Title
Aggressive regimens for multidrug-resistant tuberculosis reduce recurrence
Date Issued
15 March 2013
Access level
open access
Resource Type
journal article
Author(s)
Franke M.
Appleton S.
Mitnick C.
Furin J.
Chalco K.
Shin S.
Murray M.
Becerra M.
Socios En Salud Sucursal Peru
Abstract
Background. Recurrent tuberculosis disease occurs within 2 years in as few as 1% and as many as 29% of individuals successfully treated for multidrug-resistant (MDR) tuberculosis. A better understanding of treatment-related factors associated with an elevated risk of recurrent tuberculosis after cure is urgently needed to optimize MDR tuberculosis therapy. Methods. We conducted a retrospective cohort study among adults successfully treated for MDR tuberculosis in Peru. We used multivariable Cox proportional hazards regression analysis to examine whether receipt of an aggressive MDR tuberculosis regimen for ≥18 months following sputum conversion from positive to negative was associated with a reduced rate of recurrent tuberculosis. Results. Among 402 patients, the median duration of follow-up was 40.5 months (interquartile range, 21.2-53.4). Receipt of an aggressive MDR tuberculosis regimen for ≥18 months following sputum conversion was associated with a lower risk of recurrent tuberculosis (hazard ratio, 0.40 [95% confidence interval, 0.17-0.96]; P =. 04). A baseline diagnosis of diabetes mellitus also predicted recurrent tuberculosis (hazard ratio, 10.47 [95% confidence interval, 2.17-50.60]; P =. 004).Conclusions. Individuals who received an aggressive MDR tuberculosis regimen for ≥18 months following sputum conversion experienced a lower rate of recurrence after cure. Efforts to ensure that an aggressive regimen is accessible to all patients with MDR tuberculosis, such as minimization of sequential ineffective regimens, expanded drug access, and development of new MDR tuberculosis compounds, are critical to reducing tuberculosis recurrence in this population. Patients with diabetes mellitus should be carefully managed during initial treatment and followed closely for recurrent disease. © 2012 The Author 2012. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved.
Start page
770
End page
776
Volume
56
Issue
6
Language
English
OCDE Knowledge area
Enfermedades infecciosas
Subjects
Scopus EID
2-s2.0-84874775165
PubMed ID
Source
Clinical Infectious Diseases
ISSN of the container
10584838
Sponsor(s)
Potential conflicts of interest. C. D. M. has served as a board member of Otsuka Scientific Advisory Board. S. S. S. has received a grant from the Eli Lilly Foundation. All other authors report no potential conflicts.
Financial support. This work was supported by the Charles H. Hood Foundation; the David Rockefeller Center for Latin American Studies at Harvard University; the NEW AID Foundation; the von Clemm Foundation at Harvard School of Public Health; the Bill & Melinda Gates Foundation; the National Heart, Lung, and Blood Institute (K01 HL080939 to M. B. V.), the National Institute of Allergy and Infectious Diseases (K01 A1065836 to C. D. M.); and the Research Core of the Department of Global Health and Social Medicine at Harvard Medical School.
Sources of information:
Directorio de Producción Científica
Scopus