If you’ve found that your bladder is controlling you more than you’re controlling it, you could have a medical condition called Overactive Bladder, or OAB. And despite what you may have heard, it’s not an inevitable part of the aging process, and it’s not something you should ‘just have to live with.
Fortunately, there are real, effective treatments available. The first step on your path to better wellness begins with understanding the signs and symptoms:
There are lots of reasons why people don’t seek treatment for OAB. Many people don’t think that anything can be done about it. Some assume that it’s actually normal as they get older. And others are simply too embarrassed to talk about it. In fact, less than half of adults living with OAB seek help for their condition1.
That’s unfortunate, because there’s a whole range of proven, effective treatments available, including some that you can do on your own, right now. Some of these options include…
One of the most exciting therapies our office offers for the treatment of OAB is the InterStim™ system by Medtronic, one of the world’s leading healthcare innovators.
For more than 20 years, InterStim™ has been used to improve bladder and bowel function in more than 250,000 patients. One medical study found that 85% of patients who’ve had the system in place for a year saw significant improvement in their condition2,*. After 5 years, that rate was 82%, and 45% of patients with leaking had no leakage at all3,†. Device-related adverse events occurred in 30% of subjects post-implant. The most common device-related adverse effects were undesirable change in stimulation, implant site pain, and implant site infection.
InterStim™ is a form of neuromodulation called sacral neuromodulation that uses gentle nerve stimulation to correct the bladder-brain communication pathway to help restore* bladder function4,5.
Unlike other bladder control treatments, InterStim™ lets you try it first with an evaluation. The evaluation is performed right in your doctor’s office and involves placing a lead (a thin wire) in the upper part of your buttock. The lead then attaches to a small external device worn discreetly under your clothes.
Most patients can tell within just a few days if it’s working for them, though some evaluations may take up to two weeks. After the evaluation period, you and your doctor will decide if the long-term therapy is right for you. If it is, your evaluation device will be replaced with an implantable device called a neurostimulator during a short outpatient procedure.
It’s important to remember this therapy is not for everyone. This treatment is prescribed by your doctor. Please talk to your doctor to decide whether this therapy is right for you.
Implanting an InterStim™ system has risks similar to any surgical procedure, including swelling, bruising, bleeding and infection. In addition to risks related to surgery, complications from this therapy can include pain, infection, sensation of electrical shock, device problems, undesirable change in voiding function and lead migration, among others. Talk with your doctor about ways to minimize these risks.
Of those patients who have found success with InterStim™, many have told us that it has truly transformed their lives. People who had lived for years with leaks and accidents have found they can once again control their bladders, rather than having their bladders control them. No more scheduling activities based on bathroom availability. No more sense that they have to go right now. And no more unpleasant accidents.
If you think InterStim™ might be right for you, our staff is available to discuss your particular condition and treatment options.
Medtronic Bladder Control Therapy delivered by the InterStim™ system treats urinary retention (inability to completely empty the bladder) and the symptoms of overactive bladder, including urinary urge incontinence (leakage) and significant symptoms of urgency-frequency. It should be used after you have tried other treatments such as medications and behavioral therapy and they have not worked, or you could not tolerate them.
You must demonstrate an appropriate response to the evaluation to be a candidate. You cannot have diathermy (deep heat treatment from electromagnetic energy) if you have an InterStim™ device.
This therapy is not intended for patients with a urinary blockage. Safety and effectiveness have not been established for pregnancy and delivery; patients under the age of 16; or for patients with neurological disease origins.
In addition to risks related to surgery, complications can include pain at the implant sites, new pain, infection, lead (thin wire) movement/migration, device problems, interactions with certain other devices or diagnostic equipment such as MRI, undesirable changes in urinary or bowel function, and uncomfortable stimulation (sometimes described as a jolting or shocking feeling).
This therapy is not for everyone. This treatment is prescribed by your doctor. Please talk to your doctor to decide whether this therapy is right for you. Your doctor should discuss all potential benefits and risks with you. Although many patients may benefit from the use of this treatment, results may vary. For further information, please call Medtronic at 1-800-328-0810 and/or consult Medtronic’s website at www.medtronic.com. USA Rx only. Rev. 0517.
Axonics Therapy is a clinically proven solution for treating symptoms of overactive bladder (including urinary urgency incontinence), bowel (fecal) incontinence and urinary retention.1
Axonics Therapy provides gentle stimulation to the nerves that control the bladder and bowel, which can restore normal control and result in symptom improvement.
The Evaluation Step: To see if Axonics Therapy is right for you, you will undergo a short period of therapy using a temporary system. The evaluation period allows you to experience the level of symptom relief the therapy may provide before you commit to long-term therapy.
Long-term Therapy: If you and your doctor determine that Axonics Therapy is right for you, you will have an outpatient procedure where the miniaturized Axonics implant is placed just beneath the skin in the upper part of your buttock.
Backed by clinical studies, Axonics Therapy is clinically proven to regain bladder and bowel control and deliver clinically meaningful improvement in quality of life.
It is up to you and your healthcare provider to determine if you are a good candidate for Axonics Therapy.
Axonics Therapy is an approved treatment for patients suffering with:
Ready to take the first step towards symptom relief? Schedule a consultation with your doctor to discuss your symptoms and to determine if Axonics Therapy is right for you.
Jill, 45 years old and married with 4 kids, started noticing OAB symptoms 10 years ago. Having an active family, her condition impacted every part of her life. With Axonics Therapy, Jill regained control!
Important Safety Information:
Implantation and use of the Axonics System incurs risk beyond those normally associated with surgery, some of which may necessitate surgical intervention.
Results and experiences may vary and are unique to each patient. No promise or guarantee is made about specific results or experiences. Talk to your doctor about whether the Axonics System is right for you and to discuss the potential risks and benefits. For more information about safety and potential risks, go to: www.axonics.com/isi.
Caution: Federal law (USA) restricts this device to sale and use by, or on the order of, a physician.
For many patients, the hardest part of their treatment plan is getting started. It isn’t always easy to talk about incontinence, even with your physician, but it’s a necessary first step if you want to see results.
There’s no need to be embarrassed. Our medical providers work with OAB patients every single day, and we’re experts at making sure you’re comfortable having an open, honest conversation about the symptoms you’ve been experiencing.
Give us a call today and we’ll help you develop a treatment program that’s right for you.
*Success defined as a 50% or greater reduction in your troublesome bladder symptoms. Numbers reflect completers analysis defined as patients with diary data at baseline and 12 months (n=220). Clinical success was 82% at 12 months using the modified completers analysis (subjects who either had a baseline and 12 month evaluation or withdrew early due to device-related reasons and are considered failures). Device-related adverse events occurred in 30% of subjects post-implant. The most common device-related AEs were unde- sirable change in stimulation, implant site pain, and implant site infection.
† Defined as a 50% or greater reduction in your troublesome bladder symptoms. Numbers reflect completers analysis which is subjects who had evaluable diary data at both baseline and 5 years. Modified Completers analysis was 67% at 5 years. The most common AEs were: undesirable change in stimulation (22%, 60/272); implant site pain (15%, 40/272); and therapeutic product ineffective (13%, 36/272).
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