CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application claims the benefit of U.S. Provisional Patent Application No.
61/931,645, filed January 26, 2014 and entitled "A Dilating Device for Prostatic urethra", which is incorporated herein by reference in its entirety.
FIELD OF THE INVENTION
[0002] The invention relates to the field of urological medical devices.
BACKGROUND
[0003] Benign prostate hyperplasia (BPH), also known as benign prostatic hypertrophy, is a urological disease in which the prostate enlarges and constricts the urethra. BPH affects a majority of the male population over 50 years of age, and is thus of great medical and commercial importance.
[0004] Surgical treatment of hypertrophy of the prostate has been a routine procedure for many years. One method of such surgical treatment is open prostatectomy wherein the gland is totally or partially removed. Another method of surgical treatment is transurethral resection of the prostate (TURP). However, surgical treatment is an extremely invasive procedure which is debilitating, painful and often traumatic to the patient. Various complications including impotence, incontinence, bleeding, infection and other undesirable problems attendant with such surgery can result.
[0005] Another procedure to treat prostatic hypertrophy is to place a catheter at the external opening of the urethra and into the obstructed portions of the urethra, allowing urine to pass from the bladder by way of the catheter lumen. These urinary catheters typically employ a positioning or retention balloon at the distal tip which inflates at the bladder neck and prevents the expulsion of the catheter from the body.
[0006] Heat, such as produced by microwave or laser energy, may be provided in combination with such catheters for treating the enlarged portion of the prostate. However, this procedure may result in pain and discomfort to the patient
SUMMARY
[0007] The following embodiments and aspects thereof are described and illustrated in conjunction with systems, tools and methods which are meant to be exemplary and illustrative, not limiting in scope.
[0008] There is provided, in accordance with an embodiment, a dilating device for the prostatic urethra, the device comprising: at least three, laterally connected longitudinal ridges, wherein each ridge is configured to longitudinally engage with a different substantially longitudinally groove of the prostatic urethra of a patient, and wherein the at least three laterally connected ridges are configured to laterally compress to enable insertion into the prostatic urethra in a compressed configuration, and wherein the at least three laterally connected ridges are configured to laterally expand to a normally - open configuration upon deployment within the prostatic urethra, to exert a radially outwards force that dilates the prostatic urethra.
[0009] In some embodiments, the at least three laterally connected ridges comprise two peripheral ridges that are each configured to engage with a different postero-lateral groove of the prostatic urethra, and a central ridge that is configured to engage with the anterior inter-lobar groove of the prostatic urethra.
[0010] In some embodiments, there is further provided one or more connectors that laterally connect each peripheral ridge to the central ridge.
[0011] In some embodiments, the one or more connectors laterally connect each peripheral ridge to the central ridge at a point on each ridge that lies between the distal and proximal ends of the peripheral and central ridges.
[0012] In some embodiments, the one or more connectors comprise two distal connectors that laterally connect a distal end of each peripheral ridge to a distal end of the central ridge, and two proximal connectors that laterally connect a proximal end of each peripheral ridge to a proximal end of the central ridge, thereby forming two closed forms joined at the central ridge.
[0013] In some embodiments, the two closed forms comprise lengthwise oriented avoid lOOps that together form a figure-eight shape in the normally-open configuration.
[0014] In some embodiments, the two closed forms form two substantially rectangular shapes that span two substantially non-parallel planes in the normally-open configuration.
[0015] In some embodiments, the two distal connectors are substantially S-shaped, and are configured to span a portion of a cylinder in the normally-open configuration, thereby dilating the prostatic urethra at the bladder neck.
[0016] In some embodiments, the two proximal connectors are substantially S-shaped, forming a butterfly shape by the device in the normally-open configuration.
[0017] In some embodiments, all the at least three laterally connected ridges and one or more connectors are configured to maintain intimate contact with the prostate urethra mucosa.
[0018] In some embodiments, there is further provided two or more distally positioned protrusions that are configured to impinge against the postero-lateral side of the bladder neck, thereby preventing a migration of the device into the urinary bladder.
[0019] In some embodiments, the at least three laterally connected ridges are composed of wire.
[0020] In some embodiments, the at least three laterally connected ridges are composed of cut foil.
[0021] In some embodiments, the at least three laterally connected ridges are composed of super-elastic alloy.
[0022] In some embodiments, the at least three laterally connected ridges are composed of super-elastic polymer.
[0023] In some embodiments, the super-elastic polymer is a biodegradable polymer.
[0024] In some embodiments, the device is configured to allow free passage of a liquid when deployed in the prostatic urethra.
[0025] In some embodiments, the shape of the device is configured to reside within the prostate urethra.
[0026] In some embodiments, the at least three, laterally connected ridges are further configured to: laterally compress for fitting within a deployment lumen, laterally expand to a normally-open configuration upon extraction from the deployment lumen, and exert the outwards radial force upon deployment within the prostatic urethra.
[0027] In some embodiments, the deployment lumen is configured to be housed within a work channel of a cystoscope.
