Logo image
Proxy Healthcare Decision-Making for Persons With Intellectual Disability: Perspectives of Residential-Agency Directors
Journal article   Open access   Peer reviewed

Proxy Healthcare Decision-Making for Persons With Intellectual Disability: Perspectives of Residential-Agency Directors

Kathleen M Fisher, Fredrick K Orkin, Michael J Green, Vernon M Chinchilli and Anand Bhattacharya
American journal on intellectual and developmental disabilities, v 114(6), pp 401-410
01 Nov 2009
PMID: 19792056
url
https://doi.org/10.1352/1944-7558-114.6.401View
Published, Version of Record (VoR) Open

Abstract

Abstract Directors of residential agencies for persons with intellectual disability in one U.S. state completed a self-administered, mailed survey to assess relative importance of information sources and decision factors in proxy healthcare decision-making. The most important sources were physician recommendations and input from the person; family input, care staff recommendations, and medical records were less valued. The person's wishes and best interests and recommendations of medical experts were the most important decision factors. Less important were benefits and risks of the intervention, family wishes, and health status; little emphasis was accorded to religious affiliation and extra cost to agency. More research is needed on how best to elicit the wishes and determine what constitutes the “best interests” of these vulnerable individuals.

Metrics

5 Record Views
18 citations in Scopus

Details

UN Sustainable Development Goals (SDGs)

This publication has contributed to the advancement of the following goals:

#3 Good Health and Well-Being

InCites Highlights

Data related to this publication, from InCites Benchmarking & Analytics tool:

Collaboration types
Domestic collaboration
Web of Science research areas
Education, Special
Rehabilitation
Logo image