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Safety And Feasibility of Early DischargE - a Prospective And Randomized Trial of Low-risk Primary Percutaneous Coronary Intervention (PCI) Patients (SAFE-DEPART)

Primary Purpose

Myocardial Infarction

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Early hospital discharge facilitated by close nurse practitioner follow-up
Sponsored by
Hamilton Health Sciences Corporation
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional health services research trial for Myocardial Infarction focused on measuring STEMI, Primary PCI, Length of Stay, Early Discharge

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient with ST-elevation myocardial infarction (STEMI)
  • Treatment with either primary or rescue PCI
  • Zwolle risk score <= 3

Exclusion Criteria:

  • Developed MI while in hospital for another reason
  • Time from angioplasty to enrollment > 24 hours

Sites / Locations

  • Hamilton Health Sciences

Outcomes

Primary Outcome Measures

Safety: All-cause mortality
Safety: Readmission for any of CHF, unstable angina, arrhythmia, re-infarction, revascularization, stroke, or major bleeding requiring transfusion
Feasibility: Proportion of patients in the intervention group discharged within 72 hours ("feasible" if >= 70%)
Feasibility: Proportion of patients in the intervention group who saw nurse practitioner within 3 days of discharge ("feasible" if >= 80%)
Feasibility: Proportion of patients in the intervention group who saw nurse practitioner within 5 days of discharge ("feasible" if >= 90%)

Secondary Outcome Measures

Quality of life, as measured by the SF-36 questionnaire
Compliance with medications
Compliance with smoking cessation
Attendance at first cardiac rehabilitation session
Cost-effectiveness

Full Information

First Posted
May 15, 2007
Last Updated
February 22, 2010
Sponsor
Hamilton Health Sciences Corporation
Collaborators
McMaster University, Regional Medical Associates Research Scholarship Fund
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1. Study Identification

Unique Protocol Identification Number
NCT00474214
Brief Title
Safety And Feasibility of Early DischargE - a Prospective And Randomized Trial of Low-risk Primary Percutaneous Coronary Intervention (PCI) Patients
Acronym
SAFE-DEPART
Official Title
Safety And Feasibility of Early DischargE - a Prospective And Randomized Trial of Low-risk Primary PCI Patients (The SAFE-DEPART Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
February 2010
Overall Recruitment Status
Completed
Study Start Date
January 2007 (undefined)
Primary Completion Date
December 2007 (Actual)
Study Completion Date
December 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Hamilton Health Sciences Corporation
Collaborators
McMaster University, Regional Medical Associates Research Scholarship Fund

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine if early hospital discharge (at 48-72 hours), is feasible, safe, cost-effective, and/or improves compliance with medications, positive lifestyle changes and quality-of-life, in low-risk patients with ST-elevation myocardial infarction treated with primary percutaneous coronary intervention (primary PCI).
Detailed Description
Patients with acute ST-segment elevation myocardial infarction (STEMI) have traditionally been hospitalized for at least 5-7 days to monitor for serious complications, including heart failure, arrhythmias, re-infarction and death. With the advent of primary percutaneous coronary intervention (PCI) as the treatment of choice for STEMI, fewer patients are completing their infarcts and the incidence of complications is decreasing. The Zwolle Primary PCI Index is one of several externally validated risk scores that can be used to identify low-risk primary PCI patients who can safely be discharged at 48-72 hours. Recent reviews have found that a majority of primary PCI patients with risk scores that deem them "low-risk" are kept in hospital longer than predicted by these scores. SAFE-DEPART is a trial where low-risk primary and rescue PCI patients will be randomized either to an intervention arm (early hospital discharge, early outpatient follow-up with a nurse practitioner) or to standard of care (no recommended discharge date, no outpatient follow-up with a nurse practitioner). At 6 weeks time, a blinded research assistant will contact patients and collect data on feasibility, safety, quality-of-life, and cost-effectiveness outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myocardial Infarction
Keywords
STEMI, Primary PCI, Length of Stay, Early Discharge

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
54 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Behavioral
Intervention Name(s)
Early hospital discharge facilitated by close nurse practitioner follow-up
Primary Outcome Measure Information:
Title
Safety: All-cause mortality
Time Frame
6 weeks
Title
Safety: Readmission for any of CHF, unstable angina, arrhythmia, re-infarction, revascularization, stroke, or major bleeding requiring transfusion
Time Frame
6 weeks
Title
Feasibility: Proportion of patients in the intervention group discharged within 72 hours ("feasible" if >= 70%)
Title
Feasibility: Proportion of patients in the intervention group who saw nurse practitioner within 3 days of discharge ("feasible" if >= 80%)
Title
Feasibility: Proportion of patients in the intervention group who saw nurse practitioner within 5 days of discharge ("feasible" if >= 90%)
Secondary Outcome Measure Information:
Title
Quality of life, as measured by the SF-36 questionnaire
Time Frame
6 weeks
Title
Compliance with medications
Time Frame
6 weeks
Title
Compliance with smoking cessation
Time Frame
6 weeks
Title
Attendance at first cardiac rehabilitation session
Time Frame
6 weeks
Title
Cost-effectiveness
Time Frame
6 weeks

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient with ST-elevation myocardial infarction (STEMI) Treatment with either primary or rescue PCI Zwolle risk score <= 3 Exclusion Criteria: Developed MI while in hospital for another reason Time from angioplasty to enrollment > 24 hours
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark A Kotowycz, MD, MBA
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Madhu K Natarajan, MD
Organizational Affiliation
Hamilton Health Sciences Corporation
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hamilton Health Sciences
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8L 2X2
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
20102876
Citation
Kotowycz MA, Cosman TL, Tartaglia C, Afzal R, Syal RP, Natarajan MK. Safety and feasibility of early hospital discharge in ST-segment elevation myocardial infarction--a prospective and randomized trial in low-risk primary percutaneous coronary intervention patients (the Safe-Depart Trial). Am Heart J. 2010 Jan;159(1):117.e1-6. doi: 10.1016/j.ahj.2009.10.024.
Results Reference
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Safety And Feasibility of Early DischargE - a Prospective And Randomized Trial of Low-risk Primary Percutaneous Coronary Intervention (PCI) Patients

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