hepatitis b carrier

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    Hepatitis B Carrier

    By Ruby Lai

    21/7/2006

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    1. Who to screen

    2. Clarify whether a true HB carrier

    3. Counsel on contact tracing for thoseHBsAg+& HBsAb + w/o vaccination

    4. Hep B Vaccination

    5. Surveillance of hepatitis, cirrhosis, CA

    6. Current treatment available &management guideline

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    Cases discussion

    1. M/21 no Hx of blood test on Hep Bstatus

    2. M/35, Hep B vaccine 5 years ago,request check Hepatitis B status.

    3. F/34 , husband Hep B carrier 4. F/40 detected HBsAg 3 months ago as

    first time, request repeat Hepatitis B

    Status 5. M/45, Known Hep B carrier, moderate

    drinker,

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    Who to screen

    Health Care worker

    Family history of Hep B carrier

    Adolescent or Adult no hx of vaccination,esp. high risk group e.g. multiple sexualpartner, frequent blood transfusion,injecting drug, sexual partner Hep B

    carrier. People with compromised immunity post-vacc serology need for the above group

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    True Hep B carrier

    The risk of carrier rate:

    90-95% perinatal transmission

    30% children age 1-5

    5-10% older children, adolescent, adult

    Route of transmission: perinatal, paternal,sexual

    China & South East Asia high prevalence>8% Carriers

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    True Hep B carrier

    Once HBsAg detected, it should berepeated at least 6 months later to confirmthe true Hep. B Carrier Status

    So usually advise repeat HBsAg & HBsAbone year later

    Persist HBsAg confirm Carrier status.

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    Contact Tracing

    Sexual partner

    Children

    Parent Sibling

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    Hepatitis B vaccination

    Regimen 0, 1, 6 is widely used

    Efficacy >95% seroconversion rate

    Post vaccination serology usually not needexact some special group of people

    Routine boostering not recommended

    after 3 doses

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    Hepatitis B vaccination

    1st & 2nd dose not 12weeks

    3rd dose not evidence of efficacy after 10months

    More tight schedule earilar protection

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    Hypo-responder-anti-HBs titre 0-10mIU/ml

    Non-responder -anti-HBs titre

    Factor: Obesity, male sex,smoker, olderage, immunocompromised status.

    Suggest repeat 3 standard dose

    18-25% respond in 2nd course

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    When to start Surveillance

    To increase the chance of intervention andimprove survival,

    Early detection of subclinical HCC

    By AFP (Alpha-fetal protein)

    By USG Liver

    Sensitivity for AFP alone(74.2%), USGLiver Alone (81.9%)

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    How frequent

    A single tumour

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    Case 1

    M/21 no Hx of blood test on Hep B status

    Management:

    1. Born in HK?

    2. Vaccination program completed

    3. If vaccine before, low risk, no need tocheck

    4. If vaccine before high risk, check

    5. If no vaccine, check

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    Case 2

    M/35, Hep B vaccine 5 years ago, requestcheck Hepatitis B status.

    Management:

    1. Check if only high risk group

    2. Boostering usually not required because

    of natural boostering

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    Case 3

    F/34 , husband Hep B carrier

    Management:

    1. Suggest check Hep B status

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    Case 4

    F/40 detected HBsAg 3 months ago as first time,request repeat Hepatitis B Status

    Management:

    1. Suggest recheck HBsAg and HBsAb 6 to Iyear after the last blood test

    2. Advise husband and sibling, parent to check

    HBsAg status 3. Advise healthy life style and regular liver

    assessment if Hep B carrier confirmed

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    Case 5

    5. M/45, Known Hep B carrier, moderatedrinker,

    Management:

    1. Advise quit alcohol

    2. Advise family member to check Hep B

    status 3. Regular liver assessment including ALT,

    AFP, USG liver in 4-6 months interval

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    Current Management for Chronic

    Hepatitis

    Antiviral Treatment

    - Lamivudine

    - Adefovir- Interferon Alfa (IFN-)

    ? Traditional Chinese Herbal Medicine

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    Lamivudine

    Benefit:

    1. HBeAg seroconversion durability of respond aftercessation of treatment is 38%-77%

    Problem:1. Lamivudine resistent Mutant(14%, 38%, 49%,66%, 69% in first, 2nd, 3rd, 4th & 5th

    yrs of treatment )2. Relapsing rate 36-54% in 3 years, most occur in first

    year3. Duration of treatment 1 year or more

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    Adefovir

    Benefit:1. low resistent2.

    Problem:1. Cost high2. HBeAg seroconversion rate on 12%3. ALT raise again after stop the treatment

    4. Duration of treatment 1 year or more

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    Interferon Alfa

    Benefit:1. Short duration 4-6 months2. Lack of resistent mutants

    Problem:1. High cost2. Side effect (Early Flu like symptom: chill,

    headache, fever, malaise, tachycardia, myalgia,arthralgia

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    When to start Tx

    a) HBeAg+ CHB with ALT >2x ULN &compensated liver should be observed for3-6 months for spontaneous

    seroconversion from HBeAg toHBeAb(HKP7/04, AA)

    if after 3-6 months ALT remains >2xULN & HBV DNA >10^5 copies/ml

    consider Tx (HKP7/04)

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    When to start Tx

    b) HBeAg- CHB with HBV DNA >10^5 copies/ml& ALT >2x ULN on repeated testing (HKP7/04),at least 1 month between observations (AP)

    c) HBV cirrhosis with HBV DNA >10^4 (HKP7/04,AA)

    d) ALT in a rising trend or with ALT> 5xULN (AP)

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    When to start Tx

    ALT >2x ULN & HBV DNA

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    Thank You