​Updated as of 5 Aug 2026

  • Chronic Hepatitis B Care Protocol will be implemented from January 2027 – HSG GPs may refer to updates from AIC for details on the implementation of these protocols.

Chronic hepatitis B (CHB) has a prevalence of about 3–4% in Singapore and is the leading but preventable cause of liver cirrhosis and cancer in our region1. A patient with CHB lives with the hepatitis B virus (HBV) for many years. The virus can damage the liver at multiple stages of the natural cycle of a CHB infection. The patient hence requires lifelong regular surveillance. Most CHB carriers are asymptomatic with inactive infection, although viral reactivation may occur later on in life. This emphasises the need for lifelong surveillance for such patients.


Screening

In Singapore, hepatitis B vaccination is part of the National Childhood Immunisation Schedule (NCIS) and National Adult Immunisation Schedule (NAIS). An antibody titre of ≥10 IU/L is considered protective. Hepatitis B screening is recommended for populations listed below and can be performed with a blood test. These populations2 are:

1. Asymptomatic Singapore residents with no known hepatitis B carrier status born before 1987, the year Singapore’s national childhood HBV vaccination programme commenced, who did not undergo the local catch-up immunisation programmes from 2001 to 2004

2. Pregnant women

3. Healthcare workers

4. Foreigners and immigrants from countries where HBV is endemic. Hepatitis B surface Antigen (HBsAg) prevalence of ≥8% defines highly endemic areas, prevalence of 5%–7% defines high intermediate, 2%–4% low intermediate, and <2% defines low endemic areas3.

5. Individuals at increased risk for contracting hepatitis B:

a. Chronic haemodialysis patients

b. Individuals who use non-sterile needles or instruments such as people with a history of drug use, body piercing, or tattoos

c. Individuals who underwent invasive procedures in healthcare facilities with inadequate infection control practices

d. Individuals with known exposures to HBV (e.g. healthcare workers following needle stick injury involving  blood, or recipients of blood or organs from a donor)

e. Individuals with occupations involving contact with blood or blood-contaminated body fluids such as healthcare workers

f. Recipients of unscreened donated blood, blood products, or organs

g. Individuals with sexual behaviours associated with increased risk of sexually transmitted infections, including unprotected sexual intercourse, multiple sexual partners, exposure to transactional or commercial sex, or having sexual partners with known hepatitis B infection

h. Individuals newly diagnosed with HIV or hepatitis C​


The hepatitis B screening blood test serology typically consists of HBsAg and hepatitis B antibodies (Anti-HBs). If there is a high probability that patient is a CHB carrier at screening, an immunoglobulin M (IgM) hepatitis B core antibodies (anti-HBc) can be added to result in an earlier diagnosis. See results interpretation 


Diagnosis

Diagnosis of CHB requires 1 of the following:

1. Two positive HBsAg blood tests 6 months apart, OR

2. A negative test for IgM-anti-HBc and a positive HBsAg from the same blood sample4

​a. ​​A positive IgM-anti-HBc requires repeat testing of HBsAg in 6 months to determine if the hepatitis B infection is chronic in nature.​​



General Management

Once a patient is diagnosed with CHB, the clinician should ensure the following:

1. Regular surveillance of liver health by looking for signs of liver abnormalities via physical examination, blood tests, and imaging. For more details, see the section on Regular Surveillance.

2. Optimise liver health:

a. Carry out vaccination for hepatitis A if patient is not immune/previously immunised

b. Screen for and have good control of metabolic diseases, especially diabetes, hyperlipidemia and obesity

d. Avoid smoking and alcohol consumption

e. Screen for hepatitis C in patients with high-risk behaviours

f. Avoid prolonged Complementary and Alternative Medication (CAM) that may stress the liver.​

​3. Minimise the spread of hepatitis B:

a. Screen household members and sexual partners for hepatitis B and vaccinate them if not immune

b. Advise patients with CHB to:

i. Avoid sharing sharp equipment with potential for blood transmission (e.g. razors, injectables, toothbrush etc.)

ii. Clean up blood spills from infected persons with bleach

iii. Cover up cuts and scratches promptly

iv. Use barrier protection such as condoms if having sexual intercourse with a partner who has uncertain or non-immune hepatitis B status.

