Department of Cardiothoracic and Thoracic Vascular Surgery, University Hospital Würzburg, Germany.
J Thorac Cardiovasc Surg. 2012 Jan;143(1):194-200. doi: 10.1016/j.jtcvs.2011.05.035. Epub 2011 Aug 31.
Prophylactic retrosternal placement of a gentamicin-collagen sponge has been the subject of several recent clinical studies and is a matter of controversy. The present study is the first controlled, prospective, randomized, double-blind, single-center study to investigate the efficacy of a retrosternal gentamicin-collagen sponge in reducing sternal wound complications after heart surgery.
From June 2009 to June 2010, 720 consecutive patients who underwent median sternotomy were assigned to a control placebo group (collagen sponge) or an intervention group (gentamicin-collagen sponge). All patients received guideline-compliant perioperative antibiotic prophylaxis. The primary end point was the occurrence of deep sternal wound infections within 30 days of index surgery (follow-up period). Secondary end points were the occurrence of superficial sternal wound infections requiring treatment, as well as further clinical parameters, including revision, bleeding volume, and need for transfusions during the follow-up period.
A total of 720 of 994 patients (72.4%) were enrolled (control group: n = 367 vs intervention group: n = 353). Risk factors for sternal wound infection and demographic variables were comparable in the 2 groups. The incidence of deep sternal wound infections was 13 of 367 (3.52%) in the control group versus 2 of 353 (0.56%) in the intervention group (P = .014; adjusted odds ratio, 0.15; 95% confidence interval, 0.02-0.69). The numbers needed to treat relation for all sternal wound infections and deep sternal wound infections were 26 and 33, respectively. No statistically significant differences were demonstrated concerning secondary end points, such as postoperative bleeding and transfusion of red cell units, thrombocytes, and fresh-frozen plasma.
Routine prophylactic retrosternal use of a gentamicin-collagen sponge in patients undergoing cardiac surgery significantly reduces deep sternal wound infections.
预防性胸骨后放置庆大霉素-胶原海绵已成为最近几项临床研究的主题,也是一个有争议的问题。本研究是第一项对照、前瞻性、随机、双盲、单中心研究,旨在调查心脏手术后胸骨后庆大霉素-胶原海绵在减少胸骨伤口并发症方面的疗效。
2009 年 6 月至 2010 年 6 月,连续 720 例接受正中胸骨切开术的患者被分为对照组(胶原海绵)或干预组(庆大霉素-胶原海绵)。所有患者均接受了符合指南的围手术期抗生素预防。主要终点是索引手术后 30 天内深部胸骨伤口感染的发生(随访期)。次要终点是需要治疗的浅表胸骨伤口感染以及其他临床参数,包括随访期间的翻修、出血量和输血需求。
共有 994 例患者中的 720 例(72.4%)入组(对照组:n=367 例,干预组:n=353 例)。两组的胸骨伤口感染危险因素和人口统计学变量相似。对照组深部胸骨伤口感染发生率为 13/367(3.52%),干预组为 2/353(0.56%)(P=0.014;调整优势比,0.15;95%置信区间,0.02-0.69)。所有胸骨伤口感染和深部胸骨伤口感染的治疗关系数分别为 26 和 33。在次要终点方面,如术后出血和红细胞单位、血小板和新鲜冷冻血浆的输血,没有显示出统计学上的显著差异。
在接受心脏手术的患者中,常规预防性胸骨后使用庆大霉素-胶原海绵可显著减少深部胸骨伤口感染。