Dobutamine Stress Cardiac Magnetic Resonance Versus Echocardiography for the Assessment of Outcome. Are the Two Imaging Modalities Comparable?
Information source: University Hospital Heidelberg
ClinicalTrials.gov processed this data on August 20, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Coronary Artery Disease
Phase: N/A
Status: Completed
Sponsored by: University Hospital Heidelberg
Summary
Dobutamine stress echocardiography (DSE) and cardiac magnetic resonance (DCMR) are both
established non-invasive techniques, used in the clinical routine for the diagnostic
classification and risk stratification of patients with suspected or known coronary artery
disease (CAD).
In this regard, regional wall motion abnormalities (WMA) during dobutamine stress, precede
the development of ST-segment depression and anginal symptoms, enabling the detection of
anatomically significant CAD and the assessment of clinical outcomes.
In a head-to-head comparison between the 2 techniques, favourable diagnostic characteristics
in terms of higher sensitivity and accuracy were noted for DCMR compared to DSE.
Although it has been reported that stress induced WMA both in DCMR and in DSE are
independent predictors for hard cardiac events such as cardiac death or myocardial
infarction, the value of the 2 techniques for the risk stratification of patients with CAD
has not been compared to each other so far.
Comparison of these 2 non-invasive techniques is important, because referring physicians
need to know which modality is more reliable for the identification of patients at higher
risk for subsequent cardiac events, who would benefit from early invasive therapy.
In the investigators study the investigators therefore sought to compare the ability of DSE
versus DCMR to predict subsequent hard cardiac events and revascularization procedures in a
patient cohort with high CAD prevalence. Their predictive value was compared to that of
conventional atherogenic risk factors and to resting WMA. In addition, the investigators
sought to determine if both techniques are equally suitable for structuring invasive or
conservative treatment according to the presence or absence of inducible ischemia,
respectively.
Clinical Details
Study design: Observational Model: Cohort, Time Perspective: Prospective
Primary outcome: Cardiac death and nonfatal myocardial infarction (MACEs)
Secondary outcome: Late revascularization (90 days after the MR-examination)
Detailed description:
Background: Both DSE and DCMR are implemented in the daily diagnostic work-up of patients
with ischemic heart disease. Although DCMR was previously shown to aid the diagnostic
classification of patients with suspected CAD with higher sensitivity and accuracy compared
to that provided by DSE, the value of the 2 techniques for the risk stratification of
patients with CAD has not been investigated so far.
Methods: Patients with suspected or known CAD underwent either DSE or DCMR for clinical
reasons using the same standardised high-dose dobutamine/atropine protocol. Patient matching
was performed for age, gender and coronary risk factors. Wall motion was assessed at rest
and during maximum stress, and outcome data including cardiac death and non-fatal myocardial
infarction (defined as hard cardiac events) and 'late' revascularization performed >90 days
after the MR-scans were prospectively collected at least 6 months after DSE or DCMR.
Follow-up Data: Personnel unaware of the stress testing results contacts each subject or an
immediate family member and the date of this contact was used for calculating the follow-up
time duration. Outcome data is collected from a standardized questionnaire and determined
from patient interviews at the outpatient clinic or by telephone interviews. Reported
clinical events are confirmed by review of the corresponding medical records in our
electronic Hospital Information System (HIS), contact with the general practitioner,
referring cardiologist or the treating hospital. Cardiac death and nonfatal myocardial
infarction are registered as major cardiac events. Cardiac death is defined as death from
any cardiac cause (lethal arrhythmia, myocardial infarction, or congestive heart failure) or
sudden unexpected death occurring without another explanation. Myocardial infarction is
defined by angina of >30 minutes duration and either ST segment elevation of ≥2mm in 2
consecutive ECG leads or a rise in troponin T of ≥0. 03µg/l.
Other events include clinically indicated coronary arterial revascularization by
percutaneous coronary angioplasty (PCI) or coronary artery bypass graft (CABG).
In case of 2 simultaneous cardiac events, the worst event was selected (cardiac
death>non-fatal myocardial infarction>revascularization).
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- written informed consent before the DSE or DSCMR-examination
Exclusion Criteria:
- unstable angina
- severe arterial hypertension (>200/120mmHg)
- moderate or severe valvular disease
- general contraindications to dobutamine stress echocardiography: poor echogenic
windows limiting endocardial border detection in ≥2 myocardial segments
- general contraindications to dobutamine stress cardiac magnetic resonance: implanted
pacemakers or cardioverter defibrillator, claustrophobia
Locations and Contacts
University of Heidelberg, Department of Cardiology, Heidelberg, Baden-Württemberg 69120, Germany
Additional Information
Starting date: January 2001
Last updated: March 30, 2012
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