[0028] In some embodiments, the deployment lumen is further provided with a fluid delivery lumen and balloon that are configured to deliver a fluid to the bladder to allow deploying the device within the prostatic urethra via the bladder.
[0029] In some embodiments, the at least three, laterally connected ridges are provided with one or more proximally disposed protrusion that are configured to releasably connect the device to an alignment mechanism housed within the deployment lumen.
[0030] In some embodiments, the alignment mechanism comprises a releasable string that lOOps through the protrusions and runs through an alignment lumen.
[0031] In some embodiments, the device is configured for alignment within the prostatic urethra via a torque that is transferred from the alignment mechanism.
[0032] There is provided, in accordance with an embodiment, a method for dilating a prostatic urethra, the method comprising: inserting a dilating device into the urethra of a patient; aligning the dilating device within the pro static urethra; positioning the dilating device within the prostatic urethra of the patient; and deploying the dilating device within the prostatic urethra, thereby causing the dilating device to: expand to a normally-open configuration, engage with the grooves of the prostatic urethra, exert a radially outwards force on the prostatic urethra, and dilate the prostatic urethra.
[0033] In some embodiments, positioning comprises extracting the device from a deployment lumen and inserting the device into the urinary bladder of the patient.
[0034] In some embodiments, positioning comprises drawing the device from the bladder into the prostate urethra.
[0035] In some embodiments, aligning comprises transferring a torque applied to an alignment mechanism connected to the device.
[0036] In some embodiments, the torque is applied by rotating an alignment lumen that is connected to the device.
[0037] In some embodiments, aligning comprises positioning a central ridge of the device for engaging with the anterior inter-lobar groove of the prostatic urethra and positioning two peripheral ridges of the device to each engage with a different posterolateral groove of the prostatic urethra.
[0038] In some embodiments, the method further comprises causing the device to laterally compress and retreat within the deployment lumen if the alignment or position of the device is incorrect.
[0039] In some embodiments, the method further comprises causing the device to impinge against the postero-lateral side of the bladder neck, thereby preventing a migration of the device into the urinary bladder.
[0040] In some embodiments, the method further comprises disconnecting the device from a deployment lumen provided to deploy the device.
[0041] In some embodiments, the method further comprises applying a positioning balloon to secure the position of the deployed device.
[0042] There is provided, in accordance with an embodiment, a kit for dilating a prostatic urethra, the kit comprising: a deployment lumen; and a dilating device which comprises: at least three, laterally connected ridges, wherein each ridge is configured to vertically engage with a different substantially vertical groove of the prostatic urethra of a patient, and wherein the at least three laterally connected ridges are configured to laterally compress to enable insertion into the prostatic urethra, in a compressed configuration, through said deployment lumen, and wherein the at least three laterally connected ridges are configured to laterally expand to a normally-open configuration upon deployment from said deployment lumen into the prostatic urethra, to exert a radially outwards force that dilates the prostatic urethra.
[0043] In some embodiments, the at least three, laterally connected ridges are provided with one or more proximally disposed protrusion that are configured to releasably connect the device to an alignment mechanism housed within the deployment lumen.
[0044] In some embodiments, the alignment mechanism comprises a releasable string that lOOps through the protrusions and runs through an alignment lumen.
[0045] In some embodiments, the device is configured for alignment within the prostatic urethra via a torque that is transferred from the alignment mechanism.
[0046] In some embodiments, the deployment lumen is configured to be housed within a work channel of a cystoscope.
[0047] In some embodiments, the deployment lumen is further provided with a balloon that is configured to position the device within the within the prostatic urethra.
[0048] In some embodiments, the at least three laterally connected ridges comprise two peripheral ridges that are each configured to engage with a different postero-lateral groove of the prostatic urethra, and a central ridge that is configured to engage with the anterior inter-lobar groove of the prostatic urethra.
[0049] In some embodiments, the kit further comprises one or more connectors that laterally connect each peripheral ridge to the central ridge.
[0050] In some embodiments, the one or more connectors laterally connect each peripheral ridge to the central ridge at a point on each ridge that lies between the distal and proximal ends of the peripheral and central ridges.
[0051] In some embodiments, the one or more connectors comprises two distal connectors that laterally connect a distal end of each peripheral ridge to a distal end of the central ridge, and two proximal connectors that laterally connect a proximal end of each peripheral ridge to a proximal end of the central ridge, thereby forming two closed forms joined at the central ridge.
[0052] In some embodiments, the two closed forms comprise lengthwise oriented ovoid lOOps that together form a figure-eight shape in the normally-open configuration.
[0053] In some embodiments, the two closed forms form two substantially rectangular shapes that span two substantially non-parallel planes in the normally-open configuration.
[0054] In some embodiments, the two distal connectors are substantially S-shaped, and are configured to span a portion of a cylinder in the normally-open configuration, thereby dilating the prostatic urethra at the bladder neck.
[0055] In some embodiments, the two proximal connectors are substantially S-shaped, forming a butterfly shape by the device in the normally-open configuration.
[0056] In some embodiments, all the at least three laterally connected ridges and one or more connectors are configured to maintain intimate contact with the prostate urethra mucosa.
