Die Versorgung von Menschen mit seltenen Erkrankungen in Niedersachsen: Ergebnisse einer Ärztebefragung

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Frédéric Pauer
  • Uljana Pflaum
  • Verena Lührs
  • Martin Frank
  • J. Matthias Graf von der Schulenburg

Externe Organisationen

  • ÄKN - Ärztekammer Niedersachsen
Forschungs-netzwerk anzeigen

Details

Titel in ÜbersetzungHealthcare services for people in Lower Saxony (Germany) suffering from a rare disease: Findings from a survey among medical professionals
OriginalspracheMehrere Sprachen
Seiten (von - bis)36-44
Seitenumfang9
FachzeitschriftZeitschrift fur Evidenz, Fortbildung und Qualitat im Gesundheitswesen
Jahrgang113
Frühes Online-Datum3 Juni 2016
PublikationsstatusVeröffentlicht - 2016

Abstract

Background In the European Union, about 30 million people are affected by one of the 7,000 to 8,000 diseases being defined as rare. In Germany alone, an estimated 4 million people suffer from a rare disease. In many cases, therapeutic options and knowledge of specific rare diseases are strongly limited. Objective The aim of this study was to identify the deficits and challenges confronting healthcare services for people suffering from a rare disease from the medical professional's perspective. Method As many as 530 medical professionals were invited to complete an online questionnaire, which was also available on the website of the General Medical Council of Lower Saxony. The questionnaire focused on questions in the following fields: structure of the medical care system; diagnosis and therapy; information sources and information exchange; and improvement of healthcare situation. Data were analyzed using IBM SPSS 22. Result We received 65 completed questionnaires. The evaluation indicates deficits in the medical services provided for people with a rare disease and shortcomings in the communication between clinical disciplines. In addition, diagnostic and therapeutic options are limited, and quality-tested information is rare. Conclusion Many of the identified deficits have already been addressed in the German national plan of action for people affected by rare diseases. Furthermore, newly discovered deficits have been evaluated. The German government implemented healthcare structures to improve healthcare services for people with rare diseases. However, budget deficits for specialized structures have occurred inhibiting the expansion of healthcare services. Moreover, many patients need systemic treatment requiring the further development of interdisciplinary care.

Schlagwörter

    health policy, healthcare research, healthcare System, national plan of action, Rare diseases

ASJC Scopus Sachgebiete

Ziele für nachhaltige Entwicklung

Zitieren

Die Versorgung von Menschen mit seltenen Erkrankungen in Niedersachsen: Ergebnisse einer Ärztebefragung. / Pauer, Frédéric; Pflaum, Uljana; Lührs, Verena et al.
in: Zeitschrift fur Evidenz, Fortbildung und Qualitat im Gesundheitswesen, Jahrgang 113, 2016, S. 36-44.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Pauer, F, Pflaum, U, Lührs, V, Frank, M & Graf von der Schulenburg, JM 2016, 'Die Versorgung von Menschen mit seltenen Erkrankungen in Niedersachsen: Ergebnisse einer Ärztebefragung', Zeitschrift fur Evidenz, Fortbildung und Qualitat im Gesundheitswesen, Jg. 113, S. 36-44. https://doi.org/10.1016/j.zefq.2016.05.003
Pauer, F., Pflaum, U., Lührs, V., Frank, M., & Graf von der Schulenburg, J. M. (2016). Die Versorgung von Menschen mit seltenen Erkrankungen in Niedersachsen: Ergebnisse einer Ärztebefragung. Zeitschrift fur Evidenz, Fortbildung und Qualitat im Gesundheitswesen, 113, 36-44. https://doi.org/10.1016/j.zefq.2016.05.003
Pauer F, Pflaum U, Lührs V, Frank M, Graf von der Schulenburg JM. Die Versorgung von Menschen mit seltenen Erkrankungen in Niedersachsen: Ergebnisse einer Ärztebefragung. Zeitschrift fur Evidenz, Fortbildung und Qualitat im Gesundheitswesen. 2016;113:36-44. Epub 2016 Jun 3. doi: 10.1016/j.zefq.2016.05.003
Pauer, Frédéric ; Pflaum, Uljana ; Lührs, Verena et al. / Die Versorgung von Menschen mit seltenen Erkrankungen in Niedersachsen : Ergebnisse einer Ärztebefragung. in: Zeitschrift fur Evidenz, Fortbildung und Qualitat im Gesundheitswesen. 2016 ; Jahrgang 113. S. 36-44.
Download
@article{10c6d9b6ed3f4aa7a8a800627f3f8bb0,
title = "Die Versorgung von Menschen mit seltenen Erkrankungen in Niedersachsen: Ergebnisse einer {\"A}rztebefragung",
abstract = "Background In the European Union, about 30 million people are affected by one of the 7,000 to 8,000 diseases being defined as rare. In Germany alone, an estimated 4 million people suffer from a rare disease. In many cases, therapeutic options and knowledge of specific rare diseases are strongly limited. Objective The aim of this study was to identify the deficits and challenges confronting healthcare services for people suffering from a rare disease from the medical professional's perspective. Method As many as 530 medical professionals were invited to complete an online questionnaire, which was also available on the website of the General Medical Council of Lower Saxony. The questionnaire focused on questions in the following fields: structure of the medical care system; diagnosis and therapy; information sources and information exchange; and improvement of healthcare situation. Data were analyzed using IBM SPSS 22. Result We received 65 completed questionnaires. The evaluation indicates deficits in the medical services provided for people with a rare disease and shortcomings in the communication between clinical disciplines. In addition, diagnostic and therapeutic options are limited, and quality-tested information is rare. Conclusion Many of the identified deficits have already been addressed in the German national plan of action for people affected by rare diseases. Furthermore, newly discovered deficits have been evaluated. The German government implemented healthcare structures to improve healthcare services for people with rare diseases. However, budget deficits for specialized structures have occurred inhibiting the expansion of healthcare services. Moreover, many patients need systemic treatment requiring the further development of interdisciplinary care.",
keywords = "health policy, healthcare research, healthcare System, national plan of action, Rare diseases",
author = "Fr{\'e}d{\'e}ric Pauer and Uljana Pflaum and Verena L{\"u}hrs and Martin Frank and {Graf von der Schulenburg}, {J. Matthias}",
year = "2016",
doi = "10.1016/j.zefq.2016.05.003",
language = "Multiple languages",
volume = "113",
pages = "36--44",

