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Outcomes with a shorter multidrug-resistant tuberculosis regimen from Karakalpakstan, Uzbekistan

Cros, Philipp du, Atadjan, Khamraev, Zinaida, Tigay, Abdrasuliev, Tleubergen, Greig, Jane, Cooke, Graham, Herboczek, Krzysztof, Pylypenko, Tanya, Berry, Catherine, Ronnachit, Amrita, Lister, David, Dietrich, Sebastian, Ariti, Cono, Safaev, Hasan, Nyang'wa, Bern-Thomas, Nargiza, Parpieva, Mirzagalib, Tillasaikhov and Achar, Jay 2021. Outcomes with a shorter multidrug-resistant tuberculosis regimen from Karakalpakstan, Uzbekistan. ERJ Open Research 7 (1) , 00537-2020. 10.1183/23120541.00537-2020

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Abstract

Background In 2016, WHO guidelines conditionally recommended standardised shorter 9–12 month regimens for multidrug-resistant tuberculosis (MDR-TB) treatment. We conducted a prospective study of a shorter standardised MDR-TB regimen in Karakalpakstan, Uzbekistan. Methods Consecutive adults and children with confirmed rifampicin-resistant pulmonary TB were enrolled between 1st September 2013 and 31st March 2015; exclusions included prior treatment with second-line anti-TB drugs, and documented resistance to ofloxacin or to two second-line injectable agents. The primary outcome was recurrence-free cure at 1 year following treatment completion. Results Of 146 enrolled, 128 patients were included: 67 female (52.3%), median age 30.1 (IQR 23.8–44.4) years. At the end of treatment, 71.9% (92/128) patients achieved treatment success, with 68% (87/128) achieving recurrence-free cure at 1 year following completion. Unsuccessful outcomes during treatment included 22 (17.2%) treatment failure with fluoroquinolone resistance amplification in 8 patients (8/22, 36.4%); 12 (9.4%) loss to follow-up; 2 (1.5%) deaths. Recurrence occurred in one patient. 14 patients (10.9%) experienced serious adverse events. Baseline resistance to both pyrazinamide and ethambutol (aOR 6.13, 95% CI 2.01;18.63) and adherence<95% (aOR 5.33, 95% CI 1.73;16.36) were associated with unsuccessful outcome in multivariable logistic regression. Conclusions Overall success with a standardised shorter MDR-TB regimen was moderate with considerable treatment failure and amplification of fluoroquinolone resistance. When introducing standardised shorter regimens, baseline drug susceptibility testing and minimising missed doses are critical. High rates globally of pyrazinamide, ethambutol and ethionamide resistance raise questions of continued inclusion of these drugs in shorter regimens in the absence of DST-confirmed susceptibility.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Medicine
Additional Information: This article is open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0.
Publisher: European Respiratory Society
ISSN: 2312-0541
Date of First Compliant Deposit: 20 October 2020
Date of Acceptance: 18 September 2020
Last Modified: 11 Aug 2021 14:48
URI: http://orca.cardiff.ac.uk/id/eprint/135746

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