Urethral catheterless radical prostatectomy

Abstract

A method and device for facilitating the anastomotic healing of a patient after a radical prostatectomy surgical procedure, without a urethral catheter, comprising the steps of performing a radical prostatectomy, fixedly positioning a splinting element between the urethra and the bladder, across the urethral opening, placing the splinting element during the performing of the radical prostatectomy and prior to surgical closure. The fixed positioning is effected from a position within the bladder with anchoring the splinting element in position relative to the interior of the bladder, setting a separate urine drainage tube, and removing the splinting element, after anastomotic healing, with a retrieval element on the splinting element or with dissolving of the splinting element.

Claims

1. A splinting element for facilitating anastomotic healing of a male patient after a radical prostatectomy, comprising: an elongated cylinder having a diameter ranging from about 5 mm to about 10 mm, wherein the splinting element is configured to be positioned across a urethral opening between a urethra and bladder of the patient, wherein the elongated cylinder of the splinting element is sized and dimensioned for positioning across the urethral opening between the urethra and bladder of a male patient, wherein the elongated cylinder is hollow and formed to have an open end and an opposing closed end, wherein the splinting element further comprises a wing element providing the splinting element a diameter greater than a diameter of the urethral opening, wherein the wing element is attached to the open end of the elongated cylinder, wherein the splinting element prevents urine drainage therethrough, and wherein a suture is attached to the wing element that allows the splinting element to be sutured to an inner wall of the bladder.

2. The splinting element of claim 1, wherein the splinting element has a length ranging from about 30 to about 35 mm.

3. The splinting element of claim 1, further comprising a retrieval line having a sufficient length to pass through and out of the urethra when positioned across the urethral opening, wherein the retrieval line is attached to the closed end.

4. The splinting element of claim 1, wherein the wing element is integrally formed with the elongated cylinder.

5. The splinting element of claim 1, comprising an inert material.

6. The splinting element of claim 5, wherein the inert material comprises a bio-absorbable material.

7. The splinting element of claim 1, capable of being used with a separate urine drainage tube.

8. The splinting element of claim 1, wherein the open end is configured to be inserted proximate to the bladder relative to the opposing closed end.

Description

SHORT DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is a schematic cross sectional view of a bladder during a prostatectomy and placement of a splinting tube of the present invention and the position of a separate urine drainage tube, and

(2) FIG. 2 is a second embodiment of the splinting tube with anchoring wings.

(3) FIG. 3 shows a cross-sectional view of an embodiment of the splinting element.

DETAILED DESCRIPTION OF THE INVENTION AND DRAWINGS

(4) In accordance with the present invention the discomfort, pain and embarrassment of a urethral catheter is effectively eliminated by the combination of a drainage tube or suprapubic catheter commonly utilized for fluid drainage, in combination with a separate splinting element. The splinting element is emplaced with fixed anchoring suturing without additional surgery, during the prostatectomy procedure with forceps already within the bladder for the prostatectomy. Preferably, the drainage tube is positioned at the same time as well.

(5) The material of the splinting element is preferably comprised of an inert material and the connecting sutures which anchor the splinting element to the bladder are of bioabsorbable materials such as used with drug eluting stents, MUSE, and antibiotic coatings used for penile prosthesis. The splinting element is made with structural integrity and the ability to resist stricture forces exerted thereon. The splinting element or tube is dimensioned and positioned to form a liquid tight external seal at the urethral opening and is closed ended to prevent external urinary leakage. The splinting element is preferably comprised of inert flexible materials such as of latex or silicone. Removal of the splinting element is effected by absorption of the anchoring sutures within the body after the seven day healing period. A retrieval line is attached to the tube, preferably to the closed end. At the appropriate time, the line, which is thin and extended through the urethra with minimal discomfort, is pulled to remove the splinting tube from the suturing anchor and to draw it from the urethral opening and through the urethra for full removal.