[0057] In some embodiments, the kit further comprises two distally positioned protrusion that are configured to impinge against the postero-lateral side of the bladder neck, thereby preventing a migration of the device into the urinary bladder.
[0058] In some embodiments, the at least three laterally connected ridges are composed of wire.
[0059] In some embodiments, the at least three laterally connected ridges are composed of cut foil.
[0060] In some embodiments, the at least three laterally connected ridges are composed of super-elastic alloy.
[0061] In some embodiments, the at least three laterally connected ridges are composed of super-elastic polymer.
[0062] In some embodiments, the super-elastic polymer is a biodegradable polymer.
[0063] In some embodiments, the device is configured to allow free passage of a liquid when deployed in the prostatic urethra.
[0064] There is provided, in accordance with an embodiment, a dilating device for the prostatic urethra, the device comprising: at least two dilating means of the prostate urethra, wherein the dilating means are connected by ridges that are configured to fix the dilating means in place within the prostate urethra and prevent their movements or dislodgement and wherein the dilating means are configured to laterally expand to a normally-open configuration upon deployment within the prostatic urethra, to exert a lateral outwards force that dilates the prostatic urethra.
[0065] In some embodiments, the dilating means comprise arcs that exert lateral forces on the lateral lobes.
[0066] In some embodiments, the dilating means comprise rings.
[0067] In some embodiments, the shape of the device in a normally open configuration is configured to reside within a delimiting surface of a longitudinally oriented tube.
[0068] In some embodiments, the device is shaped to reside within the prostate urethra.
[0069] In some embodiments, the dilating means and connecting ridges of the device are configured to maintain intimate contact with the prostate urethra mucosa.
[0070] In addition to the exemplary aspects and embodiments described above, further aspects and embodiments will become apparent by reference to the figures and by study of the following detailed description.
BRIEF DESCRIPTION OF THE FIGURES
[0071] Exemplary embodiments are illustrated in referenced figures. Dimensions of components and features shown in the figures are generally chosen for convenience and clarity of presentation and are not necessarily shown to scale. The figures are listed below.
Fig. 1A-B illustrates a dilating device for the prostatic urethra from a perspective view and a top view, respectively, in accordance with an embodiment;
Fig. 1C shows a profile view of the device of Fig. 1A, according to an embodiment;
Fig. 1D shows a frontal view of the device of Fig. 1A, according to an embodiment;
Figs. 2A-B, together show an exemplary deployment of a device for dilating a prostatic urethra, according to an embodiment;
Figs. 3A-B together illustrate a deployment apparatus for a dilating device for the prostatic urethra, in accordance with an embodiment;
Figs. 4A-B show a cystoscope configured to deploy a dilating device for the prostatic urethra, in accordance with an embodiment; and
Fig. 5 shows a flowchart of a method for dilating the prostatic urethra, according to an embodiment.
DETAILED DESCRIPTION
[0072] Disclosed herein is a device that is configured to dilate the prostatic urethra by engaging with the three grooves of the prostatic urethra and exerting a radially outwards force upon deployment within the urethra. The device may be normally open, and made of a resilient material allowing it to laterally compress for fitting within a deployment lumen, and to laterally expand to a normally-open configuration upon extraction from the deployment lumen, and exert the outwards radial force that dilates the prostatic urethra upon deployment.
[0073] Figs. 1 through 5, wherein like parts are designated by like reference numerals throughout, illustrate a dilating device for the prostatic urethra, and a method of use according to the present invention. Although the present invention will be described with reference to the figures, it should be understood that many alternative forms can embody the present invention. One of ordinary skill in the art will additionally appreciate different ways to alter the parameters disclosed, such as the size, shape, or type of elements or materials, in a manner still in keeping with the spirit and scope of the present invention.
[0074] Reference is now made to Figs. 1A-B which illustrates a dilating device
100 for the prostatic urethra, from a perspective view and a top view, respectively, in accordance with an embodiment. Device
100 may comprise at least three laterally connected ridges
100a, 100b, 100c, each of which is configured to longitudinally engage with a different substantially longitudinal groove of the prostatic urethra of a patient. Device
100 may be normally-open, and may be configured to laterally compress, causing the distance between ridges
100a, 100b, 100c to decrease, thereby enabling the insertion of device
100 into the prostatic urethra in a compressed configuration, and to laterally expand to its normally-open configuration, causing the distance between ridges
100a, 100b, 100c to increase, upon deployment within the prostatic urethra. The lateral expansion of device
100 when deployed within the prostatic urethra may exert a radially outward force that causes ridges
100a, 100b, 100c to engage with the grooves of the urethra and push them outwards, thereby dilating the prostatic urethra, and allowing a free flow of a liquid, such as urine, to pass from the bladder through the urethra and out of the patient's body.
[0075] Peripheral ridges
100a, 100b may each be configured to engage with a different postero-lateral groove of the prostatic urethra, and central ridge
100c may be configured to engage with the anterior inter-lobar groove of the prostatic urethra.
