I am a first-year medical resident in General Medicine. I want an algorithm for how to approach any kind of jaundice, from basic diagnosis of obstruction to complex diagnosis of malignancy or bone marrow failure. Give me an algorithm from the latest guidelines and latest textbooks of medicine, like Harrison and Davidson . Make the notes easy for me to remember and how to approach it in wards and ER. Things should be on my fingertips for easy recognition. How to do a general physical examination of a patient with jaundice what can be the most common possible presenting complaints present in the patient in addition to jaundice and how to approach each case accordingly: what relevant examination to be done to reach a pet differential diagnosis and what history points should be elicited from the patient ..

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"jaundice"[MeSH Terms] AND "diagnosis"[MeSH Terms] AND "algorithm"

I am a first-year medical resident in General Medicine. I want an algorithm for how to approach any kind of jaundice, from basic diagnosis of obstruction to complex diagnosis of malignancy or bone marrow failure. Give me an algorithm from the latest guidelines and latest textbooks of medicine, like Harrison and Davidson . Make the notes easy for me to remember and how to approach it in wards and ER. Things should be on my fingertips for easy recognition. How to do a general physical examination of a patient with jaundice what can be the most common possible presenting complaints present in the patient in addition to jaundice and how to approach each case accordingly: what relevant examination to be done to reach a pet differential diagnosis and what history points should be elicited from the patient .. Searched 1 source Now let me run comprehensive parallel searches across the medical library. Searching... (4/5) Finding Sources show Finding Sources show Finding Sources show Searching PubMed show "jaundice"[MeSH Terms] AND "diagnosis"[MeSH Terms] AND "algorithm" Reading File Excellent findings. Now let me read the key sections from Harrison's 22E and Sleisenger in parallel: Ask Orris

I am a first-year medical resident in General Medicine. I want an algorithm for how to approach any kind of jaundice, from basic diagnosis of obstruction to complex diagnosis of malignancy or bone marrow failure. Give me an algorithm from the latest guidelines and latest textbooks of medicine, like Harrison and Davidson . Make the notes easy for me to remember and how to approach it in wards and ER. Things should be on my fingertips for easy recognition. How to do a general physical examination of a patient with jaundice what can be the most common possible presenting complaints present in the patient in addition to jaundice and how to approach each case accordingly: what relevant examination to be done to reach a pet differential diagnosis and what history points should be elicited from the patient .. The notes should be in the orientation, such as for wards patient treatment and care and also for my FCPS Part 2 exam TOACS section and MRCP exams. What viva questions must be mind , what most common mistake and blunders are made which we should not make

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"jaundice"[MeSH Terms] AND "diagnosis" AND "evaluation"

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PMID: 39823630

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Here is your complete, ward-ready, exam-ready algorithm - sourced directly from Harrison's 22E (2025), Goldman-Cecil Medicine, Sleisenger & Fordtran, Schwartz's Surgery, and the 2025 Am Fam Physician review (Nelson et al., 2025, PMID 39823630).

THE COMPLETE JAUNDICE ALGORITHM

For Ward, ER, FCPS Part 2 TOACS & MRCP


THE MASTER FLOWCHART (Harrison's 22E, Fig. 52-1)

Harrison's Jaundice Diagnostic Flowchart

SECTION 1: THE GOLDEN RULE - FIRST 3 QUESTIONS IN YOUR HEAD

When a jaundiced patient walks in, IMMEDIATELY ask yourself:
1. Is bilirubin elevated alone, or are other LFTs also elevated? 2. Is it conjugated (direct) or unconjugated (indirect)? 3. Is the pattern hepatocellular or cholestatic?
These three questions drive everything. Everything else is detail.

