Strategies for treating latent multiple-drug resistant tuberculosis: a decision analysis

PLoS One. 2012;7(1):e30194. doi: 10.1371/journal.pone.0030194. Epub 2012 Jan 17.

Abstract

Background: The optimal treatment for latent multiple-drug resistant tuberculosis infection remains unclear. In anticipation of future clinical trials, we modeled the expected performance of six potential regimens for treatment of latent multiple-drug resistant tuberculosis.

Methods: A computerized Markov model to analyze the total cost of treatment for six different regimens: Pyrazinamide/ethambutol, moxifloxacin monotherapy, moxifloxacin/pyrazinamide, moxifloxacin/ethambutol, moxifloxacin/ethionamide, and moxifloxacin/PA-824. Efficacy estimates were extrapolated from mouse models and examined over a wide range of assumptions.

Results: In the base-case, moxifloxacin monotherapy was the lowest cost strategy, but moxifloxacin/ethambutol was cost-effective at an incremental cost-effectiveness ratio of $21,252 per quality-adjusted life-year. Both pyrazinamide-containing regimens were dominated due to their toxicity. A hypothetical regimen of low toxicity and even modest efficacy was cost-effective compared to "no treatment."

Conclusion: In our model, moxifloxacin/ethambutol was the preferred treatment strategy under a wide range of assumptions; pyrazinamide-containing regimens fared poorly because of high rates of toxicity. Although more data are needed on efficacy of treatments for latent MDR-TB infection, data on toxicity and treatment discontinuation, which are easier to obtain, could have a substantial impact on public health practice.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antitubercular Agents / therapeutic use*
  • Aza Compounds / therapeutic use
  • Cost-Benefit Analysis
  • Decision Support Techniques*
  • Drug Therapy / economics
  • Drug Therapy / methods
  • Drug Therapy, Combination
  • Ethambutol / therapeutic use
  • Fluoroquinolones
  • Humans
  • Isoniazid / therapeutic use
  • Markov Chains*
  • Mice
  • Models, Theoretical
  • Moxifloxacin
  • Outcome Assessment, Health Care
  • Quality-Adjusted Life Years
  • Quinolines / therapeutic use
  • Rifampin / therapeutic use
  • Tuberculosis, Multidrug-Resistant / drug therapy*

Substances

  • Antitubercular Agents
  • Aza Compounds
  • Fluoroquinolones
  • Quinolines
  • Ethambutol
  • Moxifloxacin
  • Isoniazid
  • Rifampin