Abstract
Introduction and objectives:
Overactive bladder syndrome (OAB) is defined as urinary urgency, with or without urgent urinary incontinence; it is often associated with urinary frequency and nocturia, in the absence of any pathological or metabolic conditions that may cause or mimic OAB. The aim of this study was to evaluate the long-term real-life adherence of transcutaneous tibial nerve stimulation (TTNS) in the treatment of OAB, patient satisfaction of the treatment, and reasons for quitting therapy.
Materials and methods:
In this single center study, all patients who had a positive effect on percutaneous tibial nerve stimulation (PTNS) and continued to receive home-based treatment with TTNS since 2012 were included for analysis. Patients were retrospectively asked to fill out a questionnaire regarding satisfaction, reasons for quitting, and additional or next line of therapy.
Results:
We included 42 patients for this study, 81% of these patients were female (
Conclusion:
TTNS, although effective in the short-term, is not effective in the long-term. In combination with a low satisfaction rate among patients, there is a need for improvement in terms of OAB treatment modalities.
Keywords
Introduction
Overactive bladder syndrome (OAB) is defined by the International Continence Society (ICS) as urinary urgency, with or without urgent urinary incontinence, and often associated with urinary frequency and nocturia, in the absence of any pathological or metabolic conditions that may cause or mimic OAB.
1
OAB treatment starts, according to guidelines, with behavioral therapy and if needed, is supplemented with drug treatment. When drug treatment is unsuccessful, the next line of treatment consists of percutaneous tibial nerve stimulation (PTNS) or intravesical Onabotulinum Toxin A injections or sacral nerve stimulation (SNS).
2
Success rates of PTNS were described by Peters
Home-based treatment with transcutaneous stimulation of the tibial nerve (TTNS) could solve these problems. TTNS uses a surface electrode, instead of a needle, to stimulate the tibial nerve, which can be self-applied by patients.
5
Previous studies showed that TTNS in the study context is an effective treatment option in the treatment of idiopathic OAB.5–8 In particular, Ramírez-García
The aim of this study was to evaluate the long-term, real-life adherence of patients to TTNS for the treatment of OAB, including patient satisfaction and reasons for stopping TTNS.
Material and methods
In this single center study, all patients who had positive effect on PTNS and who continued to receive home-based treatment with TTNS since 2012 were included. Patients were retrospectively asked to fill out a questionnaire (supplementary data) regarding satisfaction, reasons for quitting, and additional or next line therapy. All patients were included in our single center university hospital. All patients started with at least 7 treatment sessions of PTNS (median 18, range 7–49 weeks) once a week, followed by an evaluation session with their urologist. If there was a subjective improvement of their OAB complaints, patients were asked to continue to receive home-based TTNS treatment. Instructions for home-based TTNS were given by a specialized nurse and evaluation was performed two weeks after the start of TTNS therapy. During this follow up moment, it was evaluated if they required additional training. After this, patients continued to receive maintenance therapy with TTNS at home, led by themselves, without any specific follow up.
Inclusions criteria for this study were patients with PTNS followed by TTNS. All patients who started PTNS and/or TTNS under the age of 18 were excluded for analysis, as were patients with mental or physical limitations for filling out the questionnaire [i.e., Alzheimer’s, post cerebrovascular accident (CVA) with physical limitations, illiterate]. Before the questionnaires were sent, patients were called to participate in the study. When patients could not be reached, they were defined as lost to follow up.
Baseline criteria and extra study details were retrieved from patient electronical files after receiving their informed consent. The questionnaire, which was sent to all patients, is included in the supplementary data. Statistical analysis was performed by using SPSS 22.0 (SPSS, Chicago, IL). Kaplan–Meier curves were used to estimate the survival of TTNS. Discontinuation of TTNS was used as an endpoint. The T-test was performed to determine statistical significance between the mean satisfaction score (scale 1–10) of both patient groups: patients who continued the treatment
Results
Baseline criteria
A total of 78 patients underwent PTNS followed by TTNS in our University Medical Center. Questionnaires were sent to 50 patients. The reasons and numbers for not being included in the study were as follows: 15 patients were lost to follow up, 6 patients had died, and 7 patients were determined to not be physically or mentally competent to fill out the questionnaire. Out of our 50 patients who met the inclusion and exclusion criteria, 8 patients did not respond to our request to fill out the questionnaires. As a result, we included 42 patients for this study (response rate intention to treat 55%, response rate per protocol 84%). Figure 1 shows the patient flow.

Study flow, patient inclusion/exclusion and number of patients final analysis.
42 Patients were included; of these, 81% were female (
PTNS analysis
All patients received weekly PTNS sessions prior to their treatment with TTNS. The median duration of their PTNS treatment was 18 weeks (range 7–49 weeks). We could not determine the duration of treatment for 3 patients, as these patients were treated in a hospital near their home instead of at our referral center.
TTNS analysis
All patients continued with TTNS after their PTNS treatment. The median TTNS treatment persistence was 16 months (ranges 1–112 months). Figure 2(a) illustrates the overall survival (OS) of TTNS treatment in all patients. Figure 2(b) illustrates the survival per category of OAB (OAB wet, OAB dry, and neurogenic origin). Unfortunately, due to the low numbers we could not perform any other statistical analysis. During treatment, 45% of the patients used TTNS on a daily basis, followed by 27.5% of the patients who were using it 3–6 times a week, and 22.5% who were using the system 1–2 times per week. Only a small percentage, 5%, used it less than once a week. Twenty-one percent continued treatment; reasons for and percentages for quitting therapy are shown in Figure 3. The main reason to discontinue TTNS was a loss of effect (55%).

