Servicio de Cardiología, Hospital Clínico Universitario, Universidad de Valencia, Valencia, España.
Rev Esp Cardiol. 2010 Sep;63(9):1035-44. doi: 10.1016/s1885-5857(10)70207-3.
Little is known about how prognosis is influenced by readmission for acute heart failure (AHF) following non-ST-segment elevation acute coronary syndrome (NSTEACS). The aim of this study was to determine the prognostic effect of a first admission for AHF on the risk of acute myocardial infarction (AMI) or death in patients who survived an episode of high-risk NSTEACS.
The study involved 972 consecutive patients with high-risk NSTEACS who survived after hospital admission. Readmission for AHF was selected as the main exposure variable, and its association with subsequent AMI or all-cause death was assessed using Cox proportional hazards models for time-dependent covariates that also included adjustment for competing risks.
After a median follow-up period of 30 [interquartile range, 12-48] months, 82 patients (8.4%) were admitted for AHF, 146 (15%) had an AMI, and 202 (20.8%) died. The median time to readmission for AHF was 203 [56-336] days after NSTEACS. Patients readmitted for AHF had an increased risk of subsequent death (hazard ratio [HR]=1.67; 95% confidence interval [CI], 1.13-2.45; P=.009) or AMI (HR=2.15; 95% CI, 1.41-3.27; P< .001), which was independent of baseline prognostic and time-dependent variables.
Readmission for AHF after high-risk NSTEACS was associated with an increased risk of subsequent death or AMI.
对于非 ST 段抬高型急性冠状动脉综合征(NSTEACS)后因急性心力衰竭(AHF)再次入院如何影响预后,目前知之甚少。本研究旨在确定首次因 AHF 入院对高危 NSTEACS 患者存活后发生急性心肌梗死(AMI)或死亡的风险的预后影响。
该研究纳入了 972 例高危 NSTEACS 后存活的连续患者。将因 AHF 再次入院作为主要暴露变量,并使用时间依赖性协变量的 Cox 比例风险模型评估其与随后的 AMI 或全因死亡的相关性,该模型还包括对竞争风险的调整。
中位随访期为 30 个月[四分位距(IQR),12-48]后,82 例(8.4%)患者因 AHF 再次入院,146 例(15%)发生 AMI,202 例(20.8%)死亡。NSTEACS 后因 AHF 再次入院的中位时间为 203 天[IQR,56-336]。因 AHF 再次入院的患者随后发生死亡(风险比[HR]=1.67;95%置信区间[CI],1.13-2.45;P=.009)或 AMI(HR=2.15;95% CI,1.41-3.27;P<.001)的风险增加,这与基线预后和时间依赖性变量无关。
高危 NSTEACS 后因 AHF 再次入院与随后发生死亡或 AMI 的风险增加相关。