Muszyńska-Radska Katarzyna, Szwed Krzysztof, Falkowski Adrian, Sadowska-Krawczenko Iwona
Department of Clinical Microbiology and Molecular Biology, Jan Biziel University Hospital No. 2, Ujejskiego 75, 85-168 Bydgoszcz, Poland.
Center for Methodological Support of Scientific Research, Clinic of General and Minimally Invasive Surgery, Jan Biziel University Hospital No. 2, Ujejskiego 75, 85-168 Bydgoszcz, Poland.
J Clin Med. 2024 Dec 24;14(1):5. doi: 10.3390/jcm14010005.
Neonatal sepsis, a severe infection in newborns, remains one of the leading causes of morbidity and mortality among preterm infants. This study aimed to investigate the distribution of pathogens responsible for early-onset sepsis (EOS) and late-onset sepsis (LOS), the annual variability of pathogens responsible for each type of infection, and potential trends in their profiles in preterm infants from a tertiary care neonatal intensive care unit over a ten-year period. We analyzed 177 episodes of confirmed bloodstream infection between 1 January 2014 and 31 December 2023. An episode of confirmed bloodstream infection was defined by the growth of a single potential pathogen in the blood of an infant who met four criteria: showing clinical symptoms of infection, having abnormal hematologic parameters, receiving appropriate antibiotics for less than 5 days, and being born before 37 weeks of gestation. Pathogens were isolated from aseptically collected blood samples, processed within 2 h, incubated using the BACTEC system, and identified by Gram stains and selective media cultures. Pathogen identification was performed using standardized biochemical tests or MALDI-TOF MS. Sepsis was classified as EOS if it occurred within the first 72 h of life and as LOS if it occurred after 72 h. Among the confirmed bloodstream infections, EOS accounted for 31 cases, while LOS accounted for 146 cases. Escherichia coli was identified as the primary pathogen responsible for early-onset sepsis (EOS), while Coagulase-negative Staphylococcus (CoNS) was most commonly associated with late-onset sepsis (LOS). The differences in the prevalence of these bacteria between EOS and LOS were statistically significant. However, no significant differences were found in the distribution of pathogens across different years, nor were there significant trends in their frequency over the study period. Our results demonstrate significant stability in the distribution of pathogens causing sepsis over the ten-year observation period, even during the COVID-19 pandemic. Understanding the temporal distribution of pathogens in neonatal sepsis can help prevent the overuse of antibiotics and support the implementation of screening programs, empiric therapy, and strategies to prevent healthcare-associated infections.
新生儿败血症是新生儿期的一种严重感染,仍是早产儿发病和死亡的主要原因之一。本研究旨在调查早发型败血症(EOS)和晚发型败血症(LOS)的病原体分布、每种感染类型病原体的年度变异性,以及在一家三级护理新生儿重症监护病房的早产儿中,其病原体谱在十年期间的潜在趋势。我们分析了2014年1月1日至2023年12月31日期间177例确诊的血流感染病例。确诊的血流感染病例定义为,在一名符合以下四项标准的婴儿血液中培养出单一潜在病原体:出现感染临床症状、血液学参数异常、接受适当抗生素治疗少于5天、孕周小于37周。病原体从无菌采集的血样中分离出来,在2小时内进行处理,使用BACTEC系统进行培养,并通过革兰氏染色和选择性培养基培养进行鉴定。病原体鉴定采用标准化生化试验或基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)。败血症若发生在出生后72小时内则分类为EOS,若发生在72小时后则分类为LOS。在确诊的血流感染病例中,EOS占31例,而LOS占146例。大肠杆菌被确定为早发型败血症(EOS)的主要病原体,而凝固酶阴性葡萄球菌(CoNS)最常与晚发型败血症(LOS)相关。EOS和LOS之间这些细菌的患病率差异具有统计学意义。然而,不同年份病原体的分布没有显著差异,在研究期间其频率也没有显著趋势。我们的结果表明,在十年观察期内,即使在新冠疫情期间,引起败血症的病原体分布也具有显著稳定性。了解新生儿败血症病原体的时间分布有助于防止抗生素的过度使用,并支持筛查计划、经验性治疗以及预防医疗相关感染策略的实施。