Background: Multiple sclerosis (MS) is a common neurologic disease in
young and middle-aged adults affecting approximately 35,000 Canadians,
The objectives of this study were to estimate the annual and lifetime
costs of MS from the Canadian societal perspective. Methods: Patients
were consecutively recruited by neurologists in 14 MS outpatient clin
ics across Canada. They were classified according to the Expanded Disa
bility Status Scale (EDSS) into three groups: mild (EDSS less than or
equal to 2.5), moderate (EDSS = 3.0-6.0) and severe (EDSS greater than
or equal to 6.5), Sociodemographic, clinical and resource utilization
data were collected retrospectively for the three months prior to pat
ient inclusion, Costing of resources was performed from Ministry of He
alth, private third party payers, patient and societal perspectives, A
verage Canadian costs ($CDN 1995) were valued from available provincia
l data, Results: A total of 198 patients were included in the analysis
(mild: n = 62, moderate: n = 68 and severe: n = 68), Costs increased
with increasing EDSS scores, from all perspectives, The annualized soc
ietal costs per patient were $CDN14,523, $CDN21,698 and $CDN37,024 for
the mild, moderate and severe groups, respectively, In all severity g
roups, most of the financial burden is borne by patients, from 74% to
88%, Indirect costs, namely lost daily activity/leisure time and lost
productivity, were the major societal cost drivers. The lifetime cost
of MS, including patient institutionalization, was estimated to be $CD
N1,608,000 per patient. Conclusions: In Canada, MS is associated with
enormous direct and indirect costs, Patients carry most of the economi
c burden of this disease. The results of this burden of illness study
provide a basis for cost-effectiveness analyses of new therapeutic int
erventions for MS.