• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

评估 C 反应蛋白诊断试验在新生儿迟发性感染中的准确性:系统评价和荟萃分析。

Assessment of C-Reactive Protein Diagnostic Test Accuracy for Late-Onset Infection in Newborn Infants: A Systematic Review and Meta-analysis.

机构信息

Centre for Reviews and Dissemination, University of York, York, United Kingdom.

出版信息

JAMA Pediatr. 2020 Mar 1;174(3):260-268. doi: 10.1001/jamapediatrics.2019.5669.

DOI:10.1001/jamapediatrics.2019.5669
PMID:32011640
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7042944/
Abstract

IMPORTANCE

Rapid and accurate diagnosis of late-onset infection in newborn infants could inform treatment decisions and avoid unnecessary administration of antibiotics.

OBJECTIVE

To compare the accuracy of serum C-reactive protein (CRP) with that of microbiological blood culture for diagnosing late-onset infection in newborns.

DATA SOURCES

MEDLINE (1946-2019), Embase (1946-2019), and Science Citation Index (1900-2019) databases were searched for references (any language). The MeSH search terms included were "exp infant, newborn/" or "premature birth/" plus free text synonyms; and "C-reactive protein/" plus free text synonyms; and "exp sepsis/" or "exp bacterial infections/" plus free text synonyms. The proceedings from relevant conferences and references of identified papers were scrutinized. Authors were contacted to request missing data.

STUDY SELECTION

Cohort and cross-sectional studies were included that compared the accuracy of serum CRP levels with microbiological culture results to diagnose late-onset (>72 hours after birth) infection in newborns (any gestational age) hospitalized after birth. Two reviewers assessed study eligibility. Among 10 394 records, 148 studies were assessed as full texts.

DATA EXTRACTION AND SYNTHESIS

The Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guideline extension for Diagnostic Test Accuracy (DTA) reviews was followed. Two reviewers assessed the method quality of each study using guidance from the Cochrane Screening and Diagnostic Test Methods Group (adapted from the Quality Assessment of Diagnostic Accuracy Studies 2).

MAIN OUTCOMES AND MEASURES

The primary meta-analysis outcome was diagnostic test accuracy of serum CRP level taken at initial investigation of an infant with suspected late-onset infection. The median specificity (proportion of true-negative results) and calculated pooled sensitivity (proportion of true-positive results) were determined by generating hierarchical summary receiver characteristic operating curves.

RESULTS

In total, 22 studies with 2255 infants were included (sample size range, 11-590 infants). Participants in most studies were preterm (<37 weeks) or very low-birth weight (<1500 g) infants. Two studies additionally enrolled infants born at term. Most studies (16) used a prespecified CRP level cutoff for a "positive" index test (5-10 mg/L), and most studies (17) used the culture of a pathogenic microorganism from blood as the reference standard. Risk of bias was low with independent assessment of index and reference tests. At median specificity (0.74), pooled sensitivity was 0.62 (95% CI, 0.50-0.72). Adding serum CRP level to the assessment of an infant with a 40% pretest probability of late-onset infection (the median for the included studies) generated posttest probabilities of 26% for a negative test result and 61% for a positive test result.

CONCLUSIONS AND RELEVANCE

The findings suggest that determination of serum CRP level at initial evaluation of an infant with suspected late-onset infection is unlikely to aid early diagnosis or to select infants to undergo further investigation or treatment with antimicrobial therapy or other interventions.

