Concurrent and Predictive Validity of the Mann Assessment of Swallowing Ability in Belgian Acute Stroke Patients Based on a 1-Year Follow-Up Study.

IF 1.1 4区 医学 Q3 AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY
Folia Phoniatrica et Logopaedica Pub Date : 2024-01-01 Epub Date: 2023-09-04 DOI:10.1159/000533884
Ingeborg Sylvia Simpelaere, Tina Hansen, Ella Roelant, Jan Vanderwegen, Marc De Bodt, Gwen Van Nuffelen
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引用次数: 0

Abstract

Introduction: The Mann Assessment of Swallowing Ability (MASA) is a standardized clinical swallowing examination, specifically developed as a diagnostic test for the presence of oropharyngeal dysphagia and aspiration in the early period after stroke onset. In the original validation study, cutoff scores of <178 and <170 points, respectively, for the identification of dysphagia and aspiration risk are reported. However, a literature search revealed that alternative cutoff scores for dysphagia and/or aspiration provide better diagnostic accuracy. The aim of this secondary data analysis study was to evaluate the concurrent and predictive validity of the MASA.

Methods: Data were derived from a Belgian cohort study of an acute stroke population (n = 151). The MASA total score (MASA-TS), which is the sum of weighted scores on the 24 items, was evaluated against the Fiberoptic Endoscopic Dysphagia Severity Scale (FEDSS) to assess concurrent validity. To assess predictive validity of the MASA-TS, pneumonia during hospitalization and over 1 year and mortality acted as a future criterion. Analyses included receiver operating characteristic curves and area under the curve (AUC).

Results: Diagnostic accuracy of the MASA-TS was good for dysphagia (AUC = 0.85) and for the presence of relevant aspiration risk (AUC = 0.84). Using the original cutoff scores, the MASA-TS showed perfect sensitivity (Se = 1.00) for the identification of dysphagia and aspiration but inadequate specificity (Sp) for dysphagia (Sp = 0.16) and aspiration (Sp = 0.43). After determining new MASA cutoff scores, the optimal MASA cutoff scores were ≤146 for both dysphagia and aspiration with adequate thresholds (Se = 0.71 and Sp = 0.81 for dysphagia; Se = 0.73 and Sp = 0.80 for aspiration). The MASA-TS was a significant predictor of pneumonia during hospitalization (AUC = 0.85) and 1-year follow-up (AUC = 0.86), and of mortality (AUC = 0.79).

Conclusion: The MASA-TS showed good concurrent validity with the FEDSS. Furthermore, using new cutoff scores (≤146 for the identification of dysphagia and aspiration) lead in general to more accurate diagnostic indexes. The MASA-TS is a good predictor of aspiration pneumonia during hospitalization and 1-year follow-up and of mortality.

基于 1 年随访研究的比利时急性脑卒中患者吞咽能力曼氏评估的并发和预测有效性。
简介曼氏吞咽能力评估(MASA)是一项标准化的临床吞咽检查,专门用于诊断中风发病后早期是否存在口咽吞咽困难和误吸。在最初的验证研究中,用于识别吞咽困难和吸入风险的截断分数分别为 178 分和 170 分。然而,文献检索显示,吞咽困难和/或吸入的其他临界值能提供更好的诊断准确性。这项二手数据分析研究旨在评估 MASA 的并发和预测有效性:数据来自比利时一项针对急性中风患者的队列研究(n = 151)。MASA 总分(MASA-TS)是 24 个项目的加权分数总和,与纤维内镜吞咽困难严重程度量表(FEDSS)进行对比评估,以评估并发有效性。为了评估MASA-TS的预测有效性,住院期间和一年内的肺炎以及死亡率成为未来的标准。分析包括接收者操作特征曲线和曲线下面积(AUC):结果:MASA-TS对吞咽困难(AUC = 0.85)和存在相关吸入风险(AUC = 0.84)的诊断准确性良好。使用原来的截断分数,MASA-TS 在识别吞咽困难和吸入方面显示出完美的灵敏度(Se = 1.00),但在吞咽困难(Sp = 0.16)和吸入(Sp = 0.43)方面显示出不足的特异性(Sp)。在确定了新的 MASA 临界值后,吞咽困难和吸入的最佳 MASA 临界值均为≤146,且具有足够的阈值(吞咽困难为 Se = 0.71,Sp = 0.81;吸入为 Se = 0.73,Sp = 0.80)。MASA-TS 是住院期间(AUC = 0.85)和随访 1 年(AUC = 0.86)肺炎以及死亡率(AUC = 0.79)的重要预测指标:结论:MASA-TS与FEDSS具有良好的并发有效性。此外,使用新的截断分数(≤146 分用于识别吞咽困难和吸入)可获得更准确的诊断指标。MASA-TS能很好地预测住院期间和1年随访期间的吸入性肺炎以及死亡率。
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来源期刊
Folia Phoniatrica et Logopaedica
Folia Phoniatrica et Logopaedica AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY-OTORHINOLARYNGOLOGY
CiteScore
2.30
自引率
10.00%
发文量
28
审稿时长
>12 weeks
期刊介绍: Published since 1947, ''Folia Phoniatrica et Logopaedica'' provides a forum for international research on the anatomy, physiology, and pathology of structures of the speech, language, and hearing mechanisms. Original papers published in this journal report new findings on basic function, assessment, management, and test development in communication sciences and disorders, as well as experiments designed to test specific theories of speech, language, and hearing function. Review papers of high quality are also welcomed.
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