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Wilt TJ, Shamliyan T, Shaukat A, et al. Management of Chronic Hepatitis B. Rockville (MD): Agency for Healthcare Research and Quality (US); 2008 Oct. (Evidence Reports/Technology Assessments, No. 174.)

  • This publication is provided for historical reference only and the information may be out of date.

This publication is provided for historical reference only and the information may be out of date.

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Management of Chronic Hepatitis B.

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Appendix E Tables and Figures

Figure 1. Flow Chart for Key Questions

Figure 2. Effects of interferon alfa-2b and reverse transcriptase inhibitors on clinical outcomes compared to placebo or no active treatment—Relative risk from four individual RCTs

Figure 3. Comparative effectiveness of interferon alfa-2b and reverse transcriptase inhibitors on mortality, results from individual randomized controlled clinical trials

Figure 4. Comparative effectiveness of active drugs on clinical outcomes, results from individual RCTs

Figure 5. Effects of active treatments compared to placebo on HBsAg loss at the end of the treatment (results from individual RCTs )

Figure 6. Effects of active treatments compared to placebo on HBsAg loss at followup off the treatment (results from individual RCTs)

Figure 7. Comparative effectiveness of active treatments on HBsAg loss at the end of the treatments (results from individual RCTs)

Figure 8. Comparative effectiveness of active treatments on HBsAg loss at followup off the treatments (results from individual RCTs)

Figure 9. HBsAg loss combined with other criteria of resolved hepatitis B at followup off the therapy (results from individual RCTs)

Figure 10. HBV DNA loss at the end of the drug therapies for chronic hepatitis B (significant risk differences from individual RCTs and pooled with random effects model)

Figure 11. HBV DNA loss at followup off the drug therapies for chronic hepatitis B (significant risk differences from individual RCTs and pooled with random effects model)

Figure 12. Significant effects on HBeAg loss for chronic hepatitis B (significant risk differences from individual RCTs and pooled with random effects model)

Figure 13. Significant relative risk of virological, histological and biochemical outcomes after drug therapies for chronic hepatitis B (results from individual RCT and pooled consistent results using random effects model)

Figure 14. Significant effects on HBeAg seroconversion for chronic hepatitis B (significant risk differences from individual RCTs and pooled with random effects model)

Figure 15. Significant effects on combined virological and biochemical outcomes at the end of the drug therapies for chronic hepatitis B (significant risk differences from individual RCTs and pooled with random effects model)

Figure 16. Significant effects on combined virological and biochemical outcomes at follow up after drug therapies for chronic hepatitis B (significant risk differences from individual RCTs and pooled with random effects model)

Figure 17. Histological outcomes at the end of the drug therapies for chronic hepatitis B (significant risk differences from individual RCTs and pooled with random effects model)

Figure 18. ALT normalization at the end of the drug therapies for chronic hepatitis B (significant risk differences from individual RCTs and pooled with random effects model)

Figure 19. ALT normalization at followup off the drug therapies for chronic hepatitis B (significant risk differences from individual RCTs and pooled with random effects model)

Figure 20. Combined outcomes at the end of the treatments by baseline ALT levels (individual RCTs)

Figure 21. The effects of lamivudine, 100mg/day compared to placebo at the end of the treatment depending on baseline ALT level (4 lamivudine-controlled Phase III trials)

Figure 22. HBV DNA loss at followup off the drug therapies for chronic hepatitis B by patient pretreatment status, baseline HBeAg positivity, and the proportion of the patients with baseline cirrhosis, the results from individual studies

Figure 23. HBeAg loss and seroconversion at followup off drug therapies for chronic hepatitis B by patient pretreatment status, baseline HBeAg positivity, and the proportion of the patients with baseline cirrhosis, results from individual studies

Figure 24. ALT normalization at followup off drug therapies for chronic hepatitis B by patient pretreatment status, baseline HBeAg positivity, and the proportion of the patients with baseline cirrhosis, results from individual studies

Table E1. Evidence table: Observational studies of the natural history of chronic hepatitis B in adults

Table E2. Evidence table: Randomized controlled trials for treatment of hepatitis B

Table E3. Reported clinical and intermediate outcomes after comparisons of antiviral drugs for chronic hepatitis B (randomized controlled clinical trials)

Table E4. Evidence tables of the effects of antiviral drugs on patient outcomes (individual randomized controlled clinical trials)

Table E5. Summary tables of the effects of drug therapies for chronic hepatitis B on outcomes

Table E6. Levels of viral load, biochemical, or histologic outcomes after antiviral drugs in adults with chronic hepatitis B

Table E7. Number of subjects experiencing adverse events from RCTs

Table E8. Number of subjects with laboratory abnormalities from RCTS

Table E9. Evidence tables of the effects of drug interventions on outcomes among patient subgroups (individual RCTs)

Table E10. Summary tables of the effects of therapies for CHB in patient subpopulations by baseline status of chronic hepatitis B

Table E11. Rates of clinical, intermediate, and adverse outcomes after antiviral treatment / no treatment by baseline HBeAg status at the end of treatment and at followup off treatment. (results from individual RCTs and pooled analyses with random effects models. Rates pooled from RCTs that reported outcomes independent of active or control regime)

Table E12. Summary of study IDs meeting eligibility for question 4

Table E13. Evidence table of the studies that examined the association between changes in intermediate outcomes to predict treatment effectiveness (n=4)

Table E14. Other baseline factors as predictors of outcomes, and other outcomes (n=3)

Table E15. Ongoing interventional randomized studies in patients with chronic hepatitis B (underlined outcomes assessment in patient subpopulations relevant to question 3)

Table E16. Completed unpublished RCTs in patients with chronic hepatitis B

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