TY - JOUR
T1 - Comparing Advance Care Planning in Young-Onset Dementia in the USA vs Belgium
T2 - Challenges Partly Related to Societal Context
AU - Van Rickstal, Romy
AU - De Vleminck, Aline
AU - Morrison, Sean R.
AU - Koopmans, Raymond T.
AU - van der Steen, Jenny T.
AU - Engelborghs, Sebastiaan
AU - Neugroschl, Judith
AU - Aldridge, Melissa D.
AU - Sano, Mary
AU - Van den Block, Lieve
N1 - Funding Information:
This work was supported by the Research Foundation Flanders (Fonds voor Wetenschappelijk Onderzoek - Vlaanderen) through a predoctoral Strategic Basic Research Fellowship granted to R.V.R. (1S75919N) and through a postdoctoral fellowship granted to A.D.V. (12V9718N). This study was also supported by a Fulbright Scholarship granted to A.D.V. (2015).
Publisher Copyright:
© 2020 AMDA – The Society for Post-Acute and Long-Term Care Medicine
PY - 2020/6
Y1 - 2020/6
N2 - Objectives: Advance care planning in young-onset dementia largely remains a blind spot within current literature. This study aimed to explore the engagement in and the conceptualization of advance care planning from the perspective of family caregivers of persons with young-onset dementia and to identify potential similarities and differences in this area between American and Belgian persons with young-onset dementia and their family caregivers. Design: An exploratory qualitative study. Setting and participants: We purposively sampled adult family caregivers of persons with young-onset dementia; our respondents were 13 American and 15 Belgian caregivers with varying familial relationships to the patient. Methods: We conducted 28 semi-structured interviews, using the same interview guide for American and Belgian respondents. Verbatim transcripts were analysed through the method of constant comparative analysis. Results: Important similarities between American and Belgian respondents were restricted knowledge of advance care planning, limited communication about advance directives, and their recommendation for professionals to timely initiate advance care planning. Major differences were attention paid to those end-of-life decisions depicted in the legislature of their respective countries, American caregivers placed higher emphasis on financial planning than their Belgian peers, and, in the case of consulting professionals for advance directives, American caregivers turned to lawyers, whereas Belgian caregivers relied on physicians. Conclusions and implications: Specific nuances and challenges in terms of advance care planning in young-onset dementia arise from a particular societal and legal context on the one hand, and from patients' and caregivers' younger age on the other. Professionals' awareness of and responsiveness to these specificities could facilitate the advance care planning process. Based on our interpretation of results, several recommendations for practice and policy are made.
AB - Objectives: Advance care planning in young-onset dementia largely remains a blind spot within current literature. This study aimed to explore the engagement in and the conceptualization of advance care planning from the perspective of family caregivers of persons with young-onset dementia and to identify potential similarities and differences in this area between American and Belgian persons with young-onset dementia and their family caregivers. Design: An exploratory qualitative study. Setting and participants: We purposively sampled adult family caregivers of persons with young-onset dementia; our respondents were 13 American and 15 Belgian caregivers with varying familial relationships to the patient. Methods: We conducted 28 semi-structured interviews, using the same interview guide for American and Belgian respondents. Verbatim transcripts were analysed through the method of constant comparative analysis. Results: Important similarities between American and Belgian respondents were restricted knowledge of advance care planning, limited communication about advance directives, and their recommendation for professionals to timely initiate advance care planning. Major differences were attention paid to those end-of-life decisions depicted in the legislature of their respective countries, American caregivers placed higher emphasis on financial planning than their Belgian peers, and, in the case of consulting professionals for advance directives, American caregivers turned to lawyers, whereas Belgian caregivers relied on physicians. Conclusions and implications: Specific nuances and challenges in terms of advance care planning in young-onset dementia arise from a particular societal and legal context on the one hand, and from patients' and caregivers' younger age on the other. Professionals' awareness of and responsiveness to these specificities could facilitate the advance care planning process. Based on our interpretation of results, several recommendations for practice and policy are made.
KW - Advance care planning
KW - Belgium
KW - United States of America
KW - family caregivers
KW - qualitative study
KW - young-onset dementia
UR - http://www.scopus.com/inward/record.url?scp=85081925232&partnerID=8YFLogxK
U2 - 10.1016/j.jamda.2020.01.007
DO - 10.1016/j.jamda.2020.01.007
M3 - Article
C2 - 32173310
AN - SCOPUS:85081925232
SN - 1525-8610
VL - 21
SP - 851
EP - 857
JO - Journal of the American Medical Directors Association
JF - Journal of the American Medical Directors Association
IS - 6
ER -