Deng Donna Y, Rutman Matthew, Raz Shlomo, Rodriguez Larissa V
Department of Urology, University of California, San Francisco School of Medicine, San Francisco, California, USA.
Neurourol Urodyn. 2007;26(1):46-52. doi: 10.1002/nau.20357.
Midurethral slings have become the mainstay of stress urinary incontinence (SUI) treatment due to their efficacy and low complication rates. The purpose of this study was to report the presentation and treatment of major complications from these minimally invasive treatments presented to a tertiary referral practice and to highlight a discrepancy in major complications between literature and the food and drug administration (FDA) device failure database.
From 2001 through 2005, we reviewed all cases of midurethral sling complications that presented to our institution. A literature review of all complications due to midurethral slings during the same time period was performed as was the FDA manufacturer and user facility device experience (MAUDE) database queried for self-reported complications.
A total of 26 patients referred to UCLA with voiding dysfunction after sling placement was found to have mesh in the urethra or bladder. Treatments required a combination of urethrolysis with mesh removal, urethral reconstruction with graft, and bladder excision. These were compared to major complications reported in the world literature of <1%. The MAUDE database contained 161 major complications out of a total of 928 complications reported for suburethral slings. There was significantly more major complications reported in MAUDE than in published literature.
Although rare, major complications of midurethral slings are more common than appear in literature. Devastating complications involving urethral and bladder perforations can present with mild urinary symptoms and thus are likely under-diagnosed and under-reported. Most of these cases need to be managed with additional reconstructive surgery.
由于疗效显著且并发症发生率低,中段尿道吊带已成为压力性尿失禁(SUI)治疗的主要手段。本研究的目的是报告在三级转诊机构中这些微创治疗出现的主要并发症的表现及治疗情况,并强调文献报道与食品药品监督管理局(FDA)设备故障数据库中主要并发症存在差异。
回顾2001年至2005年期间我院收治的所有中段尿道吊带并发症病例。对同一时期中段尿道吊带所致的所有并发症进行文献回顾,并查询FDA制造商和用户设施设备经验(MAUDE)数据库中自我报告的并发症情况。
共有26例在吊带置入后出现排尿功能障碍而转诊至加州大学洛杉矶分校的患者,被发现尿道或膀胱中有网片。治疗需要联合尿道松解术并取出网片、用移植物进行尿道重建以及膀胱切除术。这些与世界文献报道的主要并发症发生率<1%进行了比较。MAUDE数据库在总共报告的928例尿道下吊带并发症中有161例主要并发症。MAUDE数据库中报告的主要并发症明显多于已发表文献中的报道。
尽管罕见,但中段尿道吊带的主要并发症比文献中显示的更为常见。涉及尿道和膀胱穿孔的严重并发症可能仅表现为轻微的泌尿系统症状,因此很可能诊断不足且报告不足。大多数此类病例需要通过额外的重建手术进行处理。