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Cost of illness in patients with Gilles de la Tourette’s syndrome

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Abstract

We evaluated the health economic burden of patients with Gilles de la Tourette’s syndrome (GTS) in Germany over a 3-month observation period. Direct and indirect costs were evaluated in 200 outpatients with GTS (mean age 35 ± 11.5 years) in Germany. Patients were recruited from three outpatient departments that specialized in GTS and completed a semi-structured and self-rating interview with questionnaires screening for direct and indirect medical and non-medical costs, health status, depression, amount and severity of symptoms. Costs were obtained from various German medical economic resources. Indirect costs for lost productivity were calculated using the human capital approach. Costs were calculated from the point of view of healthcare and transfer payment providers and the individual patient. Multivariate regression analyses were performed to identify independent cost predictors. Costs are in year 2006–2007 values. Direct costs were 620 ± 1,697.1€, including rehabilitation 98.8 ± 993.6€, hospitalization 195.8 ± 1,267.8€, outpatient treatment 14.0 ± 40.6€, ancillary treatment 51.9 ± 137.4€. Drug costs were 223.1 ± 430.4. The indirect medical costs amounted to 2,511.3 ± 3,809.5€ for productivity loss and to 220.0 ± 1,092€ for absenteeism. The following variables were found to impact on direct costs: employment status, occupational advancement, depression, quality of life, age. Disease severity had no influence on cost. Because of the earlier age of disease onset, indirect costs are higher than direct costs. Interestingly, disease severity did not influence the resource need in this population. Unfortunately, no cost of illness studies are available for comparison. Further health economic studies, especially cost-effectiveness studies, are necessary for a basis for rational resource allocation.

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Correspondence to Richard Dodel.

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I. Dodel and J. P. Reese contributed equally.

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Dodel, I., Reese, J.P., Müller, N. et al. Cost of illness in patients with Gilles de la Tourette’s syndrome. J Neurol 257, 1055–1061 (2010). https://doi.org/10.1007/s00415-010-5458-y

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  • DOI: https://doi.org/10.1007/s00415-010-5458-y

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