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CLINICAL PRACTICE GUIDELINES ON

ABNORMAL LABOR AND DELIVERY

Jo-An Marie G. Aguedan, M.D.

ELECTRONIC FETAL MONITORING


DURING ABNORMAL LABOR AND
DELIVERY

Definition of Terms:

A.
B.
C.
D.
E.
F.
G.
H.

Baseline
Baseline variability
Acceleration
Early deceleration
Late deceleration
Variable deceleration
Prolonged deceleration
Sinusoidal pattern

BASELINE
The mean fetal heart rate (FHR) rounded
to increments of 5 beats per minute
during a 10-minute segment, excluding:
Periodic or episodic changes
Periodic of marked FHR variability
Segments of baseline that defer by more than
25 beats per minute

BASELINE
The baseline must be for a minimum of 2
minutes in any 10-minute segment, or the
baseline for that time period is
indeterminate.
In this case, one may refer to the prior 10minute window for determination of
baseline.

BASELINE
Normal FHR baseline: 110-160 beats per
minute
Tachycardia: FHR baseline is greater than
160 beats per minute
Bradycardia: FHR baseline is less than
110 beats per minute

BASELINE VARIABILITY
Fluctuations in the baseline FHR that are
irregular in amplitude and frequency.
Variability is visually quantified as the
amplitude of peak-to-trough in beats per
minute.

BASELINE VARIABILITY
Absent amplitude range undetectable
Minimal amplitude range detectable but
5 beats per minute or fewer
Moderate (Normal) amplitude range 625 beats per minute
Marked amplitude range greater than 25
beats per minute

ACCELERATION
A visually apparent abrupt increase (onset
to peak in less than 30 seconds) in the
FHR.
At more than or equal to 32 weeks of
gestation, acceleration has a peak of 15
beats per minute or more above baseline,
with duration of 15 seconds or more but
less than 2 minutes from onset to return.

ACCELERATION
Before 32 weeks of gestation, an
acceleration has a peak of 10 beats per
minute or more above baseline, with a
duration of 10 seconds or more but less
than 2 minutes from onset to return.
Prolonged acceleration lasts 2 minutes or
more but less than 10 minutes in duration.
If an acceleration lasts 10 minutes or
longer, it is a baseline change.

EARLY DECELERATION
Visually apparent usually symmetrical
gradual decrease and return of the FHR
associated with a uterine contraction.
Gradual FHR decrease is defined as from
the onset to the FHR nadir of 30 seconds
or more.
The decrease in FHR is calculated from
the onset to the nadir of the deceleration.

EARLY DECELERATION
The nadir of the deceleration occurs at the
same time as the peak of the contraction.
In most cases the onset, nadir, and
recovery of the deceleration are coincident
with the beginning, peak, and ending of
the contraction, respectively.

LATE DECELERATION
Visually apparent usually symmetrical
gradual decrease and return of the FHR
associated with a uterine contraction.
A gradual FHR decrease is defined as
from the onset to the FHR nadir of 30
seconds or more.
The decrease in FHR is calculated from
the onset to the nadir of the deceleration.

LATE DECELERATION
The deceleration is delayed in timing, with
the nadir of the deceleration occurring
after the peak of the contraction.
In most cases the onset, nadir, and
recovery of the deceleration occur after the
beginning, peak, and ending of the
contraction, respectively

VARIABLE DECELERATION
Visually apparent abrupt decrease in FHR.
An abrupt FHR decrease is defined as
from the onset of the deceleration to the
beginning of the FHR nadir less than 30
seconds.
The decrease in FHR is calculated from
the onset to the nadir of the deceleration.

VARIABLE DECELERATION

The decrease in FHR is 15 beats per


minute or greater, lasting 15 seconds or
greater, and less than 2 minutes in
duration.
When variable decelerations are
associated with uterine contractions, their
onset, depth and duration commonly vary
with successive uterine contractions

PROLONGED DECELERATION
Visually apparent decrease in FHR below
the baseline.
Decrease in FHR from the baseline that is
15 beats per minute or more, lasting 2
minutes or more but less than 10 minutes
in duration.
If a deceleration lasts 10 minutes or
longer, it is a baseline change.

