http://orcid.org/0000-0002-3972-4589
Figures
Abstract
Objective
To systematically review outcomes in patients with refractory overactive bladder (OAB) patients who underwent sacral neuromodulation therapy (SNM) therapy after unsuccessful onabotulinumtoxinA (BTX) therapy, and to compare outcomes with those who SNM as initial therapy.
Methods
A systematic search of Cochrane Library, Pubmed and Embase databases from July 2002 to November 2019, to analyze randomized controlled trials and retrospective studies of SNM therapy after failed initial BTX therapy. Two reviewers independently screened the studies and extracted data. A quality assessment of the included literature was conducted using Newcastle-Ottawa Scale (NOS), and Stata 12.0 software was used to conduct a meta-analysis of the collected data.
Results
A total of seven studies involving 319 patients were finally included. The success rate in refractory OAB patients who used SNM therapy after failed BTX therapy was 58.5%, 95% CI (0.47–0.70). There was no significant difference between refractory OAB patients who chose SNM as replacement therapy after failed BTX therapy and those who used SNM therapy as first choice [RR = 0.96, 95%CI (0.72–1.26), P = 0.735].
Citation: Yang G, Xu Y, Qu G, Zhang Y (2020) Refractory overactive bladder patients who chose sacral neuromodulation therapy after failed OnabotulinumtoxinA treatment: A systematic review and meta-analysis. PLoS ONE 15(3): e0230355. https://doi.org/10.1371/journal.pone.0230355
Editor: Robert Hurst, University of Oklahoma Health Sciences Center, UNITED STATES
Received: May 21, 2019; Accepted: February 27, 2020; Published: March 30, 2020
Copyright: © 2020 Yang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All the data are available from the PubMed, Embase, and Cochrane library databases.
Funding: Yulong Zhang has received the Science and Technology Innovation Project of Hunan Province, 2017SK51003. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
The International Continence Society (ICS) committee has defined OAB as “a syndrome characterized by symptoms of urgency, with or without urgency incontinence, usually with increased daytime frequency and nocturia (increased night time urination). OAB includes detrusor instability and hyperreflexia, both of which are described as neurogenic detrusor overactivity (NDO)[1]. In a telephonic survey of six European countries[2], the overall prevalence of OAB among individuals 40 years and older of both genders was 16.6%. Its incidence surpassed that of Alzheimer disease and osteoporosis. An overall 6.0% prevalence rate of OAB (5.9% of males, 6.0% of females) was reported from China’s first large-scale survey of communicable diseases[3].
Traditional treatment options for OAB’s include: ① Behavioral therapy with bladder training, biofeedback, pelvic floor muscle exercise, and hypnotherapy. ② Pharmacological therapy with anticholinergics and muscarinic receptor antagonists. When these treatments become ineffective or unsuitable, injections of BTX into the detrusor muscle and SNM are the third line treatment. Both methods have their own advantages and disadvantages.
Amundsen et al.[4] reported a multicenter random trial of BTX therapy for refractory urgency urinary incontinence and found that the efficacy was higher than of SNM; however, BTX therapy often led to urinary tract infections and the need for transient self-catheterizations. Dowson et al.[5] found that at least 37% of patients stopped using BTX therapy after the first two injections, and that the most commonly reported reasons for doing so were that it was ineffective and that there were related problems caused by intermittent urinary catheters. As for refractory OAB patients who initially chose BTX therapy, but for whom it was later ineffective or they stopped using it due to adverse reactions, whether or not to continue choosing SNM therapy is a clinical issue that must be addressed. After failure of BTX therapy for refractory OAB, there is a possibility that an even more resistant form of OAB will appear[6]. This creates limitations as to the purposes for using SNM replacement therapy. In the present study, we performed a meta-analysis to address the question of whether or not patients with refractory OAB can continue to use SNM therapy after the initial choice and failure of BTX therapy.
Materials and methods
Inclusion and exclusion criteria
Inclusion criteria were as follows: randomized controlled trials and observational studies involving refractory OAB patients who chose SNM therapy after ending BTX therapy; urodynamic tests confirmed that the patients had detrusor overactivity; other related types of diagnoses were excluded; the control group included refractory OAB patients who initially chose SNM therapy. There were no limitations regarding gender, ethnicity, or nationality. If there were identical studies from the same research group, the most recent and most comprehensive study was chosen. Observation indexes were as follows: the success rate in patients with refractory OAB after receiving therapy, including recordings of voiding diary, quality of life (QOL), OAB symptom scores (OABSS), residual urine volume (bladder ultrasound measurement), maximum flow rate, and others. The level of improvement of the main symptoms reached or exceeded 50%, while the therapeutic efficacy met the patients’ expectations, and was regarded as successful treatment of refractory OAB. Exclusion criteria were as follows: OAB combined with other urinary diseases (including stones, tumors, urinary tract infections, and others.); non-English or duplicate publications; data reported in the literature that were incomplete, unusable, or could not be acquired by contacting the author.
