福州市2012 - 2021年新生儿侵袭性B族链球菌病流行病学及耐药性回顾性研究

IF 0.7 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Clinical laboratory Pub Date : 2025-01-01 DOI:10.7754/Clin.Lab.2024.240742
Hui Zhong, Huiyu Chen, Huahong Qiu, Zhihui Wu, Chen Liu, Chengwen Que
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引用次数: 0

摘要

背景:B群链球菌(GBS)引起新生儿侵袭性疾病,主要是败血症和脑膜炎。了解GBS侵袭性感染的临床特征、实验室检查和抗生素耐药模式,为预防和治疗GBS感染提供可靠的流行病学数据。方法:分析福建省妇幼保健院2012年1月至2021年12月收治的86例新生儿侵袭性疾病(早发性疾病45例,晚发性疾病41例)的临床特点和实验室检查结果。结果:新生儿侵袭性GBS感染10年呈下降趋势。呼吸道症状是EOD的首要临床表现(71.1%),包括呻吟、呼吸急促和发绀,而LOD更常表现为发烧(78%)。肺炎是最常见的并发症(57.0%)。EOD组肺炎35例(77.8%),呼吸衰竭18例(40.0%),均多于LOD组。与LOD组相比,EOD组新生儿更易发生心肌损伤、脑损伤和代谢性酸中毒。LOD中化脓性脑膜炎(63.4%)和贫血(29.3%)的比例高于EOD。EOD组白细胞计数高于LOD组,而白细胞减少的患者比例(24.4%)低于LOD组(46.3%)。所有GBS菌株均对青霉素、氨苄西林、利奈唑胺、奎努普汀、万古霉素和替加环素敏感。红霉素和克林霉素耐药率分别为82.6%和84.9%。d检验显示iMLSB表型(诱导克林霉素耐药)为48.6%,cMLSB表型(47.3%),l -表型(2.7%)和m -表型(1.4%)也被发现。结论:近年来,新生儿侵袭性GBS感染的病例数有所下降。侵袭性GBS-EOD感染患者发病症状隐匿,应根据临床症状和实验室检查结果及早诊断。GBS菌株对红霉素和克林霉素耐药,不适合在本地区新生儿人群中进行预防性和经验性治疗。
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Epidemiology and Antibiotic Resistance of Neonatal Invasive Group B Streptococcus Disease: a Retrospective Study in Fuzhou, China, 2012 - 2021.

Background: Group B streptococcus (GBS) causes neonatal invasive disease, mainly sepsis and meningitis. Understanding the clinical characteristics, laboratory tests, and antibiotic resistance patterns of GBS invasive infections provides reliable epidemiological data for preventing and treating GBS infections.

Methods: Clinical characteristics and laboratory test results from 86 patients with neonatal invasive disease (45 cases of early-onset disease [EOD] and 41 cases of late-onset disease [LOD]) recruited from Fujian Maternity and Child Health Hospital between January 2012 and December 2021 were analyzed.

Results: The number of neonates with invasive GBS infections declined for 10 years. Respiratory symptoms, the first clinical presentation in EOD, were predominant (71.1%), including groan, tachypnea, and cyanosis, whereas LOD more often presented with fever (78%). Pneumonia was the most common complication (57.0%). There were 35 patients (77.8%) with pneumonia and 18 patients (40.0%) with respiratory failure in the EOD cases, which were more than those in LOD cases. Neonates in the EOD cases were more prone to myocardial damage, cerebral injury, and metabolic acidosis than those in the LOD cases. The proportion of purulent meningitis (63.4%) and anemia (29.3%) in LOD was higher than those in EOD. White blood cell count of the EOD group was higher than that of the LOD group, whereas the proportion of patients with leukopenia was lower in the EOD group (24.4%) than in the LOD group (46.3%). All the GBS strains were susceptible to penicillin, ampicillin, linezolid, quinupristin, vancomycin, or tigecycline. Erythromycin and clindamycin resistance rates were 82.6% and 84.9%, respectively. A D-test revealed 48.6% iMLSB phenotype (inducible clindamycin resistant), and cMLSB phenotype (47.3%), L-phenotypes (2.7%), and M-phenotypes (1.4%) were also found.

Conclusions: The number of cases of neonatal invasive GBS infections has decreased in recent years. Patients with invasive GBS-EOD infections have insidious onset symptoms and should be diagnosed early based on clinical symptoms and laboratory examination results. GBS strains are resistant to erythromycin and clindamycin, which is not suitable for prophylactic and empirical treatment in the neonatal population in this region.

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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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