Padre Antero Micone Hospital, ASL 3 "Genovese", Genova, Italy.
Institute of Cardiology, Department of Experimental, Diagnostic, and Specialty Medicine, Policlinico S. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Heart Rhythm. 2021 Mar;18(3):411-418. doi: 10.1016/j.hrthm.2020.11.024. Epub 2020 Nov 27.
Device replacement is the ideal time to reassess health care goals regarding continuing implantable cardioverter-defibrillator (ICD) therapy. Only few data are available on the decision making at this time.
The goals of this study were to identify factors associated with poor prognosis at the time of ICD replacement and to develop a prognostic index able to stratify those patients at risk of dying early.
DEtect long-term COmplications after implantable cardioverter-DEfibrillator replacement (DECODE) was a prospective, single-arm, multicenter cohort study aimed at estimating long-term complications in a large population of patients who underwent ICD/cardiac resynchronization therapy - defibrillator replacement. Potential predictors of death were investigated, and all these factors were gathered into a survival score index (SUSCI).
We included 983 consecutive patients (median age 71 years (63-78)); 750 (76%) were men, 537 (55%) had ischemic cardiomyopathy; 460 (47%) were implanted with cardiac resynchronization therapy - defibrillator. During a median follow-up period of 761 days (interquartile range 628-904 days), 114 patients (12%) died. In multivariate Cox regression analysis, New York Heart Association class III/IV, ischemic cardiomyopathy, body mass index < 26 kg/m, insulin administration, age ≥ 75 years, history of atrial fibrillation, and hospitalization within 30 days before ICD replacement remained associated with death. The survival score index showed a good discriminatory power with a hazard ratio of 2.6 (95% confidence interval 2.2-3.1; P < .0001). The risk of death increased according to the severity of the risk profile ranging from 0% (low risk) to 47% (high risk).
A simple score that includes a limited set of variables appears to be predictive of total mortality in an unselected real-world population undergoing ICD replacement. Evaluation of the patient's profile may assist in predicting vulnerability and should prompt individualized options, especially for high-risk patients.
在进行器械更换时,重新评估与植入式心律转复除颤器(ICD)治疗相关的健康目标是理想的选择。目前仅有少量数据可用于决策。
本研究旨在确定与 ICD 更换时预后不良相关的因素,并开发一种能够对早期死亡风险较高的患者进行分层的预后指数。
DEtect long-term COmplications after implantable cardioverter-DEfibrillator replacement(DECODE)是一项前瞻性、单臂、多中心队列研究,旨在评估大量接受 ICD/心脏再同步治疗-除颤器更换的患者的长期并发症。研究调查了死亡的潜在预测因素,并将所有这些因素纳入生存评分指数(SUSCI)。
我们纳入了 983 例连续患者(中位年龄 71 岁(63-78));750 例(76%)为男性,537 例(55%)患有缺血性心肌病;460 例(47%)植入心脏再同步治疗-除颤器。在中位随访 761 天(四分位间距 628-904 天)期间,114 例(12%)患者死亡。多变量 Cox 回归分析显示,纽约心脏协会心功能分级 III/IV 级、缺血性心肌病、体质指数(BMI)<26kg/m、使用胰岛素、年龄≥75 岁、心房颤动史和 ICD 更换前 30 天内住院与死亡相关。生存评分指数具有良好的判别能力,风险比为 2.6(95%置信区间 2.2-3.1;P<.0001)。死亡风险根据风险谱的严重程度而增加,范围从 0%(低危)到 47%(高危)。
一种简单的评分,包含一组有限的变量,似乎可以预测接受 ICD 更换的未选择人群的全因死亡率。评估患者的情况可以帮助预测脆弱性,并应提示个体化选择,尤其是对高危患者。