YouTube-videos for patient education in lymphangioleiomyomatosis?


Journal

Respiratory research
ISSN: 1465-993X
Titre abrégé: Respir Res
Pays: England
ID NLM: 101090633

Informations de publication

Date de publication:
27 Apr 2022
Historique:
received: 17 02 2022
accepted: 12 04 2022
entrez: 28 4 2022
pubmed: 29 4 2022
medline: 30 4 2022
Statut: epublish

Résumé

The Internet is commonly used by patients to acquire health information. To date, no studies have evaluated the quality of information available on YouTube regarding lymphangioleiomyomatosis (LAM). Our aim was to determine the quality and content of YouTube videos regarding LAM and to compare the information provided with current knowledge and guidelines about the disease. The first 200 video hits on YouTube in English for the search term "lymphangioleiomyomatosis" were recorded. All videos suitable for patient education on LAM were included. Video quality was analyzed independently by two investigators utilizing the Health on the Net (HONcode) score, which assesses whether websites provide understandable, accessible, and trustworthy health information; the DISCERN score, which evaluates the quality of information about treatment decisions; and a newly developed LAM-related content score (LRCS) with 31 guideline elements. The search identified 64 eligible videos. The "engagement rate" of 0.3 was low, with a median number of views of 408 (range 42-73,943), a median of 4 likes (range 0-2082), and the majority (53%) receiving a low HONcode score (≤ 2) and only 10% of videos achieving a high score (> 5). The median DISCERN score was 28 (range 15-61, maximum possible score 80), indicating poor video quality and reliability. The median LRCS was 8 (range 0-29, maximum possible score 31) and videos frequently failed to provide sources of information. Online resources could contribute to the limited and often inaccurate information available to patients with LAM, with only a few YouTube videos providing high-quality patient-relevant information.

Sections du résumé

BACKGROUND BACKGROUND
The Internet is commonly used by patients to acquire health information. To date, no studies have evaluated the quality of information available on YouTube regarding lymphangioleiomyomatosis (LAM). Our aim was to determine the quality and content of YouTube videos regarding LAM and to compare the information provided with current knowledge and guidelines about the disease.
METHODS METHODS
The first 200 video hits on YouTube in English for the search term "lymphangioleiomyomatosis" were recorded. All videos suitable for patient education on LAM were included. Video quality was analyzed independently by two investigators utilizing the Health on the Net (HONcode) score, which assesses whether websites provide understandable, accessible, and trustworthy health information; the DISCERN score, which evaluates the quality of information about treatment decisions; and a newly developed LAM-related content score (LRCS) with 31 guideline elements.
RESULTS RESULTS
The search identified 64 eligible videos. The "engagement rate" of 0.3 was low, with a median number of views of 408 (range 42-73,943), a median of 4 likes (range 0-2082), and the majority (53%) receiving a low HONcode score (≤ 2) and only 10% of videos achieving a high score (> 5). The median DISCERN score was 28 (range 15-61, maximum possible score 80), indicating poor video quality and reliability. The median LRCS was 8 (range 0-29, maximum possible score 31) and videos frequently failed to provide sources of information.
CONCLUSIONS CONCLUSIONS
Online resources could contribute to the limited and often inaccurate information available to patients with LAM, with only a few YouTube videos providing high-quality patient-relevant information.

Identifiants

pubmed: 35477513
doi: 10.1186/s12931-022-02022-9
pii: 10.1186/s12931-022-02022-9
pmc: PMC9043877
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

103

Informations de copyright

© 2022. The Author(s).

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Auteurs

Finn M Wilkens (FM)

Center for Interstitial and Rare Lung Diseases, Dep. Pneumology, Thoraxklinik, University of Heidelberg, Heidelberg, Germany.
German Center for Lung Research, Heidelberg, Germany.

Claudia Ganter (C)

Center for Interstitial and Rare Lung Diseases, Dep. Pneumology, Thoraxklinik, University of Heidelberg, Heidelberg, Germany.
German Center for Lung Research, Heidelberg, Germany.

Katharina Kriegsmann (K)

Department for Hematology, Oncology and Rheumatology, University of Heidelberg, Heidelberg, Germany.

Heinrike Wilkens (H)

Department of Pneumology, Allergology and Critical Care Medicine, University Medical Centre, Saarland University, Homburg/Saar, Germany.

Nicolas Kahn (N)

Center for Interstitial and Rare Lung Diseases, Dep. Pneumology, Thoraxklinik, University of Heidelberg, Heidelberg, Germany.
German Center for Lung Research, Heidelberg, Germany.

Gillian C Goobie (GC)

Clinician Investigator Program, Department of Medicine, University of British Columbia, Vancouver, BC, Canada.
Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
Simmons Center for Interstitial Lung Disease, Division of Pulmonary, Allergy and Critical Care Medicine, University of Pittsburgh, Pittsburgh, PA, USA.

Christopher J Ryerson (CJ)

Department of Medicine, University of British Columbia and St. Paul's Hospital, Vancouver, BC, Canada.
Centre for Heart Lung Innovation, University of British Columbia and St. Paul's Hospital, Vancouver, BC, Canada.

Michael Kreuter (M)

Center for Interstitial and Rare Lung Diseases, Dep. Pneumology, Thoraxklinik, University of Heidelberg, Heidelberg, Germany. kreuter@uni-heidelberg.de.
German Center for Lung Research, Heidelberg, Germany. kreuter@uni-heidelberg.de.

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