Publication:
Cardiovascular outcomes in adults with coronary artery disease and obstructive sleep apnea with versus without excessive daytime sleepiness in the RICCADSA cinical trial

dc.contributor.coauthorEulenburg, Christine
dc.contributor.coauthorRedline, Susan
dc.contributor.coauthorThunstrom, Erik
dc.contributor.coauthorGlantz, Helena
dc.contributor.coauthorStrollo, Patrick J., Jr.
dc.contributor.departmentKUTTAM (Koç University Research Center for Translational Medicine)
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorÇelik, Yeliz
dc.contributor.kuauthorPeker, Yüksel
dc.contributor.schoolcollegeinstituteResearch Center
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2025-01-19T10:29:45Z
dc.date.issued2023
dc.description.abstractRationale: Recent randomized controlled trials did not show cardiovascular benefits of continuous positive airway pressure (CPAP) in adults with coronary artery disease (CAD) and obstructive sleep apnea (OSA) in intention-to-treat analyses. It has been argued that exclusion of patients with OSA with excessive daytime sleepiness (EDS), who may be most likely to benefit from CPAP treatment, may be a reason for the null results. Objectives: We addressed 1) the effect of concomitant EDS on adverse outcomes in patients with CAD and OSA; and 2) whether the cardiovascular benefit of CPAP adherence differs between individuals with versus without EDS. Methods: This was a secondary analysis of the RICCADSA (Randomized Intervention with CPAP in CAD and Obstructive Sleep Apnea) trial, conducted in Sweden between 2005 and 2013. Data were analyzed from 155 patients with CAD with OSA (apnea-hypopnea index> 15/h) and EDS (Epworth Sleepiness Scale score> 10), who were allocated to CPAP and 244 patients without EDS (ESS, 10), who were randomized to CPAP or no CPAP. Patients who were allocated to no CPAP or were nonadherent (CPAP usage, 4 h/night) were compared with adherent patients (CPAP usage> 4 h/night) at 1-year follow-up. Inverse probability of treatment weighting was applied to mimic randomization of EDS. The primary endpoint was the first event of repeat revascularization, myocardial infarction, stroke, or cardiovascular mortality. Results: The median follow-up was 52.2 months. The incidence of the primary endpoint did not differ significantly between the EDS versus no-EDS groups in the entire cohort. Within the adherent group, patients without EDS had a significantly decreased risk compared with patients with EDS (adjusted hazard ratio, 0.41; 95% confidence interval, 0.20-0.85; P = 0.02). Conclusions: Adverse cardiovascular outcomes did not differ by degrees of EDS for patients with CAD with OSA who were untreated or nonadherent to treatment. CPAP use, at least 4 h/night, was associated with reduced adverse outcomes in participants without EDS. Clinical trial registered with www.
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue7
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipSupported by Swedish Research Council grants 521-2011-537 and 521-2013-3439; Swedish Heart and Lung Foundation grants 20080592, 20090708, and 20100664; the "Agreement concerning research and education of doctors" of Vastra Gotalandsregionen grants ALFGBG-11538 and ALFGBG-150801; Research Fund at Skaraborg Hospital grants VGSKAS-4731, VGSKAS-5908, VGSKAS-9134, VGSKAS-14781, VGSKAS-40271, and VGSKAS-116431; Skaraborg Research and Development Council grant VGFOUSKB-46371; the Heart Foundation of Karnsjukhuset; ResMed Foundation; ResMed; and National Institutes of Health grant R35 HL1358181 (S.R.). ResMed Sweden provided some of the sleep recording devices and technical support. None of the funders had any direct influence on the design of the study, the analysis of the data, the data collection, the drafting of the manuscript, or the decision to publish.
dc.description.volume20
dc.identifier.doi10.1513/AnnalsATS.202208-676OC
dc.identifier.eissn2325-6621
dc.identifier.issn1546-3222
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85167479591
dc.identifier.urihttps://doi.org/10.1513/AnnalsATS.202208-676OC
dc.identifier.urihttps://hdl.handle.net/20.500.14288/25944
dc.identifier.wos1028827800017
dc.keywordsObstructive sleep apnea
dc.keywordsCoronary artery disease
dc.keywordsCardiovascular outcomes
dc.keywordsExcessive sleepiness
dc.language.isoeng
dc.publisherAmerican Thoracic Society
dc.relation.grantnoSwedish Research Council [521-2011-537, 521-2013-3439]; Swedish Heart and Lung Foundation [20080592, 20090708, 20100664]; Research Fund at Skaraborg Hospital [VGSKAS-4731, VGSKAS-5908, VGSKAS-9134, VGSKAS-14781, VGSKAS-40271, VGSKAS-116431]; Skaraborg Research and Development Council [VGFOUSKB-46371]; Heart Foundation of Karnsjukhuset; ResMed Foundation; ResMed; National Institutes of Health [R35 HL1358181]; "Agreement concerning research and education of doctors" of Vastra Gotalandsregionen grants [ALFGBG-11538, ALFGBG-150801]
dc.relation.ispartofAnnals of the American Thoracic Society
dc.subjectRespiratory system
dc.titleCardiovascular outcomes in adults with coronary artery disease and obstructive sleep apnea with versus without excessive daytime sleepiness in the RICCADSA cinical trial
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorÇelik, Yeliz
local.contributor.kuauthorPeker, Yüksel
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit1Research Center
local.publication.orgunit2KUTTAM (Koç University Research Center for Translational Medicine)
local.publication.orgunit2School of Medicine
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