Literature DB >> 29791302

Preferences of adults with spinal cord injury for widely used health-related quality of life and subjective well-being measures.

Alina Ionela Palimaru1, William E Cunningham1,2, Marcus Dillistone3, Arturo Vargas-Bustamante1, Honghu Liu4, Ron D Hays1,2.   

Abstract

OBJECTIVE: To describe preferences for survey instruments on health-related quality of life (HRQOL) and subjective well-being (SWB) among adults with spinal cord injury (SCI), and compare perspectives on the instruments between the United States and the United Kingdom.
DESIGN: We conducted 20 in-depth interviews.
SETTING: Participants were interviewed in their homes, some in person and some via Skype. PARTICIPANTS: A convenience sample of 20 adults with SCI (10 in the US and 10 in the UK) were recruited via print and on-line advertisements.
INTERVENTIONS: Not applicable. MAIN OUTCOME MEASURES: Interviewees reviewed six instruments and rated how important it was for their medical providers to know answers to each survey. Two coders analyzed verbatim transcriptions independently using an inductive approach. Keyword-in-context (KWIC) analysis identified the most frequently used words by interviewees to discuss the merits of each instrument.
RESULTS: Participants in both samples identified the Fatigue Severity Scale (FSS) as "vital" that their medical providers know about it. This was followed by the Spinal Cord Injury Independence Measure III, and a stand-alone Eudaimonic Well-Being question. The KWIC analysis showed that the most distinctive words used to discuss FSS were "fatigue" and "pain."
CONCLUSIONS: Understanding what HRQOL and SWB measures are valued by adults living with SCI can lead to selection of informative instruments, which could help clinicians to complement and tailor established care and rehabilitation protocols for individual needs. Participants identified fatigue as a significant issue, and the FSS as a vitally important instrument to share with medical providers.

Entities:  

Keywords:  Fatigue; Health-related quality of life; Outcomes; Quality of life; Spinal cord injury; Subjective well-being

Mesh:

Year:  2018        PMID: 29791302      PMCID: PMC6522975          DOI: 10.1080/10790268.2018.1474691

Source DB:  PubMed          Journal:  J Spinal Cord Med        ISSN: 1079-0268            Impact factor:   1.985


  28 in total

1.  Performance of health-related quality-of-life instruments in a spinal cord injured population.

Authors:  E M Andresen; B S Fouts; J C Romeis; C A Brownson
Journal:  Arch Phys Med Rehabil       Date:  1999-08       Impact factor: 3.966

2.  Use of the SF-36 and other health-related quality of life measures to assess persons with disabilities.

Authors:  Ron D Hays; Harlan Hahn; Grant Marshall
Journal:  Arch Phys Med Rehabil       Date:  2002-12       Impact factor: 3.966

3.  Variability in the treatment of acute spinal cord injury in the United Kingdom: results of a national survey.

Authors:  Melissa C Werndle; Argyro Zoumprouli; Philip Sedgwick; Marios C Papadopoulos
Journal:  J Neurotrauma       Date:  2011-10-26       Impact factor: 5.269

4.  The MOS 36-item short-form health survey (SF-36). I. Conceptual framework and item selection.

Authors:  J E Ware; C D Sherbourne
Journal:  Med Care       Date:  1992-06       Impact factor: 2.983

5.  Dependence of weighted kappa coefficients on the number of categories.

Authors:  H Brenner; U Kliebsch
Journal:  Epidemiology       Date:  1996-03       Impact factor: 4.822

6.  A comparison of perceptions of quality of life among adults with spinal cord injury in the United States versus the United Kingdom.

Authors:  Alina Palimaru; William E Cunningham; Marcus Dillistone; Arturo Vargas-Bustamante; Honghu Liu; Ron D Hays
Journal:  Qual Life Res       Date:  2017-07-15       Impact factor: 4.147

7.  The fatigue severity scale. Application to patients with multiple sclerosis and systemic lupus erythematosus.

Authors:  L B Krupp; N G LaRocca; J Muir-Nash; A D Steinberg
Journal:  Arch Neurol       Date:  1989-10

8.  Subjective well-being measures for children were developed within the PROMIS project: presentation of first results.

Authors:  Ulrike Ravens-Sieberer; Janine Devine; Katherine Bevans; Anne W Riley; Jeanhee Moon; John M Salsman; Christopher B Forrest
Journal:  J Clin Epidemiol       Date:  2013-12-02       Impact factor: 6.437

9.  Dimensions of Subjective Well-Being.

Authors:  Arie Kapteyn; Jinkook Lee; Caroline Tassot; Hana Vonkova; Gema Zamarro
Journal:  Soc Indic Res       Date:  2014-09-13

10.  Perceptions of individuals living with spinal cord injury toward preference-based quality of life instruments: a qualitative exploration.

Authors:  David G T Whitehurst; Nitya Suryaprakash; Lidia Engel; Nicole Mittmann; Vanessa K Noonan; Marcel F S Dvorak; Stirling Bryan
Journal:  Health Qual Life Outcomes       Date:  2014-04-14       Impact factor: 3.186

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