کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
988906 | 935374 | 2008 | 4 صفحه PDF | دانلود رایگان |

ObjectivesThe European Transparency Directive requires that reimbursement decisions of member states are taken in a transparent, objective, and verifiable way within strict timelines. We investigated whether evidence of therapeutic value was a factor affecting the Belgian pharmaceutical reimbursement decision without compromising the respect of strict timelines.MethodsWe analyzed 824 reimbursement submissions within the period 2002 to 2004.ResultsOnly 67 submissions claimed added therapeutic value versus available alternatives: if the applicant failed to prove added value the odds ratio (OR) for a negative decision increased significantly: OR = 9.1 (2.3–35.6). There were 399 “limited evidence” submissions (new medicinal products or new indications) and 425 “extended evidence” submissions (mainly line extensions). The OR for a negative decision decreased significantly for submissions with extended evidence: OR = 0.18 (0.12–0.27). The median time to decision was 175 days.ConclusionsBoth factors suggest that evidence plays a role in the decision-making process.
Journal: Value in Health - Volume 11, Issue 4, July–August 2008, Pages 784-787