neobookRx

Hepatitis, Viral

Description Hepatitis B, Acute Hepatitis B, Chronic (Non-HIV Co-infection) Hepatitis B, Chronic (HIV Co-infection) *Notifiable medical condition. DESCRIPTION Hepatitis caused by one of the hepatotropic viruses, hepatitis A, B, C, D and E. HEPATITIS B, ACUTE ICD-10 code:  B16.0-2/B16.9 GENERAL MEASURES Bed-rest until acute phase has resolved. Avoid alcohol during the illness and for ≥ 6 month

Description

Hepatitis B, Acute

Hepatitis B, Chronic (Non-HIV Co-infection)

Hepatitis B, Chronic (HIV Co-infection)


*Notifiable medical condition.

DESCRIPTION

Hepatitis caused by one of the hepatotropic viruses, hepatitis A, B, C, D and E.

HEPATITIS B, ACUTE

ICD-10 code: B16.0-2/B16.9

GENERAL MEASURES

  • Bed-rest until acute phase has resolved.
  • Avoid alcohol during the illness and for ≥ 6 months after clinical recovery.
  • Screen sexual contacts of patients with acute hepatitis B. Non-immune contacts (negative for hepatitis B surface antibodies) should receive hepatitis B active immunisation (see: Adult vaccination).

MEDICINE TREATMENT

For nausea and vomiting: (R11)

  • Metoclopramide, IV/oral, 10 mg 8 hourly as required.

Hepatitis B virus: prophylaxis following exposure e.g. needle stick injury S61.0 + (W46.22+Z20.5+Z29.8)

  • Persons at risk can be protected by passive immunisation with hyper immune serum globulin prepared from blood containing anti-HBs.
  • It is essential that all categories of healthcare workers (HCW) at risk of contact with bodily fluids, including cleaning staff and home-based or family caregivers, are screened and fully vaccinated against hepatitis B if nonimmune.
  • All occupational exposure incidents must be adequately documented for possible subsequent compensation.
  • Recommended post-exposure management for HCW exposed to infectious material from patients with infectious hepatitis B (either surface antigen or e antigen positive).

Check vaccination status and antibody response of HCW (See table below for management depending on immunity):

Table 1.1: Prophylaxis following Hepatitis B exposure

Vaccination status and antibody response status of HCW Source patient status & treatment
HBsAg positive HBsAg negative HBsAg unknown
Unvaccinated
OR
vaccination incomplete
- HBIG, IM, 500 units*
- Hep B vaccine (3 doses at monthly intervals)
- Initiate Hep B vaccination (month 0, 1 and 6) - HBIG, IM, 500 units*
- Hep B vaccine (3 doses at monthly intervals)
Vaccinated
AND
HBsAb ≥10 units/mL#
No treatment No treatment No treatment
Vaccinated
AND
HBsAb <10 units/mL
- HBIG, IM, 500 units*
- Repeat Hep B vaccine (3 doses at monthly intervals)
- Initiate Hep B vaccination (month 0, 1 and 6) - HBIG, IM, 500 units*
- Repeat Hep B vaccine (3 doses at monthly intervals)

* HBIG and first dose of vaccine to be given simultaneously, but at different sites.
# If the delay in obtaining HBsAb results is more than 24 hours initiate treatment as for vaccinated AND HBsAb <10 units/mL.

HEPATITIS B, CHRONIC (NON-HIV COINFECTION)

ICD-10 code: B18.0-2/B18.8-9


Consult the most recent Hepatitis Guidelines from the National Department of Health for comprehensive monitoring recommendations.


DESCRIPTION

  • HBV is most commonly transmitted horizontally in children <5 years of age. Vertical mother to child transmission and adult transmission, sexually or through a parenteral route, can also occur.
  • Acute infection may be asymptomatic or present as acute hepatitis.
  • A proportion of patients develop chronic hepatitis (defined as abnormalities listed in the table below persisting for >6 months), which can result in cirrhosis and hepatocellular carcinoma.
  • It is essential to know the HIV status of all patients with chronic hepatitis B before considering therapy.
  • Antiviral therapy is not indicated for acute hepatitis B infection.