[0076] Two distal connectors
100d, 100e may branch out from a V-shaped distal end of central ridge
100c and laterally connect to the distal ends of peripheral ridges
100a and
100b, respectively. Additionally, two proximal
100f, 100g may branch out from a proximal end of central ridge
100c and laterally connect to the proximal ends of peripheral ridges
100a, and
100b, thereby forming two closed forms that are joined at central ridge
100c. In one embodiment, proximal connectors
100f and
100g may branch out from a V-shaped proximal end of central ridge
100c, as illustrated in Fig. 1A. In the embodiment of Fig. 1A, connectors
100d, 100e, 100f, and
100g may be substantially S-shaped, forming a butterfly shape by device
100 when in the normally-open configuration, where proximal connectors
100f, and
100g may be configured for positioning towards the distal end of the prostate urethra..
[0077] Device
100 may be provided with two, or more distally positioned protrusions
102a and
102b that are configured to impinge against the postero-lateral side of the bladder neck, and prevent a migration of device
100 into the urinary bladder. Protrusions
102a and
102b may be integrally formed with distal connectors
100d, 100e, such as forming a portion of the S-shape of distal connectors
100d, 100e that are shown in Figs. 1A, 2.
[0078] Device
100 may additionally be configured for alignment within the prostatic urethra via two proximally disposed protrusions
104a and
104b that are provided with device
100 to releasably connect device
100 to an alignment mechanism provided with the deployment lumen, and which will be described in greater detail below. Protrusions
104a and
104b may be integrally formed with proximal connectors
100f, 100g. For example, an operator may be guided by an external marker provided with device
100, and apply a torque that is transferred to device
100 and that causes it to rotate, thereby aligning central ridge
100c with the anterior inter-lobar groove of the prostatic urethra.
[0079] Device
100 may be integrally formed, and may be made of a suitably flexible material, such as wire or cut foil made of a super-elastic alloy such as Nitinol. Alternatively, device may be made of a super-elastic polymer or biodegradable polymer. This memory-retaining flexibility may allow distal connectors
100d and
100e and proximal connectors
100f and
100g to bend in a manner that decreases the distance between ridges
100a, 100b and
100c, thereby compressing device
100 to enable its insertion into the prostatic urethra. Additionally, distal connectors
100d and 100e and proximal connectors
100f and
100g may be normally unbent, and may revert to their normally unbent configuration upon deployment within the prostatic urethra, thereby increasing the distance between ridges
100a, 100b and
100c and expanding device
100 to enable dilating the prostatic urethra.
[0080] Reference is made to Fig. IC, which shows a profile view of the device of Figs. 1A-B, according to an embodiment. The closed form that is formed by peripheral ridge
100b, central ridge
100c, distal connector
100e, and proximal connector
100g resembles a 'butterfly wing'. An identical and symmetric butterfly wing (not shown) is formed by peripheral ridge
100a, central ridge
100c, distal connector
100d, and proximal connector
100f.
[0081] Reference is now made to Fig. ID, which shows a frontal view of the device of Figs. 1A-B, according to an embodiment. When normally-open, S-shaped distal connectors
100d, 100e, comprising a distal end of device
100, may be configured to span an arc, such as a portion of a circle to dilate the prostatic urethra at the bladder neck.
[0082] In one embodiment, the shape of the device in the normally-open configuration may reside within the delimiting surface of a longitudinally oriented tube, such as a free-form longitudinally-oriented lumen. The shape of the lumen may be a cylinder, prism, or trunk-conical shape, to name a few, and may comprise a combination of shapes. For example, the lumen may have a cylindrical shape at the tubular ends, and a triangular prism shape at the midsection. The profile, or cross section of such shape may be circular ovoid, triangular, and may be uniform or may change in size and/or shape along the axial length. In the example given above, the cross-section at the ends of the open device may be circular due to the normally-open circular arc-shape of connector pairs
100d, 100e, and
100f, 100g, whereas the cross-section at the middle of 30 the device may be triangular due to the three ridges
100d, 100e, 100c that are 'pulled apart' by the normally open connectors. The device may have a varying cross-sectional size. For example, a portion of the device may reside within a fraction, such as 50%, 66%, or 75% of the longitudinally oriented tube.
[0083] Similarly, in the normally-open configuration, S-shaped proximally connectors
100f, 100g, comprising a proximal end of device
100 may be configured to reside within the circular delimiting surface of a cylinder to dilate the prostatic urethra at the proximal end of device
100.
[0084] The device may be shaped for residing within the prostate urethra and for positioning on the longitudinal axis between the external sphincter of the urethra distally and the bladder neck proximally.
