<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fregonese F</submitter><funding>World Health Organization</funding><funding>Intramural CDC HHS</funding><funding>CIHR</funding><pagination>265-275</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9017096</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6(4)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Isoniazid-resistant, rifampicin-susceptible (INH-R) tuberculosis is the most common form of drug resistance, and is associated with failure, relapse, and acquired rifampicin resistance if treated with first-line anti-tuberculosis drugs. The aim of the study was to compare success, mortality, and acquired rifampicin resistance in patients with INH-R pulmonary tuberculosis given different durations of rifampicin, ethambutol, and pyrazinamide (REZ); a fluoroquinolone plus 6 months or more of REZ; and streptomycin plus a core regimen of REZ.&lt;h4>Methods&lt;/h4>Studies with regimens and outcomes known for individual patients with INH-R tuberculosis were eligible, irrespective of the number of patients if randomised trials, or with at least 20 participants if a cohort study. Studi</pubmed_abstract><journal>The Lancet. Respiratory medicine</journal><pubmed_title>Comparison of different treatments for isoniazid-resistant tuberculosis: an individual patient data meta-analysis.</pubmed_title><pmcid>PMC9017096</pmcid><funding_grant_id>001</funding_grant_id><funding_grant_id>CC999999</funding_grant_id><pubmed_authors>Jacobson KR</pubmed_authors><pubmed_authors>Tabarsi P</pubmed_authors><pubmed_authors>Cegielski P</pubmed_authors><pubmed_authors>Yoshiyama T</pubmed_authors><pubmed_authors>Bastos M</pubmed_authors><pubmed_authors>Munang M</pubmed_authors><pubmed_authors>Trajman A</pubmed_authors><pubmed_authors>Goldberg S</pubmed_authors><pubmed_authors>Escalante P</pubmed_authors><pubmed_authors>Nguyen VN</pubmed_authors><pubmed_authors>Erkens C</pubmed_authors><pubmed_authors>Lee JH</pubmed_authors><pubmed_authors>Baghaei P</pubmed_authors><pubmed_authors>Skrahina A</pubmed_authors><pubmed_authors>Reves R</pubmed_authors><pubmed_authors>Cattamanchi A</pubmed_authors><pubmed_authors>Li PZ</pubmed_authors><pubmed_authors>Fregonese F</pubmed_authors><pubmed_authors>Ayakaka I</pubmed_authors><pubmed_authors>Menzies D</pubmed_authors><pubmed_authors>Griffith D</pubmed_authors><pubmed_authors>Maciel EL</pubmed_authors><pubmed_authors>Merle CSC</pubmed_authors><pubmed_authors>Ponnuraja C</pubmed_authors><pubmed_authors>Benedetti A</pubmed_authors><pubmed_authors>Arakaki-Sanchez D</pubmed_authors><pubmed_authors>Seung K</pubmed_authors><pubmed_authors>Schaaf HS</pubmed_authors><pubmed_authors>Jones-Lopez EC</pubmed_authors><pubmed_authors>Chien JY</pubmed_authors><pubmed_authors>Koh WJ</pubmed_authors><pubmed_authors>Garcia-Prats AJ</pubmed_authors><pubmed_authors>Ahuja SD</pubmed_authors><pubmed_authors>Narendran G</pubmed_authors><pubmed_authors>Bang D</pubmed_authors><pubmed_authors>Galliez RM</pubmed_authors><pubmed_authors>Ohkado A</pubmed_authors><pubmed_authors>Glynn JR</pubmed_authors><pubmed_authors>Bonnet M</pubmed_authors><pubmed_authors>Gillespie SH</pubmed_authors><pubmed_authors>Johnston JC</pubmed_authors><pubmed_authors>Soolingen DV</pubmed_authors><pubmed_authors>Romanowski K</pubmed_authors><pubmed_authors>Falzon D</pubmed_authors><pubmed_authors>Khan A</pubmed_authors><pubmed_authors>Trieu L</pubmed_authors><pubmed_authors>Dedicoat M</pubmed_authors><pubmed_authors>Wang JY</pubmed_authors><pubmed_authors>Park JS</pubmed_authors><pubmed_authors>Cox H</pubmed_authors><pubmed_authors>Banurekha VV</pubmed_authors><pubmed_authors>Nunn A</pubmed_authors><pubmed_authors>Akkerman OW</pubmed_authors><pubmed_authors>Kritski A</pubmed_authors><pubmed_authors>Viiklepp P</pubmed_authors><pubmed_authors>Gegia M</pubmed_authors><pubmed_authors>Lan ZY</pubmed_authors><pubmed_authors>Phillips PPJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comparison of different treatments for isoniazid-resistant tuberculosis: an individual patient data meta-analysis.</name><description>&lt;h4>Background&lt;/h4>Isoniazid-resistant, rifampicin-susceptible (INH-R) tuberculosis is the most common form of drug resistance, and is associated with failure, relapse, and acquired rifampicin resistance if treated with first-line anti-tuberculosis drugs. The aim of the study was to compare success, mortality, and acquired rifampicin resistance in patients with INH-R pulmonary tuberculosis given different durations of rifampicin, ethambutol, and pyrazinamide (REZ); a fluoroquinolone plus 6 months or more of REZ; and streptomycin plus a core regimen of REZ.&lt;h4>Methods&lt;/h4>Studies with regimens and outcomes known for individual patients with INH-R tuberculosis were eligible, irrespective of the number of patients if randomised trials, or with at least 20 participants if a cohort study. Studi</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Apr</publication><modification>2026-06-03T10:17:48.74Z</modification><creation>2025-02-18T23:35:47.492Z</creation></dates><accession>S-EPMC9017096</accession><cross_references><pubmed>29595509</pubmed><doi>10.1016/S2213-2600(18)30078-X</doi><doi>10.1016/s2213-2600(18)30078-x</doi></cross_references></HashMap>