摘要

重要性

快速准确地诊断新生儿晚期感染可以为治疗决策提供信息,并避免不必要地使用抗生素。

目的

比较血清 C 反应蛋白 (CRP) 与微生物血培养对诊断新生儿晚期感染的准确性。

数据来源

对 MEDLINE(1946-2019 年)、Embase(1946-2019 年)和科学引文索引(1900-2019 年)数据库进行了检索,检索语言不限。使用的 MeSH 检索词包括“新生儿/早产”或“婴儿,新生/”加上同义词的自由文本;和“C 反应蛋白/”加上同义词的自由文本;和“败血症/”或“细菌感染/”加上同义词的自由文本。还仔细审查了相关会议的会议记录和已确定论文的参考文献。联系作者以请求缺失的数据。

研究选择

纳入了比较血清 CRP 水平与微生物培养结果以诊断出生后住院的晚期(出生后>72 小时)感染(任何胎龄)新生儿的准确性的队列研究和横断面研究。两名审查员评估了研究的合格性。在 10394 条记录中,有 148 项研究被评估为全文。

数据提取和综合

遵循了系统评价和荟萃分析(PRISMA)诊断测试准确性(DTA)扩展指南。两名审查员使用 Cochrane 筛查和诊断测试方法小组的指导(改编自诊断准确性研究 2 的质量评估)评估了每项研究的方法质量。

主要结果和措施

主要的荟萃分析结果是在疑似晚期感染婴儿的初始检查中进行血清 CRP 水平的诊断测试准确性。通过生成分层总结接收者特征工作曲线确定中位数特异性(真阴性结果的比例)和计算的 pooled 敏感性(真阳性结果的比例)。

结果

共纳入 22 项研究,涉及 2255 名婴儿(样本量范围为 11-590 名婴儿)。大多数研究的参与者是早产儿(<37 周)或极低出生体重儿(<1500 克)。两项研究还招募了足月出生的婴儿。大多数研究(16 项)使用了预先指定的 CRP 水平截断值(5-10mg/L)作为“阳性”指标测试,大多数研究(17 项)使用血液中致病微生物的培养作为参考标准。独立评估指标和参考测试的偏倚风险较低。在中位数特异性(0.74)时,pooled 敏感性为 0.62(95%CI,0.50-0.72)。在考虑了一个患有 40%晚期感染可能性的婴儿的预测试验概率(包括研究的中位数)后,阴性试验结果的后测试概率为 26%,阳性试验结果的后测试概率为 61%。

结论和相关性

研究结果表明,在疑似晚期感染的婴儿初始评估时测定血清 CRP 水平不太可能有助于早期诊断,也不太可能选择婴儿进行进一步检查或接受抗生素治疗或其他干预措施。

相似文献

1
Assessment of C-Reactive Protein Diagnostic Test Accuracy for Late-Onset Infection in Newborn Infants: A Systematic Review and Meta-analysis.评估 C 反应蛋白诊断试验在新生儿迟发性感染中的准确性:系统评价和荟萃分析。
JAMA Pediatr. 2020 Mar 1;174(3):260-268. doi: 10.1001/jamapediatrics.2019.5669.
2
C-reactive protein for diagnosing late-onset infection in newborn infants.用于诊断新生儿晚发型感染的C反应蛋白
Cochrane Database Syst Rev. 2019 Jan 14;1(1):CD012126. doi: 10.1002/14651858.CD012126.pub2.
3
Presepsin for the Diagnosis of Neonatal Early-Onset Sepsis: A Systematic Review and Meta-analysis.降钙素原在新生儿早发性败血症诊断中的应用:系统评价和荟萃分析。
JAMA Pediatr. 2022 Aug 1;176(8):750-758. doi: 10.1001/jamapediatrics.2022.1647.
4
Cell-Surface Biomarkers, C-Reactive Protein and Haematological Parameters for Diagnosing Late Onset Sepsis in Pre-term Neonates.用于诊断早产儿晚发性败血症的细胞表面生物标志物、C 反应蛋白和血液学参数。
J Trop Pediatr. 2021 Jan 29;67(1). doi: 10.1093/tropej/fmab016.
5
C-reactive protein for late-onset sepsis diagnosis in very low birth weight infants.C反应蛋白用于极低出生体重儿晚发性败血症的诊断
BMC Pediatr. 2018 Jan 30;18(1):16. doi: 10.1186/s12887-018-1002-5.
6
Serial serum C-reactive protein levels in the diagnosis of neonatal infection.连续血清C反应蛋白水平在新生儿感染诊断中的应用
Pediatrics. 1998 Oct;102(4):E41. doi: 10.1542/peds.102.4.e41.
7
Diagnosis of late onset neonatal sepsis with cytokines, adhesion molecule, and C-reactive protein in preterm very low birthweight infants.细胞因子、黏附分子及C反应蛋白用于诊断早产极低出生体重儿迟发型新生儿败血症
Arch Dis Child Fetal Neonatal Ed. 1997 Nov;77(3):F221-7. doi: 10.1136/fn.77.3.f221.
8
Diagnostic test accuracy of procalcitonin and C-reactive protein for predicting invasive and serious bacterial infections in young febrile infants: a systematic review and meta-analysis.降钙素原和 C 反应蛋白预测发热婴幼儿侵袭性和严重细菌感染的诊断准确性:系统评价和荟萃分析。
Lancet Child Adolesc Health. 2024 May;8(5):358-368. doi: 10.1016/S2352-4642(24)00021-X. Epub 2024 Mar 16.
9
Diagnostic Test Accuracy of the Red Reflex Test for Ocular Pathology in Infants: A Meta-analysis.《婴幼儿眼部病变的红反射试验的诊断准确性:Meta 分析》
JAMA Ophthalmol. 2021 Jan 1;139(1):33-40. doi: 10.1001/jamaophthalmol.2020.4854.
10
The future of Cochrane Neonatal.考克兰新生儿协作网的未来。
Early Hum Dev. 2020 Nov;150:105191. doi: 10.1016/j.earlhumdev.2020.105191. Epub 2020 Sep 12.

