Cost Comparison of Cardiac Magnetic Resonance Imaging (MRI) Use in Emergency Department (ED) Patients With Chest Pain
Primary Purpose
Acute Coronary Syndrome, Chest Pain
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Observation unit care, coupled with cardiac MRI
Sponsored by
About this trial
This is an interventional diagnostic trial for Acute Coronary Syndrome focused on measuring ACS, Acute Coronary Syndrome, Chest pain, Cardiac MRI, CMR, Risk Stratification, Emergency Department
Eligibility Criteria
Inclusion Criteria:
- Age greater than or equal to 18 years of age at the time of enrollment
- Chest discomfort or other symptoms consistent with possible Acute Coronary Syndrome (ACS) as indicated by the treating physician after obtaining an Electrocardiogram (ECG) and cardiac biomarkers for the patient's evaluation
- Patient requires an inpatient evaluation for their chest pain
- The treating physician feels the patient could be discharged home if cardiac disease was excluded
- Thrombolysis in Myocardial Infarction (TIMI) risk score ≥ 2 OR physician clinical impression of intermediate or high likelihood that the symptoms represent ACS
- Negative pregnancy test (if sexually active, female, and of childbearing age)
Exclusion Criteria:
- Initial troponin I > 1.0 ng/ml
- New ST-segment elevation on any electrocardiogram (≥ 1 mV)
- New ST-segment depression on any electrocardiogram (≥ 2 mV)
- Unable to lie flat
- Hypotension (systolic < 90 mm Hg)
- Contra-indications to MRI(Pacemaker, defibrillator, cerebral aneurysm clips, metallic ocular foreign body, implanted devices, claustrophobia)
- Patient refusal of medical record review and telephone follow-up at 30 days
- Terminal diagnosis with life expectancy less than 3 months
- Pregnancy per patient report or positive pregnancy test (Center for Medicare & Medicaid Services (CMS) exclusion criteria)
- Renal insufficiency(done prior to enrollment)or end stage renal disease
- Chronic liver disease (ex. hepatitis, cirrhosis)
- History of liver, heart, or kidney transplant
Sites / Locations
- Wake Forest University Baptist Medical Center - Emergency Department
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Emergency Department (ED) Observation unit
Usual care
Arm Description
Emergency Department observation unit- Cardiac Magnetic Resonance Imaging (MRI) Protocol. Patients will be transferred to the observation unit and undergo a stress cardiac MRI evaluation.
This is the comparison arm. Patients are admitted to the hospital and undergo usual care.
Outcomes
Primary Outcome Measures
Cost of Index Hospitalization
Index hospitalization refers to the hospital visit during which the participant was enrolled in the trial. The primary outcome is examining the cost for this visit.
Secondary Outcome Measures
Correct Admission Decision, Based Upon the Reference Standard of Acute Coronary Syndrome (ACS) at 30 Days
Participants with ACS and admitted or not experiencing ACS and discharged will be considered a correct admission decision. Remaining participants will be considered to have incorrect admission decisions.
The Number of Participants Randomized to the OU and Were Able to Complete CMR Imaging
The number of participants able to complete the planned imaging sequences will be measured.
Number of Participants Who Utilized the Indicated Health Care Procedures
Measured as self report, assessed during telephone follow-up.
Adverse Events During Magnetic Resonance Imaging (MRI) Scanning
Any event leading to early termination of the MRI acquisition, or requiring intervention by a physician, will be considered an adverse event related to MRI, excluding physician termination of image acquisition due to concerns of cardiac ischemia.
Full Information
NCT ID
NCT00678639
First Posted
May 8, 2008
Last Updated
August 13, 2018
Sponsor
Wake Forest University Health Sciences
1. Study Identification
Unique Protocol Identification Number
NCT00678639
Brief Title
Cost Comparison of Cardiac Magnetic Resonance Imaging (MRI) Use in Emergency Department (ED) Patients With Chest Pain
Official Title
Randomized Cost Comparison of Cardiac MRI Use in ED Patients With Chest Pain
Study Type
Interventional
2. Study Status
Record Verification Date
August 2018
Overall Recruitment Status
Completed
Study Start Date
January 2008 (undefined)
Primary Completion Date
March 2009 (Actual)
Study Completion Date
March 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Wake Forest University Health Sciences
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to investigate the best way to evaluate patients with chest pain in the emergency department. It compares receiving treatment in an observation unit with admission to the hospital. Patients treated in the observation unit will undergo cardiac Magnetic Resonance Imaging (MRI) testing. Patients treated with hospital admission will undergo the testing their doctor determines is best for them. All patients will undergo follow up to find out if they have had any heart related events.
Detailed Description
Almost half of patients presenting to the Emergency Department (ED) with possible cardiac chest pain are at intermediate risk for short term death or infarction. Most are admitted to the hospital for serial ECG's, cardiac biomarkers, cardiology consultation, and stress testing or coronary angiogram. However, the 2007 ACC/AHA guidelines suggest that these patients can be managed in an observation unit (OU). Recently, cardiac magnetic resonance imaging (CMR) has proven more accurate than traditional testing modalities for the diagnosis of acute coronary syndrome (ACS), and has also received endorsement from the American College of Cardiology (ACC)/American Heart Association (AHA) guidelines. Immediate application of CMR in an OU may improve health care utilization compared to standard hospital admission for intermediate risk patients.
