About this trial
The proportion of noncardiac surgeries performed as same-day surgery is increasing worldwide, with more complex surgeries being performed on higher risk patients in the outpatient setting. Little is known on the risk factors, incidence and prognosis of patients undergoing same-day noncardiac surgery. The main objective of this study is to inform on the incidence and risk factors of cardiovascular and other adverse events after same-day surgery and to develop risk prediction tools to better inform on the risk and selection of patients undergoing same-day surgery.
Eligibility criteria
Qualifiers
45-64 years of age with at least one risk factor, or ≥65 years of age;
undergoing elective noncardiac same-day surgery;
planned duration in the operating room 60 minutes or more;
provided written consent.
Disqualifiers
intervention does not require the presence of an anesthesiologist;
procedure is performed by a nonsurgical specialty (e.g., gastroenterology, pneumology, radio-oncology or radiology);
intervention is an ophthalmologic procedure;
previously enrolled in the VALIANCE study.
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
Centre hospitalier de l'Université de Montréal (CHUM)
Lead sponsor
Canadian Institutes of Health Research (CIHR)
Collaborator
Université de Montréal
Collaborator
Fonds de la Recherche en Santé du Québec
Collaborator