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ORIGINAL RESEARCH article

Front. Neurol., 08 December 2025

Sec. Pediatric Neurology

Volume 16 - 2025 | https://doi.org/10.3389/fneur.2025.1706698

Urodynamic evaluation of neurogenic lower urinary tract dysfunction in children with Guillain-Barre syndrome within 6 months

  • 1. West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China

  • 2. Sichuan Provincial Children’s Hospital, Meishan, Sichuan, China

  • 3. Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, Chengdu, Sichuan, China

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Abstract

Objective:

This study aimed to evaluate urodynamic characteristics, identify high-risk and unfavorable urodynamic findings in children with neurogenic lower urinary tract dysfunction (NLUTD) secondary to Guillain-Barre syndrome (GBS) within 6 months since the onset of illness.

Methods:

This study conducted a retrospective observational analysis of 16 children diagnosed with GBS complicated by NLUTD. Clinical data collected included demographic information, lower urinary tract symptoms, uroflowmetry results, post-void residual urine (PVRU), and urodynamic parameters. Follow-up assessments focused on high-risk urodynamic features-such as high detrusor pressure during the filling phase and low bladder compliance-as well as unfavorable findings, including detrusor overactivity, detrusor underactivity, or an acontractile bladder.

Results:

The majority of patients presented with clinical symptoms of urinary retention. Characterized by a decreased Qmax on uroflowmetry and elevated PVRU. Urodynamic study (UDS) revealed two predominant findings: reduced bladder sensation during the filling phase and detrusor underactivity during the voiding phase. At the 8-week follow-up, low bladder compliance and detrusor overactivity were observed in only 2 of the 16 patients (12.5%). During the filling phase, none of the patients exhibited high detrusor pressure (>40 cmH₂O), while all cases demonstrated underactive bladder function during the voiding phase. By the 24-week follow-up, 12 patients (12/16, 75.0%) had achieved normal bladder compliance, with only one case persisting with low bladder compliance and detrusor overactivity. Additionally, 10 patients (10/16, 62.5%) who had presented with an underactive bladder during the voiding phase showed recovery by the 24-week assessment.

Conclusion:

The prognosis of autonomic dysfunction involving the urinary system in pediatric GBS was generally favorable, with most cases of GBS-associated NLUTS showing substantial reversibility, as confirmed by the normalization of urodynamic parameters over time.

1 Introduction

Guillain-Barre syndrome (GBS) is an acute-onset immune-mediated, inflammatory disease of the peripheral nervous system (PNS) and is one of the common causes of acute flaccid paralysis (1). It is a monophasic illness that typically presents with relatively symmetrical weakness of the limbs, which rapidly progresses over time (1, 2). The annual incidence of the disease is reported to be 1–2/100,000 per year, with male predominance (1.5:1). Children are reported to be less affected (0.34–1.34 per 100,000 per year) than adults (3, 4).

In patients with GBS, autonomic dysfunction may involve the urinary system, characterized by neurogenic lower urinary tract dysfunction (NLUTD). Some patients exhibit urinary retention in the early stages, primarily due to transient autonomic dysregulation or somatic nerve involvement (4, 5). The detrusor muscle weakness results from impaired parasympathetic input (pelvic splanchnic nerves, S2-S4), while sympathetic overactivity (T11-L2) may increase bladder outlet resistance. In addition, inflammation affecting the pudendal nerve (S2-S4) can lead to external sphincter dyssynergia, further contributing to functional obstruction (57). Although urinary retention is typically transient and resolves with disease stabilization, temporary catheterization may be required to prevent complications (6, 7).

Urodynamic study (UDS) is the primary objective method for evaluating NLUTD, such as urinary retention, urinary incontinence (8, 9). Unfavorable urodynamic parameters showed in UDS are widely recognized as high-risk indicators for renal complications, and initiating proper management of NLUTD could mitigate the upper urinary tract complications in children (9, 10). This study aimed to evaluate urodynamic characteristics, detect unfavorable urodynamic findings of children with GBS presenting NLUTD and follow up these findings at different time intervals.

2 Materials and methods

We conducted a retrospective chart review of 16 children diagnosed with GBS who had complicated with NLUTD at our hospital from June 2021 to December 2024. A comprehensive medical history, physical examinations, cerebrospinal fluid (CSF), nerve conduction studies (NCS) consistent with polyneuropathy, were performed to ensure accurate diagnosis of GBS. All of patients showed clinical symptoms of lower urinary tract dysfunction, including urinary retention, urgency and/or urinary incontinence. Exclusion criteria included urinary tract infections, non-neurogenic bladder, structural bladder abnormalities (e.g., bladder cancer, bladder calculi), or psychogenic urinary frequency. Informed consent was obtained from all of the children’s parents. The study was conducted in accordance with the ethical principles of the Declaration of Helsinki, and was approved by the Independent Ethics Committee/Institutional Review Board of our hospital.

