Feifer Andrew, Corcos Jacques
Urology Department, Jewish General Hospital, McGill University, 3755 Côte Ste-Catherine, Montreal, Quebec, H3T 1E2, Canada.
Int Urogynecol J Pelvic Floor Dysfunct. 2007 Sep;18(9):1087-95. doi: 10.1007/s00192-007-0347-3. Epub 2007 Apr 27.
We set out to review the existing literature regarding the use of synthetic suburethral sling products for the treatment of female stress urinary incontinence. Products currently implanted are examined and scrutinized, and evidence regarding their efficacy and complication rates is noted. Additionally, specifics of presently utilized synthetic materials, including construction method and biocompatibility, are explored and directly correlated to currently marketed products. This investigation was undertaken with the use of the Medline database. Studies pertaining to synthetic or surgical mesh, as well as each specific suburethral sling product, are included. Our findings and ultimately our recommendations stem from the preponderance of evidence supporting the continued use of knitted, macroporous polypropelene mesh slings. Several existing marketed products detailed in the study fit this description. Specific reference is made to recent reports of vaginal erosions and deep space infections related to several specific products. A cautionary note is also made regarding the implantation of transobturator sling products currently marketed without the necessary pre-market testing, potentially placing the public at risk. From the currently available literature on biomaterials, it seems clear that knitted macroporous polypropylene is the material of choice for suburethral implantation. With respect to the means and techniques by which these mesh materials are suburethrally implanted, the surgeon's choice often dictates which method is used, but recent experience has demonstrated that the transobturator approach can be equally as effective as the traditional tension-free vaginal tape, with less-associated morbidity. Ongoing randomized controlled trials will further clarify and distinguish between methods.
我们着手回顾关于使用合成尿道下吊带产品治疗女性压力性尿失禁的现有文献。对目前植入的产品进行检查和详细审查,并记录有关其疗效和并发症发生率的证据。此外,探讨目前使用的合成材料的具体情况,包括构建方法和生物相容性,并将其与目前市场上销售的产品直接关联。这项调查是通过使用Medline数据库进行的。纳入了与合成或手术网片以及每种特定尿道下吊带产品相关的研究。我们的研究结果以及最终建议源于支持继续使用针织大孔聚丙烯网片吊带的大量证据。该研究中详细介绍的几种现有市场产品符合这一描述。特别提到了与几种特定产品相关的阴道糜烂和深部空间感染的近期报告。对于目前市场上销售的经闭孔吊带产品在没有必要的上市前测试情况下进行植入也提出了警示,这可能使公众面临风险。从目前关于生物材料的现有文献来看,似乎很明显针织大孔聚丙烯是尿道下植入的首选材料。关于这些网片材料尿道下植入的方法和技术,外科医生的选择通常决定使用哪种方法,但最近的经验表明,经闭孔方法与传统无张力阴道吊带同样有效,且相关发病率较低。正在进行的随机对照试验将进一步阐明并区分不同方法。