice results not
attached) and presumptive antirelapse therapy (PART) as indicated
A 127C must be issued and used w ithin s ix months of COS. It w ill not be honored
after that time has ela psed.
A 127C may be iss ued by a PCMO, RMO, or VS staff.
The 127C form has three parts. The origina l (hea lth recor d copy) is placed in the
Volunteers health record under In-Ser vice or COS/Post-Service care
depending on when it was issued. The f irst copy (provider copy) is given to the
provider by the Volunteer and the second copy (patie nt copy) is for the Volunteer's
persona l records. The PCMO should ensure that all three copies are legible pr ior to
issue.
After COS, if a Volunteer has questions or pr oble ms with his/her 127C
author ization, he/she should contact the Post-Service Unit in VS.
TG 340 PC-127C For m Author ization for Payment of Medical/Denta l Services
conta ins additiona l guidance on the use of 127C author izations.
3.2 FECA Be ne fits
FECA provides medica l and denta l treatment for health conditions re lated to
Volunteers overseas service.
FECA benef its are administered by the Office of Wor kers Compensation Programs
at the U.S. Department of Labor (DOL). The Post-Service Unit in VS ass ists
Volunteers in f iling c la ims with DOL.
FECA benef its are not guaranteed. The DOL must determine that a health condition
is service-related before a cla im for benef its is accepted.
DOL claims process ing usua lly takes from s ix to 12 weeks. This pr ocess can be
expedited if Volunteers contact the Post-Service Unit as soon as they be lieve they
have a service-related condition requir ing treatment and if they respond quickly to
requests for infor mation from the Post-Service Unit or DOL.
Cla ims must be made within three years of COS or within three years of recognition
of a service-related hea lth condition.
Health pr oble ms resulting from injur ies or illnesses that deve lop in the U.S. while
on vacation, home leave , emergency leave, or on medevac when the Volunteer is
not directly engaged in Peace Corps activity, are not eligible for FECA benef its (see
AfterCorps Insurance in section 3. 3 be low).
The PCMO or Post-Service Unit can provide inf or mation on FECA cla ims
processing and copies of The Post-Service Health Benefits at Glance inf ormation
sheet for Volunteers.
January 2016
Page 4
TG 330
Post-Service Benefits
January 2016
Page 5
TG 330
Post-Service Benefits
The post staff member who pr ovides AfterCorps inf ormation to Volunteers at COS
should hold the AfterCorps broc hure/extens ion f orms. That person should ma intain
a one-year supply of br ochures. Brochures may be reor dered from Post Logistics
and Support D ivis ion (M/AS/PLS) in Washington, DC.
Because the AfterCorps brochure conta ins an AfterCorps Ins urance Identif ication
Card, the br ochures should not be distr ibuted f or inf ormationa l purposes. Persons
who request a brochure for inf ormationa l purposes should be given photocopies of
the brochure.
3.4 He alth Be ne fits Information for Re turne d Voluntee rs
For questions regarding 127C author izations, FECA benef its, or other servicerelated hea lth issues , returned Volunteers should contact the VS Post-Service Unit.
In the U.S., they may dia l 800- 424-8580 (extens ion 1500) , toll free. Outside the
U.S., they ma y call 202- 692-1500.
Volunteers with questions regarding the use of the Health Benefits identif ication
card should contact the Peace Corps Health Benefits Program at 800-544- 1802. For
infor mation on network providers in a particular geographic location, Volunteers
should contact Seven Corners at 800-544- 1802 or vis it Seven C orners online at
www.peacecorps.sevencorners.com.
PCMOs with questions regarding the Health Benef its ide ntif ication card should
contact VS by phone at 202- 692-1500 and ask to be transferred to the Health Care
Resources Program Manager, or by fax at 202-692-1541.
To extend AfterCor ps insura nce coverage, Volunteers should contact the pla n
adminis trator , Seven Cor ners. Their phone numbers are 800-544-1802 in the U.S.,
or 317-582- 2609 outs ide the U.S. Volunteers may use Seven Cor ners' web site to
see a copy of the AfterCorps policy or to check persona l coverage as follows. Go to
www.peacecorps.sevencorners.com; clic k the AfterCor ps button.
For inf ormation or assistance with a medical e mergency or a non-service-related
health problem, retur ned Volunteers enrolled in AfterCorps should contact
AfterCorps. In the U.S., they may dia l 800- 544-1802. Outs ide the U.S., they may
call 317-582- 2609.
January 2016
Page 6
TG 330
Post-Service Benefits
Evaluate, document, and, where poss ible, complete treatment of curre nt medica l
proble ms;
Provide 127C author izations for necessary post-service medical and denta l eva luations;
COS health evaluation is not required for PCT who c loses service dur ing staging, unless
extenuating c ircumsta nces exist. VS will be consulted f or specia l s ituations where a COS
health evaluation may be necessary.
4.1 He alth His tory
The PCMO is respons ible for completing the review and update of the Volunteers
health record, eve n if a loca l consultant is used to perfor m the phys ical exa mination.
Steps
1. Volunteer completes Section 1 of PC-1790 (COS/EXT) C lose of Service or
Extens ion of Service Medica l Eva luation form (ATTACHMENT C).
2. PCMO reviews the health record and completes the health history w ith the
Volunteer in order to:
Ask the Volunteer whether he/she has any other hea lth concerns; and
January 2016
Page 7
TG 330
Post-Service Benefits
January 2016
Page 8
TG 330
Post-Service Benefits
On a case-by-case basis, laborator y screening be yond the required tests is occasiona lly
indicated. Such screening may be warranted if there is a r isk of exposure to a particular
condition and early diagnos is of the condition would be be nefic ia l, e.g., STDs. Refer to
the appropr iate TG for advice on screening for s pecif ic conditions. Consult the RMO or
VS for questions regarding additiona l screening tests at COS.
4.3 HIV Tes ting at COS
HIV Testing
All Volunteers, if more tha n 12 months s ince pre-service examination, should be
encouraged to have HIV testing at COS. HIV testing is not mandatory.
COS HIV testing can be accomplis hed us ing the rapid test kits or at a reputable medica l
laborator y.
If rapid test or screening test performed in country is indeterminate or pos itive for HIV,
medical off icers must inf or m and counse l the Volunteer and perfor m conf ir mator y HIV
test. Medical off icers should als o inf orm VS.
For ms 127C and PC-209B Author ization f or Medical Examination and Labs should
not be used to author ize HIV testing at COS unless it is impossible to obta in a sample
in country.
Schistosomiasis Testing
Routine screening testing f or Schistosomiasis at COS is no longer required or
recommended. All PCVs who have served in endemic areas, unless a medica l
contra indication exis ts, should be empir ically treated no greater than 72 hours pr ior to
departure from post. If there is uncertainty as to whether a post is in an endemic area,
check with the Chief of Epidemiology and Surve illance in VS.
4.4 Phys ical Exam
Use PC-1790 (COS/EXT) (ATTACHMENT C) for the COS phys ical exam.
Perform a comprehens ive phys ica l examination. This should be performe d by the
PCMO (if the PCMO is a phys ic ian, nurse practitioner , or phys ic ian ass istant) or by
the RMO or a referral consultant. Referral consultants used for COS examinations
must pr ovide a thor ough eva luation.
Have the PC-1790 (COS/EXT) for m co-s igned by an RMO or a Medical Advisor in
VS if the phys ica l examination is perfor med by a Nurse Practitioner or Phys icia n
Assistant. The Department of Labor (DOL) requires all documentation submitted
for FECA cla ims to be s igned or co-s igned by a phys ic ian.
January 2016
Page 9
TG 330
Post-Service Benefits
Steps
1. Complete PC 1790 (COS/EXT) section 2, parts A and F, even if a loca l consultant
performs the phys ica l exam.
2. Address all items reported on the health his tor y dur ing the phys ical exam. For
example , if the Volunteer reports a histor y of thyroid abnorma lities, a thyr oid exa m
should be perfor med and documente d.
3. Provide treatment for any medica l pr oble m that needs immediate attention.
Whenever poss ible, establis h a treatment plan that a llows the pr oble m to be
addressed before the Volunteers departure.
4. Issue a 127C for any hea lth condition that w ill require post-service evaluation in the
U.S. Expla in the use of the 127C and the Health Benefits Program identif ication
card.
5. If a Volunteer is advised to return to the U.S. for additional eva luation or treatment
within a certain period of time after COS, docume nt this infor mation in PC-1790
(COS/EXT) section 2, Part F. Other travel recommendations or functiona l
restrictions should a lso be recorded.
Medications
Immunizations
Booster doses of appr ove d vaccines ma y be given to Volunteers at COS who do not
plan to retur n to the U.S. within 30 days of COS and who me dically require the
vaccine for trave l in a destination countr y (see TG 300 Technical Reference
Infor mation on individua l vaccines).
A primary series of an approved vaccine may be initiate d for Volunteers at COS
who do not plan to return to the U.S. within 30 days of COS and medica lly require
the vaccine for trave l in a destination countr y. The vaccine must be ava ilable in the
Health Unit or thr ough another relia ble local source, e.g., Departme nt of State or
Ministr y of Health clinic.
Yellow fever vaccine can only be given at off ic ia l ye llow fever vaccination centers.
Peace Corps Health Units are not off ic ia l ye llow fever vaccination centers.
Malaria Prophylaxis/Suppression
For the Volunteer serving in a ma laria endemic area, PCMOs should pr ovide the
Volunteer with the follow ing:
June 2012
Page 10
TG 330
Post-Service Benefits
Handout titled Instr uctions for Volunteers: COS Guide lines for Preventing
Malar ia (see TG 330, Attachment G).
G6PD testing: PCMOs must follow the guidance in TG 840 G6PD
Testing when issuing pr imaquine to Volunteers. All Volunteers should
have been tested for G6PD def ic iency pr ior to enter ing PC. Testing should
only be repeated at COS if the pre-service results are not docume nted in the
medical recor d and those results are not obta ina ble. Volunteers who ha ve
not been tested for G6PD def icie ncy pr ior to COS should not be iss ued
pr imaquine and they should be pr ovided w ith a 127C author ization for ,
Primary care consultation for G6PD testing and presumptive anti-rela pse
therapy (PART) as indicated.
June 2012
Page 11
TG 330
Post-Service Benefits
June 2012
Page 12
TG 330
Post-Service Benefits
Update the Wor ld Hea lth Organization (WHO) Internationa l Certif icate of
Vaccination and return it to the Volunteer.
Obtain any medical equipment previous ly issued to the Volunteer.
Ensure the Volunteer has received a 30-da y supply of all prescription and required
OTC medications.
Ensure the Volunteer has received immunizations required f or post-service trave l
(see Section 4.4 above)
Ensure Volunteers serving in ma lar ia endemic areas have received me dications for
malar ia pr ophyla xis/suppress ion (see Section 4. 4 above)
If the Volunteer has refused to have blood drawn for HIV testing, this will be
documented in the hea lth record.
If the Volunteer has refused to undergo a COS health eva luation, he/she must read
and sign a copy of Ref usal to Undergo a COS Health Eva luation
(ATTACHMENT I).
If medically indicated, advise the Volunteer to return pr omptly to the U.S.
Document this advice in the health record.
Have the Volunteer read, complete, and sign a copy of V olunteer Health Program
COS Checklis t (ATTACHMENT B ).
Final Documentation in the Health Record
Document pending la bs. Record where each specimen was sent and the date sent.
Document denta l exams , mammography, and other eva luations to be done after
COS.
Comment on all unresolved medical conditions requir ing f ollow-up in the U.S.
File the health record copy of a ll 127Cs and any 209B issued.
Update the problem list.
File the Volunteer Health Program COS Checklis t.
Document the dispos ition of medica l x-rays.
Return Health Record to VS
Within 30 days of COS, package health record, mark "Me dical Eyes Only," and
send to:
Peace Corps Office of Volunteer Support
Medical Records Department
1111 20th Street, NW
Washington, DC 20526
June 2012
Page 13
TG 330
Post-Service Benefits
When laboratory test results are received after a Volunteer has closed service,
PCMOs should use the chart be low to determine how to document results and
initiate follow-up. When ava ilable , PCMOs should provide VS w ith the Volunteer's
SSN, home address, and te lephone number if follow-up is needed.
FOLLOW-UP OF POST-COS TEST RESULTS
Health Record Is Still In the
Health Unit
Urgent Follow-Up
Required
Follow -Up
Not Required
Post-COS Laboratory
Test Results
June 2012
Page 14
TG 330
Post-Service Benefits
5.1 He alth His tory, Scree ning Labs and Phys ical Examination
Use PC-1790 (COS/EXT) (ATTACHMENT C). The extension of service table on
page 4 of PC-1790 must be completed in a ll cases.
Perform all screening labs and tests indicated in PC-1790 (COS/EXT) section 2, parts
D and E, except HIV. Some required screening tests, e.g., mammography, may not be
Office of Volunteer Support
June 2012
Page 15
TG 330
Post-Service Benefits
available in country. This may require issuing a 127C and having the Volunteer
complete a test while on home leave.
5.2 HIV tes ting
HIV testing is not required for extens ion or transfer. HIV testing at extens ion of service
follows the same criter ia as all in-service HIV testing, and should be cons idered based
on r isk factors or c linica l f indings (see TG 710 STD/HIV Prevention).
5.3 Me dical Approval to Exte nd or Trans fe r
Medical approval f or extens ion or transfer uses criter ia establis hed in TG 160 Medica l
Separation. VS must be consulte d for any undia gnosed, unresolved, or potentia lly
recurrent health conditions that ma y interfere with the Volunteers ability to rema in in
countr y or transfer.
If a Volunteer is transferr ing to another country, the PCMO should disc uss with VS and
the receiving countrys PCMO any s ignif icant past me dical his tor y, spec ia l medica l
needs, or accommodation require ments.
