A CANADIAN STUDY OF THE TOTAL MEDICAL COSTS FOR PATIENTS WITH SYSTEMIC LUPUS-ERYTHEMATOSUS AND THE PREDICTORS OF COSTS

Citation
Ae. Clarke et al., A CANADIAN STUDY OF THE TOTAL MEDICAL COSTS FOR PATIENTS WITH SYSTEMIC LUPUS-ERYTHEMATOSUS AND THE PREDICTORS OF COSTS, Arthritis and rheumatism, 36(11), 1993, pp. 1548-1559
Citations number
48
Categorie Soggetti
Rheumatology
Journal title
ISSN journal
00043591
Volume
36
Issue
11
Year of publication
1993
Pages
1548 - 1559
Database
ISI
SICI code
0004-3591(1993)36:11<1548:ACSOTT>2.0.ZU;2-O
Abstract
Objective. We conducted a cost identification analysis on 164 consecut ive patients with systemic lupus erythematosus (SLE) who entered the M ontreal General Hospital Lupus Registry between January 1977 and Janua ry 1990, compared their costs to the population of Quebec, and determi ned the predictors of cost. Methods. In January 1990 and 1991, partici pants completed questionnaires on health services utilization and on e mployment history over the preceding 6 months, as well as on functiona l, psychological, and social well-being. The societal burden of SLE wa s determined in terms of direct costs (all resources consumed in patie nt care) and indirect costs (wages lost due to lack of work force part icipation because of morbidity). Results. The mean total annual cost f or 1989, as assessed in January 1990 and expressed in 1990 Canadian do llars, was $13,094. Although only 44% of the patients were fully emplo yed, indirect costs were responsible for 54% of this total ($7,071). A mbulatory costs, primarily diagnostic procedures, medications, and vis its to health care professionals, comprised 55% of direct costs ($3,33 1). The results of the 1990 cost determination were similar. On averag e, hospitalizations among SLE patients were 4 times more frequent than among the general population of Quebec (matched for age and sex), and the number of ambulatory visits to physicians was double that for the average resident of Quebec. Higher 1989 values of creatinine and a po orer level of physical functioning were the best predictors of higher 1990 direct costs (R2 = 0.29). A poorer SLE well-being score, a combin ation of education and employment status, and a weaker level of social support were the best predictors of higher indirect costs (R2 = 0.29) . Conclusion. The direct and indirect costs for patients with SLE are substantial, and their respective predictors are distinct. Direct cost s arise from organic complications which induce functional disability. Predictors of indirect costs are potentially amenable to psychologica l or social interventions and may be more easily modified than the det erminants of direct costs, thereby improving patient outcome while sim ultaneously reducing disease costs.