引用本文的文献

1
Critical appraisal of presepsin for diagnosing late-onset sepsis in critically ill neonates.对前降钙素原在诊断危重新生儿晚发性败血症中的批判性评价。
Clin Chem Lab Med. 2025 Sep 8. doi: 10.1515/cclm-2025-1131.
2
Neonatal leucocyte cell population data: reference intervals and relevance for detecting sepsis and necrotizing enterocolitis.新生儿白细胞细胞群体数据:参考区间及对检测败血症和坏死性小肠结肠炎的相关性
Pediatr Res. 2025 Jun 6. doi: 10.1038/s41390-025-04159-x.
3
Comparative analysis of inflammatory biomarkers for the diagnosis of neonatal sepsis: IL-6, IL-8, SAA, CRP, and PCT.用于新生儿败血症诊断的炎症生物标志物的比较分析:白细胞介素-6、白细胞介素-8、血清淀粉样蛋白A、C反应蛋白和降钙素原
Open Life Sci. 2025 Jan 28;20(1):20221005. doi: 10.1515/biol-2022-1005. eCollection 2025.
4
Theoretical impact of a bedside decision-making tool on antibiotic use for suspected neonatal healthcare-associated infection: an observational study.床边决策工具对疑似新生儿医疗保健相关感染抗生素使用的理论影响:一项观察性研究。
BMC Pediatr. 2025 Jan 21;25(1):52. doi: 10.1186/s12887-024-05323-8.
5
The impact of early speech and language cognitive training care on the developmental quotient of children with language impairments: A retrospective study.早期言语和语言认知训练护理对语言障碍儿童发育商的影响:回顾性研究。
Medicine (Baltimore). 2024 Oct 25;103(43):e39898. doi: 10.1097/MD.0000000000039898.
6
Multicentre external validation of the Neonatal Healthcare-associated infectiOn Prediction (NeoHoP) score: a retrospective case-control study.多中心新生儿医疗保健相关感染预测(NeoHoP)评分的外部验证:一项回顾性病例对照研究。
BMJ Paediatr Open. 2024 Oct 1;8(1):e002748. doi: 10.1136/bmjpo-2024-002748.
7
Diagnosis and Management of Neonatal Bacterial Sepsis: Current Challenges and Future Perspectives.新生儿细菌性败血症的诊断与管理:当前挑战与未来展望
Trop Med Infect Dis. 2024 Aug 28;9(9):199. doi: 10.3390/tropicalmed9090199.
8
The potential role of heparin-binding protein in neonatal sepsis: research progress.肝素结合蛋白在新生儿败血症中的潜在作用:研究进展。
Front Cell Infect Microbiol. 2024 Aug 13;14:1422872. doi: 10.3389/fcimb.2024.1422872. eCollection 2024.
9
The spectrum of pneumonia among intubated neonates in the neonatal intensive care unit.新生儿重症监护病房中气管插管新生儿肺炎的谱。
J Perinatol. 2024 Sep;44(9):1235-1243. doi: 10.1038/s41372-024-01973-9. Epub 2024 May 2.
10
Impact of Physician Characteristics on Late-Onset Sepsis (LOS) Evaluation in the NICU.医师特征对新生儿重症监护病房迟发性败血症(LOS)评估的影响。
Healthcare (Basel). 2024 Apr 17;12(8):845. doi: 10.3390/healthcare12080845.

