Comparison of prognostic significance of mean platelet volume/platelet count with GRACE for long-term prognosis in patients with non-ST-segment elevation myocardial infarction undergoing percutaneous coronary intervention
详细信息    查看全文
文摘
Mean platelet volume to platelet count ratio (MPV/P ratio) has been demonstrated to be a predictor of adverse outcome in patients with non-ST-segment elevation myocardial infarction (NSTEMI). We aimed to assess whether MPV/P ratio is a useful marker to predict long-term prognosis in NSTEMI patients undergoing PCI. Moreover, the prognostic accuracy of MPV/P ratio was compared with MPV and GRACE score.MethodsIn a retrospective cohort study, according to the baseline MPV/P values, 887 consecutive NSTEMI patients undergoing PCI were divided into two groups: the high MPV/P group (n = 296, MPV/P ≥ 0.054) and the low MPV/P group (n = 591, MPV/P < 0.054). Clinical endpoints were all-cause mortality and all-cause mortality/nonfatal reinfarction.ResultsMultivariate analysis showed that high MPV/P was an independent predictor of all-cause mortality [HRs: 1.973, 95% CI: 1.528–2.549, P < 0.001], and all-cause mortality/nonfatal myocardial reinfarction [HRs: 1.289, 95% CI: 1.181–1.408, P < 0.001]. MPV/P ratio has good accuracy for predicting clinical endpoints. The discriminatory performance of MPV/P ratio was similar to GRACE score but better than MPV (for all-cause mortality: MPV/P vs. GRACE: z = 0.205, p = 0.837; MPV/P vs. MPV: z = 2.677, p = 0.008; GRACE vs. MPV: z = 3.017, p = 0.003; for all-cause mortality/nonfatal myocardial: MPV/P vs. GRACE: z = 1.098, p = 0.272; MPV/P vs. MPV: z = 4.026, p < 0.001; GRACE vs. MPV: z = 4.962, p < 0.001).ConclusionsMPV/P ratio was similar to GRACE score but better than MPV for predicting all-cause mortality and all-cause mortality/nonfatal myocardial reinfarction in NSTEMI patients undergoing PCI. However, MPV/P ratio is easier to calculate than GRACE score.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700