(6) A hollow, close ended tube is preferred for the splinting element since the hollow can readily retain anchoring knotting of the removing line (which insures that the line does not disengage from the tube during withdrawal of the splinting device). In addition, a hollow tube provides for greater control and minimized. Solid tubes made of appropriate materials may however also be used in the effecting of anastomotic healing. An appropriate tube size is one with a diameter of about 5-10 mm (a bevel gradation in diameter may facilitate initial placement) and a length of about 30-35 mm. Though more difficult to work with than hollow tubes, the solid cylindrical configuration may also be used with appropriate connection of the retrieval line to the solid material. A suturing line to the interior of the bladder is used to anchor the splinting elements from being dislodged as a result of urine pressure. The same urine pressure however eliminates any need for preventing the splinting element from being dislodged inwardly. Alternatively, the splinting element itself may be comprised of a bio-absorbable or dissolving material which results, in time, with automatic self removal, without the necessity of a retrieval line.

(7) In another embodiment a splinting element with wing elements may be used anchor the splinting element in place, with the wings preventing outward dislodgement. The wings are sutured to the inner walls of the bladder, with bio-absorable sutures.

(8) There are several theoretical advantages of the approach of the present invention including early ambulation and reduced risk of urethral stricture. Use of a conventional urethral catheter is painful during first few days and often moves with the thigh movement. This movement causes more pain at the penis and may possibly be an impediment for early ambulation. All the patients with the catheterless approach of the present invention did not have penile pain and were quite ambulatory following surgery. This early ambulation may pay many dividends in terms of reduced risk for deep vein thrombosis and enhanced overall sense of well being. It was discovered that the most significant benefits included less penile tip and shaft pain and less discomfort in the postoperative period as compared to the standard method. The patients had earlier return to a normal functional status and earlier return to normal activity.

(9) The device in the procedure of the present invention serves two purposes a) to splint the anastomosis and b) to divert urine. In order to avoid the urethral route, several custom made prototypes were tried in human cadaveric experiments which entered the bladder anteriorly and had a distal elongated splint to bridge the anastomosis. The final prototype had a suprapubic drainage tube with a retention mechanism, drainage holes for diverting urine from the bladder and a distal splinting tip to keep the anastomosis patent. This tube was easy to deploy during surgery and to remove after 7 days.

EXAMPLE

(10) A pilot study was undertaken for the procedure and device of the present invention involving a total of 30 patients (10 subjects and 20 controls), who completed 6 months follow-up.

(11) This was a prospective, non-randomized pilot study to evaluate the feasibility of the urethral catheterless technique in patients undergoing robotic prostatectomy. Over a period of three month, the feasibility of the urethral catheterless approach was tested in 10 patients who specifically requested this modification and signed an informed consent. The data were compared with 20 contemporary patients who did not undergo this modification.

(12) Eligibility criteria—Patients with early prostate cancer who were scheduled to undergo robotic prostatectomy were candidates for this procedure. Patients who had large prostate volumes (>75 cc), median lobe, high body mass index (>30), high risk cancers (Gleason-8, 9 and 10, clinical stage T3 and beyond) and patients with relatively abnormal coagulation parameters were excluded from this pilot study.

(13) Preoperative, intraoperative and postoperative data were collected prospectively. The duration of the catheterization was 7 days in all 30 patients.

(14) The study was used to: 1) evaluate the technique of urethral catheterless robotic radical prostatectomy using this modification, 2) to compare the immediate outcome of the catheterless approach with the standard technique of robotic prostatectomy in terms of discomfort, pain, penile tip irritation, need for urethral catheterization and clot retention, 3) evaluate early urinary continence between two groups and 4) measure the incidence of 6 month bladder neck contracture rates.

(15) Preoperative, intraoperative and postoperative data were collected prospectively. The duration of the catheterization was 7 days in all 30 patients.

(16) Outcomes Measurement:

(17) Demographic, laboratory, oncological, intraoperative and outcomes data were measured and entered in an IRB approved database. Urethral symptoms were recorded using a specifically developed questionnaire. The questionnaire comprised 12 questions pertaining to a) pain at suprapubic site, in penile shaft and penile tip, testicular pain and use of pain medications; b) discomfort while walking and sleeping c) fever; d) erosion/encrustation at tip of penis; e) bladder spasms.

(18) Additional 3.sup.rd party telephone interviews were conducted at 10, 14, 21 and 30 days to determine early continence status. Patients were considered continent if they were either using 0 pad or 1 security liner during stressful activities. International Prostate Symptom Scores (IPSS) were obtained preoperatively and at 1, 3 and 6 months postoperatively.