5.4 Provis ional Me dical Approval to Exte nd
Provis ional medica l approva l to extend is given by VS only, and ma y be give n pending
treatment or tests results if the Volunteer is asymptomatic and can complete all
screening tests in a reasonable per iod of time.
Provis ional medica l approva l should not be granted when:
signs or symptoms suggestive of an undiagnosed condition exist;
pending eva luation of an undiagnosed or unresolved medical problem; or
for transfer to another countr y pr ogram.
Provis ional medica l approva l may be rescinded if a screening test result requires
follow- up unava ilable in country or the result precludes medica l appr ova l to extend. In
this case, the Volunteer should be granted e ither a COS or a medical separation.
Consult VS for guidance.
June 2012
Page 16
TG 330 ATTACHMENT A
Covers
Time Limit
How Accessed
PC-127C
Authorizations
FECA
Benefits
AfterCorps
Insurance
PC 127C Authorizations
A 127C is used to authorize payment of expenses for medical and dental evaluations of health
conditions that are related to your overseas service.
May 2015
TG 330 ATTACHMENT A
Only evaluations are covered, and only the specific evaluation authorized will be reimbursed. A 127C
cannot be used for medical treatment.
You must use a 127C within 6 months of your close of service (COS) date. It will not be honored
after that time has elapsed.
A 127C may be issued by a PCMO, a Regional Medical Officer (RMO) or Office of Health Services
(OHS) staff. The form has three parts. The one copy is kept with your Peace Corps health record. You
should give a copy to the healthcare provider with whom you consult and keep a copy for your
personal records.
For questions regarding 127C authorizations, FECA benefits or other service-related health issues,
you should contact the OHS Post-Service Unit at psu@peacecorps.gov. In the U.S., you may call (toll
free) 855-855-1961, extension 1540, option 7. Outside the U.S. you may call 202-692-1540, option 7.
A 127C authorization should be used in conjunction with your Peace Corps Health Benefits
identification card. For questions regarding the use of the Health Benefits ID card, you should contact
OHS Post-Service Unit at psu@peacecorps.gov or 855-855-1961, extension 1540, option 7. For
information on network providers in a particular geographic location, you should contact Seven
Corners at 800-544-1802 or visit their website at www.peacecorps.sevencorners.com.
To extend AfterCorps insurance coverage, you should contact the plan administrator, AfterCorps.
Their phone numbers are 800-544-1802 in the U.S. or 317-582-2609 outside the U.S. You may use
Seven Corners website to see a copy of the AfterCorps policy or to check personal coverage (go to
www.peacecorps.gov.sevencorners.com and click the AfterCorps button).
For information or assistance with a medical emergency or a non-service-related health problem, returned
Volunteers enrolled in AfterCorps should contact AfterCorps directly. In the U.S. they should call 800544-1802. Outside the U.S., they may call 317-582-2609.
Federal Employees Compensation Act Benefits (FECA)
FECA pays for medical treatment for health conditions related to your overseas service.
FECA benefits are administered by the Office of Workers Compensation Program at the U.S.
Department of Labor (DOL). The Post-Service Unit in OHS can assist you in filing claims for
benefits.
FECA benefits are not guaranteed. The DOL must determine that your health condition is
service-related before a claim for benefits is accepted.
DOL claims processing usually takes from six to twelve weeks. This process can be expedited if
you contact the Post-Service Unit as soon as you believe you have a service-related condition
requiring treatment and if you respond quickly to requests for information from the Post-Service
Unit or DOL.
Claims must be made within 3 years of COS or within 3 years of recognition of a service-related
health condition.
Health problems resulting from injuries or illnesses that develop in the U.S. while you are on
vacation, home leave, emergency leave or on medevac but not directly engaged in Peace Corps
activity are not eligible for FECA benefits (see AfterCorps insurance below).
The Post-Service Unit in OHS can provide information on FECA claims processing. You can get
additional information at www.peacecorps.gov/resources/returned/healthben/feca/
May 2015
TG 330 ATTACHMENT A
AfterCorps Insurance
Peace Corps pays only for the first months premium on your AfterCorps insurance. Before you leave
service, you will be given an insurance card and an application that allows you to purchase up to 2
(two) months additional coverage for yourself and for your qualified dependents.
Peace Corps strongly encourages you to sign-up for extended AfterCorps coverage before you leave
country. If this policy lapses, for even one month, you will not be eligible to rejoin the plan. You
may alternatively transition immediately into private insurance through the Affordable Care Act
(www.healthcare.gov) or your parents insurance plan (if eligible).
May 2015
TG 330 ATTACHMENT A
For questions regarding 127C authorizations, FECA benefits or other service-related health issues,
contact the Post-Service Unit in OHS at psu@peacecorps.gov. In the U.S. call 1-855-855-1961,
extension 1540, option 7 (toll free). Outside the U.S. call 202-692-1540, option 7.
For questions regarding the use of the Seven Corners Health Benefits identification card. Contact
the Peace Corps Health Benefits Program at 800-544-1802. For information on Network providers
in a particular geographic location, see www.peacecorps.sevencorners.com. Numbers are also
listed on the Health Benefits identification card and the Instructions for Use information sheet.
To extend AfterCorps insurance coverage, contact the plan administrator, Seven Corners. Their
phone numbers are 800-544-1802 in the U.S. or 317-582-2609 outside the U.S. You may use
Seven Corners website to see a copy of the AfterCorps policy or to check personal coverage. (Go
to www.peacecorps.sevencorners.com and click the AfterCorps button.)
For information or assistance with a medical emergency or a non-service-related health problem,
returned Volunteers enrolled in AfterCorps should contact AfterCorps Assistance at 800-544-1802
or 317-582-2609.
May 2015
TG 330 ATTACHMENT B
Health Information (please initial each statement and sign and date below)
I have received and reviewed Attachment A Post-Service Health Information for Returning Volunteers. I understand my postservice health benefits.
I have been given PC-127C forms for medical/dental evaluations after return to the US. I understand that it is my responsibility
to have these evaluations performed within six (6) months of my close-of-service date.
I have received a Health Benefits Program identification card to be used with the PC-127C forms.
I have been shown the Post-Service/FECA video and/or have received information on Post-Service Health Benefits Program
available at the following internet address: www.peacecorps.gov/resources/returned/healthben/feca/
_____
_____
If serving in a malaria endemic area: I have received and reviewed Attachment G Instructions for Volunteers: COS
Guidelines for Preventing Malaria. I have been instructed in, and understand, the necessity of continuing my malaria
prophylaxis after leaving malaria endemic areas:
Chloroquine, Doxycycline or Mefloquine: fourteen days after leaving malaria endemic areas
_____
If serving in a schistosomiasis endemic area: I have received and reviewed Attachment J Praziquantel Medication
Information Sheet. I have received and taken anti-schistosomal medication within 72 hours of my departure from country.
I have been given my yellow WHO International Health Card, and it is up to date.
I have not had a significant change in my health since my close-of-service health evaluation. (If change has occurred, please
check ____ and comment on the reverse of this form.)
Signature
________
May 2015
Date
PC-1790 (COS/EXT)
Peace Corps
Close-of-Service or
Extension-of-Service
Medical Evaluation
Sex M
Country of Service
Telephone No.
Home/permanent address
To be completed by volunteer
Section One
I. Health History
A. Instructions to Volunteer
Please answer each question by indicating if you have experienced any of the following during Peace Corps
service by checking No, Yes (Resolved), or Yes (Current). Comment in the space provided.
Symptoms or problems during Peace Corps service
Weight gain or loss of more than 10 pounds
Frequent or severe headaches
Fainting spells or blackouts
Vision problems, eye injuries or disorders
Hearing problems
Persistent cough
Chest pain or chest pressure
Shortness of breath or wheezing
Repeated episodes of indigestion, heartburn, or stomach pain
Frequent diarrhea
Frequent constipation
Frequent or painful urination
Blood in your urine
Repeated episodes of back or neck pain
Muscle, bone, or joint injuries
Painful or swollen joints
Breast lump or mass, or nipple discharge
Skin problems (e.g. eczema, dermatitis)
Change in color or size of a mole or other growth
A sore which does not heal
Frequent sadness or feelings of depression
Frequent or severe nervousness or anxiousness
Frequent sleeplessness or insomnia
Use of cigarettes or other tobacco products
(Females) Gynecologic symptoms or disorders
No
Yes
(Resolved)
Yes
(Current)
Volunteer Comments
SSN
Section Two
Pulse
Hearing
Gross Vision
Uncorrected
Right 20/___
Left 20/____
feet/inches
lbs.
mmHg
(resting)
bpm (resting)
Corrected
Right 20/___
Left 20/____
(whisper test
of other
gross test)
Page 2 of 4
SSN
C. Clinical Examination
To be completed by PCMO or examining physician
Normal
Abnormal
D. Laboratory Findings (PCMO: For any test not performed/ordered document rationale in Section F on page 4)
Urinalysis
Hematocrit OR Hemoglobi
G6PD Status
Tuberculin Test (5 IU PPD)
(check one)
n
If terminal prophylaxis with
Date read
mm of induration
Albumin
primaquine is indicated.
Sugar
Normal Deficient
If deficient, do not dispense
primaquine.
Blood
Other
Grams
Schistosomiasis
serology
PAP smear
cytology results
Chlamydia/GC
HIV serology
(check one)
If intestinal parasites are
endemic
(check one)
Indicated if PCV is leaving
or has traveled to an
endemic area
(check one)
(check one)
(check one)
Specimens to
_____________________
On Date:______________
127C issued
209B issued
Results attached
Specimens to CDC
On Date:______________
Specimens to
_____________________
On Date:______________
Specimens to
_____________________
On Date:______________
Specimens to
_____________________
On Date:______________
127C issued
209B issued
Results attached
127C issued
209B issued
Results attached
127C issued
209B issued
Results attached
127C issued
209B issued
Results attached
Page 3 of 4
SSN
Pos
Pos
1. Date ________________________
Pos
2. Date ________________________
3. Date ________________________
Neg
Neg
Neg
127C issued
209B issued
*Important*
PCMO/Physician Signature
(Must be signed or co-signed by a licensed M.D. or
D.O. if exam performed by PA or NP)
State
Medically cleared by PCMO for extension of service or transfer. No significant undiagnosed, unresolved,
or potentially recurrent health conditions.
Medically cleared or provisionally medically cleared by OMS for extension of service or transfer.
Consultation by PCMO with OMS is required for undiagnosed, unresolved, or potentially recurrent health
conditions.
Not medically cleared for extension of service or transfer due to significant unresolved or potentially
recurrent health conditions. Consultation by PCMO with OMS is required.
Page 4 of 4
TG 330 Attachment D
Peace Corps
Report of
Dental Evaluation
PC-1790 (Dental)
Sex M F
/
PEACE CORPS USE ONLY
Check one:
Country of service
Home/permanent address
Telephone No.
OR
Comment on findings:
OR
Comment on findings:
Page 1 of 4
Applicant SSN:
Lingual
Lingual
Buccal
Lingual
Buccal
Calculus Deposits:
Light
Moderate
Heavy
None
Areas of suppuration
None
Furcation involvement
None
None
C. Periodontal Classification:
No Disease
Class I: Gingivitis
Class II: Early Periodontitis
Class III: Moderate Periodontitis
Class IV: Advanced Periodontitis
Page 2 of 4
Applicant SSN:
V. Bruxism
No history of bruxism
History of bruxism
Please describe any bruxism habit, presence of wear facets or need for occlusal guard:
VI. Prosthesis
No prosthesis present
Prosthesis present
Please describe the nature and extent of the prosthesis (e.g. full or partial dentures, bridge, etc.)
and the need for repair or replacement:
VII. Treatment
List all treatment completed after this examination. Do not include treatment planned but not yet completed.
Treatment
Date
Signature
Page 3 of 4
Applicant SSN:
* Important *
Dental examination is
complete only when:
2
3
Dentists signature
Date
Dentists License number
State
Applicants only:
The dentist has included one of the
following sets of x-rays:
1) A full mouth series, or
2) A Panorex with bitewing x-rays.
Periapical or Panorex films must be
less than two years old.
Bitewing x-rays must be less than
one year old.
All films must be original films,
not duplicates.
Close-of-service only:
The dentist has included bitewing x-rays.
Date
Dental Clearance
Date
Date
Specify restrictions:
Page 4 of 4
PC-OMS-127C
(PCMO: SeeTG340)
For Additional services, dial 855-855-1961, option 1, and ask for
the extension listed below:
OMS PCMO
Pre-Service: Ext. 1500
In-Service trainees and Volunteers: medevac,
home leave, medical hold: Ext. 1500
Post-Service (after COS or ET): Ext: 1540
Expires 6 months after date of COS or ET
Name:
Last
First
Social Security #
Country of Service
MI
Specialty:
Problems/Symptoms/HX:
Services Authorized:
Authorized by:
Date:
(dd-mon-yy)
Signature:
The Peace Corps uses a health benefits program fee schedule. The Peace
Corps does not pay fees in excess of this schedule. In using this
authorization, the provider and patient agree to accept the health benefits
program fee schedule as full payment for services. Providers may not bill
patients for any balance in excess of the fee schedule.
Date
TG 330 ATTACHMENT F
Volunteer Name:
(PCMO signature)
Date of Issue:
Volunteer SSN:
Country:
COS/ET Date:
Hematocrit or Hemoglobin
Chlamydia Testing
G6PD Status
TB Test/5 IU PPD
Mammogram
Shistosomiasis Serology
FEES FOR SERVICES: Peace Corps guarantees payment in accordance with its Health Benefits Program Fee
Schedule. Billing of Peace Corps Volunteers for any outstanding balance is not permitted under this plan. If
you have a question about the Health Benefits Program Fee Schedule please call1-800-544-1802.
CLAIMS PAYMENT INSTRUCTIONS:
The following items must be enclosed with your
claim:
1) This authorization form
2) A completed PC-1790 and lab results
3) An itemized bill. Please use UB-92,
HCFA-1500 or SF-1080.
