Compara mètodes

	Questionari de Qualitat de Vida en la Deglució	Escala d'Evolució i Gravetat de la Disfàgia
Camp	Logopèdia	Logopèdia
Família	Process / pipeline	Process / pipeline
Any d'origen	2002	1999
Autor original	McHorney, C. A., et al.	O'Neil, K. H., et al.
Tipus	Self-report	Clinician-rated
Font seminal	McHorney, C. A., Bricker, D. E., Kramer, A. E., et al. (2000). The SWAL-QoL Outcomes Tool for Oropharyngeal Dysphagia in Adults: I. Conceptualization and Item Development. Dysphagia, 15(3), 115–121.	O'Neil, K. H., Purdy, M., Falk, J., & Gidas, L. (1999). The Dysphagia Outcome and Severity Scale. Dysphagia, 14(3), 139–145.
Àlies	SWAL-QoL, SWAL-CARE	DOSS
Relacionats	2	2
Resum	The Swallowing Quality of Life (SWAL-QoL) Questionnaire is a comprehensive 44-item self-report measure of the psychosocial and functional impact of dysphagia across 11 quality-of-life domains, including eating burden, food selection, social participation, emotional impact, and fatigue. Developed by McHorney and colleagues (2002), SWAL-QoL captures the patient perspective on swallowing-related disability, complementing objective clinical measures (dysphagia severity, aspiration risk) with data on lived experience and psychological burden. A brief 15-item version, SWAL-CARE, enables efficient monitoring of treatment response.	The Dysphagia Outcome and Severity Scale (DOSS) is a 7-point clinician-rated ordinal scale that measures the severity of swallowing dysfunction and functional swallowing outcomes across two dimensions: safety (penetration-aspiration risk) and efficiency (oral intake adequacy and diet level tolerance). Developed by O'Neil and colleagues in 1999, DOSS integrates clinical observation with videofluoroscopic findings to provide a standardized, functionally meaningful classification of swallowing status from normal to non-functional.