Beyond Antimuscarinics: A Review of Pharmacological and Interventional Options for Overactive Bladder Management in Men.


Journal

European urology
ISSN: 1873-7560
Titre abrégé: Eur Urol
Pays: Switzerland
ID NLM: 7512719

Informations de publication

Date de publication:
04 2021
Historique:
received: 26 10 2020
accepted: 17 12 2020
pubmed: 7 1 2021
medline: 23 2 2022
entrez: 6 1 2021
Statut: ppublish

Résumé

The role of overactive bladder (OAB) treatment in women beyond antimuscarinics has been evaluated extensively. Beta-3 agonists, botulinum toxin-A (BTX-A), and nerve stimulation are indicated in these patients. However, data on male patients in this clinical scenario are scarce. The aim of this systematic review was to evaluate the evidence on treatment options beyond antimuscarinics in men with OAB. A search of PubMed, EMBASE, Scopus, Web of science, Cochrane Central Register of Controlled Trials, and Cochrane Central Database of Systematic Reviews databases was performed for relevant articles published between January 2000 and October 2020, using the following Medical Subject Headings: "male/man," "LUTS," "overactive bladder," "storage symptoms," "urgency," "nocturia," "incontinence," "beta-3 agonist," "PDE-5 inhibitors," "botulinum toxin," "sacral nerve stimulation/neurostimulation," "percutaneous/transcutaneous tibial nerve stimulation," "PTENS," and "combination therapy." Evidence acquisition was performed according to Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines. PROSPERO registration number is CRD42020201223. Overall, 24 studies were retrieved. In male OAB, mirabegron (MIRA) is the most intensively investigated pharmacological option. A pooled analysis of five randomized clinical trials (RCTs), including 1187 patients, concluded that MIRA 50 mg was associated with a greater reduction in frequency versus placebo (-0.37, 95% confidence interval [CI]: -0.74, -0.01, p <  0.05). A pooled analysis of three RCTs, including 1317 male patients, has also shown that the addition of MIRA 50 mg in men receiving the α MIRA has the most robust data in terms of safety and efficacy in this patient population. Preliminary data in men suggest that BTX-A is indicated as an interventional treatment. Evidence for PDE-5 inhibitors and nerve stimulation is too limited to provide recommendations. Future studies in this population should aim to better define the best treatment sequence and to identify predictors for treatment response and failure, to determine a therapeutic approach tailored to patients' characteristics. Overactive bladder is highly prevalent in men. Mirabegron 50 mg is the treatment option supported by the highest level of evidence when antimuscarinics failed. Botulinum toxin A injections seems to be an effective treatment as interventional option. Roles of nerve stimulation and phosphodiesterase inhibitors in male OAB patients are still to be defined.

Identifiants

pubmed: 33402296
pii: S0302-2838(20)31018-6
doi: 10.1016/j.eururo.2020.12.032
pii:
doi:

Substances chimiques

Acetanilides 0
Muscarinic Antagonists 0
Phosphodiesterase 5 Inhibitors 0
Botulinum Toxins, Type A EC 3.4.24.69
Tamsulosin G3P28OML5I

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

492-504

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2020 European Association of Urology. Published by Elsevier B.V. All rights reserved.

Auteurs

Cosimo De Nunzio (C)

Urology Unit, Ospedale Sant'Andrea, Sapienza University of Rome, Rome, Italy. Electronic address: cosimodenunzio@virgilio.it.

Benjamin Brucker (B)

New York University Langone Health, New York, NY, USA.

Thomas Bschleipfer (T)

Clinic for Urology, Andrology and Pediatric Urology, Clinics of Nordoberpfalz AG, Weiden, Germany.

Jean-Nicolas Cornu (JN)

Urology Department, Charles Nicolle University Hospital, University of Rouen F-76000, Rouen, France.

Marcus J Drake (MJ)

Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK; Bristol Urological Institute, North Bristol NHS Trust, Bristol, UK.

Ferdinando Fusco (F)

Urology Unit, University of Campania L. Vanvitelli, Naples, Italy.

Stavros Gravas (S)

Department of Urology, Faculty of Medicine, School of Health Sciences, University of Thessaly, Larissa, Greece.

Matthias Oelke (M)

Department of Urology, Pediatric Urology & Urological Oncology, St. Antonius Hospital, Gronau, Germany.

Benoit Peyronnet (B)

Department of Urology, University of Rennes, Rennes, France.

Manuela Tutolo (M)

Division of Oncology, Unit of Urology, Urological Research Institute, IRCCS Ospedale San Raffaele, Milan, Italy.

Gommert van Koeveringe (G)

Department of Urology, Maastricht University Medical Center, Maastricht, The Netherlands.

Stephan Madersbacher (S)

Department of Urology, Clinic Favoriten and Sigmund Freud Private University, Vienna, Austria.

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Classifications MeSH