Searching for just a few words should be enough to get started. If you need to make more complex queries, use the tips below to guide you.
Article type: Research Article
Authors: Schweda, Marka; 1; * | Kögel, Annaa; 1 | Bartels, Claudiab | Wiltfang, Jensb; c; d | Schneider, Anjae; f | Schicktanz, Silkea
Affiliations: [a] Department for Medical Ethics and History of Medicine, University Medical Center Göttingen, Göttingen, Germany | [b] Department of Psychiatry and Psychotherapy, University Medical Center Göttingen, Göttingen, Germany | [c] German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany | [d] Department of Medical Sciences, iBiMED, University of Aveiro, Aveiro, Portugal | [e] German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany | [f] Department for Neurodegenerative Diseases and Gerontopsychiatry, University Hospital Bonn, Bonn, Germany
Correspondence: [*] Correspondence to: PD Dr. Mark Schweda, Department for Medical Ethics and History of Medicine, University Medical Center Göttingen, Humboldtallee 36, 37073 Göttingen, Germany. Tel.: +49 551 39 22116; E-mail: [email protected].
Note: [1] These authors contributed equally to this work.
Abstract: Background:Biomarker-supported testing for preclinical and prodromal Alzheimer’s disease (AD) finds its way into clinical practice. Professional attitudes and practices regarding disclosure and ethical issues are controversial in many countries. Objectives:Against this background, the objective was to survey the actual practice and the attitudes of physicians in German hospitals and memory clinics in order to explore possible practical insecurities and ethical concerns. Methods:A detailed survey with 37 items was conducted among medical professionals at German hospitals and memory clinics (n = 108). Analyses were performed using SPSS 21.0 (IBM). Findings were based on frequency and percentage distribution. Results:Nearly half of the respondents stated that persons with mild cognitive impairment and pathological cerebrospinal fluid biomarkers were informed they had or would soon develop AD. While 81% acknowledged a ‘right not to know’, 75% said that results were always communicated. A majority agreed there was a benefit of prediction or later life planning [end-of-life, financial, family, housing (73–75%)] but also expected high psychological stress (82%) and self-stigmatization (70%) for those tested. Conclusions:There is considerable heterogeneity and insecurity regarding prediction and early detection in the context of AD in Germany. Information of professionals and standardization of professional testing and disclosure practices are needed.
Keywords: Alzheimer’s disease, dementia, disclosure, ethics, Germany, questionnaires, surveys
DOI: 10.3233/JAD-170443
Journal: Journal of Alzheimer's Disease, vol. 62, no. 1, pp. 145-155, 2018
IOS Press, Inc.
6751 Tepper Drive
Clifton, VA 20124
USA
Tel: +1 703 830 6300
Fax: +1 703 830 2300
[email protected]
For editorial issues, like the status of your submitted paper or proposals, write to [email protected]
IOS Press
Nieuwe Hemweg 6B
1013 BG Amsterdam
The Netherlands
Tel: +31 20 688 3355
Fax: +31 20 687 0091
[email protected]
For editorial issues, permissions, book requests, submissions and proceedings, contact the Amsterdam office [email protected]
Inspirees International (China Office)
Ciyunsi Beili 207(CapitaLand), Bld 1, 7-901
100025, Beijing
China
Free service line: 400 661 8717
Fax: +86 10 8446 7947
[email protected]
For editorial issues, like the status of your submitted paper or proposals, write to [email protected]
如果您在出版方面需要帮助或有任何建, 件至: [email protected]