Bridging Implantable Cardioverter-Defibrillator Patients Undergoing Radiotherapy with a Wearable Cardioverter-Defibrillator

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Abstract

Background: Chest radiation therapy (RT) in patients with an implantable cardioverter defibrillator (ICD) can be problematic and cause transitory malfunction or permanent damage to the device. If the ICD cannot be properly shielded from the radiation necessary for the treatment, then it may be necessary to turn off certain aspects (i.e. tachy-therapy) of the device or to temporarily remove the device leaving the patient without protection and exposing to high risk of complications. The wearable cardioverter defibrillator (WCD) is guideline recommended as bridging therapy in patients requiring temporary removal or inactivation of an ICD. Objectives: The objective of this analysis was to assess the wearable cardioverter defibrillator as a tool in high-risk implantable cardioverter defibrillator patients with cancer during the weeks to months of radiation therapy. Methods: Two retrospective cohorts were analyzed from the University of Padova (Italy) and from the manufacturer’s US registry. Patients undergoing RT who had their ICD removed or deactivated and were prescribed a WCD were included. Demographic, medical history and device usage data collected. Results: Eighty patients were analyzed (76 US, 4 Padova). The median age was 69 years and 56% were female. The most common cancer types were breast (44%) and lung (33%). Median wear time of the WCD was 22.2 hours/day over 57 days. Strategies to protect ICDs from RT involved either removing the device (82.5%) or turning off therapy in the remaining 14 (17.5%). Ventricular arrhythmias (VA) were recorded by the wearable cardioverter defibrillator in four patients, with two sustained episodes in a patient that were successfully cardioverter by the wearable cardioverter defibrillator, and three patients with non-sustained ventricular arrhythmias that did not receive shocks. Five deaths occurred four with an asystole event and one while not wearing the device. Conclusions: This study supports a role for the wearable cardioverter defibrillator in protecting implantable cardioverter defibrillator patients while undergoing radiation therapy. Back-up pacing considered for patients at risk of Bradyarrhythmias.
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桥接植入式心律转复除颤器患者接受放疗与可穿戴心律转复除颤器
背景:植入式心律转复除颤器(ICD)患者的胸部放射治疗(RT)可能会出现问题,并导致设备的短暂功能障碍或永久性损伤。如果ICD不能适当地屏蔽治疗所需的辐射,则可能有必要关闭该装置的某些方面(即速疗)或暂时移除该装置,使患者没有保护并暴露于并发症的高风险中。可穿戴式心律转复除颤器(WCD)被指南推荐为需要暂时移除或停用ICD的患者的桥接治疗。目的:本分析的目的是评估可穿戴式心律转复除颤器作为高风险植入式心律转复除颤器患者在几周到几个月的放射治疗期间的工具。方法:两个回顾性队列分析来自帕多瓦大学(意大利)和制造商的美国注册。接受放射治疗的患者,其ICD已被移除或停用,并开了WCD。收集的人口统计、病史和设备使用数据。结果:共分析80例患者(76例US, 4例Padova)。中位年龄为69岁,56%为女性。最常见的癌症类型是乳腺癌(44%)和肺癌(33%)。57天内,WCD的中位磨损时间为22.2小时/天。保护icd不受RT影响的策略包括移除设备(82.5%)或在其余14例(17.5%)中停止治疗。可穿戴式心律转复除颤器记录了4例患者的室性心律失常(VA),其中1例患者通过可穿戴式心律转复成功,2例持续发作,3例非持续性室性心律失常患者未接受电击。有5人死亡,其中4人死于心脏骤停,1人死于未佩戴该装置。结论:本研究支持可穿戴式心律转复除颤器在放射治疗中保护植入式心律转复除颤器患者的作用。缓发性心律失常风险患者的备用起搏。
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