SINUSOIDAL PATTERN
Visually apparent, smooth, sine wave-like
undulating pattern in FHR baseline with a
cycle frequency of 3-5 per minute which
persists for 20 minutes or more.

Classification of FHR
Tracings Three
Tiered System for the
Categorization of FHR
Patterns

Categ FHR
ory
Tracin
gs

Definition

Norm Category I FHR tracings


al
are strongly predictive of
normal fetal acid-base
status at the time of
observation.
Category I FHR tracings
may be monitored in a
routine manner, and no

Catego
FHR
ry
Tracings
II

Definition

not predictive of abnormal fetal


Indeter acid-base status, yet presently
mi-nate there is no adequate evidence to
classify these as Category I or
Category III.
require
evaluation
and

continued
surveilance
and
reevaluation, taking into account
the entire associated clinical
circumstances.
In some circumstances, either
ancillary tests to ensure fetal well
being
or
intrauterine

Catego
FHR
Definition
ry
Tracings
III
Abnorm associated with abnormal fetal
al
acid-base status at the time of
observation.
require clinical evaluation
on
the
clinical
Depending
situation, efforts to expeditiously
resolve the abnormal FHR pattern
may include but are not limited
to provision of:
1.maternal oxygen
2.change in maternal position
3.
discontinuation
of
labor
stimulation
4.treatment
of
maternal

Categ
ory

III

FHR
Tracings

Definition

Abnor If
category
III
mal tracing does not
resolve with these
measures, delivery
should
be
undertaken.

Clinical Consideration and


Recommendations
1. Fetal surveillance in labor, whether by
intermittent auscultation (IA) or by EFM
should be recommended to all women.

(Level III, Grade C)

Frequency of IA is as follows:

For low risk patients every 30 minutes for 1st


stage, then every 15 minutes for the 2nd stage

For high risk patients every 15 minutes for 1st


stage, then every 5 minutes for the 2nd stage

2. Based on available data, there is no clear


benefit for the use of EFM over IA. Either
option is acceptable in patients without
complications.

(Level III, Grade C)

A meta-analysis synthesizing results of


randomized
control trials (RCTs) comparing modalities
had the
following conclusions: (Level I, Grade A)
The use of EFM compared with IA increased
the overall cesarean delivery rate (RR, 1.66,
95% CI 1.30-2.13) and the cesarean delivery
rate for abnormal FHR or acidosis or both (RR
2.37, 95% CI 1.88-3.00).
The use of EFM increased the risk of both
vacuum and forceps operative vaginal
delivery (RR 1.16, 95% CI 1.01-1.32).

The use of EFM did not reduce perinatal


mortality (RR 0.85, 95% CI 0.59-1.23).
The use of EFM reduced the risk of
neonatal seizures (RR 0.50, 95% CI 0.310.80).
The use of EFM did not reduce the risk of
cerebral palsy (RR 1.74, 95% CI 0.973.11).

3. In ideal settings, continuous EFM should


be offered and is recommended for high
risk pregnancies where there is increased
risk of perinatal death, cerebral palsy or
neonatal encephalopathy.
(Level II-2 to III, Grade C)

4. Current evidence does not support the use


of admission tocogram in low risk
pregnancy.
(Level III, Grade C)

5. Based on careful review of available


terminologies, a three-tiered system of
categorization of FHR interpretation is
recommended.

(Level III, Grade C)

Category

II

Baseline 110-160 Bradycardia not


FHR
beats per accompanied by
minute
absent baseline
variability or
Tachycardia

III

Bradycar
dia

Baseline Moderate Minimal baseline Absent


variabilit
variability
y
Absent baseline
variability with no
recurrent
decelerations
Marked baseline
variability

Category

Decelerati Absent
ons
early, late
or
variable

II
Recurrent
variable
decelerations
accompanied by
minimal or
moderate
baseline
variability
Prolonged
deceleration
more than 2
minutes but less
than 10 minutes
Recurrent late

