176
Views
35
CrossRef citations to date
0
Altmetric
Original Article

Economic analysis of micafungin versus liposomal amphotericin B for treatment of candidaemia and invasive candidiasis in Germany

, , , , &
Pages 1743-1753 | Accepted 17 Apr 2008, Published online: 08 May 2008
 

ABSTRACT

Objective: To investigate the economic impact of micafungin (MICA) for treatment of invasive candidiasis and candidaemia (systemic Candida infections), a health economic analysis was conducted comparing MICA with liposomal amphotericin B (L-AMB).

Research design and methods: The model was based on a phase III, randomised, double-blind, clinical trial which compared MICA with L-AMB. The model entailed a period of 14–20 weeks starting from initiation of treatment and was analysed from a German hospital perspective.

Main outcome measures: The main outcome measures were defined as the percentage of patients achieving clinical and mycological response after initial treatment and who were alive at the end of the study (EOS), and the total treatment-associated costs over the study period.

Results: The health economic analysis shows that with MICA, 52.9 % of patients are successfully treated and were alive at EOS compared to 49.1 % for L-AMB. In addition, MICA has, on average, lower treatment-associated costs than L-AMB with [euro]43 243 and [euro]49 216 per patient, respectively. Because the costs are lower and the effectiveness is higher for MICA in comparison with L-AMB, MICA is more cost-effective than L-AMB. However, the results of the probabilistic sensitivity analysis show that the differences cannot be considered significant due to a large variance, although MICA remained the most cost-effective option throughout the one-way sensitivity analyses.

Conclusions: The lower costs and higher effectiveness reported for MICA versus L-AMB in this analysis indicate that MICA may be a more cost-effective therapy in the treatment of invasive candidiasis and candidaemia when compared with L-AMB.

Acknowledgments

Declaration of interest: The research described in this article, and the drafting of the manuscript, were funded by Astellas Pharma Europe Ltd. O.A.C. is supported by the German Federal Ministry of Research and Education (BMBF grant 01KN0706).

Notes

* AmBisome is a registered trade name of Gilead Sciences, Inc, Foster City, USA

† Cancidas is a registered trade name of Merck & Co., Inc., Whitehouse Station, USA

‡ Ecalta is a registered trade name of Pfizer Ltd., Sandwich, UK

§ Mycamine is a registered trade name of Astellas Pharma US, Inc., Deerfield, USA

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.