O veractive bladder (OAB) is a condition defined by the International Continence Society (ICS) as urgency with or without urgency incontinence, usually with increased daytime frequency and nocturia. 1 Patients with OAB have significantly reduced quality of life.2 Population-based surveys done in Canada have shown high prevalence (14%) in both sexes.3 In a survey of over 19 000 adults in Canada and Europe, the overall prevalence of OAB was 12.8% in women and 10.8% in men. 4 The similar study in United States showed that overall, 16.5% of the U.S. population aged ≥18 years (about 33 million people) have symptoms of OAB. 5 The initial treatment of the OAB includes anticholinergic medications. Compliance and satisfactory results, however, are low after 1 year and range from 18% to 65%. 6,7 Patients with medication refractory OAB have the option of sacral neuromodulation (SNM), intravesical injection of Botulinum Toxin type A (BTX A) or surgery, such as bladder augmentation or diversion.I strongly belief the most appropriate option for these patients is SNM. It is the most innovative treatment modality developed in recent years for the management of OAB and other voiding dysfunctions; it has also been approved by Health Canada for this indication since 1999. The ideal treatment should be effective, safe and financially sound. There is no question that SNM is effective. Brazzelli and colleagues systematic review found that 80% (4 randomized controlled trials) and 67% (30 case series) of patients became dry or achieved a >50% improvement in symptoms after implantation. 8 Our own data showed 84.8% success rate with a median follow-up of 50 months (Fig. 1). 10 Furthermore, in a recent study, overall satisfaction was reported as high as 90%.9 There are very little initial complications with the device. The infection rate is under 5%; in our series of 96 implants, no infection was reported at all. There is a possibility of seroma formation which was described occasionally. In our experience, the reoperation rate due to malfunction of the device or lack of improvement was initially high at 40%. The main reason for revisions (50%) was poor response. The second most common indication (17%) for revision was local pain from the device. The median time for revision was 24 months. Review of the literature of 855 patients, showed 33% revision rate. Most of the studies, including ours, consist of sacral nerve stimulation non-tined lead data, which have higher complication rates associated with the open fasciotomy procedure and lead migration.
10With the advances in the equipment and surgical technique, this rate was reduced to 26% with a combined revision rate of 32% in our experience. The biggest improvement was in the introduction of the tined-lead which can be implanted through percutaneus, minimal invasive technique. Some patients also complained of unpleasant sensations or pain. This, however, was usually resolved with reprogramming. Patients are followed on a regular basis the third and sixth month mark, and then yearly. The ...