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Download the full report (116 p.) - KCE

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<strong>KCE</strong> Reports 82 Multislice CT in Coronary Heart Disease 37<br />

Figure 3: Clinical path of patients studied in trials and those deemed<br />

appropriate for MSCT by current guidelines<br />

Shaded area: patients studied in clinical trials so far. Dark grey area: patients in whom MSCT is<br />

CHEST PAIN ANGINA<br />

ATYPICAL CHEST PAIN<br />

NEGATIVE ECG STRESS TEST POSITIVE<br />

INCONCLUSIVE<br />

NEGATIVE MPS/DSE POSITIVE<br />

INCONCLUSIVE<br />

APPROPRIATE<br />

CANDIDATE FOR MSCT ?<br />

STANDARD CARE.<br />

CCA if APPROPRIATE.<br />

STANDARD CARE.<br />

CCA if APPROPRIATE.<br />

STANDARD CARE.<br />

CCA if APPROPRIATE.<br />

currently advocated in international guidelines. 108, 109 Bottom area: terra icognita. MPS: myocardial<br />

perfusion scintigraphy. DSE: dobutamine stress echocardiogram. CCA: conventional (invasive)<br />

coronary angiography.<br />

The most decisive evidence for judging <strong>the</strong> effectiveness of MSCT should come from<br />

randomised controlled trials. MSCT can affect patient outcome when <strong>the</strong> information<br />

obtained from it is used to guide decisions to start, withhold, modify or stop<br />

treatment. 113 Only patients in whom coronary imaging is deemed appropriate but <strong>the</strong><br />

likelihood for revascularisation is low, should be enrolled in such a trial. If <strong>the</strong> potential<br />

need for revascularisation is high, invasive CCA is a more efficient first step because it<br />

allows to proceed to <strong>the</strong> <strong>the</strong>rapeutic intervention (PCI) within <strong>the</strong> same procedure.<br />

Noninvasive imaging by MSCT can e.g. be envisaged for reassurance of a patient (or<br />

his/her cardiologist) or for making an early decision for discharge of a patient admitted<br />

with acute chest pain from <strong>the</strong> emergency department. Randomisation of such patients<br />

in a trial can take place at different decision points in <strong>the</strong> clinical path (after stress<br />

testing, MPS, or DSE) and against several alternative diagnostic options (MPS, DSE,<br />

CCA, sequential biomarkers). The outcome of such a trial should not focus on <strong>the</strong><br />

correctness of <strong>the</strong> anatomical diagnosis but on endpoints that are relevant to patients,<br />

such as symptom control, prevention of MI, and prolongation of survival. From a<br />

societal perspective, long term downstream costs differences between different<br />

pathways should be obtained.<br />

Key point<br />

• There is an urgent need for evidence on (1) <strong>the</strong> diagnostic<br />

performance of MSCT in real world clinical practice, (2) its effect on<br />

patient outcomes (QoL, prevention of infarction, prolongation of<br />

life) and (3) its cost-effectiveness as compared to diagnostic<br />

pathways in which MSCT is not embedded.

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