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==Treatment==
==Treatment==
Shown below is an algorithm summarizing the treatment of <nowiki>Jaundice</nowiki> according the the [...] guidelines.
Based on the liver function tests and CBC,patients with Jaundice will typically fall into one of 3 categories.<ref name="pmid15684121">{{cite journal |vauthors=Giannini EG, Testa R, Savarino V |title=Liver enzyme alteration: a guide for clinicians |journal=CMAJ |volume=172 |issue=3 |pages=367–79 |date=February 2005 |pmid=15684121 |pmc=545762 |doi=10.1503/cmaj.1040752 |url=}}</ref>
{{familytree/start |summary=PE diagnosis Algorithm.}}
{{familytree/start |summary=PE diagnosis Algorithm.}}
{{familytree | | | | | | | |A01| | |A01= ''' Jaundice''' }}  
{{familytree | | | | | | | |A01| | |A01= ''' Jaundice''' }}  
Line 139: Line 139:
{{familytree | | | | | | G01 | | G02 | | | | | | G03 | | G04 | |G01=Preoperative biliary decompression (ERCP or PTC)<br>Cholecystectomy<br>endoscopic stenting,surgery<br>excision of cyst |I02=If resecteable, consult surgery<br> If unresectable<br> Pallative therapy,biliary decompression ||G02=If resectable,fit for surgery<br>If unresecatable,pallative therapy |G03=Compensated Cirrhosis Mangament<br>Alochol abstinence<br> Antiviral medications for viral hepatitis<br> avoidance of hepatotoxic medications<br>vaccination|G04=Decompensated Cirrhosis Managment(with complications)<br>Managment of complications:<br>Varices,Asciets,Hepatorenal syndrome,Hepatic encephalopathy }}
{{familytree | | | | | | G01 | | G02 | | | | | | G03 | | G04 | |G01=Preoperative biliary decompression (ERCP or PTC)<br>Cholecystectomy<br>endoscopic stenting,surgery<br>excision of cyst |I02=If resecteable, consult surgery<br> If unresectable<br> Pallative therapy,biliary decompression ||G02=If resectable,fit for surgery<br>If unresecatable,pallative therapy |G03=Compensated Cirrhosis Mangament<br>Alochol abstinence<br> Antiviral medications for viral hepatitis<br> avoidance of hepatotoxic medications<br>vaccination|G04=Decompensated Cirrhosis Managment(with complications)<br>Managment of complications:<br>Varices,Asciets,Hepatorenal syndrome,Hepatic encephalopathy }}
{{familytree/end}}
{{familytree/end}}


==Do's==
==Do's==

Revision as of 23:11, 15 August 2020

Jaundice
Resident Survival Guide
Overview
Causes
Diagnosis
Treatment
Do's
Don'ts


Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:

Synonyms and keywords:

Overview

The classic definition of Jaundice is a serum bilirubin level higher than 2.5 to 3 mg per dL (42.8 to 51.3 μper L) in conjunction with a clinical picture of yellow skin and sclera. Bilirubin metabolism takes place in three phases; "prehepatic", "intrahepatic", and "posthepatic". The causes of jaundice can be classified under these categories by measuring total bilirubin and its conjugated and unconjugated levels determine where is the dysfunction of bilirubin metabolism.

Causes

Life Threatening Causes

Life-threatening causes include conditions that may result in death or permanent disability within 24 hours if left untreated.

Common Causes

of acute Jaundice[2]

of chronic progressive Jaundice

Diagnosis

Shown below is an algorithm summarizing the diagnosis of [[disease name]] according the the [...] guidelines.

 
 
 
 
 
 
 
 
 
 
 
 
 
Characterize the jaundice duration and frequency
❑ Duration: short versus long
❑ Frequency: episodic vesus constant
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Ask about assoaciated symptoms

Abdominal pain (episodic or constant)
Abdominal distension
Fever
❑ Clay colored stool
❑ Dark urine
Weight gain or loss
Anorexia
Dyspepsia
Arthralgia
Myalgia
Back pain
❑ Rash
Confusion
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Inquire about

❑ Past medical history
Blood disorder
Liver diseases
biliary diseases
Pancreatic disease
Cardiac disease
Infectious disease
HIV
Malaria
❑ Etc

❑ Family history of

Hemolytic anemias
Congenital hyperbilirubinemia
Wilson disease

Medication history
Parentral exposure

Blood transfusion
Iv drug abuse

❑ Recent travel history
❑ Social history

❑ Excess alcohol intake
❑ Sexual history
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Examine the patient

General Appearance
❑ Check for:
Pale skin (hemolysis/cancer/cirrhosis)
❑ Gross weight loss (cancer/severe malabsorption)
❑ Fetor hepaticus
❑ Flapping tremor (impending hepatic coma)

Skin exam
❑ Check for:

❑ Scratch marks
❑ Melanin pigmentation
Xanthoma of eyelids (chronic cholestasis)
❑ Signs of liver disease: spider nevi, palmar erythema
❑ Bruising, purpuric spots, clotting defects due to thrombocytopenia of cirrhosis

Cariac exam
❑ Check JVP (right sided heart failure)
full abdominal exam
❑ Size and consistency of liver and spleen

❑ A grossly enlarged nodular liver or an obvious abdominal mass suggests malignancy
❑ Small liver can be seen in (severe hepatitis/cirrhosis)
❑ An enlarged tender liver could be due to:
❑ Viral hepatitis
❑ Alcoholic hepatitis
❑ An infiltrative process such as amyloidosis
❑ Acutely congested liver secondary to right-sided heart failure)

❑ Check gall bladder area if it is tender

❑ Positive murphy sign due to choledocholithiasis
❑ Palpable, visibly enlarged GB can be due to pancreatic ca

❑ Splenomegaly can be seen in hemolytic states, hodgkin’s, portal hypertension
❑ Ascites due to cirrhosis/ abdominal malignancy
caput medosa
Extremity examination

❑ Ankle edema due to cirrhosis/IVC obstruction due to hepatic or pancreatic malignancy
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Order

❑ Blood tests
CBC
❑ Total Bilirubin
❑ Conjugated or unconjugated bilirubin
❑ Metabolic panel
LFT
INR

Urine

Bilirubin
Urobilinogen
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Isolated conjugated billirubin
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
H01
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
H03
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Treatment

Based on the liver function tests and CBC,patients with Jaundice will typically fall into one of 3 categories.[1]

 
 
 
 
 
 
 
Jaundice
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Managment of isolated unconjugated hyperbilirubinemia

If no eveidence of hemolytic anemia consider
Gilbert syndrome
OR
Crigler-Najjar type I, II
 Work-up and detect the cause of hemolysis, if low Hb,High LDH,Low haptoglobulin, and reticulocytes present
 G6PD deficiency - mostly recover on its own,if progresses to hemolytic anaemia, oxygen therapy or blood transfusion may be required.Avoid of precipitants and etiological factors
 Spherocytosis ,phototherapy and/or exchange transfusion for infants, Folic acid for maaintaing erythropoiesis.Splenectomy is the definitive treatment
 Sickle cell anemia reduce pain and prevent complications, blood transfusions and supplemental oxygen, as well as a bone marrow transplant.
 Immune related hemolysis – corticosteroids, folic acid is main line of treatment
 Parasitic Infections like malaria are treated with antimalarial drugs like chloroquine, artesunate, lumefantrine,amodiaquine
 Ineffective erythropoiesis- iron and folic acid & B12 supplementation, repeated blood transfusions
 
Managment of isolated conjugated hyperbilirubinemia
 
Unconjugated & Conjugated hyperbilirubinemia managment
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Hepatocellular pattern,⇈AST/ALT out of proportion to ALK-P

Treatment depends on causes
 Hepatitis A :mostly self limiting
 Hepatitis B treated with antiviral medications
 Hepatitis C is treated with interferons
Other Viral infections like EBV, CMV, HSV are treated with Antiviral medications
Alcohl hepatitis: Alcohol abstinence,glucocorticoids, pentoxifylline
 Wilson"s disease:chelating agents such as D-penicillamine
 Managmenof Acute liver failure
 Drug toxicity treatment(e.g. Acteaminophen, Isoniazid
Primary biliary cholangitis management
 Auroimmune hepatitis
 enviromental toxin:kavakava
 
 
Cholestatic pattern managment,⇈ Alk-P out of proportion to AST/ALT,predominantly conjugated
 
 
 
 
 
Managment of cirrhosis,Predominantly conjugated,↑ INR,↓ Alb,↓ PLt
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Dilated Bile ducts
 
Non-dilated Bile ducts
 
 
 
MELD Score
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Consider Intrahepatic injury
 
>15
 
<15
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
CBD stones
Stricture/choldochal cyst
 
Solid mass(Extrahepatic)
 
 
 
Consider reffering patient to a transplant center
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Preoperative biliary decompression (ERCP or PTC)
Cholecystectomy
endoscopic stenting,surgery
excision of cyst
 
If resectable,fit for surgery
If unresecatable,pallative therapy
 
 
 
 
 
Compensated Cirrhosis Mangament
Alochol abstinence
Antiviral medications for viral hepatitis
avoidance of hepatotoxic medications
vaccination
 
Decompensated Cirrhosis Managment(with complications)
Managment of complications:
Varices,Asciets,Hepatorenal syndrome,Hepatic encephalopathy
 

Do's

  • The content in this section is in bullet points.

Don'ts

  • The content in this section is in bullet points.


References

  1. Giannini EG, Testa R, Savarino V (February 2005). "Liver enzyme alteration: a guide for clinicians". CMAJ. 172 (3): 367–79. doi:10.1503/cmaj.1040752. PMC 545762. PMID 15684121.