NOTE TO VOLUNTEER: You may pay for authorized services out-of-pocket and request reimbursement
from Peace Corps. To receive reimbursement you must mail the following items to the address shown above:
White - Provider Copy
TG 330 ATTACHMENT F
(1) this authorization form; (2) a completed PC-1790; (3) bills for lab fees and test results; and (4) proof of
payment (i.e., a canceled check or receipt).
PRIVACY ACT NOTICE: The information requested is collected under authority of the Peace Corps Act for the purpose of documenting the basis
for requested payments. Disclosure of this information is voluntary. However, failure to disclose the information will make it impossible for Peace
Corps to pay for these services. This information will be maintained under the provisions of the Privacy Act for the routine uses described in the
Federal Register of August 27, 1984 (relating to Peace Corps Volunteer medical records).
TG 330 ATTACHMENT G
DOSE
FREQUENCY
DURATION
Mefloquine
Weekly
4 weeks
Chloroquine
Weekly
4 weeks
Doxycycline
Daily
4 weeks
Malarone
(1) tablet
Daily
1 week
If you plan to travel in a malaria endemic area following COS, you must take with you enough
anti-malarial medication for the duration of your travels and for post-departure prophylaxis.
December 2013
Page 1
TG 330 ATTACHMENT G
POST-DEPARTURE
PROPHYLAXIS
Mefloquine
Chloroquine
Doxycycline
Malarone
Before service you were tested for G6PD, an enzyme necessary to metabolize primaquine. If
your G6PD level is normal or adequate, your PCMO will give you primaquine and you may
commence terminal prophylaxis as outlined above. If your G6PD level is low or absent, you
should not take primaquine. You should contact your health care provider when you arrive
home. Individuals with low or absent G6PD levels should only take primaquine if
recommended, and supervised, by a medical professional.
Adverse effects of primaquine in individuals with normal levels of G6PD are infrequent.
However, if your urine becomes very dark or red while taking primaquine, stop taking the drug
and consult a physician. You may also contact the Peace Corps Office of Health Services at 1855-855-1961, extension 1540, option 7 for advice. Primaquine should not be taken during
pregnancy.
December 2013
Page 2
TG 330 ATTACHMENT H
I,
having a blood specimen drawn at completion of service for human immunodeficiency virus
(HIV) antibody testing. I fully understand that this may jeopardize my benefits under the
Federal Employees Compensation Act and AfterCorps insurance should I later be found to
be infected with HIV.
(Volunteer Signature)
(Date)
Volunteer ID Number)
(Country of Service)
March 2014
TG 330 ATTACHMENT I
I,
having a Close of Service (COS) health evaluation. I fully understand that refusal of this
evaluation may adversely affect my eligibility for or coverage by post-service benefits,
including those under the Federal Employees Compensation Act, AfterCorps, and Peace
Corps-authorized post-service evaluations of service-related conditions.
(Volunteer Signature)
(Date)
-
(Volunteer SSN)
(Country of Service)
TG 330 ATTACHMENT J
Praziquantel (Biltricide)
(Schistosomiasis Medication)
Medication Information Sheet
What is praziquantel?
Praziquantel is a medication used to treat schistosomiasis (and infection with a type of worm
that lives in the bloodstream). It is a class of medication called anthelmintic which works by
killing the worms. Praziquantel is used for both treatment of individual patients and in mass
community treatment programs.
What is schistosomiasis?
Schistosomiasis, also known as bilharzias, is a disease caused by parasitic worms from the
Schistosoma genus. Schistosoma. mansoni, S. haematobium, S. japonicum, S. mekongi, and S.
intercalatum cause illness in humans. Different clinical complications are associated with the
various species. The clinical features also differ in acute and chronic infections.
Why should I take praziquantel?
You have been living in a Schistosoma endemic area. Any freshwater (lakes, rivers, streams,
even rainwater overflow) must be considered contaminated. It is almost impossible not to come
into contact with presumptively contaminated water during service. Long term kidney and bowel
complications can be severe in untreated infections. In order to avoid these complications,
Peace Corps policy is to treat all Volunteers who have lived in endemic areas as they COS.
How do I take the tablets?
The dose of praziquantel is based on weight and will be individualized for each Volunteer, then
divided in two. The two doses are taken in one day four to six hours apart. Take the tablets and
portion of tablets by water with a meal. Do not crush, chew or hold the tablets in your mouth. Do
not eat grapefruit or drink grapefruit juice while taking praziquantel.
Are there any side effects (adverse reactions)?
Adverse effects of praziquantel are generally mild, but occur in approximately one third of
people. Side effects include dizziness, malaise, headache, vomiting, abdominal pain diarrhea
and itching. These symptoms may be partly related to the drug itself and may be partly related
to host immune responses to dying worms. Call the PCMO (or your doctor) if they become
severe or do not go away, or if you develop hives.
Praziquantel may make you drowsy. Do not drive a car or operate machinery on the day you
take praziquantel and the day after you take it.
What special precautions should be followed?
Before taking praziquantel,
Tell your PCMO if you are allergic to praziquantel or any other medications
Page 1
December 2013
TG 330 ATTACHMENT J
Page 2
December 2013
TG 330 ATTACHMENT K
Primaquine Phosphate
(Anti-Malarial Medication)
Medication Information Sheet
What is primaquine phosphate?
I t is one of sev eral types of drugs used to prevent and treat malaria.
Primaquine phosphate is the specific drug used to eliminate P. ovale and P. vivax
parasites from your liv er. These species may reside harmlessly in your liv er for
months or years w ithout causing any symptoms, but they can cause malaria
months or years later (called relapsing malaria). Special treatment called
Presumptive Anti-Relapse Therapy (PART), formerly known as terminal
prophylaxis, is required to eliminate these parasites from your system. While the
malaria infection these species cause is not as serious as malaria caused by P.
falciparum, it can be v ery uncomfortable.
How do I take the tablets?
You hav e been giv en 28 tablets (15 mg) by your prov ider
Take tw o (2) tablets by mouth daily for 14 days
I t may be taken w ith food if stomach upset occurs, but not w ith antacids
For best results, take each dose at the same time ev ery day. This w ill
ensure a constant lev el of medication in your blood
Take this medication for the full time prescribed. Stopping therapy too
soon may result in a re-infection
Store at room temperature aw ay from sunlight and moisture
Do not share medications w ith others
PART
POST-DEPARTURE PROPHYLAXIS
Mefloquine
Chloroquine
Doxycycline
Malarone
12/2013
You may hav e an upset stomach, stomach cramps, nausea, v omiting, loss
of appetite, or muscle w eakness, especially during the first several days as
you body adjusts to the medication. I f any of these symptoms persists or
become sev ere, inform your health provider.
Notify your health prov ider if you dev elop a rash, rapid heart rate,
changes in v ision, hearing trouble, ringing in the ears, or dark urine w hile
taking this medication.
I f your G6PD lev el is low or absent, you should NOT take primaquine.
I f your G6PD is low or absent, consult w ith your health care provider when
you arriv e home.
I ndividuals with low or absent G6PD levels should only take primaquine if
recommended, and supervised, by a medical professional
I f you hav e arthritis, psoriasis, lupus, liver disease or allergies to primaquine
I f you are pregnant or breast-feeding. Discuss the risks and benefits with
your Peace Corps health prov ider while in country or your health care
prov ider at home. The CDC recommends postponing primaquine until
after deliv ery or breast feeding (unless the infant has been tested for
G6PD deficiency).
I f you miss one or more doses for any reason, take ONE dose as soon as
possible and then continue on your usual dosing schedule. DO NOT
double-up the dose to catch up unless instructed to by a health care
prov ider.
12/2013
TG 330 ATTACHMENT L
Time Limit:
Peace Corps pays one month's premium for all Volunteers. Volunteers may purchase up to 2 months of
additional coverage for themselves, their spouse, and all qualified dependents (younger than 18 years
old) while transitioning into private insurance (Affordable Care Act - www.healthcare.gov or parents plan).
How Accessed:
Contact AfterCorps Customer Service for:
1. Emergency medical assistance
2. Referrals to Multiplan hospitals, physicians, and other health services
3. Insurance coverage extensions
To extend or confirm coverage, preauthorize emergency and non-emergency medical treatment, inquire
about the status of your medical claim or find a US network provider call 800-690-6295 or 317-818-2809
(collect calls accepted).
Additional information can be found at:
http://www.peacecorps.gov/resources/returned/benefits/healthben/aftercorps/
PC-127c Authorization
Benefit Covers:
Authorizes payment for evaluation of medical and dental health conditions related to Volunteer service
Time Limit:
Must be issued and used within six months after service.
How Accessed:
May be issued by Peace Corps Medical Officers (PCMO) or the Peace Corps Office of Health Services
(OHS) Post-Service Unit
Call 855-855-1961, ext. 1540, option 7 or e-mail psu@peacecorps.gov
Additional information can be found at:
http://www.peacecorps.gov/resources/returned/benefits/healthben/medical/
FECA
Benefit Covers:
Treatment for most medical and dental conditions related to Volunteer service and conditions incurred or
contracted while overseas during service
Time Limit:
Claims must be filed within three years after service, or within three years of recognition that a health
condition is service-related.
How Accessed:
Claims should be filed through the OHS Post-Service Unit. Call 855-855-1961, ext. 1540, option 7 or
202-692-1540, option 7, or e-mail psu@peacecorps.gov
Additional information can be found at:
http://www.peacecorps.gov/resources/returned/benefits/healthben/feca/
February 2014
Peace Corps
Technical Guideline 340
1. PURPOSE
To provide instructions on the use of the Health Benefits Program identification card
(ATTACHMENT B).
2. BACKGROUND
Form PC-127C (127C) authorizes payment of medical and dental services. The 127C is
designed for use in the U.S. For information on the use of the 127C outside of the U.S., see
Section 5 below.
Peace Corps utilizes a Health Benefits Program fee schedule. Peace Corps does not pay fees
in excess of this schedule and providers who accept the 127C have agreed to accept the Peace
Corps Health Benefits fee schedule as full payment for services. Providers may not bill
Volunteers for any fees in excess of the fee schedule. Volunteers are not expected to pay copayments charged by providers. The Health Benefits identification card is designed to
facilitate access to care and payment for services.
A 127C authorization should be used in conjunction with a Peace Corps Health Benefits
identification card (see section 6 below).
A 127C must be signed by both the Peace Corps medical staff member authorizing
service and the Volunteer seeking care. The staff member signature authorizes payment
of services and the Volunteer signature authorizes the release of medical and dental
reports to the Office of Medical Services (OMS) for the services associated with the
127C.
The 127C form has three parts. The original (health record copy) is placed in the
Volunteers health record under In-Service or Close of Service (COS)/Post-Service
care depending on when it was issued. The first copy (provider copy) is given to the
provider by the Volunteer and the second copy (patient copy) is for the Volunteer's
personal records. The Peace Corps Medical Officer (PCMO) should ensure that all three
copies are legible prior to issue.
A 127C may be issued by a PCMO, Area Peace Corps Medical Officer (APCMO), or
OMS staff.
September 2008
Page 1
TG 340
PC-127C Form
A separate 127C authorization should be issued for each provider. A single authorization,
however, may request that one provider evaluate several conditions.
If a Volunteer has multiple conditions that require specialist evaluation, care should be
coordinated through a primary care physician (family practitioner or internist).
The 127C should be issued for an initial evaluation, to include diagnosis and management
recommendations, of the conditions. A 127C form may be used during service and at
COS (see sections 3.1 and 3.2 below).
During Service
At Close of
Service
After COS
Issued by PCMO
Issued by OMS
* For use of the PC-127C outside the U.S.; see section 5 below.
3.1
During Service
3.2
PCMO will contact the Field Support Unit in OMS when Trainees and Volunteers
require evaluation and/or treatment for medical or dental conditions while they are
traveling to the U.S. 1 on home leave, emergency leave, or vacation. PCMOs in the
Africa Region should coordinate medical and dental care with APCMO before
contacting the Field Support Unit.
At Close of Service
1 For information on the use of the 127C outside the U.S.; see section 5 below.
September 2008
Page 2
TG 340
PC-127C Form
127Cs issued at COS should be issued for physicians, clinical psychologists, and
dentists only, i.e., Department of Labor (DOL) criteria of an authorized provider. A
127C may be issued at COS for other types of licensed healthcare providers;
however, if the medical problem results in a Federal Employees Compensation Act
(FECA) claim the evaluation will not be accepted by DOL and the Volunteer will
be required to obtain additional evaluation.
The Volunteer must have a 127C authorization prior to receiving medical or dental
evaluation or treatment.
The Volunteer should use the 127C authorization with his/her Health Benefits Program
identification card.
For questions regarding the use of the Health Benefits identification card, Volunteers
should contact the Peace Corps Health Benefits Program at 1-800-544-1802. For
information on network providers in a particular geographic location, Volunteers should
contact Health Systems International (HSI) at 800-726-0766. Numbers are listed on the
Health Benefits identification card and the Instructions for Use information sheet.
September 2008
Page 3
TG 340
PC-127C Form
4.1
4.2
During Service
The International Health Coordinator(IHC) in the Field Support Unit will issue
127C for Volunteers requiring a medical or dental evaluation/treatment while they
are in the U.S.
The Volunteer is responsible for obtaining medical reports from his/her providers
and communicating medical information to the IHC. The Volunteer will also bring
a copy of the reports to post for inclusion in his/her health record.
The Volunteer must contact OMS if a new health problem develops or a previous
health problem becomes unstable while he/she is in the U.S. Evaluation and
treatment of illnesses or injuries that develop while a Volunteer is in the U.S. are
authorized and managed by OMS.
If the nature of the illness prevents the Volunteer from returning to country as
scheduled, OMS may place the Volunteer on medical hold status (see TG 370
Field Consultation section 13.3 Medical Hold) pending the outcome of the
evaluation and treatment.
At Close of Service
Emphasize to the Volunteer that a 127C covers evaluation only, not treatment.
