Heller Aaron, McIff Terence E, Lai Sue-Min, Burton Douglas C
Departments of *Orthopedic Surgery †Preventive Medicine and Public Health, University of Kansas Medical Center, Kansas City, KS.
J Spinal Disord Tech. 2015 Dec;28(10):E584-9. doi: 10.1097/BSD.0000000000000045.
A retrospective historical cohort design.
To determine what effect the addition of intrawound vancomycin powder to the prophylactic regimen of posterior instrumented spinal arthrodesis procedures has had on acute surgical site infections (SSIs).
SSIs are known complications in instrumented spinal arthrodesis procedures, and are predominately caused by Staphylococcus aureus. Recent reports have suggested that placing vancomycin powder into the surgical wound before closure prevents SSIs in spinal surgery. Risk factors for SSIs in the setting of intrawound vancomycin powder use have not been previously reported on.
SSI rates after 342 posterior instrumented spinal arthrodeses (October 2008-September 2011) in which intrawound vancomycin powder was used in addition to the standard antimicrobial prophylaxis (Vanco cohort) were compared with 341 posterior instrumented spinal arthrodeses (April 2005-October 2008) in which no vancomycin powder was added (non-Vanco cohort). Both 2 sample t test and χ test (Fisher where appropriate) were used for group comparisons. A subanalysis of the Vanco cohort was undertaken to identify risk factors for SSIs despite intrawound vancomycin use.
There was a significant reduction in the number of acute staphylococcal SSIs in the Vanco cohort (1.1%) compared with the non-Vanco cohort (3.8%; P=0.029). Deep staphylococcal infections decreased to 0 compared with 7 in the non-Vanco cohort (2.1%; P=0.008). Deep methicillin-resistant S. aureus infections decreased to 0 compared with 5 in the non-Vanco cohort (1.5%; P=0.031). A subanalysis of the Vanco cohort identified that being discharged to an inpatient rehabilitation or skilled nursing facility was associated with developing a SSI.
Intrawound vancomycin powder use has decreased the rate of acute staphylococcal SSIs in our posterior instrumented spine arthrodesis surgeries. Patients who are discharged to skilled nursing or rehabilitation facilities are at an increased risk for developing SSIs despite intrawound vancomycin use.
回顾性历史队列研究设计。
确定在脊柱后路器械固定融合手术的预防方案中添加伤口内万古霉素粉末对急性手术部位感染(SSIs)有何影响。
SSIs是脊柱器械固定融合手术中已知的并发症,主要由金黄色葡萄球菌引起。最近的报告表明,在关闭手术伤口前将万古霉素粉末置于手术伤口内可预防脊柱手术中的SSIs。此前尚未有关于使用伤口内万古霉素粉末情况下SSIs的危险因素的报告。
将2008年10月至2011年9月期间342例脊柱后路器械固定融合手术(使用伤口内万古霉素粉末加标准抗菌预防措施,即万古霉素组)后的SSI发生率与2005年4月至2008年10月期间341例未添加万古霉素粉末(非万古霉素组)的脊柱后路器械固定融合手术进行比较。两组比较采用双样本t检验和χ检验(适当情况下采用Fisher检验)。对万古霉素组进行亚分析以确定尽管使用了伤口内万古霉素但发生SSIs的危险因素。
与非万古霉素组(3.8%)相比,万古霉素组急性葡萄球菌性SSIs的数量显著减少(1.1%;P = 0.029)。深部葡萄球菌感染降至0,而非万古霉素组为7例(2.1%;P = 0.008)。耐甲氧西林金黄色葡萄球菌深部感染降至0,而非万古霉素组为5例(1.5%;P = 0.031)。对万古霉素组的亚分析确定,出院后入住住院康复机构或专业护理机构与发生SSI相关。
在我们的脊柱后路器械固定融合手术中,使用伤口内万古霉素粉末降低了急性葡萄球菌性SSIs的发生率。尽管使用了伤口内万古霉素,但出院后入住专业护理或康复机构的患者发生SSIs的风险增加。