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A novel leadless, miniature implantable Tibial Nerve Neuromodulation System for the management of overactive bladder complaints.
Heesakkers, John P F A; Digesu, Guiseppe A; van Breda, Jetske; Van Kerrebroeck, Philip; Elneil, Sohier.
Afiliación
  • Heesakkers JPFA; Department of Urology 610, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Digesu GA; Department of Gynaecology, St. Mary's Hospital, London, UK.
  • van Breda J; Department of Urology 610, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Van Kerrebroeck P; Department of Urology, Maastricht University Medical Center, Maastricht, The Netherlands.
  • Elneil S; Department of Uro-Neurology, National Hospital of Neurology and Neurosurgery, London, UK.
Neurourol Urodyn ; 37(3): 1060-1067, 2018 03.
Article en En | MEDLINE | ID: mdl-28892221
BACKGROUND: Overactive bladder is a chronic condition affecting lower urinary tract function that has a significant negative impact on QoL. OBJECTIVE: Evaluation of the BlueWind implantable tibial nerve system performance and safety in refractory OAB. DESIGN, SETTING, AND PARTICIPANTS INTERVENTION: A 6-month multi-center prospective intervention study. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Objective assessment was done by voiding diary parameters including voids/day, volume voided/day, urgency assessment, leaking episodes/day, pads used/day, leak severity, and clinical success defined as a ≥50% reduction in the number of leaks/day or number of voids/day or number of episodes with degree of urgency >2 or a return to <8 voids/day on a 3 Day diary. Subjective assessment was based on OAB-q including HRQL and symptom severity score. Safety was evaluated by adverse event (AE) analysis. RESULTS AND LIMITATIONS: Thirty-four of the 36 implanted subjects completed the study. One subject withdrew voluntarily and one developed inflammation necessitating removal of the system. In the remaining subjects, 71% experienced clinical success at 6 months. Leaks/day, leak severity, and pad changes/day decreased significantly over time with 27.6% of urge incontinence subjects that became "dry." Voids/day, degree of urgency, volume/void, pads changed improved significantly. All quality of life aspects (concern, coping, sleep, and social) improved as well as symptom severity scores measured by the OAB-q. Adverse events included: implant site pain (13.9%), suspected infection (22.2%), and procedural wound complications (8.3%). CONCLUSIONS: The BlueWind implantable tibial nerve stimulator is a safe, minimally invasive system that affords OAB patients significant improvements. PATIENT SUMMARY: The performance and safety of the BlueWind RENOVA™ implantable tibial nerve neuromodulator for OAB was tested. Our preliminary results demonstrate that the system has a low risk safety profile and may be considered an effective treatment option for OAB management.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Calidad de Vida / Nervio Tibial / Terapia por Estimulación Eléctrica / Vejiga Urinaria Hiperactiva / Incontinencia Urinaria de Urgencia / Neuroestimuladores Implantables Tipo de estudio: Clinical_trials / Observational_studies Aspecto: Patient_preference Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Neurourol Urodyn Año: 2018 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Calidad de Vida / Nervio Tibial / Terapia por Estimulación Eléctrica / Vejiga Urinaria Hiperactiva / Incontinencia Urinaria de Urgencia / Neuroestimuladores Implantables Tipo de estudio: Clinical_trials / Observational_studies Aspecto: Patient_preference Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Neurourol Urodyn Año: 2018 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Estados Unidos