(19) Technique of Robotic Prostatectomy:

(20) All patients underwent the athermal trizonal nerve sparing technique of robotic prostatectomy with total reconstruction of the continence mechanism. The continence preservation technique involves seven key elements: (i) Preservation of the puboprostatic ligaments and arcus tendineus; (ii) Creation of a muscular flap behind the bladder neck (which is later sutured to the distal end of Denonvilliers' fascia behind the sphincter); (iii) Control of the dorsal venous complex using a puboprostatic ligament sparing suture which also provides anterior suspension; (iv) Preparation of a thick and long urethral stump during apical dissection; (v) The ‘Pagano principle’, reinforcing of the flap behind the bladder neck; (vi) The ‘Rocco principle’, suturing of the retrotrigonal flap to the distal end of Denonvilliers' fascia, close to the urethral stump, to prevent caudal retraction of the central tendon, thus providing posterior support; and (vii) Re-attachment of the arcus tendineus and puboprostatic plate to the bladder neck after anastomosis is completed.

(21) Technique of Deployment of Device and Anastomosis:

(22) Urethrovesical anastomosis was performed in multiple layers using two 3-0 monocryl sutures on a RB needle. Once the two posterior layers of anastomosis were completed, (Rocco stitch followed by posterior bladder) the device was introduced through a suprapubic puncture made under direct vision and entered the bladder 2-3 inches proximal to the bladder neck and advanced the distal attached tip of the device through the anastomosis. It took 2-3 minutes to complete this phase of the surgery and the anterior anastomosis was completed in two layers (bladder followed by reconstruction of the puboprostatic-arcus tendineus complex).

(23) Post Operative Care:

(24) On the 7.sup.th day, the suprapubic device was removed following a cystogram. The degree of pain, discomfort and bother were assessed by a self administered questionnaire.

(25) Statistical Analysis:

(26) The data were entered into an Excel spreadsheet and the chi-square test and Student t test were applied to compare the group characteristics as well as the incidence of complications between the groups, with critical values and statistical significance at P<0.05.

(27) Results:

(28) Group 1 was the study group of 10 patients in whom robotic radical prostatectomy was performed using catheter less approach. Group 2 comprised of 20 age, tumor stage, and prostate volume matched patients undergoing the conventional urethral catheterization technique performed in same time period. The two groups were also comparable in terms of console times, amount of bleeding, or volume of blood transfusion (0), anastomotic leakage (0) and post operative retention rates (0) (P>0.05). In Group 1 which was the study group of 10 subjects, we used a custom made suprapubic catheter which provided a small anastomotic splint, two balloons to prevent either upward or downward migration, multiple holes for drainage and the ability to retract the splint to give a voiding trial before removing the drainage device. Group 2 was the control group of 20 patients in whom standard urethral catheterization was performed with an 18F Silastic Foley catheter. Demographic, intraoperative and outcomes data were measured and entered in an IRB approved database. Urethral symptoms were recorded using a specially developed questionnaire.

(29) These values are shown in Table 1.

(30) TABLE-US-00001 TABLE 1 Baseline, intraoperative and post operative outcomes in two matched cohorts MEAN (RANGE) GROUP 2 GROUP 1 (N = 20) (N = 10) URETHRAL CATHETER CATHETER P VARIABLES LESS COHORT VALUE BASELINE PARAMETERS AGE 60.76 (52.8-67.3) 59.99 (55.8-66.3) NS BMI 26.10 (22.9-33.2)  27.25 (23.08-34.16) NS Serum (PSA) ng/ml 4.2 (2-6.8)    5.5 (3.2-12.1) NS IPSS Prostate Volume ml Biopsy Gleason NS score 2-6 8 8 7 (3 + 4) 2 2 7 (4 + 3) — — 8-10 — — Clinical stage NS T1b — — T1c 9 9 T2a 1 1 T2b — — T3 INTRA- NS OPERATIVE PARAMETERS Estimated Blood 170  155  NS loss (cc) Console time in  80 (52-108)  78 (46-110) NS minutes Extra time for  3 (2-5) — NS procedure (minutes) Intraoperative blood Nil Nil NS transfusion POST OPERATIVE NS PARAMETERS Pathological Stage NS T2a 1 2 T2b 1 — T2c 7 8 T3a 1 — Duration of 7 7 NS catheterization or device removal (days) Clinical urinary leak Nil Nil NS Post operative Nil Nil NS retention Bladder neck Nil Nil NS contracture

(31) As is seen in the table 2, most patients achieved continence in 6-12 weeks. The catheter-less group had a greater percentage of patients who became continent almost immediately, however this was not statistically significant (50% v/s 20% p=0.09).

