ong Term Cardiovascular Disease Event Risk for Patients undergoing Non-Cardiac Surgery. A pilot study.

• Conditions: Cardiovascular disease events; 10011082; 10003216

• Registration Number: NL-OMON56737
• Lead Sponsor: niversity Health Network Toronto

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 18 June 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 25

Inclusion Criteria

1. Age 45 - 75 years
2. Scheduled for intermediate- to high risk non-cardiac surgery (intra-thoracic
or intra-abdominal surgery, all vascular surgery, intra-cranial neurosurgery,
spine surgery)
3. Expected postoperative length of stay of at least two days, according to the
surgeon*s expectation
4. At least two of the following CVD risk factors:
o History of: Hypertension, Diabetes, Coronary artery disease, Chronic heart
failure, Chronic kidney disease, Cerebrovascular disease, Peripheral vascular
disease
o Obesity (BMI >25 kg/m2), Current smoking, Poor exercise capacity (<4 METS)

Exclusion Criteria

1. Currently participating in a CVD risk reduction program
2. Patient is scheduled to undergo transplant or has undergone emergency
surgery
3. Life expectancy <1 year (palliative surgery)
4. Recent (<6 months) myocardial infarction or stroke
5. Inability to effectively communicate

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The primary study outcome is (change in) estimated 10 year CVD event risk.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>A secondary outcome is number of patients that complete the study.</p><br>