III
Recurrent
late
deceleratio
ns
Recurrent
variable
deceleratio
ns

Category

Decelerat Absent
ions
early,
late
or
variable

II

III

Variable
decelerations with
other
characteristics such
as slow return to
baseline,
overshoots, or
shoulders

Recurrent
late
decelerati
ons
Recurrent
variable
decelerati
ons

Accelerati Present
Absence of
ons
or Absent induced
accelerations
after fetal

Sinusoidal
pattern

Based on careful review of available


terminologies, a three-tiered system of
categorization of FHR interpretation is
recommended. (Level III, Grade C)
The false-positive rate of EFM for
predicting cerebral palsy is high, at
greater than 99%.
(Level II-2 to III, Grade C)

The use if EFM is associated with an


increased rate of both vacuum and
forceps operative vaginal delivery, and
cesarean delivery for abnormal FHR
patterns or acidosis or both.
(Level II-2 to III, Grade C)

When the FHR tracing includes recurrent


variable decelerations, amnioinfusion to
relieve umbilical cord compression should
be considered.
(Level II-1, Grade B)

Pulse oximetry has not been demonstrated


to be a clinically useful test in evaluating
fetal status.
(Level III, Grade C)

There is high interobserver and intraobserver


variability in interpretation of FHR tracing.
(Level III, Grade C)

Reinterpretation of the FHR tracing, especially


if the neonatal outcome is known, may not be
reliable.

(Level III, Grade C)

The use of EFM does not result in


reduction of cerebral palsy.
(Level III, Grade C)

A three-tiered system for the


categorization of FHR patterns is
recommended.
(Level III, Grade C)

The labor of women with high-risk


conditions should be monitored with
continuous FHR monitoring.
(Level III, Grade C)

The terms hyperstimulation and


hypercontractiliy should be abandonded. It
is now calles uterine tachysystole (i.e. more
than 5 contractions in 10 minutes, averaged
over a 30-minute window).

(Level III, Grade C)

Clinical Consideration and


Recommendations
6. Ancillary tests available that can aid in the
management of Category II or Category III
fetal heart tracings include fetal scalp pH
sampling, Allis clamp stimulation,
vibroacoustic stimulation and digital scalp
stimulation.

(Level II-3, Grade B)

Because vibroacoustic stimulation and


digital scalp stimulation is less invasive
than the other two methods, they are
preferred methods.

(Level I, Grade A)

7. A Category II or Category III FHR Tracing


requires initial evaluation and treatment
may include the following:
a. Discontinuation of any labor stimulating
agent
b. Cervical examination to determine
umbilical cord prolapsed, rapid cervical
dilatation, or descent of the fetal head
(Level III, Grade C)

Changing maternal position to left or right


lateral recumbent position, reducing
compression of the vena cava and
improving uteroplacental blood flow.

Monitoring maternal for evidence of


hypotension, especially in those with
regional anesthesia (if present, treatment
with volume expansion or with ephedrine
or both or phenylephrine may be
warranted).

DYSTOCIA

Definition of Abnormal Patterns of Labor


LABOR PATTERN

Diagnostic Criteria
Nulliparas Multiparas

Prolongaton Disorder
1. Prolonged Latent
> 20 hrs
Phase
Protraction Disorder
1. Protracted Active
< 1.2 cm/hr
Phase Dilation (Phase
of maximum slope of
dilatation)
2. Protracted Descent
< 1 cm/hr
(maximum slope of
descent during the pelvic

> 14 hrs

< 1.5 cm/hr

< 2cm/hr

LABOR PATTERN
Arrest Disorder
1.
Prolonged
Deceleration
Phase
(cervical dilatation arrested
at 8 to 9 cm)
2. Secondary Arrest of
Dilatation
(progressive
cervical dilatation stops at
the phase of maximum
slope)
3. Arrest of Descent
(progressive descent stops
during pelvic division of
labor, station + 1)

Diagnostic Criteria
Nulliparas Multiparas
> 3 hrs

> 1 hr

> 2 hrs

> 1 hr

LABOR PATTERN

Diagnostic Criteria
Nulliparas Multiparas

4. Failure of Descent Lack of expected descent


(station 0)
during deceleration phase
or second stage of labor
5. Prolonged
Stage