[0085] In an embodiment, connectors
100d, 100e with ridge
100c may, in the normally-open configuration, may create an arc that exerts a lateral force on the lateral prostate lobes and dilates the prostate. Similarly, connectors
100f, 100g with
100c may create another arc that exerts a lateral force on the lateral prostate lobes and may dilate the prostate at a region situated distally. Thus, the device may provide two or more arcs that each exert a lateral force on a different region of the lateral prostate lobes. In another embodiment additional connectors (not shown), similar and substantially parallel to connectors
100d, 100e, 100f, and
100g, may be provided to laterally connect each peripheral ridge
100a, 100b, to the central ridge
100c at a point on each ridge that lies between the distal and proximal ends of the peripheral and central ridges
100a, 100b, 100c, such as at a midpoint along the ridge. The distance along the long axis of the device between any such pair of connectors may be between 0.5 cm to 3 cm, or more explicitly between 1 cm to 2 cm. The shape of the device in the normally-open configuration may reside within the delimiting surface of an longitudinally oriented tube, such as a free-form longitudinally-oriented lumen.
[0086] In an embodiment, the length of the device may range between 1 cm to 7 cm. There may be different sizes suitable for different lengths of prostate urethra.
[0087] In an embodiment, the diameter of the expanded device may be between 10 mm to 30 mm, and more explicitly between 15 mm and 25 mm.
[0088] In an embodiment, the device may be compressed to a minimal diameter of 0.5 mm to 3 mm and more explicitly of 1 mm to 2 mm.
[0089] In an embodiment, in case of a Nitinol device, the wire or ribs size may range from 0.2 to 0.8 mm and more explicitly between 0.3mm to 0.6 mm. In an embodiment, the dilating action of the device on the prostate urethra may be performed by the radial outward force exerted by the longitudinally oriented ridges on the prostate grooves and by an additional force exercised on the lateral lobes by the arc formed by the connection of components
100d, 100c, 100e, and the arc formed by the connection of components
100f, 100c, 100g.
[0090] In an embodiment, the components of the device, such as the ridges and connectors, or alternatively, the dilating means and connecting ridges of the device may be configured to maintain intimate contact with the mucosa of the prostate urethra when the device is in the open congifuration.
[0091] Alternatively, the arcs formed by connectors
100d, 100e, 100f, and
100g of device
100 may comprise at least two dilating means of the prostate urethra. Connectors
100d, 100e, 100f, and
100g may be connected with longitudinally oriented ridges
100a, 100b, and
100c that may be configured to fix the dilating means in place within the prostate urethra and prevent their movement or dislodgement.
[0092] In one embodiment, any of connectors
100d, 100e, 100f, and
100g may comprise closed rings, and any of connecting ridges may have an oblique or sinusoidal orientation. Reference is now made to Figs. 2A-B, which together show an exemplary deployment of a device for dilating a prostatic urethra, according to an embodiment. Fig. 3A shows a cross-section of prostatic urethra
200 that is obstructed by an enlarged prostate
202. Fig. 3B shows the cross-section of the prostatic urethra of Fig. 3A upon deploying a dilating device, in accordance with an embodiment of the invention. The three laterally connected ridges of the device that are illustrated at a midsection view along the axially oriented device and labeled as points
204a, 204b, and
204c, are shown in the normally-open configuration and engaged within the grooves of prostatic urethra 200, thereby dilating urethra
200 to allow a free passage of fluid therethrough.
[0093] Reference is now made to Figs. 3A-B which together illustrate an apparatus for deploying a dilating device for the prostatic urethra, in accordance with an embodiment. Fig. 3A shows a dilating device
300 in the normally-open configuration such as after deployment, and Fig 3B shows device
300 in the compressed configuration while housed within a deployment lumen
308, prior to deployment. The apparatus for deployment and the dilating device may be jointly referred to as a "kit".30 Turning to Fig. 3B, to deploy device
300, deployment lumen
308 may be retracted relative to device
300 to expose device
300 from the distal end
314 of lumen
308, allowing device
300 to protrude from lumen
308 and expand to its normally-open configuration, as shown in Fig. 4A. Upon protruding from lumen
308 and during the expansion of device
300, the ridges of device
300 may engage with the grooves of the prostatic urethra and cause it to dilate, as described above. To reposition device
300 within the prostatic urethra after its exposure from lumen
308, device
300 may be retracted relative to lumen
308, such as by pulling a string
312 that is releasably attached to device
300 and that is exposed from a proximal end of deployment lumen
308. The distal opening
314 of lumen
308 may press on the expanded ridges of device
300, causing device
300 to compress and allowing its retreat into lumen
308 where it may be housed for subsequent redeployment.
[0094] The retraction of either deployment lumen
308 or device
300 in relation to each other may be performed mechanically by a practitioner, such as via a work channel of a cystoscope, and which will be described in greater detail below.
[0095] Dilating device
300 may be provided with one or more proximally disposed protrusions
304a and
304b that are that may be integrally formed with the proximal end of device
300 and that are configured to releasably connect device
300 to an alignment mechanism
306 that is configured for being housed within deployment lumen
308.