SECTION 2: THE "3 ZONES" CLASSIFICATION - PREHEPATIC / HEPATIC / POSTHEPATIC

Memory Mnemonic: "PRE-HEP-POST" or think of a factory analogy:

  • PRE = Too much raw material (excess bilirubin production)
  • HEP = Factory broken (liver can't process)
  • POST = Pipe blocked (can't export what's made)
FeaturePrehepatic (Pre)Hepatic (Hep)Posthepatic (Post)
Bilirubin typeUnconjugated (indirect)Both (mixed)Conjugated (direct)
Urine colourNormal/paleDarkDark (bilirubinuria)
Stool colourNormalNormal-palePale/clay-coloured
UrobilinogenIncreasedVariableAbsent
PruritusAbsentVariableProminent
Key labRaised indirect bili, anaemia, reticulocytosisRaised ALT/AST >> ALPRaised ALP >> ALT/AST
Typical causeHaemolysis, ineffective erythropoiesisHepatitis, cirrhosisCBD stone, Ca head of pancreas

SECTION 3: HISTORY TAKING - THE STRUCTURED APPROACH

The "DRUG-FAT-SIS" Mnemonic for history:

D - Drugs - ALL medications, herbal, OTC, anabolic steroids, contraceptives, anti-TB drugs (rifampicin, INH, pyrazinamide), statins, paracetamol dose/overdose R - Risk factors for viral hepatitis - IV drug use, tattoos, sexual history, blood transfusion, healthcare worker, travel U - Urine & stool change - Dark urine = conjugated; pale/clay stool = obstruction; ask specifically G - Gallstones/prior surgery - Previous biliary surgery, RUQ pain attacks, prior cholecystectomy
F - Fever + Pain - Fever + RUQ pain + jaundice = Charcot's triad = CHOLANGITIS (emergency) A - Alcohol - Quantify units/week; duration; AST:ALT ratio >2:1 = alcoholic hepatitis T - Travel/tainted food - Travel to endemic area = Hep A/E; raw shellfish; Leptospirosis (Weil's disease)
S - Symptoms suggesting malignancy - Painless jaundice + weight loss + anorexia = Red flag for Ca head of pancreas/cholangiocarcinoma I - Itching (pruritus) - Suggests cholestasis; bile salts deposited in skin S - Systemic/family - Family history of jaundice/liver disease (Wilson's, haemochromatosis, Gilbert's); autoimmune history

Additional HIGH-YIELD History Points:

Symptom clusterThink of
Jaundice after fasting/stress/illness, mild, no other symptomsGilbert's syndrome (most common benign cause)
Young patient, neuropsychiatric + jaundice + Kayser-Fleischer ringsWilson's disease
Jaundice + arthralgia/myalgia BEFORE jaundiceViral hepatitis (prodrome)
Jaundice + sudden severe RUQ pain + rigor + feverCholedocholithiasis + cholangitis
Painless progressive jaundice + weight loss + new-onset diabetesCarcinoma head of pancreas
Jaundice + fatigue + pruritus in middle-aged womanPBC (Primary Biliary Cholangitis)
Jaundice + inflammatory bowel diseasePSC (Primary Sclerosing Cholangitis)
Jaundice in a returning traveller with fever, rigorsMalaria, Hep A/E, Leptospirosis
Jaundice + pallor + splenomegaly, NO hepatomegalyHaemolytic anaemia
Jaundice + pancytopeniaThink bone marrow failure, lymphoma infiltration, leukaemia
Jaundice + right heart failure symptoms, JVD, pulsatile liverCongestive hepatopathy (Budd-Chiari or CCF)
Post-operative jaundiceIschaemic hepatitis, haemolysis, drug reaction, cholestasis

SECTION 4: GENERAL PHYSICAL EXAMINATION - THE STRUCTURED HEAD-TO-TOE APPROACH

STEP 1: GENERAL INSPECTION (look before you touch)

Assess from the foot of the bed:
  • Nutritional state - Temporal wasting, muscle wasting = chronic disease (cirrhosis, malignancy)
  • Depth of jaundice - Mild yellowing (sclera only) vs deep orange-green (chronic obstruction)
  • Consciousness - Encephalopathy? (flapping hands, confusion)
  • Build - Cachexia = malignancy, chronic liver disease

STEP 2: SKIN SIGNS - "Spider Farmer Has Dupuytren And Leuconychia, He Bruises Easily"

