Acute effect of sacral neuromodulation on video-urodynamic parameters of neurogenic lower urinary tract dysfunction in a patient with vesicoureteral reflux: a case report
Introduction
“Neurogenic bladder” is referred to as lower urinary tract dysfunction caused by nerve injury or nervous system disease (1). Although the terminologies of such diseases have not been unified worldwide, it is recommended to use “neurogenic lower urinary tract dysfunction (NLUTD)” instead of “neurogenic bladder”. The term NLUTD was proposed by the International Continence Society (ICS) and is defined as “lower urinary tract dysfunction caused by disorders in the regulation of the nervous system” (2-4). This broad definition provides a more comprehensive summary of different severities of the disease; thus, the term NLUTD was used in this study.
The most common symptoms of NLUTD are dysuria and urinary retention (5). If not treated properly, NLUTD can cause damage even to upper urinary tract function and have a negative effect on patient’s life expectancy (6). Therefore, the primary treatment goal is to protect the upper urinary tract function and prevent the occurrence of pyelonephritis, hydronephrosis, and chronic renal failure. The secondary goal is to improve the symptoms of urinary dysfunction to alleviate pain (7).
Current research shows that restoring the lost nerve function through sacral neuromodulation (SNM) is a feasible treatment strategy for NLUTD (8,9). While most previous studies have focused mainly on the efficacy and safety of SNM in the treatment of NLUTD, some focused less on changes in urodynamic parameters in patients with NLUTD before and after SNM.
The ICS recommends urodynamics (UDS) as an important examination method for the diagnosis of lower urinary tract disorders, and it has been widely used (10). Video-urodynamics (VUDS) is based on the traditional UDS examination, combined with real-time image analysis of morphological changes in the lower urinary tract. VUDS can show the anatomical structure and functional status of the bladder and urethra simultaneously. It is currently the most accurate method for diagnosing the pathophysiological changes in the upper and lower urinary tract in patients with NLUTD (11).
Herein, we present the case of a 63-year-old, female NLUTD patient with vesicoureteral reflux (VUR) who was treated with SNM in Beijing Hospital in February 2021, and the changes in VUDS before and after surgery were evaluated. This study aimed to explore the effect of short-term SNM treatment on the anatomy and function of the lower urinary tract in a patient with NLUTD. We present the following case in accordance with the CARE reporting checklist (available at https://apm.amegroups.com/article/view/10.21037/apm-21-1132/rc).
Case presentation
Ethics statements
All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committee(s) and with the Helsinki Declaration (as revised in 2013). Written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the editorial office of this journal.
Patient information
A 63-year-old woman presented with dysuria, urinary incontinence for 4 years, and urinary retention for 1 month. The patient has no other comorbid diseases. In the past, the patient was treated in other hospitals and received treatment such as behavior adjustment and oral drugs, but the effect was poor or ineffective. In January 2021, she was admitted to the outpatient clinic of our hospital and was examined using VUDS (Figure 1A-1C). Before the examination, the patient’s residual urine volume after free urination was 160 mL.
UDS evaluation
UDS evaluation was performed in accordance with the ICS guidelines and by the same doctor (10,12). Before beginning the examination, the patient was instructed to take the lithotomy position for disinfection and catheterization after urination, and the residual urine volume was recorded. The perfusion rate at the time of the examination was 30 mL/min and stopped when the patient had a strong desire to urinate or felt uncomfortable. At the end of VUDS, the retractor was connected, pressure measurement catheter was pulled out at a uniform speed of 1 mm/s, and urethral pressure was recorded.
The following bladder function parameters were recorded: bladder compliance, bladder capacity and pressure when VUR occurs, maximum cystometric capacity, presence or absence of uninhibited detrusor contraction, presence or absence of detrusor contraction and contraction force, maximum urethral pressure, and maximum urethral closure pressure.
Clinical findings
The VUDS examination showed that the bladder sensitivity and compliance (4.48 mL/cmH2O) decreased during the storage period. Right ureteral reflux began to appear when the bladder pressure was 52 cmH2O after perfusion to 90 mL (Figure 1B). There was no active contraction of the detrusor during the voiding period and abdominal pressure-assisted micturition, and the maximum change in detrusor contractility compared with the baseline was 14.4 cmH2O. The patient’s functional cystometric capacity was 231.7 mL, with first sensation, first desire, and strong desire capacity of 138, 146, and 230 mL, respectively, and the residual urine volume was approximately 110 mL. The patient’s maximum urethral pressure was 84 cmH2O, and the maximum urethral closure pressure was 43 cmH2O. On synchronous X-ray images during the filling period, the bladder was abnormal in shape, showing a Christmas-tree shape, and the bladder wall was rough. During the voiding period, the opening of the bladder neck was satisfactory, and the urethra was well visualized. The level of right ureteral reflux increased with an increase in abdominal pressure (Figure 1C).
