Hypothesis / aims of study
Sacral neuromodulation (SNM) is an established treatment for refractory overactive bladder (OAB) and urinary retention, according to American Urologic Association Guidelines. It achieves long-term symptom relief in approximately 60–80% of patients and significantly improves quality of life [1, 2]. This study aims to evaluate a pragmatic approach to the management medically refractory overactive bladder patients. We also aimed to evaluate the regional and cultural limitations on outcome of SNM in our patients population.
Study design, materials and methods
This single-centre retrospective cohort study included 21 patients who underwent the two phases of SNM implantation (completed treatment) between January 2019 and January 2025. Inclusion criteria were adults (≥18 years) with OAB or urinary retention who had received SNM and had a minimum of six months of follow-up. Patients with incomplete records or prior major bladder surgery were excluded. Patient demographics and clinical data, including preoperative bladder treatments such as Botox injections, were extracted from the EPIC system. Outcomes measured were symptom improvement (≥50% improvement), device longevity, re-interventions, complications, and changes in post-SNM medication use. Data were analysed using SPSS.
Results
A total of 21 patients underwent SNM therapy for refractory OAB, urinary retention, and mixed symptoms. The cohort included 12 OAB patients, 6 with urinary retention, and 3 with mixed features. The overall mean follow-up duration was 23.28 ± 22.49 months, and the mean test phase duration was 11.33 ± 4.43 days. Prior to SNM, 33.33% (4/12) of OAB patients had undergone bladder Botox injections. Initial test stimulation was successful in 91.7% (11/12) OAB patients, 83.3% (5/6) urinary retention patients, and 66.7% (2/3) mixed patients, leading to permanent implantation. In the OAB subgroup, 1-month postoperative symptom improvement averaged 70.0% ± 10.0%, with 91.7% (11/12) achieving ≥50% symptom improvement at last follow-up. Medication use decreased significantly, with 72.7% (8/11) discontinuing anticholinergic/bladder medications postoperatively. All retention patients experienced restoration of voiding function, with mean PVR volume decreasing from 579.33 ± 187.89 mL to 139.00 ± 128.57 mL. Complete bladder emptying success by 6 months was achieved in 66.7% (4/6). The mixed group saw 33.3% (1/3) achieving full bladder emptying without catheterization. SNM device re-interventions were required in 22.2% (4/18), including four explantations and one revision/replacement. Mild postoperative pain was reported by 11.1% (2/18). No infections or lead migrations occurred.
Interpretation of results
Our cohort analysis were comparable to previously reported data including complications and re-intervention rates. More importantly, we data suggests that SNM offers similar efficacy and safety and durable