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095 VISUAL AND QUANTITATIVE ANALYSIS OF MYOCARDIAL PERFUSION IN LEFT MAIN STEM DISEASE: A CE-MARC SUBSTUDY
  1. J P Greenwood1,
  2. A Kidambi1,
  3. N Maredia1,
  4. K Mohee1,
  5. S Sourbron1,
  6. M Motwani1,
  7. A Uddin1,
  8. D P Ripley1,
  9. B Herzog1,
  10. A Zaman1,
  11. C J Dickinson2,
  12. J M B Brown1,
  13. J Nixon1,
  14. C C Everett1,
  15. S Plein1
  1. 1 University of Leeds
  2. 2 Leeds Teaching Hospitals NHS Trust

    Abstract

    Background Left main stem (LMS) disease occurs in approximately 5% of patients with stable angina. It confers adverse prognosis, with potential for prognostic gain with revascularization. Single-photon emission CT (SPECT) and cardiovascular magnetic resonance (CMR) fail to detect ischaemia in 41% and 18% of patients with significant LMS stenosis respectively, likely in part because of balanced reduction in coronary perfusion. It is not known whether quantitative assessment of myocardial blood flow (MBF) can improve diagnostic rates. The CE-MARC study prospectively enrolled 752 patients with suspected coronary artery disease, scheduled to undergo CMR, SPECT and X-ray coronary angiography. We assessed the diagnostic performance of visual and quantitative perfusion CMR in CE-MARC patients with LMS disease.

    Methods All patients from the CE-MARC population with LMS disease ≥50%, or LMS equivalent disease (proximal LAD and proximal LCx ≥70%) on quantitative angiography were studied. A control group (matched for age and gender, excluding LMS or 3-vessel disease) was randomly selected from the CE-MARC population. Visual SPECT and CMR analyses were from the original, blinded read of CE-MARC. Only perfusion components of the CE-MARC CMR and SPECT protocols were analysed. MBF was calculated offline (PMI v0.4) using the Fermi model from CMR stress perfusion images, with arterial input defined in LV blood pool, and LAD and LCx segments in the mid-LV short axis myocardial slice as tissue response.

    Results 47 patients were included in the analysis (22 LMS, 1 LMS equivalent, 24 controls); 1 LMS patient did not have CMR. Visual detection rates for ischsemia in LMS disease were non-significantly higher for CMR than SPECT (83% vs 61%, p=0.19). On quantitative CMR perfusion analysis, stress MBF was significantly lower in LMS patients than controls (2.67±0.94 ml/g/min vs 3.97±1.25 ml/g/min, p<0.01). ROC AUC for MBF was 0.81. An MBF cut-off of 3.78 ml/g/min was derived by Youdens Index (to objectively find optimal sensitivity and specificity). This cut-off point had sensitivity 0.96, specificity 0.67 and accuracy 0.81 for LMS disease over controls. Using this cut-off, stress MBF had higher sensitivity in LMS disease than visual SPECT analysis (96% vs 61%, p=0.01, figure 1), but was not significantly superior to visual CMR analysis (p=0.35).

    Figure 1

    Detection rates of ischaemic heart disease for CMR visual analysis, CMR MBF quantitation, and SPECT in 23 patients with LMS or LMS equivalent disease.

    Conclusions Quantitative CMR identifies LMS disease with higher sensitivity than visual SPECT analysis. Quantitative CMR analysis of MBF compared to visual CMR analysis did increase diagnostic sensitivity numerically; however this did not reach statistical significance in this small population from CE-MARC.

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