分析由无乳链球菌和大肠杆菌引起的新生儿败血症的差异。

IF 0.7 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Clinical laboratory Pub Date : 2024-07-01 DOI:10.7754/Clin.Lab.2024.231233
Chengwen Que, Huiyu Chen, Huahong Qiu, Hui Zhong
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引用次数: 0

摘要

背景:无乳链球菌(GBS)和大肠杆菌(E. coli)是新生儿败血症的主要致病菌。因此,我们对这两种细菌的临床特征、非特异性指标和药物敏感性进行了研究:方法:选取 2012 年 5 月至 2023 年 7 月期间我院新生儿科收治的分别由 GBS 和大肠杆菌感染引起的败血症患儿 81 例和 80 例,分析两组患儿的临床特征。回顾性分析非特异性指标和药敏试验结果:结果:GBS组的出生体重、呼吸急促、呻吟、心动过速或过缓,以及肺炎、呼吸衰竭、化脓性脑膜炎等并发症的发生率均高于大肠杆菌组。患儿均为早产儿,母亲胎膜早破。黄疸、腹胀、不典型临床表现和坏死性小肠结肠炎并发症的发生率低于大肠杆菌组,差异有统计学意义(P < 0.05)。GBS 组的 WBC、NE#、NE#/LY#、hs-CRP 和 PCT 均高于大肠杆菌组,而 MPV、D-D 和 FDP 水平则低于大肠杆菌组,差异均有统计学意义(P<0.05)。这些差异均有统计学意义(P < 0.05)。81 珠 GBS 对四环素(95%)、红霉素(48.8%)和克林霉素(40%)的耐药率较高,没有出现对万古霉素、利奈唑胺、青霉素或氨苄西林耐药的菌株,而 80 株大肠杆菌对青霉素的耐药率较高。大肠杆菌对青霉素和第三代头孢菌素的耐药率较高,其中对氨苄西林(68.30%)、三甲氧苄青霉素/磺胺甲噁唑(53.6%)和环丙沙星(42.90%)的耐药率较高。对碳青霉烯类和氨基糖苷类药物的耐药率极低:结论:GBS 和大肠杆菌新生儿败血症都有特定的临床特征,尤其是在临床表现、并发症、非特异性指标和耐药性方面。早期识别对临床诊断和治疗非常重要。
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Analysis of Differences in Neonatal Sepsis Caused by Streptococcus Agalactiae and Escherichia Coli.

Background: Streptococcus agalactiae (GBS) and Escherichia coli (E. coli) are the main pathogenic bacteria in neonatal sepsis. Therefore, the clinical characteristics, nonspecific indicators, and drug susceptibilities of these two bacteria were studied.

Methods: In total, 81 and 80 children with sepsis caused by GBS and E. coli infection, respectively, admitted to the neonatal department of our hospital between May 2012 and July 2023, were selected, and the clinical characteris-tics of the two groups were analyzed. Nonspecific indicators and drug sensitivity test results were analyzed retrospectively.

Results: Birth weight, tachypnea, groan, tachycardia or bradycardia, and the incidence of complications, such as pneumonia, respiratory failure, and purulent meningitis, were higher in the GBS group than in the E. coli group. The children were born prematurely, and the mother had a premature rupture of membranes. The incidence of jaundice, abdominal distension, atypical clinical manifestations, and complications of necrotizing enterocolitis was lower than of the E. coli group, and the differences were statistically significant (p < 0.05). The WBC, NE#, NE#/LY#, hs-CRP, and PCT of the GBS group were higher than those of the E. coli group, whereas the MPV, D-D, and FDP levels were lower than those in the E. coli group. The differences were all statistically significant (p < 0.05). The 81-bead GBS had high resistance rates against tetracycline (95%), erythromycin (48.8%), and clindamycin (40%), and no strains resistant to vancomycin, linezolid, penicillin, or ampicillin appeared, whereas 80 strains of E. coli were more resistant to penicillin and third-generation cephalosporins, with the higher resistance rates to ampicillin (68.30%), trimethoprim/sulfamethoxazole (53.6%), and ciprofloxacin (42.90%). Resistance rates to carbapenems and aminoglycosides were extremely low.

Conclusions: Both GBS and E. coli neonatal sepsis have specific clinical characteristics, especially in terms of clinical manifestations, complications, non-specific indicators, and drug resistance. Early identification is important for clinical diagnosis and treatment.

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来源期刊
Clinical laboratory
Clinical laboratory 医学-医学实验技术
CiteScore
1.50
自引率
0.00%
发文量
494
审稿时长
3 months
期刊介绍: Clinical Laboratory is an international fully peer-reviewed journal covering all aspects of laboratory medicine and transfusion medicine. In addition to transfusion medicine topics Clinical Laboratory represents submissions concerning tissue transplantation and hematopoietic, cellular and gene therapies. The journal publishes original articles, review articles, posters, short reports, case studies and letters to the editor dealing with 1) the scientific background, implementation and diagnostic significance of laboratory methods employed in hospitals, blood banks and physicians'' offices and with 2) scientific, administrative and clinical aspects of transfusion medicine and 3) in addition to transfusion medicine topics Clinical Laboratory represents submissions concerning tissue transplantation and hematopoietic, cellular and gene therapies.
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