Treatment and outcome
After reviewing the examination results and obtaining informed consent from the patient, we performed the first stage of SNM on the patient in January 2021. After a 2-week experience period, the VUDS findings were reviewed in the same month (Figure 2A-2C). Before the examination, the patient’s residual urine volume after free urination was 380 mL. The VUDS examination showed that bladder compliance was significantly improved during the storage period (10.5 mL/cmH2O). When perfused to 340 mL, right ureteral reflux began to occur when the bladder pressure was 72 cmH2O (Figure 2B). The performance during the voiding period was the same as earlier, and there was no obvious active contraction of the detrusor. The patient’s functional cystometric capacity was 446.3 mL, with first sensation, first desire, and strong desire volume of 275, 402, and 413 mL, respectively, and the residual urine volume was about 110 mL. The urethral pressure of the patient was approximately the same as before. Simultaneous X-ray images suggested that with the increase in abdominal pressure, the level of right ureteral reflux also increased (Figure 2C), and the reflux volume and level improved remarkably compared with before the operation. The patient was satisfied with the curative effect and received permanent implantation of SNM (PINS, G132) in February 2021.
Discussion
Studies have confirmed that the low bladder compliance in patients with NLUTD not only causes clinical symptoms of frequent urination, urgency, and dysuria but also leads to intravesical hypertension during the filling period and may even impair the upper urinary tract function (13). Therefore, for patients with NLUTD, the golden principle of treatment is to ensure that the detrusor pressure remains within the low-pressure safe range during both the storage and voiding periods, which will significantly reduce the fatality rate due to urinary complications in these patients (14). The European Association of Urology has proposed a more specific treatment goal for patients with NLUTD, that is, to convert an overactive, unstable, high-pressure bladder into a passive, low-pressure, storage allantoic (although it will cause a large amount of residual urine) bladder so that urinary incontinence can be controlled and then to use low-pressure urination methods, such as intermittent catheterization, to empty the bladder (15).
SNM is a new method developed in recent years to treat lower urinary tract dysfunction (including NLUTD), and its effectiveness and safety have been well established (16-19). In addition, a meta-analysis published in 2010 showed that SNM is effective and safe for the treatment of NLUTD (8). However, the analysis included a small number of patients, showed high heterogeneity among studies and lacked support from randomized controlled clinical trials. At the same time, the study did not describe the UDS parameters, so the neurological patient population category that is most suitable for SNM was unclear (8,20-22).
In animal experiments, SNM has been shown to increase bladder capacity and reduce bladder pressure (23). Literature search found that Chaabane et al. began to explore the effects of SNM on the UDS of patients with NLUTD as early as 2011, but they did not make judgments and assessments of the possible combined VUR (24). Therefore, on this basis, Chen et al. retrospectively included 19 patients with NLUTD and evaluated the improvement in SNM during the storage period of patients with NLUTD using VUDS (25). These results suggest that SNM can improve urinary storage function of the bladder in patients with NLUTD to a certain extent. For patients with VUR, SNM can cure or reduce VUR by improving detrusor overactivity and/or bladder compliance.
The conclusion of the present study is similar to that of the study by Chen et al. (25), that is, after receiving SNM treatment, the storage period of the patient was significantly improved, but the voiding period did not significantly improve. Specifically, as reflected in bladder compliance, the safe capacity of the bladder significantly increased and VUR significantly decreased. SNM successfully transformed the patient’s small-volume, high-pressure bladder into a large-volume, low-pressure bladder, which reduced the number of intermittent catheterizations and greatly improved her quality of life.
To our knowledge, only one study by Groenendijk et al. presented the acute effects of SNMs on the UDS parameters (26). Specifically, 10 patients with overactive bladder underwent UDS examination before SNM treatment and 1 week after SNM treatment. The results showed no significant difference in the UDS parameters at the two time points, so Groenendijk et al. speculated that the UDS parameters were not affected by short-term SNM. The above conclusions are quite different from those of the present study, because the VUDS parameters of our patient improved to varying degrees or showed a trend of improvement after 2 weeks of SNM. We speculate that there could be two reasons for the different conclusions. First, the patients included in the earlier study were diagnosed with overactive bladder, so the indication of SNM treatment might have been different. Second, in the present study, the duration of SNM treatment was 2 weeks, and the patient had a relatively longer stimulation time to observe improvement in clinical symptoms.
The main limitation of this study is that during the VUDS examination, some of the patient’s urine leaked out of the collector, which could not be directly reflected in the examination image. In this case, it can only be calibrated by the examination doctor, which may affect the accuracy of the objective examination results to a certain extent. Another limitation is that we had no follow-up data after SNM permanent implantation as the patient was not due for reexamination by the time this manuscript was communicated.
In conclusion, this study confirmed the satisfactory efficacy of short-term SNM in a patient with NLUTD with VUR; short-term SNM effectively improved lower urinary tract function and reduced VUR. In general, clinicians should have a more positive attitude toward the first stage of SNM implantation in patients with NLUTD.
Acknowledgments
Funding: This work was supported by the National Key R&D Program of China (2018YFC2002202) and the National Key R&D Program of China (2016YFC0105505).
Footnote
Reporting Checklist: The authors have completed the CARE reporting checklist. Available at https://apm.amegroups.com/article/view/10.21037/apm-21-1132/rc
Peer Review File: Available at https://apm.amegroups.com/article/view/10.21037/apm-21-1132/prf
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://apm.amegroups.com/article/view/10.21037/apm-21-1132/coif). The authors have no conflicts of interest to declare.
Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committee(s) and with the Helsinki Declaration (as revised in 2013). Written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the editorial office of this journal.
Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
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