SignMeaning
Spider naevi (>5, upper body)Chronic liver disease (CLD)
Palmar erythemaCLD (hyperestrogenism)
Dupuytren's contractureAlcoholic liver disease
Leuconychia (white nails)Hypoalbuminaemia
Terry's nails (white proximal, pink distal)Cirrhosis
Bruising / purpuraCoagulopathy
Scratch marks (excoriations)Cholestasis - pruritus
Xanthelasma / xanthomataPBC, chronic cholestasis
GynaecomastiaCLD (hyperestrogenism)
Testicular atrophyCLD (alcohol)
Parotid enlargementAlcoholic liver disease
Caput medusaePortal hypertension
Kayser-Fleischer rings (slit lamp)Wilson's disease

STEP 3: EYES & FACE

  • Scleral icterus - Best place to detect early jaundice (bilirubin >2.5-3 mg/dL). Look in good daylight, pull down lower lid, compare to healthy person's sclera.
  • Anaemia - Conjunctival pallor (haemolysis, bone marrow failure, chronic disease)
  • Kayser-Fleischer rings - Brown-gold rings at corneal periphery (Wilson's disease - use slit lamp to confirm)
  • Xanthelasma - PBC

STEP 4: HANDS

  • Flapping tremor (asterixis) - hepatic encephalopathy
  • Leuconychia - hypoalbuminaemia
  • Palmar erythema - CLD
  • Clubbing - CLD, IBD (PSC), hepatopulmonary syndrome
  • Dupuytren's - alcoholic liver disease
  • Bruising - coagulopathy

STEP 5: LYMPH NODES - KEY ONES TO FEEL

NodeClinical Significance
Virchow's node (left supraclavicular)Intra-abdominal malignancy (Ca stomach, pancreas, colon)
Sister Mary Joseph's nodule (periumbilical)Intra-abdominal malignancy with peritoneal spread
Generalised lymphadenopathyLymphoma, leukaemia, EBV, CMV

STEP 6: ABDOMINAL EXAMINATION - THE CORE EXAM

Inspection first:
  • Distension = ascites
  • Caput medusae = portal hypertension
  • Surgical scars = prior biliary surgery
Palpation:
FindingClinical Significance
Hepatomegaly - smooth, tenderViral/alcoholic hepatitis, CCF, early cirrhosis
Hepatomegaly - hard, nodularMalignancy (HCC, metastases), cirrhosis (later)
Hepatomegaly - pulsatileTricuspid regurgitation / right heart failure
Splenomegaly + jaundice, NO hepatomegalyHaemolysis, portal hypertension
HepatosplenomegalyPortal hypertension, lymphoma, haematological malignancy
Murphy's sign positiveAcute cholecystitis
Palpable non-tender gallbladder + jaundiceCourvoisier's sign = malignant obstruction (Ca head of pancreas)
Hard, irregular mass RUQMalignancy
AscitesCirrhosis, malignancy, CCF
Courvoisier's Law (HIGH-YIELD EXAM POINT):
"A palpable, non-tender gallbladder in a jaundiced patient suggests malignant obstruction of the common bile duct, NOT gallstones" - because gallstones cause chronic fibrosis and a shrunken non-distensible gallbladder.
Percussion:
  • Dullness in flanks + shifting dullness = ascites
  • Liver dullness span: Normal 8-12 cm in mid-clavicular line. Dullness reduced = small/shrunken liver (late cirrhosis, acute liver failure)

STEP 7: CARDIOVASCULAR

  • JVD + peripheral oedema + jaundice = Congestive hepatopathy (CCF causing hepatic congestion)
  • Right pleural effusion without obvious ascites = advanced cirrhosis (hepatic hydrothorax)

STEP 8: NEUROLOGICAL

  • Asterixis (flapping tremor) = hepatic encephalopathy
  • Confusion, slurring, behavioural change = encephalopathy
  • Kayser-Fleischer rings + neuropsychiatric features = Wilson's disease

SECTION 5: THE INVESTIGATION ALGORITHM - STEP BY STEP

FIRST-LINE INVESTIGATIONS (Order immediately on any jaundiced patient):

