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Chapter 3
41
Surgical Approaches in Pediatric Neurogenic Low Urinary Tract Dysfunction
José AntonioMarch-Villalba
This chapter explores surgical treatment modalities in pediatric urology for patients with lower urinary tract dysfunction due to neurogenic etiologies. Specific surgical strategies and innovative approaches are examined to enhance urinary function and improve the quality of life in this pediatric population. The discussion emphasizes the importance of comprehensive assessment and careful planning to tai­lor surgical interventions to the individual needs of each patient. Additionally, recent advances in understanding and treating these conditions are addressed, providing a comprehensive overview of available surgical options and their implications for pre­serving renal function and improving the quality of life for children with neurogenic lower urinary tract dysfunction.
Keywords: pediatric, neurogenic, urinary tract dysfunction, treatment, surgery
. Introduction
Neurogenic lower urinary tract dysfunction (NLUTD) is a common complication in children with neurological disorders such as spina bifida, cerebral palsy, and spinal cord injuries [–].
NLUTD involves an alteration in the coordination between the nervous system and the urinary tract, affecting the child’s ability to control urination. It is often associated with neurological dysfunction that impacts the nerves controlling the bladder and urinary tract muscles, resulting in hyperactivity and a non-compliant bladder, which leads to abnormalities in bladder filling or emptying. This is a common problem in children, accounting for  of pediatric urology consultations. Therapeutic man­agement focuses on improving symptoms and preventing damage to renal function caused by recurrent infections or vesicoureteral reflux [, ].
While most children with NLUTD can be managed with conservative therapies, such as anticholinergics, intermittent bladder catheterization, oral autoimmune vaccines, and so on, surgical interventions may be necessary in some cases to improve urinary tract function and prevent long-term complications [–].
Before considering surgical intervention, it is crucial to conduct a thorough evalu­ation of the pediatric patient with NLUTD. This includes a detailed medical history,
and Rosa MaríaGras-Martínez
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a comprehensive physical examination, and diagnostic tests such as urodynamic studies, renal ultrasound, and voiding cystourethrography to assess the severity and nature of the urinary tract dysfunction [–].
In this chapter, we will review the surgical approaches used in the management of NLUTD in pediatric patients, focusing on reducing intravesical pressure, modifying urethral resistance, and considering urinary diversion.
. Procedures to reduce intravesical pressure
. Botulinum toxin detrusor injection
Botulinum toxin has emerged as a promising therapeutic option in the manage­ment of NLUTD in pediatric patients. Its use has become widespread as an effective alternative for controlling detrusor overactivity and reducing urethral resistance in this population [, –]. Botulinum toxin works by blocking the release of acetylcho­line at nerve endings, resulting in the relaxation of the detrusor muscle and a decrease in uncontrolled contractile activity. This therapeutic approach has proven particularly useful in cases refractory to other forms of conservative treatment, offering signifi­cant improvements in urinary symptoms and quality of life for pediatric neuropathic patients. However, careful preoperative evaluation and postoperative follow-up are required to optimize outcomes and minimize potential risks associated with the procedure [–].
The use of botulinum toxin-A (Botox/BoNT-A) intradetrusor injections in the neuropathic pediatric bladder (Figure ) has been the subject of numerous studies
Figure 1. Scheme of the puncture and injection points of BOTOX in the bladder. Injecting 10units per kg of body weight up to a maximum of 300units, with a dilution of 10units per ml of saline solution. 20 to 30 different trigger points are injected in the detrusor with 1ml of dilution per point, respecting the trigone.
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that have evaluated different aspects of its efficacy and safety. Published results have consistently demonstrated a significant improvement in urinary symptoms and quality of life following botulinum toxin injection into the detrusor. However, there is some variability in reported outcomes, which may be partly attributed to differences in injection techniques [–].
The reviewed studies have demonstrated that BoNT-A injections into the detru­sor muscle are effective in reducing overactivity and involuntary contractions in children with bladder neuropathy. This leads to a decrease in voiding frequency, urinary urgency, and episodes of incontinence. Additionally, the reduction in detrusor overactivity can improve urinary retention capacity and the quality of life for patients [–].
Bladder compliance refers to the ability of the bladder to distend and store urine efficiently without experiencing excessive increases in intravesical pressure. In patients with a neuropathic bladder, loss of bladder compliance can result in diminished storage capacity and an increased risk of complications such as incon­tinence and renal dysfunction. Botulinum toxin can improve bladder compliance by reducing detrusor muscle activity and decreasing involuntary contractions. This allows for more effective bladder distension during filling, resulting in increased urinary retention capacity and a decrease in symptoms of overactive bladder. Consequently, the risk of incontinence is reduced, and long-term renal function is improved [–].