Literature retrieval strategy
Search words were: ‘botulinum toxin’, ‘botulin’, ‘botulinum neurotoxin’, ‘botulinum’, ‘botulinum toxin’, ‘botulinum neurotoxins’, ‘botulism toxin’, ‘botulin toxin’, ‘botulinum toxin’, ‘botulinum a toxin’, ‘sacral neuromodulation’, ‘sacral nerve electrostimulation’, ‘sacral nerve stimulation’, ‘OAB’, ‘overactive bladder’, and ‘urinary bladder hyperactivity’. A comprehensive literature search was carried out on November 11, 2019 using PubMed, Embase, and Cochrane Library databases. Simultaneously, we looked up relevant studies by referencing other literature. The literature publication dates were limited to the period between July 2002 to November 2019. The study selection process is summarized in Fig 1.
From: Moher D, Liberate A, Tetzlaff J, Altman DG. The PRISMA Group (2009). Preferred Reporting items for Systematic Reviews and Analyses: The PRISMA Statement. PLoS Med 6(7): e1000097. doi: 10.1371/journal.pmed1000097. For more information, visit www.prisma-statement.org.
Literature screening and data extraction
Two researchers independently screened the literature and extracted the data. They cross-checked the data, and if they encountered differences of opinion, they discussed with each other to resolve disputes of opinion or submitted the issue to a third party for resolution. A self-made data extraction chart was adopted to extract the following data: ① the basic information included in the study, including research objective, authors, the publication where the literature was published and the time of publication, and others; ② the baseline characteristics of the research participants, including each group’s average age and gender distribution; ③ the primary factors of bias risk assessment; ④ all relevant outcome indicators and data related to results measurement.
Bias risk assessment for research inclusion
The quality of the nonrandomized studies was assessed using NOS with some modifications to match this study’s needs. The NOS included observational studies, specifically including patient selection, comparability and results assessments of the research participants, with the highest score at 9 points (Table 1).
Statistical analysis
Stata 12.0 software was used to conduct a meta-analysis of the data. Publication bias was estimated based on the funnel plot. Effect size was expressed as point estimation value and 95% confidence interval (CI). Studies with an I2 statistic>50% or p< 0.1 were considered to have significant heterogeneity. A fixed-effects model was used if there was no significant heterogeneity. Otherwise, random-effects model were employed in the meta-analysis.
Results
An initial search produced 612 relevant articles, and after strict screening for inclusion and exclusion criteria. Eventually, seven retrospective studies[6–12] were involved in this study. The literature screening process and results are shown in Fig 1. The seven included retrospective studies included 319 patient cases. The baseline characteristics and NOS score results for research inclusion are illustrated in Table 2.
Meta-analysis results
The success rate of refractory OAB patients choosing SNM as replacement therapy after ending BTX therapy. The results of meta-analysis are shown in Fig 2. There was a total of six included studies[6–12] tested for heterogeneity: each index where there was significant heterogeneity (p = 0.014, I2 = 62.4%). A randomized effects model was adopted to conduct a synthesized analysis of the data. We used a fixed effects model to synthesize the size of each index’s group mean. The overall results and those of the random effects model were similar, demonstrating that the synthesized outcomes had good stability and were reliable. Synthesis of the effects size was as follows: After the six included studies were weighted and synthesized, the success rate of refractory OAB patients who used SNM therapy after ending BTX therapy was 58.5%, 95% CI (0.47–0.70).
We compared outcomes in patients with refractory OAB who chose SNM therapy after ending BTX therapy and those for whom the initial choice was SNM therapy. The results of meta-analysis are shown in Fig 3. There was a total of four included studies[6–9] tested of heterogeneity: For each index, the magnitude of heterogeneity was zero (p > 0.10, I2 = 0); therefore, a fixed effects model was adopted to conduct a synthesized analysis of the data. Synthesis of the effect size: After the four included studies were weighted and combined, the resulting statistic RR was 0.96, [95% CI: 0.72–1.26], and there was no significant difference between the two groups (p = 0.735).
Publication bias is defined as the problem that results from systematic differences between the results of all the completed studies on a topic and the results of the subset of those studies that are published[13]. The plot in Fig 4 resembles a symmetrical inverted funnel (95% CI), inside which are all studies included in our meta-analysis. There was no evidence of publication bias as revealed by the distribution of the funnel plot.
