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| Scala di Valutazione e Gravità della Disfagia× | Questionario sulla Qualità della Vita legata alla Deglutizione× | |
|---|---|---|
| Campo | Logopedia | Logopedia |
| Famiglia | Process / pipeline | Process / pipeline |
| Anno di origine≠ | 1999 | 2002 |
| Ideatore≠ | O'Neil, K. H., et al. | McHorney, C. A., et al. |
| Tipo≠ | Clinician-rated | Self-report |
| Fonte seminale≠ | O'Neil, K. H., Purdy, M., Falk, J., & Gidas, L. (1999). The Dysphagia Outcome and Severity Scale. Dysphagia, 14(3), 139–145. DOI ↗ | 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. link ↗ |
| Alias≠ | DOSS | SWAL-QoL, SWAL-CARE |
| Correlati | 2 | 2 |
| Sintesi≠ | 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. | 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. |
| ScholarGateInsieme di dati ↗ |
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