Second > 3 hrs with > 2 hrs with


regional
regional
anesthesia or anesthesia or
> 2 hrs
without
regional
anesthesia

> 1 hr
without
regional
anesthesia

Recommendations
1. Prolonged Latent Phase
2. Protracted Active Phase Dilatation
3. Arrest Disorders

Prolonged Latent Phase


Avoid admission to the labor and
delivery area until active labor is
established.
(Level III, Grade C)

Develop a plan to meet the womans


need either at home or in a nonlaboring hospital unit.
(Level III, Grade C)

Prolonged Latent Phase


Friedman (1972) reported that
prolongation of the latent phase did not
adversely influence fetal or maternal
morbidity and mortality.
(Level III, Grade C)

Data show that patients with prolonged


latent phase are no more prone to
develop problems than gravidas with
normal latent phase.
(Level III, Grade C)

Prolonged Latent Phase


Observation, rest and therapeutic
analgesia/strong sedatives are
favored over a more active approach
of amniotomy and oxytocin induction.
(Level III, Grade C)

Support and information from


caregivers to provide coping
strategies.
(Level III, Grade C)

Prolonged Latent Phase


A patient who has a latent
phase longer than 20 hrs
should be expected to evolve a
normal subsequent dilatation
and descent if allowed to do
so.
(Level III, Grade C)

Prolonged Latent Phase


- It cannot be too strongly stated that
patients who are delivered by
cesarean section (CS) during the
latent phase for no other reason than
their lack of progress are being
subjected to this operation
unnecessarily most of the time.
(Level III, Grade C)

Prolonged Latent Phase


CS has no place as a method of
treatment for prolonged latent phase
without other clear indications like
documented cephalopelvic disproportion
(CPD) or abnormal FHR pattern (category
III).

(Level III, Grade C)

Friedmans recommended approach is


support and therapeutic rest by the use of
large doses of narcotic analgesics.

(Level III, Grade C)

Prolonged Latent Phase


Exceptionally, oxytocin may be undertaken
directly if additional 6 to 10 hours delay by
rest would be clinically unacceptable as in
the presence of chorioamnionitis.

(Level III, Grade C)

Recommendations
1. Prolonged Latent Phase
2. Protracted Active Phase Dilatation
3. Arrest Disorders

Protracted Active Phase


Dilatation
Physical and emotional support.
(Level I, Grade A)

Continuous support during labor from


caregivers should be encouraged because it is
beneficial for women and their newborns.
(Level I, Grade A)

Amniotomy with early oxytocin


augmentation shortens labor by as much
as 2 hours compared to expectant care but
has not been shown to change cesarean
delivery rates.

(Level I, Grade A)

Protracted Active Phase


Dilatation
Amniotomy may enhance progress in the
active phase and negate the need for oxytocin
augmentation but may increase the risk of
chorioamnionitis.
(Level I, Grade A)

Oxytocin should be used to achieve adequate


contractions (at least 200 Montevideo units)
before operative delivery is considered.
(Level I, Grade B)

High-dose oxytocin regimens result in


shorter labors than low dose regimens
without adverse effects to the fetus.
(Level I, Grade B)

Rule out CPD.


(Level III, Grade B)

If with CPD, do CS.


(Level III, Grade B)

Recommendations
1. Prolonged Latent Phase
2. Protracted Active Phase Dilatation
3. Arrest Disorders

Arrest Disorders
Continuous support during labor from
caregivers should be encouraged because it
is beneficial for women and their newborns.
(Level I, Grade A)

X-ray pelvimetry alone as a predictor of


dystocia has not been shown to have benefit,
and therefore is not recommended.
(Level I, Grade B)

Rule out CPD


(Level III, Grade B)

Arrest Disorders
If with CPD, do CS.
(Level III, Grade B)

Before an arrest disorder can be


diagnosed in the first stage of labor, the
latent phase should be completed, and the
uterine contraction pattern exceeds 200
Montevideo units for 2 hours without
cervical change.
(Level III, Grade C)

Arrest Disorders
The 2-hour rule for the diagnosis of arrest in
active labor has been challenged.
In a clinical trial, 542 women were managed
by a protocol in which, after active phase
arrest was diagnosed, oxytocin was initiated
with the intent to achieve a sustained uterine
contraction pattern of greater than 200
Montevideo units.

