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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

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          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.

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          Most cited references3

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          Qualitative content analysis: basis and techniques

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            An introduction into qualitative social sciences

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              European network of rare disease help lines (ENRDHLs)—caller profile analysis 2013

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                Author and article information

                Contributors
                ab@cherh.de
                mf@cherh.de
                frp@cherh.de
                sl@cherh.de
                dr@cherh.de
                verena.luehrs@aekn.de
                Lisa.Biehl@achse-online.de
                hartz@uni-mainz.de
                holger.storf@uni-mainz.de
                franziska.schauer@uniklinik-freiburg.de
                t.wagner@em.uni-frankfurt.de
                jms@ivbl.uni-jannover.de
                Journal
                BMC Health Serv Res
                BMC Health Serv Res
                BMC Health Services Research
                BioMed Central (London )
                1472-6963
                9 February 2018
                9 February 2018
                2018
                : 18
                : 99
                Affiliations
                [1 ]ISNI 0000 0001 2163 2777, GRID grid.9122.8, CHERH - Centre for Health Economics Research Hannover, , Leibniz University Hannover, ; Otto-Brenner-Straße 1, 30159 Hannover, Germany
                [2 ]ZQ - Centre for Quality and Management in Healthcare, Medical Association of Lower Saxony, Berliner Allee 20, 30175 Hannover, Germany
                [3 ]ISNI 0000 0001 1093 4868, GRID grid.433743.4, ACHSE – Alliance for Chronic Rare Diseases, , DRK-Clinics Berlin, ; Drontheimer Straße 39, 13359 Berlin, Germany
                [4 ]IMBEI - Institute for Medical Biometry, Epidemiology and Informatics, Obere Zahlbacher Str. 69, 55131 Mainz, Germany
                [5 ]Department of Dermatology, Freiburg Center for Rare Diseases, University Medical Center, University of Freiburg, Hauptstraße 7, 79104 Freiburg, Germany
                [6 ]ISNI 0000 0004 1936 9721, GRID grid.7839.5, University Centre for Thorax Oncology, , University Clinic of the Johann Wolfgang-Goethe University, ; Theodor-Stern-Kai 7, 60559 Frankfurt am Main, Germany
                Author information
                http://orcid.org/0000-0002-0210-5370
                Article
                2872
                10.1186/s12913-018-2872-9
                5807836
                29426339
                b07fc103-2c89-4059-8c67-3f83ebc8acc6
                © The Author(s). 2018

                Open AccessThis 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.

                History
                : 21 November 2016
                : 22 January 2018
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100003107, Bundesministerium für Gesundheit;
                Award ID: IIA5-2513FSB801
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2018

                Health & Social care
                rare diseases,telemedicine,health-seeking behaviour,helpline,health information

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