Dent Arlene, Toltzis Philip
Divisions of aInfectious Disease, Department of Pediatrics, Rainbow Babies and Children's Hospital, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106, USA.
Curr Opin Infect Dis. 2003 Jun;16(3):279-83. doi: 10.1097/00001432-200306000-00016.
The critically ill neonate is particularly prone to life threatening bacterial infections compared with other patient populations. Current patterns of neonatal sepsis caused by Gram-negative bacilli are reviewed to enable the clinician to better anticipate and effectively respond to neonatal infection by these serious pathogens.
With increasing use of intrapartum antibiotics for prophylaxis against early-onset group B streptococcal infection, there is growing concern that the incidence of neonatal sepsis by Gram-negative pathogens may rise. Although several surveys indicate no such increase to date, studies in selected neonatal intensive care unit populations have suggested a recent elevation in newborn infection caused by Escherichia coli and other bacillary pathogens. Most recent investigations reveal growing antibiotic resistance in those Gram-negative bacilli causing neonatal infection. Modern molecular genotyping methods have been applied to Gram-negative bacilli in the neonatal intensive care unit in order to understand their epidemiology in greater detail. In most instances these techniques have been used to identify the sources and prevalence of an outbreak strain, and to devise rational interventions to control the epidemic. Studies utilizing molecular genotyping during non-outbreak periods indicate that Gram-negative bacilli, even those expressing antibiotic resistance, may be acquired very early in the intensive care unit course, and that different clones are introduced and lost in the infants' indigenous flora throughout their stay. These studies further indicate that cross-transmission of bacillary pathogens occurs regularly even in the absence of a recognized epidemic.
Gram-negative bacilli are prominent causes of infection in the neonatal intensive care unit. Their incidence, antibiotic susceptibility pattern, and modes of acquisition continue to evolve in the modern intensive care unit setting.
与其他患者群体相比,危重新生儿尤其容易发生危及生命的细菌感染。本文综述了由革兰氏阴性杆菌引起的新生儿败血症的当前模式,以使临床医生能够更好地预测并有效应对这些严重病原体引起的新生儿感染。
随着产时抗生素越来越多地用于预防早发型B族链球菌感染,人们越来越担心革兰氏阴性病原体引起的新生儿败血症发病率可能会上升。尽管几项调查表明迄今为止尚无此类增加,但对选定新生儿重症监护病房人群的研究表明,最近大肠杆菌和其他杆菌病原体引起的新生儿感染有所增加。最新调查显示,那些引起新生儿感染的革兰氏阴性杆菌的抗生素耐药性不断增强。现代分子基因分型方法已应用于新生儿重症监护病房的革兰氏阴性杆菌,以便更详细地了解其流行病学。在大多数情况下,这些技术已用于确定暴发菌株的来源和流行情况,并制定合理的干预措施来控制疫情。在非暴发期间利用分子基因分型进行的研究表明,革兰氏阴性杆菌,即使是那些表现出抗生素耐药性的杆菌,也可能在重症监护病房病程的早期就被感染,并且在婴儿住院期间,不同的克隆会在其原生菌群中引入和消失。这些研究进一步表明,即使在没有公认疫情的情况下,杆菌病原体的交叉传播也经常发生。
革兰氏阴性杆菌是新生儿重症监护病房感染的主要原因。在现代重症监护病房环境中,它们的发病率、抗生素敏感性模式和感染方式不断演变。