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- W4286294570 abstract "Amyotrophic lateral sclerosis (ALS) is a degenerative disease of unknown origin that affects the motor neurons. It has a rapid, fatal course. For this study, an initial questionnaire of eleven items was developed by experts in the field, who evaluated the suitability and relevance of the items. The questionnaire was then applied to a pilot group of 22 patients diagnosed with ALS. Confirmatory factor analysis, based on estimating maximum likelihood, confirmed the three domains detected in the exploratory factor analysis. The reliability of the scale was tested using Cronbach's α (0.801) and the Kaiser–Meyer–Olkin test (0.770) confirmed the construct validity. The DEREDELA questionnaire is valid, in terms of its content, for monitoring the neurological dysphagia and respiratory deterioration suffered by patients diagnosed with ALS. La esclerosis lateral amiotrófica (ELA) es una enfermedad degenerativa, de origen desconocido, que afecta a las neuronas motoras. Su evolución es rápida y mortal. Para este estudio, desarrollamos un cuestionario inicial de 11 ítems, que fue evaluado por expertos en la materia, valorando la idoneidad y pertinencia de los ítems. A continuación se aplicó el cuestionario a un grupo piloto de 22 pacientes diagnosticados con ELA. El análisis factorial confirmatorio, basado en la estimación de máxima verosimilitud, confirmó los tres dominios detectados en el análisis factorial exploratorio. La confiabilidad de la escala se probó mediante el α de Cronbach (0,801) y la prueba de Kaiser-Meyer-Olkin (0,770) confirmó la validez de constructo. El cuestionario DEREDELA es válido, en cuanto a su contenido, para la monitorización del deterioro neurológico digestivo y el deterioro respiratorio que sufren los pacientes diagnosticados de ELA." @default.
- W4286294570 created "2022-07-21" @default.
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- W4286294570 date "2022-06-01" @default.
- W4286294570 modified "2023-10-14" @default.
- W4286294570 title "Design and validation of a questionnaire for monitoring neurological dysphagia and respiratory deterioration in patients with amyotrophic lateral sclerosis (DEREDELA)" @default.
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- W4286294570 doi "https://doi.org/10.1016/j.nrl.2022.03.010" @default.
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