Cost of Illness and Health-Related Quality of Life for Stuttering: Two Systematic Reviews.


Journal

Journal of speech, language, and hearing research : JSLHR
ISSN: 1558-9102
Titre abrégé: J Speech Lang Hear Res
Pays: United States
ID NLM: 9705610

Informations de publication

Date de publication:
09 11 2023
Historique:
medline: 10 11 2023
pubmed: 27 9 2023
entrez: 26 9 2023
Statut: ppublish

Résumé

For those who stutter, verbal communication is typically compromised in social situations. This may attract negative responses from listeners and stigmatization by society. These have the potential to impair health-related quality of life across a range of domains, including qualitative and quantitative impacts on speech output, mental health issues, and failure to attain educational and occupational potential. These systematic reviews were designed to explore this matter using traditional health economics perspectives of utility measures and cost of illness. Studies were included if they involved children, adolescents, or adults with stuttering as a primary diagnosis. The quality of life search strategy identified 2,607 reports, of which three were included in the quality of life analysis. The cost of illness search strategy identified 3,778 reports, of which 39 were included in the cost of illness analysis. Two of the three studies included in the quality of life analysis had a high risk of bias. When measured using utility scores, quality of life for people who stutter was in the range of those reported for chronic health conditions such as diabetes mellitus, cardiovascular disease, and cancer. However, there is little such evidence of quality of life impairment during the preschool years. Studies included in the cost of illness analysis carried considerable risk of bias overall. For people who stutter, there are substantive direct and indirect costs of illness. These include impairment, challenges, and distress across many domains throughout life, including income, education, employment, and social functioning. Evidence of quality of life impairment using utility measures is extremely limited. If this situation is not remedied, the lifetime impairment, challenges, and distress experienced by those who stutter cannot be documented in a form that can be used to influence health policy and health care spending. https://doi.org/10.23641/asha.24168201.

Identifiants

pubmed: 37751681
doi: 10.1044/2023_JSLHR-23-00072
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4414-4431

Auteurs

Alicia Norman (A)

Macquarie University Centre for the Health Economy, Macquarie University Business School, North Ryde, New South Wales, Australia.
Australian Institute for Health Innovation, Macquarie University, North Ryde, New South Wales, Australia.

Robyn Lowe (R)

Australian Stuttering Research Centre, University of Technology Sydney, New South Wales, Australia.

Mark Onslow (M)

Australian Stuttering Research Centre, University of Technology Sydney, New South Wales, Australia.

Sue O'Brian (S)

Australian Stuttering Research Centre, University of Technology Sydney, New South Wales, Australia.

Ann Packman (A)

Australian Stuttering Research Centre, University of Technology Sydney, New South Wales, Australia.

Ross Menzies (R)

Australian Stuttering Research Centre, University of Technology Sydney, New South Wales, Australia.

Liz Schroeder (L)

Macquarie University Centre for the Health Economy, Macquarie University Business School, North Ryde, New South Wales, Australia.
Nuffield Department of Primary Care Health Sciences, University of Oxford, United Kingdom.

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