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首页> 外文期刊>Obstetrics and Gynecology: Journal of the American College of Obstetricians and Gynecologists >Surgical staples compared with subcuticular suture for skin closure after cesarean delivery: A randomized controlled trial
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Surgical staples compared with subcuticular suture for skin closure after cesarean delivery: A randomized controlled trial

机译:剖宫产术后外科手术吻合钉与表皮下缝线缝合的对比:一项随机对照试验

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OBJECTIVE: To compare the risk of cesarean wound disruption or infection after closure with surgical staples compared with subcuticular suture. METHODS: Women with viable pregnancies at 24 weeks of gestation or greater undergoing scheduled or unscheduled cesarean delivery were randomized to wound closure with surgical staples or absorbable suture. Staples were removed at postoperative days 3-4 for low transverse incisions and days 7-10 for vertical incisions. Standardized wound evaluations were performed at discharge (days 3-4) and 4-6 weeks postoperatively. The primary outcome was a composite of wound disruption or infection within 4-6 weeks. Secondary outcomes included operative time, highest pain score on analog scale, cosmesis score, and patient scar satisfaction score. Analyses were by intent to treat. RESULTS: Of 398 patients, 198 were randomized to staples and 200 to suture (but four received staples). Baseline characteristics including body mass index, prior cesarean delivery, labor, and type of skin incision were similar by group. The primary outcome incidence at hospital discharge was 7.1% for staples and 0.5% for suture (P<.001, relative risk 14.1, 95% confidence interval [CI] 1.9-106). Of 350 (87.9%) with follow-up at 4-6 weeks, the cumulative risk of the primary outcome at 4-6 weeks was 14.5% for staples and 5.9% for suture (P=.008, relative risk 2.5, 95% CI 1.2-5.0). Operative time was longer with suture closure (median time of 58 versus 48 minutes; P<.001). Pain scores at 72-96 hours and at 6 weeks, cosmesis score, and patient satisfaction score did not differ by group. CONCLUSION: Staples closure compared with suture is associated with significantly increased composite wound morbidity after cesarean delivery. CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov, www.clinicaltrials.gov, NCT01008449. LEVEL OF EVIDENCE: I
机译:目的:比较使用缝合钉和皮下缝线缝合后剖宫产伤口破裂或感染的风险。方法:将在妊娠24周或更早时进行了计划内或计划外剖宫产的可行妊娠妇女随机分配为使用手术吻合钉或可吸收缝合线闭合伤口。对于低横向切口,术后3-4天除去钉书钉,对于垂直切口,在7-10天除去钉书钉。在出院时(3-4天)和术后4-6周进行标准化伤口评估。主要结局是4-6周内伤口破裂或感染的复合物。次要结果包括手术时间,类似评分下的最高疼痛评分,美容评分和患者疤痕满意度评分。分析是出于治疗目的。结果:在398例患者中,有198例被随机分配为吻合钉,而200例被缝合(但有4例接受了吻合钉)。各组的基线特征包括体重指数,先兆剖宫产,分娩和皮肤切口类型相似。钉书钉出院时的主要结局发生率为7.1%,缝合时为0.5%(P <.001,相对危险度14.1,95%置信区间[CI] 1.9-106)。在4-6周进行随访的350名患者中(87.9%),主钉在4-6周时的主要结局累积风险为14.5%,缝线为5.9%(P = .008,相对风险2.5、95% CI 1.2-5.0)。缝线缝合的手术时间更长(中位时间为58分钟,相对于48分钟; P <.001)。各组在72-96小时和6周时的疼痛评分,美容评分和患者满意度评分没有差异。结论:与缝合相比,缝合闭合与剖宫产术后复合伤口发病率显着增加有关。临床试验注册:ClinicalTrials.gov,www.clinicaltrials.gov,NCT01008449。证据级别:我

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