女性室性心律失常和植入式心律转复除颤器治疗:倾向评分匹配分析

G. Maglia, M. Giammaria, G. Zanotto, A. D'Onofrio, P. Della Bella, M. Marini, G. Rovaris, S. Iacopino, V. Calvi, E. Pisanò, F. Caravati, G. Balestri, D. Giacopelli, A. Gargaro, M. Biffi
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引用次数: 0

摘要

资金来源类型:无。植入式心律转复除颤器(ICD)是一种既定的治疗方法,用于预防某些患者的心源性猝死。虽然目前的指导方针适用于女性和男性,但人们越来越认识到心律失常和器械干预的发生率受性别的影响。利用icd和心脏再同步化除颤器(CRT-Ds)的远程监测数据,研究性别特异性的持续性室性心律失常(SVAs)风险和器械治疗。研究终点为第一次适当SVA的时间,第一次适当SVA器械治疗的时间,以及第一次ICD休克的时间。设备检测sva的适当性由三位电生理学专家裁决。将结果在女性和1:1倾向评分(PS)匹配的男性亚组之间进行比较。在2532例ICD或CRT-D患者(中位年龄70岁)中,488例(19.3%)为女性。与男性相比,女性更常发生CRT-D(51%对40%,p<0.001)和非缺血性心肌病(65%对45%,p<0.001)。中位随访2.1年后,有123名女性(25.2%)和488名ps匹配的男性中有174名(35.6%)出现SVAs,校正风险比(HR)为0.65(95%可信区间[CI], 0.51-0.81;p < 0.001)。女性也显示出任何器械治疗的风险降低(HR, 0.59;CI, 0.45 - -0.76;p<0.001)和冲击(HR, 0.66;CI, 0.47-0.94, p=0.021)。在CRT-D患者中,未证实性别特异性SVA风险谱的差异(HR, 0.78;CI, 0.55 - -1.09;p=0.14)和射血分数<30% (HR, 0.80;CI, 0.52 - -1.23;p = 0.31)。在我们对远程监测数据的分析中,在ICD或/和射血分数≥30%的患者亚组中,女性的SVA风险比ps匹配的男性低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ventricular arrhythmias and implantable cardioverter-defibrillator therapy in women: a propensity score-matched analysis
Type of funding sources: None. The implantable cardioverter-defibrillator (ICD) is an established therapy for the prevention of sudden cardiac death in selected patients. Although current guidelines apply to both women and men, there is a growing awareness that the incidence of cardiac arrhythmias and device interventions is influenced by sex. To investigate sex-specific risk of sustained ventricular arrhythmias (SVAs) and device therapies, using remote monitoring data from ICDs and cardiac resynchronization therapy defibrillators (CRT-Ds). Study endpoints were time to the first appropriate SVA, time to the first appropriate device therapy for SVA, and time to the first ICD shock. Appropriateness of device-detected SVAs was adjudicated by three expert electrophysiologists. Results were compared between women and a 1:1 propensity score (PS)-matched subgroup of men. In a cohort of 2,532 patients with an ICD or CRT-D (median age, 70 years), 488 patients (19.3%) were women. As compared to men, women more frequently had a CRT-D (51% vs. 40%, p<0.001), and nonischemic cardiomyopathy (65% vs. 45%, p<0.001). After a median follow-up of 2.1 years, SVAs occurred in 123 women (25.2%) and in 174 of the 488 PS-matched men (35.6%) with an adjusted hazard ratio (HR) of 0.65 (95% confidence interval [CI], 0.51-0.81; p<0.001). Women also showed a reduced risk of any device therapy (HR, 0.59; CI, 0.45-0.76; p<0.001) and shocks (HR, 0.66; CI, 0.47-0.94, p=0.021). Differences in sex-specific SVA risk profile were not confirmed in CRT-D patients (HR, 0.78; CI, 0.55-1.09; p=0.14) and in those with an ejection fraction <30% (HR, 0.80; CI, 0.52-1.23; p=0.31). In our analysis of remote monitoring data, women exhibited a lower SVA risk profile than PS-matched men in the subgroup of patients with an ICD or/and ejection fraction ≥30%.
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