Trauma and Orthopedic Department, Saint Philibert Hospital Center-Lomme, Rue du Grand But-BP 249, 59462, Lomme Cedex, France.
Transveral Infectious Disease Department, Saint Philibert Hospital Center-Lomme, Lomme, France.
Eur J Orthop Surg Traumatol. 2021 Jan;31(1):155-160. doi: 10.1007/s00590-020-02755-7. Epub 2020 Aug 2.
Analyze the diagnostic performance of suction drainage fluid culture for acute surgical site infection, which has not been specifically reported in spine surgery patients.
This was a retrospective single-center observational study including data from 363 patients who underwent aseptic instrumented spine surgery between 2015 and 2017. A suction drain was inserted in all cases. Data analyzed were patient age, gender, ASA score, indication for surgery (degenerative disease, tumor, trauma), spine level (cervical, thoracic, lumbar), procedure performed and spine level, operative time, body temperature, postoperative C-reactive protein time-curve, clinical aspect of surgical scar, bacteriology results of suction drainage fluid, and in case of revision surgery, lavage fluid. Major criteria for periprosthetic infection proposed by the Musculoskeletal Infection Society (MSIS) were accepted as the gold standard for the diagnosis of acute surgical site infection.
The overall rate of surgical site infection was 6.9% (5.76% for 1- or 2-level fusion, 5.81% for 3- or 4-level fusion, and 15.6% for 5-level fusion and above). The suction drain was withdrawn on the second postoperative day in 44.1% of cases and the third day in 39.1%. The sensitivity of suction drainage fluid culture for the diagnosis of surgical site infection was 20% [95%CI 6.8-40.7%] with a 96.2% [95%CI 93.2-97.9] specificity.
The diagnostic performance of suction drainage fluid culture after aseptic instrumented spine surgery for acute surgical site infection is insufficient to warrant its use in routine practice.
分析抽吸引流液培养在急性手术部位感染诊断中的表现,而抽吸引流液培养在脊柱外科患者中尚未得到专门报道。
这是一项回顾性单中心观察性研究,纳入了 2015 年至 2017 年间 363 例接受无菌器械脊柱手术的患者数据。所有患者均插入了引流管。分析的数据包括患者年龄、性别、ASA 评分、手术指征(退行性疾病、肿瘤、创伤)、脊柱节段(颈椎、胸椎、腰椎)、手术操作和脊柱节段、手术时间、体温、术后 C 反应蛋白时间曲线、手术疤痕的临床特征、抽吸引流液的细菌学结果,以及在翻修手术时的冲洗液。美国矫形外科感染协会(MSIS)提出的假体周围感染主要标准被接受为急性手术部位感染诊断的金标准。
手术部位感染的总发生率为 6.9%(1-2 个节段融合为 5.76%,3-4 个节段融合为 5.81%,5 个节段及以上融合为 15.6%)。44.1%的病例在术后第 2 天、39.1%的病例在术后第 3 天拔除引流管。抽吸引流液培养对手术部位感染的诊断敏感性为 20%[95%CI 6.8-40.7%],特异性为 96.2%[95%CI 93.2-97.9%]。
无菌器械脊柱手术后抽吸引流液培养对急性手术部位感染的诊断性能不足,不能常规应用于临床实践。