Adopting Quality Criteria for Websites Providing Medical Information About Rare Diseases

Downloadstatistik des Dokuments (Auswertung nach COUNTER):

Pauer, Frederic; Gobel, Jens; Storf, Holger; Litzkendorf, Svenja; Babac, Ana et al.: Adopting Quality Criteria for Websites Providing Medical Information About Rare Diseases. In: Interactive Journal of Medical Research 5 (2016), Nr. 3, e24. DOI: http://dx.doi.org/10.2196/ijmr.5822

Version im Repositorium

Zum Zitieren der Version im Repositorium verwenden Sie bitte diesen DOI: https://doi.org/10.15488/525

Zeitraum, für den die Download-Zahlen angezeigt werden:

Jahr: 
Monat: 

Summe der Downloads: 335




Kleine Vorschau
Zusammenfassung: 
BACKGROUND: The European Union considers diseases to be rare when they affect less than 5 in 10,000 people. It is estimated that there are between 5000 and 8000 different rare diseases. Consistent with this diversity, the quality of information available on the Web varies considerably. Thus, quality criteria for websites about rare diseases are needed. OBJECTIVE: The objective of this study was to generate a catalog of quality criteria suitable for rare diseases. METHODS: First, relevant certificates and quality recommendations for health information websites were identified through a comprehensive Web search. Second, all considered quality criteria of each certification program and catalog were examined, extracted into an overview table, and analyzed by thematic content. Finally, an interdisciplinary expert group verified the relevant quality criteria. RESULTS: We identified 9 quality certificates and criteria catalogs for health information websites with 304 single criteria items. Through this, we aggregated 163 various quality criteria, each assigned to one of the following categories: thematic, technical, service, content, and legal. Finally, a consensus about 13 quality criteria for websites offering medical information on rare diseases was determined. Of these categories, 4 (data protection concept, imprint, creation and updating date, and possibility to contact the website provider) were identified as being the most important for publishing medical information about rare diseases. CONCLUSIONS: The large number of different quality criteria appearing within a relatively small number of criteria catalogs shows that the opinion of what is important in the quality of health information differs. In addition, to define useful quality criteria for websites about rare diseases, which are an essential source of information for many patients, a trade-off is necessary between the high standard of quality criteria for health information websites in general and the limited provision of information about some rare diseases. Finally, transparently presented quality assessments can help people to find reliable information and to assess its quality.
Lizenzbestimmungen: CC BY 2.0 Unported
Publikationstyp: Article
Publikationsstatus: publishedVersion
Erstveröffentlichung: 2016
Die Publikation erscheint in Sammlung(en):Wirtschaftswissenschaftliche Fakultät

Verteilung der Downloads über den gewählten Zeitraum:

Herkunft der Downloads nach Ländern:

Pos. Land Downloads
Anzahl Proz.
1 image of flag of Germany Germany 181 54,03%
2 image of flag of United States United States 44 13,13%
3 image of flag of Sweden Sweden 16 4,78%
4 image of flag of Russian Federation Russian Federation 16 4,78%
5 image of flag of No geo information available No geo information available 12 3,58%
6 image of flag of China China 8 2,39%
7 image of flag of Netherlands Netherlands 7 2,09%
8 image of flag of Ukraine Ukraine 5 1,49%
9 image of flag of France France 4 1,19%
10 image of flag of Czech Republic Czech Republic 4 1,19%
    andere 38 11,34%

Weitere Download-Zahlen und Ranglisten:


Hinweis

Zur Erhebung der Downloadstatistiken kommen entsprechend dem „COUNTER Code of Practice for e-Resources“ international anerkannte Regeln und Normen zur Anwendung. COUNTER ist eine internationale Non-Profit-Organisation, in der Bibliotheksverbände, Datenbankanbieter und Verlage gemeinsam an Standards zur Erhebung, Speicherung und Verarbeitung von Nutzungsdaten elektronischer Ressourcen arbeiten, welche so Objektivität und Vergleichbarkeit gewährleisten sollen. Es werden hierbei ausschließlich Zugriffe auf die entsprechenden Volltexte ausgewertet, keine Aufrufe der Website an sich.