Annals of Surgery · 2010 · 350 citations · 61 references
MedicineSurgeryUrologyNeurourologyUrogenital SurgeryUrologic SurgeryBladder Function AssessmentContinence AssessmentPelvic Floor DisordersUrinary ContinenceUrinary Continence AssessmentUrinary IncontinenceChronic ImplantationEfficacy Of Implantable StimulationElectrical Stimulation For ContinenceIncontinence Severity MeasurementInformed ConsentInstitutional Review Board ApprovalPrimary Efficacy Endpoints
Sacral nerve stimulation is approved in the U.S. for urinary incontinence since 1997 and in Europe for both urinary and fecal incontinence since 1994. This study aimed to assess the safety and efficacy of sacral nerve stimulation in a large cohort, with the primary goal of demonstrating at least 50% therapeutic success—defined as a 50% reduction in incontinent episodes at 12 months—under FDA‑approved investigational protocol. In a multicenter prospective trial, 133 patients underwent test stimulation, 120 of whom (90% success) received chronic implantation of Medtronic’s InterStim Therapy, with a mean follow‑up of 28 months.
Sacral nerve stimulation has been approved for use in treating urinary incontinence in the United States since 1997, and in Europe for both urinary and fecal incontinence (FI) since 1994. The purpose of this study was to determine the safety and efficacy of sacral nerve stimulation in a large population under the rigors of Food and Drug Administration-approved investigational protocol.Candidates for SNS who provided informed consent were enrolled in this Institutional Review Board-approved multicentered prospective trial. Patients showing > or =50% improvement during test stimulation received chronic implantation of the InterStim Therapy (Medtronic; Minneapolis, MN). The primary efficacy objective was to demonstrate that > or =50% of subjects would achieve therapeutic success, defined as > or =50% reduction of incontinent episodes per week at 12 months compared with baseline.A total of 133 patients underwent test stimulation with a 90% success rate, and 120 (110 females) of a mean age of 60.5 years and a mean duration of FI of 6.8 years received chronic implantation. Mean follow-up was 28 (range, 2.2-69.5) months. At 12 months, 83% of subjects achieved therapeutic success (95% confidence interval: 74%-90%; P < 0.0001), and 41% achieved 100% continence. Therapeutic success was 85% at 24 months. Incontinent episodes decreased from a mean of 9.4 per week at baseline to 1.9 at 12 months and 2.9 at 2 years. There were no reported unanticipated adverse device effects associated with InterStim Therapy.Sacral nerve stimulation using InterStim Therapy is a safe and effective treatment for patients with FI.
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Fecal incontinence quality of life scale
Todd Rockwood, James M. Church, James W. Fleshman et al. · Diseases of the Colon & Rectum · 2000 · 1.2K citations
Third degree obstetric anal sphincter tears: risk factors and outcome of primary repair
Abdul H. Sultan, Michael A. Kamm, C. N. Hudson et al. · BMJ · 1994 · 766 citations
Medicine, Obstetrics, Surgery +16
Defecation frequency and timing, and stool form in the general population: a prospective study.
K W Heaton, J Radvan, H. Cripps et al. · Gut · 1992 · 740 citations · Full text
Community-Based Prevalence of Anal Incontinence
Richard L. Nelson · JAMA · 1995 · 671 citations
Medicine, Community Health, Urology +12