Risk factors associated with mortality and pathogen characteristics of bloodstream infection-induced severe sepsis in the pediatric intensive care unit: a retrospective cohort study.
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引用次数: 0
Abstract
Background: Bloodstream infection (BSI)-induced severe sepsis is a common cause of mortality, frequently resulting in septic shock and multiple organ dysfunction syndrome (MODS). This study aimed to analyze mortality risk factors and summarize pathogen characteristics associated with BSI-induced severe sepsis in the pediatric intensive care unit (PICU).
Methods: This retrospective study was conducted at a tertiary pediatric hospital between January 2015 and December 2023, encompassing children with BSI-induced severe sepsis in the PICU. Clinical characteristics, laboratory parameters, pathogen characteristics, and drug resistance profiles of the patients were collected. Clinical and laboratory indicators along with pathogen characteristics were summarized. Logistic regression analysis was employed to identify independent risk factors associated with 28-day mortality.
Results: A total of 192 patients with bloodstream infection (BSI)-induced severe sepsis were identified, with a 28-day in-hospital mortality rate of 36.98% (71/192). The incidence of septic shock (42.1% vs. 69%, P < 0.001) and AKI (14% vs. 31%, P = 0.005) was significantly lower in the survival group compared to the non-survival group. In multivariate analysis, independent risk factors for 28-day mortality were the pediatric sequential organ failure assessment (pSOFA) score (OR 1.176; 95% CI: 1.046-1.321, p = 0.007) and the P/F value (OR 0.994; 95% CI: 0.991-0.997, P < 0.001). Double organism growth was detected in 8 cultures, and a total of 200 pathogenic bacteria were isolated from all blood cultures. Of these, 110 strains (55.0%) were Gram-negative bacteria, 88 strains (44.0%) were gram-positive bacteria, and 2 strains (1.0%) were Candida albicans. The most commonly isolated pathogens were Staphylococcus aureus, Coagulase-negative Staphylococcus, and Escherichia coli. The detection rate of carbapenem resistance (CR) in Acinetobacter baumannii (66.7%) was higher than that in Pseudomonas aeruginosa (15.4%). The detection rates of extended-spectrum cephalosporin resistance (ECR) and fluoroquinolone resistance (FQR) in Escherichia coli (E. coli) were higher than those in Klebsiella pneumoniae.
Conclusion: In the PICU, higher mortality was observed in children with BSI-induced severe sepsis who presented with elevated pSOFA scores and low P/F values. Acinetobacter baumannii exhibited the highest levels of CR and FQR, while Escherichia coli demonstrated the highest level of ECR.
背景:血流感染(BSI)引起的严重脓毒症是一种常见的死亡原因,经常导致感染性休克和多器官功能障碍综合征(MODS)。本研究旨在分析儿童重症监护病房(PICU) bsi致严重脓毒症的死亡危险因素,并总结与之相关的病原体特征。方法:本回顾性研究于2015年1月至2023年12月在一家三级儿科医院进行,纳入PICU中bsi诱发的严重脓毒症患儿。收集患者的临床特征、实验室参数、病原菌特征及耐药情况。总结临床、实验室指标及病原菌特点。采用Logistic回归分析确定与28天死亡率相关的独立危险因素。结果:共发现192例血流感染(BSI)所致严重脓毒症患者,住院28天死亡率为36.98%(71/192)。生存组脓毒性休克发生率(42.1% vs. 69%, P < 0.001)和AKI发生率(14% vs. 31%, P = 0.005)显著低于非生存组。在多因素分析中,28天死亡率的独立危险因素是儿童序事性器官衰竭评估(pSOFA)评分(OR 1.176;95% CI: 1.046-1.321, p = 0.007), p /F值(OR 0.994;95% ci: 0.991-0.997, p 0.001)。8个培养物检测到双菌生长,所有血培养物共分离病原菌200株。其中革兰氏阴性菌110株(55.0%),革兰氏阳性菌88株(44.0%),白色念珠菌2株(1.0%)。最常见的分离病原体是金黄色葡萄球菌、凝固酶阴性葡萄球菌和大肠杆菌。鲍曼不动杆菌碳青霉烯类耐药检出率(66.7%)高于铜绿假单胞菌(15.4%)。大肠杆菌的广谱头孢菌素耐药(ECR)和氟喹诺酮类药物耐药(FQR)检出率高于肺炎克雷伯菌。结论:在PICU中,以pSOFA评分升高和P/F值较低为表现的bsi诱导的严重脓毒症患儿死亡率较高。鲍曼不动杆菌的CR和FQR最高,大肠杆菌的ECR最高。
期刊介绍:
Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.