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基于全国注册数据的静态球囊房间隔造口术的实践与安全性。

Practice and Safety of Static Balloon Atrial Septostomy Based on a Nationwide Registry Data.

机构信息

Department of Pediatrics, The University of Tokyo Hospital.

Department of Clinical Data Science, Clinical Research & Education Promotion Division, National Center of Neurology and Psychiatry.

出版信息

Circ J. 2022 Nov 25;86(12):1990-1997. doi: 10.1253/circj.CJ-22-0185. Epub 2022 Sep 1.

DOI:10.1253/circj.CJ-22-0185
PMID:36047087
Abstract

BACKGROUND

Balloon atrial septostomy (BAS) is an essential catheterization procedure for congenital heart lesions. Recently, a balloon catheter for static BAS was approved for the first time in Japan as an alternative to the conventional pull-through BAS. Despite the expected increase in the use of static BAS, reports on its safety are scarce worldwide.

METHODS AND RESULTS

Data on static and pull-through BAS registered in a national registry between 2016 and 2018 were collected. During the study period, 247 sessions of static BAS and 588 sessions of pull-through BAS were performed on a total of 674 patients. Patients who underwent static BAS were older (P<0.001). The incidence of serious adverse events (4.3% vs. 0.9%, P=0.03) and the overall incidence of adverse events (8.1% vs. 3.2%, P=0.03) were higher in static BAS than in pull-through BAS. Among patients who underwent static BAS, the risk factor for adverse events was a body weight <3 kg at the time of the procedure (odds ratio: 4.3 [confidence interval: 1.7-11], P=0.003).

CONCLUSIONS

This nationwide study revealed differences in patient background between static and pull-through BAS, as well as a higher incidence of adverse events related to static BAS. Patients weighing <3 kg are at high risk for adverse events after static BAS and may require surgical and circulatory support backup.

摘要

背景

球囊房间隔造口术(BAS)是先天性心脏病变介入治疗的重要程序。最近,日本首次批准了一种用于静态 BAS 的球囊导管,作为传统经皮 BAS 的替代方法。尽管预计静态 BAS 的使用会增加,但全球范围内关于其安全性的报告却很少。

方法和结果

收集了 2016 年至 2018 年在全国注册中心注册的静态和经皮 BAS 数据。在研究期间,共有 674 名患者接受了 247 次静态 BAS 和 588 次经皮 BAS。接受静态 BAS 的患者年龄较大(P<0.001)。与经皮 BAS 相比,严重不良事件的发生率(4.3%对 0.9%,P=0.03)和不良事件的总发生率(8.1%对 3.2%,P=0.03)更高。在接受静态 BAS 的患者中,不良事件的危险因素是手术时体重<3 公斤(优势比:4.3[置信区间:1.7-11],P=0.003)。

结论

这项全国性研究揭示了静态 BAS 和经皮 BAS 之间患者背景的差异,以及与静态 BAS 相关的不良事件发生率较高。体重<3 公斤的患者在接受静态 BAS 后发生不良事件的风险较高,可能需要手术和循环支持的后备。

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