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心脏植入式电子设备植入过程中远程参数测试的临床应用:一项单中心、随机、开放标签、非劣效性试验。

The clinical use of remote parameter testing during cardiac implantable electronic devices implantation procedures: a single center, randomized, open-label, non-inferiority trial.

作者信息

Xiong Shiqiang, Qin Shujuan, Tong Lin, Long Yu, Luo Yan, Feng Qiao, Peng Xiufen, Jiang Maoling, Xiong Feng, Li Jin, Zhang Yangchun, Zhang Zhen, Liu Hanxiong, Cai Lin

机构信息

Department of Cardiology, The Third People's Hospital of Chengdu, Affiliated Hospital of Southwest Jiaotong University, Chengdu Cardiovascular Disease Research Institute, Chengdu, Sichuan, China.

出版信息

Front Cardiovasc Med. 2024 Mar 22;11:1364940. doi: 10.3389/fcvm.2024.1364940. eCollection 2024.

Abstract

BACKGROUND

A novel non-contact system for remote parameter testing and reprogramming offers an alternative method for assessing device parameters during cardiac implantable electronic devices (CIEDs) implantation without the need for physical contact with the manufacturer's clinical service technician. The safety and feasibility of using this system in CIEDs implantation procedures remains to be determined.

OBJECTIVE

Evaluate the safety and feasibility of remote parameter testing in CIEDs implantation procedures.

METHODS

A single center, randomized, open-label, non-inferiority trial (ChiCTR2200057587) was conducted to compare the two approaches for interrogating CIEDs during implantation procedures: routine interrogation performed by on-site technicians or remote interrogation performed by technicians using the 5G-Cloud Technology Platform. Patients aged ≥18 years and elected to receive CIEDs were eligible for inclusion. The primary endpoint was the completion rate of the parameter test. Safety and efficiency were evaluated in all randomly assigned participants.

RESULTS

A total of 480 patients were finally enrolled and were randomly assigned to routine group ( = 240) or remote group ( = 240). The primary endpoint was achieved by 100% in both groups ( = 0.0060 for noninferiority). The parameters of sensing, threshold, and impedance regarding the right atrium, right ventricle, and left ventricle had no statistical significance between the two groups ( > 0.05). Procedure time, parameter testing time, and both duration and dose of x-ray irradiation were not significantly different between the two groups ( > 0.05). Shut-open door frequency was significantly higher in the routine group than the remote group [6.00 (4.00, 8.00) vs. 0,  < 0.0001]. Notably, no clinical or technical complications were observed in the remote group.

CONCLUSIONS

Remote parameter testing is safe and feasible across various devices implantation procedures. The utilization of remote parameter testing and reprogramming could represent an innovative approach to improve healthcare accessibility and unlock the full potential of secondary centers in managing CIEDs.

THE REGISTRATION IDENTIFICATION

ChiCTR2200057587.

摘要

背景

一种用于远程参数测试和重新编程的新型非接触系统提供了一种替代方法,可在心脏植入式电子设备(CIED)植入期间评估设备参数,而无需与制造商的临床服务技术人员进行身体接触。在CIED植入手术中使用该系统的安全性和可行性仍有待确定。

目的

评估在CIED植入手术中进行远程参数测试的安全性和可行性。

方法

进行了一项单中心、随机、开放标签、非劣效性试验(ChiCTR2200057587),以比较植入手术期间询问CIED的两种方法:由现场技术人员进行的常规询问或由技术人员使用5G云技术平台进行的远程询问。年龄≥18岁且选择接受CIED的患者符合纳入条件。主要终点是参数测试的完成率。在所有随机分配的参与者中评估安全性和效率。

结果

最终共纳入480例患者,随机分为常规组(n = 240)或远程组(n = 240)。两组的主要终点达成率均为100%(非劣效性P = 0.0060)。两组之间右心房、右心室和左心室的感知、阈值和阻抗参数无统计学意义(P>0.05)。两组之间的手术时间、参数测试时间以及X射线照射的持续时间和剂量均无显著差异(P>0.05)。常规组的开关门频率显著高于远程组[6.00(4.00,8.00)对0,P<0.0001]。值得注意的是,远程组未观察到临床或技术并发症。

结论

远程参数测试在各种设备植入手术中是安全可行的。远程参数测试和重新编程的应用可能代表一种创新方法,可提高医疗可及性并释放二级中心在管理CIED方面的全部潜力。

注册识别号

ChiCTR2200057587。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d668/10995217/1fe1c483203f/fcvm-11-1364940-g001.jpg

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