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

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.A computerized Markov model to analyz...

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Main Authors: David P Holland, Gillian D Sanders, Carol D Hamilton, Jason E Stout
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3260212?pdf=render
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spelling doaj-87f5b154989847f7a9fbe7ac548aa1aa2020-11-25T00:23:25ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0171e3019410.1371/journal.pone.0030194Strategies for treating latent multiple-drug resistant tuberculosis: a decision analysis.David P HollandGillian D SandersCarol D HamiltonJason E StoutThe 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.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.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."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.http://europepmc.org/articles/PMC3260212?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author David P Holland
Gillian D Sanders
Carol D Hamilton
Jason E Stout
spellingShingle David P Holland
Gillian D Sanders
Carol D Hamilton
Jason E Stout
Strategies for treating latent multiple-drug resistant tuberculosis: a decision analysis.
PLoS ONE
author_facet David P Holland
Gillian D Sanders
Carol D Hamilton
Jason E Stout
author_sort David P Holland
title Strategies for treating latent multiple-drug resistant tuberculosis: a decision analysis.
title_short Strategies for treating latent multiple-drug resistant tuberculosis: a decision analysis.
title_full Strategies for treating latent multiple-drug resistant tuberculosis: a decision analysis.
title_fullStr Strategies for treating latent multiple-drug resistant tuberculosis: a decision analysis.
title_full_unstemmed Strategies for treating latent multiple-drug resistant tuberculosis: a decision analysis.
title_sort strategies for treating latent multiple-drug resistant tuberculosis: a decision analysis.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description 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.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.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."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.
url http://europepmc.org/articles/PMC3260212?pdf=render
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