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Telephone health services in the field of rare diseases : a qualitative interview study examining the needs of patients, relatives, and health care professionals in Germany

  • Background: Rare diseases are, by definition, very serious and chronic diseases with a high negative impact on quality of life. Approximately 350 million people worldwide live with rare diseases. The resulting high disease burden triggers health information search, but helpful, high-quality, and up-to-date information is often hard to find. Therefore, the improvement of health information provision has been integrated in many national plans for rare diseases, discussing the telephone as one access option. In this context, this study examines the need for a telephone service offering information for people affected by rare diseases, their relatives, and physicians. Methods: In total, 107 individuals participated in a qualitative interview study conducted in Germany. Sixty-eight individuals suffering from a rare disease or related to somebody with rare diseases and 39 health care professionals took part. Individual interviews were conducted using a standardized semi-structured questionnaire. Interviews were analysed using the qualitative content analysis, triangulating patients, relatives, and health care professionals. The fulfilment of qualitative data processing standards has been controlled for. Results: Out of 68 patients and relatives and 39 physicians, 52 and 18, respectively, advocated for the establishment of a rare diseases telephone service. Interviewees expected a helpline to include expert staffing, personal contact, good availability, low technical barriers, medical and psychosocial topics of counselling, guidance in reducing information chaos, and referrals. Health care professionals highlighted the importance of medical topics of counselling—in particular, differential diagnostics—and referrals. Conclusions: Therefore, the need for a national rare diseases helpline was confirmed in this study. Due to limited financial resources, existing offers should be adapted in a stepwise procedure in accordance with the identified attributes.

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Author:Ana BabacORCiDGND, Martin FrankORCiDGND, Frédéric PauerORCiD, Svenja LitzkendorfORCiD, Daniel Rosenfeldt, Verena LührsORCiD, Lisa BiehlORCiD, Tobias HartzORCiD, Holger StorfORCiDGND, Franziska SchauerORCiDGND, Thomas O. F. WagnerORCiDGND, Johann-Matthias von der SchulenburgORCiDGND
URN:urn:nbn:de:hebis:30:3-456868
DOI:https://doi.org/10.1186/s12913-018-2872-9
ISSN:1472-6963
Pubmed Id:https://pubmed.ncbi.nlm.nih.gov/29426339
Parent Title (English):BMC health services research
Publisher:BioMed Central
Place of publication:London
Document Type:Article
Language:English
Year of Completion:2018
Date of first Publication:2018/02/09
Publishing Institution:Universitätsbibliothek Johann Christian Senckenberg
Release Date:2018/02/15
Tag:Health information; Health-seeking behaviour; Helpline; Rare diseases; Telemedicine
Volume:18
Issue:1, Art. 99
Page Number:14
First Page:1
Last Page:14
Note:
© The Author(s). 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
HeBIS-PPN:427855586
Institutes:Medizin / Medizin
Dewey Decimal Classification:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Sammlungen:Universitätspublikationen
Licence (German):License LogoCreative Commons - Namensnennung 4.0