Influence of frailty and health status on outcomes in patients with coronary disease undergoing percutaneous revascularization.
Influence of frailty and health status on outcomes in patients with coronary disease undergoing percutaneous revascularization.
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DOI:
10.1161/circoutcomes.111.961375
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发表时间:
2011-09
期刊:
影响因子:
--
通讯作者:
Roger VL
中科院分区:
文献类型:
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作者:
Singh M;Rihal CS;Lennon RJ;Spertus JA;Nair KS;Roger VL
While older patients frequently undergo percutaneous coronary interventions (PCI), frailty, comorbidity, and quality of life (QOL) are seldom part of risk prediction approaches. We assessed their incremental prognostic value over and above the risk factors in the Mayo Clinic risk score (MCRS). Patients ≥ 65 years who underwent PCI were assessed for frailty (Fried criteria), comorbidity (Charlson index), and QOL [SF-36]. Of the 628 discharged [median follow-up of 35.0 months (IQR, 22.7-42.9)], 78 died and 72 had an MI. Three year mortality was 28% for frail patients, 6% for non-frail patients. The respective 3-year rates of death or MI were 41% and 17%. Following adjustment, frailty [hazard ratio (HR) 4.19 [95% confidence interval (CI), 1.85, 9.51], physical component score of the SF-36 (HR, 1.59; 95% CI, 1.24-2.02), and comorbidity, (HR, 1.10; 95% CI, 1.05, 1.16) were associated with mortality. Frailty was associated with mortality/MI (HR, 2.61, 1.52, 4.50). Models with conventional MCRS had C-statistics of 0.628, 0.573 for mortality and mortality/MI respectively. Adding frailty, QOL, and comorbidity, the C statistic was (0.675, 0.694, 0.671) for mortality, and (0.607, 0.587, 0.576) for mortality/MI respectively. Including frailty, comorbidities, and SF-36, conferred a discernible improvement to predict death and death/MI (integrated discrimination improvement 0.027 and 0.016 and net reclassification improvement of 43% and 18% respectively). Following PCI, frailty, comorbidity and poor QOL are prevalent and are associated with adverse long-term outcomes. Their inclusion improves the discriminatory ability of the MCRS derived from the routine cardiovascular risk factors.