(Level III, Grade C)

Arrest Disorders
Cesarean delivery is not performed for
labor arrest until there were at least 4
hours of sustained uterine contraction
pattern of greater than 200 Montevideo
units, or a minimum of 6 hours of oxytocin
augmentation if the contraction pattern
could not be achieved.

(Level III, Grade C)

Arrest Disorders
The protocol resulted in a high rate of
vaginal delivery (92%) with no severe
adverse maternal or fetal outcomes.
Extending the minimum period of oxytocin
augmentation for active phase arrest from 2
hours appears effective.
(Level III, Grade C)

DYSTOCIA SECONDARY TO
PROBLEMS IN PASSENGER

BREECH PRESENTATION
EXTERNAL CEPHALIC VERSION
PERSISTENT OCCIPUT POSTERIOR,
OCCIPUT TRANSVERSE
BROW PRESENTATION
FACE PRESENTATION
FETAL MACROSOMIA
SHOULDER DYSTOCIA
TRANSVERSE LIE/OBLIQUE LIE
COMPOUND PRESENTATION

BREECH PRESENTATION

BREECH PRESENTATION
Recommendations:
Planned cesarean section (CS) for babies in
breech presentation has a reduced risk for
perinatal death and neonatal morbidity
compared to planned vaginal birth.
(Level I, Grade A)

Planned CS for babies in breech presentation


is associated with a modest increase in short
term maternal morbidity

(Level I, Grade A)

Recommendations:
Information is limited about the potential for
problems with future pregnancies.

(Level I, Grade C)

After two years, there were no differences in


the combined outcome death or
neurodevelopmental delay. Maternal
outcomes were also similar.

(Level I, Grade A)

Recommendations:
There is no data to quantify risks of CS to
the mother (scar dehiscence in a
subsequent pregnancy, increased risk to
repeat CS, placenta accreta).
(Level III, Grade C)

There is no evidence that the long term


health of babies with a breech
presentation delivered at term is
influenced by how the baby is born.
(Level I, Grade A)

Recommendations:
Planned vaginal breech delivery remains a
viable option, provided the criteria are met,
a skilled obstetrician and facilities for CS
are immediately available, and the women
is informed of all possible risks.

(Level I, Grade B)

Recommendations:
For a woman with suspected breech
presentation, pre- or early labor ultrasound
should be performed to assess type of
breech presentation, fetal growth and
estimated weight, and attitude of fetal
head. If ultrasound is not available, CS is
recommended.

(Level II, Grade A)

Recommendations:

Contraindications to labor
include:
a) Cord presentation. (Level II, Grade A)
b) Fetal growth restriction or macrosomia
(Level I, Grade A)

c) Any presentation other than a frank or


complete breech with a flexed or
neutral head attitude
(Level III, Grade B)

Recommendations:

Contraindications to labor
include:
d)Clinically inadequate maternal pelvis

(Level

III, Grade B)

e)Fetal anomaly incompatible with vaginal


delivery.
(Level III, Grade B)

Recommendations:
Vaginal breech delivery can be offered when the
estimated fetal weight is between 2500 g and
4000 g.
(Level II, Grade B)

Clinical pelvic examination should be performed to


rule out pathological pelvic contraction. Radiologic
pelvimetry is not necessary for a safe trial of labor;
good progress in labor is the best indicator of
adequate fetal-pelvic proportions.
(Level III, Grade B)

Recommendations:
Continuous electronic fetal heart monitoring (EFM)
is preferable in the first stage and mandatory in
the second stage of labor.
(Level I, Grade A)

When membrane rupture, immediate vaginal


examination is recommended to rule out
prolapsed cord.
(Level III, Grade B)

In the absence of adequate progress in labor, CS


is advised.
(Level II-1, Grade A)

Recommendations:

