Literature DB >> 19844839

Validation of the SF-36 in Jamaicans with sickle-cell disease.

Monika R Asnani1, Garth E Lipps, Marvin E Reid.   

Abstract

Quality-of-life (QOL) measurements are becoming a vital part of health outcome appraisal. Sickle-cell disease (SCD) places a substantial burden on those afflicted. No QOL measure has been validated for use in Jamaica. The SF-36 version 2 was administered to two samples of patients with SCD: the 'Cohort' (n = 233), and the 'Main' samples (n = 256). All patients were also administered the World Health Organization Quality of Life-Bref (WHOQOL-Bref), Flanagan's Quality-of-Life Scale (QOLS), and the UCLA Loneliness Scale. All measures were found to be reliable with coefficient alphas' ranging from 0.70 to 0.93. The total SF-36 score showed a strong positive correlation with the total WHOQOL-Bref (0.78) and a moderate one with the total QOLS score (0.57). The correlations of the total scores from the SF-36 scale with those from the Loneliness Scale were negative but moderate in size (-0.59). This study provides fair evidence for the concurrent, and some evidence for the discriminant, validity of the SF-36 in Jamaicans with SCD.

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Year:  2009        PMID: 19844839     DOI: 10.1080/13548500903016567

Source DB:  PubMed          Journal:  Psychol Health Med        ISSN: 1354-8506            Impact factor:   2.423


  7 in total

1.  Depression, quality of life, and medical resource utilization in sickle cell disease.

Authors:  Soheir S Adam; Charlene M Flahiff; Shital Kamble; Marilyn J Telen; Shelby D Reed; Laura M De Castro
Journal:  Blood Adv       Date:  2017-10-12

Review 2.  What is the future of patient-reported outcomes in sickle-cell disease?

Authors:  Sharon A Singh; Nitya Bakshi; Prashant Mahajan; Claudia R Morris
Journal:  Expert Rev Hematol       Date:  2020-10-15       Impact factor: 2.929

3.  Utility of WHOQOL-BREF in measuring quality of life in sickle cell disease.

Authors:  Monika R Asnani; Garth E Lipps; Marvin E Reid
Journal:  Health Qual Life Outcomes       Date:  2009-08-10       Impact factor: 3.186

4.  Adult sickle cell quality-of-life measurement information system (ASCQ-Me): conceptual model based on review of the literature and formative research.

Authors:  Marsha J Treadwell; Kathryn Hassell; Roger Levine; San Keller
Journal:  Clin J Pain       Date:  2014-10       Impact factor: 3.442

5.  Preference-based measure of health-related quality of life and its determinants in sickle cell disease in Nigeria.

Authors:  Adedokun Oluwafemi Ojelabi; Afolabi Elijah Bamgboye; Jonathan Ling
Journal:  PLoS One       Date:  2019-11-18       Impact factor: 3.240

6.  External validation of the priapism impact profile in a Jamaican cohort of patients with sickle cell disease.

Authors:  Belinda F Morrison; Wendy Madden; Monika Asnani; Ayodeji Sotimehin; Uzoma Anele; Yuezhou Jing; Bruce J Trock; Arthur L Burnett
Journal:  PLoS One       Date:  2021-10-15       Impact factor: 3.240

7.  Health-related quality of life in hemoglobinopathies: A systematic review from a global perspective.

Authors:  Francesca Rodigari; Giorgia Brugnera; Raffaella Colombatti
Journal:  Front Pediatr       Date:  2022-08-25       Impact factor: 3.569

  7 in total

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