Blood tests:
  1. Total bilirubin + fractionation (direct vs indirect)
  2. ALT, AST, ALP, GGT
  3. Albumin, Prothrombin time / INR
  4. Full blood count (CBC)
  5. Blood urea, creatinine, electrolytes
Urine:
  • Urine bilirubin (dipstick) - present = conjugated hyperbilirubinemia (hepatic/posthepatic)
  • Urobilinogen - increased in haemolysis/hepatitis, absent in complete obstruction

INTERPRETING THE PATTERN - THE "ENZYME COMPASS":

HEPATOCELLULAR INJURY             CHOLESTATIC PATTERN
ALT/AST very high (>500 IU)   vs.  ALP very high + ALT/AST mildly raised
Bilirubin raised (mixed)            Bilirubin raised (conjugated)
PT prolonged (doesn't correct       PT may correct with Vit K
with Vit K in severe disease)       (bile needed for Vit K absorption)
Specific patterns:
PatternThink
ALT/AST >1000 IUAcute viral hepatitis, drug-induced (paracetamol), ischaemic hepatitis
AST:ALT ratio >2:1Alcoholic liver disease
ALP very high, ALT/AST mildly elevatedCholestasis, infiltrative disease, bone disease
GGT elevated WITH ALPLiver source confirmed (not bone); also elevated in alcohol
Isolated unconjugated hyperbilirubinemia, normal restGilbert's syndrome
Prolonged PT + low albuminAdvanced/chronic liver disease
PT prolonged + corrects with Vit KObstructive jaundice (malabsorption of fat-soluble vitamins)

SECOND-LINE INVESTIGATIONS (based on pattern):

If hepatocellular pattern:
  1. Hepatitis A IgM, Hepatitis B sAg + core Ab (IgM), Hepatitis C RNA
  2. Toxicology screen, paracetamol level
  3. ANA, ASMA, anti-LKM1 = Autoimmune hepatitis
  4. Ceruloplasmin + 24hr urine copper = Wilson's (in patients <40)
  5. Serum ferritin + transferrin saturation = Haemochromatosis
  6. CMV DNA, EBV capsid antigen, Hepatitis D Ab, Hepatitis E IgM
If cholestatic pattern:
  1. USS abdomen FIRST (cheap, accessible, non-invasive) - look for dilated biliary ducts
  2. If ducts dilated (extrahepatic cholestasis): CT abdomen / MRCP / ERCP
  3. If ducts NOT dilated (intrahepatic cholestasis): AMA (antimitochondrial Ab) for PBC, hepatitis serologies, drug review
  4. AMA positive = PBC - proceed to liver biopsy
  5. AMA negative, no cause found = MRCP or liver biopsy
If isolated unconjugated hyperbilirubinemia:
  • Blood film, reticulocyte count, LDH, haptoglobin, Coombs test = haemolysis screen
  • No haemolysis + otherwise well = Gilbert's syndrome (no further workup needed)
If malignancy suspected:
  • CT chest/abdomen/pelvis with contrast
  • CA 19-9 (pancreatic cancer), AFP (HCC), CEA (colorectal metastases)
  • ERCP/MRCP for biliary obstruction characterisation
  • Biopsy/EUS for tissue diagnosis
If bone marrow failure suspected (pancytopenia + jaundice):
  • Blood film (dysplastic cells, blasts?)
  • Reticulocyte count
  • Bone marrow aspirate + trephine biopsy
  • LFTs pattern (usually hepatic infiltration pattern - raised ALP, mild bilirubin)

SECTION 6: DISEASE-SPECIFIC APPROACH - MATCHING PRESENTATION TO DIAGNOSIS

SCENARIO-BASED QUICK GUIDE FOR WARD ROUNDS:

Young patient, jaundice + fever + arthralgia 2 weeks before:
  • Think viral hepatitis - send Hep serology, ALT/AST pattern
Young patient, exam stress/fasting, mild jaundice, nothing else:
  • Gilbert's syndrome - fractionated bili (indirect up, direct normal), otherwise normal LFTs - REASSURE
Middle-aged alcoholic, tender hepatomegaly, fever, high AST:ALT >2:1:
  • Alcoholic hepatitis - Maddrey's Discriminant Function = 4.6 x (PT patient - PT control) + bilirubin (mg/dL); if >32 = severe, consider steroids
Middle-aged woman, pruritus, fatigue, xanthelasma:
  • PBC - AMA, ALP high, check cholesterol
Young patient, neuropsychiatric + Kayser-Fleischer rings:
  • Wilson's disease - ceruloplasmin, 24hr urine copper, slit-lamp
Elderly patient, painless progressive jaundice + weight loss + new-onset diabetes:
  • Carcinoma head of pancreas - CT triple phase, CA19-9, ERCP/MRCP
RUQ pain + fever + jaundice (Charcot's triad) + hypotension + confusion (Reynolds' pentad):
  • ASCENDING CHOLANGITIS - EMERGENCY - blood cultures, IV antibiotics, urgent ERCP
Jaundice + pallor + no hepatomegaly + splenomegaly + raised reticulocytes:
  • Haemolytic anaemia - blood film, Coombs test, haemoglobin electrophoresis
Jaundice + IBD (UC) + ALP raised + PSC on MRCP:
  • Primary Sclerosing Cholangitis - MRCP (beading of ducts), p-ANCA, colonoscopy
Jaundice + ascites in a young patient after exertion:
  • Think Budd-Chiari syndrome - Doppler USS of hepatic veins (absent flow)

SECTION 7: CLINICAL SIGNS TABLE - "WHAT SIGN POINTS TO WHAT"

Clinical SignDiagnosis to Think Of
Kayser-Fleischer ringsWilson's disease
Xanthelasma + scratch marksPBC, chronic cholestasis
Spider naevi + gynaecomastia + parotid enlargementAlcoholic cirrhosis
Pulsatile hepatomegaly + JVDTricuspid regurgitation, CCF
Hepatomegaly + hard/nodularHCC, metastases, lymphoma
Virchow's nodeGI malignancy
Sister Mary Joseph's nodulePeritoneal malignancy
Courvoisier's signMalignant biliary obstruction
Murphy's signAcute cholecystitis
AsterixisHepatic encephalopathy
Dupuytren's + parotid + spider naeviAlcohol-related CLD
Fever + rigors + RUQ pain + jaundiceCholangitis (Charcot's triad) - EMERGENCY

