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Strategies for Treating Latent Multiple-Drug Resistant Tuberculosis: A Decision Analysis
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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3260212/ https://www.ncbi.nlm.nih.gov/pubmed/22272302 http://dx.doi.org/10.1371/journal.pone.0030194 |
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author | Holland, David P. Sanders, Gillian D. Hamilton, Carol D. Stout, Jason E. |
author_facet | Holland, David P. Sanders, Gillian D. Hamilton, Carol D. Stout, Jason E. |
author_sort | Holland, David P. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3260212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32602122012-01-23 Strategies for Treating Latent Multiple-Drug Resistant Tuberculosis: A Decision Analysis Holland, David P. Sanders, Gillian D. Hamilton, Carol D. Stout, Jason E. PLoS One Research Article 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. Public Library of Science 2012-01-17 /pmc/articles/PMC3260212/ /pubmed/22272302 http://dx.doi.org/10.1371/journal.pone.0030194 Text en Holland et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Holland, David P. Sanders, Gillian D. Hamilton, Carol D. Stout, Jason E. Strategies for Treating Latent Multiple-Drug Resistant Tuberculosis: A Decision Analysis |
title | 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_short | Strategies for Treating Latent Multiple-Drug Resistant Tuberculosis: A Decision Analysis |
title_sort | strategies for treating latent multiple-drug resistant tuberculosis: a decision analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3260212/ https://www.ncbi.nlm.nih.gov/pubmed/22272302 http://dx.doi.org/10.1371/journal.pone.0030194 |
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