N/A N=483

Perioperative Management of Patients With Coronary Stents Undergoing Noncardiac Surgery

Acute Coronary Syndrome · Coronary Stent Occlusion · Surgery

Bottom Line

View on ClinicalTrials.gov: NCT01171612 ↗

Enrolled (actual)

483

Serious AEs

14.1%

Results posted

Nov 2013

Primary outcome: Primary: Major Adverse Cardiac and Cerebrovascular Events (MACCEs) — 63 participants

Study Design & Population

Study type: Observational
Phase: N/A
Interventions: —
Age: Adult, Older Adult · 18+ yrs
Sex: All
Sponsor: Corporacion Parc Tauli
Primary completion: Feb 2010

Outcome Measures

Outcome	Result	p-value
PRIMARY Major Adverse Cardiac and Cerebrovascular Events (MACCEs)	63	—
SECONDARY Major Haemorrhagic Events	161	—
SECONDARY Number of Patients With Adverse Events Related With Antiplatelet Therapy Management	38; 10; 9	0.479

Summary

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

Eligibility Criteria

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

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01171612). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.