First non-invasive device for stress incontinence approved by FDA

Published On 2018-12-12 14:40 GMT   |   Update On 2024-01-27 11:11 GMT

First non-invasive device for stress incontinence approved by The US Food and drug administration, FDA. The new, device developed by a Creighton University professor could help women take control of their problem rather than simply managing it.Innovo® therapy device, for pelvic floor weakness, will soon be available in the United States.


The device, manufactured by Atlantic Therapeutics in Galway, Ireland, is the first non-invasive transcutaneous electrical stimulation continence device to be cleared by the FDA in the U.S. The product has been available in Europe for several years.


Stress urinary incontinence, caused by a weakened pelvic floor can have a tremendously negative effect on women’s lives and about one in three women in their lifetime will be affected by it. stress urinary incontinence is a condition that results in intermittent urinary leakage during laughing, coughing, sneezing and exercise.

Stress urinary incontinence, caused by a weakened pelvic floor can have a tremendously negative effect on women’s lives, says Ruth Maher, assistant professor of physical therapy at Creighton and director of the Women’s Health Residency Program.


“The burden associated goes far beyond the cost of pads as medical and psychological morbidity in addition to the quality of life are profoundly impacted,” says Maher. “It has a huge impact on the quality of life for women. Women will plan outings around available restrooms, choose not to wear certain clothes for fear of ruining them from leakage and severely curtail their exercise regimens which can have a severe impact on their health across their lifespan. Additionally, this type of incontinence can impede intimacy for up to 65 per cent of women because of leakage during sex.”


The non-invasive INNOVO® shorts send targeted impulses to integrated conductive panels to safely and effectively activate the muscles of the pelvic floor via patented technology. The shorts can be used in the privacy and comfort of home to enhance coordination and strength of the pelvic floor muscles. The device is controlled by a handheld device that attaches to the garment.


According to the research, more than 87 per cent of patients were dry or had mild leakage after a 12-week treatment period, with 93 per cent of patients experiencing improvement in just four weeks.


Maher says it can be difficult to teach women how to do pelvic floor exercises correctly because the muscles don’t move a joint, but instead aid in controlling pressure in the lumbopelvic region and of course in bowel and bladder function. Consequently, clinicians can have trouble determining if a patient is using the right muscles unless they perform a digital pelvic floor exam or use some type of imaging


Maher, in her research and teaching, uses ultrasound imaging and noticed when many women said they were doing pelvic floor exercises also known as Kegels, they were actually doing inappropriate contractions using muscle groups other than the pelvic floor groups. She notes about 40 per cent of women is unable to voluntarily contract the pelvic floor muscles.


“The Innovo® therapy shorts facilitate a pelvic floor contraction and reproduce the same contraction consistently,” says Maher. “The benefit of this is two-fold: the strength and coordination of the pelvic floor improves, but more importantly the device improves the users awareness of their pelvic floor and improves their ability to perform appropriate contractions without the device, In fact, I encourage users to try to contract their pelvic floor muscles while using the shorts.”


The device will be available beginning in January by prescription only, but Maher says it will be available over the counter in the near future.


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