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Treatment correlates of successful outcomes in pulmonary multidrug-resistant tuberculosis: an individual patient data meta-analysis

Authors :
Parvaneh Baghaei
Nicolas Veziris
Nesri Padayatchi
Anete Trajman
Timothy H. Holtz
Ying Cai
Janice Westenhouse
Ignacio Monedero
Sarah Smith
Vija Riekstina
Dick Menzies
Maria I. Rodriguez
Payam Tabarsi
Lia D'Ambrosio
Maia Kipiani
Didi Bang
Norbert Ndjeka
Suzanne M. Marks
Maryline Bonnet
Medea Gegia
Jan-Willem C. Alffenaar
James C.M. Brust
Ethel Leonor Noia Maciel
Zarir F Udwadia
Tae Sun Shim
Phil Lowenthal
Lorenzo Guglielmetti
Domingo Palmero
Carole D. Mitnick
Chi-Chiu Leung
Gerard de Vries
Shama D. Ahuja
Faiz Ahmad Khan
Sue Gu
Rafael Laniado-Laborín
Lawrence Mbuagbaw
Nakwon Kwak
Margareth Pretti Dalcolmo
Russell R. Kempker
Erika Mohr
Christoph Lange
Kathleen F. Walsh
Serena P. Koenig
Vladimir Milanov
Sundari Mase
Liga Kuksa
Tjip S. van der Werf
Kwok-Chiu Chang
Mayara Lisboa Bastos
Andrea Benedetti
Payam Nahid
Gregory P. Bisson
Geisa Fregona
Zhiyi Lan
Simon Tiberi
Won-Jung Koh
Eric Caumes
Jennifer Hughes
Maria Tarcela Gler
Keertan Dheda
Martin J. Boeree
Piret Viiklepp
Macarthur Charles
Nicola M. Zetola
Chawangwa Modongo
Barbara Seaworth
Eric Chung Ching Leung
Kathryn Schnippel
Ann C. Miller
Giovanni Battista Migliori
J. Peter Cegielski
Matteo Zignol
Kwonjune J. Seung
Digamber Behera
Salmaan Keshavjee
Laura F Anderson
Nafees Ahmad
Jérôme Robert
Afranio Lineu Kritski
Wing Wai Yew
Rupak Singla
Aliasgar Esmail
Mathilde Fréchet-Jachym
Ganzaya Sukhbaatar
Onno W. Akkerman
Rosella Centis
Stalz Charles Vilbrun
Pei-Chun Chan
Laura Jean Podewils
Edward D. Chan
Pei Zhi Li
Leah G. Jarlsberg
Sarah K. Brode
Charlotte Kvasnovsky
Jean W. Pape
Gregory J. Fox
Lisa Trieu
Ian R Reynolds
Petros Isaakidis
Pennan M. Barry
Vaira Leimane
Max R. O'Donnell
Andra Cirule
Myungsun Lee
Jae-Joon Yim
Giovanni Sotgiu
Jennifer Flood
Regina Gayoso
Microbes in Health and Disease (MHD)
Source :
The Lancet (London), 392, 821-834, The Lancet (London), 392, 10150, pp. 821-834, LANCET, 392(10150), 821-834. ELSEVIER SCIENCE INC
Publication Year :
2018

Abstract

Item does not contain fulltext BACKGROUND: Treatment outcomes for multidrug-resistant tuberculosis remain poor. We aimed to estimate the association of treatment success and death with the use of individual drugs, and the optimal number and duration of treatment with those drugs in patients with multidrug-resistant tuberculosis. METHODS: In this individual patient data meta-analysis, we searched MEDLINE, Embase, and the Cochrane Library to identify potentially eligible observational and experimental studies published between Jan 1, 2009, and April 30, 2016. We also searched reference lists from all systematic reviews of treatment of multidrug-resistant tuberculosis published since 2009. To be eligible, studies had to report original results, with end of treatment outcomes (treatment completion [success], failure, or relapse) in cohorts of at least 25 adults (aged >18 years). We used anonymised individual patient data from eligible studies, provided by study investigators, regarding clinical characteristics, treatment, and outcomes. Using propensity score-matched generalised mixed effects logistic, or linear regression, we calculated adjusted odds ratios and adjusted risk differences for success or death during treatment, for specific drugs currently used to treat multidrug-resistant tuberculosis, as well as the number of drugs used and treatment duration. FINDINGS: Of 12 030 patients from 25 countries in 50 studies, 7346 (61%) had treatment success, 1017 (8%) had failure or relapse, and 1729 (14%) died. Compared with failure or relapse, treatment success was positively associated with the use of linezolid (adjusted risk difference 0.15, 95% CI 0.11 to 0.18), levofloxacin (0.15, 0.13 to 0.18), carbapenems (0.14, 0.06 to 0.21), moxifloxacin (0.11, 0.08 to 0.14), bedaquiline (0.10, 0.05 to 0.14), and clofazimine (0.06, 0.01 to 0.10). There was a significant association between reduced mortality and use of linezolid (-0.20, -0.23 to -0.16), levofloxacin (-0.06, -0.09 to -0.04), moxifloxacin (-0.07, -0.10 to -0.04), or bedaquiline (-0.14, -0.19 to -0.10). Compared with regimens without any injectable drug, amikacin provided modest benefits, but kanamycin and capreomycin were associated with worse outcomes. The remaining drugs were associated with slight or no improvements in outcomes. Treatment outcomes were significantly worse for most drugs if they were used despite in-vitro resistance. The optimal number of effective drugs seemed to be five in the initial phase, and four in the continuation phase. In these adjusted analyses, heterogeneity, based on a simulated I(2) method, was high for approximately half the estimates for specific drugs, although relatively low for number of drugs and durations analyses. INTERPRETATION: Although inferences are limited by the observational nature of these data, treatment outcomes were significantly better with use of linezolid, later generation fluoroquinolones, bedaquiline, clofazimine, and carbapenems for treatment of multidrug-resistant tuberculosis. These findings emphasise the need for trials to ascertain the optimal combination and duration of these drugs for treatment of this condition. FUNDING: American Thoracic Society, Canadian Institutes of Health Research, US Centers for Disease Control and Prevention, European Respiratory Society, Infectious Diseases Society of America.

Details

Language :
English
ISSN :
01406736
Database :
OpenAIRE
Journal :
The Lancet (London), 392, 821-834, The Lancet (London), 392, 10150, pp. 821-834, LANCET, 392(10150), 821-834. ELSEVIER SCIENCE INC
Accession number :
edsair.doi.dedup.....da5589835d62745cbc34faee59b9dc46