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本文引用的文献

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Early-onset sepsis in very low birth weight neonates: a report from the National Institute of Child Health and Human Development Neonatal Research Network.极低出生体重新生儿早发型败血症:美国国立儿童健康与人类发展研究所新生儿研究网络的报告
J Pediatr. 1996 Jul;129(1):72-80. doi: 10.1016/s0022-3476(96)70192-0.
2
Reliability of observation variables in distinguishing infectious outcome of febrile young infants.观察变量在区分发热婴幼儿感染性结局方面的可靠性。
Pediatr Infect Dis J. 1993 Feb;12(2):111-4. doi: 10.1097/00006454-199302000-00001.
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Significance of serial C-reactive protein responses in neonatal infection and other disorders.新生儿感染及其他疾病中连续C反应蛋白反应的意义。
Pediatrics. 1993 Sep;92(3):431-5.
4
Hematologic scoring system in early diagnosis of sepsis in neutropenic newborns.中性粒细胞减少新生儿脓毒症早期诊断中的血液学评分系统
Pediatr Infect Dis J. 1993 May;12(5):372-6. doi: 10.1097/00006454-199305000-00004.
5
Users' guides to the medical literature. III. How to use an article about a diagnostic test. B. What are the results and will they help me in caring for my patients? The Evidence-Based Medicine Working Group.医学文献用户指南。III. 如何使用一篇关于诊断试验的文章。B. 结果是什么,它们对我照顾患者有帮助吗?循证医学工作组。
JAMA. 1994 Mar 2;271(9):703-7. doi: 10.1001/jama.271.9.703.
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Users' guides to the medical literature. III. How to use an article about a diagnostic test. A. Are the results of the study valid? Evidence-Based Medicine Working Group.医学文献用户指南。III. 如何使用关于诊断试验的文章。A. 研究结果是否有效?循证医学工作组。
JAMA. 1994 Feb 2;271(5):389-91. doi: 10.1001/jama.271.5.389.
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C-reactive protein as a diagnostic tool of sepsis in very immature babies.
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Guidelines for meta-analyses evaluating diagnostic tests.评估诊断试验的Meta分析指南。
Ann Intern Med. 1994 Apr 15;120(8):667-76. doi: 10.7326/0003-4819-120-8-199404150-00008.
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Role of tumor necrosis factor in neonatal sepsis.
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Diagnostic value of leukocyte indices in late neonatal sepsis.白细胞指标在晚期新生儿败血症中的诊断价值。
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从出生到90天的细菌感染诊断测试——一项系统综述

Diagnostic tests for bacterial infection from birth to 90 days--a systematic review.

作者信息

Fowlie P W, Schmidt B

机构信息

Department of Child Health, University of Dundee, Scotland.

出版信息

Arch Dis Child Fetal Neonatal Ed. 1998 Mar;78(2):F92-8. doi: 10.1136/fn.78.2.f92.

DOI:10.1136/fn.78.2.f92
PMID:9577277
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1720763/
Abstract

AIM

To determine the clinical value of common diagnostic tests for bacterial infection in early life.

METHODS

A Medline search (1966-95) was undertaken to identify studies that reported the assessment of a diagnostic "test," predicting the presence or absence of bacterial infection in infants up to 90 days of age. The quality of each selected study was assessed using defined criteria. Data were extracted twice to minimise errors.

RESULTS

Six hundred and seventy articles were identified. Two independent investigators agreed that 194 studies met the inclusion criteria (kappa = 0.85), 52 of which met primary quality criteria; 23 studies reported data on (a) haematological indices, (b) C reactive protein evaluation, and (c) surface swab assessment. For haematological indices, the likelihood ratios for individual tests ranged from 20.4 (95% confidence interval 7.3 to 56.8) for a white cell count < 7000/mm3 to 0.12 (0.04 to 0.37) for an immature:total (I:T) white cell ratio < 0.2. For C reactive protein evaluation, the likelihood ratios ranged from 12.56 (0.79 to 199.10) for a value of > 6 mg/l to 0.22 (0.08 to 0.65) for a negative value. For surface swab assessment, the likelihood ratios ranged from 33.6 (2.1 to 519.8) for a positive gastric aspirate culture to 0.08 (0.006 to 1.12) for microscopy of ear swab material that did not show any neutrophils. Likelihood ratios for combinations of these individual tests ranged from 10.17 (3.64 to 28.41) to 0.47 (0.22 to 1.00).

CONCLUSIONS

The methodological quality of studies assessing the accuracy of diagnostic tests is generally poor. Even in rigorous studies, the reported accuracy of the tests varies enormously and they are of limited value in the diagnosis of infection in this population.

摘要

目的

确定早期生活中细菌感染常见诊断检测的临床价值。

方法

进行了一项Medline检索(1966 - 1995年),以识别报告了对一种诊断“检测”进行评估的研究,该检测用于预测90日龄以内婴儿是否存在细菌感染。使用既定标准评估每项入选研究的质量。数据提取了两次以尽量减少误差。

结果

共识别出670篇文章。两名独立研究者一致认为194项研究符合纳入标准(kappa = 0.85),其中52项符合主要质量标准;23项研究报告了关于(a)血液学指标、(b)C反应蛋白评估和(c)表面拭子评估的数据。对于血液学指标,各项检测的似然比范围为:白细胞计数<7000/mm³时为20.4(95%置信区间7.3至56.8),未成熟:总(I:T)白细胞比值<0.2时为0.12(0.04至0.37)。对于C反应蛋白评估,似然比范围为:值>6mg/l时为12.56(0.79至199.10),阴性值时为0.22(0.08至0.65)。对于表面拭子评估,似然比范围为:胃吸出物培养阳性时为33.6(2.1至519.8),耳拭子材料显微镜检查未显示任何中性粒细胞时为0.08(0.006至1.12)。这些个体检测组合的似然比范围为10.17(3.64至28.41)至0.47(0.22至1.00)。

结论

评估诊断检测准确性的研究方法质量普遍较差。即使在严格的研究中,所报告的检测准确性差异也极大,且它们在该人群感染诊断中的价值有限。