Indeed, botulinum toxin (BoNT-A) has been shown to temporarily decrease detrusor contractility and improve bladder compliance in children with neuropathic bladder, potentially delaying the need for surgical interventions aimed at increasing bladder capacity. However, it is important to consider that the effects of BoNT-A are temporary, typically lasting around  to months, after which repeat injections may be necessary to maintain therapeutic benefits. Therefore, while BoNT-A injec­tions can provide valuable symptom relief and improve bladder function in pediatric patients with neuropathic bladder, they may not eliminate the need for long-term management strategies, including surgical interventions to address bladder capacity issues. Ultimately, the decision to pursue surgical intervention should be individual­ized based on the patient’s clinical presentation, response to treatment, and overall treatment goals, with consideration given to both short-term and long-term out­comes [–].
Specifically, in a recent systematic review involving pediatric patients with neu­rogenic bladder, it was found that continence rates ranged from  to , with a reduction in maximum detrusor pressure of –, an increase in maximum cysto­metric capacity of –, and improvement in bladder compliance (–) []. Onabotulinum toxin A (administered at a maximum dose of IU injected at – different sites) appears to be more effective in bladders exhibiting detrusor muscle overactivity, while bladders that are non-compliant and lack detrusor overactivity are less likely to respond [, ].
In summary, BoNT-A offers significant benefits in the treatment of detrusor over­activity and the improvement of bladder compliance in children with neuropathic bladder. These benefits translate into a reduction in symptoms of overactive bladder, improvement in urinary retention capacity, and enhanced quality of life for pediatric patients [–].
The adverse effects of BOTOX use in children can vary depending on the study and population studied, but some common adverse effects mentioned in the reviewed articles include [–]:
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• Urinary retention: Following BOTOX treatment, some children may experience difficulties in urination due to excessive relaxation of the detrusor muscle. This may manifest as decreased urinary flow or the need for intermittent catheteriza­tion to empty the bladder.
• Urinary tract infections (UTIs): There is an increased risk of UTIs following BOTOX treatment, especially in those requiring intermittent catheterization or having trouble completely emptying the bladder.
• Incontinence: Although BOTOX is used to treat urinary incontinence, some chil­dren may experience overflow incontinence due to the inability to fully empty the bladder following treatment.
• Dysuria: Irritation of the bladder mucosa due to BOTOX treatment can cause discomfort during urination, such as pain or burning (dysuria).
• Fecal retention: In some cases, BOTOX may also affect the function of the anal sphincter, leading to fecal retention and constipation in children.
The systemic effects of BOTOX after bladder injection in children are a critical consideration in the management of pediatric patients undergoing this treatment. While BOTOX is primarily localized to the site of injection and exerts its therapeutic effects by blocking nerve signals to the targeted muscle, there is potential for systemic absorption and distribution of the toxin [–].
Some systemic effects that have been reported in the literature include [–]:
• Systemic spread of toxin: Although rare, systemic spread of BOTOX beyond the injection site can occur, leading to distant muscle weakness or paralysis. This can manifest as weakness in adjacent muscles or more generalized weakness, depending on the extent of systemic absorption.
• Flu-like symptoms: Children may experience flu-like symptoms such as fever, malaise, and muscle aches following BOTOX injection, which are typically mild and transient.
• Allergic reactions: While uncommon, allergic reactions to BOTOX, such as rash, itching, or swelling at the injection site, have been reported in pediatric patients.
• Systemic toxicity: In rare cases, systemic toxicity due to excessive systemic absorp­tion of BOTOX can occur, leading to symptoms such as difficulty breathing, swallowing, or speaking, and generalized weakness or paralysis.
It is essential for healthcare providers to be vigilant for signs of systemic effects following BOTOX injection in children and to monitor patients closely for any adverse reactions. Additionally, healthcare providers should discuss the potential risks and benefits of treatment with parents and caregivers before proceeding with BOTOX injection and ensure that appropriate precautions are taken to minimize the risk of systemic effects [, –].
Studies have compared the efficacy and side effects of a single intradetru­sor injection versus multiple injections distributed throughout the bladder wall.
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While some studies suggest that a single intradetrusor injection may be sufficient to achieve similar results with lower risks of complications, others have found that multiple injections may be more effective in certain patient subgroups. It is crucial to consider these differences in injection technique when interpreting the results and planning individualized treatment for neuropathic pediatric patients with bladder dysfunction.
