Abstract
Objective:
In Finland, regional rates of schizophrenia exceed those in most countries, impacting the healthcare burden. This study determined the cost-effectiveness of long-acting antipsychotic (LAI) drugs paliperidone palmitate (PP-LAI), olanzapine pamoate (OLZ-LAI), and risperidone (RIS-LAI) for chronic schizophrenia.
Method:
This study adapted a decision tree analysis from Norway for the Finnish National Health Service. Country-specific data were sought from the literature and public documents, guided by clinical experts. Costs of health services and products were retrieved from literature sources and current price lists. This simulation study estimated average 1-year costs for treating patients with each LAI, average remission days, rates of hospitalization and emergency room visits and quality-adjusted life-years (QALY).
Results:
PP-LAI was dominant. Its estimated annual average cost was €10,380/patient and was associated with 0.817 QALY; OLZ-LAI cost €12,145 with 0.810 QALY; RIS-LAI cost €12,074 with 0.809 QALY. PP-LAI had the lowest rates of hospitalization, emergency room visits, and relapse days. This analysis was robust against most variations in input values except adherence rates. PP-LAI was dominant over OLZ-LAI and RIS-LAI in 77.8% and 85.9% of simulations, respectively. Limitations include the 1-year time horizon (as opposed to lifetime costs), omission of the costs of adverse events, and the assumption of universal accessibility.
Conclusion:
In Finland, PP-LAI dominated the other LAIs as it was associated with a lower cost and better clinical outcomes.
Acknowledgements
Declaration of funding
This article was supported by Janssen Pharmaceutica NV, Beerse, Belgium.
Declaration of financial/other relationships
RJ is an employee of Janssen. TE, HP, RZ, and CV have received consultant/advisory board fees from Janssen. TE has received funding from the sponsor for this research. He has also received travel funding to present a portion of these results at the Latin American ISPOR conference in Mexico City, 2011. In the past, he has received funding for unrelated work from Novo Nordisk, Lundbeck, BMS, Generex, and Janssen-Ortho. This was not a clinical trial; it was a pharmacoeconomic analysis. Therefore, the protocol is presented in the Methods section of this paper.
Acknowledgements
The authors would like to thank the following persons for medical advice and clinical input into this project. MD, PhD Jari Tiihonen, Hospital of Niuvaniem; MD, Antti Liuska, Hospital district of Pohjois-Karjala; MD, Ilkka Larmo, HUS; MD, Sirpa Lindroos, Health care district of Forssa.