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.