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Hepatology
Infectious Diseases
Gastroenterology
Travel Medicine

Hepatitis A

High EvidenceUpdated: 2025-12-22

On This Page

Red Flags

  • Acute liver failure (encephalopathy, coagulopathy)
  • Fulminant hepatitis
  • Prolonged cholestasis (>3 months)
Overview

Hepatitis A

1. Clinical Overview

Summary

Hepatitis A is an acute, self-limiting viral hepatitis caused by the Hepatitis A Virus (HAV), a non-enveloped RNA virus. It is transmitted via the faecal-oral route, typically through contaminated water, food (especially shellfish), or close contact. Unlike hepatitis B and C, hepatitis A does NOT cause chronic infection. Most cases are mild and self-limiting, particularly in children. Symptomatic infection is more common and more severe in adults. Diagnosis is confirmed by IgM anti-HAV antibody. Treatment is supportive. Vaccination is highly effective for prevention and is recommended for travellers to endemic areas.

Key Facts

  • Virus: Hepatitis A Virus (HAV) - RNA picornavirus
  • Transmission: Faecal-oral (contaminated food/water, shellfish, close contact)
  • Chronicity: NEVER chronic - always acute, self-limiting
  • Incubation: 15-50 days (average 28 days)
  • Diagnosis: IgM anti-HAV (acute); IgG anti-HAV (past infection/immunity)
  • Treatment: Supportive (no specific antiviral)
  • Prevention: Highly effective vaccine

Clinical Pearls

"Hepatitis A = Acute Only": Unlike Hep B and C, Hepatitis A NEVER causes chronic infection. One episode confers lifelong immunity.

"Sicker Adults, Mild Kids": Children often have asymptomatic or mild infection. Adults are more likely to have icteric hepatitis and take longer to recover.

"Shellfish and Travellers": Classic epidemiological clues - ask about recent travel to endemic regions and raw shellfish consumption.

"Fulminant Hepatitis is Rare": <0.5% develop acute liver failure, but risk increases with age and pre-existing liver disease.


2. Epidemiology

Global Burden

  • 1.4 million cases annually worldwide
  • Highly endemic in developing countries
  • Low endemicity in developed countries

Demographics

  • All ages; severity increases with age
  • Equal M:F
  • High seroprevalence in endemic regions (>90% by adulthood)

Risk Factors

FactorMechanism
Travel to endemic areasAfrica, Asia, Central/South America
Contaminated food/waterPoor sanitation
Shellfish consumptionFilter feeders concentrate virus
MSMClose contact transmission
IVDUShared needles (rare)
Close contacts of casesHousehold transmission
Childcare workersFaecal-oral in nurseries

UK Context

  • Rare (imported cases, outbreaks)
  • Travel-related or MSM outbreaks

3. Pathophysiology

Virology

  • Hepatitis A Virus (HAV)
  • Picornaviridae family
  • Non-enveloped RNA virus
  • Single serotype (only one genotype clinically relevant)

Transmission

  • Faecal-oral route
  • Contaminated water, food (raw shellfish), person-to-person
  • Viral shedding peaks 2 weeks before symptoms onset

Pathogenesis

  1. Ingestion of contaminated food/water
  2. Intestinal uptake → Viraemia
  3. Hepatocyte infection → Viral replication
  4. Immune response → Hepatocyte destruction (T-cell mediated)
  5. Recovery → Viral clearance, lifelong immunity

Why Self-Limiting?

  • Robust immune response clears virus
  • No viral integration into host DNA
  • No persistence mechanism

4. Clinical Presentation

Phases

PhaseDurationFeatures
Incubation15-50 daysAsymptomatic
Prodrome1-7 daysFlu-like: Fever, malaise, fatigue, anorexia, nausea
Icteric phase2-4 weeksJaundice, dark urine, pale stools, RUQ discomfort
ConvalescenceWeeks-monthsGradual recovery

Symptoms

FeatureFrequency
Fatigue/malaise80%+
Nausea/vomiting70%
Anorexia70%
Abdominal pain (RUQ)60%
Jaundice70% adults, <10% children
Fever60%
Dark urine80%
Pale stools50%

Age-Related Severity


Children <6
Usually asymptomatic (70%)
Older children/adults
More likely icteric and symptomatic
Elderly/chronic liver disease
Higher risk of severe/fulminant disease
5. Clinical Examination

General

  • Jaundice (scleral icterus, skin)
  • Mild fever
  • Dehydration (if vomiting)

Abdominal

  • Hepatomegaly (tender)
  • RUQ tenderness
  • Splenomegaly (occasionally)
  • No ascites (acute infection)

Signs of Severe Disease

  • Encephalopathy (confusion, asterixis)
  • Coagulopathy (bruising, bleeding)
  • Signs of hepatic decompensation

6. Investigations

First-Line Tests

TestFinding
IgM anti-HAVPositive = Acute infection (diagnostic)
IgG anti-HAVPositive = Past infection or vaccination (immunity)
LFTsALT/AST markedly elevated (>000); Bilirubin elevated
FBCUsually normal; mild lymphocytosis
CoagulationINR usually normal; elevated = severe

Serology Interpretation

IgMIgGInterpretation
+-Acute infection
++Acute infection (recent)
-+Past infection or vaccination (immune)
--Susceptible

Additional Tests

  • Ultrasound abdomen: Exclude biliary obstruction, assess liver
  • Blood glucose: Hypoglycaemia in liver failure