The clinical data collected encompassed demographic details, lower urinary tract symptoms, and a 2-day frequency volume chart. Additionally, each participant underwent uroflowmetry, post-voided residual urine (PVRU) measurement, and UDS. A standardized urodynamic detector (Laborie®) was utilized, with all procedures were conducted according to the standard methods recommended by the International Continence Society by the same physician, and results of UDS interpreted by experienced pediatric nephrologists who specifically trained in pediatric urodynamics and participated actively in UDS.

The outcome measures were evaluated through urodynamic parameters, including the results of filling cystometry (bladder capacity, bladder compliance, detrusor overactivity), the results of the voiding phase (maximum detrusor pressure during the voiding phase), and PVRU. Cystometric bladder capacity was defined as the bladder volume at the end of the filling cystogram. The expected bladder capacity (EBC) for children was calculated using the formula: EBC (ml) = [age (years) + 1] × 30. The EBC is applicable for children between 4 and 12 years as it reaches a level of 390 mL at 12 years. Based on this calculation, bladder capacity was classified as: “Increased”: if the measured maximum cystometric capacity was >150% of the EBC; Decreased: if the measured maximum cystometric capacity was <65% of the EBC (11). Bladder compliance was calculated by dividing the change in volume by the change in detrusor pressure during filling cystometry. The maximum detrusor pressure during the voiding phase and PVRU at the end of micturition were recorded.

High-risk findings (high detrusor pressure during the filling phase, low-compliance bladder) and unfavorable findings (detrusor overactivity, underactive or acontractile bladder) were observed and followed up within 6 months since the onset of illness. High detrusor pressure exceeding 40cmH2O during the filling phase was considered as a high-risk finding of urodynamic parameter to pose significant risk to the upper urinary tract (8, 11). Low bladder compliance was recognized as a compliance value lower than 20 mL/cmH2O, while high compliance was higher than 40 mL/cmH2O (11, 12). Detrusor overactivity was defined as involuntary detrusor contraction during the filling phase, with a pressure rise exceeding 15cmH2O above baseline (8, 11, 12). During the voiding phase, detrusor function was classified into three categories: normal, underactive, or acontractile bladder. An underactive bladder was defined as reduced detrusor pressure (<40cmH₂O), leading to prolonged bladder emptying or the inability to achieve complete emptying. An acontractile bladder was characterized by the absence of any increase in detrusor pressure during voluntary voiding (11).

All the pediatric participants and their parents received personalized lifestyle recommendations, focusing on balanced fluid intake and dietary adjustments. Furthermore, specialists provided guidance on clean intermittent catheterization (CIC) and behavioral modifications to improve voiding habits. Besides, 16 patients received biofeedback lasting 30 min each time, administered twice weekly using a specialized apparatus (Laborie®). During the procedure, children were positioned laterally, with a myoelectric probe inserted into the anus and surface electromyography electrodes attached to the perianal skin. They were then guided by multimedia animations displayed on a computer screen to perform pelvic floor muscle contractions and relaxations, ensuring proper and effective exercise.

Continuous variables with a normal distribution were presented as mean ± standard deviation, while continuous variables with a skewed distribution were presented as median and interquartile range. Categorical variables were summarized as frequencies and percentages. Statistical analyses were performed with SPSS software (version 18.0). Clinical variables were compared across groups using the Pearson chi-square test for categorical data. All reported p values <0.05 were considered statistically significant.

3 Results

3.1 Baseline characteristics of the study cohort

Sixteen participants (9 males and 7 females), with a median age of 10.5 ± 2.2 years, met the inclusion criteria. Detailed clinical features, including age, sex, lower urinary tract symptoms, uroflowmetry results and urodynamic parameters were summarized in Table 1.

Table 1

Patient No. Age (years) Sex Lower urinary tract symptoms Uroflowmetry Filling cystometry Voiding phase PVRU (ml)
Urinary retention Urgency Urinary incontinence Qmax (ml/min) Bladder capacity (ml) Bladder compliance (ml/cmH₂O) Detrusor overactive Maximum detrusor pressure (mmH2O)
1 11.7 Male Yes No No 9.5 470 23 No 16 230
2 9.6 Male Yes No No 10.3 410 45 No 10 190
3 10.2 Female Yes No Yes 9.7 500 46 No 12 220
4 9.4 Male Yes No No 8.4 460 42 No 15 180
5 8.3 Female Yes No No 7.3 350 34 No 13 170
6 12.6 Male Yes No No 10.2 560 27 No 23 270
7 12.7 Male Yes No No 9.8 590 46 No 15 160
8 8.7 Female Yes No No 6.3 350 25 No 16 170
9 9.5 Female No Yes Yes 6.9 150 10 Yes 24 80
10 10.5 Male Yes No No 9.1 430 22 No 18 220
11 11.4 Female Yes No Yes 10.2 540 48 No 14 210
12 8.4 Male Yes No No 5.8 410 45 No 12 150
13 9.0 Female Yes No No 6.0 370 21 No 17 230
14 12.2 Female No Yes Yes 11.7 190 9 Yes 28 70
15 11.8 Male Yes No No 6.3 470 21 No 19 240
16 10.9 Male Yes No No 7.1 490 44 No 18 160

