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Jaundice Algorithm
Jaundice Algorithm
Jaundice Algorithm
Hyperbilirubinemia
B1>B2
B1<B2
Hepatocellular/
Cholecysta:c
Pre-hepa:c
Cholecysta:c
Congenital
defect
Hemolysis
Hepatocellular
Check
present
Gilberts
syndrome
Consider
RBC:
B-thalassemia
Sickle
cell
disease
Hereditary
spherocytosis
G6PD
deciency
Hypersplenism
Autoimmune
hepa::s
ABO
incompa:bility
WBC:
Malaria
absent
Consider:
drug
toxicity
hematoma
present
Crigler-Najan
syndrome
Extrahepa:c Cholestasis
Recheck
ALT/AST
Elevated,
<300UI
Consider
AST:ALT>2
Check
Chronic
Hepatocellular
disease
Pa:ent
History
Age
Sexual
Ac:vity
Medica:ons
(Drug-induced
liver
damage)
Serologic
Markers
IgMAn:-HAV
(Hepa::s
A)
HbsAg
and
IgM
An:-HBV
(Hepa::s
B)
An:-HCV
(Hepa::s
C)
SMA
ANA
(Autoimmune
disease)
Ceruloplasmin
(Wilsons
disease)
Intrahepa:c Cholestasis
Acute
Hepatocellular
disease
absent
Check
Alcoholic
liver
diseases/Cirrhosis
Check
Alcohol
intake
(alcoholic
liver
disease)
-an:
trypsin
(cirrhosis)
Malignant
Cholangiocarcinoma
Pancrea:c
cancer
Gallbladder
cancer
Ampullary
cancer
Malignant
involvement
of
the
porta
hepa:s
lymph
nodes
Benign
Choledolithiasis
Post-op
biliary
structures
Primary
sclerosing
cholangi:s
Chronic
pancrea::s
AIDS
cholangiopathy
Mirfzzis
syndrome
Parasi:c
disease
(ascariasis)
Serologic
tes:ng
AMA
Hepa::s
serologies
Hepa::s
A,
CMV,
EBV
Drugs
Results
posi:ve
Results nega:ve
MRCP
Liver
biopsy
Liver biopsy
Consider
Viral
hepa::s
Alcoholic
hepa::s
Drug
toxicity
Chloropromazine
Erythromycin
estolate
Prochloroperazine
Primary
biliary
cirrhosis
Primary
sclerosing
cholangi:s
Vanished
bile
duct
syndrome
Inherited
Cholestasis
of
pregnancy
Total
parenteral
nutri:on
Non-hepatobiliary
sepsis
Benign
post-opera:ve
cholestasis
Paraneoplas:c
syndrome
Veno-occlusive
disease
Grae-vs-host
disease
Inltra:ve
disease
Infec:ons
Malaria
Leptospirosis
(serological
assays
MAT
and
ELISA)