Surgical Staples vs. Absorbable Subcuticular Suture for Wound Closure of Cesarean Deliveries
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 398
- 试验地点
- 2
- 主要终点
- Percent of Subjects With Composite Wound Morbidity.
研究概览
简要总结
The objective of this randomized controlled trial is to compare wound morbidity (including disruption and infection) in surgical staples versus absorbable subcuticular suture for wound closure in cesarean deliveries.
详细描述
Cesarean delivery (CD) is a common surgical procedure with over 1 million performed annually in the United States. The rate of CD is steadily increasing. In 2006, an estimated 31.1% of U.S. births were by CD. Approximately two thirds of these are primary procedures and 90% of CD will later undergo a repeat cesarean delivery. The rise in CD has been attributed to changes in physician and patient expectations, attitudes about risk, and changes in clinical practice. These include decreased vaginal birth after cesarean delivery (VBAC), breech vaginal deliveries, and operative vaginal deliveries as well as an increase in maternal request, failed induction of labor, and elective repeat CD. The CD rate is expected to rise as high as 40-50% in the next decade if the increasing trend continues unabated.
Despite the large number of CD performed, there is no agreed standard for skin closure. The most commonly used materials are surgical staples and absorbable subcuticular suture. Staples have a clear benefit in decreasing operating time. In theory, staples also have a decreased chance of bacterial migration into the wound, decreased tension at the incision edges, and less damage to capillaries in the subcuticular layer of skin than absorbable subcuticular suture. However, some argue that staples are more painful and have a worse cosmetic appearance. This is especially the case for staples that remain in place longer than recommended and leave "track marks." Staples are also less visually appealing to patients.
The Cochrane Collaboration identified one randomized controlled trial (RCT) that addressed skin closure for CD (Alderice, 2003). This study included 66 women and compared absorbable subcuticular suture versus surgical staples for skin closure of CD. Surgical staples had shorter operating time but absorbable subcuticular suture had decreased post-operative pain and better cosmesis at the 6 week post-operative visit (Frishman, 1997). Rousseau, J. presented opposing findings in her RCT "A Randomized Study Comparing Subcuticular Sutures Versus Staples for Skin Closure at Cesarean Sections". In this study, staples had better cosmesis, decreased pain at the post-operative visit, and shorter operating time (Rousseau, 2009). Neither study assessed wound disruption or infection directly. With such widely varying findings and lack of data there is a need to identify the cesarean section skin closure which provides the best outcomes for the most common major surgical procedure in women.
We have undertaken a RCT to compare surgical staples vs. absorbable subcuticular suture for the closure of the skin in cesarean sections. Our primary outcome is a composite wound morbidity outcome (including wound disruption or infection). Assuming a baseline wound morbidity of 8%, Power of 80%, and a decrease of wound morbidity to 4%, a sample size of 1,204 will be required. Our secondary outcomes will include cosmesis, post-operative pain, health service use/cost, procedure time, and patient satisfaction.
The study was terminated after recruitment of approximately 400 subjects after administrative review (see publication: Figueroa et al. Obstet Gynecol. 2013 Jan;121(1):33-8.)
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 16 Years 至 —(Child, Adult, Older Adult)
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •cesarean delivery
排除标准
- •chronic use of immunosuppressive agents ( e.g.po steroids > 2 weeks)
- •significant immune compromising disease (e.g. AIDS, CD4<200)
- •contraindication to standard post operative pain management (acetaminophen, ibuprofen, oxycodone)
- •refusal or inability to give consent
结局指标
主要结局
Percent of Subjects With Composite Wound Morbidity.
时间窗: 4-6 weeks post partum
this outcome measure included a composite of either disruption and/ or infection of the wound at 4 - 6 weeks post partum. The number of subjects experiencing wound disruption and or wound infection at 4 - 6 weeks post delivery was assessed
次要结局
- Composite Cosmesis Score (Stony Brook Scar Evaluation Score - SBSES) Core - SBSES))(at the end of follow up, 4 - 6 weeks post partum)
- Operative Procedure Time.(Intraoperative, at time of intervention.)
- Post Operative Pain - 4 - 6 Weeks Post Delivery(at end of follow-up, 4 - 6 weeks post partum)
- Post Operative Pain - 72 - 96 Hours Post Delivery(72 - 96 hours post delivery)
- Subject Reported Satisfaction With Appearance of Scar(4 - 6 weeks post delivery)
- Subject Satisfaction With Comfort With Scar(at end of follow-up, 4 - 6 weeks post partum)
- Subject Satisfaction With Location of Scar(at end of follow-up, 4 - 6 weeks post partum)
研究者
Alan Tita
Physician
University of Alabama at Birmingham
