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舌下神经刺激器植入后的器械相关结果。

Device-related outcomes following hypoglossal nerve stimulator implantation.

机构信息

Department of Otolaryngology-Head and Neck Surgery, Thomas Jefferson University Hospital, Philadelphia, Pennsylvania.

Department of Neurology and Jefferson Sleep Disorders Center, Thomas Jefferson University Hospital, Philadelphia, Pennsylvania.

出版信息

J Clin Sleep Med. 2024 Sep 1;20(9):1497-1503. doi: 10.5664/jcsm.11176.

Abstract

STUDY OBJECTIVES

Hypoglossal nerve stimulation (HGNS) has been widely used to treat obstructive sleep apnea in selected patients. Here we evaluate rates of revision and explant related to HGNS implantation and assess types of adverse events contributing to revision and explant.

METHODS

Postmarket surveillance data for HGNS implanted between January 1, 2018 and March 31, 2022, were collected. Event rates and risk were calculated using the postmarket surveillance event counts and sales volume over the same period. Indications were categorized for analysis. Descriptive statistics were reported and freedom from explant or revision curves were grouped by year of implantation.

RESULTS

Of the 20,881 HGNS implants assessed, rates of explant and revision within the first year were 0.723% and 1.542%, respectively. The most common indication for explant was infection (0.378%) and for revision was surgical correction (0.680%). Of the 5,820 devices with 3-year postimplantation data, the rate of explant was 2.680% and of revision was 3.557%. During this same interval, elective removal (1.478%) was the most common indication, and for revisions, surgical correction (1.134%).

CONCLUSIONS

The efficacy of HGNS is comparable in the real world setting to published clinical trial data. Rates of explant and revision are low, supporting a satisfactory safety profile for this technology.

CITATION

Moroco AE, Wei Z, Byrd I, et al. Device-related outcomes following hypoglossal nerve stimulator implantation. . 2024;20(9):1497-1503.

摘要

研究目的

舌下神经刺激(HGNS)已广泛用于治疗选定患者的阻塞性睡眠呼吸暂停。在这里,我们评估与 HGNS 植入相关的修订和取出率,并评估导致修订和取出的不良事件类型。

方法

收集了 2018 年 1 月 1 日至 2022 年 3 月 31 日期间植入的 HGNS 上市后监测数据。使用同期的上市后监测事件计数和销售量计算事件发生率和风险。按分析进行分类。报告描述性统计数据,并按植入年份分组绘制免取出或修订曲线。

结果

在评估的 20881 例 HGNS 植入中,植入后第一年的取出和修订率分别为 0.723%和 1.542%。取出的最常见原因是感染(0.378%),修订的最常见原因是手术矫正(0.680%)。在具有 3 年植入后数据的 5820 个设备中,取出率为 2.680%,修订率为 3.557%。在同一时期,择期取出(1.478%)是最常见的原因,而修订的最常见原因是手术矫正(1.134%)。

结论

HGNS 的疗效在真实世界环境中与已发表的临床试验数据相当。取出和修订的比例较低,支持该技术具有令人满意的安全性。

引文

Moroco AE, Wei Z, Byrd I, et al. 植入后与设备相关的结果。 2024;20(9):1497-1503.

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