Сравнение на методи

	Скала за изход и тежест на дисфагията	Въпросник за качеството на живот при преглъщане	Индекс на гласова инвалидност
Област	Логопедия	Логопедия	Логопедия
Семейство	Process / pipeline	Process / pipeline	Process / pipeline
Година на възникване	1999	2002	1997
Създател	O'Neil, K. H., et al.	McHorney, C. A., et al.	Jacobson, B. H., et al.
Тип	Clinician-rated	Self-report	Self-report
Основополагащ източник	O'Neil, K. H., Purdy, M., Falk, J., & Gidas, L. (1999). The Dysphagia Outcome and Severity Scale. Dysphagia, 14(3), 139–145.	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.	Jacobson, B. H., Johnson, A., Grywalski, C., Silbergleit, A., Jacobson, G., Benninger, M. S., & Newman, C. W. (1997). The Voice Handicap Index (VHI): Development and Validation. American Journal of Speech-Language Pathology, 6(3), 66–70.
Други названия	DOSS	SWAL-QoL, SWAL-CARE	VHI, VHI-30
Свързани	2	2	2
Резюме	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.	The Voice Handicap Index (VHI) is a 30-item self-report questionnaire that measures the impact of voice disorders on quality of life and functional communication. Developed by Jacobson and colleagues in 1997, it quantifies the psychosocial, physical, and emotional burden of dysphonia across functional, physical, and emotional domains. Widely used in otolaryngology and speech-language pathology to assess treatment outcomes and monitor disease progression.