[0096] Alignment mechanism
306 may comprise an alignment lumen
310 concentrically housed within deployment lumen
308, as well as releasable string
312. String
312 may lOOp through protrusions
304a and
304b of device
300 and may run through alignment lumen
310 and may be exposed from a proximal end of alignment lumen
310 for subsequent removal upon deployment of device
300. Device
300 may be configured for alignment within the prostatic urethra via a torque that is transferred from alignment mechanism
306 to device
300. For example, an operator may rotate alignment lumen
310 to align alignment lumen
310 with an externally provided alignment mark, thereby applying a torque to alignment lumen
310 that is transferred by alignment mechanism
306 to device
300 and causes device
300 to be aligned within the prostatic urethra.
[0097] Alternatively, referring to Figs. 4A-B a cystoscope
420 disposed with a work channel
422 may be used for deploying device
300 of Figs. 3A-B from the distal end
428 of cystoscope
420. Device
300 housed within deployment lumen
308 and optionally with alignment lumen
310 may be inserted into work channel
422. The deployment and alignment of device
300 may be controlled from a proximal end
428 of work channel
422.
[0098] In an embodiment, cystoscope
420 may be provided with a fluid delivery lumen and a balloon (not shown) that are configured to deliver a fluid to inflate the patient's bladder. The device may be configured for delivery into the inflated bladder, where it may be extracted from the deployment lumen to expand within the bladder, and then retracted for final deployment within the prostate urethra.
[0099] Reference is made to to Fig. 4B which shows a close-up view of distal end
428 of cystoscope
420, a camera
424 and illuminator
426 provided with cystoscope
420 may be utilized, in an embodiment, for aligning and deploying device
300 using conventional techniques. Deployment lumen
308 housing device
300 and alignment mechanism
306, and optionally the fluid delivery lumen and balloon, may be inserted into work channel
422 of cystoscope
420 and may be manipulated from a proximal end
428 of work channel
422 to deploy device
300 within the pro static urethra. The patient's bladder may be filled via the fluid delivery lumen and ballOOn, allowing deployment of device
300 within the prostatic urethra via the bladder.
[0100] Reference is now made to Fig. 5 which is a flowchart of a method for deploying a dilating device into a prostatic urethra.
[0101] The laterally compressed dilating device may by inserted into the urethra of a patient via a deployment lumen that is releasably connected to the device (Step
500). The patient's bladder may be filled according to conventional techniques, such as via a fluid delivery lumen disposed with a balloon (Step
502). The device may be extracted from the deployment lumen and inserted into the urinary bladder, such as by retracting 20 the deployment lumen relative to the device, and, upon exiting from the deployment lumen, the dilating device may expand to a normally-open configuration in the partially filled urinary bladder of the patient (Step
504). A torque may be applied to align the device via an alignment mechanism connected to the device, such as by rotating an alignment lumen of the alignment mechanism and transferring the torque to the device, where alignment may comprise aligning a central ridge of the device for engaging with the anterior inter-lobar groove of the prostatic urethra and aligning two peripheral ridges of the device to each engage with a different postero-lateral groove of the prostatic urethra (Step
506). The application of the torque may be guided via a cytoscope, or alternatively, via an external mark indicating that the device is aligned. The aligned device may be positioned in the prostate urethra, such as by pulling on the deployment mechanism to draw the device in from the bladder into the prostate urethra (Step
508). Two protrusions disposed at the distal end of the device may be caused to impinge against the postero-lateral side of the bladder neck, thereby securing the position of the device, and preventing a migration of the device into the urinary
bladder (Step
510). The device, thus deployed and aligned within the prostatic urethra, may exert an outwards radial force that pushes the inter-lobar grooves of the urethra outwards, and dilate the urethra (Step
512).
[0102] If the positioning or alignment of the device is incorrect, the device may be retracted relative to the deployment lumen, causing the device to laterally compress and retreat within the deployment lumen (Step
514). The retreated device may be repositioned or realigned within the prostatic urethra and redeployed (Steps
504-512). If the positioning and alignment of the device is correct, The device may be disconnected from the deployment and alignment lumens (Step
518), such as by removing a string that releasably connects the device to the alignment lumen.
[0103] Numerous modifications and alternative embodiments of the present invention will be apparent to those skilled in the art in view of the foregoing description. Accordingly, this description is to be construed as illustrative only and is for the purpose of teaching those skilled in the art the best mode for carrying out the present invention. Details of the structure may vary substantially without departing from the spirit of the present invention, and exclusive use of all modifications that come within the scope of the appended claims is reserved. Within this specification embodiments have been described in a way which enables a clear and concise specification to be written, but it is intended and will be appreciated that embodiments may be variously combined or separated without parting from the invention. It is intended that the present invention be limited only to the extent required by the appended claims and the applicable rules of law.
[0104] It is to be understood that the following claims are to cover all generic and specific features of the invention described herein, and all statements of the scope of the invention which, as a matter of language, might be said to fall therebetween.
Examples
[0105]
- 1. A dilating device for the prostatic urethra, the device comprising:
at least three, laterally connected longitudinal ridges,
wherein each ridge is configured to longitudinally engage with a different substantially longitudinally groove of the prostatic urethra of a patient,
and wherein the at least three laterally connected ridges are configured to laterally compress to enable insertion into the prostatic urethra in a compressed configuration,
and wherein the at least three laterally connected ridges are configured to laterally expand to a normally-open configuration upon deployment within the prostatic urethra, to exert a radially outwards force that dilates the prostatic
urethra.
