Surgery – Body inserted urinary or colonic incontinent device or...
Reexamination Certificate
1998-09-04
2001-05-15
Gilbert, Samuel G. (Department: 3736)
Surgery
Body inserted urinary or colonic incontinent device or...
Reexamination Certificate
active
06231501
ABSTRACT:
FIELD OF INVENTION
The present invention relates to devices to control and regulate urinary incontinence in women.
BACKGROUND OF THE INVENTION
Urinary incontinence in women is a relatively common problem which exists in three primary forms. Stress urinary incontinence occurs as a result of physical stress, such as lifting, coughing, or sneezing. Urge urinary incontinence is a result of gradual loss of control of the nerves that control the micturition process. Mixed urinary incontinence is a combination of symptoms of stress urinary incontinence and urge urinary incontinence.
The problem is often a source of difficulty or embarrassment to the affected woman. One solution, in relatively mild cases, has been the use of pads or diapers to absorb the uncontrolled seepage of urine. This can be undesirable as it sometimes results in restricting the type or style of clothing wished to be worn, as well as requiring frequent changing of absorbent devices. Uncomfortability and irritation due to the lingering presence of captured urine in enforced close proximity to tender urogenital tissues is another problem existing with external absorbent systems.
More severe cases require the temporary use of an intraurethral device to control the involuntary seepage or flow of urine. Several devices are known in the prior art for dealing with the problems of urinary incontinence in women. One device as claimed in U.S. Pat. No. 5,352,182, comprises a relatively rigid valved catheter having an extendible sealing portion on the interior end of the catheter. The sealing portion must be relatively rigid as it secures the device in the patient and defines at least one aperture to allow the passage of urine into the device. A manually operable valve is located between the internal and external ends of the catheter to enable the woman to selectively control elimination of urine at desired places and times. Other types of valved devices are known, and these generally comprise rigid tubular casings with valves inserted at various locations.
Still other prior art devices comprise solid plugs which are inserted into the urethra to block the involuntary seepage or flow of urine. Several such devices are known in the prior art. As claimed in U.S. Pat. No. 5,082,006, one prior art device comprises a relatively thin, solid shaft having at least one knob or thickening of the shaft along its length. Another device, as claimed in U.S. Pat. No. 5,090,424 comprises a flexible urethral plug which has a soft molded inflatable plastic catheter and a transportable fluid. The device is inserted into the urethra, and pressure applied to an external bellows which causes the fluid to be transported into the interior end of the device. The interior or distal end of the device increases in diameter as a result, securely implanting the plug on a temporary basis, until the interior or distal end of the device is deflated. Removal is then accomplished after deflation.
All known devices employ some kind of enlargement of the interior end of the catheter or shaft to secure the device within the urethra following placement. This can result in discomfort to the woman, and may lead to a sensation of a necessity to void the bladder when it may not be necessary. Additionally, many women suffering from stress urinary incontinence have bladder necks and proximal urethras that will open up during a stress event. This condition exists when the bladder neck becomes deformed from its normally perpendicular state to one which sags downward. When this condition is encountered, securing of the device via an enlarged distal end within the urethra may be negatively affected due to the enlargement occurring at the wrong position on the device. Further, all known prior art devices utilize a form stable catheter or shaft which remains temporarily implanted in the urethra As a result, the urethra will necessarily be deformed from its normally collapsed configuration which is naturally assumed at all times except during urination, when it will be open. Additional problems, such as bladder and urethral infections may also develop from the extended presence of a relatively rigid artificial body in the urethra, and associated open urethra.
What is clearly needed is a device which will allow women suffering from stress or mixed urinary incontinence to live as normal a life as possible. Such a device would ideally be secured in the urethra by means other than a thickening of the interior end, and contain a valve mechanism to allow elimination of urine from the bladder without the necessity of frequent removal followed by subsequent reimplantation of the device. Finally, such a device would comprise a thin walled and flexible catheter, so as to be able to conform as closely as possible to the natural non elimination configuration of the woman's urethra.
SUMMARY OF THE INVENTION
The present invention is directed to a device which comprises a thin walled, flexible tube which minimizes any dilatation effect on the urethra and having a length sufficient to traverse the length of the patient's urethra and into the bladder. At least the portion of the device which contacts the inner surfaces of the patient's urethra is externally coated in foam. Together, the foam and the thin flexible tube may be manufactured in three different diameter sized devices to fit the variation of diameter sizes of the urethra. These sizes would include small (14 Fr.), medium (17 Fr.), and large (20-22 Fr.) diameter sized devices. The foam serves several functions. Because of its pliable nature, it is able to be compressed with the flexible tube when under the relatively constant pressure exerted by the urethra when in the closed, non-urination configuration. Another function provided by the foam coating is that it is able to expand freely in the bladder neck, allowing it to assume the natural shape of the bladder neck. This enhances securing the device in the patient, as well as providing the additional advantage of absorbing abdominal pressure spikes during stress events. Examples of stress events are coughing, sneezing, and strenuous physical activity. Additionally, a foamed tube assuming the shape of the bladder neck creates a bottleneck effect helping to prevent the passage of urine except through the device at desired times and places for the large sized diameter devices. Or, the device offers enough obstruction to prevent leakage during a stress event but not during micturition for the small and medium sized diameter devices. Finally, a foamed tube serves to increase patient comfort during use, as well as providing a degree of structural support on the distal or internal end necessary for eventual successful elimination of urine. Extending beyond the urethra into the bladder neck is the distal portion of the device, which is provided with at least one aperture to permit the flow of urine through the device.
At the proximal end of its length, the tube is surrounded by a meatal flange which has an outer diameter which is significantly greater than that of the tube. The meatal flange helps to secure the position of the device by being normally entrapped between the labia minora and the vestibular floor. Another function of the meatal flange is to prevent migration of the device into the urethra following implantation. In one embodiment, the meatal flange comprises a relatively flat structure in another it comprises a concave structure, and in yet another, it comprises a convex structure. In the case where the meatal flange is concave towards the body, a co-axial tube may be added to direct the flow of urine that passes around the outside diameter of the urethral tube of the device through the inner diameter of the flange.
Located within the tube are valve means to enable the user to selectively eliminate urine from the bladder at an appropriate time without removing the device. This permits the user to insert the device for an extended period of time without having to remove or replace it. This would be done preferably once daily, but longer periods of implantation and
Crompton Seager & Tufte, LLC.
Gilbert Samuel G.
Tama Medical, Inc.
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