Objective: To review the evidence surrounding Sacral Neuromodulation therapy and delineate areas that will need more research. Methods: An extensive search was performed on the available literature on SNM for lower urinary tract dysfunction. Based on the results of the search, the mechanisms of action, indications, technique, and patient characteristics of therapy failures and success are presented and discussed. Results: SNM is accepted by the FDA since 1997 for the treatment of lower urinary tract dysfunction. As it is a relatively new procedure, there are variations in the technique of lead placement, generator choice, testing interval, patient selection, time to explantation, and definitions of therapy failures and successes. Conclusions: SNM is a safe and therapeutic option for the treatment of urgencyfrequency syndrome, urge incontinence, and idiopathic urinary retention. However, there are multiple unanswered questions that require extensive research.
Sacral neuromodulation (SNM) received approval from the US Food and Drug Administration in 1997 for the treatment of urgency-frequency syndrome, refractory urge incontinence, and idiopathic urinary retention. It has become a valuable therapeutic option for patients that have failed anticholinergic therapy, behavioral modifications and pelvic floor rehabilitation. Several studies reported positive responses with SNM treatment in refractory lower urinary tract issues. However, there are also reports of treatment failures and explants. Not much is known at this time regarding the predictors of success or failure with SNM. There is limited literature that indicates higher failure in neurogenic voiding dysfunction, older populations and those with longer duration of symptoms. Several trials have evaluated InterStim Therapy and have provided the data from which surgeons decide optimal treatment protocols for their patients. However, there are many unanswered questions. It is not clear what is the most efficient and cost effective approach to select patients for SNM. Staged approach seems to be superior with close to 80% success of implanting a generator, however data is limited by small numbers. The optimum length of test phase is yet to be determined. Length of time is balanced by potential for infection at the leads. It is also not clear how long the device will stay effective and if there is deterioration in function over time either due to reaction in leads or changes in generator. The purpose of this article is to review the evidence surrounding SNM therapy and delineate areas that need more research.
Sacral neuromodulation (SNM) is FDA approved for urge incontinence, non-obstructive urinary retention and urinary urgency and frequency. It is unclear how SNM works in patients with urinary dysfunction but possible explanations rely on modulating the micturition reflex pathway, rather than directly modulating the motor response of the urethral sphincter or detrusor. Normal detrusor functioning depends on sympathetic and parasympathetic neural pathways. The sympathetic nervous system allows for urinary retention and storage while the parasympathetic nervous system allows for detrusor contraction and bladder emptying. Supraspinal inputs from the pontine micturition center influence the micturition reflex pathway. It is hypothesized that SNM modulates signaling from the somatic and afferent nerves that control the micturition reflex pathway. Simultaneously, detrusor, sphincter and urethral vesica are affected. In patients with overactive bladder, SNM inhibits detrusor activity without affecting the strength of detrusor contractions or urethral resistance. For urinary retention, SNM suppresses the guarding reflex to decrease urethral sphincter tone and allow voiding.
SNM therapy is considered when the patient with OAB has exhausted conservative therapies which include lifestyle changes, pelvic floor physiotherapy, bladder training and anticholinergic medications. As of 2013, SNM has FDA approval for overactive bladder (including urgency and frequency with or without urgency incontinence), urinary retention and fecal incontinence. Clinical benefit has been documented in cases of interstitial cystitis, and chronic pelvic pain. This article focuses on SNM use pertaining to lower urinary tract.
Sacral neuromodulation can be accomplished either as a staged implantation with tined leads or a peripheral nerve evaluation (PNE) with temporary electrodes followed by full system implantation. The peripheral nerve evaluation is done as an outpatient procedure using a monopolar electrode. After correct placement of the electrode in the sacral foramina, the temporary electrode is attached to the skin with adhesives for the duration of the 4 to 7 day test period. If the patient has a successful test phase, then the temporary electrode is removed and the patient is taken to the operating room for implantation of the permanent tined lead and the implantable pulse generator (IPG).
The staged technique consists of an initial test stage (acute and subchronic neuromodulation) and then an implantation stage (chronic neuromodulation). In contrast to PNE, the staged technique uses quadripolar tined leads that contain an intrinsic retention mechanism. Prior to the introduction of the self-anchoring “tined” lead in 2002, the older leads required implantation during an open surgical procedure with the leads being secured to the sacral periosteum. The introduction of tined leads allowed for percutaneous placement under radiological guidance. The use of tined leads enabled physicians to directly evaluate sensory responses to stimulation while the patient was under local anesthesia. Other advantages included shorter operative time and post operative recovery time, less infection and less pain. More importantly, tined leads have reduced the incidence of lead migration.