}

Download

TY - JOUR

T1 - Die Versorgung von Menschen mit seltenen Erkrankungen in Niedersachsen

T2 - Ergebnisse einer Ärztebefragung

AU - Pauer, Frédéric

AU - Pflaum, Uljana

AU - Lührs, Verena

AU - Frank, Martin

AU - Graf von der Schulenburg, J. Matthias

PY - 2016

Y1 - 2016

N2 - Background In the European Union, about 30 million people are affected by one of the 7,000 to 8,000 diseases being defined as rare. In Germany alone, an estimated 4 million people suffer from a rare disease. In many cases, therapeutic options and knowledge of specific rare diseases are strongly limited. Objective The aim of this study was to identify the deficits and challenges confronting healthcare services for people suffering from a rare disease from the medical professional's perspective. Method As many as 530 medical professionals were invited to complete an online questionnaire, which was also available on the website of the General Medical Council of Lower Saxony. The questionnaire focused on questions in the following fields: structure of the medical care system; diagnosis and therapy; information sources and information exchange; and improvement of healthcare situation. Data were analyzed using IBM SPSS 22. Result We received 65 completed questionnaires. The evaluation indicates deficits in the medical services provided for people with a rare disease and shortcomings in the communication between clinical disciplines. In addition, diagnostic and therapeutic options are limited, and quality-tested information is rare. Conclusion Many of the identified deficits have already been addressed in the German national plan of action for people affected by rare diseases. Furthermore, newly discovered deficits have been evaluated. The German government implemented healthcare structures to improve healthcare services for people with rare diseases. However, budget deficits for specialized structures have occurred inhibiting the expansion of healthcare services. Moreover, many patients need systemic treatment requiring the further development of interdisciplinary care.

AB - Background In the European Union, about 30 million people are affected by one of the 7,000 to 8,000 diseases being defined as rare. In Germany alone, an estimated 4 million people suffer from a rare disease. In many cases, therapeutic options and knowledge of specific rare diseases are strongly limited. Objective The aim of this study was to identify the deficits and challenges confronting healthcare services for people suffering from a rare disease from the medical professional's perspective. Method As many as 530 medical professionals were invited to complete an online questionnaire, which was also available on the website of the General Medical Council of Lower Saxony. The questionnaire focused on questions in the following fields: structure of the medical care system; diagnosis and therapy; information sources and information exchange; and improvement of healthcare situation. Data were analyzed using IBM SPSS 22. Result We received 65 completed questionnaires. The evaluation indicates deficits in the medical services provided for people with a rare disease and shortcomings in the communication between clinical disciplines. In addition, diagnostic and therapeutic options are limited, and quality-tested information is rare. Conclusion Many of the identified deficits have already been addressed in the German national plan of action for people affected by rare diseases. Furthermore, newly discovered deficits have been evaluated. The German government implemented healthcare structures to improve healthcare services for people with rare diseases. However, budget deficits for specialized structures have occurred inhibiting the expansion of healthcare services. Moreover, many patients need systemic treatment requiring the further development of interdisciplinary care.

KW - health policy

KW - healthcare research

KW - healthcare System

KW - national plan of action

KW - Rare diseases

UR - http://www.scopus.com/inward/record.url?scp=84971671147&partnerID=8YFLogxK

U2 - 10.1016/j.zefq.2016.05.003

DO - 10.1016/j.zefq.2016.05.003

M3 - Article

C2 - 27480187

AN - SCOPUS:84971671147

VL - 113

SP - 36

EP - 44

JO - Zeitschrift fur Evidenz, Fortbildung und Qualitat im Gesundheitswesen

JF - Zeitschrift fur Evidenz, Fortbildung und Qualitat im Gesundheitswesen

SN - 1865-9217

ER -