A 127C must be used within six months of the Volunteers COS date. It will not be
honored after that time has elapsed.
After COS, a Volunteer with questions or problems with his/her 127C authorization
should contact the Post-Service Unit in OMS.
Advise the Volunteer to retain a copy of the 127C for his/her records.
Obtaining routine health care outside the U.S. using a 127C is not encouraged. When
necessary, a 127C may be issued to a Volunteer for use outside of the U.S.
The Volunteer should be informed that providers in countries other than the U.S. may not
accept the 127C form. In these cases, the Volunteer will be required to pay for services at
the time of the visit and seek reimbursement from the Peace Corps Health Benefits
Program in a timely manner. The procedures for reimbursement are clearly outlined on
the 127C form.
September 2008
Page 4
TG 340
PC-127C Form
During service and after COS, all 127Cs issued by post and used outside the U.S. should
be submitted to the Peace Corps Health Benefits Program for reimbursement (see section
7 below).
The Volunteer should be informed that he/she is responsible for obtaining all medical
reports for care received outside the U.S. During service, these reports should be brought
to post to be included in the Volunteers health record. For services received after COS, a
copy of all reports should be retained by the Volunteer as this information may be needed
to facilitate payment by the Health Benefits Program or to document eligibility for postservice health benefits.
Provide the Volunteer or Returned Peace Corps Volunteer (RPCV) with access to
a network of medical providers in the U.S. willing to accept the 127C and/or the
PC-209B Authorization for Medical Examination and Labs form (see TG 330
Post-Service Health Benefits and Close of Service or Extension of Service
Health Evaluations section 4.5, for information on the use of the 209B form).
Facilitate proper and timely payment of medical bills associated with medical and
dental services authorized on the 127C and 209B.
The Health Benefits identification card should be presented along with the 127C or 209B
whenever the Volunteer or RPCV seeks to access medical care in the U.S. Use of the
Health Benefits identification card in this manner will:
Ensure that the provider agrees to accept the Peace Corps Health Benefits
Program fee schedule as full payment for services;
Protect the Volunteer from having to pay for care at the time of service;
Protect the Volunteer from being billed directly by the provider for full or partial
payment of services, or for fees in excess of the fee schedule.
The Health Benefits identification card must only be used with a 127C or 209B
authorization. Use of the health benefit card without a 127C or 209B does not authorize
payment of medical services. Volunteers or RPCVs who obtain medical services in the
U.S. without a 127C or 209B authorization may not be reimbursed by Peace Corps.
Because Volunteers and RPCVs should present the Health Benefits identification card
whenever medical services are sought using a 127C or 209B, Volunteers must have the
card in their possession whenever they travel to the U.S., regardless of the reason, e.g.,
vacation, home leave, emergency leave, medevac, etc., and at COS.
September 2008
Page 5
TG 340
PC-127C Form
At post, the PCMO is responsible for issuing the Health Benefits identification card and
ensuring that Volunteers understand its use.
The PCMO, and the post administrative staff, are responsible for ensuring that Volunteers
have their cards whenever a 127C or 209B is issued and when travel to the U.S. is
planned. Therefore, posts should treat the card like other important travel documents and
store the card with the Volunteers passport or in the Volunteers health record. In certain
circumstances, post may require Volunteers to be responsible for their own cards.
Volunteers and RPCVs may use a provider of their choice; however, in light of the
benefits outlined above, the OMS Health Benefits Program strongly encourages
Volunteers to use providers who are members of the network. For information on
network providers in a particular geographic location in the U.S., Volunteers should
contact HSI at 800-726-0766 or on the web at www.peacecorps.sevencorners.com.
The Health Benefits card is valid during Peace Corps service and up to the expiration
date on an accompanying 127C or 209B authorization.
The Health Benefits identification card is separate and distinct from the CorpsCare PostService health insurance program and the CorpsCare insurance card.
Peace Corps utilizes a Health Benefits Program fee schedule that is consistent with
recognized fee schedules used by health care insurers in the U.S. Providers who accept
the 127C form agree to accept the Peace Corps Health Benefits Program fee schedule as
full payment for services (see information highlighted in red on the 127C form). Peace
Corps does not pay charges in excess of this schedule.
The standard method of payment of medical or dental care authorized by a 127C is for
the provider to accept the 127C, with the Health Benefits identification card, and to
submit a claim directly to the Peace Corps Health Benefit Program.
In the event that a Volunteer cannot locate a provider who will accept the 127C form, the
Volunteer may pay for the medical care at the time of service and submit a claim for
reimbursement to the Peace Corps Health Benefits Program. In most cases, the Volunteer
will be reimbursed according to the Peace Corps Health Benefits Program fee schedule.
All 127C authorizations should be submitted to the Peace Corps Health Benefits Program
for payment or reimbursement. This includes 127Cs issued by post or by OMS, 127Cs
issued for use in the U.S. or overseas, and 127Cs issued for use during service or after
COS.
Prior to receiving care, the Volunteer should read and understand the information on the
127C, including the specific services authorized and bill payment information.
September 2008
Page 6
TG 340
PC-127C Form
8. AUTHORIZING SERVICES
The specific services authorized must be clearly described in the section Services
Authorized on the 127C. Common examples include the following:
During Service
Evaluation by a Specialist
Dermatologist
Problems/Sx/Hx:
Services Authorized:
At COS
Problems/Sx/Hx:
Services Authorized:
Evaluation by a Specialist
Dermatologist
Problems/Sx/Hx:
Services Authorized:
September 2008
Page 7
TG 340
PC-127C Form
Problems/Sx/Hx:
Services Authorized:
Evaluation by a Dentist
Dentist
Problems/Sx/Hx:
Services Authorized:
September 2008
Page 8
TG 340
PC-127C Form
Service Level
Mark an X in the appropriate box. For Volunteers going to the U.S. on vacation, home
leave, or emergency leave, mark In-Service.
Provider
Print name of provider if known.
Specialty
Designate Primary Care Physician, Dentist or type of specialist.
September 2008
Page 9
PC-OMS-127C
(PCMO: SeeTG340)
For Additional services, dial 800-424-8580 and ask for the
extension listed below:
OMS PCMO
Pre-Service: Ext. 1500
*PCSTART127C*
Name:
Last
First
Social Security #
Country of Service
MI
Specialty:
Problems/Symptoms/HX:
Services Authorized:
Authorized by:
Date:
(dd-mon-yy)
*PCEND127C*
Signature:
The Peace Corps uses a health benefits program fee schedule. The Peace
Corps does not pay fees in excess of this schedule. In using this
authorization, the provider and patient agree to accept the health benefits
program fee schedule as full payment for services. Providers may not bill
patients for any balance in excess of the fee schedule.
Date
Date:
MEMBER:
PEACE CORPS ID#
DATE ISSUED
http://peacecorps.sevencorners.com
Provide you access to a network of medical/dental providers in the United States willing to accept a PC-127C Authorization
for Payment of Medical/Dental Services and/or a PC-209B Authorization for Volunteer Medical Evaluation and Labs form.
Facilitate proper and timely payment of medical bills associated with the medical services authorized on your PC-127C form
and/or your PC-209B form.
The Health Benefits identification card must only be used with a PC-127C or a PC-209B authorization. Volunteers or RPCVs
who obtain medical services in the US without a PC-127C or PC-209B may not be reimbursed by Peace Corps.
The card is valid during your Peace Corps service and up to the expiration date on your accompanying PC-127C or PC-209B
authorization form.
Present the Health Benefits identification card anytime you seek medical services using a PC-127C or PC-209B authorization
form.
Have the card on your person when traveling to the United States for any reason, e.g.,vacation, home leave, emergency leave,
medevac, and at Close of Service (COS)
You may use a provider of choice, however, in light of the benefits outlined above, the Peace Corps Health Benefits Program
strongly encourages you to use providers who are members of the network to avoid out of pocket expenses.
For information on Medical or Dental network providers in a particular geographic location in the U.S., you should contact
Equian at 1(800)726-0766 or on the website http://peacecorps.sevencorners.com.
The Health Benefits identification card is separate and distinct from the AfterCorps medical insurance program and the AfterCorps insurance card that is provided to you at COS.
Rev PC (04/14)
Rev PC (04/14)
Peace Corps
Technical Guideline 355
1. PURPOSE
To provide guidance on breast imaging and the evaluation of breast masses.
2. BACKGROUND
A mammogram is an x-ray picture of the breast. Screening mammograms are used to check
for breast cancer in women who have no signs or symptoms of the disease. Diagnostic
mammograms are used to check for breast cancer after a lump or other sign or symptom of
the disease has been found. A sonogram, also called an ultrasound, is a computerized picture
taken using sound waves.
3. SCREENING GUIDELINES
Several organizations have published recommendations for screening mammograms. Peace
Corps follow the recommendations of the U.S. Preventive Services Task Force (USPSTF) as
they are the US government agency charged with creating such guidelines. These guidelines
can be found at:
http://www.uspreventiveservicestaskforce.org/uspstf09/breastcancer/brcanrs.htm
A summary of the 2009 USPSTF recommendations for screening mammography are as
follows:
Women aged 50 to 74 should receive screening mammography for breast cancer
every two years.
The decision to start regular, biennial screening mammography before the age of 50
years should be an individual one and take patient context into account, including the
patient's values regarding specific benefits and harms.
There is insufficient evidence to assess the benefits and harms of screening
mammography in women 75 years or older.
Routine annual mammograms are not recommended by the USPSTF, but the decision to
perform mammography is individual and should take patient context into account, including
the patient's values regarding specific benefits and harms.
Screening mammograms performed in-country may be sent to OHS for review by a U.S.
radiologist according to the procedures outlined in section 9 below. Any mammogram
reported through the Breast Imaging-Reporting and Data System (BI-RADS) as BI-RADS
Category 3, must be sent to OHS for a second read by a US radiologist.
A field consultation must always be obtained for the evaluation of an abnormal breast
finding, e.g., breast mass, nipple discharge, and skin changes. ATTACHMENT A is a
standard Mammogram Field Consult form. The PCMO, together with OHS/RMO, is
June 2013
Page 1
TG 355
Mammography
responsible for the evaluation, monitoring, and follow-up of women with any abnormal
breast findings.
4. DIAGNOSTIC MAMMOGRAPHY
Mammography is of limited usefulness in women under age 40 due to higher breast tissue
density. Ultrasound is preferred to evaluate breast lesions in younger women. Mammography
should only be performed in a woman younger than 40 if indicated by her particular
circumstances.
A diagnostic mammogram, in a woman older than 40 years, is indicated in women with the
following conditions:
Signs or symptoms of breast disease including, but not limited to, mass, induration, axillary
lymphadenopathy, some types of nipple discharge, skin changes, or persistent focal areas of pain
or tenderness.
Asymptomatic women who have breast implants or who have a history of treatment for breast
cancer may have a screening mammogram, instead of diagnostic mammogram, at the discretion
of the mammography facility 1.
Diagnostic mammograms performed in-country may be sent to OHS for review by a U.S.
radiologist according to the procedures outlined in section 9 below. All mammograms reported
as BI-RADS 3 must be sent to OHS for a second read by a US radiologist.
A negative diagnostic mammogram does not rule out malignancy in the presence of a palpable
mass or other breast abnormality. The purpose of mammography in this setting is to further
define the mass and to rule out the presence of an unexpected nonpalpable breast cancer in the
ipsilateral or contralateral breast. PCMOs should ensure that a Volunteer with a palpable breast
mass understands the purpose of mammography.
5. MAMMOGRAPHY ACCOMMODATION
As of August 2012, screening mammography is required for women age 50 and over
prior to entering Peace Corps service.
All female applicants who will be 50 years or older during their service are offered an
accommodation to a country where screening mammography is available. They may
choose to waive this accommodation, however, if certain risk factors are present, the
applicant will be assigned to a country with access to mammography.
If an applicant has waived the mammogram accommodation, Peace Corps will not
medevac her for screening mammography or issue a PC-127C for screening
mammography in the US or another country. However, if a PCV who had waived the
American College of Radiology. ACR Practice Guideline for the Performance of Screening
and Diagnostic Mammography. 2008.
http://www.acr.org/~/media/ACR/Documents/PGTS/guidelines/Screening_Mammography.pdf
Office of Health Services
June 2013
Page 2
TG 355
Mammography
All applicants are asked to obtain, and bring to country, copies of their most recent
mammogram(s). If, for any reason, a Volunteer arrives in country without her films, the
Peace Corps Medical Officers (PCMOs) should work with the Volunteer to obtain the
films and have them sent to post.
June 2013
Page 3
TG 355
Mammography
7. SPECIAL CONSIDERATIONS
Female Volunteers should be accompanied by the PCMO or by a female attendant for
screening or diagnostic mammograms performed in-country.
Women should be scheduled for screening mammography when they are not
experiencing cyclic breast tenderness or conditions that increase breast
tenderness.
8.
All mammogram films should be returned to the Volunteer at COS. The PCMO
should document in the Health Record that the films have been returned (see
Technical Guideline (TG) 330 Post-Service Benefits section 4.6).
MAMMOGRAPHY REPORTS
Mammography reports should include a brief statement about the reason for the
examination, a description of the breast composition, a description of significant
findings, and a statement regarding comparison with prior examinations. These reports
should be signed and dated by the consulting radiologist and translated into English if
necessary. The American College of Radiology promotes the use of a standardized
reporting system, the Breast Imaging-Reporting and Data System (BI-RADS). Peace
Corps requires that all mammograms are reported using the BI-RADS system. It
includes one of the following overall assessments and recommendations:
June 2013
Page 4
TG 355
Mammography
BI-RADS
Category
Assessment
Recommendations
Negative
Benign Finding
Suspicious Finding
Highly Suggestive of
Malignancy
June 2013
Page 5
TG 355
Mammography
OHS will:
Ensure that the films are read by a U.S.-based radiologist;
Fax stateside results and, if indicated, a field consult report to country within one week of
receipt of the field consult and mammograms if previous films are readily available.
