Brief Article
Copyright ©2012 Baishideng Publishing Group Co.
World J Gastroenterol. Nov 14, 2012; 18(42): 6106-6113
Published online Nov 14, 2012. doi: 10.3748/wjg.v18.i42.6106
Table 1 General assumptions of the Markov model of the B positive hepatocellular cancer prevention program
AssumptionHow addressed and rationale
Participant recruitmentTarget population age ≥ 35 yr, HBsAg +ve for ≥ 6 mo, born in China, Hong Kong, Vietnam
Contact testing and immunisationNot factored into the model
Seroprevalence in target populations10.7% for people born in China
10.5% for people born in Vietnam
7.7% for people born in Hong Kong (Nguyen et al[16])
Initial testing to confirm chronic hepatitis BNot factored in the GP consultation calculations
Program participation ratesBase case assumption: 25% of eligible people are enrolled
HCC screeningAll participants have AFP and liver US at enrolment
Participants receiving enhanced surveillance have 6-monthly AFP and US
Participants receiving treatment also have liver biopsy
Follow up requirementsRoutine surveillance arm: 2 GP appointments/yr
Enhanced HCC surveillance arm: 2 GP appointments/yr
Interferon treatment: 6 specialist appointments/yr
Entecavir treatment: 4 specialist appointments/yr
Patients with HCC: assumed two monthly follow up
Viral load distributionBased upon Risk Evaluation of Viral Load Elevation and Associated Liver Disease study data (Chen et al[20])
ALT level distributionBased upon Hong Kong data (Yuen et al[18])
Progression rates through different disease stagesConstant
Treatment protocol30% receive first line interferon (weekly for 12 mo); 30% seroconvert and receive no further treatment; 70% commence entecavir the following year 70% receive entecavir as first-line treatment; 20% seroconvert in first year and receive no further treatment; 80% continue lifelong entecavir
Patients with liver failureReceive lifelong entecavir
Table 2 Participant distribution by disease stage at initial enrolment and management pathways, according to the B positive algorithm and hepatitis B treatment published guidelines n (%)
Treatment guidelineB positiveModified B positiveEASL, United States expertsAPASLAASLD
HBV DNA level to treat> 2000 if > 50> 2000> 2000> 2000> 20 000
> 20 000 if < 50
ALT (ULN)> 1.5> 1.5> 1> 2> 2
Number receiving interferon61 (4)81 (6)108 (8)54 (4)33 (2)
Number receiving entecavir143 (10)190 (13)253 (17)126 (9)76 (5)
Total on treatment204 (14)271 (19)361 (25)181 (12)109 (8)
Total under enhanced surveillance340 (23)452 (31)361 (25)542 (37)326 (23)
Total under routine surveillance907 (63)728 (50)728 (50)728 (50)1016 (70)
Total1451 (100)1451 (100)1451 (100)1451 (100)1451 (100)
Table 3 Calculated costs (in Australian dollars) of implementing a program of chronic hepatitis B management in hepatitis B e antigen-negative patients according to the B positive algorithms and published hepatitis B treatment guidelines, n (%)
Discounted costs of management strategiesB positiveModified B positiveAPASLEASL, United States expertsAASLD
Cost/QALY (discounted)13 46515 77011 74619 6228867
Total program cost (discounted)13 979 22416 372 32012 194 90520 371 1179 205 680
Cost components
Initial CHB screening cost767 728 (5.5)800 792 (4.9)755 971 (6.2)845 613 (4.2)720 357 (7.8)
Drug treatment costs9 347 662 (66.9)11 493 535 (70.2)7 360 940 (60.4)15 447 510 (75.8)4 951 419 (53.8)
CHB surveillance costs2 827 093 (20.2)2 866 053 (17.5)2 866 053 (23.5)2 866 053 (14.1)2 767 073 (30.1)
HCC surveillance costs917 783 (6.6)1 092 983 (6.7)1 092 983 (9.0)1 092 983 (5.4)647 874 (7.0)
Total cost per person in the program963411 283840414 0396344
% change with equivalent unit costs/QALY1001178714666