Use and importance of different information sources among patients with rare diseases and their relatives over time: a qualitative study

被引:0
作者
Svenja Litzkendorf
Martin Frank
Ana Babac
Daniel Rosenfeldt
Franziska Schauer
Tobias Hartz
J.-Matthias Graf von der Schulenburg
机构
[1] Leibniz University Hannover,Center for Health Economics Research Hannover (CHERH)
[2] Ostfalia University of Applied Science,Faculty of Public Health Services
[3] University of Freiburg,Department of Dermatology, Medical Center
[4] Faculty of Medicine,undefined
[5] University of Freiburg,undefined
[6] Clinical Cancer Registry of Lower Saxony,undefined
来源
BMC Public Health | / 20卷
关键词
Rare diseases; Information sources; Informants; Health information seeking; Qualitative research; Content analysis; Self-help; Online information; Written information;
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[1]  
Litzkendorf S(2016)Information needs of people with rare diseases – what information do patients and their relatives require? Journal of Rare Disorders: Diagnosis & Therapy 2 1-11
[2]  
Babac A(2010)Multiple sclerosis: patients’ information sources and needs on disease symptoms and management Patient Prefer Adherence 4 157-161
[3]  
Rosenfeldt D(2016)Implementing ‘self-help friendliness’ in German hospitals: a longitudinal study Health Promot Int 31 303-313
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