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进餐时间评估量表(MAS):第2部分 - 初步心理测量分析。

The Mealtime Assessment Scale (MAS): Part 2 - Preliminary Psychometric Analysis.

作者信息

Pizzorni Nicole, Valentini Debora, Gilardone Marco, Scarponi Letizia, Tresoldi Martina, Barozzi Stefania, Corbo Massimo, Schindler Antonio

机构信息

Department of Biomedical and Clinical Sciences "L. Sacco," Università degli Studi di Milano, Milan, Italy,

Department of Neurorehabilitation Sciences, Casa di Cura del Policlinico, Milan, Italy,

出版信息

Folia Phoniatr Logop. 2020;72(3):182-193. doi: 10.1159/000494136. Epub 2019 Apr 17.

Abstract

AIMS

The Mealtime Assessment Scale (MAS) was developed to assess swallowing safety and efficacy during the meal. The study aims to perform a preliminary validation of MAS by investigating internal consistency, inter-rater agreement, concurrent and known-group validity, and responsiveness.

METHODS

MAS was tested on 100 persons without dysphagia (group 1) and 100 persons with dysphagia (group 2). Fifty subjects were simultaneously evaluated at mealtime using MAS by two independent clinicians to test inter-rater agreement. For concurrent validity, MAS was correlated with the Mann Assessment of Swallowing Ability (MASA) and American Speech-Language-Hearing Association National Outcomes Measurement System (ASHA NOMS) swallowing scale. MAS scores of groups 1 and 2 were compared for known-group validity. Responsiveness was tested reassessing 36 patients from group 2 after diet improvement.

RESULTS

Internal consistency and responsiveness were established for efficacy but not for safety. For inter-rater agreement, an average deviation index <0.66 was found for all items. MAS showed strong correlations with MASA and ASHA NOMS. MAS scores were significantly different between groups 1 and 2.

CONCLUSION

Preliminary evidence of the validity and reliability of MAS was established, except for the internal consistency and the responsiveness of the safety subscale. Further studies need to complete the validation process.

摘要

目的

进餐时间评估量表(MAS)旨在评估进餐期间的吞咽安全性和有效性。本研究旨在通过调查内部一致性、评分者间信度、同时效度和已知组效度以及反应度来对MAS进行初步验证。

方法

对100名无吞咽困难者(第1组)和100名有吞咽困难者(第2组)进行MAS测试。50名受试者在进餐时间由两名独立的临床医生同时使用MAS进行评估,以测试评分者间信度。为了评估同时效度,将MAS与吞咽能力曼恩评估量表(MASA)和美国言语语言听力协会国家结局测量系统(ASHA NOMS)吞咽量表进行相关性分析。比较第1组和第2组的MAS评分以评估已知组效度。通过对第2组36例患者在饮食改善后重新评估来测试反应度。

结果

确立了MAS在有效性方面的内部一致性和反应度,但在安全性方面未确立。对于评分者间信度,所有项目的平均偏差指数均<0.66。MAS与MASA和ASHA NOMS显示出很强的相关性。第1组和第2组的MAS评分有显著差异。

结论

除安全性子量表的内部一致性和反应度外,确立了MAS有效性和可靠性的初步证据。需要进一步的研究来完成验证过程。

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