US20160249976A1

Movatterモバイル変換

Info

Publication number: US20160249976A1
Application number: US15/151,223
Authority: US
Inventors: Gamal Ghoniem
Original assignee: University of California San Diego UCSD
Current assignee: University of California San Diego UCSD
Priority date: 2012-09-17
Filing date: 2016-05-10
Publication date: 2016-09-01
Also published as: USD972135S1; US20140081257A1; US9339329B2

Abstract

A device and method for transvaginal or transrectal treatment of a bladder pathology. The device includes an elongate body that includes a longitudinal axis, a handle at one end of the body, a head at the other end of the body, and a shaft between the handle and the head. The head includes a substantially flat surface and one or more retractable needle electrodes extending through the flat surface. The method includes inserting a probe into a vagina or rectum of a patient, where the probe includes a head portion comprising one or more retractable needle electrodes; heating one or more pelvic nerves supplying the patient's bladder by emitting radiofrequency energy from the one or more needle electrodes; and as a result of the heating, damaging the one or more pelvic nerves.

Description

BACKGROUND

1. Field of the Invention

The invention relates to an apparatus and treatment for bladder pathologies.

Problems of bladder overactivity are typically resolved using medications to pharmacologically reduce over activity of the bladder's nerves. These medications, including anticholinergic medications, are used by a very large population of patients. The medications are effective in most, but not all cases. Additionally, the medications have significant systemic side effects and the majority of patients stop taking it by one year (decreased patient compliance). This could be reduced by a localized treatment strategy. Surgical denervation using the Ingelman-Sundberg procedure have also been used to treat urge incontinence.

SUMMARY

In one aspect, a device for transvaginal or transrectal treatment of a bladder pathology is provided. The device includes an elongate body that includes a longitudinal axis, a handle at one end of the body, a head at the other end of the body, and a shaft between the handle and the head. The head includes a substantially flat surface and one or more retractable needle electrodes extending through the flat surface. The shaft and the head are sized and configured to be received in a patient's vagina or rectum.

In the device, the head can contain an array of needle electrodes arranged in rows transverse to the longitudinal axis, and in some embodiments, the rows can be spaced about 1 cm apart. The one or more needle electrodes in some embodiments are curved. The flat surface of the device can be about 3 mm in length in a direction parallel to the longitudinal axis, and/or can be from about 1 to about 2 cm in width in a direction transverse to the longitudinal axis.

In some embodiments, the shaft includes one or more markers for guiding depth of insertion into the patient. In some embodiments, the handle includes controls for turning the device off and on and for regulating radiofrequency energy levels, and/or a slider for extending and retracting the needle electrodes.

In another aspect, a method is provided for treating a bladder pathology involving pelvic nerves. The method includes: inserting a probe into a vagina or rectum of a patient, where the probe includes a head portion comprising one or more retractable needle electrodes; heating one or more pelvic nerves supplying the patient's bladder by emitting radiofrequency energy from the one or more needle electrodes; and as a result of the heating, damaging the one or more pelvic nerves. The head portion of the probe can include a substantially flat surface through which the one or more retractable needle electrodes extend.

In the method, the damaging can include causing a heat lesion in the one or more pelvic nerves, and/or destroying the one or more pelvic nerves. In some embodiments, the damaging results in bladder denervation, and/or the damaging reduces overactivity of the bladder.

In the method, the bladder pathology can involve urinary frequency, urinary urgency, and urge incontinence, overactive bladder, painful bladder syndrome, interstitial cystitis, chronic pelvic pain, pelvic pain because of levator ani trigger points, levator ani and puborectalis spasm, constipation, levator muscle spasm, pelvic floor trigger point, pelvic pain, constipation secondary to puborectalis muscle spasm, anal pain and proctitis, or symptoms of chronic prostatitis without infection. In some embodiments, the bladder pathology is overactive bladder.

The radiofrequency energy can be applied to a central location proximal to the level of the patient's trigone, and can be applied to alocation 30 degrees from the midline to either side of the central location.

BRIEF DESCRIPTION OF THE DRAWINGS

For a more complete understanding of the present invention, reference is now made to the following descriptions taken in conjunction with the accompanying drawings, in which:

FIG. 1 is drawing of a device for treating bladder pathologies.

FIG. 2A is a top plan view of a head for a bladder treatment device.

FIG. 2B is a side view of a head for a bladder treatment device.

FIGS. 3A and 3B are drawings of various features of a handle for a bladder treatment device.

FIGS. 4A-4C are schematic drawings of an embodiment.FIG. 4A is a top plan view,FIG. 4B is a side view, andFIG. 4C is a front view from the head toward the handle.

FIGS. 5A-5C are 3D drawings of an embodiment.FIG. 5A is a perspective view of the device,FIG. 5B is perspective view of the head and shaft, andFIG. 5C is a perspective view of the handle.

