Literature DB >> 1583931

Assessing quality of life. Moral implications for clinical practice.

R Faden1, A Leplège.   

Abstract

The purpose of this paper is to examine some of the moral implications for clinical practice of the move toward measuring or assessing quality of life. For purposes of this presentation, discussions of the good life or quality of life have at least two "conceptual" preconditions. First is biologic life; second is a minimum cognitive apparatus to attach meaning to life (or a capacity for self-awareness). Quality of life measurement in clinical care has three principal uses: screening, monitoring, and decisionmaking. The paper discusses how increasing reliance on quality of life measures is potentially morally appealing in all these cases, but also how moral "downsides" may be created that should be recognized and confronted with appropriate moral constraints.

Keywords:  Analytical Approach; Health Care and Public Health; Professional Patient Relationship

Mesh:

Year:  1992        PMID: 1583931     DOI: 10.1097/00005650-199205001-00014

Source DB:  PubMed          Journal:  Med Care        ISSN: 0025-7079            Impact factor:   2.983


  11 in total

1.  Oncologists' use of quality of life information: results of a survey of Eastern Cooperative Oncology Group physicians.

Authors:  A Bezjak; P Ng; R Skeel; A D Depetrillo; R Comis; K M Taylor
Journal:  Qual Life Res       Date:  2001       Impact factor: 4.147

Review 2.  The problem of (non-)compliance: is it patients or patience?

Authors:  G R Scofield
Journal:  HEC Forum       Date:  1995 Mar-May

3.  Health outcomes by self-report: validity of the SF-36 among Australian hospital patients.

Authors:  B Shadbolt; J McCallum; M Singh
Journal:  Qual Life Res       Date:  1997-05       Impact factor: 4.147

4.  Intellectual property considerations in the development and use of HRQL measures for clinical trial research.

Authors:  R Berzon; D Patrick; G Guyatt; J M Conley
Journal:  Qual Life Res       Date:  1994-08       Impact factor: 4.147

5.  Clinical validity of the SWAL-QOL and SWAL-CARE outcome tools with respect to bolus flow measures.

Authors:  Colleen A McHorney; Bonnie Martin-Harris; JoAnne Robbins; John Rosenbek
Journal:  Dysphagia       Date:  2006-07       Impact factor: 3.438

6.  Schooling of the patients and clinical application of questionnaires in osteoarthitis.

Authors:  Gustavo Constantino De Campos; Marcelo Tomio Kohara; Marcia Uchoa Rezende; Olga Fugiko Magashima Santana; Merilu Marins Moreira; Olavo Pires De Camargo
Journal:  Acta Ortop Bras       Date:  2014       Impact factor: 0.513

Review 7.  Outcome measures and needs assessment tools for schizophrenia and related disorders.

Authors:  S M Gilbody; A O House; T A Sheldon
Journal:  Cochrane Database Syst Rev       Date:  2003

8.  Quality of life, gender and schizophrenia: a cross-national survey in Canada, Cuba, and U.S.A.

Authors:  V L Vandiver
Journal:  Community Ment Health J       Date:  1998-10

9.  Patients' rights, quality of life, and health care system performance.

Authors:  Ivan Barofsky
Journal:  Qual Life Res       Date:  2003-08       Impact factor: 4.147

Review 10.  Psychometric characteristics of health-related quality-of-life questionnaires in oropharyngeal dysphagia.

Authors:  Angelique A Timmerman; Renée Speyer; Bas J Heijnen; Iris R Klijn-Zwijnenberg
Journal:  Dysphagia       Date:  2014-03-05       Impact factor: 3.438

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