Surgery for Posterior Urethral Valves
ROSALIA MISSERI
KENNETH I. GLASSBERG
A posterior urethral valve (PUV) is the most common cause of congenital bladder outlet obstruction in boys. It is associated with a dilated posterior urethra, poor urinary stream, and incomplete bladder emptying. Bilateral hydroureteronephrosis of varying degrees is almost always present and frequently accompanied by vesicoureteral reflux and/or bladder diverticula.
DIAGNOSIS
With the widespread use of antenatal ultrasound, PUVs are often diagnosed prenatally. The condition is suspected in utero when a male fetus is found to have bilateral hydroureteronephrosis and a thick-walled bladder that does not empty completely on sonography. In addition, there may be a keyhole deformity noted on sonography. This is noted when a dilated bladder and posterior urethra is seen. In severely affected fetuses, oligohydramnios, pulmonary hypoplasia, and Potter syndrome may occur. Newborns may present with abdominal masses representing a distended bladder or hydronephrotic kidney, dry diapers, nonspecific gastrointestinal symptoms, respiratory distress, or urinary ascites. Younger boys usually present with urinary tract infection, respiratory distress, abdominal distention, sepsis, or azotemia, while older boys may present with dysfunctional voiding symptomatology, incontinence, poor urinary stream, urinary tract infections, or hematuria.
If a PUV is suspected in an infant based on antenatal ultrasound evaluation, prophylactic antibiotics should be initiated, and the bladder should be drained with a 5Fr or 8Fr feeding tube securely taped in place with a clear transparent dressing. Positioning is best confirmed with an abdominal radiograph as the tube may coil in the dilated posterior urethra. The feeding tube is left in place until a voiding cystourethrogram (VCUG) is obtained to make the diagnosis. A baseline postnatal ultrasound is routinely obtained to evaluate the renal parenchyma and degree of hydronephrosis. Serum chemistries, blood urea nitrogen and creatinine, should be obtained after 24 hours of life because labs in the first 24 hours reflect the mother’s serum values. In patients with severe hydroureteronephrosis and/or azotemia, the catheter should be left in place until the azotemia resolves/stabilizes and hydroureteronephrosis improves.
The VCUG of a boy with a PUV will reveal a posterior urethra that appears dilated, often taking on a “shield shape” or squared-off appearance. The bladder neck is often clearly demarcated and may appear as a thick collar, and the urethra distal to the obstruction will appear less full or more narrow than normal (Fig. 97.1). Vesicoureteral reflux may be present in about 25% to 50% of boys with vesicoureteral reflux and is most often related to bladder outlet obstruction due to PUVs (1,2,3,4).
INDICATIONS FOR SURGERY
Although some controversy still exists as to what to do once the bladder has been drained with a catheter, almost all valves are currently treated with transurethral ablation (Fig. 97.2). For severe hydronephrosis, some report better long-term outcomes when these infants are temporarily diverted, while most feel that primary valve ablation is the treatment of choice (5). For those who believe temporary diversion is best, many methods of vesical and supravesical diversion of the obstructed bladder exist.
ALTERNATIVE THERAPY
There is no effective alternative to surgical therapy. Antenatal attempts at valve ablation, transurethral stenting, and percutaneous vesicoamniotic shunting are offered at few select centers and remain quite controversial.
SURGICAL TECHNIQUE
Transurethral Valve Ablation
Valve ablation is most commonly accomplished transurethrally. The size of the infant’s fossa navicularis usually limits the size of cystoscope that may be used. Typically, a 7.5Fr or 8.5Fr scope is used in infants, while a larger scope may be used
in older children. The cystoscope should be well lubricated and advanced under direct vision. Gentle dilation of the distal urethra may be required to advance the cystourethroscope. With the bladder full and applying gentle suprapubic pressure, the valve leaflets are more easily seen coming off the verumontanum and extending distally to fuse anteriorly (Fig. 97.3). The goal of valve ablation is to disrupt the leaflet, hence destroying the obstruction.
in older children. The cystoscope should be well lubricated and advanced under direct vision. Gentle dilation of the distal urethra may be required to advance the cystourethroscope. With the bladder full and applying gentle suprapubic pressure, the valve leaflets are more easily seen coming off the verumontanum and extending distally to fuse anteriorly (Fig. 97.3). The goal of valve ablation is to disrupt the leaflet, hence destroying the obstruction.
A PUV may be ablated or incised in several ways. The decision to proceed with one technique over another is often based on surgeon preference, availability of equipment, and the size of the child’s urethra. The valve may be ablated using a 3Fr Bugbee electrode through a cystoscope. Alternatively, the wire insert of a 3Fr ureteral catheter with the distal end connected to electrocautery may be used. All but the tip of the wire is insulted by the catheter to avoid thermal injury. Once in position, the Bugbee or wire is advanced and pushed into the valve at the 5 and 7 o’clock positions while employing a cutting current of 20 to 25 W. (Note that power settings may vary from machine to machine.) When using cautery, care must be taken to ensure that thermal energy is targeted at the valves alone. The holmium:YAG laser may also be used to incise the valves (6). These techniques may be particularly useful if the infant resectoscope is too large for the child’s urethra.
