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儿童药物诱导睡眠内镜分级系统(PedDISE-8)的可靠性和有效性

Reliability and Validity of a Pediatric Drug-Induced Sleep Endoscopy Grading System (PedDISE-8).

作者信息

Jaffal Hussein, Coutras Steven W, Dewey John, McArdle Erica, Cui Ruifeng

机构信息

Department of Otolaryngology-Head and Neck Surgery, West Virginia University, Morgantown, WV, USA.

出版信息

Ann Otol Rhinol Laryngol. 2025 Jun;134(6):420-426. doi: 10.1177/00034894251318158. Epub 2025 Feb 9.

Abstract

OBJECTIVES

Drug-induced sleep endoscopy (DISE) is increasingly being used in children with obstructive sleep apnea (OSA) to identify specific sites of upper airway obstruction and plan surgical interventions. This study aims to test the reliability and validity of a new grading system for pediatric DISE procedures (PedDISE-8).

METHODS

We conducted a retrospective chart review of children 0 to 18 years old with OSA who underwent DISE. Four independent raters reviewed and graded each video recording twice using the PedDISE-8. Eight upper airway sites were evaluated: inferior turbinates, adenoid, velum, tonsils/lateral pharyngeal walls, lingual tonsils, tongue base, epiglottis, and supra-arytenoid tissue. Intraclass correlation coefficients were calculated to determine inter-rater and intra-rater rating reliability for each site. External validity was assessed by analyzing the correlation between the number of sites with severe obstruction and polysomnographic data.

RESULTS

DISE recordings were reviewed for 86 pediatric patients, 59.5% of whom were male and 26.7% were obese. The median age was 3.5 (IQR 2.4-5.3) years, and the median obstructive apnea-hypopnea index (oAHI) was 5.5 (IQR 3.1-10.4). Moderate to good inter-rater and intra-rater reliability were found for all eight sites (intraclass correlation coefficient 0.67 to 0.88 and 0.71 to 0.87, respectively). The number of sites with severe obstruction correlated positively with the oAHI (τ = 0.119,  = .004).

CONCLUSIONS

The PedDISE-8 grading system demonstrated good inter-rater and intra-rater reliability and external validity. It can be used in children undergoing DISE for OSA.

摘要

目的

药物诱导睡眠内镜检查(DISE)越来越多地用于阻塞性睡眠呼吸暂停(OSA)患儿,以确定上气道阻塞的具体部位并规划手术干预措施。本研究旨在测试一种新的儿科DISE程序分级系统(PedDISE-8)的可靠性和有效性。

方法

我们对0至18岁接受DISE的OSA患儿进行了回顾性病历审查。四名独立评估者使用PedDISE-8对每个视频记录进行两次审查和分级。评估了八个上气道部位:下鼻甲、腺样体、软腭、扁桃体/咽侧壁、舌扁桃体、舌根、会厌和杓状软骨上组织。计算组内相关系数以确定每个部位的评估者间和评估者内评分可靠性。通过分析严重阻塞部位数量与多导睡眠图数据之间的相关性来评估外部有效性。

结果

对86例儿科患者的DISE记录进行了审查,其中59.5%为男性,26.7%为肥胖患者。中位年龄为3.5(IQR 2.4-5.3)岁,中位阻塞性呼吸暂停低通气指数(oAHI)为5.5(IQR 3.1-10.4)。所有八个部位均发现了中度至良好的评估者间和评估者内可靠性(组内相关系数分别为0.67至0.88和0.71至0.87)。严重阻塞部位的数量与oAHI呈正相关(τ = 0.119,P = 0.004)。

结论

PedDISE-8分级系统显示出良好的评估者间和评估者内可靠性以及外部有效性。它可用于接受DISE治疗OSA的儿童。

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