Acute Myocardial Infarction Quality Assurance Project (AMIQA)

Cohort study aimed at evaluating the incidence of left ventricular (LV) dysfunction after myocardial infraction (MI) and assessing the prognostic utility of change in ejection fraction (EF) over the initial 12 months after MI.

Study Overview

• Status: Unknown
• Conditions: Myocardial Infarction; Heart Failure; Death
• Intervention / Treatment: Other: Standard of Care; Other: Quality Assurance Implementation

Detailed Description

Background

Patients suffering a myocardial infraction (MI) may have from minimal to extensive myocardial damage. While severe left ventricular (LV) dysfunction that persists beyond the initial 2-3 months of an MI is a predictor of sudden death, the prognostic significance of less severe LV dysfunction after MI is unclear.

There is significant clinical value in quantifying LV function after the recovery phase of an MI. This information is vital in guiding the breadth and duration of therapies known to improve prognosis (beta-blockers, ACE inhibitors, angiotensin blockers, anticoagulants, and others). Further, it will identify patients in whom other therapies, such as an implantable cardioverter defibrillator (ICD), are recommended. Yet, no guidelines to guide clinical decision making in terms of collecting follow-up ejection fraction (EF) data in such patients who do not also have overt heart failure.

Purpose The Acute Myocardial Infarction Quality Assurance (AMIQA) project proposes to

1. document clinical practice by collecting data on the proportion of patients with initial LV dysfunction after MI without a follow-up EF assessment arranged,
2. collect follow-up EF data in patients with initial LV dysfunction post-MI and evaluate the prognostic significant of EF early and late after MI as well as factors associated with the change in value, and
3. educate physicians regarding the importance of EF reassessment after MI.

Follow up LV assessment

The current guidelines do not clearly provide clear indications to the appropriate timing or modality of follow up left ventricular assessments. We have chosen to define an adequate follow up LV assessment to occur within 2 to 12 months post-myocardial infarction, measured by any modality such as echocardiography, cardiac MRI, or nuclear perfusion scan.

Overall Study Objectives

1. To evaluate the relationship of changes in EF after MI with clinical variables such as age, gender, co-morbid conditions, MI characteristics, and the prescription of pharmacological agents after MI.
2. To assess the relationship of changes in EF after MI with clinical outcomes.

Study Methodology and Data Collection

This study will be conducted in three phases:

1. determining the existing practice of assessing left ventricular ejection fraction following myocardial infarction within the Calgary region (Quality Assurance);
2. determining the factors associated with LVEF improvement, stability and decline post-MI and the relationship of these with outcome (Prognostic Factor Study);
3. educating the clinical community about the importance of follow up LVEF assessments and reporting the findings of this through presentations, educational materials and/or academic publications (Knowledge Dissemination)

Study Population

The study population will include patients presenting with an acute myocardial infarction (NSTEMI or STEMI) undergoing cardiac catheterization at the Foothills Medical Center, who have significant left ventricular impairment upon initial LV assessment as defined as at least:

• At least mod dysfunction (LVEF < 0.40) if no prior history of MIs (i.e. first MI)
• More than mild-moderate dysfunction (LVEF < 0.45) if prior history of MI Exclusion criteria include: patients lost to follow up by their family physician or primary cardiologist, and patients who are deceased who do not have a follow-up EF.

Patients will be identified using the APPROACH (Alberta Provincial Project for Outcome Assessment in Coronary Heart Disease (www.approach.org)) database. All patients will have provided written, informed consent as part of their participation in APPROACH.

AMIQA Phase I: Quality Assurance

Part One (Quality Assurance) will include patients with an MI occurring between July 1, 2010 to November 30, 2011 (15 months). The list of patients who have had myocardial infarctions undergoing cardiac catheterization at the Foothills Medical Center between these dates can be obtained through the APPROACH database. For the patients that meet the initial inclusion criteria for significant LV dysfunction post-MI, the study group will determine if a follow up LVEF assessment has been performed within 2 to 12 months post-MI by contacting the patient's family physician and/or primary cardiologist for any records of LVEF measurements, and searching through the following electronic databases.