When using a small pediatric resectoscope, the valves are incised with a right-angle hook, loop electrode, or hook-shaped cold knife. When using a loop electrode, a narrow, more oblong loop is preferable to a wider, more circular loop. Some debate exists as to the best location for valve incision. Williams et al. (4) preferred incising at the 12 o’clock position, while Gonzales (7) advocated cutting at the 4, 8, and 12 o’clock positions. However, many prefer incising at the 4 to 5 o’clock and 7 to 8 o’clock positions using a hook-shaped cold knife or with the cutting current set at 20 to 25 W pure cut.
Additional methods of PUV ablation have also been described for use in patients with small-caliber urethras that do not allow passage of even the smallest cystoscope. With the advent of smaller scopes, perineal urethrostomy is now rarely necessary for valve ablation. Zaontz and Firlit (8) have described percutaneous antegrade ablation of PUV as well as antegrade incision of PUV in infants with small-caliber urethras. At our institutions, small or premature infants who are critically ill and cannot be successfully catheterized have had percutaneous suprapubic catheters placed at the bedside.
Once the valves are endoscopically ablated, the bladder should be cystoscoped to evaluate for diverticula, trabeculations, and the appearance of the ureteral orifices. A full stream should be noted at the end of the procedure while applying gentle pressure to the suprapubic area. A small urethral catheter is left in place for 1 to 2 days following the procedure or until an elevated creatinine nadirs. Repeat serum electrolytes and creatinine should be obtained 24 hours after catheter removal while the boy is still hospitalized. A renal ultrasound is useful in the postoperative period to evaluate for improvements in hydronephrosis. Its timing should be dictated by the surgeon’s level of concern. A VCUG may be performed after the catheter is removed to assess the success of the procedure. Timing of the VCUG is determined by the surgeon based on his or her confidence in the adequacy of ablation. The urethra, degree of reflux, and bladder appearance should be evaluated on VCUG. A VCUG and urodynamics or preferably videourodynamics should be delayed no longer than 6 to 8 weeks after ablation. If there is suspicion of inadequate ablation or continued obstruction, “second-look” cystoscopy with ablation of residual leaflets should be considered. Some have recommended routine cystoscopy a few weeks after valve ablation because of the high incidence of residual obstruction (9).
Follow-up renal ultrasound and serum creatinine and electrolytes should be performed at the time of the VCUG and urodynamics but may be obtained sooner based on the child’s renal function and clinical presentation.
If the child is found to have diminished compliance or detrusor hyperactivity, anticholinergic therapy should be considered. Anticholinergic therapy may also be instituted immediately after valve ablation or prior to closure or reversal of vesical or supravesical diversion. Alpha-blocker therapy may be considered even in the first months of life in the face of high detrusor voiding pressures and in the absence of residual valve obstruction or postvalve ablation stricture (10,11).
Vesicostomy
While most patients with PUV are treated with primary valve ablation, a vesicostomy may be useful in neonates whose urethra will not accommodate a cystoscope or in those whose creatinine rises despite adequate valve resection.
With the patient in the supine position, the lower abdominal skin is prepared and draped in the typical fashion. The procedure is more easily performed with a full bladder. A 2-cm transverse incision is then made midway between the pubic symphysis and umbilicus. The rectus fascia is exposed and a 2 cm × 2 cm cruciate incision is made. Alternately, a triangle or circle of rectus fascia measuring 2 cm may be excised. One must remember that the size of the fascial opening ultimately determines the caliber of the stoma. The rectus muscles are then retracted laterally, exposing the bladder. A 3-0 suture is placed near the dome of the bladder and used for traction. Using the traction suture, the bladder is mobilized superiorly. The peritoneum is gently swept off the superior aspect of the bladder. Additional cephalad sutures may be placed in a
stepwise fashion to help bring the dome into the surgical field. Care is taken to avoid the peritoneal contents. With gentle traction, one should be able to visualize the urachus or obliterated hypogastric artery.
stepwise fashion to help bring the dome into the surgical field. Care is taken to avoid the peritoneal contents. With gentle traction, one should be able to visualize the urachus or obliterated hypogastric artery.
The vesicostomy may be created in one of two ways. In the first method, a stay suture is placed proximal to the urachus. The urachus is then transected and excised. In the second method, the portion of the bladder cephalad to the urachal remnant is used as the site for the vesicostomy. The bladder is incised and the fascial edges are sewn to the outer bladder wall using 3-0 or 4-0 polyglactin sutures approximately 0.5 to 1 cm from the opening created in the bladder. The vesicostomy should be calibrated to 24Fr or large enough to allow passage of the surgeon’s fifth digit. If the fascial defect is too large, interrupted 3-0 polyglactin sutures may be used to narrow the opening. The edges of the detrusor are then sewn to the skin using 4-0 polyglactin sutures in an interrupted fashion. If the skin incision is wider than the stoma created, the skin is approximated with a suture of choice (Fig. 97.4).
FIGURE 97.4 Blocksom vesicostomy. A: A 2-cm transverse incision is made midway between the pubic symphysis and umbilicus. B: A 2 cm × 2 cm cruciate fascial incision is made. C: Using the traction suture the bladder is mobilized superiorly. The peritoneum is gently swept off the superior aspect of the bladder. D: The urachus is incised and the bladder is further mobilized. E: The urachus is excised. F and G: The outer bladder wall is sewn to the edges of the incised rectus fascia. H: The edges of the detrusor are sewn to the skin. (Modified with permission from Belman AB, King LR. Vesicostomy: useful means of reversible urinary diversion in selected infant. Urology 1973;1:208-213. Copyright © 1973. Published by Elsevier Inc.)
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