Gorlitzer Michael, Wagner Florian, Pfeiffer Steffen, Folkmann Sandra, Meinhart Johann, Fischlein Theodor, Reichenspurner Hermann, Grabenwoeger Martin
Hospital Hietzing, Vienna, Austria.
Interact Cardiovasc Thorac Surg. 2013 Sep;17(3):515-22. doi: 10.1093/icvts/ivt240. Epub 2013 Jun 11.
A prospective randomized multicentre trial was performed to analyse the efficacy of a vest (Posthorax support vest®) to prevent sternal wound infection after cardiac surgery, and to identify risk factors.
From September 2007 to March 2010, 2539 patients undergoing cardiac surgery via median sternotomy were prospectively randomized into those who received a Posthorax® vest and those who did not. Patients were instructed to wear the vest postoperatively for 24 h a day for at least 6 weeks; the duration of follow-up was 90 days. Patients who did not use the vest within a period of 72 h postoperatively were regarded as study dropouts. Statistical calculations were based on an intention-to-treat (ITT) analysis. Further evaluations comprised all subgroups of patients.
Complete data were available for 2539 patients (age 67 ± 11years, 45% female). Of these, 1351 were randomized to receive a vest, while 1188 received no vest. No significant differences were observed between groups regarding age, gender, diabetes, body mass index, chronic obstructive pulmonary disease (COPD), renal failure, the logistic EuroSCORE and the indication for surgery. The frequency of deep wound complications (dWC: mediastinitis and sternal dehiscence) was significantly lower in vest (n = 14; 1.04%) vs non-vest (n = 27; 2.27%) patients (ITT, P < 0.01), but superficial complications did not differ between groups. Subanalysis of vest patients revealed that only 933 (Group A) wore the vest according to the protocol, while 202 (Group BR) refused to wear the vest (non-compliance) and 216 (Group BN) did not use the vest for other reasons. All dWC occurred in Groups BR (n = 7) and BN (n = 7), although these groups had the same preoperative risk profile as Group A. Postoperatively, Group BN had a prolonged intubation time, a longer stay in the intensive care unit, greater use of intra-aortic balloon pump, higher frequency of COPD and a larger percentage of patients who required prolonged surgery.
Consistent use of the Posthorax® vest prevented deep sternal wounds. The anticipated risk factors for wound complications did not prove to be relevant, whereas intra- and postoperative complications appear to be very significant.
进行一项前瞻性随机多中心试验,以分析一种背心(Posthorax support vest®)预防心脏手术后胸骨伤口感染的疗效,并确定危险因素。
2007年9月至2010年3月,2539例接受正中胸骨切开术的心脏手术患者被前瞻性随机分为接受Posthorax®背心组和未接受组。患者被指示术后每天佩戴背心24小时,至少佩戴6周;随访时间为90天。术后72小时内未使用背心的患者被视为研究失访者。统计计算基于意向性分析(ITT)。进一步评估包括所有患者亚组。
2539例患者(年龄67±11岁,45%为女性)有完整数据。其中,1351例被随机分配接受背心,1188例未接受背心。两组在年龄, 性别, 糖尿病, 体重指数, 慢性阻塞性肺疾病(COPD), 肾衰竭, 逻辑欧洲心脏手术风险评估系统(EuroSCORE)和手术指征方面未观察到显著差异。背心组(n = 14;1.04%)的深部伤口并发症(dWC:纵隔炎和胸骨裂开)发生率显著低于未穿背心组(n = 27;2.27%)(ITT,P < 0.01),但两组浅表并发症无差异。对背心组患者的亚分析显示,只有933例(A组)按方案佩戴了背心,而202例(BR组)拒绝佩戴背心(不依从),216例(BN组)因其他原因未使用背心。所有dWC均发生在BR组(n = 7)和BN组(n = 7),尽管这些组术前风险状况与A组相同。术后,BN组插管时间延长,在重症监护病房停留时间更长,主动脉内球囊泵使用更多,COPD发生率更高,需要长时间手术的患者比例更大。
持续使用Posthorax®背心可预防深部胸骨伤口。伤口并发症的预期危险因素未被证明具有相关性,而术中及术后并发症似乎非常显著。