SECTION 8: VIVA HOT QUESTIONS - FOR FCPS TOACS & MRCP

Q1: What is the first investigation in a jaundiced patient?
Fractionated serum bilirubin (total + direct/indirect) PLUS LFT panel (ALT, AST, ALP, albumin, PT). Also urine for bilirubin and urobilinogen. First imaging = USS abdomen.
Q2: What is Courvoisier's law?
A palpable, non-tender gallbladder in a jaundiced patient suggests malignant obstruction of the bile duct, NOT gallstones. Gallstones cause chronic inflammation and fibrosis of the GB wall, making it unable to distend.
Q3: What is Charcot's triad and why is it an emergency?
Fever + RUQ pain + Jaundice = Ascending cholangitis. Reynolds' pentad adds hypotension + altered consciousness. It is septic shock from biliary sepsis. Requires immediate blood cultures, IV broad-spectrum antibiotics, and urgent biliary decompression (ERCP).
Q4: How do you distinguish obstructive jaundice from parenchymal liver disease on labs?
Obstructive: ALP >> ALT/AST, conjugated bilirubin, PT corrects with Vit K, dilated ducts on USS. Parenchymal: ALT/AST >> ALP, mixed bilirubin, PT may not correct with Vit K, no duct dilation.
Q5: What is Gilbert's syndrome and when do you say "nothing more needed"?
Benign inherited condition, reduced UGT1A1 enzyme activity. Presents with mild isolated unconjugated (indirect) hyperbilirubinemia during fasting, stress, or illness. ALL other LFTs are normal. Blood film normal. No haemolysis. REASSURE - no treatment needed.
Q6: A 25-year-old with jaundice, low ceruloplasmin, Kayser-Fleischer rings - what test confirms Wilson's disease?
24-hour urine copper (>100 mcg/day is diagnostic). Liver biopsy with copper quantification (>250 mcg/g dry weight) is gold standard if uncertain.
Q7: What is the Maddrey Discriminant Function?
Used in alcoholic hepatitis: 4.6 x (PT_patient - PT_control) + serum bilirubin (mg/dL). Score >32 = severe alcoholic hepatitis = consider prednisolone 40 mg/day. Score <32 = conservative management.
Q8: What is the MELD score used for?
Model for End-stage Liver Disease. Used to prioritise liver transplant. = 3.78 x ln[bilirubin mg/dL] + 11.2 x ln[INR] + 9.57 x ln[creatinine mg/dL] + 6.43. Score >15 = consider transplant listing.
Q9: In PBC, what is the diagnostic antibody and what is the treatment?
Anti-mitochondrial antibody (AMA) in >90% cases. Treatment = Ursodeoxycholic acid (UDCA) 13-15 mg/kg/day. If inadequate response: Obeticholic acid.
Q10: When do you do liver biopsy in jaundice?
When etiology remains unclear despite full biochemical and imaging workup. Also for: autoimmune hepatitis confirmation, grading/staging of chronic hepatitis, unexplained cholestasis with non-dilated ducts and negative serology.

SECTION 9: COMMON MISTAKES & BLUNDERS TO AVOID

THE "8 DEADLY SINS" IN JAUNDICE MANAGEMENT:

1. Missing cholangitis (the most dangerous mistake)
  • Mistake: Calling RUQ pain + jaundice "gallstones" and sending home or waiting
  • Correct: Charcot's triad = EMERGENCY. Start IV antibiotics immediately. Arrange urgent ERCP. Do NOT delay.
2. Missing the drug history
  • Mistake: Not asking about herbal medicines, supplements, OTC drugs, recent antibiotics (flucloxacillin causes cholestatic jaundice weeks later), statins, OCP
  • Correct: ALWAYS ask a detailed drug history including herbals and recent changes. Drug-induced liver injury is one of the most commonly missed diagnoses.
3. Reassuring a patient with "painless jaundice + weight loss" without malignancy workup
  • Mistake: Attributing painless jaundice in an elderly patient to Gilbert's or viral hepatitis
  • Correct: Painless progressive jaundice + weight loss = Ca head of pancreas until proven otherwise. Order CT triple phase + CA19-9.
4. Forgetting to check PT/INR in an acutely jaundiced patient
  • Mistake: Only checking bilirubin and transaminases
  • Correct: PT/INR is a marker of SYNTHETIC FUNCTION. A prolonged PT that does NOT correct with Vitamin K = severe parenchymal disease / acute liver failure. This changes management urgently.
5. Giving Vitamin K without checking whether it corrects the PT
  • Mistake: Just giving Vit K without checking effect
  • Correct: Give IV Vit K 10 mg and recheck PT in 24 hours. Correction = obstructive; no correction = liver synthetic failure.
6. Ordering ERCP before USS in a new jaundiced patient
  • Mistake: Jumping to invasive investigation
  • Correct: USS abdomen is ALWAYS the first imaging modality. Cheap, non-invasive, excellent for gallstones and ductal dilation. Reserve ERCP for therapeutic intervention.
7. Not checking blood film and reticulocyte count in unconjugated hyperbilirubinemia
  • Mistake: Treating unconjugated jaundice as Gilbert's without ruling out haemolysis
  • Correct: ALWAYS check blood film + reticulocyte count + LDH + haptoglobin before diagnosing Gilbert's. Haemolysis must be excluded.
8. Forgetting that jaundice in cirrhosis may not be from the liver
  • Mistake: Assuming new jaundice in a known cirrhotic = disease progression
  • Correct: Known cirrhotic + new/worsening jaundice = rule out superimposed cause: hepatocellular carcinoma (AFP, triphasic CT), spontaneous bacterial peritonitis, portal vein thrombosis, drug hepatotoxicity, or superimposed viral hepatitis.

