<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(6)</volume><submitter>Ramirez-Venegas A</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>COPD due to biomass exposure (COPD-B) is highly prevalent in low- and middle-income countries, and there are no clinical trials designed to evaluate the effectiveness of the treatments currently recommended for patients with COPD due to cigarette smoking (COPD-C). The purpose of the study was to compare the efficacy of fluticasone furoate/vilanterol (FF/V) 100/25 μg and umeclidinium/vilanterol (UMEC/VI) 62.5/25 μg on the rate of exacerbations, the time to first exacerbation, on dyspnoea, health-related quality of life (HRQL), forced expiratory volume in 1 s (FEV&lt;sub>1&lt;/sub>) and inspiratory capacity (IC) during a period of 6 months in patients with COPD-B and COPD-C, at a third level referral centre in Mexico City.&lt;h4>Methods&lt;/h4>A pilot, single-centre, open-label, parallel-group study included 132 patients with a history of at least two exacerbations. They were randomised to receive one of four treatment groups: 33 COPD-B patients received FF/VI 100/25 μg, 31 COPD-B patients received UMEC/VI 62.5/25 μg, 34 COPD-C patients received FF/V and 34 COPD-C patients received UMEC/VI.&lt;h4>Results&lt;/h4>There were no differences in exacerbation rates between patients receiving FF/VI or UMEC/VI in either the COPD-B (0.07 (95% CI 0.03-0.13), 0.06 (95% CI 0.03-0.12)) or COPD-C group (0.06 (95% CI 0.04-0.11), 0.08 (95% CI 0.05-0.13)), nor in the time of first exacerbation, nor FEV&lt;sub>1&lt;/sub> and IC. All groups showed improvement in dyspnoea and HRQL, independently of medication used.&lt;h4>Conclusions&lt;/h4>Among patients with COPD-B and COPD-C with a history of exacerbation, FF/VI was equally effective as UMEC/VI in preventing exacerbations and improving dyspnoea and HRQL.</pubmed_abstract><journal>ERJ open research</journal><pagination>00154-2024</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11587136</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Effectiveness of ICS/LABA and LAMA/LABA in COPD due to biomass.</pubmed_title><pmcid>PMC11587136</pmcid><pubmed_authors>Robles-Hernandez RE</pubmed_authors><pubmed_authors>Gonzalez-Gonzalez C</pubmed_authors><pubmed_authors>Hernandez-Morales AP</pubmed_authors><pubmed_authors>Mayar-Maya ME</pubmed_authors><pubmed_authors>Montiel-Lopez F</pubmed_authors><pubmed_authors>Cassou-Martinez M</pubmed_authors><pubmed_authors>Falfan-Valencia R</pubmed_authors><pubmed_authors>Hernandez-Zenteno RJ</pubmed_authors><pubmed_authors>Perez-Bautista O</pubmed_authors><pubmed_authors>Ramirez-Venegas A</pubmed_authors><pubmed_authors>Celli BR</pubmed_authors><pubmed_authors>Sansores RH</pubmed_authors><pubmed_authors>Lara-Albisua JLP</pubmed_authors><pubmed_authors>Thirion-Romero I</pubmed_authors><pubmed_authors>Perez-Padilla R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effectiveness of ICS/LABA and LAMA/LABA in COPD due to biomass.</name><description>&lt;h4>Background&lt;/h4>COPD due to biomass exposure (COPD-B) is highly prevalent in low- and middle-income countries, and there are no clinical trials designed to evaluate the effectiveness of the treatments currently recommended for patients with COPD due to cigarette smoking (COPD-C). The purpose of the study was to compare the efficacy of fluticasone furoate/vilanterol (FF/V) 100/25 μg and umeclidinium/vilanterol (UMEC/VI) 62.5/25 μg on the rate of exacerbations, the time to first exacerbation, on dyspnoea, health-related quality of life (HRQL), forced expiratory volume in 1 s (FEV&lt;sub>1&lt;/sub>) and inspiratory capacity (IC) during a period of 6 months in patients with COPD-B and COPD-C, at a third level referral centre in Mexico City.&lt;h4>Methods&lt;/h4>A pilot, single-centre, open-label, parallel-group study included 132 patients with a history of at least two exacerbations. They were randomised to receive one of four treatment groups: 33 COPD-B patients received FF/VI 100/25 μg, 31 COPD-B patients received UMEC/VI 62.5/25 μg, 34 COPD-C patients received FF/V and 34 COPD-C patients received UMEC/VI.&lt;h4>Results&lt;/h4>There were no differences in exacerbation rates between patients receiving FF/VI or UMEC/VI in either the COPD-B (0.07 (95% CI 0.03-0.13), 0.06 (95% CI 0.03-0.12)) or COPD-C group (0.06 (95% CI 0.04-0.11), 0.08 (95% CI 0.05-0.13)), nor in the time of first exacerbation, nor FEV&lt;sub>1&lt;/sub> and IC. All groups showed improvement in dyspnoea and HRQL, independently of medication used.&lt;h4>Conclusions&lt;/h4>Among patients with COPD-B and COPD-C with a history of exacerbation, FF/VI was equally effective as UMEC/VI in preventing exacerbations and improving dyspnoea and HRQL.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2026-06-14T05:27:51.101Z</modification><creation>2026-06-14T03:08:24.217Z</creation></dates><accession>S-EPMC11587136</accession><cross_references><pubmed>39588082</pubmed><doi>10.1183/23120541.00154-2024</doi></cross_references></HashMap>