Discussion
The American Urological Association (AUA) and the Society of Urodynamics, Female Pelvic Medicine & Urogenital Reconstruction (SUFU)’s updated guidelines classify BTX and SNM as third-line treatment options for refractory OAB[14]. Henriet et al.[15] performed a systematic retrospective study and found that injecting BTX inside the detrusor muscle effectively increased bladder capacity, improved OAB symptoms, and enhanced QOL. Nevertheless, the most commonly seen side-effect was incomplete emptying and intermittent urinary catheterization with accompanying increased risk of urinary tract infections. After undergoing BTX therapy, the possibility that refractory OAB patients may require insertion of an intermittent urinary catheter varied from 16% to 42%[16,17]. For patients in whom BTX therapy for refractory OAB failed or the patients appeared unwilling to continue receiving BTX therapy, SNM was the only minimally invasive replacement therapy method.
Our meta-analysis revealed that the success rate of SNM therapy after the initial choice and failure of BTX therapy was 58.5%, 95% CI (0.47–0.70). Furthermore, there was no significant difference in terms of the effectiveness of SNM therapy after the initial choice and failure of BTX therapy as compared to the initial choice of SNM therapy, with an RR of 0.96, [95% CI: 0.72–1.26] (not significant, p = 0.735). This may be related to the differences created between the preceding research results and the action of BTX and SNM on the mechanism of action of OAB. BTX quickly binds the neuromuscular end-plate to inhibit the release of acetylcholine from presynaptic membranes, thereby removing innervation in the form of muscle relaxation and paralysis. It also has the therapeutic effect of alleviating spasms and stiffness. It is also related to the mechanism of SNM therapy in treatment of OAB and adjusting micturition reflexes with sacral cord afferent impulses. Compared to the local response to BTX, SNM has an even more central role.
In terms of treating OAB, SNM therapy has long-term and stable healing effects; its most commonly seen side-effect is regional pain at the implant site, with an incidence of 3–42%. Its side-effects include impaired defecation (4–7%), infection (4–10%), and electrode malposition (1–21%)[18,19]. Among refractory OAB patients who initially chose SNM therapy, there were some who abandoned SNM therapy because it was ineffective or they could no longer tolerate the side-effects. There is currently a major controversy regarding whether they could continue to use BTX as second line therapy for SNM therapy. Kirkpatrick et al.[20] performed a retrospective analysis and found that when patients with urge incontinence OAB received BTX therapy after failure of SNM therapy, it was even more effective than was BTX therapy. By contrast, recent studies reported that the success rate when OAB patients chose BTX therapy after the initial choice and ineffectiveness of SNM therapy was only 27%–39%[21,22]. Currently, there is a need for more high-quality research before one can confirm the efficacy of OAB in those who receive BTX therapy after the failure of initially undergoing SNM therapy.
This research’s advantages are demonstrated in the wide-ranging literature retrieval, and the included standard can be reproducibly operated. The methodology is feasible, and the assessment and data collection are reproducible. Our research is the first systematic review with meta-analysis assessing refractory overactive bladder patients who chose sacral neuromodulation therapy after failed onabotulinumtoxinA treatment, which guides clinical practice and future research. There were several limitations of this study: 1) there was a limited amount of pertinent research, and most of the research samples were relatively small and there is a paucity of randomized controlled trials; 2) despite the fact that we selected relatively better examples of recently published literature, there remained problems with homogeneity and sensitivity. As a result, there is a need for more comprehensive studies with acceptable homogeneity and sensitivity; 3) there were also linguistic limitations. We included only English publications; therefore, we might have missed pertinent research published in other languages. Large scale and multi-center studies are needed to further validate our results.
Conclusion
Current evidence suggests that patients with refractory OAB who either failed or were dissatisfied with BTX therapy can chose SNM therapy. It is effective and shows no substantial differences in terms of outcomes from SNM initial therapy.
References
- 1. Abrams P, Cardozo L, Fall M, et al. The standardisation of terminology of lower urinary tract function: report from the Standardisation Sub-committee of the International Continence Society[J]. Am J Obstet Gynecol, 2002, 187(1): 116–126. pmid:12114899
- 2. Milsom I, Abrams P, Cardozo L, et al. How widespread are the symptoms of an overactive bladder and how are they managed? A population-based prevalence study[J]. BJU Int, 2001, 87(9): 760–766. pmid:11412210
- 3. Wang Y, Xu K, Hu H, et al. Prevalence, risk factors, and impact on health related quality of life of overactive bladder in China[J]. Neurourol Urodyn, 2011, 30(8): 1448–1455. pmid:21826714
- 4. Amundsen C L, Richter H E, Menefee S A, et al. Onabotulinumtoxin a vs sacral neuromodulation on refractory urgency urinary incontinence in women: A randomized clinical trial[J]. JAMA—Journal of the American Medical Association, 2016, 316(13): 1366–1374.
