Rockford Spine Center, Rockford, IL 61103, USA.
Spine (Phila Pa 1976). 2011 Nov 15;36(24):2084-8. doi: 10.1097/BRS.0b013e3181ff2cb1.
A retrospective cohort study from a single institution of a consecutive series of spine surgery patients.
To evaluate the safety and efficacy of adjunctive local application of vancomycin for infection prophylaxis in posterior instrumented thoracic and lumbar spine wounds compared to IV cephalexin alone.
Cephalosporin resistant strains of staphylococcus (MRSA and coagulase negative staph) have diminished the efficacy of intravenous antibiotic prophylaxis for instrumented spine fusion. Intravenous vancomycin prophylaxis has not been shown to decrease wound infection rates compared to IV cephalosporins. Adjunctive application of vancomycin powder in wounds for instrumented spinal fusion surgery may decrease infection rates.
Since 2000, 1732 consecutive thoracic and lumbar posterior instrumented spinal fusions have been performed with routine 24 hours of perioperative intravenous antibiotic prophylaxis with cephalexin. Since 2006, 911 of these instrumented thoracic and lumbar cases had 2 g of vancomycin powder applied to the wound before closure in addition to intravenous antibiotics. A retrospective review for infection rates and complications was performed. Oswestry and SF-36 outcomes instruments were completed before surgery, immediately after surgery, and at latest follow-up. The average follow-up is 2.5 years, range 1 to 7 years.
Eight hundred twenty-one posterior instrumented thoracic and lumbar fusions were preformed using intravenous cephalexin prophylaxis with a total of 21 deep wound infections (2.6%). Coag negative staph was the most commonly isolated organism. Nine hundred eleven posterior instrumented thoracic and lumbar fusions have been performed with IV cephalexin plus adjunctive local vancomycin powder with two deep wound infections (0.2%). The reduction in wound infections was statistically significant (P < 0.0001). There were no adverse clinical outcomes or wound complications related to the local application of vancomycin.
Adjunctive local application of vancomycin powder decreases the postsurgical wound infection rate with statistical significance in posterior instrumented thoracolumbar spine fusions.
单中心回顾性队列研究,连续系列脊柱手术患者。
评估与单独静脉注射头孢菌素相比,局部应用万古霉素辅助预防后路胸腰椎脊柱伤口感染的安全性和有效性。
头孢菌素耐药的葡萄球菌(MRSA 和凝固酶阴性葡萄球菌)降低了静脉抗生素预防用于器械脊柱融合的疗效。静脉万古霉素预防与静脉头孢菌素相比并未显示出降低伤口感染率。在器械脊柱融合手术的伤口中局部应用万古霉素粉末可能会降低感染率。
自 2000 年以来,已对 1732 例连续的胸腰椎后路器械脊柱融合术进行了常规的 24 小时围手术期静脉抗生素头孢菌素预防。自 2006 年以来,在静脉抗生素的基础上,911 例器械胸腰椎病例将 2 克万古霉素粉末应用于伤口,然后关闭伤口。对感染率和并发症进行了回顾性回顾。术前、术后即刻和最新随访时完成 Oswestry 和 SF-36 结果量表。平均随访时间为 2.5 年,范围为 1 至 7 年。
821 例后路胸腰椎融合术采用静脉头孢菌素预防,共发生 21 例深部伤口感染(2.6%)。凝固酶阴性葡萄球菌是最常见的分离菌。911 例后路胸腰椎融合术采用静脉头孢菌素加局部万古霉素粉末辅助治疗,发生深部伤口感染 2 例(0.2%)。伤口感染的减少具有统计学意义(P<0.0001)。局部应用万古霉素无不良临床结局或伤口并发症。
后路胸腰椎器械脊柱融合术中局部应用万古霉素粉末可显著降低术后伤口感染率。