7. Management

Supportive Care

┌──────────────────────────────────────────────────────────┐
│   HEPATITIS A MANAGEMENT                                 │
├──────────────────────────────────────────────────────────┤
│                                                          │
│  MOST CASES: SUPPORTIVE CARE (Outpatient)                │
│  • Rest                                                  │
│  • Adequate hydration                                    │
│  • Antiemetics (if needed)                               │
│  • Avoid alcohol (hepatotoxic)                           │
│  • Avoid paracetamol if liver severely affected          │
│  • No specific antiviral therapy                         │
│                                                          │
│  MONITORING:                                              │
│  • Check LFTs weekly until improving                     │
│  • INR if severe symptoms                                │
│  • Warn about signs of deterioration                     │
│                                                          │
│  ADMISSION CRITERIA:                                      │
│  • Unable to tolerate oral fluids                        │
│  • INR &gt;1.5 or encephalopathy (fulminant hepatitis)      │
│  • Elderly or pre-existing liver disease                 │
│                                                          │
│  FULMINANT HEPATITIS (RARE):                              │
│  • Liver transplant centre referral                      │
│  • ICU care, N-acetylcysteine, transplant evaluation     │
│                                                          │
└──────────────────────────────────────────────────────────┘

Public Health

  • Notifiable disease in UK
  • Contact tracing
  • Vaccination/immunoglobulin for close contacts within 14 days
  • Hygiene advice (handwashing, food safety)

Return to Work

  • Exclude food handlers for 7 days after jaundice onset
  • Children: Exclude from school/nursery for 7 days after jaundice

8. Complications

Rare Complications

  • Fulminant hepatitis/acute liver failure (<0.5%)
  • Prolonged cholestasis (>3 months)
  • Relapsing hepatitis (10-15%)
  • Post-hepatitic syndrome (prolonged fatigue)

Risk Factors for Severe Disease

  • Age >50
  • Pre-existing chronic liver disease (especially Hep B/C)
  • Immunosuppression

No Chronic Sequelae

  • No chronic hepatitis, cirrhosis, or hepatocellular carcinoma

9. Prognosis & Outcomes

Natural History

  • Self-limiting in >99% of cases
  • Complete recovery expected
  • No chronic carrier state

Recovery Timeline

  • Symptoms resolve: 2-6 weeks
  • LFTs normalise: 2-3 months
  • Full recovery: 3-6 months (adults may take longer)

Mortality

  • Overall: <0.3%
  • Age >50 or chronic liver disease: Up to 1-2%
  • Fulminant hepatitis: High mortality without transplant

10. Evidence & Guidelines

Key Guidelines

  1. EASL: Hepatitis A Guidelines
  2. Green Book: Immunisation Against Infectious Disease (UK)
  3. CDC: Hepatitis A Prevention

Key Evidence

Vaccination

  • Highly effective (95%+ protection after 2 doses)
  • Long-lasting immunity (possibly lifelong)

Post-Exposure Prophylaxis

  • Vaccine effective if given within 14 days of exposure
  • Immunoglobulin for immunocompromised or >40 years

11. Patient/Layperson Explanation

What is Hepatitis A?

Hepatitis A is a liver infection caused by a virus. It's spread by eating or drinking something contaminated with the virus, often from poor sanitation or raw shellfish. It causes a short illness and then gets better completely - unlike some other types of hepatitis, it does NOT cause long-term liver damage.

What Are the Symptoms?

  • Feeling tired and unwell
  • Loss of appetite, nausea
  • Stomach ache (right side)
  • Yellowing of the skin and eyes (jaundice)
  • Dark urine, pale poo

Is it Serious?

For most people, hepatitis A is mild and you recover fully within a few weeks to months. Very rarely, it can cause serious liver problems, especially in older people or those with existing liver disease.

How is it Treated?

There's no specific medicine - your body fights off the virus on its own. Treatment is rest, fluids, and avoiding alcohol. Most people recover at home.

How Can I Prevent It?

  • Wash hands thoroughly after using the toilet and before eating
  • Avoid raw/undercooked shellfish in high-risk areas
  • Get vaccinated before travelling to endemic countries
  • Drink bottled or boiled water in high-risk areas

Is There a Vaccine?

Yes! The hepatitis A vaccine is very effective. It's recommended for travellers to Africa, Asia, South America, and other high-risk regions.


12. References

Primary Guidelines

  1. European Association for the Study of the Liver. EASL Clinical Practice Guidelines on Hepatitis A.
  2. Public Health England. Immunisation Against Infectious Disease (Green Book). Chapter 17: Hepatitis A.

Key Studies

  1. Jacobsen KH, Wiersma ST. Hepatitis A virus seroprevalence by age and world region, 1990 and 2005. Vaccine. 2010;28(41):6653-6657. PMID: 20723630
  2. Fiore AE. Hepatitis A transmitted by food. Clin Infect Dis. 2004;38(5):705-715. PMID: 14986256

Last updated: 2025-12-22

At a Glance

EvidenceHigh
Last Updated2025-12-22

Red Flags

  • Acute liver failure (encephalopathy, coagulopathy)
  • Fulminant hepatitis
  • Prolonged cholestasis (&gt;3 months)

Clinical Pearls

  • **"Hepatitis A = Acute Only"**: Unlike Hep B and C, Hepatitis A NEVER causes chronic infection. One episode confers lifelong immunity.
  • **"Sicker Adults, Mild Kids"**: Children often have asymptomatic or mild infection. Adults are more likely to have icteric hepatitis and take longer to recover.
  • **"Shellfish and Travellers"**: Classic epidemiological clues - ask about recent travel to endemic regions and raw shellfish consumption.
  • **"Fulminant Hepatitis is Rare"**: &lt;0.5% develop acute liver failure, but risk increases with age and pre-existing liver disease.

Guidelines

  • NICE Guidelines
  • BTS Guidelines
  • RCUK Guidelines