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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-...

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Autores principales: Babac, Ana, Frank, Martin, Pauer, Frédéric, Litzkendorf, Svenja, Rosenfeldt, Daniel, Lührs, Verena, Biehl, Lisa, Hartz, Tobias, Storf, Holger, Schauer, Franziska, Wagner, Thomas O. F., Graf von der Schulenburg, J-Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5807836/
https://www.ncbi.nlm.nih.gov/pubmed/29426339
http://dx.doi.org/10.1186/s12913-018-2872-9
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author Babac, Ana
Frank, Martin
Pauer, Frédéric
Litzkendorf, Svenja
Rosenfeldt, Daniel
Lührs, Verena
Biehl, Lisa
Hartz, Tobias
Storf, Holger
Schauer, Franziska
Wagner, Thomas O. F.
Graf von der Schulenburg, J-Matthias
author_facet Babac, Ana
Frank, Martin
Pauer, Frédéric
Litzkendorf, Svenja
Rosenfeldt, Daniel
Lührs, Verena
Biehl, Lisa
Hartz, Tobias
Storf, Holger
Schauer, Franziska
Wagner, Thomas O. F.
Graf von der Schulenburg, J-Matthias
author_sort Babac, Ana
collection PubMed
description 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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spelling pubmed-58078362018-02-15 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 Babac, Ana Frank, Martin Pauer, Frédéric Litzkendorf, Svenja Rosenfeldt, Daniel Lührs, Verena Biehl, Lisa Hartz, Tobias Storf, Holger Schauer, Franziska Wagner, Thomas O. F. Graf von der Schulenburg, J-Matthias BMC Health Serv Res Research Article 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. BioMed Central 2018-02-09 /pmc/articles/PMC5807836/ /pubmed/29426339 http://dx.doi.org/10.1186/s12913-018-2872-9 Text en © 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.
spellingShingle Research Article
Babac, Ana
Frank, Martin
Pauer, Frédéric
Litzkendorf, Svenja
Rosenfeldt, Daniel
Lührs, Verena
Biehl, Lisa
Hartz, Tobias
Storf, Holger
Schauer, Franziska
Wagner, Thomas O. F.
Graf von der Schulenburg, J-Matthias
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
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
title_full 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
title_fullStr 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
title_full_unstemmed 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
title_short 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
title_sort 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
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5807836/
https://www.ncbi.nlm.nih.gov/pubmed/29426339
http://dx.doi.org/10.1186/s12913-018-2872-9
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