Literature DB >> 19681006

A content analysis from a US statewide survey of memorable healthcare decisions for individuals with intellectual disability.

Kathleen M Fisher1, Michael J Green, Fredrick K Orkin, Vernon M Chinchilli.   

Abstract

BACKGROUND: Little is known about surrogate healthcare decision-making for individuals with intellectual disability (ID). This study examined healthcare decision-making by residential-agency directors to learn their process and the extent to which the individual is included.
METHOD: Content analysis of qualitative data from a mailed survey of residential-agency directors in a large US northeastern state.
RESULTS: Narrative comments of 102 directors (65% of respondents) are reported. Three themes emerged: (a) Identifying someone else's "best interest" is challenging; (b) Perceptions of the healthcare community, especially related to quality of life, can influence care provided; and (c) Surrogate decision-making is a team effort.
CONCLUSIONS: With knowledge of how decisions are made, the healthcare community can better interact with the complex array of service agencies and persons who determine care for this vulnerable population.

Entities:  

Mesh:

Year:  2009        PMID: 19681006      PMCID: PMC2862000          DOI: 10.1080/13668250903083332

Source DB:  PubMed          Journal:  J Intellect Dev Disabil        ISSN: 1366-8250


  12 in total

1.  The capacity of people with a 'mental disability' to make a health care decision.

Authors:  J G Wong; C H Clare; A J Holland; P C Watson; M Gunn
Journal:  Psychol Med       Date:  2000-03       Impact factor: 7.723

2.  The ethics of surrogate decision making.

Authors:  Ben A Rich
Journal:  West J Med       Date:  2002-03

3.  Health care decision-making by adults with mental retardation.

Authors:  Christine D Cea; Celia B Fisher
Journal:  Ment Retard       Date:  2003-04

4.  Evaluation of qualitative research studies.

Authors:  Cynthia K Russell; David M Gregory
Journal:  Evid Based Nurs       Date:  2003-04

5.  Physical and behavioral health of adults with mental retardation across residential settings.

Authors:  Ruth I Freedman; Deborah Chassler
Journal:  Public Health Rep       Date:  2004 Jul-Aug       Impact factor: 2.792

Review 6.  Physical activity of adults with mental retardation: review and research needs.

Authors:  Viviene A Temple; Georgia C Frey; Heidi I Stanish
Journal:  Am J Health Promot       Date:  2006 Sep-Oct

7.  Capacity issues related to the health care proxy.

Authors:  Martin Lyden
Journal:  Ment Retard       Date:  2006-08

8.  The limitations of "vulnerability" as a protection for human research participants.

Authors:  Carol Levine; Ruth Faden; Christine Grady; Dale Hammerschmidt; Lisa Eckenwiler; Jeremy Sugarman
Journal:  Am J Bioeth       Date:  2004       Impact factor: 11.229

9.  The challenges for nurses communicating with and gaining valid consent from adults with intellectual disabilities within the accident and emergency care service.

Authors:  Margaret Sowney; Owen Barr
Journal:  J Clin Nurs       Date:  2007-04-24       Impact factor: 3.036

10.  Proxy healthcare decision-making for persons with intellectual disability: perspectives of residential-agency directors.

Authors:  Kathleen M Fisher; Fredrick K Orkin; Michael J Green; Vernon M Chinchilli; Anand Bhattacharya
Journal:  Am J Intellect Dev Disabil       Date:  2009-11
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.