کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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6239962 | 1279015 | 2013 | 12 صفحه PDF | دانلود رایگان |
ObjectiveTo investigate the desirability and feasibility of a cyclic reimbursement process to address uncertainty accompanying initial decision making.MethodsWe performed desk research for three expensive outpatient drugs: imatinib, pegfilgrastim, and adalimumab. We analysed the evidence base at the time of decision making (TÂ =Â 0) and May 2011 (TÂ =Â 1). For TÂ =Â 0, public reports of the Dutch reimbursement agency were investigated regarding available clinical and economic evidence, and a systematic review was performed to retrieve additional economic evidence. For TÂ =Â 1, the systematic review was extended till May 2011.ResultsThe evidence base at TÂ =Â 0 lacked information on clinically relevant outcomes such as mortality, morbidity, and quality of life (5/8 reports), (long-term) adverse events (2/8 reports) and experience in use (1/8 reports). One budget impact analysis and one economic evaluation were available but no pharmacoeconomic dossiers. The systematic review identified 39 cost-utility studies (of 52 economic evaluations) for TÂ =Â 1, characterised by methodological heterogeneity.ConclusionsGiven the considerable uncertainty accompanying initial decision-making, a more cyclic reimbursement process seems feasible to reduce uncertainty regarding the therapeutical and economical value of expensive drugs. A mandatory evidence development requirement seems desirable to sufficiently meet decision makers' needs.
Journal: Health Policy - Volume 112, Issue 3, October 2013, Pages 285-296