Induction of labor is not recommended for breech


presentation.
(Level II, Grade B)

Oxytocin augmentation is acceptable in the


presence of hypotonic uterine dysfunction.
(Level II, Grade A)

A passive second stage without active pushing


may last up to 90 minutes, allowing the breech to
descend well into the pelvis. Once active pushing
commences, if delivery is not imminent after 60
minutes, CS is recommended.
(Level I, Grade A)

The active second stage of labor should take place


in or near an operating room with equipment and
personnel available to perform a timely CS section
if necessary.
(Level I, Grade A)

Recommendations:
A health care professional skilled in neonatal
resuscitation should be in attendance at the time of
delivery.
(Level III, Grade A)

The health care provider for a planned vaginal


breech delivery needs to possess the requisite
skills and experience.
(Level II, Grade A)

Recommendations:
An experienced obstetrician-gynecologist comfortable
in the performance of vaginal breech delivery should be
present at the delivery to supervise other health care
providers, including a trainee.
(Level I, Grade A)

The health care provider should have rehearsed a plan


of action and should be prepared to act promptly in the
rare circumstance of a trapped aftercoming head or
irreducible nuchal arms: symphysiotomy or emergency
abdominal rescue can be life saving.
(Level III, Grade B)

Recommendations:
Total breech extraction is inappropriate for term
singleton breech delivery
(Level II, Grade A)

Effective maternal pushing efforts are essential to


safe delivery and should be encouraged.
(Level II, Grade A)

At the time of delivery of the aftercoming head, an


assistant should be present to apply suprapubic
pressure to favor flexion and engagement of the
fetal head.

(Level II, Grade B)

Recommendations:

Spontaneous or assisted breech


delivery is acceptable. Fetal traction
should be avoided, and fetal
manipulation must be applied only
after spontaneous delivery to the level
of the umbilicus.

(Level III, Grade A)

Nuchal arms may be reduced by


Lovset maneuver.

(Level III, Grade B)

Recommendations:
The fetal head may deliver spontaneously, with the
assistance of suprapubic pressure, by MauriceauSmellie-Veit maneuver, or with the assistance of
Piper forceps.

(Level III, Grade B)

Recommendations:

In the absence of a contraindication


to vaginal delivery, a woman with a
breech presentation should be
informed of the risks and benefits of
a trial of labor and elective CS, and
informed consent should be
obtained. A womans choice of
delivery mode should be respected.

(Level III, Grade A)

Recommendations:
The consent discussion and chosen plan
should be well documented and
communicated to labor room staff.
(Level III, Grade B)

Hospitals offering a trial of labor should


have a written protocol for eligibility and
intrapartum management.
(Level III, Grade B)

Recommendations:

Women with a contraindication to a trial


of labor should be advised to have a
CS. Women choosing to labor despite
this recommendation have right to do
so and should not be abandoned. They
should be provided the best possible
in-hospital care.

(Level III, Grade A)

Recommendations:
A physician is free to choose whom he will serve.
He may refuse calls, or other medical services for
reasons satisfactory to his professional
conscience.

He should, however, always respond to any


request for his assistance in an emergency. Once
he undertakes a case, he should not abandon nor
neglect it.

If for any reason he wants to be released from it,


he should announce his desire previously, giving
sufficient time or opportunity to the patient or his
family to receive another medical attendant.

Recommendations:

Theoretical and hands-on breech birth


training simulation should be part of
basic obstetrical skills taining programs
such as ALARM, to prepare health care
providers for unexpected vaginal breech
births

(Level III, Grade B)

Recommendations:
Not enough evidence to support the
intervention of helping a breech baby to be
born in one pushing contraction following
the birth of the babys umbilicus.
(Level III, Grade B)

Epidural anesthesia is not routinely


advised.

(Level III, Grade C)

EXTERNAL CEPHALIC VERSION

EXTERNAL CEPHALIC VERSION


is a procedure of manipulation of the fetus
through the maternal abdomen to a
cephalic presentation.

The rationale behind ECV is to reduce the


incidence of breech presentation at term
and therefore the associated risks,
particularly of avoiding CS.

