Cookies?
Library Header Image
LSE Research Online LSE Library Services

Multicriteria decision analysis applied to the clinical use of pharmacotherapy for overactive bladder symptom complex

Chapple, Christopher R., Mironska, Emma, Wagg, Adrian, Milsom, Ian, Diaz, David Castro, Koelbl, Heinz, Pushkar, Dmitry, Tubaro, Andrea, De Ridder, Dirk, Chartier-Kastler, Emmanuel and Phillips, Lawrence D. (2020) Multicriteria decision analysis applied to the clinical use of pharmacotherapy for overactive bladder symptom complex. European Urology Focus, 6 (3). pp. 522-530. ISSN 2405-4569

Full text not available from this repository.

Identification Number: 10.1016/j.euf.2019.09.020

Abstract

Context: The nonspecific storage symptom complex overactive bladder (OAB) is an important clinical condition in functional urology. Until recently, pharmacological therapy comprised antimuscarinic drugs, but more recently beta 3 agonists have added to the available agents. Traditional reporting of efficacy and safety of these agents relies upon regulatory placebo-controlled studies. There remains no head-to-head comparison of existing agents in the contemporary literature. Contemporary conclusions on comparative efficacy and safety drawn from the use of these agents are based on systematic reviews of the literature and associated meta-analyses. Objective: In this study, we used the analytical model of multicriteria decision analysis (MCDA) to compare contemporary pharmacotherapy for OAB. Evidence acquisition: Efficacy and safety data from published, randomised, placebo-controlled trials of antimuscarinic antagonists, the beta 3 agonist, and the combination of an antimuscarinic and beta 3 agonist were used to populate the MCDA model. Evidence synthesis: Experts assessed weights of the relative importance of favourable and unfavourable effects, which provided a common measure of benefits and safety that were combined in the MCDA model to give an overall ranking of the OAB drugs. Results: When benefits are judged as more important than safety, fesoterodine 4 or 8 mg used in a flexible dosing pattern provides the most favourable therapeutic option, over a wide sensitivity analysis relating to benefits and harms. Conclusions: In our analysis using an MCDA model, in both the flexible dosing pattern of fesoterodine and the solifenacin combination with mirabegron, the benefit-safety balance is better in terms of benefits and/or safety than any of the other available OAB drugs. Caution in interpretation of the data has to be expressed as the fesoterodine data are based on a flexible dosing regimen, which adds an additional dimension of personalising therapy. Patient summary: Overactive bladder (OAB) is a common condition with a significant impact on the quality of life. Possible symptoms include the following: (1) urgency—a compelling desire to urinate, which is difficult to defer; (2) urgency urinary incontinence—urgency leading to incontinence episodes; (3) frequency—increased frequency of wanting to pass urine; and (4) nocturia—increase in instances of getting up at night to urinate. To date, the mainstay of therapy for OAB has been antimuscarinic drugs and, more recently, the beta 3 agonist mirabegron. Ten international experts in urology, obstetrics, gynaecology, healthy ageing, and data analysis compared the benefit-risk balance of 14 OAB drugs licensed in Europe. The experts considered the importance of a favourable effect on the above four symptoms and also potential for side effects, but only three of these side effects, constipation, dry mouth, and dizziness, showed clinically relevant differences among the six drugs they considered. The observations recorded here suggest interesting differences between drugs across a wide range of possible trade-offs between benefit and safety. The different recruitment criteria used for each study may influence the results seen, so they need to be treated with caution. Comparison of flexibly dosed fesoterodine studies with fixed-dose fesoterodine studies introduces an additional potential bias; definitive conclusions can be drawn only if enough comparable placebo-controlled flexible dosing studies with other drugs were available.

Item Type: Article
Additional Information: © 2019 European Association of Urology.
Divisions: Management
Subjects: R Medicine > RA Public aspects of medicine > RA0421 Public health. Hygiene. Preventive Medicine
Date Deposited: 30 Aug 2022 12:21
Last Modified: 18 Apr 2024 02:00
URI: http://eprints.lse.ac.uk/id/eprint/116405

Actions (login required)

View Item View Item