Single lesion
Hard
Immovable
Irregular borders
If the initial physical examination does not confirm the presence of a dominant mass,
thickening or asymmetry, close observation with a follow-up examination in two to three
months should be arranged to assure resolution or stability of findings. Alternatively, the
patient can be referred to a breast specialist, depending on the confidence and expertise of the
examiner.
If the initial physical exam indicates that further evaluation is indicated, then arrangements
should be made for breast imaging and OHS should be notified of the breast mass through a
field consult.
June 2013
Page 6
TG 355
Mammography
10.3 Imaging
A mammogram should be the first diagnostic test ordered in a woman over the age of 30 with
a new breast complaint. Even if the patient had a recent negative screening mammogram, if
she has a focal complaint, a diagnostic mammogram should be obtained. Mammography is
not routinely ordered in women under age 30 years. Ultrasound is the first line of imaging in
a woman who is pregnant or less than 30 years old with focal breast symptoms or findings.
However, it is not inappropriate to order a mammogram as part of a diagnostic evaluation of
a clinically suspicious mass in younger women.
Certain mammographic features such as asymmetry, clustered pleomorphic calcification,
increasing density, or a new mass with irregular borders or spiculation are suggestive of
malignancy. However, mammography cannot determine whether a mass is benign.
A negative mammogram does not eliminate the need for further evaluation of a suspicious
mass. Mammography misses 10 to 20 percent of clinically palpable breast cancers. Thus, a
negative mammogram should not stop further investigation if a suspicious mass is felt on
clinical examination. Targeted ultrasonography is a useful diagnostic test to evaluate a
palpable mass or an area of abnormality detected on mammogram. It is particularly useful for
assessing whether a mass is solid or cystic in nature.
Breast magnetic resonance imaging (MRI) is not indicated for the work-up of an
undiagnosed mass. MRI is best reserved for diagnostic dilemmas and used with discretion as
there is a significant false positive rate, which dramatically increases the rate of benign
biopsies. Diagnostic breast MRIs should only be performed in institutions that have capacity
for MRI directed biopsy, as lesions seen on MRI may not be visible on other imaging
modalities.
The findings of breast imaging will dictate the next steps in the evaluation of the breast mass.
OHS should be made aware of any imaging reports that indicate a finding of BI-RADS
category 3, 4 or 5.
REFERENCES
American College of Radiology. ACR Practice Guideline for the Performance of Screening and
Diagnostic Mammography. 2008.
http://www.uspreventiveservicestaskforce.org/uspstf09/breastcancer/brcanrs.htm
http://www.uptodate.com/contents/breast-masses-and-other-common-breastproblems?source=search_result&search=breast+mass&selectedTitle=1%7E41#H19
June 2013
Page 7
Most major health organizations recommend that women over the age of 40 receive regular,
comprehensive screening for breast cancer, including mammography every one to two years.
The Peace Corps strongly supports these recommendations and is able to provide screening
mammography in some but not all of its overseas posts. The Peace Corps would like to
facilitate access to screening mammography by recommending an overseas assignment for
you in a country where you can receive a routine screening mammogram. After discussing
the matter with your phys ician, please choose one of the two options outlined below under
Instructions to Peace Corps Applicant.
I have discussed with the above-named person the consensus medical opinion that
regular, comprehensive screening for breast cancer, including screening mammography
every one to two years, is medically indicated for her age group and I concur with the
Peace Corps Office of Volunteer Support willingness to recommend that she serve in a
country where she can receive a routine screening mammogram for breast cancer.
I have reviewed and assisted in the completion of the Mammogram Health Assessment
Questionnaire with the above-named person.
I have discussed with the above-named person the fact that foregoing a routine screening
mammogram for more than two years may subject her to risk of delayed diagnosis of
breast cancer, which could cause major adverse health consequences, including death.
______________________
(Physician Printed Name)
_______________________
(Physician Signed Name)
_____________
(Date)
After discussing these matters with my doctor, I have decided that I wish to ensure that I
receive a routine screening mammogram during my 27 months of Volunteer service.
(You do not need to fill out the Mammogram Health Assessment Questionnaire)
After discussing these matters with my doctor, I have decided that I do not wish to
ensure that I receive a routine screening mammogram during my 27 months of Volunteer
service. You must complete the attached Mammogram Health Assessment Questionnaire.
Based on that information and/or your mammogram report, you may be given a
mammogram accommodation and will be considered for placement in a country where
this resource is available.
________________________
(Applicant Printed Name)
________________________
(Applicant Signed Name)
____________
(Date)
No
N/A
N/A
No
N/A
No
N/A
OPTIONAL
#_______
Yes
#_______
Yes
TG 355 ATTACHMENT B
DOB:
COS DATE:
[
[
[
[
[
]
]
]
]
]
YES
YES
YES
YES
YES
[
[
[
[
[
]
]
]
]
]
NO
NO
NO
NO
NO
[
[
[
[
[
]
]
]
]
]
YES
YES
YES
YES
YES
[
[
[
[
[
]
]
]
]
]
NO
NO
NO
NO
NO
CLINICAL EXAM:
LMP: ...........................................................................................................
On oral contraceptives or hormone replacement therapy ....................
Palpable lump or mass ...............................................................................
Breast tenderness or pain .........................................................................
Nipple discharge.........................................................................................
Lymph nodes ..............................................................................................
If YES to any of the above, please describe below. For palpable abnormalities, include specific location,
i.e., breast (left or right), quadrant (upper outer, upper inner, lower outer, lower inner). A graphic
representation of the breast may be used.
RIGHT
PREVIOUS MAMMOGRAMS
Available in country ..........................................................................
[ ] YES
LEFT
[ ] NO
If yes, send previous mammograms and report to VS with the current mammogram study.
If no, please initiate the process of having Volunteer's previous mammogram films sent from her HOR to VS
as soon as possible (see TG 355 section 6).
TG 355 ATTACHMENT C
Patient's name:
DOB:
Country of service:
LOCATION WHERE PREVIOUS MAMMOGRAMS MAY BE OBTAINED:
Clinic name:
Address:
Telephone number:
Fax number:
I,
Office of Volunteer Support. Please send original films and reports to:
Peace Corps
Office of Volunteer Support
1111 20th Street, N.W.
Washington D.C. 20526
Attn:
International Health Coordinator
(202) 692-1500
Privacy Act Statement: I understand that all information in my record will be released, including
dates, history of illness, and diagnostic and therapeutic information related to my condition.
Patient Signature:
Date
Witness:
Date
Peace Corps
Technical Guide line 3 60
1 . PURPOSE
To prov ide P eace Corps Medical Officers (P CMOs) with guidance on :
2 . B ACKGROUND
The Office of Health Services (OHS) arranges and pays for laboratory serv ices for all P eace
Corps p osts at the laboratories referenced below (see section 3).
P CMOs may use local laboratory services when in-cou ntry facilities are adequate. The
P CMO together wit h the Regional Medical Officers (RMOs) are responsible for mak ing th is
determinat ion. Costs for in-country laboratory services are paid from the country bu dget.
SERVICES
General purpos e laboratory
s ervic es (see Quest
Direc tory of Servic es )
HIV testing
February 2013
ADDRESS
Quest Diagnostics Nichols Institute
14225 Newbrook Drive PO Box 10841
Chantilly, VA 20153-0841
P ag e 1
TG 3 60
U.S . Labo ra to ries
LABORATORY
Centers for Dis ease Control
and Prevention (CDC)
(c ontinued)
SER VIC ES
Malaria slide ex amination
Mefloquine blood levels
DASH-Parasitology
CDC MS G-12
1600 Clifton Road
Atlanta, GA 30333
Hepatitis E antibody
ADDRESS
4 .1 Specimen Preservation
February 2013
P ag e 2
TG 3 60
U.S . Labo ra to ries
specimens requiring refrigerat ion, they should send t hem directly to the lab oratory
via an express mail system, i.e., DHL or other. Specimens sent t hro ugh an express
mail system may be subject to delay at the U.S. port of entry f or custo ms clearance.
P CMOs should consult t he Quest Directory of Services for specific informat ion on
specimen preparation and preservat ion of indiv id ual tests (see section 5. 1 below).
4 .2 Specimen Pack aging
By federal regulat ion, diagnostic specimens and bio logic products sh ip ped within the
U.S. must be packaged to withstand leakage of contents, sh ocks,pressure changes, and
ot her cond it ions incident to ordinary hand ling in transportation (42 Code of federal
Regulat ions (CFR) P art 72).
P CMOs should package specimens of b lood or other potentially infectious material
being ship ped to the U.S. in the following way:
Requisition slip: P lace the requisition slip in a zip lock plastic bag. This protects the
requisition slip from leakage or contaminat io n.
Secondary co ntainer: P lace the primary container and the requisition slip inside
the zip lock bag in a second watertight container with absorbent material. A
Styrofoam packing container, malaria kit container, or ot her container placed in a
leak proof (ziplock) bag is sufficient.
For addit io nal information, see also Technical Guideline (TG) 2 60 sect io n 5.2
S pecimen P ackaging and TG 2 60 Attachment A P ackaging Specimens.
4 .3 Specimen Labe ling
Specimen Labels: P osts may create preprinted labels to be added to the chart
of incoming trainees. If labels are not availab le specimens and slides should be
labeled as follows:
Date o f Birth
Please note that use of adhesive labels is not acceptable for use on specimens that
are placed on slides. Information must be written in pencil on the frosted glass
portion of the slide.
February 2013
P ag e 3
TG 3 60
U.S . Labo ra to ries
4 .4
Specimen Biohaza rd Labels: Specimens and ot her infectious material being sh ipped
to the U.S. must be appropriately labeled as a bio hazard.
Eit her the primary or t he secondary container describe d abo ve must have a
warning label that includes the universal biohazard symbol followed, by t he
term biohazard. A red bag or red container ma y be subst it uted f or a label.
P lastic specimen bags with the red biohazard symbol may also be used and
can be procured through OSD. See TG 260.5 f or add it ional information on
specimen handling and labeling.
The P CMO may label both the primary and secondary containers but is not
requ ired to do so.
Specimen Shipment
P rior to shipment, secondary container(s) must be placed inside one or two cardb oard
boxes as follows:
Double Box: Specimens sent b y diplo mat ic pouch or hand carried to the US mail
room for forwarding to U.S. laboratories must be do ub le boxed.The outer b ox
should be addressed to:
P eace Corps Mail Roo m
1111 20the Street, N.W.
Washingt on, D.C. 20526
Attention: Lab Specimens
Each inner bo x must be accurately addressed to its final dest inat ion, e.g., Quest
Diagnostics ; CDC, etc. (see addresses in section 3 above). Each inner package must
contain specimens samples dest ined f or one and only one U.S. laboratory.
S ingle Bo x: Double boxing is not required if t he package is sent d irect ly from post
to a U.S. lab. A single cardboard box addressed directly to the reference lab (see
addresses in section 3 above) is sufficient.
Rigid mailing sleeves, if properly reinforced for o verseas shipment , may be used
instead of boxes for shipment of specimens.
February 2013
P ag e 4
TG 3 60
U.S . Labo ra to ries
Shipping Supplies
Q u e s t mailers / Sty rofo am
Plastic zip lo ck bags
Cardboard bo xes
A bso rben t p ap er
Forms
Clien t Supp ly Order Re quest Fo rm
Cy to logy / His tology Request Fo rm
These supp lies are provided only upon request from post to PLS. P CMOs shou ld order
Quest supplies through PLS using the Quest Supp ly Order Request For m or
by email request. Request forms can be obtained from PLS. Supp ly req uests sh ou ld not
b e sent directly to Quest.
February 2013
P ag e 5
TG 3 60
U.S . Labo ra to ries
Hepatitis E antibody
Send specimens to the Centers for Disease Control and P revent io n. See section 3 above for
addresses.
February 2013
P ag e 6
TG 3 60
U.S . Labo ra to ries
In-service indeterminate or posit ive HIV results are received by the P CMO and reported
by the P CMO to OHS
COS lab reports are received, evaluated and filed in t he medical record by t he P CMO
prior to packaging of t he health record for shipment to P eace Corps headquarters
All medical records are required to be received at P eace Corps headquarters with in 30
days after COS
Any abn ormal COS test resu lts that are received after the Volunteer has closed serv ice
must be reported to t he P ost Service Un it (P SU) mailbox v ia secure file transfer (SFT) :
psu@peacecorps.gov
February 2013
P ag e 7
TG 360 ATTACHMENT A
Page 1
TG 360 ATTACHMENT A
Page 2
TG 360 ATTACHMENT B
Lab Number:
Date
Age
1.______________________________________________________________________________________________
2.______________________________________________________________________________________________
3.______________________________________________________________________________________________
4.______________________________________________________________________________________________
5.______________________________________________________________________________________________
6.______________________________________________________________________________________________
7.______________________________________________________________________________________________
8.______________________________________________________________________________________________
9.______________________________________________________________________________________________
10._____________________________________________________________________________________________
Signature of Submitter:_________________________________________Date:______________________
If a separate billing address is desired, please note.
Opened by:____________ Processed by:____________ Computer Entry:____________ Verified by:____________ Reviewed by:____________
Peace Corps
Technical Guideline 370
1. PURPOSE
To provide guidance on the use of field consultation in the Volunteer Health System.
To outline the methods of communication between the Office of Medical Services (OMS)
and Peace Corps Medical Officers (PCMOs).
2. BACKGROUND
Clinical care overseas relies on the following resources:
Medical evacuation when an illness or injury requires evaluation and/or treatment beyond
the scope of care available locally.
A field consult is a clinical inquiry by overseas medical personnel to OMS. OMS in turn
utilizes all necessary medical resources and specialists in the U.S. to inform and respond to
the inquiry. Field consultation is used when a medical condition: (1) involves the potential
for significant complications; (2) requires resources or expertise that exceeds the PCMO's
training, skills and qualifications; or (3) approaches the limits of diagnostic and/or
therapeutic care available in country. The field consultation process is an integral component
of the Volunteer Health System, and PCMOs should use the process when indicated.
