Literature DB >> 18179663

Introducing evidence-based medicine in reimbursement procedures: does it affect the outcome?

Philippe Van Wilder1, Alain Dupont.   

Abstract

OBJECTIVES: The 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.
METHODS: We analyzed 824 reimbursement submissions within the period 2002 to 2004.
RESULTS: Only 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.
CONCLUSIONS: Both factors suggest that evidence plays a role in the decision-making process.

Mesh:

Substances:

Year:  2007        PMID: 18179663     DOI: 10.1111/j.1524-4733.2007.00299.x

Source DB:  PubMed          Journal:  Value Health        ISSN: 1098-3015            Impact factor:   5.725


  4 in total

1.  Relative efficacy and effectiveness assessment of new pharmaceuticals in three EU member states: current practices and outcome agreement between Belgium, the Netherlands and France.

Authors:  P B Van Wilder; V V Bormans; A G Dupont
Journal:  Eur J Clin Pharmacol       Date:  2013-09-01       Impact factor: 2.953

2.  Access to orphan drugs despite poor quality of clinical evidence.

Authors:  Alain G Dupont; Philippe B Van Wilder
Journal:  Br J Clin Pharmacol       Date:  2011-04       Impact factor: 4.335

3.  How to assess the value of medicines?

Authors:  Steven Simoens
Journal:  Front Pharmacol       Date:  2010-09-07       Impact factor: 5.810

4.  Valorising and creating access to innovative medicines in the European union.

Authors:  Lieven Annemans; Irina Cleemput; Frank Hulstaert; Steven Simoens
Journal:  Front Pharmacol       Date:  2011-10-11       Impact factor: 5.810

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.