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Clinical Trials/NCT02672137
NCT02672137
Completed
Not Applicable

Knowledge Translation to Promote Evidence-based Medical Therapy in Acute Coronary Syndromes

Montreal General Hospital0 sites4,604 target enrollmentJanuary 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acute Coronary Syndromes
Sponsor
Montreal General Hospital
Enrollment
4604
Primary Endpoint
Proportion of patients who received evidence-based medical therapy at hospital discharge (mean of 4 days)
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

Cluster randomized open-label experimental study multi-center of 24 hospitals to either knowledge translation vs usual care to improve care of patents hospitalized for acute coronary syndromes.

Detailed Description

The AMI-OPTIMA study was a cluster randomized controlled trial of 24 hospitals to one-year knowledge translation (KT) vs usual care. Prior to randomization, we reviewed charts of 100 consecutive acute coronary syndromes (ACS) patients at each participating hospital in 2009. During one year, hospitals randomized to KT completed: 1) revision of the most recent American Heart Association Guidelines of ACS management, 2) focus groups to identify and solve local care gaps, and 3)local champion team to promote evidence-based medical therapy (EBMT). At the end of 12-month of KT/usual care, we reviewed discharge prescriptions of 100 consecutive ACS patients at each participating hospital (year 2012). EBMT was pre-defined as in-hospital anticoagulation and discharge prescription of dual anti-platelets, beta-blockers, statins, and angiotensin pathway modulating agents (for patients with impaired left ventricular systolic function). Refusal, impaired cognitive function, allergy or intolerance of patients to any of EBMT were considered valid reasons for withholding EBMT.

Registry
clinicaltrials.gov
Start Date
January 2010
End Date
January 2016
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Thao Huynh

Cardiologist, associate professor of medicine

Montreal General Hospital

Eligibility Criteria

Inclusion Criteria

  • Had a final discharge diagnosis of one of the following categories:
  • Myocardial infarction with ST-segment elevation
  • Myocardial infarction without ST-segment elevation
  • Unstable angina
  • Acute coronary syndromes -

Exclusion Criteria

  • Non-atherosclerotic coronary artery disease (as confirmed by coronary angiograms or other non-invasive tests such as stress test, coronary CT-scan, nuclear scans)
  • Hospital stay of less than 48 hours -

Outcomes

Primary Outcomes

Proportion of patients who received evidence-based medical therapy at hospital discharge (mean of 4 days)

Time Frame: at hospital discharge (average of 4 days)

Evidence-based medical therapy is defined as aspirin,dual-antiplaquelets, beta-blockers, statins.

Secondary Outcomes

  • Discharge prescription of individual evidence-based medical therapy: aspirin, dual antiplatelets, beta-blockers(at hospital discharge (average of 4 days))
  • Safety endpoints (mortality, reinfarction, strokes and bleeding outcomes (TIMI major and minor bleeds))(in-hospital (average of 4 days))

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