(32) TABLE-US-00002 TABLE 2 Continence outcomes in two cohorts of patients (0 pad status) Group 1 Group 2 P Zero pad status N = 10 N = 20 value Continence within 1 6 (50%)  4 (20%) <0.5 week Continence within 6 10 (100%) 16 (80%) NS weeks Continence within 12 10 (100%) 18 (98%) NS weeks

(33) Table 3 summarizes data regarding pain, discomfort and early ambulation. No patient in group 1 had pain in penile shaft or tip as compared to 18/20 patients in group 2. (p<0.05)). 2 patients in group 1 complained of minimal pain at the suprapubic puncture site. 2 patients in group 1 had discomfort walking and sleeping as compared to 14 patients in group 2 (p<0.05) and 3 patients in group 1 had bladder spasms compared to 8 patients in group 2. No patient either group had hematuria or clot retention requiring irrigation. No patient in either group had symptoms suggestive of a bladder neck contracture at 6 months follow-up.

(34) TABLE-US-00003 TABLE 3 Pain and discomfort outcomes Group 1 Group 2 P n = 10 n = 20 value Pain at site of 2 18 <0.5 Suprapubic catheter or penile shaft Pain at tip of 0 10 <0.5 penis Erosion at penile 0 5 <0.5 tip Discomfort 2 14 <0.5 walking and sleeping
Conclusions:

(35) Urethral catheterless robotic radical prostatectomy is feasible. The advantages are decreased penile shaft and tip pain and decreased patient discomfort and an earlier return of continence. In this pilot study there was no late term complication such as bladder neck contracture.

(36) Results:

(37) The two groups were comparable in terms of age, serum prostate specific antigen (PSA) values, body mass index (BMI), Gleason scores, tumor stage, operating time, amount of bleeding, console times, anastomotic leakage and post operative retention rates. The study group had significantly less penile shaft or tip pain and discomfort during walking or sleeping. No patient in either group had hematuria or clot retention requiring irrigation.

(38) With reference to the drawings, In FIG. 1, the interior of bladder 10, is shown during a robotic prostatectomy procedure. Laparoscopically inserted forceps 20 carry and position splinting element 30, shown as a tube formed of medical grade latex with a closed forward end 30a and a removal string 31 sutured to the forward end 30a. The inner or distal end 30b (or an extension thereof as shown) is provided with suture material 32. Forceps 20 position the splinting element 30 across the anatomotic opening 11 between the bladder 10 and the urethra 12.

(39) The removal string 31 is snaked through the urethra for external access when necessary for removal of the splinting tube. During surgery a Foley catheter is placed through the urethra 12 to assist in anastomosis. At the end, before anastomotic stitches are tied, the Foley catheter is pulled outside through the anterior gap in anastomosis and string 31 is tied through the tip of the Foley catheter. The Foley catheter is pulled out (with string) and the string then protrudes outside the urethra. Splinting element 30 is positioned across the anastomosis and is secured using a 4-O Chromic catgut to the bladder wall (which dissolves over net few days). Anastomosis is closed once a suprapubic catheter 40 is properly positioned.

(40) Suture material 32 is sutured to an internal wall of the bladder to anchor the splinting element 30, once positioned. The separate suprapubic drainage catheter 40 is positioned through a wall of the bladder 10 for urine drainage.

(41) The splinting element with integral anchoring members is shown in FIG. 2. The splinting element 33 is provided with wing elements 34a and 34b which are used with the suture material 32. The wing elements 34a and 34b engage the bladder wall, peripheral to the bladder opening to provide an anchor for the splinting element 33. The splinting element 33 is removed by the dissolving of the sutures holding the wing element 34a and 34b and by pulling the splinting element through the urethra with the string 31 as in the first embodiment. Alternatively, splinting elements 30 and 33 may be comprised of a self dissolving material whereby the bladder “plug” is automatically opened over time without need for a retrieval line or string. It is however preferred, for ensuring removal, that the splinting element be provided with externally accessible retrieval means such as string 31.

(42) It is understood that the above Example and description of the preferred embodiment are exemplary of the present invention and that changes in material, components, structure, method steps and the like may be made without departing from the scope of the present invention as defined in the following claims.