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Peroneal Electric Transcutaneous NeuroModulation (eTNM®): A Novel Method for the Treatment of the Overactive Bladder
J. Krhut, L. Peter, M. Rejchrt, M. Slovak, B. Skugarevska, P. Zvara
Language English Country Great Britain
Document type Journal Article
NLK
PubMed Central
from 2016
Europe PubMed Central
from 2016
Open Access Digital Library
from 2010-01-01
Open Access Digital Library
from 2010-01-01
Open Access Digital Library
from 2016-01-01
Medline Complete (EBSCOhost)
from 2015-12-01 to 2023-06-29
Wiley-Blackwell Open Access Titles
from 2010
ROAD: Directory of Open Access Scholarly Resources
from 2010
PubMed
34659685
DOI
10.1155/2021/4016346
Knihovny.cz E-resources
- MeSH
- Electrodes MeSH
- Electric Stimulation Therapy * MeSH
- Urinary Bladder, Overactive * therapy MeSH
- Quality of Life MeSH
- Humans MeSH
- Telemedicine * MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- United States MeSH
Overactive bladder syndrome (OAB) is a prevalent medical problem with a significant impact on the quality of life of the affected individuals. Pharmacotherapy is considered the main treatment method, although it is discontinued in a significant proportion of patients due to inefficacy or associated side effects. If pharmacotherapy fails, patients can undergo peripheral neuromodulation of the somatic nerves of the lower limb or sacral neuromodulation; however, neither of these represents an ideal therapeutic tool. The Peroneal electric Transcutaneous NeuroModulation (Peroneal eTNM®), based on the selective stimulation of the peroneal nerve, is the new fully noninvasive neuromodulation method intended to treat OAB. The URIS® neuromodulation system, engineered to provide Peroneal eTNM®, consists of the URIS® device, URIS® active electrodes, and the biofeedback foot sensor (BFS). The unique design of the URIS® device and URIS® active electrodes allows for the use of a low voltage and current during neuromodulation, which significantly reduces the unpleasant sensations. The BFS allows for precise localization of the active electrodes and for continuous adjustment of the voltage and frequency to achieve the optimal therapeutic effect. The URIS® system adopts several principles of telemedicine, which makes it compatible with the US Food and Drug Administration (FDA) and European Union (EU) regulations for home-based use. This article describes both the Peroneal eTNM® method and the URIS® neuromodulation system, including its technical specifications and data from laboratory testing. Preclinical and early clinical data demonstrate the feasibility of this new method for noninvasive OAB treatment and possible implications for clinical practice.
Department of Surgical Studies Medical Faculty Ostrava University Ostrava Czech Republic
Department of Urology Odense University Hospital Odense Denmark
Department of Urology University Hospital Ostrava Czech Republic
References provided by Crossref.org
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