August 2008
Page 1
TG 370
Field Consultation
Routine
(Non-Urgent)
OMS Fax
(202-692-1501)
Urgent
These numbers are up to date as of the publication of this TG. Posts should ensure that their
contact information is accurate and up to date.
4.2
General Indications
Volunteer requests a second opinion and post does not have a qualified provider.
Local resources cannot provide safe, efficient, and timely care that conforms to U.S.
standards and norms.
To establish the technical merits or reliability of local resources including, but not
limited to radiology, laboratory, medical and dental facilities and personnel.
Volunteer has a new onset or poor control of a major or chronic medical condition,
e.g., diabetes, asthma, hypertension, angina.
August 2008
Page 2
TG 370
Field Consultation
When a condition may lead to significant cosmetic deformity, e.g., large facial
lacerations, facial leishmaniasis.
5.2
5.3
Copy of relevant diagnostic test reports, e.g., x-rays, laboratory studies, ECGs, etc.;
Radiographic studies and photographs if post has the ability to transmit digitally.
OMS Response
The IHC, in consultation with the Chief of Clinical Programs, reviews all field consults.
Following review, field consults are answered directly by medical professionals in
OMS or are referred to outside specialists in the Washington, DC area.
August 2008
Page 3
TG 370
Field Consultation
Urgent field consults for an acute medical problem or an urgent medevac consideration
are handled as an emergency, and a response is sent to post as quickly as possible.
Non-urgent field consults are answered within two business days. If outside specialist
consultation is required by OMS, a response will be sent to country within two days of
OMS receipt of the specialists opinion.
All consults are sent to post immediately via cable, fax or telephone. If PCMOs do not
receive a response from OMS within a reasonable time frame, they should follow-up
with their IHC directly.
6. METHODS OF COMMUNICATION
Field consults and other communication with OMS may be by fax, cable, or telephone. The
method of communication should be determined by the urgency of the medical problem, the
time of day, the day of the week, the confidentiality of the material being communicated, and
the reliability of communication services at post.
The health unit should maintain a log or tracking system for outgoing cables and faxes.
Health unit staff should be able to verify from their logs that a communication was
transmitted and the date of transmission.
6.1
Non-Urgent Communication
Fax Transmissions
Faxes should indicate clearance by the originator and any clearing officials.
All faxes that identify an individual Volunteer and contain medical information
should be designated as Medical Eyes Only. A cover sheet indicating that the
information on the following pages is Medically Confidential should be used as a
safeguard when sending medically confidential information.
August 2008
Page 4
TG 370
Field Consultation
PCMOs should contact OMS if the health unit does not have a Medical Eyes Only
fax and there are concerns about the security of medically confidential information.
Telephone
The PCMO may obtain a medical consultation via telephone, i.e., a telcon.
PCMOs calling from overseas during business hours should use the main OMS
switchboard number (202-692-1500). The PCMO should identify him or herself as
a PCMO and indicate that he or she is calling from overseas. The administrative
assistant who answers the telephone will ensure that the call is transferred to the
appropriate OMS staff.
All confidential information should be sent using Secure File Transfer Protocol
(SFTP). Contact OMS if there are any questions regarding use of SFTP.
Cable Transmissions
6.2
Cables are only used when fax or e-mail communication is not practical. Section 7
Cable Preparation below outlines the preparation of a cable. Routine cables take
12-24 hours to reach Washington.
Urgent Communication
Telephone: During business hours (7:30 a.m. to 5 p.m. eastern time Monday
through Friday).
For urgent concerns during business hours the PCMO should contact field support
directly through the main OMS switchboard (202-692-1500). When calling the
OMS switchboard, PCMOs should identify themselves, state the urgency of the
call, and state with whom they would like to speak. The administrative assistant
who answers the phone will ensure that the call gets to the requested OMS staff.
August 2008
Page 5
TG 370
Field Consultation
the PCMO does not receive a response within 20 minutes of the call, he or she
should contact the service again.
If Communication is Impossible.
Under extraordinary circumstances immediate communication with OMS may be
impossible. In these circumstances, PCMOs should use their clinical judgment and
all available resources to provide necessary care to an ill or injured Volunteer. In
these situations, the PCMO should contact OMS as soon as possible after
communication has been restored.
Medical Eyes Only is reserved for medically confidential cables. Copies of this type of
cable are distributed to OMS staff and overseas Peace Corps medical staff only. The term
Med Channel is not used by Peace Corps.
Cable Preparation
Follow directions in the Peace Corps Cable Preparation Guide (1992) available from the
Office of Information Resources Management (M/IRM/CTIS). A summary of the parts of
a cable is provided in ATTACHMENT A.
Use Optional Forms 152(H) and 152a(H), continuation sheets, or the cable template
distributed by M/IRM/CTIS. The spacing between lines is critical as cables are optically
scanned for transmission. If the scanner can not find the information it is looking for, e.g.,
embassy city, on the correct line, the cable will be rejected.
August 2008
Page 6
TG 370
Field Consultation
The following symbols may not be used in cables: *, #, $, &, +, % as the optical scanner
will not read them.
REFERENCES
Manual Section 832 Cables and Facsimile Transmissions.
Technical Guideline 150 Medical Confidentiality.
Peace Corps Cable Preparation Guide (available from M/IRM/CTIS).
August 2008
Page 7
TG 370 ATTACHMENT A
PARTS OF A CABLE
The following description of the basic parts of a cable may be used when preparing a cable. Medical
Officers should contact the Office of Information Resources Management (M/IRM/CTIS) in Washington
or the local U.S. Embassy for post-specific procedures.
1.
2.
3.
Originator Identification
The originating (sending) facility is identified as follows:
FM AMEMBASSY LOME
Thus, this cable originated from the U.S. Embassy in Lome, Togo.
4.
Action Addressee(s)
The action addressee is the cable address of the person or office whom the writer of the cable
intends to take appropriate action on the contents of the cable. For example:
TO SEC STATE WASHDC
indicates that the cable address of the person for whom the cable is intended is the State Department
in Washington, which will forward the cable to Peace Corps (see 7, below).
5.
Precedence Designation
Cable precedence governs the order in which cables are transmitted through the system and the
actions required for delivery at the receiving post. The following precedence is used by Peace
Corps:
Routine;
TG 370 ATTACHMENT A
6.
NIACT Immediate (or Night Action Immediate): the cable will be delivered to the addressee
without regard to the time of day or night.
Information Addressee(s)
An info addressee is the cable address of a person or office whom the writer wants to have
knowledge of the contents of the cable. It is the equivalent of a carbon copy of a memorandum.
For example:
TO SECSTATE WASH, IMMEDIATE
INFO AMEMBASSY BANJUL
This designation indicates a cable to Washington with an information copy to the American Embassy
in Banjul, Gambia.
7.
8.
9.
To
This is the specific person and/or office to which the cable is intended. Therefore,
TO: DGOOTNICK, VS/MS
indicates that the cable is intended for D. Gootnick, Director of Medical Services.
10. From
This is the specific person and/or office sending the cable. Thus,
FROM: DR. H. GLUCKSBERG, APCMO/LOME
indicates that the cable was sent by Dr. H. Glucksberg, the APCMO, in Lome, Togo.
N/A
Page 2
TG 370 ATTACHMENT A
12. Tags
Tags are designations used by State Department for the filing and distribution of cables. Peace
Corps does not use this system. Therefore,
TAGS:
N/A
13. Subject
The topic of the cable. Therefore, a specific PCV would be referenced as follows:
SUBJ:
SSN 123-45-6789
14. References
References are previous cable correspondence on the same subject. For example,
REF:
LOME 0980
indicates Cable No. 0980 from Lome contains information on the same subject.
16. Signature
All official cables bear the name of the Chief of the originating facility, e.g., the Ambassador, the
Charg, the Secretary of State, etc. In the example case,
BRAY
refers to Ambassador Bray. This does not mean these cables must be approved by the individual.
17. Classification
All Peace Corps cables are unclassified and are designated as such.
18. YY
YY indicates to the optical scanner that it has reached the end of the message.
Page 3
Peace Corps
Technical Guideline 380
MEDICAL EVACUATION
1. PURPOSE
To provide Peace Corps Medical Officers (PCMOs) with the framework for developing a
comprehensive Medical Evacuation Plan that is specific to the needs and circumstances
of each post.
2. BACKGROUND
Medevac is any transfer of a Volunteer across an international border in order to reach a
higher level of care. In general, medevac is indicated when an illness or injury requires
evaluation and treatment beyond the scope of care available in-country through: (1) the Peace
Corps health unit, (2) field consultation, and (3) approved in-country consultants and
resources. In general, conditions requiring medical evacuation are of an urgent nature, and
evaluation and treatment cannot be delayed until after the Volunteer closes service.
The majority of medevacs are to the U.S. In certain circumstances, however, medevacs are to
a regional evacuation site or other non-U.S. location.
See Technical Guideline (TG) 385 Emergency Medical Evacuation for guidance on
medevac of an acute or life-threatening illness or injury that requires emergency air rescue by
a chartered aircraft to ensure timely delivery of care.
Pregnancy counseling;
Psychiatric conditions that require evaluation and treatment beyond the management
capabilities of post;
April 2013
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TG 380
Medical Evacuation
4.2
April 2013
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TG 380
Medical Evacuation
5.1
1. Medevac Procedures
Medevac checklist for the PCMO, CD and Director of Management Operations (DMO)
(see ATTACHMENT B)
TG 380 Medical Evacuation;
Peace Corps Manual Section (MS) on Medical Evacuation;
2. Emergency Contacts
OMS, including after-hours duty officer contact information;
Peace Corps staff, e.g. CD, DMO, Regional Medical Officer (RMO);
U.S. Embassy staff to include Duty Officer, Administrative Officer;
Local and regional ambulance services;
Local and regional hospitals;
Local and regional emergency providers, e.g., cardiologist and general surgeon;
Local and regional laboratories, e.g., emergency blood typing, HIV testing;
Local and regional emergency radiology facilities, e.g., ultrasound, CT scan;
Maps to important medical locations.
3. Volunteer Contact Information
Volunteer Emergency Locator Forms (see ATTACHMENT A);
Volunteer telephone numbers and addresses;
Maps to Volunteer sites.
4. Communication Systems
Sample medevac field consult;
Sample medevac estimated time of arrival (ETA) fax or cable;
Instructions for use of in country communications services, e.g., government, NGO,
missionary, and police radio networks;
Instructions for use of cell phones, pagers, beepers, and hand-held radios.
5. Transportation Systems
Procedures for emergency use of the Peace Corps vehicle;
Local ambulance services;
Airline schedules;
Government and military services for helicopter and charter aircraft;
Train and bus schedules;
Taxi services;
Contact information for airport security, customs officials, and immigration officials.
(continued)
April 2013
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TG 380
Medical Evacuation
5.2
Sources of Information
Useful sources for developing or updating a Medical Evacuation P lan may include:
April 2013
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TG 380
Medical Evacuation
5.3
Country Director
Administrative Officer (DMO)
Peace Corps staff
Volunteers
Local medical societies
Local fire department
Office of Medical Services
U.S. Embassy
Other foreign embassies and consulates
Non-Government Organizations (NGOs)
International business organizations
Medical universities and teaching hospitals
Red Cross
5.4
6. MEDEVAC DECISIONS
The decision to medevac a Volunteer to the U.S. is made by OMS, in consultation with the
PCMO and Regional Medical Officer. The decision to medevac a Volunteer to a regional
medical evacuation site is made by OMS, or the RMO in consultation with the PCMO.
PCMOs should inform OMS of all RMO medevac decisions.
April 2013
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TG 380
Medical Evacuation
This section describes standard procedures for the initiation, coordination and administration
of a medical evacuation.
6.1
Consultation
Medevac consultation is the dialogue between OMS and the PCMO in a setting
where medical evacuation is under consideration.
Consultation may occur by cable, fax, or telephone and should include the
following information:
6.2
Volunteer's name, date of birth (DOB), social security number (SSN), and
Close of Service (COS) date;
Transportation requirements;
Accompaniment requirements;
Special considerations.
Volunteers being medically evacuated often have medical problems other than the
condition necessitating the medevac. If these conditions require evaluation and
treatment beyond the scope of care available through the Peace Corps health unit,
the PCMOs should include this information in the medevac consultation
communication.
Concurrence
Upon concurrence, the PCMO, RMO and OMS will determine the following:
April 2013
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TG 380
Medical Evacuation
6.3
Authorization
In the rare event where OMS or the RMO cannot be contacted in a timely fashion,
the PCMO may unilaterally authorize an urgent medevac. The PCMO should
promptly notify the CD in this situation.
M EDEVAC DECISIONS : SUM M ARY
Medevac Destination
OMS or RMO
Consultation
OMS or RMO
Concurrence
OMS Authorization
U.S.
Required
Required
Required
Regional Evacuation
Site and Other NonU.S. Sites
Required
Required
Not Required
7. MEDEVAC COMMUNICATIONS
Effective communication is essential for the timely management of a medevac. During the
medevac process, the PCMO will need to communicate with the Volunteer, Peace Corps staff,
local providers, local communication and transportation services, and OMS.
7.1
7.2
April 2013
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TG 380
Medical Evacuation
Post is required to establish 24/7 access to the PCMO or a qualified medical provider
in order to ensure 24-hour emergency medical assistance for Volunteers. The
emergency contact system varies by country and availability of services. PCMOs may
carry cell phones, pagers, hand-held radios, or other devices that allow immediate
contact. Where communications services are severely limited, some counties may
provide Volunteers with cell phones or other communication devices.
7.3
7.4
7.5
Family/Parental Notification
Consistent with the Privacy Act and principles of medical confidentiality, OMS will
not, in general, notify family members or discuss the medevac with family members
unless permission from the Volunteer has been obtained.
