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Original article

Economic evaluation of pharmacological treatments for overactive bladder from the perspective of the UK National Health Service

, , , , &
Pages 390-397 | Accepted 02 Dec 2014, Published online: 19 Dec 2014
 

Abstract

Objective:

To evaluate the costs and outcomes associated with different sequences of oral anti-muscarinic agents and the selective β3-adrenoceptor agonist, mirabegron, for the treatment of overactive bladder (OAB).

Methods:

A Markov model with monthly cycle length and time horizon up to 3 years was designed to compare two different sequences of up to three lines of oral therapy for OAB. Patients who discontinued one oral medication could switch to another oral medication or could discontinue treatment. Patients whose symptoms were not controlled were considered for botulinum toxin or sacral nerve stimulation. Outcomes were measured by (a) number of patients with controlled symptoms (no incontinence episodes and <8 micturitions per 24 h); (b) patients with no incontinence episodes per 24 hours; and (c) patients with <8 micturitions per 24 h.

Results:

Including a third-line oral medication before considering other treatment options improved all patient outcomes, irrespective of the specific drugs used. A three-line sequence including two generic (oxybutynin first line and tolterodine extended-release second line) and one branded drug (solifenacin 5 mg third line) resulted in inferior patient outcomes at costs similar to a sequence of branded drugs (mirabegron first line, solifenacin 5 mg second line, solifenacin 10 mg third line): controlled patients (generic 29.6/1000 vs branded 38.7/1000); patients with no incontinence episodes (103.6/1000 vs 123.7/1000); patients with <8 micturitions (228.7/1000 vs 262.1/1000). Annual treatment costs per patient were similar (generic £1299 vs branded £1385).

Conclusions:

In the treatment of OAB, low-cost generic treatments are not necessarily more cost-effective than branded drugs, primarily because a better efficacy and tolerability balance improves both symptom control and persistence.

Transparency

Declaration of funding

The model described was developed by HERON Commercialisation, PAREXEL, with funding from Astellas Pharma Europe, Ltd. Employees of Astellas Pharma Europe, Ltd, helped to author the manuscript. All authors contributed to the study design and methodology, interpretation of the results, development and writing of the draft manuscript, and approved the final version.

Declaration of financial/other relationships

JN, IO, and AG are employed by Astellas Pharma Europe, Ltd. ZH is employed by Astellas Pharma Global Development. JP and AW are employed by HERON Commercialisation, PAREXEL, and were contracted by Astellas Pharma Europe, Ltd, to prepare the model used in this research.

Acknowledgments

Medical writing support was provided by Andy Noble of Bioscript Medical, and was funded by Astellas Pharma Europe, Ltd. This study was presented in part at the International Society for Pharmacoeconomics and Outcomes Research (ISPOR) 16th Annual European Congress, Dublin, Ireland, November 2–6, 2013.

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