DETAILED DESCRIPTION

The following is incorporated by reference herein: Provisional Patent Application No. 61/702,176, filed on Sep. 17, 2012.

Referring toFIG. 1 showing an embodiment of the device, the device includes anelongate body2 that includes a longitudinal axis4, ahandle6 at one end of the body, ahead8 at the other end of the body, and ashaft10 between the handle and the head. The head includes a substantiallyflat surface12 and an array of retractable needle electrodes (shown retracted) that can extend and project through the flat surface. InFIG. 1, the term L₁refers to the length of the shaft, while the terms L₂and L₃refer to lengths of shaft subsections, with L₂+L₃=L₁. The term L₄refers to the length of the head. The term L₅refers to the length of the handle. In general, the shaft and head are sized and configured to be received in a patient's vagina or rectum. In some embodiments, L₁can be 10 cm-20 cm. In some embodiments, L₅can be 9 cm-12 cm. In a particular embodiment, L₁is about 15 cm, L₂is about 10 cm and L₃is about 5 cm, and L₄is about 4 cm.

Positions

14 of retractable needle electrodes forming aneedle electrode array16 on aflat surface18 of the head are shown in the embodiment inFIG. 2A. The number of needle electrodes can vary depending on the size of the body portion to be exposed to radiofrequency energy. The needle electrodes can be arranged inrows20 that run transverse to the longitudinal axis of the elongate body. In the figure, the term L₆refers to the spacing between rows, and can be 0.5 cm-1.5 cm. In particular embodiments, L₆can be about: 0.5 cm, about 1 cm, or about 1.5 cm. The term L₇refers to the length of the flat surface in a direction parallel to the longitudinal axis of the device. The width of the flat surface can be measured in a direction transverse to the longitudinal axis of the device. The length and width can vary according to the size and configuration of the head and the number of needle electrodes. L₇can be 2 cm-5 cm, and in particular embodiments is about: 2 cm, 3 cm, 4 cm, or 5 cm. The width of the flat surface can range from about 1 to about 4 cm, and in some embodiments is about: 1 cm, 2 cm, 3 cm, or 4 cm. In the embodiment inFIG. 2B, an example of acurved needle electrode 22 is shown projecting through the flat surface of the head. In this example, thebase 24 of the needle electrode is covered with insulation while thetip portion 26 of the needle electrode is not insulated. The distance the base of a needle electrode can extend above the flat surface of the head is referred to as L₈inFIG. 2B, the distance the non-insulated tip portion can extend above the insulated base is referred to as L_9,and the total distance the needle electrode can extend above the flat surface is referred to as L_10,where L₈+L₉=L₁₀. L₈can be 1 mm-2 mm, and in particular embodiments is about: 1 mm, 1.5 mm, or 2 mm. L₉can be 2 mm-8 mm, and in particular embodiments is about: 2 mm, 3 mm, 4 mm, 5 mm, 6 mm, 7 mm, or 8 mm. In particular embodiments, L₈is about 2 mm, L₉is about 3 mm, and L₁₀is about 5 mm.

In some embodiments, the overall length of the portion of the needle electrode extending through the flat surface can be between 1-10 mm, and in particular embodiments can be about: 4 mm, or 5 mm.

The handle can include one or more controls, buttons, sliders, or switches, or a combination thereof, for controlling and using the device. Such features can be included, for example, for turning the device on and off, for controlling the level of radiofrequency energy emitted, or for controlling the length of the needles electrodes projecting out of the flat surface. In the various embodiments shown inFIGS. 3A and 3B, the handle includes an on-off button28, radiofrequency power controls30, and aslider32 on the side of the handle to control needle electrode extension, having an in34 and an out36 position. Referring toFIG. 1, the handle of the device can include awire38 for connecting the needle electrodes to aradiofrequency generator40. The radiofrequency generator can be battery operated and/or rechargeable, and can include a temperature monitoring feature. In addition, the shaft can include one ormore markers42 such as a pattern or guide for guiding the depth of insertion of the device into the patient. A marker can be positioned at length L₃on the shaft of the handle.

Embodiments of the device can thus include the following: an elongate body, a longitudinal axis, a handle at one end of the body, a head at the other end of the body, a shaft between the handle and the head, and an array of retractable needle electrodes on a flat surface of the head.

The device and method for treating bladder pathologies can be used to treat women or men who have urinary frequency, urgency, and urge incontinence. Other indications for the device and method are overactive bladder, painful bladder syndrome, interstitial cystitis, chronic pelvic pain, pelvic pain because of levator ani trigger points, levator ani and puborectalis spasm, constipation, levator muscle spasm, pelvic floor trigger point, pelvic pain, constipation secondary to puborectalis muscle spasm, anal pain and proctitis, or symptoms of chronic prostatitis without infection.

In particular embodiments, a vaginal probe is inserted into a patient and the needle electrodes emit radiofrequency energy, which then destroys the nerves with heat. In one embodiment, a thin wire (probe) is passed through one or more of the needles. In another embodiment, heat treatment causes a heat lesion to the pelvic nerve(s).