- 5. Dowson C, Watkins J, Khan M S, et al. Repeated botulinum toxin type A injections for refractory overactive bladder: medium-term outcomes, safety profile, and discontinuation rates[J]. Eur Urol, 2012, 61(4): 834–839. pmid:22204745
- 6. Hoag N, Plagakis S, Pillay S, et al. Sacral neuromodulation for refractory overactive bladder after prior intravesical onabotulinumtoxinA treatment[J]. Neurourology and Urodynamics, 2017, 36(5): 1377–1381. pmid:27612039
- 7. Forrest A, Eldaly A, Kenefick N, et al. The efficacy of sacral nerve stimulation, with reference to previous intravesical botulinum toxin a injection, for the treatment of refractory overactive bladder[J]. International Urogynecology Journal and Pelvic Floor Dysfunction, 2011, 22: S1771–S1772.
- 8. Morton H, Harding C. Does prior treatment with intravesical botulinum toxin a affect the outcome of sacral neuromodulation evaluation in patients with refractory detrusor overactivity?[J]. Neurourology and Urodynamics, 2015, 34: S236–S237.
- 9. Singh R, El-Nashar S, Klingele C, et al. Patients treated with sacral nerve stimulation after failure of intravesical onabotulinum toxin injection compared to those with no historyof onabotulinum toxin for treatment of overactive bladder symptoms. Is there a difference in outcomes?[J]. Female Pelvic Medicine and Reconstructive Surgery, 2014, 20: S351–S352.
- 10. Smits MA, Oerlemans D, Marcelissen TA, et al. Sacral neuromodulation in patients with idiopathic overactive bladder after initial botulinum toxin therapy[J]. J Urol, 2013, 190(6): 2148–2152. pmid:23872028
- 11. Abtahi B, Gonzales G, Digesu A, et al. Sacral neuromodulation in patients with intractable detrusor overactivity who failed to respond to treatment with botulinum toxin[J]. International Urogynecology Journal and Pelvic Floor Dysfunction, 2013, 24: S123.
- 12. Agarwal S, Zahner P, Giusto L, et al. Salvage sacral nervestimulation after inadequate response to onabotuliunumtoxin a for the treatment of overactive bladder is there hope after crossover? [J]. Neurourology and Urodynamics, 2018, 37: S646–S649
- 13. Lau J, Ioannidis JP, Terrin N, et al. The case of the misleading funnel plot[J]. Bmj, 2006, 333(7568): 597–600. pmid:16974018
- 14. Gormley E A, Lightner D J, Faraday M, et al. Diagnosis and treatment of overactive bladder (non-neurogenic) in adults: AUA/SUFU guideline amendment[J]. J Urol, 2015, 193(5): 1572–1580. pmid:25623739
- 15. Henriet B, Roumeguere T. [Botulinum toxin injection for refractory non-neurogenic overactive bladder. Systematic review][J]. Rev Med Brux, 2015, 36(1): 29–37. pmid:25856969
- 16. Sahai A, Khan M S, Dasgupta P. Efficacy of botulinum toxin-A for treating idiopathic detrusor overactivity: results from a single center, randomized, double-blind, placebo controlled trial[J]. J Urol, 2007, 177(6): 2231–2236. pmid:17509328
- 17. Brubaker L, Richter HE, Visco A, et al. Refractory idiopathic urge urinary incontinence and botulinum A injection[J]. J Urol, 2008, 180(1): 217–222. pmid:18499184
- 18. Hassouna MM, Siegel SW, Nyeholt AA, et al. Sacral neuromodulation in the treatment of urgency-frequency symptoms: a multicenter study on efficacy and safety[J]. J Urol, 2000, 163(6): 1849–1854. pmid:10799197
- 19. Hijaz A, Vasavada SP, Daneshgari F, et al. Complications and troubleshooting of two-stage sacral neuromodulation therapy: a single-institution experience[J]. Urology, 2006, 68(3): 533–537. pmid:16979724
- 20. Kirkpatrick G, Brown G, Sussman D. The efficacy of on abotulinumtoxina (Botox) in patients with urge urinary incontinence who failed sacral neuromodulation (interstim)[J]. Neurourology and Urodynamics, 2015, 34: S22.
- 21. Baron M, Delcourt C, Pfister C, et al. Efficacy and tolerance of botulinum toxin injections after sacral nerve stimulation failure for idiopathic overactive bladder[J]. European Urology, Supplements, 2018, 17(2): e1356.
- 22. Trinh H, Irish V, Diaz-Insua M, et al. Effectiveness of intradetrusor onabotulinum toxin a injections in managing overactive bladder after initial sacral neuromodulation therapy[J]. Neurourology and Urodynamics, 2018, 37: S652.