TY - JOUR
T1 - Sensitivity to change of generic quality of life instruments in patients with rheumatoid arthritis
T2 - Preliminary findings in the generic health OMERACT study
AU - Wells, George
AU - Boers, Maarten
AU - Shea, Beverley
AU - Tugwell, Peter
AU - Westhovens, Rene
AU - Saurez-Almazor, Maria
AU - Buchbinder, Rachelle
PY - 1999/2/2
Y1 - 1999/2/2
N2 - This is the initial report of the genetic health OMERACT study concerned with the sensitivity to change of genetic quality of life (QOL) measures. Our objective was to determine which QOL instrument is best able to show a statistically significant improvement in patients with rheumatoid arthritis (RA) demonstrating relevant improvement in a core set of disease activity and disease-specific disability measures. A multicenter controlled trial of a single group with repeated measurements at 0 (baseline), 3, and 6 months was conducted. All participating centers recruited 10 patients with RA who were about to start methotrexate therapy for the first time because of active disease. Assessments included disease activity measures, disease-specific disability measures, and generic QOL measures. To date, 40 patients have been recruited from 4 centers for the study. After 6 months of treatment many of the generic QOL measures showed a 20% improvement from baseline and medium standardized response means around 0.5. In particular, the Nottingham Health Profile (NHP) and the Rheumatoid Arthritis Quality of Life (RAQOL) measures had the largest percentage improvement (22 and 29%, respectively) and standardized response means (both with 0.54). Early results on the sensitivity of genetic health QOL measures are promising, in particular for the NHP and RAQOL measures.
AB - This is the initial report of the genetic health OMERACT study concerned with the sensitivity to change of genetic quality of life (QOL) measures. Our objective was to determine which QOL instrument is best able to show a statistically significant improvement in patients with rheumatoid arthritis (RA) demonstrating relevant improvement in a core set of disease activity and disease-specific disability measures. A multicenter controlled trial of a single group with repeated measurements at 0 (baseline), 3, and 6 months was conducted. All participating centers recruited 10 patients with RA who were about to start methotrexate therapy for the first time because of active disease. Assessments included disease activity measures, disease-specific disability measures, and generic QOL measures. To date, 40 patients have been recruited from 4 centers for the study. After 6 months of treatment many of the generic QOL measures showed a 20% improvement from baseline and medium standardized response means around 0.5. In particular, the Nottingham Health Profile (NHP) and the Rheumatoid Arthritis Quality of Life (RAQOL) measures had the largest percentage improvement (22 and 29%, respectively) and standardized response means (both with 0.54). Early results on the sensitivity of genetic health QOL measures are promising, in particular for the NHP and RAQOL measures.
KW - Outcome measures
KW - Quality of life
KW - Rheumatoid arthritis
KW - Sensitivity
UR - http://www.scopus.com/inward/record.url?scp=0032918353&partnerID=8YFLogxK
M3 - Article
C2 - 9918267
AN - SCOPUS:0032918353
SN - 0315-162X
VL - 26
SP - 217
EP - 221
JO - The Journal of Rheumatology
JF - The Journal of Rheumatology
IS - 1
ER -