From the Division of Pediatric Emergency Medicine, Department of Emergency Medicine, Columbia University, New York, NY.
Division of Emergency Medicine, Boston Children's Hospital and Harvard Medical School, Boston, MA.
Pediatr Emerg Care. 2024 Jul 1;40(7):e82-e88. doi: 10.1097/PEC.0000000000003188. Epub 2024 Apr 2.
To evaluate the performance of synovial fluid biomarkers to identify children with culture-positive septic arthritis.
We identified children 6 months to 18 years old presenting to a single emergency department between 2007 and 2022 undergoing evaluation for septic arthritis defined by having a synovial fluid culture obtained. Our primary outcome was septic arthritis defined by a positive synovial fluid culture. We evaluated the ability of synovial fluid biomarkers to identify children with septic arthritis using area under the receiver operating characteristic curve (AUC) analyses. We measured the sensitivity and specificity of commonly used synovial fluid biomarkers.
We included 796 children, of whom 79 (10%) had septic arthritis. Compared with synovial white blood cell count (AUC, 0.72; 95% confidence interval [CI], 0.65-0.78), absolute neutrophil count (AUC, 0.72; 95% CI, 0.66-0.79; P = 0.09), percent neutrophils (AUC, 0.66; 95% CI, 0.60-0.71; P = 0.12), and glucose (AUC, 0.78; 95% CI, 0.67-0.90; P = 0.33) performed similarly, whereas protein (AUC, 0.52; 95% CI, 0.40-0.63, P = 0.04) had lower diagnostic accuracy. Synovial fluid white blood cell count ≥50,000 cells/μL had a sensitivity of 62.0% (95% CI, 50.4%-72.7%) and a specificity of 67.0% (95% CI, 63.4%-70.4%), whereas a positive synovial fluid Gram stain had a sensitivity of 48.1% (95% CI, 36.5%-59.7%) and specificity of 99.1% (95% CI, 98.1%-99.7%) for septic arthritis.
None of the routinely available synovial fluid biomarkers had sufficient accuracy to be used in isolation in the identification of children with septic arthritis. New approaches including multivariate clinical prediction rules and novel biomarkers are needed.
评估滑液生物标志物在识别培养阳性脓毒性关节炎患儿中的性能。
我们确定了 2007 年至 2022 年间在单个急诊部门就诊的 6 个月至 18 岁儿童,这些儿童接受了脓毒性关节炎的评估,其定义为获得滑液培养阳性。我们的主要结局是通过阳性滑液培养定义的脓毒性关节炎。我们使用接受者操作特征曲线(AUC)分析评估滑液生物标志物识别脓毒性关节炎患儿的能力。我们测量了常用滑液生物标志物的灵敏度和特异性。
我们纳入了 796 名儿童,其中 79 名(10%)患有脓毒性关节炎。与滑液白细胞计数(AUC,0.72;95%置信区间[CI],0.65-0.78)相比,绝对中性粒细胞计数(AUC,0.72;95%CI,0.66-0.79;P=0.09)、中性粒细胞百分比(AUC,0.66;95%CI,0.60-0.71;P=0.12)和葡萄糖(AUC,0.78;95%CI,0.67-0.90;P=0.33)的表现相似,而蛋白质(AUC,0.52;95%CI,0.40-0.63,P=0.04)的诊断准确性较低。滑液白细胞计数≥50,000 个/μL 的敏感性为 62.0%(95%CI,50.4%-72.7%),特异性为 67.0%(95%CI,63.4%-70.4%),而滑液革兰染色阳性的敏感性为 48.1%(95%CI,36.5%-59.7%),特异性为 99.1%(95%CI,98.1%-99.7%)用于诊断脓毒性关节炎。
目前尚无一种常规可用的滑液生物标志物具有足够的准确性,可单独用于识别患有脓毒性关节炎的儿童。需要新的方法,包括多变量临床预测规则和新型生物标志物。