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中华妇幼临床医学杂志(电子版) ›› 2017, Vol. 13 ›› Issue (02) : 194 -198. doi: 10.3877/cma.j.issn.1673-5250.2017.02.013

所属专题: 文献

论著

新式阴道前壁补片修补术治疗压力性尿失禁女性患者的疗效分析
袁峥1, 尹格平1,(), 李娟1, 刘娜1, 梁静1, 武爱芳1   
  1. 1. 250031 济南军区总医院妇科
  • 收稿日期:2017-01-10 修回日期:2017-03-05 出版日期:2017-04-01
  • 通信作者: 尹格平

A new vaginal antetheca-retropubic mesh-repair for stress urinary incontinence female patients

Zheng Yuan1, Geping Yin1,(), Juan Li1, Na Liu1, Jing Liang1, Aifang Wu1   

  1. 1. Department of Gynecology, Jinan Military General Hospital, Jinan 250031, Shandong Province, China
  • Received:2017-01-10 Revised:2017-03-05 Published:2017-04-01
  • Corresponding author: Geping Yin
  • About author:
    Corresponding author: Yin Geping, Email:
引用本文:

袁峥, 尹格平, 李娟, 刘娜, 梁静, 武爱芳. 新式阴道前壁补片修补术治疗压力性尿失禁女性患者的疗效分析[J]. 中华妇幼临床医学杂志(电子版), 2017, 13(02): 194-198.

Zheng Yuan, Geping Yin, Juan Li, Na Liu, Jing Liang, Aifang Wu. A new vaginal antetheca-retropubic mesh-repair for stress urinary incontinence female patients[J]. Chinese Journal of Obstetrics & Gynecology and Pediatrics(Electronic Edition), 2017, 13(02): 194-198.

目的

探讨阴道前壁黏膜下双侧耻骨后间隙造穴植入生物补片修补术(简称为新式阴道前壁补片修补术),对压力性尿失禁(SUI)女性患者的近、远期手术疗效。

方法

选择2009年1月至2014年12月,在济南军区总医院诊断为SUI,并行新式阴道前壁补片修补术治疗的316例女性患者为研究对象,并对其随访≥12个月。本术式中使用本研究设计并获中国实用新式专利的"YGP-Ⅱ型阴道前壁穴道分离补片放置复合钳" 。采用《国际尿失禁咨询委员会尿失禁问卷简表》 (ICIQ-SF) 进行疗效主观评价,采用尿垫试验进行疗效客观评价。分析患者手术情况及术后并发症等临床资料,统计学分析该术式近、远期疗效。本手术及研究遵循的程序,得到济南军区总医院医学伦理委员会批准,并取得患者知情同意。

结果

①本研究中度SUI患者为264例,重度SUI患者为52例;平均手术时间为(15.7±4.2) min,术中平均出血量为(69.1±26.9) mL,术后平均住院时间为(1.9±1.7) d。②术后并发症包括排尿不尽、发热、小便困难、尿路感染及补片外露等,术后无严重并发症发生。③中度或重度SUI女性患者,术前ICIQ-SF评分均较术后12个月高,并且差异均有统计学意义(t=12.569,14.028;P<0.001);术后随访12个月患者的SUI治愈率(91.8%)与随访≥24个月的治愈率(94.2%)比较,差异无统计学意义(χ2=1.020,P=0.211)。

结论

本新式阴道前壁补片修补术,治疗中、重度SUI女性患者有效,远期疗效可靠,并且更微创化,是否适于临床推广应用,尚需多中心、大样本随机对照试验进一步研究、证实。

Objective

To investigate the short and long term effects of vaginal antetheca submucosal-retropubic space with mesh-repair through the implantation of biological patch (shortly as new-style vaginal mesh repair) in the treatment of the female patients with stress urinary incontinence (SUI).

Methods

From January 2009 to December 2014, 316 female patients diagnosed as SUI and with the treatment of new-style vaginal mesh repair in Jinan Military General Hospital, were chosen as study subjects, and were followed up more than 12 months. The special designed Chinese utility model patent named " YGP-Ⅱ type of composite clamp for anterior vaginal wall acupoint patch separation and patch placement" was used in this technique in this research. The International Consultation on Incontinence Questionnaire Short Form (ICIQ-SF) was used for subjective evaluation of curative effects, and the urine pad test was used for objective evaluation. The clinical data of surgery condition and postoperative complications of these patients, and short and long term curative effects of this operation were statistically analyzed. The operation and research procedures were approved by the Ethics Committee of Jinan Military General Hospital, and obtained the informed consent of each patient.

Results

①There were 264 cases of moderate SUI and 52 cases of severe SUI in this study. The average operation time was (15.7±4.2) min, the average intraoperative bleeding volume was (69.1±26.9) mL, and the average stay of hospitalization was (1.9±1.7) d. ②Postoperative complications included sensation of not emptying bladder completely finished urinating, fever, dysuria, urinary tract infection and exposure of the patch, and no serious complications were found. ③In female patients with moderate or severe SUI, preoperative ICIQ-SF scores were higher than that of 12 months after surgery, and the differences were statistically significant (t=12.569, 14.028; P<0.001). There was no significant difference of SUI recovery rate between patients with 12 months of follow-up and patients with more than 24 months of follow-up (91.8% vs 94.2%, χ2=1.020, P=0.211).

Conclusions

This new-style vaginal mesh repair in the treatment of moderate and severe SUI female patients is effective, the long term efficacy is reliable, and more minimally invasive. More multi-center, large sample randomized controlled trials need to be done and confirmed to decide whether it is suitable for clinical application.

图1 新式阴道前壁补片修补术(图1A:YGP-Ⅱ型阴道前壁穴道分离补片放置复合钳;图1B:术中分离完毕左、右侧穴道;图1C:左右侧穴道位置示意图;图1D:补片放置入左右侧穴道;图1E:手术完毕)
表1 316例SUI女性患者术前与术后12个月ICIQ-SF评分比较(分,±s)
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