Application of New Pediatric Sepsis Definition to a Multicenter Observational Cohort of Previously Enrolled Severe Sepsis Patients Defined by SIRS Plus Organ Dysfunction.

IF 3 3区 医学 Q2 CRITICAL CARE MEDICINE
Kate F Kernan, Mohammed Shaik, Christopher M Horvat, Dana Y Fuhrman, Zachary Aldewereld, Robert A Berg, David Wessel, Murray M Pollack, Kathleen Meert, Mark W Hall, Christopher J L Newth, Tom Shanley, Rick E Harrison, Joseph A Carcillo, Rajesh K Aneja
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Abstract

IntroductionIn 2024, a Society of Critical Care Medicine task force updated the pediatric sepsis definition from the presence of suspected or confirmed infection, and a systemic inflammatory response (SIRS) with organ dysfunction, to a novel definition. Our objective is to identify how many patients previously identified as having severe sepsis would continue to meet the new definition.Materials and methodsWe performed a secondary analysis of the Phenotyping Sepsis-Induced Multiple Organ Failure cohort of 401 children with suspected or confirmed infection, two of four SIRS criteria and organ dysfunction enrolled between 2015-2017. We calculated a modified Phoenix Sepsis Criteria Score (mPSC) for participants and compared those with mPSC of greater than or equal to 2 or less than 2 according to the 2024 definition.ResultsOf 401 children, 132 (33%) did not meet mPSC definitions. While children meeting mPSC had more organ dysfunction, the total mortality did not differ. One in 4 children requiring extracorporeal membrane oxygenation and 1 in 4 mortalities did not meet the mPSC definition. In logistic regression models, in the complete cohort, hematologic (OR 4.4, 95% CI: 1.8-10.2, P-value = .001), central nervous system (OR 2.3, 95% CI: 1.0-5.1, P-value = .046) and renal failure (OR: 3.2, 95% CI:1.2-7.9, P-value = .017) predicted mortality; in the mPSC subgroup pulmonary (OR: 3.6, 95% CI:1.3-13.3, P-value = .030) and hematologic failure (OR 5.6, 95% CI: 2.2-14.5, P-value = .0003) were significant predictors. In the mPSC excluded subgroup, only renal failure predicted mortality (OR 9.6, 95% CI 1.1-73.0, P-value = .028).ConclusionsFurther study of the impact of the 2024 data-driven organ dysfunction definition on pediatric sepsis research, patient safety, and clinical benchmarking efforts is warranted.

新的儿童脓毒症定义在一项多中心观察队列中的应用,该多中心观察队列由SIRS加器官功能障碍定义的先前入组的严重脓毒症患者。
2024年,美国重症医学学会(Society of Critical Care Medicine)的一个工作组更新了儿科败血症的定义,从疑似或确诊感染,以及伴有器官功能障碍的全身炎症反应(SIRS),到一个新的定义。我们的目标是确定有多少以前被确定为严重败血症的患者将继续符合新的定义。材料和方法我们对2015-2017年间纳入的401名疑似或确诊感染、4项SIRS标准中的2项和器官功能障碍的脓毒症诱导的多器官衰竭队列进行了二次分析。我们为参与者计算了修改后的Phoenix脓毒症标准评分(mPSC),并根据2024年的定义将mPSC大于等于2或小于2的患者进行比较。结果401例患儿中,132例(33%)不符合mPSC定义。虽然接受mPSC的儿童有更多的器官功能障碍,但总死亡率没有差异。四分之一需要体外膜氧合的儿童和四分之一的死亡率不符合mPSC的定义。在logistic回归模型中,在完整队列中,血液学(OR 4.4, 95% CI: 1.8-10.2, p值= 0.001)、中枢神经系统(OR 2.3, 95% CI: 1.0-5.1, p值= 0.046)和肾衰竭(OR: 3.2, 95% CI:1.2-7.9, p值= 0.017)预测死亡率;在mPSC亚组中,肺衰竭(OR: 3.6, 95% CI:1.3-13.3, p值= 0.030)和血液学衰竭(OR 5.6, 95% CI: 2.2-14.5, p值= 0.0003)是显著的预测因子。在排除mPSC的亚组中,只有肾功能衰竭预测死亡率(OR 9.6, 95% CI 1.1-73.0, p值= 0.028)。结论2024年数据驱动的器官功能障碍定义对儿童败血症研究、患者安全性和临床基准工作的影响值得进一步研究。
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来源期刊
Journal of Intensive Care Medicine
Journal of Intensive Care Medicine CRITICAL CARE MEDICINE-
CiteScore
7.60
自引率
3.20%
发文量
107
期刊介绍: Journal of Intensive Care Medicine (JIC) is a peer-reviewed bi-monthly journal offering medical and surgical clinicians in adult and pediatric intensive care state-of-the-art, broad-based analytic reviews and updates, original articles, reports of large clinical series, techniques and procedures, topic-specific electronic resources, book reviews, and editorials on all aspects of intensive/critical/coronary care.
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