TY - JOUR
T1 - A novel clinically relevant segmentation method and corresponding maximal ischemia score to risk-stratify patients undergoing myocardial perfusion scintigraphy
AU - Nudi, Francesco
AU - Pinto, Annamaria
AU - Procaccini, Enrica
AU - Neri, Giandomenico
AU - Vetere, Maurizio
AU - Tomai, Fabrizio
AU - Gaspardone, Achille
AU - Biondi-Zoccai, Giuseppe
AU - Schillaci, Orazio
PY - 2014
Y1 - 2014
N2 - Background. Myocardial perfusion scintigraphy (MPS) represents a key prognostic tool, but its predictive yield is far from perfect. We developed a novel clinically relevant segmentation method and a corresponding maximal ischemia score (MIS) in order to risk-stratify patients undergoing MPS. Methods. Patients referred for MPS were identified, excluding those with evidence of myocardial necrosis or prior revascularization. A seven-region segmentation approach was adopted for left ventricular myocardium, with a corresponding MIS distinguishing five groups (no, minimal, mild, moderate, or severe ischemia). The association between MIS and clinical events was assessed at 1 year and at long-term follow-up. Results. A total of 8,714 patients were included, with a clinical follow-up of 31 ± 20 months. Unadjusted analyses showed that subjects with a higher MIS were significantly different for several baseline and test data, being older, having lower ejection fraction, and achieving lower workloads (P <.05 for all). Adverse outcomes were also more frequent in patients with higher levels of ischemia, including cardiac death, myocardial infarction (MI), and their composites (P <.05 for all). Differences in adverse events remained significant even after extensive multivariable adjustment (hazard ratio for each MIS increment = 1.57 [1.29-1.90], P <.001 for cardiac death; 1.19 [1.04-1.36], P = .013 for MI; 1.23 [1.09-1.39], P = .001 for cardiac death/MI). Conclusions. Our novel segmentation method and corresponding MIS efficiently yield satisfactory prognostic information.
AB - Background. Myocardial perfusion scintigraphy (MPS) represents a key prognostic tool, but its predictive yield is far from perfect. We developed a novel clinically relevant segmentation method and a corresponding maximal ischemia score (MIS) in order to risk-stratify patients undergoing MPS. Methods. Patients referred for MPS were identified, excluding those with evidence of myocardial necrosis or prior revascularization. A seven-region segmentation approach was adopted for left ventricular myocardium, with a corresponding MIS distinguishing five groups (no, minimal, mild, moderate, or severe ischemia). The association between MIS and clinical events was assessed at 1 year and at long-term follow-up. Results. A total of 8,714 patients were included, with a clinical follow-up of 31 ± 20 months. Unadjusted analyses showed that subjects with a higher MIS were significantly different for several baseline and test data, being older, having lower ejection fraction, and achieving lower workloads (P <.05 for all). Adverse outcomes were also more frequent in patients with higher levels of ischemia, including cardiac death, myocardial infarction (MI), and their composites (P <.05 for all). Differences in adverse events remained significant even after extensive multivariable adjustment (hazard ratio for each MIS increment = 1.57 [1.29-1.90], P <.001 for cardiac death; 1.19 [1.04-1.36], P = .013 for MI; 1.23 [1.09-1.39], P = .001 for cardiac death/MI). Conclusions. Our novel segmentation method and corresponding MIS efficiently yield satisfactory prognostic information.
KW - maximal ischemia score
KW - Myocardial ischemia
KW - myocardial perfusion imaging
KW - myocardial perfusion scintigraphy
KW - segmentation
UR - http://www.scopus.com/inward/record.url?scp=84905084042&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84905084042&partnerID=8YFLogxK
U2 - 10.1007/s12350-014-9877-5
DO - 10.1007/s12350-014-9877-5
M3 - Article
C2 - 24890378
AN - SCOPUS:84905084042
SN - 1071-3581
VL - 21
SP - 807
EP - 818
JO - Journal of Nuclear Cardiology
JF - Journal of Nuclear Cardiology
IS - 4
ER -