Hepatitis B (sexual/BBV)
Hepatitis B virus — blood-borne / sexually transmitted
Overview
A blood-borne virus transmitted sexually, parenterally and vertically — one of the blood-borne viruses GUM screens for alongside HIV, hepatitis C and syphilis. Causes acute hepatitis; a proportion (higher if acquired perinatally) become chronic carriers at risk of cirrhosis and hepatocellular carcinoma. Vaccine-preventable.
Recognise
- Acute: malaise, anorexia, nausea, jaundice, RUQ pain (many subclinical)
- Chronic carriage (esp. perinatal acquisition) → cirrhosis, hepatocellular carcinoma
- Extrahepatic: polyarteritis nodosa, membranous nephropathy
Red flags
- Fulminant hepatic failure (acute); cirrhosis/HCC (chronic); pregnancy (vertical transmission)
Differentials & how to tell them apart
Investigations
Serology: HBsAg (current infection), anti-HBc (exposure; IgM = acute), HBeAg/HBV DNA (infectivity/viral load), anti-HBs (immunity/vaccination). LFTs. Screen for co-infection (HIV, HCV, HDV).
Management
Acute: supportive + notify; Chronic active: tenofovir/entecavir (specialist)
- 1Acute: supportive care; NOTIFIABLE — inform UKHSA; test/vaccinate contacts. Most acute adult infections clear spontaneously.
- 2Chronic (HBsAg >6 months): refer to hepatology; antiviral (tenofovir or entecavir) if active disease; HCC surveillance.Gate: In pregnancy with high viral load → maternal antiviral + neonatal vaccine AND HBIG at birth to prevent vertical transmission
- 3Prevention: HBV vaccination (at-risk groups, now universal in the UK infant schedule); post-exposure vaccine ± immunoglobulin.
Key points
GUM screens the four BBV/STIs together: HIV, hepatitis B, hepatitis C and syphilis. Risk of chronicity is highest with perinatal acquisition. Hepatitis D only co-infects with B.
Monitor & prognosis
LFTs, HBV DNA, HBeAg seroconversion; HCC surveillance in cirrhosis.
Most acute adult cases resolve; chronic carriage risks cirrhosis/HCC.
Source: NICE CKS Hepatitis B; BASHH; QuackQuackMed cross-check