Literature DB >> 17907225

Concepts important to persons with systemic lupus erythematosus and their coverage by standard measures of disease activity and health status.

Tanja A Stamm1, Bettina Bauernfeind, Michaela Coenen, Eva Feierl, Mona Mathis, Gerold Stucki, Josef S Smolen, Klaus P Machold, Martin Aringer.   

Abstract

OBJECTIVE: To explore the array of concepts important to patients with chronic systemic lupus erythematosus (SLE) and to compare these with instruments assessing disease activity, damage, and health status.
METHODS: We conducted a qualitative focus-group study of patients with SLE concerning their problems in daily functioning. The group sessions were tape recorded, transcribed, and divided into meaning units. The concepts contained in these meaning units were extracted and linked to the International Classification of Functioning, Disability and Health (ICF). We then compared the concepts from the focus groups with those concepts covered by SLE activity scores, the Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index (SDI), and the Short Form 36 Health Survey (SF-36).
RESULTS: A total of 92 concepts emerged from 5 focus groups; of these, 28 related to body functions and structures, 24 to activities and participation, and 25 to environmental factors. Two concepts were linked to the health condition itself and 6 to personal factors. Seven were not covered by the ICF. Of the 28 concepts regarding body functions and structures, 24 (86%) were covered by the combination of activity scores and the SDI. The SF-36 also addressed 3 of these concepts and contained 9 (38%) of 24 concepts in activities and participation.
CONCLUSION: Although the combination of SLE activity scores, SDI, and SF-36, as suggested for SLE studies, well covers body functions and structures and includes a significant portion of problems regarding activities and participation, neither environmental nor personal factors are covered at all.

Entities:  

Mesh:

Year:  2007        PMID: 17907225     DOI: 10.1002/art.23013

Source DB:  PubMed          Journal:  Arthritis Rheum        ISSN: 0004-3591


  15 in total

Review 1.  Top 10 recent developments in health-related quality of life in patients with systemic lupus erythematosus.

Authors:  Anisha B Dua; Zahi Touma; Sergio Toloza; Meenakshi Jolly
Journal:  Curr Rheumatol Rep       Date:  2013-12       Impact factor: 4.592

2.  Psychometric Evaluation of the National Institutes of Health Patient-Reported Outcomes Measurement Information System in a Multiracial, Multiethnic Systemic Lupus Erythematosus Cohort.

Authors:  Patricia Katz; Jinoos Yazdany; Laura Trupin; Stephanie Rush; Charles G Helmick; Louise B Murphy; Cristina Lanata; Lindsey A Criswell; Maria Dall'Era
Journal:  Arthritis Care Res (Hoboken)       Date:  2019-11-05       Impact factor: 4.794

3.  The cutaneous lupus disease activity and severity index as a validated outcome measure for cutaneous lupus erythematosus: comment on the article by Stamm et al.

Authors:  Michael Krathen; Joerg Albrecht; Victoria P Werth
Journal:  Arthritis Rheum       Date:  2008-04-15

4.  Understanding systemic lupus erythematosus patients' desired outcomes and their perceptions of the risks and benefits of using corticosteroids.

Authors:  X Ng; S dosReis; R Beardsley; L Magder; C D Mullins; M Petri
Journal:  Lupus       Date:  2017-08-31       Impact factor: 2.911

Review 5.  Patient-Reported Outcomes in Systemic Lupus Erythematosus.

Authors:  Mary Mahieu; Susan Yount; Rosalind Ramsey-Goldman
Journal:  Rheum Dis Clin North Am       Date:  2016-03-17       Impact factor: 2.670

6.  Concepts of functioning and health important to people with systemic sclerosis: a qualitative study in four European countries.

Authors:  Tanja A Stamm; Malin Mattsson; Carina Mihai; Juliane Stöcker; Alexa Binder; Bettina Bauernfeind; Georg Stummvoll; Gunvor Gard; Roger Hesselstrand; Gunnel Sandqvist; Oana Draghicescu; Ana Maria Gherghe; Malina Voicu; Klaus P Machold; Oliver Distler; Josef S Smolen; Carina Boström
Journal:  Ann Rheum Dis       Date:  2011-06       Impact factor: 19.103

7.  Do patient-reported outcome measures cover personal factors important to people with rheumatoid arthritis? A mixed methods design using the International Classification of Functioning, Disability and Health as frame of reference.

Authors:  Mona Dür; Michaela Coenen; Michaela Alexandra Stoffer; Veronika Fialka-Moser; Alexandra Kautzky-Willer; Ingvild Kjeken; Răzvan Gabriel Drăgoi; Malin Mattsson; Carina Boström; Josef Smolen; Tanja Alexandra Stamm
Journal:  Health Qual Life Outcomes       Date:  2015-02-25       Impact factor: 3.186

8.  The patients' perspective: living with lupus in Austria.

Authors:  Georg Stummvoll; Tanja Stamm
Journal:  Wien Klin Wochenschr       Date:  2017-02-22       Impact factor: 1.704

9.  Major Depression and Adverse Patient-Reported Outcomes in Systemic Lupus Erythematosus: Results From a Prospective Longitudinal Cohort.

Authors:  Brett Dietz; Patricia Katz; Maria Dall'Era; Louise B Murphy; Cristina Lanata; Laura Trupin; Lindsey A Criswell; Jinoos Yazdany
Journal:  Arthritis Care Res (Hoboken)       Date:  2020-12-06       Impact factor: 5.178

Review 10.  Health determining concepts important to people with Crohn's disease and their coverage by patient-reported outcomes of health and wellbeing.

Authors:  Mona Dür; Martina Sadloňová; Stefanie Haider; Alexa Binder; Michaela Stoffer; Michaela Coenen; Josef Smolen; Clemens Dejaco; Alexandra Kautzky-Willer; Veronika Fialka-Moser; Gabriele Moser; Tanja Alexandra Stamm
Journal:  J Crohns Colitis       Date:  2013-01-31       Impact factor: 9.071

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.