Patent Application
20100168656
The present invention relates generally to medical devices and, more particularly, to an injection apparatus to target specific anatomy and facilitate the treatment of urinary incontinence and gastroesophageal reflux disease.
One of the primary uses of the present invention is treatment of urinary incontinence. For example, many women suffer from incontinence caused by childbirth and/or obesity. Usually exercises to strengthen the pelvic floor muscles are the initial treatment for incontinence. If these exercises are ineffective, pharmacological solutions are usually attempted. As a final resort, open surgical repair of the bladder neck can be attempted. But surgical repair procedures are not successful in all patients and there is also risk associated with open surgical procedures, such as trauma, infection, and side effects of anesthesia.
As an alternative to surgical repair, urinary incontinence has been treated by injecting various substances into the tissue surrounding the urethra, i.e., the periurethral tissue, to add bulk to this tissue. The aim of this treatment is to compress the urethra at the level of the bladder neck to impede involuntary flow of urine from the bladder.
The use of sodium morrhuate for the treatment of stress incontinence has been reported (1). This material was not successful in treating incontinence, and pulmonary infarction was an observed complication. Paraffin and other sclerosing solutions have also been tried, also yielding poor results (2,3).
Polytetrafluoroethylene particles have been used as injectable balking material with a success rate from 30% to 86% in some studies (4,5,6,7,8,9). The complications associated with this procedure include foreign body granulomas that tended to migrate to distant organs, such as the lungs, liver, spleen, and brain (10).
Another injectable used recently is glutaraldehyde cross-linked bovine dermal collagen (Br. J. Urol., 75:359-363 (1995); Br. J. Urol., 75: 538-542 (1993)) (11). A major problem with the use of collagen was biodegradation with associated decrease in implant volume over time necessitating re-treatment (12) Collagen can also cause adverse immune responses and allergic reactions to bovine collagen have been described (13).
Other materials have been suggested for use in the treatment of vesicourectal reflux. These substances include polyvinyl alcohol foam, glass particles, a chondrocyte-alginate suspension, and a detachable silicone balloon (14,15,16,17).
The effectiveness of these bulking agents is often limited by the precision and circumferentialality of injection. If the injection is non-circumferential, it can produce an oblong lumen that does not adequately inhibit flow. If the injection is not made into the urinary sphincter, it will also not have the desired effect. Currently, in an effort to obtain circumferentiality and precision, time-consuming multiple injections are usually made.
Additionally, various injection apparatus and probes are described in U.S. Pat. Nos. 5,645,528; 6,090,063; 6,183,520; 6,666,848; 6,852,091; and 6,878,369; and U.S. Patent Publication Nos. 2005/0124852 and 2004/0037887; the entire disclosures of which are hereby incorporated herein by reference.
It is, therefore, an object of the present invention to provide apparatus and methods for effectively treating urinary incontinence and gastroesophageal reflux disease, with minimal to no complications.
Generally, the invention relates to apparatus and methods for accurately introducing bulking agents into tissue surrounding bodily lumens, in particular a catheter for urethral incontinence (CUI) that precisely and consistently delivers a bulking agent to the urethral sphincter for the treatment of incontinence. The CUI utilizes a balloon to precisely position injection needles into the urethral sphincter and surrounding tissue without complicated and invasive visualization tools. More importantly, the plurality of injection needles in the present invention creates a longer and more circular treatment area within the bodily lumen for the injection of the bulking agent, improving treatment of the effected area over the prior art methods.
In one aspect, the invention relates to a medical delivery device, such as a catheter, that includes an elongate body defining at least one lumen and a deployable injection assembly disposed at a distal portion of the elongate body.
In various embodiments, the elongate body can define a plurality of lumens and may include a balloon or other securing means disposed proximate the distal end of the elongate body. The plurality of lumens can be used to deliver a therapeutic agent to the body or provide drainage of bodily fluids. At least one of the lumens could be disposed about a central longitudinal axis of the elongate body. The additional lumens could be disposed radially about the central longitudinal axis of the elongate body, or in essentially an orientation as necessary to suit a particular purpose. Additionally, one or more lumens could be in fluid communication with the balloon to inflate/deflate the balloon. Further, a central lumen of the catheter can be used as a conduit to drain the contents of the bladder. The device could also include valving to isolate the lumens or regulate the flow of materials therethrough. Alternatively or additionally, the device could include other structures to position and/or secure the device in place such as, for example, a molly bolt, a metallic fan, or a malecot.
The deployable injection assembly can include a plurality of hypodermic tubes disposed about the elongate body to deliver the therapeutic materials to the body. The tubes can have a retracted position, for example recessed within the elongate body to prevent the tubes from interfering with insertion of the device, and an extended position, where a sharpened end of the tubes extend beyond the outer surface of the elongate body and into the surrounding tissue.
The tubes can be disposed about the circumference of the elongate body and can be oriented radially with respect to the central longitudinal axis. The tubes can be disposed in multiple rows along the length of the elongate body, where the orientation of the rows of tubes may be aligned, offset, or helically arranged. The use of multiple rows of needles facilitates injecting the agent over a longer section of the bodily lumen, i.e., urethra, bladder neck, or esophagus, and not just, for example, the urethral sphincter. The distal ends of the needles may be modified to decrease the penetration force required.
In another aspect, the invention relates to a method of treating urinary incontinence or gastroesophageal reflux disease (GERD). The method includes the steps of providing a medical delivery device including an elongate body defining at least one lumen and a deployable injection assembly disposed at a distal portion of the elongate body; positioning the device within the body; deploying the injection assembly; and delivering a therapeutic agent to the surrounding tissue. The method also includes retracting the injection assembly and removing the device. The method may also include repositioning the device between multiple deployments of the injection assembly and delivering of therapeutic agents, e.g., a bulking agent. In one embodiment, the bulking agent can be gently warmed prior to injection to decrease viscosity. Decreased viscosity will reduce the force required to push the bulking agent through the injection assembly.
