Improvement of coping abilities in patients with systemic lupus erythematosus: a prospective study. Issue 11 (13th April 2005)

• Record Type: Journal Article
• Authors: Haupt, M; Millen, S; Jänner, M; Falagan, D; Fischer-Betz, R; Schneider, M
• Is Part Of: Annals of the rheumatic diseases. Volume 64:Issue 11(2005)
• Page Start: 1618
• Page End: 1623
• Publication Date: 2005-04-13
• Subjects: ACR, American College of Rheumatology -- ECLAM, European consensus lupus activity measurement -- FAL, everyday life questionnaire -- FKV, Freiburg questionnaire on coping with illness -- HADS-D, hospital anxiety and depression scale–German version -- KKG, questionnaire for registration of control convictions relating to illness and health -- SCL-90-R, symptom checklist 90, revised version -- SESA, self acceptance registration scale -- SF-36, short form 36 item general health questionnaire -- SLE, systemic lupus erythematosus -- SLICC, system lupus international collaborating clinics; coping -- quality of life -- systemic lupus erythematosus; Rheumatism -- Periodicals; 616.723005
• DOI: 10.1136/ard.2004.029926
• Languages: English
• ISSNs: 0003-4967

Abstract

Abstract : Objective: To evaluate a novel specific psychological intervention aimed at improving coping in patients with systemic lupus erythematosus (SLE). Methods: 34 community living SLE patients were recruited for the study. Intervention was undertaken in groups of up to eight patients and in two blocks over six months each. Eight patients were enrolled as a waiting list group. The 18 group sessions focused on information about the disease and specific problems of SLE patients, combining psychoeducative and psychotherapeutic elements. Psychological and medical evaluations were conducted at baseline and after three, six, and 12 months, using validated instruments. Results: The 34 SLE patients (91% female, mean age 42 years) improved significantly over a six month period on most of the psychological measuring instruments applied, such as depression, anxiety, and overall mental burden. The waiting list group showed no significant changes. Conclusions: Conceptualised psychoeducational support may produce a significant and sustained improvement in coping skills of SLE patients and hence in their quality of life.