(a) Treatment duration of TTNS in months among all patients (

Reasons for discontinuation of TTNS (
During TTNS treatment, almost 62% of the patients did not use any other form of treatment, 36% of the patients used medication as additional therapy, and in 2% it was unknown. The mean satisfaction score (scale 1–10), for which all patients rated their TTNS treatment, was 5.6 [
Discussion
We report that, in this real-life study, the median treatment persistence of TTNS is only 16 months after start treatment. In addition, 55% of patients quit their therapy because of a loss of effect over time, while most of them were treating themselves on a daily base. These results illustrate the main short comings of TTNS over time. TTNS has a positive effect on OAB symptoms; this is shown for short term follow up by Booth in their sham controlled TTNS study, and Schreiner in their randomized controlled trial (RCT), where patients received TTNS in addition to standard therapy [bladder training, programme of repeated voluntary pelvic floor muscle contraction (PFMT)].9,10 Although TTNS is successful at the start, we observed that most patients do not continue with their treatment in the long term due to the numerous reasons provided above.
If we compare our real-life data regarding the long-term treatment efficacy to existing studies, we do see slightly different outcomes. Leroux
Comparing our long-term TTNS therapy adherence data to real-life PTNS data, we do not see a large difference in outcome. As previously discussed, the median treatment persistence in our study was 16 months (
The main reason for TTNS discontinuation was a loss of efficacy or a lack of sufficient symptom relief. This is in line with other publications. Leroux describes that 70% of their patients stopped treatment due to a lack of sufficient symptom relief. 7 They further mentioned compliance difficulty and becoming asymptomatic as reasons for discontinuation. This could be the reason why, in their series, 70% of patients experienced a loss of effect; this is higher compared to the 55% in our study.
In this study we could only quantify the level of satisfaction rate of patients by recall for both treatment periods with PTNS and TTNS. Patients rated their TTNS treatment generally, with an overall 5.6 (scale 1–10) report grade. This fairly low score, in addition to the fact that patients often preferred a different form of TNM (24%) suggests that other forms of TNM had more satisfactory outcomes. These observations are in contrast to a RCT published by Martin Garcia followed by a non-inferiority study by Ramírez-García.6,8 Both studies concluded that there was no statistical difference in efficacy outcome and QoL questionnaires in TTNS
Posterior tibial neuromodulation, and as a part of this TTNS, has proven its efficacy over the years in the treatment of OAB.3,9,13 However, similar to other OAB treatment modalities, long term therapy adherence is poor and alternative treatment options are scarce. For the most part, OAB patients stop these forms of therapy because of side effects or a lack of efficacy in the longer-term.11,14 In our view, this is also the case for TTNS in the real-life setting. The limitations of our study are the number of patients which were included and the single center nature of the study. As shown in Figure 2(b), there could be some differences between OAB categories. However, our numbers were too low and this poses a limitation on reaching a solid conclusion. We hope that a more patient tailored, minimally-invasive treatment modality could enhance persistence and adherence for patients utilizing the current OAB treatment modalities in the future. As a result, developments in the efficacy of tibial nerve stimulation utilizing implantable devices is, therefore, of interest.15–17
Conclusion
Although many publications report a positive effect of TTNS on patients suffering from OAB in short term follow up, TTNS in the long term is not that effective in real-life. In combination with a low satisfaction rate, the need for other OAB treatments is still persistent. In order to appreciate the value of treatment modalities, also for OAB, more research in the real-world setting is needed.
Supplemental Material
sj-pdf-1-tau-10.1177_17562872211041470 – Supplemental material for Real-life patient experiences of TTNS in the treatment of overactive bladder syndrome
Supplemental material, sj-pdf-1-tau-10.1177_17562872211041470 for Real-life patient experiences of TTNS in the treatment of overactive bladder syndrome by Manon te Dorsthorst, Michael van Balken, Dick Janssen, John Heesakkers and Frank Martens in Therapeutic Advances in Urology
Footnotes
Author contributions
MtD: data collection, analysis, writing.
MvB: writing, protocol development.
DJ: writing.
JH: writing.
FM: writing, protocol development.
Conflict of interest statement
Manon te Dorsthorst: Participation in the OASIS-trial, regarding the RENOVA implantable stimulation device for Tibial Nerve Stimulation (Firm: Bluewind) Dick Janssen: no conflict of interest.
Frank Martens: Participation in the OASIS-trial, regarding the RENOVA implantable stimulation device for Tibial Nerve Stimulation (Firm: Bluewind) Michael van Balken: Participation in the OASIS-trial, regarding the RENOVA implantable stimulation device for Tibial Nerve Stimulation (Firm: Bluewind) John Heesakkers: Participation in the OASIS-trial, regarding the RENOVA implantable stimulation device for Tibial Nerve Stimulation (Firm: Bluewind)
Ethical approval
The study has been reviewed by the Ethics Committee of the Radboud University Nijmegen Medical Centre on the basis of the Dutch Code of conduct for health research, the Dutch Code of conduct for responsible use, the Dutch Personal Data Protection Act and the Medical Treatment Agreement Act. The ethics committee has passed a
Funding
The authors received no financial support for the research, authorship, and/or publication of this article.
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References
Supplementary Material
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