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Phantom shocks in patients with implantable cardioverter defibrillator: Results from a randomized rehabilitation trial (COPE-ICD)

机译:植入式心脏复律除颤器患者的幻影休克:随机康复试验(COPE-ICD)结果

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AimsThe aim of this trial was to assess a combined rehabilitation intervention including an exercise training component and a psycho-educational component in patients treated with implantable cardioverter defibrillator (ICD). The hypothesis was that the intervention would reduce the occurrence of phantom shocks.Methods and resultsThe design was secondary explorative analyses of data from a randomized controlled trial. One hundred and ninety-six patients with first-time ICD implantation (79% male, mean age 58 years) were randomized (1: 1) to either combined rehabilitation or a control group receiving 'treatment as usual'. A total of 144 participants completed the 12-month follow-up. Intervention consisted of 12 weeks of exercise training and 1 year of psycho-educational follow-up focusing on modifiable factors associated with poor outcomes, e.g. phantom shocks. Outcome measures were ancillary questions regarding the experience of phantom shocks, date, time, and place. Twelve patients (9.4%) experienced a phantom shock, 7 in the intervention group and 5 in the control group (NS). Neither age, sex, quality of life nor perceived health at baseline was significantly related to the probability of occurrence of phantom shock.ConclusionPhantom shocks were experienced by about one in ten ICD patients, with no interventional effect found and no significant difference found regarding receiving an actual shock therapy among phantom shock patients. Trial registration: ClinicalTrials.gov (ID: NCT00569478).
机译:目的本试验的目的是评估接受植入式心脏复律除颤器(ICD)治疗的患者的综合康复干预措施,包括运动训练成分和心理教育成分。假设是干预将减少幻影电击的发生。方法和结果设计是对来自随机对照试验的数据的二次探索性分析。 196例首次植入ICD的患者(男性79%,平均年龄58岁)被随机分配(1:1)接受联合康复治疗或接受“照常治疗”的对照组。共有144名参与者完成了12个月的随访。干预包括12周的运动训练和1年的心理教育跟进,重点是与不良结局相关的可改变因素,例如:幻影冲击。结果措施是有关幻影电击的经历,日期,时间和地点的辅助问题。十二名患者(9.4%)发生了幻觉性休克,干预组7例,对照组(NS)5例。基线时的年龄,性别,生活质量或感知的健康状况与幻影电击的发生率均无显着相关。结论幻影电击发生在约十分之一的ICD患者中,未发现干预效果,并且接受幻影电击也无明显差异。幻影电击患者中的实际电击疗法。试用注册:ClinicalTrials.gov(ID:NCT00569478)。

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