Research hypotheses:
Patients in an OU CMR protocol will have lower cost for the index hospitalization than standard care.
An OU CMR protocol for patients with intermediate risk chest pain will significantly improve the frequency of correct cardiovascular admission decisions when compared to standard care.
Methods summary:
110 ED patients at intermediate risk for short-term death or infarction, with nondiagnostic Electrocardiograms (ECG) and normal initial cardiac biomarkers, will be randomized to standard care or OU CMR protocols. Subjects in the OU CMR protocol will undergo CMR perfusion and stress testing, followed by serial biomarkers. Standard care subjects will be admitted for usual cardiac testing. ACS (infarction, death, coronary revascularization, unstable angina) will be assessed by evaluation of hospital course and phone follow-up at 30 days. Cost of hospital care will be compared among groups.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Coronary Syndrome, Chest Pain
Keywords
ACS, Acute Coronary Syndrome, Chest pain, Cardiac MRI, CMR, Risk Stratification, Emergency Department
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
110 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Emergency Department (ED) Observation unit
Arm Type
Experimental
Arm Description
Emergency Department observation unit- Cardiac Magnetic Resonance Imaging (MRI) Protocol. Patients will be transferred to the observation unit and undergo a stress cardiac MRI evaluation.
Arm Title
Usual care
Arm Type
No Intervention
Arm Description
This is the comparison arm. Patients are admitted to the hospital and undergo usual care.
Intervention Type
Other
Intervention Name(s)
Observation unit care, coupled with cardiac MRI
Intervention Description
After Emergency Department (ED) evaluation, patients are randomized to Observation unit care or standard inpatient care. Patients in the observation unit will also undergo a stress cardiac MRI. Patients in the usual care arm may undergo any desired testing, including cardiac MRI, as determined by their treating physician.
Primary Outcome Measure Information:
Title
Cost of Index Hospitalization
Description
Index hospitalization refers to the hospital visit during which the participant was enrolled in the trial. The primary outcome is examining the cost for this visit.
Time Frame
Emergency Department (ED) arrival through hospital discharge, median length of stay was 28.1 hours
Secondary Outcome Measure Information:
Title
Correct Admission Decision, Based Upon the Reference Standard of Acute Coronary Syndrome (ACS) at 30 Days
Description
Participants with ACS and admitted or not experiencing ACS and discharged will be considered a correct admission decision. Remaining participants will be considered to have incorrect admission decisions.
Time Frame
30 Days
Title
The Number of Participants Randomized to the OU and Were Able to Complete CMR Imaging
Description
The number of participants able to complete the planned imaging sequences will be measured.
Time Frame
Emergency Department (ED) arrival through hospital discharge
Title
Number of Participants Who Utilized the Indicated Health Care Procedures
Description
Measured as self report, assessed during telephone follow-up.
Time Frame
30d, 3mo, 6mo, and 1 year
Title
Adverse Events During Magnetic Resonance Imaging (MRI) Scanning
Description
Any event leading to early termination of the MRI acquisition, or requiring intervention by a physician, will be considered an adverse event related to MRI, excluding physician termination of image acquisition due to concerns of cardiac ischemia.
Time Frame
Occuring in the MRI scanning suite or within 30 minutes of the last image acquisition.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age greater than or equal to 18 years of age at the time of enrollment
Chest discomfort or other symptoms consistent with possible Acute Coronary Syndrome (ACS) as indicated by the treating physician after obtaining an Electrocardiogram (ECG) and cardiac biomarkers for the patient's evaluation
Patient requires an inpatient evaluation for their chest pain
The treating physician feels the patient could be discharged home if cardiac disease was excluded
Thrombolysis in Myocardial Infarction (TIMI) risk score ≥ 2 OR physician clinical impression of intermediate or high likelihood that the symptoms represent ACS
Negative pregnancy test (if sexually active, female, and of childbearing age)
Exclusion Criteria:
Initial troponin I > 1.0 ng/ml
New ST-segment elevation on any electrocardiogram (≥ 1 mV)
New ST-segment depression on any electrocardiogram (≥ 2 mV)
Unable to lie flat
Hypotension (systolic < 90 mm Hg)
Contra-indications to MRI(Pacemaker, defibrillator, cerebral aneurysm clips, metallic ocular foreign body, implanted devices, claustrophobia)
Patient refusal of medical record review and telephone follow-up at 30 days
Terminal diagnosis with life expectancy less than 3 months
Pregnancy per patient report or positive pregnancy test (Center for Medicare & Medicaid Services (CMS) exclusion criteria)
Renal insufficiency(done prior to enrollment)or end stage renal disease
Chronic liver disease (ex. hepatitis, cirrhosis)
History of liver, heart, or kidney transplant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chadwick D Miller, MD
Organizational Affiliation
WFUBMC
Official's Role
Principal Investigator
Facility Information:
Facility Name
Wake Forest University Baptist Medical Center - Emergency Department
City
Winston-Salem
State/Province
North Carolina
ZIP/Postal Code
27157
Country
United States
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Cost Comparison of Cardiac Magnetic Resonance Imaging (MRI) Use in Emergency Department (ED) Patients With Chest Pain
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