Regarding injection numbers and doses, across the studies, the number of injec­tions and doses of BoNT-A varied depending on the specific protocol used. Typically, multiple injections were administered into the detrusor muscle of the bladder under cystoscopic guidance. Doses ranged from  to units of BoNT-A per injection, with some studies utilizing a single injection and others employing a multiple-injec­tion approach [–].
Recurrent cases may include the return of incontinence symptoms after the effects of the injection wear off. The duration of the Botox effect ranges between  and months. Repeating the injection is often necessary. Alternative treatments or adjunct therapies may be considered if responses are inadequate [–].
Botox failure may involve a lack of response to the injection or significant side effects. Alternative therapeutic options or further diagnostic evaluation may be needed. Exploring other treatments like augmentation cystoplasty or neuromodula­tion techniques might be necessary [–].
In conclusion, botulinum toxin type A has been demonstrated to be a safe and effective therapeutic option in managing neuropathic bladder in children. The reviewed studies support its use in treating incontinence, overactive bladder, and other lower urinary tract disorders in pediatric populations. However, further research is warranted to fully understand its long-term efficacy and impact on the quality of life of pediatric patients with neuropathic bladder [, –].
. Sacral neuromodulation and stimulation
Sacral neuromodulation (SNM) is a therapeutic approach used to manage lowerurinary tract dysfunction (LUTD) in children, including those with neuro­pathic bladder dysfunction. It involves the targeted delivery of electrical stimula­tion to the sacral nerves, which play a crucial role in regulating bladder function [,–].
Although there is a significant body of literature on transcutaneous neurostimu­lation in pediatric patients with idiopathic overactive bladder, studies focusing on pediatric patients with neurogenic bladder are scarce [, –].
The first step in SNM involves the surgical implantation of a neuromodulation device, often referred to as a “neurostimulator.” This device is typically placed under the skin in the upper buttock area and is connected to thin, flexible wires called “leads” that are positioned near the sacral nerves. Once the device is implanted, it delivers mild electrical impulses to the sacral nerves via the leads. These electrical impulses modulate the activity of the nerves, helping to regulate bladder function. The stimulation parameters, such as frequency, amplitude, and pulse width, can be adjusted based on the individual patient’s needs. Following implantation, the neuromodulation device can be programmed and adjusted as needed to optimize its therapeutic effects. Regular follow-up appointments with healthcare providers are essential to monitor the child’s progress, make any necessary adjustments to the stimulation parameters, and ensure the continued effectiveness and safety of the treatment [–].
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The electrical stimulation provided by sacral neuromodulation has several effects on bladder function in children with LUTD. It can help normalize bladder contractions, reduce urinary frequency and urgency, improve bladder emptying, and decrease episodes of urinary incontinence. Additionally, sacral neuromodulation may also modulate sensory pathways involved in bladder sensation, leading to improve­ments in bladder control and continence [–].
Regarding sacral anterior root stimulation implants, there are few studies provid­ing information about their application in neuropathic pediatric patients, as it is not a commonly used technique [].
Transcutaneous electrical nerve stimulation (TENS) is a non-invasive neuro­modulation technique that involves applying electrical stimulation to the skin to modulate nerve activity [, –]. Although there are numerous studies in adults and even a meta-analysis, none has specifically investigated the pediatric population. To date, only two studies have investigated the immediate effect of transcutaneous electrical nerve stimulation (TENS) on urodynamic parameters in children with myelomeningocele. Myelomeningocele is a type of spina bifida characterized by incomplete development of the spinal cord and its protective covering. Children with myelomeningocele commonly experience bladder dysfunction, including neurogenic bladder, which can lead to urinary incontinence, urinary tract infections, and renal damage [–].
In the first study, researchers aimed to assess the immediate impact of TENS on urodynamic parameters, such as detrusor pressure, maximum cystometric capacity, and bladder compliance, in children with myelomeningocele. In the second study, researchers replicated the treatment procedure two or three times weekly. The ages of the patients ranged from  to years [].
Self-adhesive surface electrodes were placed on the skin over the region of the sacral dermatomes between S and S. This location, used in other similar studies, is the closest region to the bladder innervations, which seems to facilitate nerve recruitment [, ]. The exact location of the electrodes was determined by palpation with the thumbs between the posterior superior iliac spine using an imaginary line to identify the S vertebra. The duration of the TENS intervention was the same as the urodynamic study (UDS), lasting from  to minutes, depending on the age and size of the child’s bladder. A symmetrical biphasic pulsed waveform current with a frequency of Hz, a pulse width of s, and a maximum amplitude of mA was used. The study concluded that the use of transcutaneous electrical nerve stimu­lation had a significant immediate effect on reducing maximum bladder pressure during urodynamic studies in pediatric patients with neurogenic bladder. The results were more significant among children under years of age. These findings provide insights into the potential therapeutic effects of TENS in managing bladder dysfunc­tion in children with myelomeningocele [, ].
