Baylor College of Medicine, Houston, Texas, USA,
Mount Sinai Hospital and Institute of HPME, University of Toronto, Toronto, Ontario, Canada.
Neonatology. 2020;117(6):767-770. doi: 10.1159/000510671. Epub 2021 Jan 15.
: Late-onset infection is the most common serious complication associated with hospital care for newborn infants. Because confirming the diagnosis by microbiological culture typically takes 24 to 48 hours, the serum level of the inflammatory marker C-reactive protein (CRP) measured as part of the initial investigation is used as an adjunctive rapid test to guide management in infants with suspected late-onset infection.
: To determine the diagnostic accuracy of serum CRP measurement in detecting late-onset infection in newborn infants.
: We searched electronic databases (MEDLINE, Embase, and Science Citation Index to September 2017), conference proceedings, previous reviews, and the reference lists of retrieved articles.
: We included cohort and cross-sectional studies evaluating the diagnostic accuracy of serum CRP levels for the detection of late-onset infection (occurring more than 72 hours after birth) in newborn infants.
: Two review authors independently assessed eligibility for inclusion, evaluated the methodological quality of included studies, and extracted data to estimate diagnostic accuracy using hierarchical summary receiver operating characteristic (SROC) models. We assessed heterogeneity by examining variability of study estimates and overlap of the 95% confidence interval (CI) in forest plots of sensitivity and specificity.
: The search identified 20 studies (1615 infants). Most were small, single-centre, prospective cohort studies conducted in neonatal units in high- or middle-income countries since the late 1990s. Risk of bias in the included studies was generally low with independent assessment of index and reference tests. Most studies used a prespecified serum CRP threshold level as the definition of a ‘positive’ index test (typical cut-off level between 5 mg/L and 10 mg/L) and the culture of a pathogenic micro-organism from blood as the reference standard. At median specificity (0.74), sensitivity was 0.62 (95% CI 0.50 to 0.73). Heterogeneity was evident in the forest plots, but it was not possible to conduct subgroup or meta-regression analyses by gestational ages, types of infection, or types of infecting micro-organism. Covariates for whether studies used a predefined threshold or not, and whether studies used a standard threshold of between 5 mg/L and 10 mg/L, were not statistically significant.
AUTHORS’ CONCLUSIONS:: The serum CRP level at initial evaluation of an infant with suspected late-onset infection is unlikely to be considered sufficiently accurate to aid early diagnosis or select infants to undergo further investigation or treatment with antimicrobial therapy or other interventions.
迟发性感染是与新生儿住院治疗相关的最常见严重并发症。由于通过微生物培养来确诊通常需要 24 至 48 小时,因此在初始检查中测量的炎症标志物 C 反应蛋白(CRP)的血清水平被用作辅助快速检测,以指导疑似迟发性感染婴儿的管理。
确定血清 CRP 测量在检测新生儿迟发性感染中的诊断准确性。
我们检索了电子数据库(MEDLINE、Embase 和科学引文索引,截至 2017 年 9 月)、会议录、先前的综述和检索到的文章的参考文献列表。
我们纳入了评估血清 CRP 水平检测新生儿迟发性感染(发生在出生后 72 小时以上)的诊断准确性的队列研究和病例对照研究。
两位综述作者独立评估纳入标准,评估纳入研究的方法学质量,并使用分层汇总受试者工作特征(SROC)模型提取数据以估计诊断准确性。我们通过检查森林图中敏感性和特异性的研究估计值的可变性和 95%置信区间(CI)的重叠来评估异质性。
搜索确定了 20 项研究(1615 名婴儿)。大多数研究是在 20 世纪 90 年代后期在高收入或中等收入国家的新生儿病房中进行的小型、单中心、前瞻性队列研究。纳入研究的偏倚风险通常较低,对参考和索引测试的评估是独立进行的。大多数研究使用了一个预先指定的血清 CRP 阈值水平作为“阳性”索引测试的定义(5mg/L 至 10mg/L 之间的典型截止值),并将血液中致病性微生物的培养作为参考标准。在中位数特异性(0.74)方面,敏感性为 0.62(95%CI 0.50 至 0.73)。森林图中存在异质性,但无法按胎龄、感染类型或感染微生物类型进行亚组或荟萃回归分析。是否使用预定义阈值以及是否使用 5mg/L 至 10mg/L 之间的标准阈值进行研究的协变量在统计学上没有显著性。
在疑似迟发性感染婴儿的初始评估中,血清 CRP 水平可能不太准确,无法帮助早期诊断或选择需要进一步检查或用抗生素治疗或其他干预措施的婴儿。