Recommendations
Women should be counseled that ECV
reduces the chance of breech presentation at
delivery.
(Level I, Grade A)

ECV reduces the chances of having a CS.


(Level I, Grade A)

With a trained operator about 50% of ECV


attempts will be successful
(Level III, Grade B)

Recommendations
The use of tocolysis with beta
sympathomimetic drugs may be offered to
women undergoing ECV as it has been
shown to increase the success rate.
(Level I, Grade A)

ECV before 36 weeks is not associated


with significant reduction in noncephalic
births or CS.
(Level II, Grade B)

Recommendations
There is insufficient evidence to support
the use of postural management as a
method of promoting spontaneous version
over ECV.
(Level I, Grade A)

Labor with a cephalic presentation


following ECV is associated with a higher
rate of obstetric intervention than when
ECV has not been required.
(Level I, Grade B)

Recommendations
Absolute contraindications for ECV
that are likely to be associated with
increased mortality or morbidity:

Where cesarean delivery is required


Antepartum hemorrhafe within the last 7 days
Abnormal cardiotocograph
Major uterine anomaly
Ruptured membranes
Multiple pregnancy (except delivery of
second twin)
(Level III, Grade C)

Recommendations
Relative contraindications where ECV
might be more complicated:
Small for gestational age fetus with abnormal
Doppler parameters
Proteinuric pre-eclapmsia
Oligohydramnios
Major fetal anomalies
Scarred uterus
Unstable lie

(Level III, Grade C)

PERSISTENT OCCIPUT POSTERIOR,


OCCIPUT TRANSVERSE

PERSISTENT OCCIPUT POSTERIOR,


OCCIPUT TRANSVERSE
Definition
With effective contractions, adequate
flexion of the head, and a fetus of average
size, most posteriorly positioned occiputs
route promptly as soon as they reach the
pelvic floor.

PERSISTENT OCCIPUT POSTERIOR,


OCCIPUT TRANSVERSE
Poor contractions, faulty flexion of the
head, or epidural analgesia, which
diminishes abdominal muscular pushing
and relaxes the muscles of the pelvic floor
may predispose to incomplete rotation.

PERSISTENT OCCIPUT POSTERIOR,


OCCIPUT TRANSVERSE
If rotation is incomplete, transverse arrest
may result.
If no rotation toward the symphysis takes
place.
The occiput may remain in the direct
occiput posterior position, a condition
known as persistent occiput posterior.

Recommendations
Digital rotation should be considered when
managing the labor of a fetus in the
occipito-posterior position. This maneuver
successfully rotates the fetus reducing the
need for CS, instrumental delivery, and
other complications associated with
persistent occiput posterior

(Level III, Grade B)

Recommendations
Use of hands and knees position for ten minutes
twice daily in late pregnancy or during labor to
correct occipito-posterior position cannot be
recommended as an intervention. This is not to
suggest that women should not adopt this position
if they found it confortable. The use of this position
was associated with reduced backache.

(Level I, Grade A)

BROW PRESENTATION

BROW PRESENTATION
Recommendations:
Expectant management is reasonable as
long as the fetal heart tracing remains
reassuring and dilation and descent are
progressing normally because
spontaneous conversion to vertex or face
may occur.

(Level II, Grade B)

Recommendations
The use of forceps or manual conversion
to convert a brow presentation to a more
favorable position is contraindicated.

(Level II, Grade B)

FACE PRESENTATION

FACE PRESENTATION
Recommendations
Continuous EFM is considered mandatory
by many authors because of the increased
incidence of abnormal FHR patterns
and/or fetal compromise. Careful
application of the electrode must be
ensured; the mentum is recommended site
of application.

(Level III, Grade B)

Recommendations
Oxytocin can be used to augment labor
using the same precaution as in a vertex
presentation and using the same criteria of
assessment of uterine activity, adequacy of
the pelvis, and reassuring fetal hear
tracing.

(Level III, Grade B)

Recommendations
Attempts to manually convert the face to
vertex (Thom maneuver) or to rotate a
posterior position to a more favorable anterior
mentum position are rarely successful and are
associated with high perinatal mortality and
maternal morbidity.
Internal podalic version and breech extraction
are no longer recommended in the modern
management of the face presentation.

