AIRR - ANZCA Institutional Research Repository
Skip navigation
Please use this identifier to cite or link to this item:
Full metadata record
DC FieldValueLanguage
dc.contributor.authorChan MTV,en_US
dc.contributor.authorWang CY,en_US
dc.contributor.authorSeet E,en_US
dc.contributor.authorTam S,en_US
dc.contributor.authorLai HY,en_US
dc.contributor.authorChew EFF,en_US
dc.contributor.authorWu WKK,en_US
dc.contributor.authorCheng BCP,en_US
dc.contributor.authorLam CKM,en_US
dc.contributor.authorShort TG,en_US
dc.contributor.authorHui DSC,en_US
dc.contributor.authorChung F,en_US
dc.contributor.authorPostoperative Vascular Complications in Unrecognized Obstructive Sleep Apnea (POSA) Study Investigatorsen_US
dc.identifier.citationJAMA. 2019 May 14;321(18):1788-1798en_US
dc.description.abstractIMPORTANCE: Unrecognized obstructive sleep apnea increases cardiovascular risks in the general population, but whether obstructive sleep apnea poses a similar risk in the perioperative period remains uncertain. OBJECTIVES: To determine the association between obstructive sleep apnea and 30-day risk of cardiovascular complications after major noncardiac surgery. DESIGN, SETTING, AND PARTICIPANTS: Prospective cohort study involving adult at-risk patients without prior diagnosis of sleep apnea and undergoing major noncardiac surgery from 8 hospitals in 5 countries between January 2012 and July 2017, with follow-up until August 2017. Postoperative monitoring included nocturnal pulse oximetry and measurement of cardiac troponin concentrations. EXPOSURES: Obstructive sleep apnea was classified as mild (respiratory event index [REI] 5-14.9 events/h), moderate (REI 15-30), and severe (REI >30), based on preoperative portable sleep monitoring. MAIN OUTCOMES AND MEASURES: The primary outcome was a composite of myocardial injury, cardiac death, heart failure, thromboembolism, atrial fibrillation, and stroke within 30 days of surgery. Proportional-hazards analysis was used to determine the association between obstructive sleep apnea and postoperative cardiovascular complications. RESULTS: Among a total of 1364 patients recruited for the study, 1218 patients (mean age, 67 [SD, 9] years; 40.2% women) were included in the analyses. At 30 days after surgery, rates of the primary outcome were 30.1% (41/136) for patients with severe OSA, 22.1% (52/235) for patients with moderate OSA, 19.0% (86/452) for patients with mild OSA, and 14.2% (56/395) for patients with no OSA. OSA was associated with higher risk for the primary outcome (adjusted hazard ratio [HR], 1.49 [95% CI, 1.19-2.01]; P = .01); however, the association was significant only among patients with severe OSA (adjusted HR, 2.23 [95% CI, 1.49-3.34]; P = .001) and not among those with moderate OSA (adjusted HR, 1.47 [95% CI, 0.98-2.09]; P = .07) or mild OSA (adjusted HR, 1.36 [95% CI, 0.97-1.91]; P = .08) (P = .01 for interaction). The mean cumulative duration of oxyhemoglobin desaturation less than 80% during the first 3 postoperative nights in patients with cardiovascular complications (23.1 [95% CI, 15.5-27.7] minutes) was longer than in those without (10.2 [95% CI, 7.8-10.9] minutes) (P < .001). No significant interaction effects on perioperative outcomes were observed with type of anesthesia, use of postoperative opioids, and supplemental oxygen therapy. CONCLUSIONS AND RELEVANCE: Among at-risk adults undergoing major noncardiac surgery, unrecognized severe obstructive sleep apnea was significantly associated with increased risk of 30-day postoperative cardiovascular complications. Further research would be needed to assess whether interventions can modify this risk.en_US
dc.titleAssociation of Unrecognized Obstructive Sleep Apnea With Postoperative Cardiovascular Events in Patients Undergoing Major Noncardiac Surgeryen_US
dc.typeJournal Articleen_US
dc.description.affiliatesChinese University of Hong Kong, Hong Kong Special Administrative Region, Chinaen_US
dc.description.affiliatesUniversity of Malaya, Kuala Lumpur, Malaysiaen_US
dc.description.affiliatesKhoo Teck Puat Hospital, Singaporeen_US
dc.description.affiliatesScarborough Health Network, Ontario, Canadaen_US
dc.description.affiliatesHospital Kuala Lumpur, Kuala Lumpur, Malaysia.en_US
dc.description.affiliatesTuen Mun Hospital, Hong Kong Special Administrative Region, China.en_US
dc.description.affiliatesAuckland City Hospital, Auckland, New Zealand.en_US
dc.description.affiliatesToronto Western Hospital, University Health Network, University of Toronto, Toronto, Ontario, Canadaen_US
dc.type.studyortrialClinical Trialen_US
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
Appears in Collections:Scholarly and Clinical
Show simple item record

Google ScholarTM



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.