- 2. The device of example 1, wherein the at least three laterally connected ridges comprise two peripheral ridges that are each configured to engage with a different postero-lateral groove of the prostatic urethra, and a central ridge that is configured to engage with the anterior inter-lobar groove of the prostatic urethra.
- 3. The device of example 2, further comprising one or more connectors that laterally connect each peripheral ridge to the central ridge.
- 4. The device of example 3, wherein the one or more connectors laterally connect each peripheral ridge to the central ridge at a point on each ridge that lies between the distal and proximal ends of the peripheral and central ridges.
- 5. The device of example 3, wherein the one or more connectors comprise two distal connectors that laterally connect a distal end of each peripheral ridge to a distal end of the central ridge, and two proximal connectors that laterally connect a proximal end of each peripheral ridge to a proximal end of the central ridge, thereby forming two closed forms joined at the central ridge.
- 6. The device of example 5, wherein the two closed forms comprise lengthwise oriented ovoid loops that together form a figure-eight shape in the normally- open configuration.
- 7. The device of example 5, wherein the two closed forms form two substantially rectangular shapes that span two substantially non-parallel planes in the normally-open configuration.
- 8. The device of example 5, wherein the two distal connectors are substantially S-shaped, and are configured to span a portion of a cylinder in the normally-open configuration, thereby dilating the prostatic urethra at the bladder neck.
- 9. The device of example 5, wherein the two proximal connectors are substantially S-shaped, forming a butterfly shape by the device in the normally-open configuration.
- 10. The device of example 1, wherein all the at least three laterally connected ridges and one or more connectors are configured to maintain intimate contact with the prostate urethra mucosa.
- 11. The device of example 1, further comprising two or more distally positioned protrusions that are configured to impinge against the postero-lateral side of the bladder neck, thereby preventing a migration of the device into the urinary bladder.
- 12. The device of example 1, wherein the at least three laterally connected ridges are composed of wire.
- 13. The device of example 1, wherein the at least three laterally connected ridges are composed of cut foil.
- 14. The device of example 1, wherein the at least three laterally connected ridges are composed of super-elastic alloy.
- 15. The device of example 1, wherein the at least three laterally connected ridges are composed of super-elastic polymer.
- 16. The device of example 15, wherein the super-elastic polymer is a biodegradable polymer.
- 17. The device of example 1, wherein the device is configured to allow free passage of a liquid when deployed in the prostatic urethra.
- 18. The device of example 1, wherein the shape of the device is configured to reside within the prostate urethra.
- 19. The device of example 1, wherein the at least three, laterally connected ridges are further configured to laterally compress for fitting within a deployment lumen, laterally expand to a normally-open configuration upon extraction from the deployment lumen, and
exert the outwards radial force upon deployment within the prostatic urethra. - 20. The device of example 19, wherein the deployment lumen is configured to be housed within a work channel of a cystoscope.
- 21. The device of example 19, wherein the deployment lumen is further provided with a fluid delivery lumen and balloon that are configured to deliver a fluid to the bladder to allow deploying the device within the prostatic urethra via the bladder.
- 22. The device of example 19, wherein the at least three, laterally connected ridges are provided with one or more proximally disposed protrusion that are configured to releasably connect the device to an alignment mechanism housed within the deployment lumen.
- 23. The device of example 22, wherein the alignment mechanism comprises a releasable string that loops through the protrusions and runs through an alignment lumen.
- 24. The device of example 22, wherein the device is configured for alignment within the prostatic urethra via a torque that is transferred from the alignment mechanism.
- 25. A method for dilating a prostatic urethra, the method comprising:
inserting a dilating device into the urethra of a patient;
aligning the dilating device within the prostatic urethra;
positioning the dilating device within the prostatic urethra of the patient; and
deploying the dilating device within the prostatic urethra, thereby causing the dilating device to:
expand to a normally-open configuration,
engage with the grooves of the prostatic urethra,
exert a radially outwards force on the prostatic urethra, and
dilate the prostatic urethra.
- 26. The method of example 25, wherein positioning comprises extracting the device from a deployment lumen and inserting the device into the urinary bladder of the patient.
- 27. The method of example 26, wherein positioning comprises drawing the device from the bladder into the prostate urethra.
- 28. The method of example 25, wherein aligning comprises transferring a torque applied to an alignment mechanism connected to the device.
- 29. The method of example 25, wherein the torque is applied by rotating an alignment lumen that is connected to the device.
- 30. The method of example 25, wherein aligning comprises positioning a central ridge of the device for engaging with the anterior inter-lobar groove of the prostatic urethra and positioning two peripheral ridges of the device to each engage with a different postero-lateral groove of the prostatic urethra.
- 31. The method of example 25, further comprising causing the device to laterally compress and retreat within the deployment lumen if the alignment or position of the device is incorrect.
- 32. The method of example 25, further comprising causing the device to impinge against the postero-lateral side of the bladder neck, thereby preventing a migration of the device into the urinary bladder.