The patient is placed in prone position with visualization of the anal region and feet to assess reflex response. Either general or local anesthesia can be used but muscle relaxants should be avoided in the case of general anesthesia. Localization of the sacral nerves S2, S3 or S4 are identified with or without the aid of imaging, and a needle is inserted in the sacral foramen at an angle of about 60 degrees. Medial insertion of the needle improves the chance of obtaining optimal motor and sensory response of the anus and pelvic floor [
Most commonly, the S3 foramen is targeted because it provides the best motor and sensory response to stimulation. The S3 foramen is localized halfway between the coccyx tip and the last spinous process of the lumbar spine. Govaert et al. observed similar success rates between S3 and S4 [
The needle is connected to an external stimulator and low amplitude electrical currents are applied. Correct positioning of the leads is confirmed by assessing motor and sensory responses to stimulation. Typical responses include contraction of the levator ani muscle, a tapping or vibrating sensation in the vaginal or anal region, and dorsiflexion of the great toe on the ipsilateral side of the test stimulation. Additionally, correct position of the leads can be confirmed by fluoroscopy. Once correct placement is confirmed, electrode leads are inserted through the needle and the needle removed.
The test period should last a minimum of three days and typically 1 - 2 weeks. The patient is required to keep a voiding diary before and during the test stimulation period. If the patient has a 50% improvement of symptoms both subjectively and objectively then she is eligible for a stage 2 procedure. Parameters used to evaluate the clinical effect differ depending of the nature of the initial complaint. In patients with chronic urinary retention, values assessed include reduction in the volume at catheterization and increase in voided volume. For those with OAB dry, the most important parameters include the voided volume per void and voiding frequency. Lastly, in patients with OAB wet, the number of leakages per day and the number of pads used per day are evaluated. Patients with positive response then undergo stage 2 where pulse generator is implanted in a subcutaneous pocket in the lower abdomen or buttock.
The optimal stimulation setting for the implantable neurostimulator (INS) is chosen by assessing the sensory response to different settings. The stimulation setting that gives the best sensory response at the lowest amplitude is optimal. The optimal pulse rate is generally set between 10 and 16 Hz and the pulse width is set at 210 ms. It is unclear whether different pulse rates and pulse widths have different treatment efficacies. Although patients are advised to keep the INS on at all times, they are given a remote control to turn the INS on or off when necessary and alter the stimulation amplitude.
Patients are scheduled for follow up after implantation at six weeks, six months and yearly thereafter. Patients should be assessed for symptom relief, pain, patient comfort and compliance with SNS. The INS should be checked for proper impedance levels and patient compliance with stimulation settings. If the impedance is less than 50 Ohms or more than 4000 Ohms, then there may be damaged leads. Damaged or migrated leads can result in loss of efficacy and, thus, therapy failure. Leads can be replaced or new leads can be inserted in the contralateral sacrum. Pain can be located at the implantation site or the site of perceived sensation. If the stimulator is turned off and the pain persists, then the pain is at the implantation site and likely physical discomfort. However, if the pain decreases, then it is stimulation related. Pain relief can be achieved by modifying INS settings, repositioning the INS or adjusting lead placement. Approximately thirty-three percent of patients have required surgical revision and ten percent have needed permanent removal [
The first study of staged implantation reported a 60% to 90% improvement in treatment response when using the permanent electrode in a cohort of patients with a negative PNE result [
The differences in IPG implantation rates between PNE and staged techniques are not clearly understood. However, the quadripolar leads have been shown to have greater variety of programming options and stimulation patterns that can be manipulated to benefit the patient. The success of staged implantation is likely due to the use of the permanent electrodes for evaluation. In fact, three different trials found that permanent electrodes doubled the treatment response rate of SNM [9-11]. Additionally, some patients who fail a PNE test will pass a staged trial [
To date, there are few cost-benefit analyses comparing staged implantation to PNE. A study by Nikolavsky et al. showed that in patients with Blue Cross/Blue Shield insurance the single stage procedure would be more cost effective than a two-stage implantation. In patients with Medicare, the cost differences were not seen [
There is no consensus on the placement of unilateral or bilateral tined leads. Sheepens et al. reported that there was no advantage of bilateral lead placement, although some patients with nonobstructed urinary retention required bilateral SNM for success [
There is no consensus regarding patient characteristics that should be considered contraindications for SNM. Amundsen et al. concluded that older age, the presence of neurological conditions, spinal cord disease, the presence of three or more chronic conditions, and longer duration of complaints are negatively associated with SNS success [
Additionally, two studies found that patients who had a change in their body mass index post implantation had more complications than those who did not have significant weight fluctuations [20,23]. However, obesity itself is not considered a risk factor for SNS failure and a 2012 study by Levin et al. concluded that obesity should not be a contraindication for InterStim therapy [
Intraoperative predictors of success include motor and sensory response to stimulation during lead placement. A study in 2006 concluded that sensory response was not a reliable indicator of success [
Complications with SNS are reported as adverse events that encompass change in clinical efficacy, pain, wound complication, infection, lead migration, and device failure. Many problems can be managed conservatively but some require surgical intervention. Van Kerrebroeck’s multicenter trial reported that 67% of 152 implanted patients had adverse events. Two hundred twenty one adverse events were recorded [
Another multicenter trial reported a 33% surgical revision rate in 219 implanted patients [
Yazdany et al. attempted to identify patient characteristics that would predict explantation [
Rates of adverse events, surgical revision and explantation thus vary from study to study, some variation is attributable to inconsistent use of new technology, inconsistent patient follow up with the same physician, patient compliance and surgeon preference of revision versus explantation. Thus, counseling patients about the risks and benefits of SNS becomes heavily dependent on the physician’s understanding of the literature and personal biases.
