We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

HospiMedica

Download Mobile App
Recent News AI Critical Care Surgical Techniques Patient Care Health IT Point of Care Business Focus

Battery-Free Device Implanted Through Minimally-Invasive Procedure Treats Bladder Leaks

By HospiMedica International staff writers
Posted on 24 Sep 2024

Urinary urgency incontinence (UUI), a chronic and often debilitating condition, affects millions and can greatly disrupt daily life. Current treatments aimed at improving bladder control, such as medications and surgical interventions, often come with drawbacks, including side effects or limitations Now, an innovative Implantable Tibial NeuroModulation (iTNM) device offers an exciting new treatment option that could provide relief for patients with UUI.

The Revi Implant, developed by BlueWind Medical (Park City, UT, USA), is a small, battery-free device implanted near the ankle during a minimally invasive outpatient procedure under local anesthesia. Once implanted, the device stimulates the posterior tibial nerve to help alleviate UUI symptoms. Activation of the Revi Implant is simple: a lightweight wireless wearable is placed around the ankle once or twice a day, allowing patients to receive stimulation at their convenience. The battery-free design allows the Revi Implant to be miniaturized, measuring just 3 cm in length and 3 mm in diameter, which eliminates the need for future surgeries to address issues such as battery depletion, lead fractures, or migration.


Image: The small, battery-free implant is placed near the ankle in a single-step procedure (Photo courtesy of BlueWind Medical)
Image: The small, battery-free implant is placed near the ankle in a single-step procedure (Photo courtesy of BlueWind Medical)

Last year, the U.S. Food and Drug Administration (FDA) granted De Novo marketing authorization for the Revi System for men and women suffering from UUI. This approval was based on results from the OASIS pivotal trial, where Revi showed statistically significant symptom reduction and a favorable safety profile compared to baseline. Revi stands out as the only neuromodulation therapy that gives physicians the flexibility to decide if patients should try more conservative treatments before using the Revi System, rather than advising them to undergo "step-therapy."

Related Links:
BlueWind Medical


Gold Member
POC Blood Gas Analyzer
Stat Profile Prime Plus
Flocked Fiber Swabs
Puritan® patented HydraFlock®
New
Blood Sampling System
SafeSet
New
EMR-Ready Baby Scale with WLAN Function
seca 333 i

Latest Critical Care News

Cutting-Edge Intelligent Medical Sutures Accelerate Wound Healing

Fluorescent Dye Reveals Biochemical Conversations Between Cartilage and Bone in Early Osteoarthritis

New Guideline Details Management of CVD Risk Before, During and After Noncardiac Surgery