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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 HEPATOTOXIC DRUGS WITHDRAWN :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
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
TH/
1. MUCOSAL PROTECTION
SUCRALFATE
2. ACID SECRETION
3. NEUTRALIZED ACID
ANTACIDE
4. ERADICATION OF H. PYLORI
- METRONIDAZOLE
- CLARITHROMYCIN
- OMEPRAZOLE
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
2. NONINVASIVE
-UREA BREATH TEST
-SEROLOGY : IgG
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