Perioperative Management of Patients With Coronary Stents Undergoing Noncardiac Surgery (RegistStents)

Corporacion Parc Tauli

Status: Completed

Conditions: Acute Coronary Syndrome; Surgery; Coronary Stent Occlusion

Study type: Observational

Funder types: Other

Identifiers

NCT01171612

CIR2009017

Details and patient eligibility

About

The purpose of this study is to evaluate and monitor perioperative management of patients with coronary stents undergoing noncardiac surgery.

Objectives:

• To describe the incidence and severity of adverse cardiovascular events in patients with coronary stents undergoing noncardiac surgery with admission.
• To assess the following-up of the guidelines about the perioperative management of antiplatelet therapy in these patients.
• To assess the relationship between the incidence of cardiac or neurovascular events, as well as bleeding complications with the perioperative management of antiplatelet therapy.
• Number of Participants with Adverse Events as a Measure of Safety

Full description

(Not desired)

Enrollment: 483 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• > 18 years old, with coronary stents
• American Society of Anaesthesia physical status II-V
• noncardiac surgery wiht admission
• informed consent

Exclusion criteria

• < 18 years old
• American Society of Anaesthesia physical status I
• ambulatory surgery
• pregnancy
• obstetric anaesthesia
• endoscopic procedures
• cardiac surgery
• not informed consent

Trial design

483 participants in 1 patient group

Coronary Stent

Description:

Patients with coronary Bare Metal Stent (BMS) or Drug Eluting Stent (DES) undergoing noncardiac surgery