4. Educate patients on the chronic nature of the disease that requires long term surveillance to prevent defaulting.

5. Screen for psychosocial impact at each visit, as anxiety and depression are common in individuals living with CHB and can adversely affect treatment adherence. Where clinically indicated, refer to the General Anxiety Disorder and Major Depressive Disorder CPs for further management.


Regular surveillance

1. CHB management consultation consists of 3 key areas of liver health surveillance. They should be carried out at every visit; with each visit recommended to be 6 months apart.

The 3 key areas are:

a. Physical examination

i. Check for signs of chronic liver disease or liver failure, which include but are not limited to:

      • Jaundice
      • Hepatomegaly
      • Signs of portal hypertension (ascites, splenomegaly, caput medusae, pedal edema)
      • Altered mental status
      • Stigmata of chronic liver disease (spider telangiectasias, palmar erythema, Dupuytren's contractures, gynecomastia, testicular atrophy)

b. Blood ​​tests

i. ​H​epatitis B e Antigen (HBeAg): On diagnosis and once at age 40 (or age 35 if high-risk factors for adverse outcomes present 

ii. Liver Function Tests (LFT): At first visit, and minimally alanine aminotransferase (ALT) every 6 months thereafter.

iii. Alpha-fetoprotein (AFP): At first visit and every 6 months thereafter.

iv. Full blood count (F​BC): Consider at first visit and every 6 months thereafter to monitor for thrombocytopenia.

c. Imaging 

i. Ultrasound of Hepatobiliary System (U/S HBS) to look for suspicious liver mass or cirrhosis

ii. U/S HBS should be performed 6 monthly for those at high risk of hepatocellular carcinoma (HCC), namely 

    • ​​​Asian males above 40 years of age or Asian females above 50 years of age;
    • Family history of HCC or liver cirrhosis3; or
    • Other higher risk groups requiring specialist management (Refer to Consideration for Specialist Referral Section)

iii. In other populations, U/S HBS can be done once a year

iv. While Fibrosis-4 Index (FIB-4) can be routinely calculated as an adjunct in the assessment of advanced fibrosis in patients with CHB, it is not a replacement for U/S HBS in detecting the complications of CHB (HCC, Fibrosis, Cirrhosis). Specifically, FIB-4 does not pick up early HCC which can only be detected via regular U/S HBS surveillance.

v. The decision to repeat U/S HBS less frequently than the recommended interval should be discussed between the clinician and the patient taking into account cost, patient preference and resource availability

    • ​GPs may refer patients to public ​or private providers where U/S HBS is offered, according to patients’ preference. If the patient has completed U/S HBS with providers not within Public Healthcare Institutions (PHIs), GPs should request that the patient share the results with them. Where U/S HBS was performed within PHIs, GPs may refer to National Electronic Health Record (NEHR) for the results of their patients.

​2. Modifiable risk factors (such as hepatitis A vaccination, smoking, alcohol consumption, metabolic chronic disease) should be updated and optimised at every visit.

3. Approximately 1% of patients with CHB may naturally clear the virus (i.e., seroconvert), resulting in negative HBsAg and positive anti-HBs on serology tests. Despite this, they remain at an elevated lifetime risk of developing HCC. The cost-effectiveness of HCC surveillance in these cases is not well studied. International guidelines recommend surveillance (at least with imaging) for patients with cirrhosis, a first-degree relative with HCC, or a long history of CHB infection (over 40 years for males and 50 years for females). Primary care providers should tailor surveillance recommendations for individual patients or refer them to a hepatologist for further management.​


Recommended Care Components 

Table 1: Recommended Care Components5

​​​Recommended Tests

​Minimum Frequency*

​Remarks​

​HbeAg

​At first visit

​If positive at first visit, to recheck at age 40 years, or age 35 years if high-risk factors present if still positive, to consider specialist referral.​

​Liver Function Test

(LFT)

​At first visit, and minimally alanine aminotransferase (ALT) once every 6 months thereafter

​Frequency of monitoring and specialist referral to be tailored based on previous ALT values and trends as well as HBeAg status.

