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Patterns of Palliative Care Beliefs Among Adults in the U.S.: Analysis of a National Cancer Database
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4516658
Author(s) Cheng, Brian T.; Wangmo, Tenzin; Hauser, Joshua M.
Author(s) at UniBasel Wangmo, Tenzin
Year 2019
Title Patterns of Palliative Care Beliefs Among Adults in the U.S.: Analysis of a National Cancer Database
Journal Journal of Pain and Symptom Management
Volume 58
Number 6
Pages / Article-Number 1056-1067
Keywords Palliative care; beliefs; epidemiology; information sharing; knowledge; perceptions
Abstract Palliative care (PC) is associated with increased quality of life for individuals with life-limiting illnesses. Despite growing recognition of the need for public advocacy and involvement, data on public perception of PC are limited. We sought to examine patterns of beliefs, sociodemographic differences, and the impact of information source on perceptions of PC.; Data were analyzed from the 2018 Health Information National Trends Survey, a representative sample of public knowledge on cancer-related information. Prevalence of perceptions was estimated among adults who self-identified as knowledgeable about PC; multivariable logistic regression invoking stepwise variable selection was used to determine associations with perceptions.; Overall, 42.5% automatically thought of death when thinking about PC, and 31.7% equate PC with hospice care. Lower proportions perceived PC as incompatible with curative medical therapy: 15.1% believed PC means giving up, and 14.5% believed PC requires the discontinuation of other treatments. Perceptions varied by age, race, education attainment, income, and marital status. In adjusted models, source of PC information was not related to differences in PC perception: PC is giving up (P ≥ 0.28), requirement to stop curative therapy (P ≥ 0.07), and equation with hospice care (P ≥ 0.29).; Six in every 10 American adults knowledgeable about PC have at least one documented misperception, with differential beliefs by sociodemographic groups. Source of information had little impact on PC beliefs. These findings may help focus future measures to educate the public about the role of PC in health care and address gaps in knowledge.
Publisher Elsevier
ISSN/ISBN 0885-3924 ; 1873-6513
edoc-URL https://edoc.unibas.ch/72866/
Full Text on edoc No
Digital Object Identifier DOI 10.1016/j.jpainsymman.2019.07.030
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/31408666
ISI-Number WOS:000498417300018
Document type (ISI) Article
 
   

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