在射血分数降低的情况下,舒比曲/缬沙坦是否能够改变心力衰竭患者心脏装置的植入时机?

M. Nogueira, Marisa Brochado, I. Nabais, É. Batista, Carla Matias, G. Proença
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引用次数: 0

摘要

目的:本研究的目的是评估沙库比曲/缬沙坦对左心室(LV)逆向重构的影响,可能会改变射血分数降低心力衰竭(HFrEF)患者心脏装置植入的时间,这一问题尚未得到具体解决。方法和结果:对HFrEF患者的前瞻性队列进行二次数据分析。纳入标准:2017年11月至2019年8月期间在既往最佳药物治疗后开始服用沙库必曲/缬沙坦的患者。主要终点:达到左心室射血分数(EF)>35%的时间。Kaplan–Meier用于估计中位时间,Cox回归模型用于研究与事件发生率相关的患者特征。总共包括48名患者,平均年龄72.5岁,主要为男性(70.8%)。从最初的48名LVEF≤35%的患者中,有27名(56%)达到LVEF>35%,中位时间为11.3个月(95%置信区间[95%CI]:9.4-19.6)。在多变量分析中,基线LVEF在30%至35%之间与达到LVEF>35%的累积发生率增加相关(发病率比=3.9;95%CI:1.6-9.9;p值=0.004)。我们推测,这种改善可能会延迟心脏复律除颤器/心脏再同步治疗的植入。
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Is Sacubitril/Valsartan Able to Change the Timing for Implantation of Cardiac Devices in Heart Failure with Reduced Ejection Fraction?
Aims: The aim of this study was to evaluate the impact of sacubitril/valsartan on left ventricular (LV) reverse remodeling, potentially modifying the timing for cardiac device implantation in heart failure with reduced ejection fraction (HFrEF), which has not been specifically addressed. Methods and results: A secondary data analysis of a prospective cohort of HFrEF patients was conducted. Inclusion criteria: patients who started sacubitril/valsartan between November 2017 and August 2019 after previous optimal medical therapy. Primary endpoint: time to achieve LV Ejection Fraction (EF) > 35%. Kaplan–Meier was used to estimate median time and Cox regression model to investigate the patients’ characteristics associated with event incidence rate. In total, 48 patients were included, with a mean age of 72.5 years, predominantly male (70.8%). From the initial 48 patients with LVEF ≤ 35%, 27 (56%) reached LVEF > 35%, in a median time of 11.3 months (95% confidence interval [95%CI]: 9.4–19.6). In multivariate analysis, baseline LVEF between 30 and 35% was associated with increased cumulative incidence of attaining LVEF > 35% (Incidence rate ratio = 3.9; 95%CI: 1.6–9.9; p-value = 0.004). Conclusion: We observed an improvement in LVEF to >35% in the majority of patients who switched to sacubitril/valsartan, illustrating its role in cardiac remodeling. We speculate that this improvement may allow delaying implantation of Cardioverter-Defibrillator/Cardiac Resynchronization Therapy.
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