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本文引用的文献

1
Evaluation of pathogen detection from clinical samples by real-time polymerase chain reaction using a sepsis pathogen DNA detection kit.采用脓毒症病原体 DNA 检测试剂盒的实时聚合酶链反应法对临床样本中病原体检测的评估。
Crit Care. 2010;14(4):R159. doi: 10.1186/cc9234. Epub 2010 Aug 24.
2
Multiplex blood PCR in combination with blood cultures for improvement of microbiological documentation of infection in febrile neutropenia.多重血液 PCR 联合血液培养在发热性中性粒细胞减少症中改善感染的微生物学记录。
J Clin Microbiol. 2010 Oct;48(10):3510-6. doi: 10.1128/JCM.00147-10. Epub 2010 Aug 18.
3
Therapeutic impact and diagnostic performance of multiplex PCR in patients with malignancies and suspected sepsis.多重聚合酶链反应在恶性肿瘤和疑似脓毒症患者中的治疗效果和诊断性能。
J Infect. 2010 Oct;61(4):335-42. doi: 10.1016/j.jinf.2010.07.004. Epub 2010 Jul 15.
4
Accurate and rapid identification of bacterial species from positive blood cultures with a DNA-based microarray platform: an observational study.基于 DNA 微阵列平台的阳性血培养物中细菌种属的准确快速鉴定:一项观察性研究。
Lancet. 2010 Jan 16;375(9710):224-30. doi: 10.1016/S0140-6736(09)61569-5. Epub 2009 Dec 10.
5
International study of the prevalence and outcomes of infection in intensive care units.重症监护病房感染患病率及转归的国际研究。
JAMA. 2009 Dec 2;302(21):2323-9. doi: 10.1001/jama.2009.1754.
6
Multiplex PCR to diagnose bloodstream infections in patients admitted from the emergency department with sepsis.采用多重 PCR 方法诊断因败血症而从急诊科入院的血流感染患者。
J Clin Microbiol. 2010 Jan;48(1):26-33. doi: 10.1128/JCM.01447-09. Epub 2009 Oct 21.
7
Preliminary clinical study using a multiplex real-time PCR test for the detection of bacterial and fungal DNA directly in blood.初步临床研究使用多重实时 PCR 检测直接在血液中细菌和真菌的 DNA。
Clin Microbiol Infect. 2010 Jun;16(6):774-9. doi: 10.1111/j.1469-0691.2009.02940.x. Epub 2009 Aug 18.
8
Multiplex real-time PCR and blood culture for identification of bloodstream pathogens in patients with suspected sepsis.采用多重实时聚合酶链反应和血培养法鉴定疑似脓毒症患者血流中的病原体。
Clin Microbiol Infect. 2009 Jun;15(6):544-51. doi: 10.1111/j.1469-0691.2009.02736.x. Epub 2009 Apr 21.
9
Diagnosis of bloodstream infections in immunocompromised patients by real-time PCR.通过实时聚合酶链反应诊断免疫功能低下患者的血流感染
J Infect. 2009 May;58(5):346-51. doi: 10.1016/j.jinf.2009.03.001. Epub 2009 Mar 13.
10
Comparison of broad range 16S rDNA PCR and conventional blood culture for diagnosis of sepsis in the newborn: a case control study.新生儿败血症诊断中广泛16S rDNA聚合酶链反应与传统血培养的比较:一项病例对照研究。
BMC Pediatr. 2009 Jan 19;9:5. doi: 10.1186/1471-2431-9-5.

多重聚合酶链反应可快速准确诊断疑似败血症的新生儿和儿童的血流感染。

Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis.

机构信息

Unit of Microbiology, Children's Hospital and Research Institute Bambino Gesù, Rome, Italy.

出版信息

J Clin Microbiol. 2011 Jun;49(6):2252-8. doi: 10.1128/JCM.02460-10. Epub 2011 Apr 6.

DOI:10.1128/JCM.02460-10
PMID:21471340
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3122766/
Abstract

Sepsis is a major health problem in newborns and children. Early detection of pathogens allows initiation of appropriate antimicrobial therapy that strongly correlates with positive outcomes. Multiplex PCR has the potential to rapidly identify bloodstream infections, compensating for the loss of blood culture sensitivity. In an Italian pediatric hospital, multiplex PCR (the LightCycler SeptiFast test) was compared to routine blood culture with 1,673 samples obtained from 803 children with suspected sepsis; clinical and laboratory information was used to determine the patient infection status. Excluding results attributable to contaminants, SeptiFast showed a sensitivity of 85.0% (95% confidence interval [CI] = 78.7 to 89.7%) and a specificity of 93.5% (95% CI = 92.1 to 94.7%) compared to blood culture. The rate of positive results was significantly higher with SeptiFast (14.6%) than blood culture (10.3%) (P < 0.0001), and the overall positivity rate was 16.1% when the results of both tests were combined. Staphylococcus aureus (11.6%), coagulase-negative staphylococci (CoNS) (29.6%), Pseudomonas aeruginosa (16.5%), and Klebsiella spp. (10.1%) were the most frequently detected. SeptiFast identified 97 additional isolates that blood culture failed to detect (24.7% P. aeruginosa, 23.7% CoNS, 14.4% Klebsiella spp., 14.4% Candida spp.). Among specimens taken from patients receiving antibiotic therapy, we also observed a significantly higher rate of positivity of SeptiFast than blood culture (14.1% versus 6.5%, respectively; P < 0.0001). On the contrary, contaminants were significantly more frequent among blood cultures than SeptiFast (n = 97 [5.8%] versus n = 26 [1.6%]), respectively; P < 0.0001). SeptiFast served as a highly valuable adjunct to conventional blood culture in children, adding diagnostic value and shortening the time to result (TTR) to 6 h.

摘要

败血症是新生儿和儿童的一个主要健康问题。早期发现病原体可以启动适当的抗菌治疗,这与积极的结果密切相关。多重 PCR 具有快速识别血流感染的潜力,可以弥补血培养敏感性的损失。在意大利的一家儿科医院,将多重 PCR(LightCycler SeptiFast 检测)与 1673 份来自 803 名疑似败血症儿童的常规血培养进行了比较;临床和实验室信息用于确定患者的感染状况。排除因污染而产生的结果,与血培养相比,SeptiFast 的灵敏度为 85.0%(95%置信区间 [CI] = 78.7 至 89.7%),特异性为 93.5%(95%CI = 92.1 至 94.7%)。SeptiFast 的阳性结果率(14.6%)明显高于血培养(10.3%)(P<0.0001),当两种检测结果结合时,总体阳性率为 16.1%。金黄色葡萄球菌(11.6%)、凝固酶阴性葡萄球菌(CoNS)(29.6%)、铜绿假单胞菌(16.5%)和肺炎克雷伯菌(10.1%)是最常检测到的病原体。SeptiFast 还鉴定了血培养未能检测到的 97 株额外分离株(24.7%铜绿假单胞菌、23.7% CoNS、14.4%肺炎克雷伯菌、14.4%假丝酵母菌属)。在接受抗生素治疗的患者标本中,我们还观察到 SeptiFast 的阳性率明显高于血培养(分别为 14.1%和 6.5%;P<0.0001)。相反,与 SeptiFast 相比,血培养中污染的频率明显更高(分别为 97 例[5.8%]和 26 例[1.6%];P<0.0001)。在儿童中, SeptiFast 是常规血培养的一个非常有价值的辅助手段,增加了诊断价值,并将检测结果的时间(TTR)缩短至 6 小时。