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:
Phase | Serology |
Viral load (HBV DNA) IU/mL |
ALT | Management |
---|---|---|---|---|
1. HBeAg-positive chronic HBV infection (Immune Tolerant) |
|
>20000 (usually >200000) | Normal |
routinely needed, but should be followed up. immunosuppressive therapy to prevent hepatitis B flares. |
2. HBeAg-positive chronic hepatitis B (Immune Clearance) |
|
>20000 | Elevated |
|
3. HBeAg-negative chronic HBV infection (Immune Control) |
|
<2000 | Normal |
routinely needed, but should be followed up. immunosuppressive therapy to prevent hepatitis B flares. |
4. HBeAg-negative chronic hepatitis B (Immune Escape) |
|
>2000 | Elevated |
|
5. Occult hepatitis B |
positive |
<200 | - |
required. 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 DNA level, to prevent hepatitis B flares that will lead to decompensation.
MEDICINE TREATMENT
- Tenofovir, oral, 300 mg daily, if estimated CrCl >50 mL/minute.
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.
MONITORING WHILST ON TENOFOVIR
Baseline |
FBC+diff, ALT, INR, urine protein, serum phosphate and serum creatinine |
Week 4 and every 12 weeks |
FBC+diff, ALT |
Week 4 | INR |
Week 4, then at 3, 6 and 12 months after initiation and every 12 months thereafter if on TDF |
Serum creatinine |
Every 6 months |
HBeAg-positive patients: HbsAg after anti-HBe seroconversion HBeAg-negative patients: HBsAg with persistently undetectable HBV DNA |
Every 12 months |
HBeAg-positive patients: HBeAg, anti HBe |
HBeAg-positive patients: 12 months after HBeAg seroconversion |
HBV DNA levels |
Adapted from: National Department of Health, National guidelines for the management of viral hepatitis, 2018. Available at www.health.gov.za
DISCONTINUE TREATMENT WITH TENOFOVIR WHEN:
- HBeAg-positive patients: 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.