Perioperative cardiac risk stratification
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with peripheral vascular atherosclerosis scheduled for vascular surgery involving either; a) revascularization utilizing aortic or proximal lower extremity procedures, or b) distal lower extremity vascular reconstruction, are eligible to participate.
Exclusion criteria
Exclusion criteria: No written informed consent. Unstable coronary disease. Undergoing emergency surgery. Previous participation in the DECREASE VI trial. Reoperation within 30 days of an initial surgical procedure. Participation in another clinical trial within the last 30 days. Age
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary objective of this trial is to validate the screening potential of NT-proBNP in a population of low to intermediate risk patients, i.e. patients with zero to two cardiac risk factors, scheduled for vascular surgery. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary objective is to identify prior to vascular surgery high risk patients, with three or more cardiac risk factors, with a normal stress test. | — |
Countries
Netherlands