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Hospital Healthcare Europe

Management of coronary artery disease by cardiac magnetic resonance

Juerg Schwitter
1 January, 2008  

Juerg Schwitter
MD FESC
Director Cardiac MR Centre
Cardiology Department
University Hospital Zurich
Consultant Cardiac MR Center
Children’s University Hospital Zurich
Switzerland
Chairman of EuroCMR,
the Working Group on Cardiovascular Magnetic ­Resonance of the European Society of Cardiology

Coronary artery disease (CAD) is the number-one cause of death in the Western world, and approximately 60% of all cardiac deaths in the USA in 2004 occurred in patients before they got access to adequate in-hospital treatment (ie, deaths occurred in the emergency department or even before patients reached the hospital).(1) Thus, less than half of patients with acute myocardial infarction (AMI) benefit from the latest improvements in in-hospital care. Consequently, early detection of CAD in its “pre-AMI phase” is crucial to initiate treatment of CAD before an AMI occurs, since the mortality rate of AMI is still high, particularly during the time period before the patient reaches hospital care.

Efforts have been undertaken to reduce the “time-to-needle”, the time interval from onset of AMI ­symptoms to in-hospital treatment, with some automatic external defibrillators being installed in public areas. While ­necessary, these emergency measures do have physical limitations, and they require hospital resources (infrastructure and manpower) being reserved for emergencies and consequently not available for regular cases, which decreases cost-effectiveness. By concentrating our healthcare efforts on the treatment of AMI, approximately 60% of patients do not benefit, as they die before they reach the treatment options.

How to detect CAD in the “pre-AMI phase”?
CAD causes symptoms such as angina pectoris (chest pain), dyspnoea or arrhythmias, particularly ­during exercise. However, according to the latest US statistics in 2006, 50% of men and 64% of women who die suddenly from CAD had not had previous symptoms.(1) These numbers clearly indicate that ­concentrating healthcare efforts on symptomatic patients will miss more than half of the patients ­with CAD. Myocardial ischaemia and severe stenoses are linked to a high probability of plaque rupture and, thus, future AMI.(2) Accordingly, tests for detecting ischaemia or the presence of coronary artery ­stenoses, ideally in a noninvasive fashion, would provide the solution. In addition to noninvasiveness, these tests should show high diagnostic reliability, bring no harm to patients (since they have to be repeated to monitor the patient’s health status over many years); in addition, they should be low in price and comfortable.

Both stress echocardiography and single-photon-emission computed tomography (SPECT) demonstrate­ adequate sensitivity and specificity for CAD detection. However, stress ­echocardiography shows some operator dependence and is limited in patients with suboptimal “acoustic windows”. SPECT brings some radiation burden, which translates into an increased risk for cancer ­development. In the past years, cardiac magnetic resonance (CMR) has become a robust and clinically well-accepted method. Quality of CMR images is independent of patient anatomy, and it is not associated with ­ionising radiation, so it is repeatable. At the beginning of this century, several single-centre CMR perfusion ­studies documented a high capacity of CMR to detect CAD,(3) which was confirmed in several ­multicentre CMR studies in Europe and the USA.(4) Finally, a large international programme, the MR-IMPACT (Magnetic Resonance Imaging for Myocardial Perfusion ­Assessment in Coronary artery Disease) trial was launched, which demonstrated superiority of ­perfusion CMR over SPECT for the detection of CAD – that is, significantly larger area under the receiver–operator characteristics (ROC) curve for CMR (see Figure 1).(5,6) The availability of reliable and cost-effective tests will allow the detection of patients in the “pre-AMI phase” (ie, an active strategy will become reality by utilisation of CMR).

[[HHE07_fig1_Ca3]]

The active strategy of detection and monitoring of CAD in the healthcare systems
In the END study, the workup of patients with suspected CAD was performed by SPECT or invasive X-ray coronary angiography.(7) This study convincingly demonstrated reduced costs of workup (and two-year follow-up) by approximately 40% by means of SPECT with identical outcome. This END study is likely indicating the beginning of an era where tests in a multicentre setting will be compared so that test performance can be objectively determined and, from that, cost-effectiveness can also be calculated (eg, by cost curves).

This information is invaluable in the light of the ongoing implementation of diagnosis-related groups  (DRGs) in most countries in Europe and USA. As diagnostic performance for CAD detection is currently best achieved by CMR,(4–6) it might become the first-line test in the workup of suspected CAD or in the monitoring of CAD.

While industry highlights the multidetector computed tomography (MDCT) performance for CAD detection, this technique is limited by several drawbacks such as limited diagnostic performance (about 40% dropout rate in the only multicentre trial available so far,(8) therefore not confirming single-centre studies using the same technology), and more importantly, by its substantial radiation burden causing one solid cancer per 670 examinations based on cancer incidence per mSv (unit of ­radiation ­burden) reported in the most recent BEIR VII (phase II) report.(9) Consequently, future utilisation of tests will be based on test performance indices(10) (demonstrated by multicentre ROC curves) and their cost-­effectiveness, which will also have to include costs for treatment of side-effects such as cancer. Public health services will most likely rely on these test features (as they will allow for a meaningful ­benchmarking between ­hospitals and private providers).

As high-end scanners should run at full capacity, this imaging service will most likely be provided by hospital polyclinics or private networks. In parallel, the patients will have an increasing influence on this process of test selection, in particular in the private healthcare sector. To better involve the public in this discussion, it may be necessary to provide information on test side-effects, as suggested recently (see Figure 2). The information from multinational registries on test performances will be of utmost importance to permanently adapt healthcare resources allocation to the best and most cost-effective techniques available.(10)

[[HHE07_fig2_Ca4]]

References

  1. Heart disease and stroke statistics: Update 2005/2006. AHA 2005/2006.
  2. Schwitter J. Future Cardiol 2006;2(5):555-65.
  3. Schwitter J, et al. Circulation 2001;103(18):2230-5.
  4. Giang T, et al. Eur Heart J 2004;25:1657-65.
  5. Schwitter J, et al. Eur Heart J 2005;Clinical Trial Update; abstract.
  6. Schwitter J, et al. MR-IMPACT II. Circulation 2006;Annual Scientific Meeting of the AHA, Chicago.
  7. Shaw LJ, et al. J Am Coll Cardiol 1999;33:661-9.
  8. Garcia MJ, et al. JAMA 2006;296(4):403-11.
  9. Committee to Assess Health Risks from Exposure to Low Levels of Ionizing Radiation NRCNAoS. www.nap.edu/­catalog/11340.html
  10. Fraser AG, et al. Eur Heart J 2006;27(14):1750-3.