These and other objects, along with advantages and features of the present invention herein disclosed, will become apparent through reference to the following description and the accompanying drawings. Furthermore, it is to be understood that the features of the various embodiments described herein are not mutually exclusive and can exist in various combinations and permutations.
In the drawings, like reference characters generally refer to the same parts throughout the different views. In addition, the drawings are not necessarily to scale, emphasis instead generally being placed upon illustrating the principles of the invention. In the following description, various embodiments of the present invention are described with reference to the following drawings, in which:
Embodiments of the present invention are described below. It is, however, expressly noted that the present invention is not limited to these embodiments, but rather the intention is that variations, modifications, and equivalents that are apparent to the person skilled in the art are also included.
As shown in
Just proximal to the positioning balloon is the injection assembly (C). The injection assembly lies within the central catheter (E) and contains a plurality of sharpened hypodermic tubes (J) arranged circumferentially around the catheter with the sharpened end pointed outward. In a particular embodiment, there are twelve needles; however, the number and arrangement of the needles will vary to suit a particular application.
The proximal ends of the hypodermic needles are mechanically coupled to a deployment assembly (D) via, for example, a linkage or push wire. Moving the deployment assembly distally will cause the needles to protrude from the catheter. Moving the deployment assembly proximally retracts the needles back into the catheter. The lumens of the needles communicate directly with an injection port (F) via the central lumen of the catheter, allowing the user to inject materials from the injection port through the central lumen of the catheter and out the needles.
In one possible application of use (see
Once the catheter is in proper position, the injection assembly is pushed forward, forcing the needles to deploy outwardly and distally into the urinary sphincter (located at the neck of the bladder) and smooth muscle layer of the urethra. A bulking agent is then injected through the needles into the urinary sphincter and urethra. The number of needles and their position in the device of the present invention, create a longer, more circumferential treatment area within the bodily lumen for the injection of the bulking agent, improving treatment of the effected area over the prior art. The needles are then withdrawn back into the catheter. The positioning balloon is deflated and the catheter is removed from the patient.
In one alternative embodiment, as shown in
In an alternative method of use, the device is used to treat GERD. A simple modification in the diameter of the catheter for urinary incontinence can be made to treat GERD. The material may be injected into the wall of the esophagus to thicken the wall and narrow the gastroesophageal junction into the stomach. During proper operation of the lower esophageal sphincter, the lower esophageal sphincter opens to allow food to pass into the stomach and closes to prevent food and acidic stomach fluids from flowing back up into the esophagus. Gastroesophageal reflux occurs when the lower esophageal sphincter is weak or relaxes inappropriately, allowing the stomach's contents to retrograde or flow up into the esophagus.
This retrograde flow of gastric contents back into the esophagus, through what should be a one-way valve into the stomach, can damage the esophagus. More particularly, the contents of the stomach are very acidic; and the lining of the stomach is specially designed to cope with the lower pH contents. The esophagus, on the other hand, is not suited for such exposure to highly acidic materials. Thus, when acid retrogrades from the stomach into the esophageal tissues, irritation and inflammation will often result to these tissues.
Additional uses for the device include treating ureter reflux (see
Furthermore, the device can be used for performing prostate injection. A pair of special needles are placed 180 degrees apart on the circumference of the catheter. These needles will be longer than the other needles of the injection assembly.
The invention also relates to other methods of injecting bulking agents, such as needle-less injection, injection of anesthesia first, injection by expansion, and injection by a screw mechanism. With needle-less injection, the bulking agent is injected under high pressure. Needle-less injection requires the bulking agent to be nebulized into small particles. These small particles are forced at high pressure between the cells of the inner walls of the urethra.
Prior to deploying the needles, a surface anesthesia can be sprayed onto the inside wall of the urethra or other bodily lumen. This will reduce the pain associated with the insertion of the needles.
Injection by expansion involves the needles being attached to an inflatable member, for example a balloon. In order to deploy the needles, the balloon is inflated, driving the needles outwardly, similar to a porcupine configuration. Additionally, a worm screw mechanism can be used for deploying/retracting the positioning device and/or the needles.
The shape and dimensions of the device will vary to suit a particular application; for example, a longer catheter may be required to treat ureter reflux as opposed to treating uretheral incontinence. Also, the size and shape of the device may vary as necessary depending on the physiology of the patient to be treated; for example, a smaller device would likely be used for treating a child as opposed to an adult. The device is typically manufactured of biocompatible materials, such as polymers, for example polyurethanes, silicones, polyethylenes, nylons, polyesters, and polyester elastomers.
The various devices described herein may be manufactured by, for example, injection molding or modifying an extruded tube. For example, extrusion may be used to provide a uniform polymeric tube, to which a hub is attached at one end and the other end is sealed. Insert molding or a subsequent mechanical operation can then be used to provide the desired geometry of other components. The other components, for example the positioning balloon, can be bonded to the catheter.
Having described certain embodiments of the invention, it will be apparent to those of ordinary skill in the art that other embodiments incorporating the concepts disclosed herein may be used without departing from the spirit and scope of the invention. The described embodiments are to be considered in all respects as only illustrative and not restrictive.
This patent application claims priority to U.S. patent application Ser. No. 60/721,403, filed Sep. 28, 2005, and is incorporated by reference herein as if set forth in its entirety.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/US06/37666 | 9/28/2006 | WO | 00 | 2/26/2009 |
| Number | Date | Country | |
|---|---|---|---|
| 60721403 | Sep 2005 | US |