There are 5 potential phases of chronic hepatitis B infection which determine the need for treatment:

Table 1.2: Phases of Chronic Hepatitis B infection

Serology Viral load (HBV DNA) IU/mL ALT

Management

LoE:IIIxx

1. HBeAg-positive chronic HBV infection Immune Tolerant
- HBsAg positive
- HBeAg positive
>20 000 (usually >200 000) Normal - Treatment not routinely needed, but should be followed up.
- Treat only if on immunosuppressive therapy to prevent hepatitis B flares.
2. HBeAg-positive chronic hepatitis B Immune clearance
- HBsAg positive
- HBeAg positive
>20 000 Elevated - Treatment required.
3. HBeAg-negative chronic HBV infection Immune Control
- HBsAg positive
- HBeAg negative
<2 000 Normal - Treatment not routinely needed, but should be followed up.
- Treat only if on immunosuppressive therapy to prevent hepatitis B flares.
4. HBeAg-negative chronic hepatitis B Immune Escape
- HBsAg positive
- HBeAg negative
>2 000 Elevated - Treatment required.
5. Occult hepatitis B
- HBsAg negative
- HBsAb negative
- HB IgG core Ab positive
<200  - - No follow-up required.
- Treat only if on immunosuppressive therapy to prevent hepatitis B flares.

HBsAg: hepatitis B surface antigen; HBsAb: hepatitis B surface antibody; HBIG: hepatitis B immunoglobulin

Treat all patients with cirrhosis regardless of ALT level, HBeAg status and HBV viral load, to prevent hepatitis B flares that will lead to decompensation. Screen all categories of healthcare workers (HCW) at risk of contact with bodily fluids, including cleaning staff, home-based or family caregivers and vaccinate against hepatitis B if not immune (see: Management of close contacts of patients with hepatocellular carcinoma).

MEDICINE TREATMENT

If eGFR > 50mL/min:

  • Tenofovir disoproxil fumarate (TDF), oral, 300 mg daily.

LoE:IIIxxi

If eGFR 15-50mL/min (or on haemodialysis):

  • Tenofovir alafenamide (TAF), oral, 25 mg daily.

LoE:IIbxxii

Aims of treatment

HBeAg-positive disease:

  • Sustained HBsAg loss off therapy, with/without the development of anti-HBs, and
  • Suppression of HBV DNA to undetectable or low (<2000 IU/mL) levels, and
  • Normalisation of ALT, and
  • Sustained HBeAg loss and seroconversion to anti-HBe

HBeAg-negative disease:

  • Sustained HBsAg loss off therapy, with/without the development of anti-HBs, and
  • Suppression of HBV DNA to undetectable or low (<2000 IU/mL), and
  • Normalisation of ALT.

Table 1.3: Monitoring tests whilst on tenofovir

Monitoring whilst on tenofovir

Monitoring test When to perform test
Serum phosphate and urine protein Baseline
INR Baseline, Week 4
Serum creatinine

All patients:
Baseline

Patients on TDF:
Month 3, month 10,
and every 12
months thereafter.

ALT Baseline, Week 4, and every 12 weeks thereafter
FBC+Diff Baseline, Week 4, and every 12 weeks thereafter
HBeAg and Anti-HBe HBeAg-positive patients:
Every 12 months
HBsAg

HBeAg-positive patients:
HBsAg every 6 months after anti-HBe seroconversion

HBeAg-negative patients:
HBsAg every 6 months with persistently undetectable HBV DNA

HBV DNA levels HBeAg-positive patients:
12 months after HBeAg seroconversion

Adapted from: National Department of Health, National guidelines for the management of viral hepatitis, 2019. Available at www.health.gov.za

Duration of tenofovir treatment:

  • HBeAg-positive patients: discontinue 12 months after HBeAg seroconversion and in association with persistently normal ALT levels and undetectable HBV DNA levels.
  • HBeAg-negative patients: Long-term therapy unless HBsAg seroconversion is achieved
  • Cirrhotic patients: Lifelong treatment.

REFERRAL

Failure of, or contraindications to, tenofovir disoproxil fumarate and tenofovir alafenamide.

HEPATITIS B, CHRONIC (HIV CO-INFECTION)

See chapter: HIV and AIDS.

HEPATITIS C, CHRONIC

Consult a specialist.

Click here for the pdf.

Click here for the NEMLC Recommendations for medicine treatement (2020-4 review cycle).

Click here for the 29 July 2025 circular.


Standard Treatment Guidelines And Essential Medicines List For South Africa, Adult Hospital level, 2020-4_Version 1_July 2024

Chapter 1: Alimentary tract; 1.2 Hepatic Disorders; 1.2.4 Hepatitis, Viral

Drugs mentioned

ICD-10 codes

NeoHealth® ID 17187 · updated 8/12/2025