Sacral neuromodulation in the treatment of urgency-frequency symptoms: A multicenter study on efficacy and safety

被引:241
作者
Hassouna, MM [1 ]
Siegel, SW
Nyeholt, AABLA
Elhilali, MM
van Kerrebroeck, PEV
Das, AK
Gajewski, JB
Janknegt, RA
Rivas, DA
Dijkema, H
Milam, DF
Oleson, KA
Schmidt, RA
机构
[1] Toronto Hosp, Western Div, Toronto, ON M5T 2S8, Canada
[2] Royal Victoria Hosp, Montreal, PQ H3A 1A1, Canada
[3] Queen Elizabeth II Hlth Sci Ctr NHI, Halifax, NS, Canada
[4] Metropolitan Urol Specialists, St Paul, MN USA
[5] Medtron Inc, Minneapolis, MN USA
[6] Acad Ziekenhuis Leiden, Leiden, Netherlands
[7] Acad Ziekenhuis Nijmegen, Nijmegen, Netherlands
[8] Acad Ziekenhuis Maastricht, Maastricht, Netherlands
[9] Twenteborg Ziekenhuis Almelo, Almelo, Netherlands
[10] Albany Med Coll, Albany, NY 12208 USA
[11] Thomas Jefferson Univ, Philadelphia, PA 19107 USA
[12] Vanderbilt Univ, Nashville, TN USA
[13] Univ Colorado, Hlth Sci Ctr, Denver, CO USA
关键词
sacrum; electric stimulation; urination disorders; bladder;
D O I
10.1016/S0022-5347(05)67558-1
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose: Neuromodulation of sacral nerves has shown promising results in correcting voiding dysfunction. We report the results of a multicenter trial designed to assess the efficacy of sacral nerve neuromodulation in patients presenting with refractory urinary urgency-frequency. Materials and Methods: A total of 51 patients from 12 centers underwent baseline assessment, including a detailed voiding diary, urodynamic evaluation and percutaneous test stimulation of the sacral nerves at S3 and/or S4. All patients enrolled in the study had undergone prior conventional treatment, such as pharmacotherapy, hydrodistention and surgical intervention, which failed. All patients demonstrated a satisfactory response to trial stimulation and were randomly divided into a stimulation group (25 patients) and a control group (26), A sacral nerve stimulation device was implanted after 6 months in the control group. Patients were followed at 1, 3 and 6 months, and at 6-month intervals for up to 2 years after implantation of a neuroprosthetic InterStim* system.dagger The study variables included the number of voids daily, volume voided per void and degree of urgency before void. Results: Compared to the control group, 6-month voiding diary results demonstrated statistically significant improvements (p <0.0001) in the stimulation group with respect to the number voids daily (16.9 +/- 9.7 to 9.3 +/- 5.1), volume per void (118 +/- 74 to 226 +/- 124 ml.) and degree of urgency (rank 2.2 +/- 0.6 to 1.6 +/- 0.9). Patients in the control group showed no significant changes in voiding parameters at 6 months. Significant improvements in favor of the stimulation group were noted in various parameters with respect to water cystometry and quality of life (SF-36). At 6 months after implant, neurostimulators were turned off in the stimulation group and urinary symptoms returned to baseline values. After reactivation of stimulation sustained efficacy was documented at 12 and 24 months. Conclusions: Neuromodulation of the sacral nerves is an effective, safe therapy that successfully treats significant symptoms of refractory urgency-frequency.
引用
收藏
页码:1849 / 1854
页数:6
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