AMIQA Phase II: Prognostic Factor Study

Part Two (Prognostic Factor Study) will include patients with myocardial infarctions occurring on December 5, 2011 until December 5, 2012 (12 months). The list of patients who have had myocardial infarctions undergoing cardiac catheterization at the Foothills Medical Center between these dates can be obtained through the APPROACH database. For the patients that meet the initial inclusion criteria for significant LV dysfunction post-MI (as described in section 5.1), the study group will contact the patient, the patient's family physician, and/or patient's primary cardiologist to order a follow up LVEF measurement within 2 to 12 months post- myocardial infarction. That is, all patients that have significant LV dysfunction will undergo follow up LVEF measurements between December 5, 2011 and December 5, 2012. Modalities for follow up LVEF measurements will include echocardiogram, cardiac MRI, and nuclear perfusion imaging at the discretion of the family physician or primary cardiologist.

These follow up LVEF measurements will be entered into the APPROACH database in order to allow us to evaluate the clinical significance of changes in EF after MI and prognostic significance of initial versus follow-up EF values.

Data Analysis

AMIQA Phase I: Quality Assurance

Data collected will be entered into a database and summary statistics will be created (e.g. proportion of follow up LVEF assessments completed post-MI (Aim 5.1), choice of modality for follow up LVEF assessment, etc.) Data collected from the surveys will be entered into a database and analyzed in SAS or Stata. Summary statistics will be created from the data collected in the surveys.

Acute Myocardial Infarction Quality Assurance (AMIQA) Project Research Protocol - Updated Feb 29, 2012

AMIQA Phase II: Prognostic Factor Study

As part of AMIQA Phase II, LVEF assessments will be entered into the APPROACH database. The study will compare initial LVEF measurements post-MI to follow-up LVEF measurements, and assess for improvement, stability and deterioration of LVEF and the factors associated with these changes in LVEF.

This project has received ethics approval by the Conjoint Health Research and Ethics Board of the University of Calgary. Patients will be identified using the APPROACH database have provided written, informed consent as part of their participation in APPROACH. Only the research team will know the names and contact information of the patients included in the study, and this information will be kept confidential.

• Study Type: Observational
• Enrollment (Anticipated): 6000

Contacts and Locations

Study Locations

• Canada
  • Alberta
    • Calgary, Alberta, Canada, T3H 4N4
      • Recruiting
      • Foothills Medical Centre
      • Contact: Rozsa Sas; Phone Number: 4032107398; Email: rsas@ucalgary.ca
      • Contact: Derek V Exner, MD, MPH; Phone Number: 4032203219
      • Principal Investigator: Derek S Chew, MD
      • Principal Investigator: Derek V Exner, MD,MPH

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

• Sampling Method: Non-Probability Sample

Study Population

Patients surviving an acute MI.

Description

Inclusion Criteria:

• confirmed MI

Exclusion Criteria:

• None

Study Plan

How is the study designed?

Design Details

• Observational Models: Cohort
• Time Perspectives: Prospective

Number of groups / cohorts

2

Cohorts and Interventions

Group / Cohort	Intervention / Treatment
Retrospective; MI prior to December 11, 2011	Other: Standard of Care
Prospective; MI on or after December 11, 2011	Other: Quality Assurance Implementation

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Mortality	2 years

Secondary Outcome Measures

Outcome Measure	Time Frame
Ejection Fraction	12 months
Heart Failure Hospitalization	2 years

Collaborators and Investigators

• Sponsor: Dr. Derek Exner

Study record dates

Study Major Dates

• Study Start: December 1, 2011
• Primary Completion (Anticipated): December 1, 2017
• Study Completion (Anticipated): December 1, 2017

Study Registration Dates

• First Submitted: March 23, 2015
• First Submitted That Met QC Criteria: March 23, 2015
• First Posted (Estimate): March 26, 2015

Study Record Updates

• Last Update Posted (Estimate): June 8, 2016
• Last Update Submitted That Met QC Criteria: June 7, 2016
• Last Verified: June 1, 2016

More Information

Terms related to this study

• Keywords: Prognosis; Incidence; Ejection Fraction; Remodeling; Quality Assurance; Sudden Death
• Additional Relevant MeSH Terms: Ischemia; Pathologic Processes; Necrosis; Myocardial Ischemia; Heart Diseases; Cardiovascular Diseases; Vascular Diseases; Myocardial Infarction; Infarction
• Other Study ID Numbers: QA20111211

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No