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首页> 外文期刊>Infection and Drug Resistance >Rapid diagnosis of neonatal sepsis by PCR for detection of 16S rRNA gene, while blood culture and PCR results were similar in E.coli -predominant EOS cases
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Rapid diagnosis of neonatal sepsis by PCR for detection of 16S rRNA gene, while blood culture and PCR results were similar in E.coli -predominant EOS cases

机译:PCR快速诊断新生儿败血症可检测16S rRNA基因,而以大肠杆菌为主的EOS病例的血液培养和PCR结果相似

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Purpose: To determine the bacteriological pattern and antibiotic susceptibility of bacterial isolates causing neonatal sepsis in Qena University Hospitals and compare polymerase chain reaction (PCR) and blood culture results in a trial for rapid diagnosis. Patients and methods: Blood samples from 75 clinically suspected cases of neonatal sepsis were subjected to identification of bacteria and determination of their antibiotic sensitivity through blood culture, and rapid detection of 16S rRNA and the uidA gene (to confirm the presence of E. coli ) by PCR from extracted bacterial DNA. Results: Most patients were preterm (64%) and low birth weight (LBW) (68%). In total, 42.7% presented with early onset sepsis (EOS). LBW was significantly associated with EOS ( P -value=0.03). Although the blood culture and PCR results were similar in EOS, the PCR results were significantly higher than those of blood culture in detecting bacteria (85.3% vs 68%, respectively, P -value=0.001). Blood culture showed 100% specificity. The most common pathogen was E. coli (86.2%) in EOS and Staphylococcus spp . (45.5%) in late-onset sepsis (LOS) ( P -value=0.001 and 0.02, respectively). The most effective antibiotics against Gram-negative bacteria were ofloxacin, ciprofloxacin, imipenem, and amikacin, while vancomycin, oxacillin, and imipenem were the most effective antibiotics against Gram-positive bacteria. Conclusion: EOS was mainly caused by E. coli , while LOS was mainly caused by Staphylococcus spp . The 16S rRNA PCR showed higher sensitivity with rapid and accurate diagnosis. Blood culture is the most suitable method for antimicrobial sensitivity testing.
机译:目的:确定Qena大学医院引起新生儿败血症的细菌分离株的细菌学模式和抗生素敏感性,并比较聚合酶链反应(PCR)和血液培养结果,以进行快速诊断。患者和方法:对75例临床上疑似新生儿败血症患者的血样进行细菌鉴定,并通过血液培养确定其抗生素敏感性,并快速检测16S rRNA和uidA基因(以确认大肠杆菌的存在)通过PCR从提取的细菌DNA中提取。结果:大多数患者为早产(64%)和低出生体重(LBW)(68%)。总体上,有42.7%的患者表现为早发性败血症(EOS)。 LBW与EOS显着相关(P值= 0.03)。尽管在EOS中血液培养和PCR结果相似,但在检测细菌方面,PCR结果显着高于血液培养(分别为85.3%和68%,P值= 0.001)。血液培养显示出100%的特异性。最常见的病原体是EOS和葡萄球菌属中的大肠杆菌(86.2%)。 (45.5%)在晚期发作性败血症(LOS)中(P值分别为0.001和0.02)。对革兰氏阴性菌最有效的抗生素是氧氟沙星,环丙沙星,亚胺培南和阿米卡星,而万古霉素,奥沙西林和亚胺培南是对革兰氏阳性菌最有效的抗生素。结论:EOS主要由大肠杆菌引起,而LOS主要由葡萄球菌引起。 16S rRNA PCR表现出更高的灵敏度,并具有快速准确的诊断能力。血液培养是进行抗生素敏感性测试的最合适方法。

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