Alpha-fetoprotein

(AFP)

​At first visit and once every 6 months thereafter

​AFP is a tumour marker used for HCC surveillance.

Full Blood Count

(FBC)​

​Consider at first visit and once every 6 months thereafter

​To monitor for thrombocytopenia associated with liver disease.​

​Ultrasound of Hepatobiliary System (U/S HBS)

​At first visit and annually thereafter

​Frequency of imaging to be tailored based on HCC risk. For higher risk groups ​, 6-monthly imaging may be considered. Refer to Management: Imaging for more information.

​Hepatitis A Screening/Vaccination

​Consider anti-HAV screening and vaccination

​Unless contraindicated, hepatitis A vaccination should be given to prevent superimposed acute hepatitis A in patients with CHB virus infection.​

​Sexually Transmitted Infections and Hepatitis C Screening

​Consider screening patients with high-risk behaviours

​Metabolic disease screening blood pressure measurement, lipid profile, BMI assessment, diabetes screening​

​As per guidance under Cardiovascular Risk Assessment and BMI control Care Protocols

​Development of fatty liver and metabolic risk factors further increases risk of liver cirrhosis and HCC.

​Influenza Vaccination

Annually or per season for:

- Patients with chronic hepatitis or cirrhosis aged 18 to 64 years; and

- All patients aged 65 years or older

​As recommended under the NAIS.​

​Pneumococcal Vaccination

​Pneumococcal vaccination is recommended for:

- Patients with chronic hepatitis or liver cirrhosis (does not include hepatitis carriers without liver inflammation/ dysfunction or liver cirrhosis) aged 18 to 64 years (PCV20 OR PPSV23); and

- All patients aged 65 years or older (PCV20; OR PCV13 and/or PPSV23)

 

Those who have not previously received any pneumococcal vaccine can either receive:

· PCV20; or

· PCV13 and/or PPSV23 as per prevailing recommendations.

 

For those who received PCV13 and/or PPSV23 but not completed the recommended vaccination series can either:

· Receive PCV20 to complete the vaccination series; or

· ​Complete the vaccination series as per prevailing recommendations using PCV13 and/or PPSV23.

For further details on dose schedule for PCV20; or PCV13 and/or PPSV23 based on age and medical conditions, please refer to:

- Care Protocol on Adult Vaccination;

- MOH Circular No. 51/2025 dated 21 August 2025​​

​COVID-19 Vaccination

​For unvaccinated patients:

Ages 5 years and older: one vaccine dose


Ages 6 months to 4 years: two vaccine doses, eight weeks apart


For vaccinated patients (6 months and above) receiving an additional dose:

One additional dose at an interval of around one year (and at least five months) after the last dose received

COVID-19 vaccination is recommended for:

· Patients aged 60 years and above

· Medically vulnerable patients (e.g. patients with chronic liver conditions) aged 6 month and above

· Residents of aged care facilities

 

For more information, please refer to MOH Circular No. 67/2025 dated 24 October 2025.


*More frequently if clinically indicated, except for vaccination

Refer to Primary Care Pages – Adult Vaccination Care Protocol​ for further vaccination-related information.​


Consideration for Specialist Referral

1. Raised ALT (Tables 2 and 3)​

Table 2: Referral Criteria for Raised ALT

​​​ALT levels (IU/L)​​​Action

​≥1000

​Refer to A&E immediately

​1000 > ALT ≥ 200

​Refer to a gastroenterologist as early as possible

​ALT < 200

​Repeat LFT in 3 months. See Table 3.


