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临床试验/NCT02954224
NCT02954224已完成不适用

Prevention Of Delirium in Elderly With Obstructive Sleep Apnea (PODESA)

University Health Network, Toronto3 个研究点 分布在 1 个国家目标入组 220 人开始时间: 2016年3月24日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
220
试验地点
3
主要终点
postoperative delirium

研究概览

简要总结

Delirium is a common complication in elderly patients following surgery. Patients who develop delirium after surgery are at increased risk for serious complications, and even death.This multi-centre randomized controlled trial will enroll elderly patients scheduled for elective hip/knee replacement surgery.The objective of this trial is to identify obstructive sleep apnea using ApneaLink Air and to determine whether auto-titrating CPAP treatment of obstructive sleep apnea will decrease the incidence of post-operative delirium in elderly patients undergoing elective hip and knee replacement surgery.

详细描述

Delirium is an acute and fluctuating change in cognitive function, characterized by poor attention and disorganized thinking. Recent studies show that patients with obstructive sleep apnea (OSA) - a sleep disorder characterized by repeated episodes of complete or partial blockage of the upper airway - are at greater risk to develop delirium. It is estimated that 43% of men and 27% of women aged 50-70 years old have OSA. Elderly individuals with this condition are often undiagnosed. Unrecognized OSA may be a treatable cause of postoperative delirium. However, timely access to polysomnography is usually not possible prior to surgery. This multi-centre randomized controlled trial will enroll elderly patients scheduled for elective hip/knee replacement surgery. All participants who have given the consent to participate will be assessed risks of OSA and comorbidity by 3 basic questionnaires- STOP-Bang, Epworth Sleepiness Scale and Charlson Comorbidity index, Cognitive level assess by Mini-Cog and baseline delirium assessment by CAM. STOP-Bang questionnaire is the validated questionnaire to screen the patients for OSA. Score of 3 or higher has sensitivity of detecting OSA of 93% and 100% for moderate and severe OSA respectively. If participant has STOP-Bang score 3 or higher will have a home sleep study with the ApneaLink Air and overnight oximetry. Patients identified to have OSA(AHI ≥10/h) will be randomized to 1) Auto-titrating continuous positive airway pressure (CPAP) applied 1-3 nights before surgery (if possible) and during day/night sleep for 72 hrs after surgery or 2) Control group - routine care. All patients will be evaluated for delirium for 72h after surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Investigator)

入排标准

年龄范围
60 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age more than 60 years, Scheduled for elective hip or knee replacement surgery at least 4 working days after the preadmission clinic visit
  • •Possess cognitive and physical capability necessary to comprehend and complete the study questionnaires
  • •Proficient in English, reading level at Grade 6 (patient or accompanying person),
  • •Be accessible for follow-up via telephone, or via the Internet, Ability to provide informed consent

排除标准

  • •Conditions potentially interfering with comprehension and delivery of informed consent , Schizophrenia, anxiety disorders, poorly controlled depression, multiple psychiatric disorders
  • •Active psychosis within the last 3 months
  • •Current use of antipsychotic medication
  • •Dementia, and/or clinically significant neurological disorder (stroke, epilepsy, brain tumors, Parkinson's Disease etc.)
  • •History of drug or alcohol dependence or abuse within last 3 months
  • •Surgery that is two-staged involving more than one surgical procedure to be performed within the same hospitalization period
  • •Emergency surgery when preoperative testing is not possible
  • •Patients with prior diagnosis of sleep-related breathing disorder with CPAP treatment
  • •Patients who may have had sleep studies earlier may be included, if they have been lost to follow-up by a sleep physician, are not on treatment or are non-compliant to treatment (mean CPAP nightly use <4 hours, or median nightly CPAP use <50% of total sleep time),Severe tracheal or lung disease,Contraindication to CPAP face-mask, Central Sleep Apnea, Significant Cardiac disease(New York Heart Association Functional Class III and IV Severe Valvular Heart Disease, Dilated Cardiomyopathy, Implanted Cardiac Pacemaker, unstable angina)
  • •bMyocardial Infarction or Cardiac Surgery or Percutaneous coronary interventions within 3 months

研究组 & 干预措施

CPAP therapy arm

Experimental

Auto-titrating Continuous Positive Airway Pressure (CPAP)) treatment will be given on postoperative days 1, 2, and 3.

干预措施: CPAP treatment (Other)

Control arm

No Intervention

no auto-titrating CPAP, standard care

结局指标

主要结局

postoperative delirium

时间窗: 2 MONTHS

The primary outcome is the incidence of postoperative delirium.

次要结局

  • Length of Hospital Stay(Depending on post operative recovery(2 days-2 months))
  • Perioperative Complications(10-14 days)
  • Time to ambulate(1 week to 2 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jean Wong

Dr.

University Health Network, Toronto

研究点 (3)

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