- 33. The method of example 25, further comprising disconnecting the device from a deployment lumen provided to deploy the device.
- 34. The method of example 25, further comprising applying a positioning balloon to secure the position of the deployed device.
- 35. A kit for dilating a prostatic urethra, the kit comprising:
a deployment lumen; and
a dilating device which comprises:
at least three, laterally connected ridges,
wherein each ridge is configured to vertically engage with a different substantially vertical groove of the prostatic urethra of a patient,
and wherein the at least three laterally connected ridges are configured to laterally compress to enable insertion into the prostatic urethra, in a compressed configuration, through said deployment lumen,
and wherein the at least three laterally connected ridges are configured
to laterally expand to a normally-open configuration upon deployment from said deployment lumen into the prostatic urethra, to exert a radially outwards force that dilates the prostatic urethra, expand to a normally-open configuration upon deployment from said deployment lumen into the prostatic urethra,
- 36. The kit of example 35, wherein the at least three, laterally connected ridges are provided with one or more proximally disposed protrusion that are configured to releasably connect the device to an alignment mechanism housed within the deployment lumen.
- 37. The kit of example 36, wherein the alignment mechanism comprises a releasable string that loops through the protrusions and runs through an alignment lumen.
- 38. The kit of example 36, wherein the device is configured for alignment within the prostatic urethra via a torque that is transferred from the alignment mechanism.
- 39. The kit of example 35, wherein the deployment lumen is configured to be housed within a work channel of a cystoscope.
- 40. The kit of example 35, wherein the deployment lumen is further provided with a balloon that is configured to position the device within the within the prostatic urethra.
- 41. The kit of example 35, wherein the at least three laterally connected ridges comprise two peripheral ridges that are each configured to engage with a different postero-lateral groove of the prostatic urethra, and a central ridge that is configured to engage with the anterior inter-lobar groove of the prostatic urethra.
- 42. The kit of example 41, further comprising one or more connectors that laterally connect each peripheral ridge to the central ridge.
- 43. The kit of example 42, wherein the one or more connectors laterally connect each peripheral ridge to the central ridge at a point on each ridge that lies between the distal and proximal ends of the peripheral and central ridges.
- 44. The kit of example 42, wherein the one or more connectors comprise two distal connectors that laterally connect a distal end of each peripheral ridge to a distal end of the central ridge, and two proximal connectors that laterally connect a proximal end of each peripheral ridge to a proximal end of the central ridge, thereby forming two closed forms joined at the central ridge.
- 45. The kit of example 44, wherein the two closed forms comprise lengthwise oriented ovoid loops that together form a figure-eight shape in the normally-open configuration.
- 46. The kit of example 44, wherein the two closed forms form two substantially rectangular shapes that span two substantially non-parallel planes in the normally-open configuration.
- 47. The kit of example 44, wherein the two distal connectors are substantially S- shaped, and are configured to span a portion of a cylinder in the normally-open configuration, thereby dilating the prostatic urethra at the bladder neck.
- 48. The kit of example 44, wherein the two proximal connectors are substantially S-shaped, forming a butterfly shape by the device in the normally-open configuration.
- 49. The kit of example 35, wherein all the at least three laterally connected ridges and one or more connectors are configured to maintain intimate contact with the prostate urethra mucosa.
- 50. The kit of example 35, further comprising two distally positioned protrusion that are configured to impinge against the postero-lateral side of the bladder neck, thereby preventing a migration of the device into the urinary bladder.
- 51. The kit of example 35, wherein the at least three laterally connected ridges are composed of wire.
- 52. The kit of example 35, wherein the at least three laterally connected ridges are composed of cut foil.
- 53. The kit of example 35, wherein the at least three laterally connected ridges are composed of super-elastic alloy.
- 54. The kit of example 35, wherein the at least three laterally connected ridges are composed of super-elastic polymer.
- 55. The kit of example 54, wherein the super-elastic polymer is a biodegradable polymer.
- 56. The kit of example 35, wherein the device is configured to allow free passage of a liquid when deployed in the prostatic urethra.
- 57. A dilating device for the prostatic urethra, the device comprising:
at least two dilating means of the prostate urethra,
wherein the dilating means are connected by ridges that are configured to fix the dilating means in place within the prostate urethra and prevent their movements or dislodgement
and wherein the dilating means are configured to laterally expand to a normally-open configuration upon deployment within the prostatic urethra, to exert a lateral outwards force that dilates the prostatic urethra.
- 58. The dilating device of example 57, wherein the dilating means comprise arcs that exert lateral forces on the lateral lobes.
- 59. The dilating device of example 57, wherein the dilating means comprise rings.
- 60. The dilating device of example 57, wherein the shape of the device in a normally open configuration is configured to reside within a delimiting surface of a longitudinally oriented tube.
- 61. The device of example 57, wherein the device is shaped to reside within the prostate urethra.
- 62. The device of example 57, wherein the dilating means and connecting ridges of the device are configured to maintain intimate contact with the prostate urethra mucosa.