本文引用的文献

1
Impact of intrapartum and postnatal antibiotics on the gut microbiome and emergence of antimicrobial resistance in infants.分娩期和产后抗生素对婴儿肠道微生物组和抗生素耐药性出现的影响。
Sci Rep. 2019 Jul 23;9(1):10635. doi: 10.1038/s41598-019-46964-5.
2
C-reactive protein for late-onset sepsis diagnosis in very low birth weight infants.C反应蛋白用于极低出生体重儿晚发性败血症的诊断
BMC Pediatr. 2018 Jan 30;18(1):16. doi: 10.1186/s12887-018-1002-5.
3
Molecular assays for the diagnosis of sepsis in neonates.用于诊断新生儿败血症的分子检测方法。
Cochrane Database Syst Rev. 2017 Feb 25;2(2):CD011926. doi: 10.1002/14651858.CD011926.pub2.
4
Biomarkers for the diagnosis of neonatal sepsis and necrotizing enterocolitis: Clinical practice guidelines.新生儿败血症和坏死性小肠结肠炎诊断的生物标志物:临床实践指南
Early Hum Dev. 2017 Feb;105:25-33. doi: 10.1016/j.earlhumdev.2016.12.002. Epub 2017 Jan 25.
5
Antibiotic perturbation of the preterm infant gut microbiome and resistome.抗生素对早产儿肠道微生物群和耐药基因组的干扰。
Gut Microbes. 2016 Sep 2;7(5):443-9. doi: 10.1080/19490976.2016.1218584. Epub 2016 Jul 29.
6
Assessing variability in results in systematic reviews of diagnostic studies.评估诊断性研究系统评价结果的变异性。
BMC Med Res Methodol. 2016 Jan 15;16:6. doi: 10.1186/s12874-016-0108-4.
7
Serum Calprotectin: A Potential Biomarker for Neonatal Sepsis.血清钙卫蛋白:新生儿败血症的潜在生物标志物。
J Immunol Res. 2015;2015:147973. doi: 10.1155/2015/147973. Epub 2015 Aug 26.
8
Characteristics of neonates with culture-proven bloodstream infection who have low levels of C-reactive protein (≦10 mg/L).经培养证实存在血流感染且C反应蛋白水平较低(≤10mg/L)的新生儿的特征。
BMC Infect Dis. 2015 Aug 11;15:320. doi: 10.1186/s12879-015-1069-7.
9
Validity of C-reactive protein (CRP) for diagnosis of neonatal sepsis.C反应蛋白(CRP)在新生儿败血症诊断中的有效性。
Pak J Med Sci. 2015;31(3):527-31. doi: 10.12669/pjms.313.6668.
10
Risks of Antibiotic Exposures Early in Life on the Developing Microbiome.生命早期抗生素暴露对发育中的微生物群的风险。
PLoS Pathog. 2015 Jul 2;11(7):e1004903. doi: 10.1371/journal.ppat.1004903. eCollection 2015 Jul.