In children aged –years, the use of TENS requires special consideration due to their smaller anatomical size and different physiological responses. The procedure typically involves the placement of self-adhesive surface electrodes over the sacral dermatomes between S and S, chosen for their proximity to bladder innervations, which helps facilitate nerve recruitment [–].
The standard TENS protocol for this age group involves a symmetrical biphasic pulsed waveform current with a frequency of Hz, a pulse width of s, and a maximum amplitude of mA. The duration of each session ranges from  to minutes, depending on the child’s bladder size and overall tolerance to the stimula­tion [, –].
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Clinical observations suggest that TENS is a safe and well-tolerated intervention in this young demographic. It has shown significant immediate effects on reducing maximum bladder pressure during urodynamic studies, particularly in children under years of age. Continuous monitoring and adjustments are crucial to optimize the therapeutic benefits and minimize potential discomfort or adverse effects [, –].
.. Procedure for TENS application in children aged –years
. Preparation:
Explain the procedure to the child and their caregivers to ensure understand-
ing and cooperation [, –].
Ensure the child is comfortable and relaxed, possibly allowing them to hold a
favorite toy or watch a video during the procedure.
. Electrode Placement (Figure )
Posterior Tibial Nerve Stimulation: This technique inhibits reflex bladder
contractions, potentially increasing bladder storage capacity and reducing urinary urgency. Place two electrodes: one on the inside of the ankle and the second three to four fingers above the first.
Clean the skin over the sacral dermatomes (S–S) with an alcohol swab to
ensure good electrode adhesion.
Place the self-adhesive electrodes symmetrically over the target area.
. Device Seings:
Set the TENS device to a frequency of Hz and a pulse width of s.
Figure 2. (a) Posterior tibial nerve stimulation. Place two electrodes, the first on the inside of the ankle, and the second three to four fingers up. (b) Clean the skin over the sacral dermatomes (S2–S4) with an alcohol swab to ensure good electrode adhesion. Place the self-adhesive electrodes symmetrically over the target area.
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Gradually increase the amplitude to a maximum of mA, or until the child
feels a comfortable tingling sensation.
. Session Duration:
Each session should last between  and minutes, with the duration
tailored to the child’s tolerance and response.
. Monitoring:
Monitor the child throughout the session for any signs of discomfort or
adverse effects.
After the session, check the skin under the electrodes for any signs of irritation.
. Follow-up:
Schedule regular follow-up appointments to assess the effectiveness of the
therapy and make any necessary adjustments to the treatment plan.
The findings support the potential of TENS as a valuable tool in managing bladder dysfunction in young children with neurogenic bladder conditions. Its use can signifi­cantly improve quality of life by reducing urinary symptoms and enhancing bladder function with minimal risks. Understanding the immediate impact of TENS on urody­namic parameters can inform the development of tailored treatment approaches aimed at improving bladder function and overall quality of life in this population [, , ].
However, it is important to note that sacral nerve stimulation and transcutane­ous neuromodulation are still considered experimental in children with neurogenic bladder dysfunction and cannot be recommended outside the confines of clinical trials [, ].
. Posterior sacral root Rhizotomy
Posterior Sacral Root Rhizotomy (SARS) is a surgical procedure performed to treat neurogenic bladder dysfunction, particularly in patients with conditions such as spinal cord injury or spina bifida. During the procedure, the surgeon selectively cuts or divides specific sacral nerve roots at the posterior aspect of the sacrum. This interruption of neural signals helps reduce abnormal bladder contractions, thereby improving bladder function and reducing urinary incontinence. SARS is typically considered when other treatments, such as medications or behavioral therapies, have been ineffective in managing neurogenic bladder symptoms [].
Currently, there are no studies supporting its application in pediatric patients with neurogenic bladder. The few existing studies on this procedure date back to the last decade of the twentieth century.
. Detrusor myectomy
Detrusor myectomy is a surgical procedure used to treat neurogenic bladder dysfunction (NBD) by making incisions in the detrusor muscle of the bladder.
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This procedure aims to increase bladder capacity and improve bladder compli­ance, thereby reducing urinary incontinence and other symptoms associated with NBD. During detrusor myotomy, the detrusor muscle is incised to create a bladder diverticulum, which allows for increased bladder volume. The resulting flaps are then anchored to prevent the closure of the myotomy. Detrusor myotomy is typi­cally indicated when conservative treatments have failed to adequately manage NBD symptoms [, , ].