Clinical characteristics of 16 children diagnosed with GBS who had complicated with NLUTD.

GBS, Guillain Barre syndrome; NLUTD, Neurogenic lower urinary tract dysfunction; Qmax, Maximum flow rate; PVRU, Post-voided residual urine.

Fourteen patients (14/16, 87.5%) presented with clinical symptoms of urinary retention, while two cases (2/16, 12.5%) were complicated by urinary incontinence. All patients exhibited a decreased maximum flow rate (Qmax) accompanied by an increase of PVRU. Additionally, UDS revealed a reduction in the maximum detrusor pressure during the filling phase, and abdominal straining during micturition observed. Among them, two cases (2/16, 12.5%) demonstrated clinical manifestations of urinary urgency with urge incontinence. Urodynamic evaluation in these two patients (2/16, 12.5%) indicated a decreased functional bladder capacity and the presence of detrusor overactivity during the filling phase.

3.2 Results of high-risk and unfavorable urodynamic findings in participants at follow-ups

Table 2 summarized the high-risk and unfavorable urodynamic findings of 16 patients within 6 months since the onset of illness.

Table 2

Patients No. Onset of illness At 8 weeks At 24 weeks
Bladder compliance (ml/cmH₂O) High detrusor pressure (>40 cmH2O) at the filling phase Detrusor overactive Detrusor function at voiding Bladder compliance (ml/cmH₂O) High detrusor pressure (>40 cmH2O) at the filling phase Detrusor overactive Detrusor function at voiding Bladder compliance (ml/cmH₂O) High detrusor pressure (>40 cmH2O) at the filling phase Detrusor overactive Detrusor function at voiding
1 23 No No Underactive 26 No No Underactive 28 No No Normal
2 45 No No Underactive 43 No No Underactive 35 No No Normal
3 46 No No Underactive 43 No No Underactive 42 No No Underactive
4 42 No No Underactive 35 No No Underactive 32 No No Normal
5 34 No No Underactive 32 No No Underactive 34 No No Normal
6 27 No No Underactive 28 No No Underactive 29 No No Normal
7 46 No No Underactive 44 No No Underactive 42 No No Underactive
8 25 No No Underactive 27 No No Underactive 28 No No Normal
9 10 No Yes Underactive 14 No Yes Underactive 21 No No Normal
10 22 No No Underactive 26 No No Underactive 29 No No Normal
11 48 No No Underactive 43 No No Underactive 36 No No Underactive
12 45 No No Underactive 42 No No Underactive 43 No No Underactive
13 21 No No Underactive 26 No No Underactive 28 No No Normal
14 9 No Yes Underactive 13 No Yes Underactive 16 No Yes Underactive
15 21 No No Underactive 27 L No No Underactive 26 No No Normal
16 44 No No Underactive 42 No No Underactive 34 No No Underactive

Results of high-risk and unfavorable urodynamic findings in participants at follow-ups.

At the 8-week, low bladder compliance and detrusor overactivity were observed in only 2 of the 16 patients (12.5%). None of the patients exhibited high detrusor pressure (>40 cmH₂O) during the filling phase, while all cases demonstrated underactive bladder function during the voiding phase.

By the 24-week follow-up, 12 patients (12/16, 75.0%) had achieved normal bladder compliance, with only one case (1/16, 6.3%) persisting with low bladder compliance and detrusor overactivity. Similarly, no patient showed detrusor pressure exceeding 40cmH₂O during the filling phase. Additionally, 10 patients (10/16, 62.5%) who had presented with an underactive bladder during the voiding phase showed recovery by the 24-week assessment.

4 Discussion

GBS, as an immune-mediated, rapidly progressive polyneuropathy, can be classified into several subtypes based on clinical manifestations and electrophysiological characteristics (3). During the peak phase of the illness in pediatric populations, approximately 75% of patients lose the ability to walk independently, 30% develop tetraparesis, 35–50% exhibit cranial nerve involvement, and 15–20% experience respiratory failure and/or autonomic dysfunction (3, 4). Although GBS primarily affects motor and sensory nerves, autonomic dysfunction-though less common-can lead to NLUTD, significantly affecting the patient’s quality of life (57).

