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. 2014 Oct;84(4):911-7.
doi: 10.1016/j.urology.2014.03.059. Epub 2014 Aug 2.

Sacral neuromodulation for the dysfunctional elimination syndrome: a 10-year single-center experience with 105 consecutive children

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Sacral neuromodulation for the dysfunctional elimination syndrome: a 10-year single-center experience with 105 consecutive children

Moira E Dwyer et al. Urology. 2014 Oct.

Abstract

Objective: To evaluate our initial experience using sacral neuromodulation via implanted pulse generator as a treatment for children with dysfunctional elimination syndrome and symptoms refractory to maximum medical therapy.

Materials and methods: There were 105 consecutive patients who underwent a 2-stage procedure with a trial period (n = 89) or a single procedure (n = 16) for device implantation. They were followed up prospectively for a median of 2.72 years (average, 3.18 years; range, 0.01-9.63 years) for symptom improvement and resolution.

Results: Nearly all children (99 of 105 [94%]) experienced improvement of at least 1 symptom; 12 of 105 patients (11%) had at least 1 symptom worsen. Urinary incontinence, constipation, frequency and/or urgency, and nocturnal enuresis improved in 89 of 101 (88%), 73 of 92 (79%), 54 of 81 (67%), and 59 of 89 (66%) children, respectively, and resolved in 41 of 101 (41%), 37 of 92 (40%), 23 of 81 (28%), and 25 of 89 (28%) children, respectively. Outcomes among patients who did and did not undergo the trial were not significantly different (P = .19-1.00), and only 2 of 88 patients did not undergo permanent implantation. Reoperations (n = 85) occurred in 59 of 105 children (56%), mainly for device malfunction (n = 42), whereas explantation was performed in 36 of 104 children (35%) at an average of 2.68 years since implantation (median, 2.36 years; range, 0.03-9.04 years), mainly for complete symptom resolution (n = 12). Explantation for any reason was less common after single-stage procedures (1 of 16 [6%] vs 35 of 88 [40%] patients; P = .01).

Conclusion: Sacral neuromodulation should be considered for children with dysfunctional elimination syndrome whose symptoms are refractory to maximum medical therapy understanding that the risk of reoperation is >50%. Elimination of the trial period reduces the number of general anesthetics without sacrificing outcomes.

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Comment in

  • Reply: To PMID 25096339.
    Dwyer ME, Vandersteen DR, Hollatz P, Reinberg YE. Dwyer ME, et al. Urology. 2014 Oct;84(4):918. doi: 10.1016/j.urology.2014.03.061. Epub 2014 Aug 2. Urology. 2014. PMID: 25096338 No abstract available.
  • Editorial comment.
    Cooper CS. Cooper CS. Urology. 2014 Oct;84(4):917. doi: 10.1016/j.urology.2014.03.060. Epub 2014 Aug 2. Urology. 2014. PMID: 25096340 No abstract available.

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