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通过远程康复对认知正常至轻度认知障碍患者进行临床吞咽障碍评估的有效性。

Validity of conducting clinical dysphagia assessments for patients with normal to mild cognitive impairment via telerehabilitation.

机构信息

The University of Queensland, School of Health and Rehabilitation Sciences, Brisbane, QLD, Australia.

出版信息

Dysphagia. 2012 Dec;27(4):460-72. doi: 10.1007/s00455-011-9390-9. Epub 2012 Jan 20.

DOI:10.1007/s00455-011-9390-9
PMID:22271284
Abstract

To assess the validity of conducting clinical dysphagia assessments via telerehabilitation, 40 individuals with dysphagia from various etiologies were assessed simultaneously by a face-to-face speech-language pathologist (FTF-SLP) and a telerehabilitation SLP (T-SLP) via an Internet-based videoconferencing telerehabilitation system. Dysphagia status was assessed using a Clinical Swallowing Examination (CSE) protocol, delivered via a specialized telerehabilitation videoconferencing system and involving the use of an assistant at the patient's end of the consultation to facilitate the assessment. Levels of agreement between the FTF-SLP and T-SLP revealed that the majority of parameters reached set levels of clinically acceptable levels of agreement. Specifically, agreement between the T-SLP and FTF-SLP ratings for the oral, oromotor, and laryngeal function tasks revealed levels of exact agreement ranging from 75 to 100% (kappa = 0.36-1.0), while the parameters relating to food and fluid trials ranged in exact agreement from 79 to 100% (kappa = 0.61-1.0). Across the parameters related to aspiration risk and clinical management, exact agreement ranged between 79 and 100% (kappa = 0.49-1.0). The data show that a CSE conducted via telerehabilitation can provide valid and reliable outcomes comparable to clinical decisions made in the FTF environment.

摘要

为了评估通过远程康复进行临床吞咽障碍评估的有效性,对 40 名来自不同病因的吞咽障碍患者同时由面对面的言语语言病理学家(FTF-SLP)和远程康复言语语言病理学家(T-SLP)通过基于互联网的视频会议远程康复系统进行评估。吞咽障碍状况通过临床吞咽检查(CSE)方案进行评估,该方案通过专门的远程康复视频会议系统提供,并在患者端使用助手来协助评估。FTF-SLP 和 T-SLP 之间的一致性水平表明,大多数参数达到了临床可接受的一致水平。具体而言,T-SLP 和 FTF-SLP 对口腔、口运动和喉功能任务的评分之间的一致性水平达到了 75%至 100%(kappa 值为 0.36-1.0),而与食物和液体试验相关的参数的完全一致性水平为 79%至 100%(kappa 值为 0.61-1.0)。在与吸入风险和临床管理相关的参数方面,完全一致性水平在 79%至 100%之间(kappa 值为 0.49-1.0)。数据表明,通过远程康复进行的 CSE 可以提供与 FTF 环境中做出的临床决策相媲美的有效和可靠的结果。

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