SECTION 10: THE EMERGENCY ER APPROACH - WITHIN THE FIRST 30 MINUTES

IMMEDIATE TRIAGE CHECKLIST:

RED FLAGS = Admit and act NOW:
  • Fever >38.5°C + jaundice + RUQ pain = Cholangitis - IV Abx NOW
  • Altered consciousness + jaundice = Hepatic encephalopathy / Acute Liver Failure - ICU consideration
  • Hypotension + jaundice = Septic shock (cholangitis), Acute Liver Failure, or Haemolytic crisis
  • Deep jaundice + prolonged PT not correcting with Vit K = Acute Liver Failure - liver transplant team contact
  • Massive haemolysis + severe anaemia = transfusion support needed
ER Immediate Orders on a Jaundiced Patient:
  1. IV access - take bloods at the same time: FBC, LFTs, PT/INR, renal function, blood cultures (if febrile)
  2. Fractionated bilirubin + full LFT panel
  3. Urine dipstick: bilirubin + urobilinogen
  4. USS abdomen - same day if possible
  5. Fluids if dehydrated/hypotensive
  6. IV Vitamin K 10 mg if coagulopathic
  7. Lactulose + protein restriction if encephalopathy
  8. IV broad-spectrum antibiotics (e.g., piperacillin-tazobactam or ceftriaxone + metronidazole) if cholangitis suspected

SECTION 11: WARD MANAGEMENT ORIENTATION - THE DAILY CHECKLIST

Every day on rounds for your jaundiced patient, assess:
  • Bilirubin trend (rising/falling?)
  • PT/INR trend - falling = recovery; rising = deterioration
  • Albumin - marker of synthetic function
  • Encephalopathy grade (West Haven criteria: Grade 1-4)
  • Urine output (hepatorenal syndrome risk in advanced disease)
  • Any new fever/rigors (secondary infection, cholangitis)
  • Medications - stop ALL hepatotoxic drugs
  • Nutrition - high carbohydrate, moderate protein, avoid alcohol
Grades of Hepatic Encephalopathy (West Haven):
GradeFeatures
1Trivial confusion, altered sleep
2Asterixis, moderate confusion
3Marked confusion, somnolence, incoherence
4Coma

QUICK-REFERENCE SUMMARY CARD (Laminate this for your coat pocket)

JAUNDICE FIRST 3 QUESTIONS:
1. Isolated bili rise OR other LFTs too?
2. Conjugated (direct) or Unconjugated (indirect)?
3. Hepatocellular (ALT>ALP) or Cholestatic (ALP>ALT)?

URINE DARK + STOOLS PALE = Conjugated = Obstruction
URINE NORMAL + PALLOR + SPLENOMEGALY = Haemolysis

ALARMS:
- Fever + RUQ pain + jaundice = CHOLANGITIS (emergency)
- Painless jaundice + weight loss = MALIGNANCY
- Altered consciousness + jaundice = LIVER FAILURE

COURVOISIER'S LAW:
Palpable non-tender GB + jaundice = MALIGNANT obstruction

KEY DRUG HISTORY: Herbals, OCP, anti-TB, statins, paracetamol

INVESTIGATIONS ORDER:
1. FBC + LFTs + PT/INR
2. Fractionated bilirubin
3. USS abdomen
4. Then targeted: serology / MRCP / CT / Biopsy

Sources: Harrison's Principles of Internal Medicine 22E (2025) Ch. 52; Goldman-Cecil Medicine (2023) Ch. 133; Sleisenger & Fordtran's GI & Liver Disease, Ch. 21; Schwartz's Principles of Surgery 11th Ed., Ch. 30; Nelson M et al. Evaluation of Jaundice in Adults. Am Fam Physician. 2025; Pavlovic Markovic A et al. Jaundice as a Diagnostic and Therapeutic Problem. Dig Dis. 2022.
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