The inflow Intraurethral Valve-Pump, a device intended for use in women with impaired detrusor contractility (IDC), has been given FDA marketing approval.
The U.S. Food and Drug Administration last month announced that they are allowing marketing of the inFlow Intraurethral Valve-Pump, a replaceable urinary prosthesis for use in female adults who cannot contract the muscles necessary to push urine out of the bladder (impaired detrusor contractility or IDC).
IDC is a condition where patients are unable to spontaneously urinate because of insufficient bladder muscle contraction, which can result from significant neurologic disease or injury such as stroke, multiple sclerosis, spinal cord injury, spina bifida, or diabetic neuropathy. IDC is typically managed with various types of catheters, including clean intermittent catheterization (CIC).
“The inFlow device allows women with IDC to urinate, without the need to catheterize daily or be attached to a urine drainage bag,” said William Maisel, MD, MPH, deputy director for science and chief scientist in the FDA’s Center for Devices and Radiological Health. “This may allow for increased mobility and the ability to be more self-sufficient.”
The device has four components: a sterilized, single-use urethral insert component with silicone shaft, fins, and flange; an introducer; an activator; and a sizing component. The device draws urine out to empty the bladder and blocks urine flow when continence is desired. A physician sizes the patient for an inFlow device and performs the initial insertion. After training, device insertion and removal can be performed by the patient or a caregiver. Each inserted component must be replaced at least once every 29 days.
The FDA reviewed data for inFlow through the de novo classification process, a regulatory pathway for some low-to-moderate risk medical devices that are not substantially equivalent to a legally marketed device.
The FDA granted the de novo request based on non-clinical testing and a clinical trial that enrolled 273 women with IDC using CIC. Over half of the women stopped using the device as a result of discomfort and leakage of urine. The trial showed that 98% of the 115 women that continued to use the inFlow device had comparable post-void residual urine volume (measurement of the amount of urine left in the bladder after urination is complete) with those who used the CIC.
Adverse events associated with the device included asymptomatic bacteriuria, urinary tract infection (UTI), bladder inflammation, genital and urinary (genitourinary) pain, blood in the urine (hematuria), urinary leakage (around the device), urinary frequency/urgency, bladder spasms, and vulvar, vaginal, and urethral disorders. It is noteworthy that the most significant of these adverse events-UTI-appears to occur at a lower rate with the inFlow device than with CIC. Among patients treated with the inFlow device, UTIs were stable and easily managed with antibiotics.
The inFlow Intraurethral Valve-Pump is manufactured by Vesiflo, Inc., based in Redmond, Washington.