The PCMO should determine the Volunteer's wishes regarding notification of
immediate family members. If the Volunteer wishes to notify his or her family
members, this should be done in country prior to the Volunteers departure.
Additionally, the IHC or the Medevac Coordinator at the regional site will discuss
family notification during the Volunteers medevac orientation at the medevac site.
The Volunteer may request that specific aspects of his/her current circumstances be
communicated or specifically withheld from family members. In general, the
information given to family members will be limited to pertinent facts associated with
the Volunteer's present condition.
The determination to notify family members in a serious or life-threatening situation,
where a Volunteer is incapable of providing consent, is made by OMS. Notification is
made to the individuals whom the Volunteer designated in writing for notification in
case of emergency (see TG 150 Confidentiality). PCMOs should consult OMS in
this situation.
7.6
April 2013
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TG 380
Medical Evacuation
The PCMO should send a final notification fax or cable to OMS or the medevac
coordinator at the regional destination when evacuation plans, transportation
arrangements, and other medevac logistics are final. This communication should
include the following:
The PCMO may use local airline, train, bus, and taxi transportation systems to
transport an ill or injured Volunteer.
Local ambulance service is available in many Peace Corps countries and may be used
for transporting an ill or injured Volunteer. The PCMO should consider the following
when using local ambulance services:
Hours of operation;
Method of contact;
April 2013
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TG 380
Medical Evacuation
Local government, military, and charter aircraft services are available in some Peace
Corps countries and may be used to transport an ill or injured Volunteer. Often these
organizations have various aircraft, e.g., helicopters that can be used to transport
Volunteers from remote sites.
The PCMO should be aware of security, customs and immigration procedures prior to
an urgent medical event. Airport security officials, customs officials, and immigration
officials are integral components of the evacuation process and post is encouraged to
develop relationships with these individuals.
8.2
Emergency equipment and medications (stretcher, back board, stiff cervical collar,
head stabilization equipment);
April 2013
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TG 380
Medical Evacuation
8.3
8.4
9. MEDEVAC ACCOMPANIMENT
The policies for medical, non-medical and spouse accompaniment are outlined in MS
264.4.2.6 Accompaniment and MS 264.4.2.7 Accompaniment by V/T spouses,
Dependents, and Parents of Dependents. Medical judgments concerning the need for
accompaniment and the type of accompaniment required are determined by the PCMO in
consultation with OMS.
April 2013
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TG 380
Medical Evacuation
9.1
9.2
Type of Accompaniment
There are three categories of Peace Corps-authorized medevac accompaniment:
1. Medical Accompaniment
The PCMO, in consultation with OMS, determines that the medical condition of the
Volunteer requires accompaniment by a medically qualified individual. In these cases
the PCMO determines the most appropriate individual to accompany the Volunteer.
The PCMO should promptly notify the CD of these determinations so that post can
consider staffing and program needs. The most common medically qualified
accompaniments are the PCMO, a medical assistant, or a Peace Corps medical
consultant.
Medevacs that have been sexually assaulted or injured may require a same sex
accompaniment. Medevacs with a presumed or confirmed mental illness associated
with potential suicide may require same sex or a two-person accompaniment.
2. Non-Medical Accompaniment
The PCMO, in consultation with OMS, determines: (1) that the medical condition of
the Volunteer requires monitoring or support during travel; and (2) that monitoring
may be by a non-medically trained person. In these cases the PCMO, in consultation
with the CD, determines who will accompany the Volunteer. The accompaniment may
be a spouse, a staff member, or another Volunteer.
In extraordinary circumstances, a Volunteer may provide non-medical accompaniment
to another Volunteer. In general, this is only appropriate when the basis for nonmedical accompaniment is the need for physical or logistical assistance. As with other
April 2013
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TG 380
Medical Evacuation
Medical
PCMO
(in consultation with OMS )
PCMO
(with CD notification)
Non-Medical
PCMO
(in consultation with OMS)
PCMO
(in consultation with CD)
PCMO
PCMO
Spouse
(medically indicated)
Unauthorized Accompaniment:
In certain situations a medically evacuated Volunteer may be traveling with a friend,
significant other, or spouse who has not been designated or authorized as a medevac
accompaniment under one of the four authorities described above. In these situations,
the individual traveling with the medically evacuated Volunteer is not on official
travel and is responsible for all expenses and arrangements associated with his/her
travel, e.g., lodging.
9.3
April 2013
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TG 380
Medical Evacuation
Transport of the Volunteer's health record. The health record must be hand-carried,
safeguarded and delivered to OMS staff.
9.4
Monitor vital signs, patient signs and symptoms, adverse reactions to medications
or other therapies.
Pain management.
Provide an oral report to the IHC on the first business day after arrival.
Authorizing recuperation and other benefits consistent with Agency policies and
the Foreign Affairs Manual (FAM), i.e., authorizing per diem, miscellaneous and
incidental expenses (M&IE), lodging, etc.
Determining the length the stay for accompaniments at the medevac destination.
If the accompaniment is a family member, post should determine the length of stay in
consultation with OMS. In general, family member accompaniments who are
Volunteers are expected to return to country when the patients health status is no
longer serious and the CD determines that programmatic needs outweigh the
emotional needs of the patient.
April 2013
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TG 380
Medical Evacuation
The PCMO is primarily responsible for ensuring that all necessary and appropriate medical
care is provided in a timely and efficient manner. The DMO is responsible for providing the
necessary administrative support to accomplish these tasks.
DMOs should reference the Overseas Financial Management Handbook (OFMH), Trainee
and Volunteer Medevac and Emergency Leave for detailed information on DMO
responsibilities in the medical evacuation process. In the FY 99 edition, this information is
found on pages 233-36.
DMO
April 2013
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TG 380
Medical Evacuation
10.3
10.4
Medications
All Volunteers being medically evacuated must carry their personal passport,
visas, World Health Organization (WHO) vaccination card, and Health Benefits
identification card to the medevac destination. Local identification cards and other
forms of identification should also be carried if they are considered important
immigration documents in the host country or may be needed while on medevac.
These documents should be up to date prior to departure, and should be stored in a
location that permits both the PCMO and DMO to gain access to them in an urgent
situation.
If a passport is lost or stolen, the DMO should contact the Consular Officer at the
American Embassy and local immigration officials to assist Peace Corps with
obtaining a new passport and visa. Post should maintain a centrally located
photocopy of all passports, visas, WHO cards, and identification cards for use if
originals are lost or not available.
April 2013
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TG 380
Medical Evacuation
During Peace Corps service, Peace Corps will pay for all necessary medical care for a
Volunteer who develops an illness or becomes injured while on medevac. When
medically indicated, Volunteers may remain on medevac status for a maximum of 45
days. Peace Corps will not medically separate a Volunteer who has an urgent need for
medical or psychiatric care, or an unstable medical condition (see TG 160 Medical
Separation section 3.1).
After Peace Corps service, Federal Employees Compensation Act (FECA) will cover
service-related health problems that developed while a Volunteer was on medevac.
The contracted health insurance will cover non-service related health problems that
developed while a Volunteer was on medevac. Therefore:
10.5
Volunteers do not need short-term health insurance while in the U.S. during
service.
Volunteer Briefing
The PCMO and the DMO should review the entire medevac process with the
Volunteer. If the Volunteer is coming to Washington, DC, the Volunteer should be
given a copy of the Peace Corps Medevac Guide to Washington D.C., and encouraged
to read the booklet prior to arrival in Washington. The booklet is available, and can be
ordered, through the Overseas Support Division in Administrative Services
(M/AS/OSD). Prior to departure, the PCMO should ensure the Volunteer understands
the following:
10.6
Transportation logistics;
10.7
Medevac Travel
The DMO arranges all logistics associated with transportation and travel of the
Volunteer being medically evacuated and the accompaniment. This includes:
April 2013
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TG 380
Medical Evacuation
Issues TAs to include all necessary travel and per diem expenses for the medevac
and the accompaniment (see section 9.4 above).
Medevacs to the U.S. are issued a one-way ticket. Medevacs to a regional medevac
site may be issued either a round trip or a one-way ticket depending on the preference
of post and the regional site. Accompaniments to the U.S. or a regional medevac site
are generally issued a round trip ticket unless they have prior approval from the CD for
altering their itinerary.
Volunteers and accompaniments should be advised to: (1) retain a copy of their TA;
and (2) save receipts for all transportation lodging, tax, and other expenses. The TA
and receipts should be submitted to the Medevac Assistant in Washington, DC or
Honolulu, or to the DMO at the regional medevac site. Volunteers should contact these
same individuals if additional cash or a return travel advance is needed.
10.8
10.9
Administrative Forms
The DMO should issue all medevacs to the U.S. copies of the following completed
forms:
Power of Attorney;
If the Volunteer intends to resign or will be separated from service, the following form
should also be completed:
Form PC-1485: Report of Peace Corps Service (MS 284, Early Termination
paragraph 8, 12.2 and Attachment B).
April 2013
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TG 380
Medical Evacuation
Give keys to a Peace Corps staff member or an individual that Peace Corps can
readily contact.
Pay all debts including rent and advance salaries to domestic help.
Make a list of personal belongings and separate out those items to ship home
should a Peace Corps separation occur.
If a medevac results in medical separation, the Volunteer is entitled to 100 lb. (45.5
kg) of unaccompanied baggage shipped to his/her home of record (HOR). This 100 lb.
limit includes the weight of packaging materials. The DMO should instruct the
Volunteer to make a list of personal effects, preferably prior to evacuation, clearly
identifying the items he/she wishes shipped from the remainder of his/her belongings.
The list is maintained by the DMO. Volunteers are responsible for all costs of shipping
beyond the 100 lb. limit and must arrange for payment prior to shipping. Peace Corps
is not responsible for lost or stolen items. Volunteers are encouraged to purchase a
personal property insurance policy.
11. FUNDING
Funding for international medical travel and accompaniment (U.S., regional, and other nonU.S medical travel) is allocated to post budgets from the Office of Volunteer Support Centrally Managed Accounts at the beginning of each fiscal year. These funds may not be
reprogrammed for any other purpose. Additional funds for international medical travel, if
required, should be requested from the Office of Volunteer Support by the Region or the
Budget Implementation Team (BIT). Unused funds are returned to the agency. See the
Overseas Financial Management Handbook for more detailed information.
An OMS authorization number, or fiscal coding, is required for medical evacuations to the
U.S., and for any chartered or emergency air rescue authorized by OMS.
An OMS authorization number, or fiscal coding, is not required for regional medevacs or
other non-US medevacs.
Post is responsible for in-country travel expenses including those expenses for Volunteers
who are later transported outside the country.
Thorough medical management of the condition for which the Volunteer was evacuated.
April 2013
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TG 380
Medical Evacuation
Logistical and emotional support from OMS or the staff at the regional medevac
destination.
Evaluation and treatment of health conditions unrelated to the reasons for medical evacuation
will be evaluated by OMS, or the regional site, on a case-by-case basis. In general, PCMOs
should continue to evaluate and treat routine and on-going medical conditions in country.
12.1
Medevac Orientation
All medevacs to Washington meet with the regional IHC and the Medevac
Program Specialist on the first business day after their arrival. The medical
evaluation process, appointment schedule, and relevant policies and procedures are
reviewed during this orientation. At this meeting, PC-127C Authorization of
Payment of Medical/Dental Services authorizations, which include a release of
medical information by consultants are also issued. Copies of the health record and
other case-related material are collected by the IHC from the Volunteer or the
accompaniment at this time. Copies of the health record are held and maintained
by the regional IHC throughout the medevac.
April 2013
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TG 380
Medical Evacuation
12.2
Arrival logistics;
Medevac orientation;
Monitoring care;
April 2013
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TG 380
Medical Evacuation
Medical Clearance
13.2
Volunteers who have been medically cleared are expected to return to post
promptly. Generally, travel to post is initiated within 24 hours after medical
clearance unless the CD has authorized annual leave or absence from post.
Medical Separation
Volunteers medically separated in the U.S. complete the COS process in the U.S.
in accordance with TG 330 Post-Service Health Benefits and Close of Service or
Extension of Service Health Evaluations. Volunteers medically separated from
post or a regional medevac site must complete the COS process in the field as per
TG 330.
April 2013
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TG 380
Medical Evacuation
13.3
Volunteers who have been medically separated have the right to appeal. Appeals
should be made in writing to the Director of Medical Services.
Medical Hold
PCMOs are encouraged to authorize medically necessary examinations and treatment
for Volunteers who are traveling to the U.S. on vacation, home leave or other
approved leave. A 127C authorization form is used for this purpose (see TG 340 PC127C Form Authorization for Payment of Medical/Dental Services section 3 Use
of the 127C During Service).
Prior to departure, the PCMO should inform Volunteers that they must contact OMS if
they require medical or dental attention in the U.S. beyond that previously authorized
by the PCMO. Common situations that require OMS assistance include: an acute
illness requiring medical care; evaluations or treatments recommended as follow-up to
an initial consultation authorized by the PCMO; prolonged dental interventions such as
crowns.
When a Volunteer on personal business in the U.S. contacts OMS, the IHC works with
the individual to ensure that medical needs are resolved within the allotted leave time.
The IHC monitors care through direct contact with the Volunteer and consultation
with his/her care providers. When necessary, OMS staff issues additional 127C
authorizations for medical or dental care.
If the time required for resolution of a medical problem exceeds the Volunteer's leave,
the IHC will: (1) place the Volunteer on Medical Hold at HOR or (2) have the
Volunteer travel to Washington, DC for evaluation or care.
When a Volunteer is placed on Medical Hold at his/her HOR or medically evacuated
to Washington from his/her HOR, he/she must be medically cleared by OMS prior to
return to post. Volunteers on Medical Hold are eligible for the same benefits
(excluding travel to and from post) and have the same obligations as Volunteers. The
field support staff notifies the PCMO when a Volunteer has been placed on Medical
Hold. The PCMO is then responsible for informing the CD of the Volunteers Medical
Hold status.
