2002
DOI: 10.1016/s0090-4295(02)01630-8
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Sacral neuromodulation as an effective treatment for refractory pelvic floor dysfunction

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Cited by 115 publications
(78 citation statements)
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“…After gaining popularity in Europe, the United States Food and Drug Administration approved the use of sacral neuromodulation (InterStim 1 , Medtronic, Inc., Minneapolis, MN) in 1997 for the treatment of refractory urge incontinence. The same technology was approved in 1999 for the indication of urinary frequency and urgency and urinary retention [Aboseif et al, 2002].…”
Section: Introductionmentioning
confidence: 99%
“…After gaining popularity in Europe, the United States Food and Drug Administration approved the use of sacral neuromodulation (InterStim 1 , Medtronic, Inc., Minneapolis, MN) in 1997 for the treatment of refractory urge incontinence. The same technology was approved in 1999 for the indication of urinary frequency and urgency and urinary retention [Aboseif et al, 2002].…”
Section: Introductionmentioning
confidence: 99%
“…Temporary PNE electrodes were removed in all patients who did not respond in the testing phase (based on NICE Guidelines) [5,20]. It was assumed that 7 % of patients who did not respond to SNS would have the device explanted [21][22][23][24][25][26], and that among those who did respond, 23 % would undergo surgical revision [21,[23][24][25][26][27]. It was assumed that individuals would have three physician visits for SNS device programming per year [28].…”
Section: Resource Use and Costmentioning
confidence: 99%
“…Aboseif et al . [71] reported that 18 of 20 patients had been able to stop CISC after a mean follow-up of 24 months. Swinn et al .…”
Section: Non-obstructive Urinary Retentionmentioning
confidence: 99%
“…Long-term success rates after 12-60 months of follow-up are summarized in Table 2 [40, [70][71][72][73]75] with a > 50% reduction in the number of catheterizations in 58-86%. The cure rate, being the percentage of patients not needing to perform CISC at all, was 50-55% after 41-48 months of follow-up.…”
Section: Non-obstructive Urinary Retentionmentioning
confidence: 99%