In some embodiments, the device is applied subtrigonal and lateral to the trigone in female subjects. In other embodiments, regardless of the subject's sex, the device can be applied to the painful pelvic floor muscle (as in trigger points or spasm). It can be useful in relieving constipation due to puborectalis muscle spasm. In another embodiment, the device is applied transrectally in male subjects. The device can be applied above the prostate for overactive bladder, and to the prostate for chronic prostatitis symptoms without infection.

The radiofrequency energy emitted by the device or by the needle electrodes can be sufficient to heat the tissue to about 65-80° C.; and/or can be capable of generating between 5-10 watts of power.

The device can be applied to a patient for about 30-90 seconds, and between 1-4 ablations can be applied per site.

In some embodiments, the device and method comprise a vaginal probe to deliver radiofrequency waves (RF) through the vaginal wall and posterior to the bladder, where there is dense innervation, to denervate the pelvic nerve(s) supply to the overactive bladder (OAB). OAB is a common condition in the adult (16%) and increases with age.

Some of the advantages of the method and device over previous methods include:

- One time treatment rather than medication every day. In some cases, return of symptoms may be observed due to nerve regeneration. From other denervation surgical procedures, this can happen after a year or more. A subsequent radiofrequency session can then be undertaken.
- Will likely have no systemic side effects.
- Long-term (likely more than 6 months), a single treatment will be cost effective as medication will not be required.
- Will potentially be single outpatient treatment solution for bladder overactivity, interstitial cystitis, and other forms of bladder pathology.

A particular embodiment (called DENERA) is shown inFIGS. 4A-4C. In this embodiments, marker guides44 provide guides for depth of insertion. Also shown is a protrudingguide46. This embodiment has a 9-electrode head48. InFIGS. 5A-5C, a 3D drawing of the DENERA device is shown, containing a protrudingguide46 and a 9-electrode head48.FIG. 5C is a close-up view of ahandle50.

The present invention may be better understood by referring to the accompanying examples, which are intended for illustration purposes only and should not in any sense be construed as limiting the scope of the invention.

EXAMPLE 1

The device can be used by a method involving one or more of the following steps:

- position the patient in lithotomy position,
- prepare vagina lightly with an antiseptic such as Betadine,
- apply local anaesthetic (i.e. cream or jelly) to the area proximal to level of the trigone (about 4 cm from external urethral meatus), introduce the device to the position of a “marker”,
- once in position, apply mild pressure using index finger behind the head of the device to ensure close contact between the device and patient's tissues,
- deploy the needles on the device,
- turn RF signal on and adjust RF signal if desired using controls,
- keep RF signal on for 30-90 seconds, off for 30-90 seconds for a total of about 2 to 5 minutes in each site.
- apply three times, once to the center (i.e. area proximal to level of the trigone), once 30 degrees to the left of center; and once 30 degrees right of center.

The area treated can be cooled using an ice pack, liquid or other means known in the art. The total procedure may take about 30 minutes.

In some cases, cooling may be applied to the area while the device is on, or after treatment.

REFERENCES

The following publications are incorporated by reference herein.

1. Westney, O. L., et al., Long-term results of Ingelman-Sundberg denervation procedure for urge incontinence refractory to medical therapy, J. Urol. (2002) Sep; 168(3): 1044-7.
2. U.S. Pat. No. 6,292,695

Although the present invention has been described in connection with the preferred embodiments, it is to be understood that modifications and variations may be utilized without departing from the principles and scope of the invention, as those skilled in the art will readily understand. Accordingly, such modifications may be practiced within the scope of the invention and the following claims.

Claims

What is claimed is:

1. A device for transvaginal or transrectal treatment of a bladder pathology, comprising

an elongate body comprising a longitudinal axis, a handle at one end, a head at the other end, and a shaft between the handle and the head,

the head comprising a substantially flat surface and at least one retractable needle electrode extending therethrough,

wherein the shaft and the head are sized and configured to be received in a patient's vagina or rectum.

2. The device ofclaim 1, wherein the head comprises an array of retractable needle electrodes arranged in rows transverse to the longitudinal axis.

3. The device ofclaim 2, wherein the rows are spaced about 1 cm apart.

4. The device ofclaim 1, wherein the at least one needle electrode is curved.

5. The device ofclaim 1, wherein the flat surface is about 3 mm in length in a direction parallel to the longitudinal axis, and from about 1 to about 2 cm in width in a direction transverse to the longitudinal axis.

6. The device ofclaim 1, wherein the shaft comprises one or more markers for guiding depth of insertion into the patient.

7. The device ofclaim 1, wherein the handle comprises controls for turning the device off and on and for regulating radiofrequency energy levels.

8. The device ofclaim 1, wherein the handle comprises a slider for extending and retracting the one or more needle electrodes.