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Hepatitis B

Last reviewed: 21 Nov 2024
Last updated: 11 Dec 2024
03 Sep 2024

WHO publishes new guidelines on hepatitis B

The World Health Organization (WHO) has published new guidelines on the prevention, diagnosis, and treatment of hepatitis B virus (HBV) infection. The guidelines simplify and expand eligibility for treatment in order to overcome barriers to accessing testing and treatment.

The guidelines provide new and updated evidence-based recommendations on key priority topics from three previous guidelines, including:

  • Expanded eligibility for antiviral treatment and inclusion of adolescents

  • Expanded eligibility for antiviral prophylaxis among pregnant women to prevent mother-to-child transmission

  • Improving diagnostics through use of point-of-care assays and reflex testing and testing for hepatitis D coinfection

New recommendations on who to treat have been included. The WHO recommends initiating antiviral therapy in all adults (including pregnant women) and adolescents with:

  • Evidence of significant fibrosis or cirrhosis; or

  • Hepatitis B virus (HBV) DNA levels >2000 IU/mL and an alanine aminotransferase (ALT) level above the upper limit of normal; or

  • Presence of coinfections, family history of liver cancer or cirrhosis, immunosuppression, comorbidities, or extrahepatic manifestations; or

  • Persistently abnormal ALT levels (in the absence of access to an HBV DNA assay)

More than 250 million people live with chronic hepatitis B infection. Most of the global burden of disease is due to mother-to-child transmission at, or shortly after, birth.

See Management: approach

Original source of update

Summary

Definition

History and exam

Key diagnostic factors

  • high risk of exposure
Full details

Other diagnostic factors

  • asymptomatic
  • jaundice
  • hepatomegaly
  • ascites
  • fever/chills
  • malaise
  • maculopapular or urticarial rash
  • right upper quadrant pain
  • fatigue
  • nausea/vomiting
  • arthralgia/arthritis
  • palmar erythema
  • spider angiomata
  • splenomegaly
  • asterixis
Full details

Risk factors

  • perinatal exposure in an infant born to an HBV-infected mother
  • high-risk sexual behaviors
  • injection drug use
  • male sex
  • born in highly endemic region
  • family history of HBV, hepatocellular carcinoma, and/or chronic liver disease
  • infected with HIV
  • infected with hepatitis C virus
  • blood or blood product transfusion
  • healthcare workers
  • household contact with HBV infection
  • history of incarceration
  • hemodialysis
  • solid organ transplantation
Full details

Diagnostic tests

1st tests to order

  • hepatic panel
  • CBC
  • basic metabolic panel
  • coagulation profile
  • serum hepatitis B surface antigen
  • serum antibody to hepatitis B surface antigen
  • serum antibody to hepatitis B core antigen
  • serum hepatitis B e antigen
  • serum antibody to hepatitis B e antigen
  • serum HBV DNA
Full details

Tests to consider

  • abdominal ultrasound
  • liver biopsy
  • transient elastography
  • serum liver fibrosis biomarkers
  • aspartate aminotransferase-to-platelet ratio index (APRI)
  • alpha-fetoprotein
  • CT/MRI abdomen
  • testing for hepatitis D coinfection
  • testing for other coinfections
  • drug resistance testing
  • HBV genotype
Full details

Treatment algorithm

ACUTE

acute HBV infection

ONGOING

chronic HBV infection: adult nonpregnant without coinfection or cirrhosis

chronic HBV infection: adult nonpregnant with cirrhosis

chronic HBV infection: adult nonpregnant with HIV coinfection

chronic HBV infection: adult nonpregnant with hepatitis C coinfection

chronic HBV infection: adult nonpregnant with hepatitis D coinfection

chronic HBV infection: adult pregnant or breastfeeding

chronic HBV infection: children

Contributors

Authors

Jawad Ahmad, MD, FRCP, FAASLD

Professor of Medicine

Division of Liver Diseases

Mount Sinai Hospital

New York

NY

Disclosures

JA declares that he has no competing interests.

Acknowledgements

Dr Jawad Ahmad would like to gratefully acknowledge Dr Sateesh R. Prakash, Dr Siddarth Verma, Dr Smruti R. Mohanty, and Dr Jared Hossack, previous contributors to this topic.

Disclosures

SRP, SV, and JH declare that they have no competing interests. SRM serves as a speaker bureau for Bristol-Myers Squibb regarding the use of entecavir for the treatment of chronic hepatitis B.

Peer reviewers

George Y. Wu, MD, PhD

Chief

Hepatology Section

Department of Medicine

University of Connecticut Health Center

Farmington

CT

Disclosures

GYW is on the medical advisory boards of Gilead Sciences and Bristol-Myers Squibb.

Lucieni Oliveira Conterno, MD, PhD

Director

Clinical Epidemiology Unit

Marilia Medical School

Sao Paulo

Brazil

Disclosures

LOC declares that she has no competing interests.

Mamun-Al-Mahtab, MB BS, MSc, MD

Chairman

Bangladesh Primary Care Research Network

Dhaka

Bangladesh

Disclosures

MAM declares that he has no competing interests.

  • Differentials

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