| Literature DB >> 31862767 |
Syed Abidi1,2, Jay Achar3, Mourtala Mohamed Assao Neino4, Didi Bang5, Andrea Benedetti1,2,6, Sarah Brode7, Jonathon R Campbell1,2, Esther C Casas8, Francesca Conradie9, Gunta Dravniece10, Philipp du Cros3,11, Dennis Falzon12, Ernesto Jaramillo12, Christopher Kuaban13, Zhiyi Lan1,2, Christoph Lange14,15,16,17, Pei Zhi Li2, Mavluda Makhmudova18, Aung Kya Jai Maug19, Dick Menzies1,2, Giovanni Battista Migliori20, Ann Miller21, Bakyt Myrzaliev22, Norbert Ndjeka23, Jürgen Noeske24, Nargiza Parpieva25, Alberto Piubello19,26, Valérie Schwoebel26, Welile Sikhondze27, Rupak Singla28, Mahamadou Bassirou Souleymane19, Arnaud Trébucq26, Armand Van Deun29, Kerri Viney30,31,32, Karin Weyer12, Betty Jingxuan Zhang1,2, Faiz Ahmad Khan33,2.
Abstract
We sought to compare the effectiveness of two World Health Organization (WHO)-recommended regimens for the treatment of rifampin- or multidrug-resistant (RR/MDR) tuberculosis (TB): a standardised regimen of 9-12 months (the "shorter regimen") and individualised regimens of ≥20 months ("longer regimens").We collected individual patient data from observational studies identified through systematic reviews and a public call for data. We included patients meeting WHO eligibility criteria for the shorter regimen: not previously treated with second-line drugs, and with fluoroquinolone- and second-line injectable agent-susceptible RR/MDR-TB. We used propensity score matched, mixed effects meta-regression to calculate adjusted odds ratios and adjusted risk differences (aRDs) for failure or relapse, death within 12 months of treatment initiation and loss to follow-up.We included 2625 out of 3378 (77.7%) individuals from nine studies of shorter regimens and 2717 out of 13 104 (20.7%) individuals from 53 studies of longer regimens. Treatment success was higher with the shorter regimen than with longer regimens (pooled proportions 80.0% versus 75.3%), due to less loss to follow-up with the former (aRD -0.15, 95% CI -0.17- -0.12). The risk difference for failure or relapse was slightly higher with the shorter regimen overall (aRD 0.02, 95% CI 0-0.05) and greater in magnitude with baseline resistance to pyrazinamide (aRD 0.12, 95% CI 0.07-0.16), prothionamide/ethionamide (aRD 0.07, 95% CI -0.01-0.16) or ethambutol (aRD 0.09, 95% CI 0.04-0.13).In patients meeting WHO criteria for its use, the standardised shorter regimen was associated with substantially less loss to follow-up during treatment compared with individualised longer regimens and with more failure or relapse in the presence of resistance to component medications. Our findings support the need to improve access to reliable drug susceptibility testing. The content of this work is copyright of the authors or their employers. Design and branding are copyright ©ERS 2020.Entities:
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Year: 2020 PMID: 31862767 DOI: 10.1183/13993003.01467-2019
Source DB: PubMed Journal: Eur Respir J ISSN: 0903-1936 Impact factor: 16.671