(Level III, Grade B)

Recommendations
Forceps may be used if the mentum is anterior.
Any typical forceps including Keilland forceps,
can be used.
(Level III, Grade B)

The mechanisms of labor in the term infant can


occur only if the mentum is anterior.
(Level III, Grade B)

FETAL MACROSOMIA

FETAL MACROSOMIA
The term fetal macrosomia implies fetal
growth beyond a specific weight, usually
4000 gm (8 lb 13 oz) or 4500 gm (9 lb 4
oz) regardless of the fetal gestational age.

Recommendations
The diagnosis of fetal macrosomia is
imprecise. For suspected fetal
macrosomia, the accuracy is estimated
fetal weight using ultrasound biometry is
no better than that obtained with clinical
palpation (Leopolds maneuvers).

(Level I, Grade A)

Suspected fetal macrosomia is not an


indication for induction of labor because
induction does not improve maternal or fetal
outcomes.

(Level II, Grade B)

Recommendations
Labor and vaginal delivery is not
contraindicated for women with estimated
fetal weights up to 5,000 g in the absence
of maternal diabetes.
(Level II, Grade B)

With an estimated fetal weight more than


4,500 g, a prolonged second stage of labor
or arrest of descent in the second stage is
an indication for cesarean delivery.
(Level II, Grade B)

Recommendations
Although the diagnosis of fetal
macrosomia is imprecise, prophylactic
cesarean delivery may be considered for
suspected fetal macrosomia with
estimated fetal weights more than 5,000 g
in pregnant women without diabetes and
more than 4,500 g in pregnant women with
diabetes.

(Level III, Grade C)

Suspected fetal macrosomia is not


contraindication to attempted vaginal birth
after a previous cesarean delivery.

(Level III, Grade C)

SHOULDER DYSTOCIA

SHOULDER DYSTOCIA
Recommendations
Risk assessments for the prediction of
shoulder dystocia are insufficiently
predictive to allow prevention of the large
majority of cases.
(Level II, Grade B)

Induction of labor in women with diabetes


mellitus does not reduce the maternal or
neonatal morbidity of shoulder dystocia.
(Level I, Grade A)

Recommendations
Late pregnancy ultrasound likewise displays
low sensitivity, decreasing accuracy with
increasing birth weight, and an overall
tendency to overestimate the birth weight.
(Level II, Grade B)

Fundal pressure should not be employed.

(Level III, Grade C)

Recommendations
Episiotomy is not necessary for all cases,
is reserved to facilitate maneuvers such as
delivery of posterior arm or internal
rotation of shoulders.
(Level III, Grade C)

McRoberts is the single most effective


intervention and should be performed first.

(Level III, Grade C)

Recommendations
Suprapubic pressure is useful
(Level III, Grade C)

Suprapubic pressure can be employed


together with McRoberts maneuver to
improve success rates.

(Level III, Grade C)

Recommendations
Other maneuvers such as Rubins, Woods
screw maneuver, Zavanelli, cleidotomy
and symphysiotomy have been employed
but no controlled trials have been made.

(Level III, Grade C)

Rubin Maneuver

Woods screw maneuver

Zavanelli maneuver

Symphysiotomy

TRANSVERSE LIE/OBLIQUE LIE

TRANSVERSE LIE/OBLIQUE LIE


Recommendation
Transverse lie and oblique lie will benefit
from a trial of version to cephalic
presentation following the criteria and
recommendations of ECV for breech
presentations.

(Level III, Grade C)

COMPOUND PRESENTATION

COMPOUND PRESENTATION
Recommendations
If the hand has not prolapsed beyond the
presenting part, causing the hand to
retract often is accomplished, if necessary.
It can be ignored as long as labor is
progressing normally.

(Level III, Grade C)

COMPOUND PRESENTATION
Recommendations
In contrast, if the hand or arm has
prolapsed past the presenting part,
abdominal vaginal delivery and proceeding
to cesarean delivery is wise.

(Level III, Grade C)

Thank you

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