Varma Niraj
Cardiac Electrophysiology Laboratory, Loyola University Medical Center, Maywood, IL 60153, USA.
Am Heart J. 2007 Dec;154(6):1029-34. doi: 10.1016/j.ahj.2007.07.051. Epub 2007 Sep 27.
Increased implantable cardioverter defibrillator (ICD) implant volumes (and product advisories/recalls) pose management challenges. Most device interrogations at 3- to 6-month routine follow-up visits are "nonactionable," that is, require no clinically significant reprogramming, lead revision, or initiation or up-titration of antiarrhythmic medications. Conversely, implanted devices collect important diagnostic data (eg, atrial fibrillation onset, system integrity) that remain concealed between device interrogations. Remote monitoring may resolve some of these challenges, but has not been studied in a large-scale clinical trial. Home Monitoring (HM) uses automatic (without patient intervention) data and electrogram transmissions with rapid (<24 hours) event notification of significant (including silent) events. The Lumos-T Reduces Routine Office Device Follow-Up Study (TRUST) is a multicenter, prospective, randomized study enrolling 1000 ICD patients designed to test whether HM can safely reduce the number of scheduled nonactionable office device interrogations by 50% and provide early detection and notification of cardiac and/or device problems. After enrollment, TRUST patients are randomized 2:1 to either HM or to control (ie, HM off) arms and are seen for an in-office follow-up 3 months postimplant. At subsequent 3-month intervals, control patients have conventional office visits, whereas in HM, patient data are remotely retrieved and evaluated. In HM patients, early notification may automatically occur between periodic checks for compromised system integrity (battery, lead parameters, high-voltage circuitry) or arrhythmia occurrence (eg, atrial fibrillation, ventricular arrhythmia). All study patients will have a final office visit 15 months after implant. The results of TRUST may confirm the role of remote monitoring as an intensive surveillance mechanism for device management.
植入式心脏复律除颤器(ICD)植入量的增加(以及产品咨询/召回)带来了管理挑战。在3至6个月的常规随访中,大多数设备问询结果是“无需采取行动的”,也就是说,不需要进行具有临床意义的重新编程、导线修复,或启动或增加抗心律失常药物剂量。相反,植入设备收集的重要诊断数据(如房颤发作、系统完整性)在设备问询之间仍处于隐匿状态。远程监测可能会解决其中一些挑战,但尚未在大规模临床试验中进行研究。家庭监测(HM)使用自动(无需患者干预)数据和心电图传输,并对重大(包括无症状)事件进行快速(<24小时)事件通知。Lumos-T减少常规门诊设备随访研究(TRUST)是一项多中心、前瞻性、随机研究,招募了1000名ICD患者,旨在测试HM是否能安全地将计划内无需采取行动的门诊设备问询次数减少50%,并提供心脏和/或设备问题的早期检测和通知。入组后,TRUST患者按2:1随机分为HM组或对照组(即关闭HM),并在植入后3个月进行门诊随访。在随后的3个月间隔中,对照组患者进行常规门诊就诊,而在HM组中,患者数据被远程检索和评估。在HM组患者中,在定期检查系统完整性受损(电池、导线参数、高压电路)或心律失常发生(如房颤、室性心律失常)之间可能会自动进行早期通知。所有研究患者将在植入后15个月进行最后一次门诊就诊。TRUST的结果可能会证实远程监测作为设备管理强化监测机制的作用。