Dow Division of Health Services Research and the Division of Neurology and Pelvic Reconstructive Surgery, Department of Urology, The University of Michigan, Ann Arbor, Michigan 48109-2800, USA.
Obstet Gynecol. 2013 Sep;122(3):546-52. doi: 10.1097/AOG.0b013e31829e8543.
To assess the effectiveness of mesh compared with nonmesh slings placed in different surgical settings as measured by the frequency of complications within 1 year.
We performed a retrospective cohort study of Medicare beneficiaries undergoing sling surgery from 2006 to 2008 in hospital outpatient departments and hospital-based ambulatory surgery centers. Slings were identified and categorized according to the use of mesh by Healthcare Common Procedure Coding System codes and temporary "C" Healthcare Common Procedure Coding System codes. Patients were followed for 1 year after each procedure to identify complications. Logistic models were fit to assess relationships among sling type, surgical setting, and various complications.
We identified 6,698 Medicare beneficiaries who underwent mesh sling procedures and 445 Medicare beneficiaries who underwent nonmesh sling procedures. The overall frequency of complications was similar between the two groups at 69.8% and 72.6% in the mesh and nonmesh groups, respectively (P=.22). Infectious complications were the most common complication at 45.4% and 50.1% of the mesh and nonmesh groups, respectively (P=.06). Patients undergoing mesh procedures were less likely than patients undergoing nonmesh procedures to require management for bladder outlet obstruction (13.9% compared with 19.3%, adjusted odds ratio [OR] 0.66, 95% confidence interval [CI] 0.52-0.85) and were less likely to have a subsequent sling removal and revision or urethrolysis (2.7% compared with 4.7%, adjusted OR 0.56, 95% CI 0.35-0.89).
Frequencies of most complications were similar regardless of the use of mesh except for the management of bladder outlet obstruction. These results did not differ based on the surgical setting where the sling procedure was performed.
II.
评估在不同手术环境下使用网片与非网片吊带治疗 1 年内并发症的发生频率,以此比较网片与非网片吊带的疗效。
我们对 2006 年至 2008 年在医院门诊和医院门诊手术中心接受吊带手术的 Medicare 受益人的病历进行了回顾性队列研究。通过使用医疗保健通用程序编码系统代码和临时“C”医疗保健通用程序编码系统代码,对吊带进行识别和分类。在每个手术程序后对患者进行为期 1 年的随访,以确定并发症。使用逻辑模型评估吊带类型、手术环境和各种并发症之间的关系。
我们确定了 6698 名接受网片吊带手术的 Medicare 受益人和 445 名接受非网片吊带手术的 Medicare 受益人的病历。两组的总体并发症发生率相似,网片组和非网片组分别为 69.8%和 72.6%(P=.22)。感染性并发症是最常见的并发症,分别占网片组和非网片组的 45.4%和 50.1%(P=.06)。与非网片组相比,接受网片手术的患者不太可能需要治疗膀胱出口梗阻(13.9%比 19.3%,调整后比值比 [OR] 0.66,95%置信区间 [CI] 0.52-0.85),不太可能需要进行后续吊带移除和修复或尿道切开术(2.7%比 4.7%,调整后 OR 0.56,95% CI 0.35-0.89)。
除了膀胱出口梗阻的处理外,大多数并发症的发生频率都相似,而与是否使用网片无关。这些结果与吊带手术的手术环境无关。
II 级。