Yoon Justin G, Fares Munes, Hoyt Walter, Snyder Christopher S
Case Western Reserve University School of Medicine, 2109 Adelbert Road, Cleveland, OH, USA.
Pediatric Cardiology, The Congenital Heart Collaborative, University Hospitals Rainbow Babies and Children's Hospital, Case Western Reserve University School of Medicine, 11100 Euclid Avenue, MS RBC 6011, Cleveland, OH, 44106-6007, USA.
Pediatr Cardiol. 2021 Jan;42(1):142-147. doi: 10.1007/s00246-020-02463-3. Epub 2020 Oct 9.
Insertable cardiac monitors (ICM) are subcutaneously implanted devices that monitor a patient's heart rate and rhythm (Rossano in Pediatrics 112(3):e228, 2003). The diagnostic accuracy and safety of the Confirm Rx (Abbott, Minneapolis, MN) ICM in pediatric patients is unknown. This is a single center, retrospective, IRB-approved review of patients ≤ 21 years implanted with Confirm Rx ICMs from 2017 to 2020. Data collected included demographics, indications, presence of P-wave and R-wave amplitude at implantation and follow-up, number/appropriateness of transmissions pre and post implementation of SharpSense technology, reprogramming to improve accuracy, time from implantation to arrhythmia detection, and complications. There were 29 patients (median age: 8 years, 59% females). P-waves were identified in all patients and average R-wave amplitude was 0.85 mV (0.26-1.03 mV). There was no significant difference in R-wave amplitude based on size (BSA ≥ 1.5 m: 0.76 mV, < 1.5 m: 0.91 mV) or congenital heart disease (+CHD: 0.86 mV, -CHD: 0.85 mV). Arrhythmias identified were the following: wide complex tachycardia (1), supraventricular tachycardia (4), bradycardia/sinus pause (3), and premature ventricular contraction (1). SharpSense implementation decreased the false-positive rate in device-initiated transmissions (55.4% to 0%, p < 0.00001). Average time from implantation to arrhythmia detection was 2.63 months (range: 0-8.8). A single complication of cellulitis occurred. Confirm Rx is appropriate for implant in pediatric patients regardless of age, BSA, or CHD. Implementation of SharpSense™ technology dramatically decreased the false-positive rate. Follow-up studies could utilize additional monitoring devices to provide analysis on potential events that the Confirm Rx ICM missed.
可植入式心脏监测器(ICM)是皮下植入的设备,用于监测患者的心率和心律(罗萨诺,《儿科学》112(3):e228,2003年)。Confirm Rx(雅培公司,明尼阿波利斯,明尼苏达州)ICM在儿科患者中的诊断准确性和安全性尚不清楚。这是一项单中心、回顾性、经机构审查委员会批准的对2017年至2020年植入Confirm Rx ICM的21岁及以下患者的研究。收集的数据包括人口统计学信息、植入指征、植入时和随访时P波和R波振幅的情况、SharpSense技术实施前后传输的数量/适当性、为提高准确性而进行的重新编程、从植入到心律失常检测的时间以及并发症。共有29例患者(中位年龄:8岁,59%为女性)。所有患者均能识别出P波,平均R波振幅为0.85mV(0.26 - 1.03mV)。基于体型(体表面积≥1.5平方米:0.76mV,<1.5平方米:0.91mV)或先天性心脏病(+先天性心脏病:0.86mV,-先天性心脏病:0.85mV),R波振幅无显著差异。识别出的心律失常如下:宽QRS波心动过速(1例)、室上性心动过速(4例)、心动过缓/窦性停搏(3例)和室性早搏(1例)。SharpSense技术的实施降低了设备发起传输中的假阳性率(从55.4%降至0%,p<0.00001)。从植入到心律失常检测的平均时间为2.63个月(范围:0 - 8.8个月)。发生了1例蜂窝织炎并发症。无论年龄、体表面积或是否患有先天性心脏病,Confirm Rx都适合植入儿科患者。SharpSense™技术的实施显著降低了假阳性率。后续研究可利用额外的监测设备对Confirm Rx ICM遗漏的潜在事件进行分析。