Most studies defined success of treatment as the percentage of patients who had more than 50% improvement in key voiding diary variables at last follow up visit. Siegel’s multicenter, prospective trial of 41 patients with urge incontinence, 29 patients with urgency frequency, and 42 patients with urinary retention reported persistant improvement of symptoms after 18 to 36 months of InterStim usage [
Other studies have reported that 75% of patients not improved by conservative options such as medications and biofeedback therapy can expect a therapy response with InterStim treatment [
Sacral neuromodulation has become a valuable treatment option for chronic lower urinary tract voiding dysfunction. Multiple factors are integral to the success of SNM therapy including but not limited to patient selection, surgical technique, patient compliance, insurance status, and surgeon preference. Furthermore, advancements in technology are improving rates of revision, explantation and patient satisfaction. Regardless, our understanding of how neuromodulation works is still incomplete. And, despite of the significant number of patients undergoing SNM, there are many unanswered questions.
Patient Selection: While certain patient characteristics have proven to be predictors of SNM success, it is still unclear how comorbidities influence success and what modifications would be effective in combating those issues. Furthermore, as SNM is being expanded to the pediatric population better guidelines are needed to define optimal treatment. In addition, algorithms for patient follow up and evaluations are needed. What are the predictors of success? Are there urodynamic predictors of success? Are there patient characteristics that predict success or failure? What is the efficacy in diabetics, multiple sclerosis or other neurological conditions? How effective is the devise in older populations, obese patients and those with long standing symptoms?
Staged Procedures: More data is needed to compare the benefits and risks of a two-stage sacral nerve stimulation procedure versus out patient PNE followed by full system implantation. Response rates after PNE need to be studied and ultimate chance of patient getting generator with the two approaches needs to be determined. Provider and facility costs with these two approaches need to be taken into consideration as well. Is PNE worth offering as the overall rate of getting generator is low in patients that start of with PNE compared to direct stage 1? Are there activity restrictions and recommendations, better adhesive leads to improve the efficacy of PNE?
Is the overall cost burden related to procedure less with direct stage 1 compared to PNE? What is the ideal test interval between PNE and stage 2? Is it between stage 1 and stage 2? Is there difference between the two protocols?
Lead Placement/IPG Choice: Variations of tined lead placements need to be explored. It is unclear if unilateral SNM is as effective as bilateral SNM and whether the choice of sacral foramina (S3 vs.S4) impact success rate. Is there evidence to examine effect of lead placement at S2 or S4 in patients that fail S3 lead placement?
Therapy Time/Failures: It is unclear how long a patient can stay on SNM therapy before it starts to fail. Whether there are patient and/or device indications that can signal decreasing efficacy need to be evaluated. What is the long-term success of SNM? Does the performance of device or leads decline over time? If a patient fails SNM, what are the next steps in therapy?
Alternatives to SNM: Are there viable alternatives to SNM? Would peripheral nerve stimulation via the pudendal nerve or the posterior tibial nerve and botox injection into bladder be good options in certain patient populations? Is there concrete evidence for bilateral lead placement?
Future multicenter trials will help to answer these questions and allow surgeons to provide the best care possible. A working group of high volume users of SNM, and a prospective registry will also help to answer some of these questions.