The surgical procedure involves exposing the bladder extraperitoneally through a low midline laparotomy or Pfannenstiel incision. The detrusor muscle is incised coronally in the midline to create a bladder diverticulum, and the resulting flaps are secured to prevent the myotomy from closing. The detrusor myectomy technique remains largely unchanged from its original description. Through a Pfannenstiel incision in the lower abdomen, as previously mentioned, the bladder is exposed. A -way urethral catheter is placed to easily control bladder filling and emptying. Initial bladder distention allows for clear definition and dissection of the peritoneum off the bladder dome. A scalpel is then used to incise the detrusor muscle layer. Using a combination of gentle traction and sharp dissection, the detrusor layer covering the dome and anterior wall is stripped away to expose the bulging bladder epithelium. Care is taken to avoid perforating the bladder mucosa. Although small perforations can be repaired with sutures, the outcomes are generally less satisfac­tory. After the surgery, a urethral catheter is left for gravity drainage for –days (
Figure ) [, ].
Although detrusor myectomy has been described in the scientific literature, there are relatively few studies that both detail and apply this surgical intervention. One notable study in this regard is the one conducted by Cartwright and Snow, which provided a foundational description of the operative procedure for detrusor myot­omy. This study, along with a few others, serves as a cornerstone for understanding and implementing detrusor myotomy as a surgical treatment for neurogenic bladder dysfunction.
Figure 3. Detrusor myectomy. (a) A midline opening bladder serosa incision. (b) The detrusor muscle was incised coronally in the midline to create a bladder diverticulum, (c) The resulting flaps were hitched to prevent closure of the myotomy. (d) Closure of the first serosa incision.
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The study retrospectively reviewed the medical records of  consecutive children under the age of  who underwent detrusor myotomy (DM). These children had neurogenic bladder dysfunction (NBD) due to various underlying conditions such as myelodysplasia, sacral agenesis, lumbosacral lipoma, multiple vertebral anomalies, and spinal neuroblastoma. Postoperatively, patients under­went intermittent catheterization, and follow-up assessments included cystometric bladder capacity, renal function evaluation, and clinical assessment of continence [, , ].
The results showed that surgery was performed on  girls and  boys, with a mean age of .years. The main indications for surgery were urinary incontinence and high-grade vesicoureteral reflux (VUR). The mean follow-up was .years. Bladder capacity increased significantly postoperatively, and most patients achieved full con­tinence or marked improvement. VUR was alleviated in most cases, and renal func­tion developed normally in all except one patient. The study concluded that detrusor myotomy is a viable and safe treatment option for pediatric NBD. However, optimal results may require enhancing bladder outlet resistance in addition to increasing bladder capacity [, ].
. Augmentation cystoplasty
Augmentation cystoplasty is a surgical procedure used to increase the size or capacity of the bladder. This is typically achieved by adding a segment of tissue, often from the intestines to the bladder wall, effectively enlarging its capacity to hold urine. The procedure is commonly performed in cases where the bladder has lost its ability to stretch due to conditions such as neurogenic bladder dysfunction or congenital abnormalities. Augmentation cystoplasty aims to improve bladder function, reduce urinary incontinence, and alleviate symptoms associated with bladder dysfunction [, , ].
Often, in conjunction with augmentation cystoplasty, it is necessary to create a catheterizable conduit. Additionally, when the patient also suffers from vesicoure­teral reflux, ureteral reimplantation or ureteroneocystostomy may also be required [, –].
The indications for augmentation cystoplasty in pediatric patients with neurogenic bladder include neurogenic overactive bladder, impaired compliance, and refractory urinary incontinence. These indications are based on a clinical assessment of the patient, including urodynamic studies and evaluation of renal function. Specific indications for this surgery include failure of minimally invasive treatments such as bladder BOTOX injection, bilateral high-grade ureterohydronephrosis secondary to vesicoureteral reflux associated with significant renal failure, and significant impair­ment of bladder accommodation associated with low capacity and elevated detrusor leak pressure (> cmHO) [, –].
The most common tissues used for augmentation are ileal, sigmoid, and ureteric segments. Complications from surgery can include postoperative infections (urinary tract and wound), metabolic abnormalities (such as metabolic acidosis and electrolyte imbalances), urinary continence issues, bladder stones, mucus production, hema­turia, and bladder perforation. Neoplasms are more common as the patient reaches adulthood [–].
Each bowel segment presents unique characteristics, with both advantages and disadvantages. For instance, the ileum offers greater compliance compared to the
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