Table 3: Referral Critera for Pesistently Raised ALT Over 3 Months

Repeat ALT levels after 3 months (IU/L)

​Action

​ALT ≥200

​Refer to Table 2 for management

​200 > ALT ≥ 120

​Refer to gastroenterologist within 2 to 6 weeks

​120 > ALT > Upper limit of normal

​Refer to gastroenterologist routinely


2. Other LFT (non-ALT) persistently raised over 3 months to refer to gastroenterologist routinely

3. Rising AFP or raised AFP above the upper limit of normal

4. HBeAg positive at (i) age ≥40 years or (ii) age ≥35 years with high risk factors

a. Persistent HBeAg positivity may indicate ongoing HBV replication and increased risk of progressive liver disease. Specialist referral enables comprehensive assessment of HBV DNA levels, ALT, fibrosis stage, and hepatocellular carcinoma risk factors to determine disease activity and treatment eligibility, including consideration of antiviral therapy and monitoring for HBeAg seroconversion.

5. Thrombocytopenia

6. Ultrasound findings suspicious for cirrhosis or abnormal lesions

7. Clinical findings of chronic liver disease or liver failure

8. Special populations:

a. Immunocompromised patients:

i. Patients on chemotherapy or immunotherapy

ii. Patients on immunosuppressive drugs (e.g. biologics, antimetabolites, calcineurin inhibitors, non-calcineurin inhibitors, high dose corticosteroids – more than 5mg daily of prednisolone (or equivalent) for at least 1 month).

b. Pregnant women (for discussion of suppressive therapy to reduce maternal-fetal transmission)​

The following data fields should be documented in GPs' case notes as part of good clinical practice for all patients enrolled to their practice.

Submission of data fields marked with asterisks* is required for the Healthier SG payments.

 

Diagnosis

1. Diagnosis*

2. CDMP Condition(s)*

3. Diagnosis Year

 

Markers of Liver Health

1. Alanine aminotransferase (IU/L)

2. Platelet count (x109/L)

3. Alpha-fetoprotein (ng/mL)

4. HbeAg (+/-)

5. Date

 

Ultrasound HBS

1. Date of last ultrasound (HBS/Abdomen) (dd/mm/yy)

 

Vaccination

1. SDD code*

2. Date*

3. Due Date of Next Dose 

4. I acknowledge that I have reviewed the results and care delivery provided, that the vaccinations done are clinically indicated as per MOH’s prevailing guidelines 

5. Vaccination Exception Condition(s) (if applicable)*

6. COVID-19 Vaccination Dose Type*

7. COVID-19 Vaccination Condition(s)*​


​CHAS/PG/MG cardholders who are Healthier SG enrollees can opt to use the Healthier SG Chronic Tier at their enrolled clinics, which provides percentage-based subsidies for selected chronic medications sold within the stipulated price caps.

1. Schweitzer A, Horn J, Mikolajczyk RT, Krause G, Ott JJ. Estimations of worldwide prevalence of chronic hepatitis B virus infection: a systematic review of data published between 1965 and 2013. The Lancet. 2015 Oct 17;386(10003):1546–55.

2. Ministry of Health Singapore (MOH). MOH Circular No. 08/2019. Release of new screening test view committee guidelines, including changes to diabetes mellitus, lipid disorders, and cervical cancer screening 2019.

3. Guidelines for the prevention, care and treatment of persons with chronic hepatitis B infection World Health Organization, Geneva, 2015. Available at http://apps.who. int/iris/bitstream/10665/154590/1/9789241549059_eng.pdf, accessed June 2026.

4. Terrault, N. A., Lok, A. S. F., McMahon, B. J., Chang, K.-M., Hwang, J. P., Jonas, M. M., Brown, R. S. Jr., Bzowej, N. H., & Wong, J. B. (2018). Update on prevention, diagnosis, and treatment of chronic hepatitis B: AASLD 2018 hepatitis B guidance. Hepatology, 67(4), 1560–1599. https://doi.org/10.1002/hep.29800​

5. Chronic Disease Management Programme – Handbook for healthcare professionals. Ministry of Health. 2024.​