Department of Pediatrics B, Schneider Children's Medical Center, Petach Tikva, Israel.
Pediatric Infectious Disease Unit, Schneider Children's Medical Center, Petach Tikva, Israel.
Eur J Clin Microbiol Infect Dis. 2018 Jul;37(7):1361-1371. doi: 10.1007/s10096-018-3261-3. Epub 2018 Apr 26.
Bacterial and viral infections often present with similar symptoms. Etiologic misdiagnosis can alter the trajectory of patient care, including antibiotic overuse. A host-protein signature comprising tumor necrosis factor-related apoptosis-inducing ligand (TRAIL), interferon gamma-induced protein-10 (IP-10), and C-reactive protein (CRP) was validated recently for differentiating bacterial from viral disease. However, a focused head-to-head comparison of its diagnostic performance against other biomarker candidates for this indication was lacking in patients with respiratory infection and fever without source. We compared the signature to other biomarkers and prediction rules using specimens collected prospectively at two secondary medical centers from children and adults. Inclusion criteria included fever > 37.5 °C, symptom duration ≤ 12 days, and presentation with respiratory infection or fever without source. Comparator method was based on expert panel adjudication. Signature and biomarker cutoffs and prediction rules were predefined. Of 493 potentially eligible patients, 314 were assigned unanimous expert panel diagnosis and also had sufficient specimen volume. The resulting cohort comprised 175 (56%) viral and 139 (44%) bacterial infections. Signature sensitivity 93.5% (95% CI 89.1-97.9%), specificity 94.3% (95% CI 90.7-98.0%), or both were significantly higher (all p values < 0.01) than for CRP, procalcitonin, interleukin-6, human neutrophil lipocalin, white blood cell count, absolute neutrophil count, and prediction rules. Signature identified as viral 50/57 viral patients prescribed antibiotics, suggesting potential to reduce antibiotic overuse by 88%. The host-protein signature demonstrated superior diagnostic performance in differentiating viral from bacterial respiratory infections and fever without source. Future utility studies are warranted to validate potential to reduce antibiotic overuse.
细菌和病毒感染常表现出相似的症状。病因误诊可能改变患者的治疗轨迹,包括抗生素的过度使用。最近,一种由肿瘤坏死因子相关凋亡诱导配体(TRAIL)、干扰素γ诱导蛋白-10(IP-10)和 C 反应蛋白(CRP)组成的宿主蛋白特征被验证可用于区分细菌和病毒疾病。然而,在患有呼吸道感染和无明确病因的发热的患者中,缺乏针对该适应证的其他生物标志物候选物的诊断性能的集中比较。我们使用前瞻性收集的来自两家二级医疗中心的标本比较了该特征与其他生物标志物和预测规则。纳入标准包括体温>37.5°C、症状持续时间≤12 天、有呼吸道感染或无明确病因的发热表现。比较方法基于专家小组的裁决。特征和生物标志物的截止值和预测规则是预先设定的。在 493 名潜在合格患者中,314 名患者被专家小组一致诊断,并具有足够的标本量。由此产生的队列包括 175 例(56%)病毒感染和 139 例(44%)细菌感染。特征的敏感性为 93.5%(95%可信区间 89.1-97.9%),特异性为 94.3%(95%可信区间 90.7-98.0%),或两者均显著高于 CRP、降钙素原、白细胞介素-6、人中性粒细胞明胶酶相关脂质运载蛋白、白细胞计数、绝对中性粒细胞计数和预测规则(所有 p 值均<0.01)。特征将 50/57 例病毒患者识别为病毒感染,建议潜在地将抗生素使用率降低 88%。宿主蛋白特征在区分无明确病因的呼吸道病毒和细菌感染以及发热方面具有卓越的诊断性能。需要进一步的验证性研究来验证潜在的减少抗生素过度使用的效果。