U.S. flag

An official website of the United States government

NCBI Bookshelf. A service of the National Library of Medicine, National Institutes of Health.

Cover of The Use of the Electromotive Drug Administration System in Patients with Overactive Bladder: A Review of the Clinical Effectiveness, Safety, and Cost-Effectiveness

The Use of the Electromotive Drug Administration System in Patients with Overactive Bladder: A Review of the Clinical Effectiveness, Safety, and Cost-Effectiveness

Rapid Response Report: Summary with Critical Appraisal

Overactive bladder (OAB) is a urological condition characterized by frequent urination, the need to urinate leading to disruption of sleep (nocturia), and urinating unintentionally with or without urge incontinence. OAB is often associated with overactivity of the bladder detrusor muscle, which represents the most common underlying idiopathic or neurogenic dysfunction. It has been estimated that about one in six adults (17%) have OAB, and the prevalence of OAB increases with age. Approximately 10% of children have symptoms that are severe enough to warrant a diagnosis of OAB. Treatment for OAB includes behavioral modifications, pelvic floor rehabilitation, pharmacological agents (e.g., oral medication, intravesical instillation), electrical stimulation, or reconstructive surgery. Intravesical instillation is a local drug delivery system though a catheter into the bladder that is widely used to treat bladder cancer and other conditions. However, some substances are not readily absorbed through the low permeability of the intact urothelium leading to limited effectiveness of the treatment.

Electromotive drug administration (EMDA) represents a minimally-invasive method of intravesical instillation of therapeutic agents without the need of general anesthesia. It employs a combination of iontophoresis, electrophoresis, and electroporation to deliver drugs into deep tissue layers using an electrical current created between two electrodes. The EMDA system consists of a current generator, catheter-electrodes, and accessories. The Physionizer 30 Mini is a pulse DC generator widely used for EMDA. Lidocaine and epinephrine are used for local anesthesia during the EMDA procedure. EMDA has been used to deliver drugs for a number of conditions including inflammation of the bladder (cystitis), inflammation of the prostate (prostatitis), bladder cancer, and OAB. Drug administration by EMDA in laboratory studies in the treatment of bladder pathologies and dysfunctions include botulinum toxin A, oxybutynin, mitomycin C, resiniferatoxin, verapamil, and dexamethasone. Botulinum toxin A, an acetylcholine release blocking agent, has been thought to reduce the detrusor overactivity through ephemeral detrusor smooth muscle paralysis. Delivery of verapamil and dexamethasone through EMDA has been used for treatment of Peyronie’s disease, an erectile dysfunction.

The aim of this report is to review the clinical effectiveness, safety and cost-effectiveness of EMDA for treatment of OAB.

Disclaimer: The Rapid Response Service is an information service for those involved in planning and providing health care in Canada. Rapid responses are based on a limited literature search and are not comprehensive, systematic reviews. The intent is to provide a list of sources and a summary of the best evidence on the topic that CADTH could identify using all reasonable efforts within the time allowed. Rapid responses should be considered along with other types of information and health care considerations. The information included in this response is not intended to replace professional medical advice, nor should it be construed as a recommendation for or against the use of a particular health technology. Readers are also cautioned that a lack of good quality evidence does not necessarily mean a lack of effectiveness particularly in the case of new and emerging health technologies, for which little information can be found, but which may in future prove to be effective. While CADTH has taken care in the preparation of the report to ensure that its contents are accurate, complete and up to date, CADTH does not make any guarantee to that effect. CADTH is not liable for any loss or damages resulting from use of the information in the report.

Copyright © 2014 Canadian Agency for Drugs and Technologies in Health.

Copyright: This report contains CADTH copyright material. It may be copied and used for non-commercial purposes, provided that attribution is given to CADTH.

Links: This report may contain links to other information available on the websites of third parties on the Internet. CADTH does not have control over the content of such sites. Use of third party sites is governed by the owners’ own terms and conditions.

Except where otherwise noted, this work is distributed under the terms of a Creative Commons Attribution-NonCommercial- NoDerivatives 4.0 International licence (CC BY-NC-ND), a copy of which is available at http://creativecommons.org/licenses/by-nc-nd/4.0/

Bookshelf ID: NBK253337PMID: 25392902

Views

  • PubReader
  • Print View
  • Cite this Page
  • PDF version of this title (402K)

Other titles in this collection

Related information

Similar articles in PubMed

See reviews...See all...

Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...