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In patients undergoing neuromodulation for intractable urge incontinence a reduction in 24-hr pad weight after the initial test stimulation best predicts long term patient satisfaction
被引:31
作者:
Foster, Raymond T., Sr.
Anoia, Elizabeth J.
Webster, George D.
Amundsen, Cindy L.
机构:
[1] Duke Univ, Dept Obstet & Gynecol, Med Ctr, Div Urogynecol & Pelv Reconstruct Surg, Durham, NC 27710 USA
[2] Duke Univ, Dept Surg, Med Ctr, Div Urol Surg, Durham, NC 27710 USA
关键词:
QOL;
sacral neuromodulation;
surgical satisfaction;
urge incontinence;
D O I:
10.1002/nau.20330
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:
Aims: To evaluate long-term patient satisfaction of sacral neuromodulation and to correlate satisfaction with incontinence parameters. Methods: Patients at least 1-year remote from sacral neuromodulation were mailed a questionnaire to evaluate satisfaction and assess incontinence symptoms. Results: Fifty-two patients were consecutively enrolled in the study. Forty-nine questionnaires (94.2%) were returned. The average interval between implantation and questionnaire completion was 27.2 (range 12-52) months. 83.7% of respondents were satisfied and 79.6% of patients would "do it all over again." Compared to dissatisfied subjects during test stimulation, the satisfied patients had a significant decrease in 24-hr pad weight (84.5% vs. 60.6%, P = 0.002) but did not differ in daily pad usage (4.5 fewer pads per day vs. 3.4, P = 0.190). At long-term follow-up, satisfied patients noted significantly greater improvement in their Incontinence Impact Questionnaire score versus dissatisfied patients (mean improvement 53 vs. 10 points, P = 0.0003). Using multiple logistic regression, change in 24-hr pad weight, but not change in average daily pad usage, was correlated with long-term satisfaction. Conclusions: Eighty-four percent of patients were satisfied with sacral ncuro-modulation at a mean of 27 months. An 84.5% reduction in 24-hr pad weight correlated with long-term patient satisfaction. In addition to lack of efficacy, device pain was a contributing factor to dissatisfaction.
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页码:213 / 217
页数:5
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