Boissonneault Adam, O'Toole Robert V, Hayda Roman, Reid J Spence, Caroom Cyrus, Carlini Anthony, Dagal Arman, Castillo Renan, Karunakar Madhav, Matuszewski Paul E, Hymes Robert, O'Hara Nathan N
Department of Orthopaedics, Emory University School of Medicine, Grady Memorial Hospital, Atlanta, GA.
R Adams Cowley Shock Trauma Center, Department of Orthopaedics, University of Maryland School of Medicine, Baltimore, MD.
J Orthop Trauma. 2025 Feb 1;39(2):75-81. doi: 10.1097/BOT.0000000000002933.
To determine the association between closed suction drainage and postoperative infection in patients with tibial plateau or pilon fractures. Secondarily, this study assessed whether intrawound vancomycin powder modified the association of closed surgical drains with infection.
Secondary analysis of the Effect of Intrawound Vancomycin Powder in Operatively Treated High-risk Tibia Fractures: A Randomized Clinical Trial (VANCO).
Thirty-six academic trauma centers.
All patients with high-risk tibia fractures Orthopaedic Trauma Association/Arbeitsgemeinschaft fur Osteosynthesefragen (OTA/AO classification 41B/C or 43B/C) from the VANCO trial were considered. Closed suction drains were placed based on the treating surgeon's discretion. Patients were randomly assigned to receive 1-gram intrawound vancomycin powder in the surgical wound at definitive fixation or the standard infection prevention protocol at each center.
Deep surgical site infection (SSI) within 6 months. Comparisons were made between patients treated with and without drains. Subgroup analysis also examined the effect of drains in patients with and without intrawound vancomycin powder.
Of the 978 study patients, 197 (20%) were treated with drains. Deep infection rates did not significantly differ between patients with or without surgical drains (8% vs. 8%, P = 0.88). However, intrawound vancomycin powder significantly modified the association of surgical drains on deep SSI (interaction P = 0.048). Specifically, patients with drains but no vancomycin powder had the highest deep infection rate (13%; 95% confidence interval, 6%-19%). When vancomycin powder was used in addition to a drain, deep SSI rates were reduced by 10% (95% confidence interval, 2%-17%, P = 0.01).
This study suggests that closed suction drains after operative fixation of high-risk tibia fractures may not be associated with deep infection in general. However, a secondary analysis raises the possibility that drains are associated with reduced deep infection rates if topical vancomycin powder is used but associated with increased infection rates if vancomycin powder is not used.
Therapeutic Level III. See Instructions for Authors for a complete description of levels of evidence.
确定闭合式负压引流与胫骨平台或pilon骨折患者术后感染之间的关联。其次,本研究评估伤口内应用万古霉素粉末是否会改变闭合式手术引流与感染之间的关联。
对“伤口内应用万古霉素粉末对手术治疗的高危胫骨骨折的影响:一项随机临床试验(VANCO)”进行二次分析。
36个学术创伤中心。
纳入VANCO试验中所有患有高危胫骨骨折(骨科创伤协会/骨科学术联合会分类41B/C或43B/C)的患者。根据主刀医生的判断放置闭合式负压引流管。患者被随机分配在确定性固定时于手术伤口内接受1克万古霉素粉末或各中心的标准感染预防方案。
6个月内的深部手术部位感染(SSI)。对使用和未使用引流管的患者进行比较。亚组分析还研究了引流管在使用和未使用伤口内万古霉素粉末患者中的效果。
在978例研究患者中,197例(20%)使用了引流管。使用或未使用手术引流管的患者深部感染率无显著差异(8%对8%,P = 0.88)。然而,伤口内应用万古霉素粉末显著改变了手术引流管与深部SSI之间的关联(交互作用P = 0.048)。具体而言,使用引流管但未使用万古霉素粉末的患者深部感染率最高(13%;95%置信区间,6%-19%)。当在使用引流管的基础上再使用万古霉素粉末时,深部SSI率降低了10%(95%置信区间,2%-17%,P = 0.01)。
本研究表明,高危胫骨骨折手术固定后使用闭合式负压引流管总体上可能与深部感染无关。然而,二次分析提出了一种可能性,即如果使用局部万古霉素粉末,引流管与深部感染率降低有关,但如果不使用万古霉素粉末,则与感染率增加有关。
治疗性三级。有关证据级别的完整描述,请参阅作者指南。