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可穿戴式心脏复律除颤器——日本门诊环境中的初步经验。

Wearable Cardioverter Defibrillator - Initial Experience in the Outpatient Setting in Japan.

作者信息

Horiguchi Ai, Kishihara Jun, Niwano Shinichi, Saito Daiki, Matsuura Gen, Sato Tetsuro, Shirakawa Yuki, Kobayashi Shuhei, Arakawa Yuki, Nishinarita Ryo, Nakamura Hironori, Ishizue Naruya, Oikawa Jun, Satoh Akira, Fukaya Hidehira, Ako Junya

机构信息

Department of Cardiovascular Medicine, Kitasato University School of Medicine Sagamihara Japan.

出版信息

Circ Rep. 2020 Feb 20;2(3):137-142. doi: 10.1253/circrep.CR-20-0001.

DOI:10.1253/circrep.CR-20-0001
PMID:33693220
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7921362/
Abstract

The wearable cardioverter defibrillator (WCD) has been available since 2014 in Japan, and its benefit in the in-hospital acute phase at high risk of ventricular tachyarrhythmia (VTA) has been established, but its clinical use in the outpatient setting remains unclear, especially in Japan. The subjects consisted of 43 consecutive patients with WCD use in the outpatient setting from April 2014 to October 2019 at the present institute. Event alerts and wearing compliance were checked via the remote monitoring system, and a dedicated WCD training team contacted the patients if necessary. The median observation period was 51 days (IQR, 37-68 days) and the median daily wearing time was 23.1 h/day (IQR, 22.0-23.6 h/day). WCD was prescribed for primary prevention of VTA in 7 patients (16%), and for secondary prevention in 36 (84%). The common reason for WCD use was preventive therapy and/or clinical observation. Two appropriate and one inappropriate shock were observed. Eleven patients were not indicated for ICD because of successful catheter ablation optimal medical therapy, VTA in early onset of heart disease and refusal. The remaining 32 patients, however, underwent ICD implantation. In the present real-world study, the WCD wearing compliance was well-maintained in the outpatient setting. WCD is useful for patients at high risk of VTA.

摘要

可穿戴式心脏复律除颤器(WCD)自2014年起在日本上市,其在医院内室性快速心律失常(VTA)高危急性期的益处已得到证实,但其在门诊环境中的临床应用仍不明确,尤其是在日本。本研究对象为2014年4月至2019年10月期间在本机构门诊连续使用WCD的43例患者。通过远程监测系统检查事件警报和佩戴依从性,必要时由专门的WCD培训团队联系患者。中位观察期为51天(四分位间距,37 - 68天),中位每日佩戴时间为23.1小时/天(四分位间距,22.0 - 23.6小时/天)。7例患者(16%)因VTA一级预防而开具WCD,36例(84%)用于二级预防。使用WCD的常见原因是预防性治疗和/或临床观察。观察到2次恰当电击和1次不恰当电击。11例患者因导管消融成功、最佳药物治疗、心脏病早期出现VTA及拒绝而未被推荐植入ICD。然而,其余32例患者接受了ICD植入。在本项真实世界研究中,门诊环境下WCD的佩戴依从性良好。WCD对VTA高危患者有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a18/7921362/41beb3b834d7/circrep-2-137-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a18/7921362/43e24764cd4f/circrep-2-137-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a18/7921362/0f841ff75e5a/circrep-2-137-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a18/7921362/41beb3b834d7/circrep-2-137-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a18/7921362/43e24764cd4f/circrep-2-137-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a18/7921362/0f841ff75e5a/circrep-2-137-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a18/7921362/41beb3b834d7/circrep-2-137-g003.jpg

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本文引用的文献

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Wearable Cardioverter-Defibrillator after Myocardial Infarction.心肌梗死后的可穿戴式心脏除颤器。
N Engl J Med. 2018 Sep 27;379(13):1205-1215. doi: 10.1056/NEJMoa1800781.
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Another Shock for Sudden Death Prevention after Myocardial Infarction.心肌梗死后预防猝死的又一冲击
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Clinical Usefulness of Wearable Cardioverter Defibrillator (WCD) and Current Understanding of Its Clinical Indication in Japan.可穿戴式除颤器(WCD)的临床应用及在日本的临床适应证认识现状。
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2017 AHA/ACC/HRS Guideline for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death: Executive Summary: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines and the Heart Rhythm Society.2017年美国心脏协会/美国心脏病学会/心律学会室性心律失常患者管理和心脏性猝死预防指南:执行摘要:美国心脏病学会/美国心脏协会临床实践指南工作组及心律学会的报告
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The Wearable Cardioverter-Defibrillator: Is It Now the Standard of Care?可穿戴式心脏复律除颤器:它现在是护理标准了吗?
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