The uroflowmetry is a non-invasive procedure and the first-line method for evaluating the function and dysfunction of the lower urinary tract (9). It involves measuring parameters such as flow rate, voided volume, voiding time, and analyzing the uroflow pattern (911). Based on our study, all patients exhibited a decreased Qmax along with elevated PVRU. Their flow curves consistently demonstrated an interrupted pattern, indicative of underactive bladder. Each peak in the flow curve corresponded to abdominal straining, which served as the primary driving force for urination. Flow ceased between successive straining episodes.

UDS is not routinely used to evaluate lower urinary tract function in neurologically intact children, but is regularly performed in those with suspected neurogenic bladder (NB) (7, 9). This study assesses both the filling and voiding phases of bladder function. Cystometry, in particular, refers to the urodynamic investigation conducted during the filling phase of the micturition cycle. Bladder storage function should be characterized using objective parameters, including bladder capacity, bladder compliance, and detrusor activity (11, 12). In our cohort, the bladder capacity of vast majority of patients (14/16, 87.5%) increased accompanied by reduced bladder sensation during the filling phase; only two cases (2/16, 12.5%) showed decreased bladder capacity with detrusor overactivity. Pressure-volume relationship was evaluated during the voiding phase, and an underactive bladder was the predominant finding of NLUTD during the acute phase in all 16 patients. In our study of urodynamic evaluation, high-risk and unfavorable urodynamic findings of 16 patients-such as low bladder compliance and detrusor overactivity-were observed in only two patients (2/16, 12.5%) within the 6-month period. After 6 months of follow-up, urodynamic parameters normalized in the majority of patients, an outcome facilitated in part by biofeedback therapy. Specifically, 10 patients (10/16, 62.5%) who had presented with an underactive bladder during the voiding phase showed recovery by the 24-week assessment. These results indicated that the prognosis of NLUTS for children with GBS was likely to generally more favorable (1315).

However, this study had several limitations. First, the retrospective chart review design inherently limited the availability and consistency of data. Second, the potential influence of biofeedback therapy on the urodynamic parameters could not be definitively assessed, such as maximal cystometric capacity, bladder compliance, and detrusor pressure in the context of neurogenic bladder. Third, the small sample size may restrict the generalizability of the findings. Future prospective studies incorporating larger cohorts and longitudinal repeated urodynamic evaluations are warranted to validate these results and clarify the long-term outcomes.

5 Conclusion

In conclusion, NLUTD secondary to GBS in children primarily manifested as urinary retention, characterized by a decreased Qmax on uroflowmetry and elevated PVRU. UDS revealed two predominant findings: reduced bladder sensation during the filling phase and detrusor underactivity during the voiding phase. The prognosis for pediatric GBS patients was generally favorable, with most cases of GBS-associated NLUTS showing substantial reversibility, as confirmed by the normalization of urodynamic parameters over time.

Statements

Data availability statement

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.

Ethics statement

The studies involving humans were approved by the ethics committee of West China Second University Hospital (protocol code 20250088). The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent for participation in this study was provided by the participants’ legal guardians/next of kin.

Author contributions

YL: Data curation, Formal analysis, Investigation, Methodology, Writing – review & editing. HZ: Conceptualization, Project administration, Writing – original draft, Writing – review & editing. NZ: Formal analysis, Investigation, Methodology, Writing – review & editing.

Funding

The author(s) declare that no financial support was received for the research and/or publication of this article.

Acknowledgments

We thank the Urodynamic study room. We are also very grateful to the enrolled patient and his parents, many fellows, technical and administrative staffs.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Generative AI statement

The authors declare that no Gen AI was used in the creation of this manuscript.

Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.

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Summary

Keywords

Guillain-Barre syndrome, neurogenic urinary bladder, urinary retention, urodynamics, children

Citation

Long Y, Zhang H and Zhang N (2025) Urodynamic evaluation of neurogenic lower urinary tract dysfunction in children with Guillain-Barre syndrome within 6 months. Front. Neurol. 16:1706698. doi: 10.3389/fneur.2025.1706698

Received

16 September 2025

Revised

12 November 2025

Accepted

27 November 2025

Published

08 December 2025

Volume

16 - 2025

Edited by

Federica Silvia Ricci, University of Turin, Italy

Reviewed by

Mücahit Kart, Antalya Eğitim ve Araştırma Hastanesi, Türkiye

Andrea Sartori, Harvard Medical School, United States

Updates

Copyright

*Correspondence: Hui Zhang,

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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