Kolkailah Ahmed A, Iskander Mina, Iskander Fady, Patel Priya P, Khan Rozi, Doukky Rami
Department of Medicine, Cook County Health, Chicago, IL, USA.
Division of Cardiology, Cook County Health, 1901 W. Harrison St, Chicago, IL, 60612, USA.
J Nucl Cardiol. 2022 Feb;29(1):101-110. doi: 10.1007/s12350-020-02259-1. Epub 2020 Jul 6.
There are limited data on the prognostic utility of regadenoson SPECT myocardial perfusion imaging (MPI) in patients with end-stage renal disease (ESRD).
In a single-center, retrospective study, we analyzed consecutive ESRD patients who underwent regadenoson SPECT-MPI. The severity of MPI abnormalities and ischemic burden were determined quantitatively. The primary endpoint was major adverse cardiac events (MACE), defined as the composite of cardiac death or myocardial infarction. Among 1,227 subjects (mean age 54 ± 13 years, 47% men), 60 (5%) MACE were observed during a mean follow-up of 2.5 ± 1.8 years. The presence and severity of MPI abnormalities and ischemic burden were associated with a stepwise increase in MACE risk. Abnormal MPI (SSS ≥ 4) was associated with increased MACE risk, independent and incremental to relevant clinical covariates; adjusted hazard ratio, 1.95; 95% confidence interval, 1.15-3.32; Δχ = 5.97; P = .013. Myocardial ischemia (SDS ≥ 2) was associated with a trend towards increased MACE risk; adjusted hazard ratio, 1.63; 95% confidence interval, 0.96-2.77; Δχ = 3.12; P = .072.
In the largest cohort to date, we demonstrated the incremental prognostic value of abnormal MPI in predicting MACE risk in ESRD patients. Given its size, our study provides improved risk estimates in this population compared to previous reports.
关于瑞加诺生单光子发射计算机断层扫描心肌灌注成像(MPI)在终末期肾病(ESRD)患者中的预后效用的数据有限。
在一项单中心回顾性研究中,我们分析了连续接受瑞加诺生SPECT-MPI检查的ESRD患者。定量确定MPI异常的严重程度和缺血负担。主要终点是主要不良心脏事件(MACE),定义为心脏死亡或心肌梗死的复合事件。在1227名受试者(平均年龄54±13岁,47%为男性)中,在平均2.5±1.8年的随访期间观察到60例(5%)MACE。MPI异常的存在和严重程度以及缺血负担与MACE风险的逐步增加相关。MPI异常(SSS≥4)与MACE风险增加相关,独立于相关临床协变量且具有增量作用;调整后的危险比为1.95;95%置信区间为1.15-3.32;Δχ=5.97;P=0.013。心肌缺血(SDS≥2)与MACE风险增加的趋势相关;调整后的危险比为1.63;95%置信区间为0.96-2.77;Δχ=3.12;P=0.072。
在迄今为止最大的队列中,我们证明了MPI异常在预测ESRD患者MACE风险方面具有增量预后价值。鉴于其样本量,我们的研究与先前报告相比,为该人群提供了更好的风险估计。