Preventing Mycobacterium avium complex in patients who are using protease inhibitors: a cost-effectiveness analysis

AIDS. 1998 Aug 20;12(12):1503-12. doi: 10.1097/00002030-199812000-00013.

Abstract

Background: Practice guidelines recommending Mycobacterium avium complex (MAC) prophylaxis for patients with HIV disease were based on clinical trials in which individuals did not receive protease inhibitors.

Objective: To estimate the cost-effectiveness of strategies for MAC prophylaxis in patients whose treatment regimen includes protease inhibitors.

Design: Decision analysis with Markov modelling of the natural history of advanced HIV disease. Five strategies were evaluated: no prophylaxis, azithromycin, rifabutin, clarithromycin and a combination of azithromycin plus rifabutin.

Main outcome measures: Survival, quality of life, quality-adjusted survival, health care costs and marginal cost-effectiveness ratios.

Results: Compared with no prophylaxis, rifabutin increased life expectancy from 78 to 80 months, increased quality-adjusted life expectancy from 50 to 52 quality-adjusted months and increased health care costs from $233000 to $239800. Ignoring time discounting and quality of life, the cost-effectiveness of rifabutin relative to no prophylaxis was $44300 per life year. Adjusting for time discounting and quality of life, the cost-effectiveness of rifabutin relative to no prophylaxis was $41500 per quality-adjusted life year (QALY). In comparison with rifabutin, azithromycin was associated with increased survival, increased costs and an incremental cost-effectiveness ratio of $54300 per QALY. In sensitivity analyses, prophylaxis remained economically attractive unless the lifetime chance of being diagnosed with MAC was less than 20%, the rate of CD4 count decline was less than 10 x 10(6) cells/l per year, or the CD4 count was greater than 50 x 10(6) cells/l.

Conclusion: MAC prophylaxis increases quality-adjusted survival at a reasonable cost, even in patients using protease inhibitors. When not contraindicated, starting azithromycin or rifabutin when the patient's CD4 count is between 50 and 75 x 10(6) cells/l is the most cost-effective strategy. The main determinants of cost-effectiveness are CD4 count, viral load, place of residence and patient preference.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AIDS-Related Opportunistic Infections / economics
  • AIDS-Related Opportunistic Infections / mortality
  • AIDS-Related Opportunistic Infections / prevention & control*
  • Adult
  • Anti-Bacterial Agents
  • Antibiotic Prophylaxis / economics*
  • Antibiotics, Antitubercular
  • Azithromycin
  • Clarithromycin
  • Cost-Benefit Analysis
  • Drug Therapy, Combination
  • HIV Infections / drug therapy*
  • HIV Infections / mortality
  • HIV Protease Inhibitors / therapeutic use*
  • Health Care Costs
  • Humans
  • Male
  • Markov Chains
  • Mycobacterium avium Complex*
  • Mycobacterium avium-intracellulare Infection / economics
  • Mycobacterium avium-intracellulare Infection / mortality
  • Mycobacterium avium-intracellulare Infection / prevention & control*
  • Quality of Life
  • Rifabutin
  • United States

Substances

  • Anti-Bacterial Agents
  • Antibiotics, Antitubercular
  • HIV Protease Inhibitors
  • Rifabutin
  • Azithromycin
  • Clarithromycin