Arcispedale Santa Maria Nuova, Viale Risorgimento, 80, 42123 Reggio Emilia, Italy.
Erlanger Medical Center, 975 E 3rd St, Chattanooga, TN 37403, USA.
Europace. 2023 May 19;25(5). doi: 10.1093/europace/euad068.
Insertable cardiac monitors (ICMs) are indicated for long-term monitoring of unexplained syncope or palpitations, and for detection of bradycardia, ventricular tachycardia, and/or atrial fibrillation (AF). The aim of our study was to evaluate the safety and clinical value associated with a new generation ICM (Confirm Rx™, Abbott, Illinois, USA), featuring a new remote monitoring system based on smartphone patient applications.
The SMART Registry is an international prospective observational study. The main endpoints were ICM safety (incidence of serious adverse device and procedure-related events (SADEs) at 1 month), ICM clinical value (incidence of device-detected true arrhythmias and of clinical diagnoses and interventions), and patient-reported experience measurements (PREMs). A total of 1400 subjects were enrolled. ICM indications included syncope (49.1%), AF (18.8%), unexplained palpitations (13.6%), risk of ventricular arrhythmia (6.6%), and cryptogenic stroke (6.0%). Freedom from SADEs at 1 month was 99.4% (95% Confidence Interval: 98.8-99.7%). In the 6-month monitoring period, the ICM detected true cardiac arrhythmias in 45.7% of patients and led to clinical interventions in a relevant proportion of patients; in particular, a pacemaker implant was performed after bradycardia detection in 8.9% of subjects who received an ICM for syncope and oral anticoagulation therapy was indicated after AF detection in 15.7% of subjects with cryptogenic stroke. PREMs showed that 78.2% of subjects were satisfied with the remote monitoring patient app.
The evaluated ICM is associated with an excellent safety profile and high diagnostic yield. Patients reported positive experiences associated with the use of their smartphone for the device remote monitoring.
可植入式心脏监测器(ICM)适用于不明原因晕厥或心悸的长期监测,以及检测心动过缓、室性心动过速和/或心房颤动(AF)。我们的研究目的是评估一种新型 ICM(Confirm Rx™,雅培,伊利诺伊州,美国)的安全性和临床价值,该 ICM 具有基于智能手机患者应用程序的新型远程监测系统。
SMART 登记研究是一项国际前瞻性观察性研究。主要终点是 ICM 安全性(1 个月时严重不良设备和程序相关事件(SADEs)的发生率)、ICM 临床价值(设备检测到的真实心律失常发生率以及临床诊断和干预)和患者报告的体验测量(PREMs)。共纳入 1400 例患者。ICM 适应证包括晕厥(49.1%)、AF(18.8%)、不明原因心悸(13.6%)、室性心律失常风险(6.6%)和隐源性卒中(6.0%)。1 个月时无 SADEs 发生率为 99.4%(95%置信区间:98.8-99.7%)。在 6 个月监测期间,ICM 在 45.7%的患者中检测到真实的心脏心律失常,并在相当一部分患者中进行了临床干预;特别是,在因晕厥而接受 ICM 的 8.9%患者中因心动过缓检测到需要植入起搏器,在因隐源性卒中而接受 ICM 的 15.7%患者中需要进行口服抗凝治疗。PREMs 显示,78.2%的患者对远程监测患者应用程序感到满意。
评估的 ICM 具有出色的安全性和高诊断率。患者报告了与使用智能手机进行设备远程监测相关的积极体验。