4.7 Article

Aggressive Regimens for Multidrug-Resistant Tuberculosis Reduce Recurrence

Journal

CLINICAL INFECTIOUS DISEASES
Volume 56, Issue 6, Pages 770-776

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/cid/cis1008

Keywords

resistance; recurrence; relapse; Peru; regimen

Funding

  1. Charles H. Hood Foundation
  2. David Rockefeller Center for Latin American Studies at Harvard University
  3. NEW AID Foundation
  4. von Clemm Foundation at Harvard School of Public Health
  5. Bill & Melinda Gates Foundation
  6. National Heart, Lung, and Blood Institute [K01 HL080939]
  7. National Institute of Allergy and Infectious Diseases [K01 A1065836]
  8. Research Core of the Department of Global Health and Social Medicine at Harvard Medical School
  9. Eli Lilly Foundation

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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.

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