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Postoperative vascular complications in unrecognised Obstructive Sleep apnoea (POSA) study protocol: an observational cohort study in moderate-to-high risk patients undergoing non-cardiac surgery
  1. Matthew T V Chan1,
  2. Chew-Yin Wang2,
  3. Edwin Seet3,
  4. Stanley Tam4,
  5. Hou-Yee Lai2,
  6. Stuart Walker5,
  7. Timothy G Short6,
  8. Richard Halliwell7,
  9. Frances Chung8,
  10. for the POSA Investigators
  1. 1Department of Anaesthesia and Intensive Care, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, People's Republic of China
  2. 2Faculty of Medicine, Department of Anaesthesiology, University Malaya, Kuala Lumpur, Malaysia
  3. 3Department of Anaesthesia, Khoo Teck Puat Hospital, Singapore, Singapore
  4. 4Department of Anesthesia, Scarborough General Hospital, Ontario, Canada
  5. 5Department of Anaesthesia, Middlemore Hospital, Manukau City, New Zealand
  6. 6Department of Anaesthesia, Auckland City Hospital, Auckland, New Zealand
  7. 7Department of Anaesthesia, Westmead Hospital, Sydney, Australia
  8. 8Department of Anesthesia, Toronto Western Hospital, University Health Network, University of Toronto, Ontario, Canada
  1. Correspondence to Matthew T V Chan; mtvchan{at}cuhk.edu.hk

Abstract

Introduction Emerging epidemiological data suggest that obstructive sleep apnoea (OSA) is common in the general surgical population. Unfortunately, the majority of these patients are unrecognised and untreated at the time of surgery. There is substantial biological rationale to indicate that patients with unrecognised OSA are at a higher risk of postoperative vascular events. However, the extent of this morbidity is currently unknown. We have initated the postoperative vascular complications in the unrecognised obstructive sleep apnoea (POSA) study to determine the associations between OSA, nocturnal hypoxia and major postoperative vascular events in 1200 moderate-to-high risk patients undergoing major non-cardiac surgery.

Methods and analysis The POSA study is an international prospective observational cohort study. Using a type 3 portable sleep monitoring device and ambulatory oximetry, we will quantify the severity of OSA. The primary outcome is a composite of vascular death, myocardial infarction; non-fatal cardiac arrest; stroke; pulmonary embolism; congestive heart failure and new arrhythmia within 30 days of surgery. As of November 2013, we have recruited over 700 patients from nine centres in six countries. The mean age is 68 years, the mean body mass index is 27 kg/m2 and 55% of patients are men. 27.9% of patients have known coronary artery disease, over 76% have diabetes. The majority of patients underwent orthopaedic surgery (28%) and colorectal resection (18.5%).

Ethics and dissemination The POSA study has received ethics approval from all study sites before patient recruitment. Informed consent will be obtained from all patients. The POSA study will determine the risk of unrecognised OSA in major non-cardiac surgery. We will publish these findings in peer-reviewed journals.

Trial Registration: ClinicalTrials.gov Identifier: NCT01494181

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This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/

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