The field support staff maintains a record of all communication and 127C
authorizations for Volunteers on Medical Hold. This documentation is sent to post to
be included in the Volunteer's health record following the Volunteers return to
country. Volunteers are responsible for obtaining copies of their medical reports for
care received at their HOR and bringing them back to country to be included in their
health record.
April 2013
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TG 380
Medical Evacuation
April 2013
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TG 380
Medical Evacuation
April 2013
Page 25
TG 380 ATTACHMENT A
Name:
DOB:
5) Contact person at site willing to go to your home in an emergency; name, address and telephone number:
6) Name, address and telephone number of the Volunteer who lives closest to you:
9) Name address and telephone number of Chief of Police, police station, or security official near your site:
Page 1
TG 380 ATTACHMENT A
11) Communication options available at site including procedures for use, i.e., availability, hours.
12) Name and contact information for nearest airport or landing strip. Specify small or large aircraft capacity.
_________
_________
_________
_________
Page 2
TG 380 ATTACHMENT B
DOB:
Medevac Date:
COS:
o
o
To Volunteer:
o
o
o
o
o
o
o
PCMO Signature
2. ADMINISTRATIVE OFFICE
To Volunteer:
o
o
o
o
o
Transportation from post to medevac site, i.e., airline ticket, transportation to airport
o
o
o
o
Description of Service: Report of Peace Corps service completed if Volunteer intends to resign or be
separated from service
Peace Corps
Technical Guideline 385
1. PURPOSE
To establish procedures for the medical evacuation of Peace Corps Volunteers and Trainees
requiring emergency medical evacuation (medevac).
2. BACKGROUND
Emergency medical evacuation is used for acute, life- limb- and organ-threatening
emergencies that require emergency medical evacuation by a chartered aircraft to ensure
timely delivery of care. Such emergencies among Peace Corps Volunteers are rare.
Nevertheless, Peace Corps Medical Officers (PCMOs) must be prepared to manage these
emergencies. In these situations, Peace Corps will request the services of an international air
rescue company or the U.S. military to evacuate the Volunteer. Emergency air evacuations
require a coordinated effort between the post, the PCMO, the Office of Medical Services
(OMS), and the air rescue company.
The telephone numbers, fax numbers, email addresses, mailing addresses, and
other contact information listed below are up-to-date as of the publication of this
Technical Guideline (TG). Posts should ensure that their contact information is
accurate and up-to-date.
Capabilities of local operating suites, intensive care units, and emergency departments;
The PCMO should ensure that all individuals who may participate in an emergency medevac
are familiar with emergency medical procedures.
July 2010
Page 1
TG 385
Emergency Evacuation
Telephone: During business hours (7:30 a.m. to 5 p.m. eastern time, Monday through
Friday)
For urgent concerns during business hours the PCMO should contact field support
directly through the main OMS switchboard (202-692-1500). When calling the OMS
switchboard, PCMOs should identify themselves, state the urgency of the call, and state
with whom they would like to speak. The administrative assistant who answers the
telephone will ensure that the call is transferred to the appropriate OMS staff.
OSS
(202-692-1470)
If Communication is Impossible:
Under extraordinary circumstances immediate communication with OMS may be impossible.
In these circumstances, PCMOs should use their clinical judgment and all available resources
to provide necessary care to an ill or injured Volunteer. Peace Corps Manual Section (MS)
264 states that in no circumstances should a PCMO hesitate to evacuate an individual if that
is the medically sound course of action.
July 2010
Page 2
TG 385
Emergency Evacuation
Start basic and advanced life support measures, including the ABCs of cardiac
and trauma life support, specifically:
July 2010
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TG 385
Emergency Evacuation
6.2
Stabilize back and/or neck injuries. Patients should have full head stabilization gear,
stiff cervical collar and a long backboard in place.
Control seizures.
Ensure that a complete head to toe evaluation is completed, including mental status,
neurological, cardiovascular, and trauma exams as appropriate.
Obtain basic laboratory and diagnostic studies when possible and applicable, i.e.,
complete blood count, chemistry profile, toxicology and alcohol screens, arterial
blood gases, prothrombin and partial thrombin times, blood type, cross and match,
electrocardiogram, chest x-ray and other radiological studies as indicated.
Patient information, i.e., Volunteer's name, date of birth (DOB), social security
number (SSN), and Close of Service (COS) date;
Case summary, i.e., patient status, presumptive diagnosis, and treatment initiated;
Volunteer permission to notify parents or next of kin, to include contact name and
telephone numbers.
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TG 385
Emergency Evacuation
6.3
6.4
6.5
A Medical Services (MS) reference number is not provided to post for emergency
medevacs. For accounting purposes, an MS reference number is provided to the air
rescue company.
In the rare event where OMS can not be contacted, the PCMO may authorize an
emergency medevac. The PCMO must promptly notify the Country Director (CD)
in this situation.
The PCMO should give the CD and Administrative Officer (AO) preliminary notice
when an emergency medevac is likely or under active consideration.
PCMOs must notify the CD and the AO upon OMS concurrence to emergency
medevac.
The PCMO should provide the CD and the AO with periodic updates throughout
the emergency evacuation process.
Medevac Communications
After the emergency medevac has been initiated, the coordinating physician of the air
rescue company will usually contact the PCMO to verify contact information, obtain a
more detailed summary of the case, and assess the current status of the patient. Often
the air rescue company will also contact the attending physician managing the case.
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TG 385
Emergency Evacuation
Once the air rescue has been initiated, OMS will relay the following information to
post:
7.2
Confirmation of air rescue company's intent to contact post and name of their
coordinating physician;
Medevac Communications
The OMS regional International Health Coordinator (IHC) is primarily responsible for
maintaining and facilitating communication between the PCMO, OMS, and the
physician coordinator at the emergency air rescue company, throughout the evacuation
process.
If authorized, or as appropriate, OMS will contact and maintain communications with
the Volunteers family.
7.3
Case Management
OMS will provide interim case management direction to the PCMO throughout the
evacuation process. If needed, OMS will provide case consultation and interim
management advice to local physicians.
Case Management
The air rescue company, in consultation with OMS and the PCMO, is primarily
responsible for the medical management of the case. Most air rescue services have a
consulting medical advisor who will provide case consultation and interim management
advice to the PCMO and local specialists.
8.2
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TG 385
Emergency Evacuation
Post staff involved with an emergency medevac should be prepared to assist the air
rescue company in obtaining the following logistical information. Posts should be
familiar with this information prior to an emergency medevac situation.
8.3
Local airport facilities, e.g., hours of operation, length of runway, runway surface,
availability of night lights.
Flight permission and landing rights, e.g., procedures for obtaining airspace,
immigration, and landing rights. Assistance from the U.S. Embassy may be
required if local government permission to land is required.
Landing fees, e.g., required landing fees at the national airport, required method of
payment.
Ambulance protocols, e.g., procedures for getting an ambulance and attendants onto
the runway.
8.4
8.5
Accompaniment
Medical judgments concerning the need for accompaniment and the type of
accompaniment are made by the air rescue company. Space on air rescue aircraft is
frequently limited and accompaniments cannot be accommodated.
8.6
Medevac Communications
The air rescue company is responsible for maintaining communications with the post,
the PCMO, and OMS throughout the air evacuation process.
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TG 385
Emergency Evacuation
In general, after the emergency medevac has been initiated, the coordinating physician
of the air rescue company will contact the PCMO to verify contact information, obtain
a more detailed summary of the case, and to assess the current status of the patient.
Often the air rescue company will also contact the attending physician managing the
case.
The air rescue company will provide OMS and the post with the following information:
Following departure:
9. ADMINISTRATIVE SUPPORT
In an urgent situation, post administrative staff should make every effort to accomplish as
many administrative support tasks as circumstances and time safely allow. These procedures
are outlined in the table below. As time permits, see TG 380 Medical Evacuation, section
10 Administrative Support for a more detailed description of medevac support procedures.
Post administrative staff is also responsible for providing logistical and communication
support during an emergency medevac. A special consideration is the Volunteers passport.
In an urgent situation, the Volunteers passport may not be in the same location as the ill or
injured Volunteer. Post should make an immediate effort to obtain the Volunteers passport
and ensure that it is available to accompany the Volunteer.
ADMINISTRATIVE SUPPORT PROCEDURES
NON-EMERGENT MEDEVAC
PCMO
EMERGENCY MEDEVAC
The health record is not sent with an
emergency medevac. A case summary, copies
of all case-related notes, x-rays and diagnostic
studies should be sent. The health record
should be prepared and kept at post until
requested from OMS.
As time permits.
Provides supply of
medications.
As time permits.
As time permits.
As time permits.
As time permits.
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TG 385
Emergency Evacuation
Benefits identification card.
As time permits.
Prepares personal
documents, e.g., passport,
visas.
Arranges transportation.
As time permits.
As time permits.
Completes necessary
paperwork:
- PC-505 Volunteer
Trainee Readjustment
Allowance;
- PC-477 Certification of
Non-Indebtedness and
Accountability for
Property;
- Power of Attorney;
- PC 1485 Release of
Medical Information.
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TG 385
Emergency Evacuation
The Embassy medical unit staff or emergency medical supplies are required.
Most requests for diplomatic assistance should go through the Consular Officer during
working hours or the Duty Officer after hours. The Consular or Duty Officer will notify other
American officials, if necessary, including the Ambassador. Generally requests for the
Embassys assistance should come from the CD.
Arrange repatriation of the Volunteer to the U.S. or return of the Volunteer to post;
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TG 385 ATTACHMENT A
Volunteer:
SSN:
DOB:
Medevac Date:
Country:
IHC:
COS:
1. PCMO RESPONSIBILITIES
Medical case management.
Obtain OMS field consultation and concurrence. Have the following information available prior to consult:
Case Summary.
TG 385 ATTACHMENT A
Following Departure:
4. ADMINISTRATIVE RESPONSIBILITIES
Administrative tasks should only be accomplished as time and circumstances
safely permit. All important documents should be sealed in an envelope and given
to the Volunteer or SOS medical personnel.
PCMO
To SOS medical personnel: A case summary, copies of all case-related notes, x-rays and diagnostic
studies. The Volunteer Health Record does not accompany an SOS medevac.
Two week supply of routine medications and malaria prophylaxis, if indicated.
WHO vaccination card.
Health Benefits identification card.
Medevac instructions and While Youre Enroute to Washington D.C.
Explanation of personal effects shipment policy, i.e., weight limits, personal property insurance.
Review status of personal belongings left in country, i.e., secure, itemized list received?
COUNTRY DIRECTORS OFFICE
Form PC-1485: Report of Peace Corps service completed if Volunteer intends to resign or be separated
from service.
Authorizations for leave or vacation following medical clearance.
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Peace Corps
Technical Guideline 390
This TG uses the term Volunteer to refer to both Volunteers and Trainees for the purpose of evacuations.
____________________________________________________________________________________________________
Office of Medical Services
September 2006
Page 1
____________________________________________________________________________________________________
Office of Medical Services
September 2006
Page 2
____________________________________________________________________________________________________
Office of Medical Services
September 2006
Page 3
REFERENCES
Peace Corps Volunteer Safety Council, Evacuation Support Guide, September 2004
Laycock, Jane, Farmer, Bill. Evacuation Advice for PCMOs: A Fact Sheet of Suggestions, Peace
Corps, 2002.
____________________________________________________________________________________________________
Office of Medical Services
September 2006
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Peace Corps
Technical Guideline 395
PLANNED COUNTRY/POST CLOSURE OF HEALTH UNIT
(Non-Emergency Post Closing)
1.
PURPOSE
The purpose of this guideline is to provide the PCMO with information needed to
effectively close a post health unit after the program is suspended.
2.
BACKGROUND
Once a decision has been made to close a post, there are a number of activities that
must be completed to ensure a smooth exit from the country. This technical
guideline will assist the PCMO and health unit staff with accomplishing these tasks.
3.
GENERAL CONSIDERATIONS
The areas for review and consideration when closing a health unit include
coordination of a timeline with post staff, notification of consultants, medical
facilities, laboratories, pharmacies, etc., proper disposal of medications, supplies,
office supplies, and durable equipment. This guidance will focus on each area and
list specific tasks to be performed.
Health Records
Volunteer/Trainee health records in PCMEDICS should be relinquished to OHS
in the same process as COS. Outstanding Volunteer/Trainee reports received
after the health record has been relinquished should be reviewed to assess the
need for follow-up, then, initialed and dated. Write no follow-up needed on
those that do not require further attention. Send all reports to the Post-Service
Unit via SFTP.
Vendor Notification:
Notify consultants and other vendors (i.e. pharmacy, laboratories, etc.) as soon as
possible to facilitate payment of any outstanding bills.
Medications:
Keep all medications, supplies, and equipment until the last volunteer has closed
service.
Destroy or transfer unexpired meds to the Embassy health unit or a neighboring
post (refer to MS 341: Non-emergency Post Closing, Section 7.3).
Narcotics should be transferred to the U.S. Embassy medical unit and transfer
should be done in the presence of a PCMO, CD or designee AND Embassy
medical personnel. The narcotics log should also be transferred.
Medications and supplies cannot be donated to non-US government agencies or
organizations.
Destroy all expired medications. Medications must be destroyed in the presence
of the PCMO and the CD, or designee, in accordance with local waste disposal
and air and water pollution control standards.
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Office of Health Services
December 2015
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Medical Supplies:
For perishable supplies with an expiration date (band aids, gauze, condoms, etc.)
offer to Embassy or neighboring post and document the disposition
If not able to transfer, document and destroy
Office Supplies:
Offer excess office supplies to Embassy or neighboring post
Destroy log books that contain non-narcotic documentation
Destroy outdated Peace Corps forms; send other forms to another post
Durable Medical Equipment (beds, centrifuge, exam tables, etc.):
Work with AO to coordinate auction or other property disposal method
__________________________________________________________________________________
Office of Health Services
December 2015
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