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ENCEPHALOPATHY
DISORDER OF CEREBRAL
FUNCTION ==> Inflammation (-)
DIGESTIVE TRACT
1. Hepatic Encephalopathy
2. Kernicterus
3. Reye Syndrome
4. Dehydration +disorder of consciousness
5. Hypo/hypernatremia
severe hypophosphatemia
GE + SEVERE DEHYDRATION
CIRCULATORY DISTURBANCES
OXYGENATION
CONSCIOUSNESS
GE+SEVERE DEHYDRATION+ENCEPHALOPATHY
COMA SHOCK
P
< 1 mg %
Energy
Dysfunction of
leucocytes &
thrombocytes
RBC
O2 delivery
Cerebral Anoxia
Rhabdomyolisis
KERNICTERUS
= BILIRUBIN ENCEPHALOPATHY
Unconsciousness
Spasme
Convulsion
Mortality 75%
Recovery - Blind
- Deafness
- Neuromusc. Incoord.
(chorea athetosis)
Th
HEPATIC ENCEPHALOPATHY
= LIVER FAILURE
= HEPATOCELLULER FAILURE
= HEPATOCYTIC FAILURE
= GAGAL HATI
HEPATIC COMA
PORTO SYSTEMIC ENCEPH
FULMINANT 2 WEEKS
SUBFULMINANT 2-8 WEEKS
CONFUSED
II.
DROWSY
III.
STUPOROUS
IV.
- COMA
- DEEP COMA
HEPATIC COMA
Systemic
t
a
p
He
.
V
ic
Inferior v. cava
liver
portal v.
t
gu
LIVER FAILURE
ENCEPHALOPATHY
COAGULOPATHY
HALLMARK
DYSFUNCTION
INTRAHEPATIC
METABOLISM
THERAPY :
1. VENTILATION
2. WATER & ELECTROLYTES
3. COAGULOPATHY:
- Vitamin K
- Transfusion : Fresh Frozen Plasma
4. BLOOD AMMONIA (NH3) :
- lactulose
- neomycine Nephrotoxic
5. REDUCING INTRACRANIAL PRESSURE :
- cerebral edem : steroid, mannitol, etc.
- hypokarbia Cerebral Blood Flow
6. MONITORED CLOSELY FOR INFECTION
7. HEPATOTOXIC DRUGS WITHDRAWN :
- eg : Sedative
ENCEPHALOPATHY
REYE SYNDROME
FATTY DEGENERATION
BLOOD NH3
Mitochondrial dysfunction
HYPOGLYCEMIA
ACUTE
SALICYLIC ACID
Th
5. COAGULOPATHY IS MANAGED
6. EXCHANGE TRANSFUSION
GASTROINTESTINAL
HEMORRHAGE
Atan Baas Sinuhaji
Department of ChildHealth
School of Medicine,University Of Sumatera Utara
Medan
GI BLEEDING
GUT
OUT
- BLOOD DISORDERS :
LEUKEMIA
IN
BLOOD PER OS
- SYSTEMIC
- RUPTURE OF THE
AORTA
HEMATEMESIS
BLOOD PER
ANUM
HEMATEMESIS
DIGESTIVE
TRACT
INGESTION
INFANTS
-NIPPLES
-HEMORRHAGIC DISEASE
CHILDREN
EPISTAXIS
OF THE NEWBORN
-INGESTION OFMATERNAL BLOOD
(MATERNAL SWALLOWED BLOOD
SYNDR.)
- MUCOSAL LESION
- VARICEAL BLEEDING
NEW BORN
Hb F
50-90 %
ALKALI RESISTENT
Hb A
Hb A2
HEMATEMESIS
MUCOSAL LESION PORTAL HYPERTENSION
PEPTIC
ULCER
ESOPHAGEAL
VARICES
GASTRITIS
DRUGS
- SALICYLIC ACID
PEPTIC ULCER
PROLONGED
EXCESS ACID
BREAKDOWN IN
BARRIER
INFECTION
H. PYLORI
ACETYLCHOLINE
PROSTAGLANDIN
ZOLLINGER ELLISON
SYNDR. NON B ISLET
CELL
HISTAMIN
GASTRIN
MUSCARINIC
RECEPTOR
H2 RECEPTOR
(-)
ADENYLCYCLASE
c AMP
PROTEINKINASE
Na K ATP ase
HCL
GASTRIN
RECEPTOR
TREATMENT
1. MUCOSAL PROTECTION
SUCRALFATE
2. ACID SECRETION
3. NEUTRALIZED ACID
ANTACIDE
4. ERADICATION OF H. PYLORI
- AMOXICILLIN 50 mg/Kg/day
- CLARITHROMYCIN 15 mg/Kg/day
- OMEPRAZOLE 1 mg/Kg/day
2 WEEKS
ACID SECRETION
1. H2 RECEPTOR BLOCKER : CIMETIDINE
RANITIDINE
2. PROTON PUMP INHIBITOR :
OMEPRASOLE
3. PROSTAGLANDIN SYNTHETASE:
MISOPROSTOL
4. ANTICHOLINERGIC : PIRENZEPINE
INFECTION OF H. PYLORI
1. INVASIVE
=TISSUE
MICROSCOPIC
CULTURE
UREA TEST
=BLOOD : IgG
2. NONINVASIVE
-UREA BREATH TEST
-STOOL-BASED TEST
=H.pylori Ag
=H.pylori DNA
OCCULT
HEMOCCULT TEST
OVERT
MELENA
HEMATOCHEZIA
Materials
Heme protein
Hydrogen peroxidase
Colorless guaiac
Blue quinone
25
HEMATOCHEZIA
WITH
DIARRHOEA
WITHOUT
DIARRHOEA
DYSENTERY
- ANAL FISSURE
SYNDROME
- RECTAL POLYP
WITHOUT
STOOLS
INVAGINATION