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

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dc.identifier.uri http://dx.doi.org/10.15488/3198
dc.identifier.uri http://www.repo.uni-hannover.de/handle/123456789/3228
dc.contributor.author Babac, Ana
dc.contributor.author Frank, Martin
dc.contributor.author Pauer, Frederic
dc.contributor.author Litzkendorf, Svenja
dc.contributor.author Rosenfeldt, Daniel
dc.contributor.author Lührs, Verena
dc.contributor.author Biehl, Lisa
dc.contributor.author Hartz, Tobias
dc.contributor.author Storf, Holger
dc.contributor.author Schauer, Franziska
dc.contributor.author Wagner, Thomas O.F.
dc.contributor.author Schulenburg, Johann-Matthias Graf von der
dc.date.accessioned 2018-04-27T12:18:20Z
dc.date.available 2018-04-27T12:18:20Z
dc.date.issued 2018
dc.identifier.citation Babac, A.; Frank, M.; Pauer, F.; Litzkendorf, S.; Rosenfeldt, D. et al.: 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. In: BMC Health Services Research 18 (2018), Nr. 1, 99. DOI: https://doi.org/10.1186/s12913-018-2872-9
dc.description.abstract 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. © 2018 The Author(s). eng
dc.language.iso eng
dc.publisher London : BioMed Central Ltd.
dc.relation.ispartofseries BMC Health Services Research 18 (2018), Nr. 1
dc.rights CC BY 4.0 Unported
dc.rights.uri https://creativecommons.org/licenses/by/4.0/
dc.subject Health information eng
dc.subject Health-seeking behaviour eng
dc.subject Helpline eng
dc.subject Rare diseases eng
dc.subject Telemedicine eng
dc.subject.ddc 610 | Medizin, Gesundheit ger
dc.title 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 eng
dc.type Article
dc.type Text
dc.relation.issn 1472-6963
dc.relation.doi https://doi.org/10.1186/s12913-018-2872-9
dc.bibliographicCitation.issue 1
dc.bibliographicCitation.volume 18
dc.bibliographicCitation.firstPage 99
dc.description.version publishedVersion
tib.accessRights frei zug�nglich


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