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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorOFORI, SANDRA
dc.contributor.authorWang, Michael K.
dc.contributor.authorPopova, Ekaterine
dc.contributor.authorMcIntyre, William F
dc.contributor.authorChan, Matthew
dc.contributor.authorSessler, Daniel
dc.contributor.authorGonzalez Tallada, Anna
dc.date.accessioned2025-09-29T10:42:40Z
dc.date.available2025-09-29T10:42:40Z
dc.date.issued2025-04
dc.identifier.citationOfori S, Wang M, Popova E, McIntyre WF, Chan M, Sessler DI, et al. Smoking, Colchicine and Postoperative Outcomes in Thoracic Surgery: Post Hoc Analysis of the COP-AF Randomized Controlled Trial. CJC Open. 2025 Apr;7(7):860-70.
dc.identifier.issn2589-790X
dc.identifier.urihttp://hdl.handle.net/11351/13746
dc.descriptionSmoking; Colchicine; Thoracic surgery
dc.description.abstractBackground To determine, among patients who underwent major noncardiac thoracic surgery, the association between smoking and perioperative atrial fibrillation (AF) and myocardial injury after noncardiac surgery (MINS), and whether the effect of colchicine use on these outcomes varied by smoking status. Methods This study is a subgroup analysis of the Colchicine for the Prevention of Perioperative Atrial Fibrillation (COP-AF) randomized clinical trial. A total of 3209 participants who underwent major noncardiac thoracic surgery were randomized to receive colchicine, 0.5 mg twice daily, or identical placebo, for 10 days starting 2-4 hours before surgery. The co-primary outcomes were clinically significant perioperative AF and MINS during the 14-day follow-up. Results A total of 687 (21.4%) were current smokers, 1577 (49.1%) were former smokers, and 945 (29.5%) were never smokers. AF occurred in 7.7%, 7.6%, and 5.3%, and MINS occurred in 21.0%, 19.7%, and 17.6% of current, former, and never smokers, respectively. Compared to never smokers, the adjusted hazard ratio for AF was 1.72 (95% confidence interval [CI] 1.07-2.77, P = 0.02) in current smokers and 1.46 (95% CI 0.99-2.16, P = 0.06) in former smokers, and the adjusted hazard ratio for MINS was 1.16 (95% CI 0.87-1.54, P = 0.32) in current smokers and 1.02 (95% CI 0.81-1.28, P = 0.88) in former smokers. No interaction occurred between smoking status and colchicine allocation for AF (interaction P, 0.82) or MINS (interaction P, 0.08). Conclusions Current smoking was associated with a small but increased risk of perioperative AF but not MINS after thoracic surgery. The effect of colchicine use on either outcome was not modified by smoking status. Clinical Trial Registration NCT03310125.
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofseriesCJC Open;7(7)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectAvaluació de resultats (Assistència sanitària)
dc.subjectTabaquisme
dc.subjectTòrax - Cirurgia
dc.subjectFibril·lació auricular
dc.subject.meshAntimitotic Agents
dc.subject.mesh/therapeutic use
dc.subject.meshThoracic Surgery
dc.subject.meshSmoking
dc.subject.meshTreatment Outcome
dc.subject.meshAtrial Fibrillation
dc.titleSmoking, Colchicine and Postoperative Outcomes in Thoracic Surgery: Post Hoc Analysis of the COP-AF Randomized Controlled Trial
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.cjco.2025.04.008
dc.subject.decsantimitóticos
dc.subject.decs/uso terapéutico
dc.subject.decscirugía torácica
dc.subject.decsfumar
dc.subject.decsresultado del tratamiento
dc.subject.decsfibrilación atrial
dc.relation.publishversionhttps://doi.org/10.1016/j.cjco.2025.04.008
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Ofori S, Wang MK, McIntyre WF] Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada. Department of Medicine, McMaster University, Hamilton, Ontario, Canada. [Popova E] Institut de Recerca Sant Pau, Barcelona, Spain. Centro Cochrane Iberoamericano, Barcelona, Spain. [Chan M] The Chinese University of Hong Kong, Hong Kong Special Administrative Region, Hong Kong, China. [Sessler DI] Outcomes Research Consortium, Houston, Texas, USA. [Gonzalez Tallada A] Vall d’Hebron Hospital Universitari, Barcelona, Spain
dc.identifier.pmid40698308
dc.identifier.wos001536454100001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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