Jesseca A. Paulsen, Karen M. Wang, Isabella M. Masler, Jessica Hicks, S. Green, Jeremy M. Loberger
{"title":"Beyond Vital Signs: Pediatric Sepsis Screening that Includes Organ Failure Assessment Detects Patients with Worse Outcomes","authors":"Jesseca A. Paulsen, Karen M. Wang, Isabella M. Masler, Jessica Hicks, S. Green, Jeremy M. Loberger","doi":"10.1055/s-0042-1753536","DOIUrl":null,"url":null,"abstract":"Pediatric sepsis screening is recommended. The 2005 Goldstein criteria, the basis of our institutional sepsis screening tool (ISST), correlate poorly with clinically diagnosed sepsis. The study objective was to retrospectively evaluate the ISST sensitivity compared with the Pediatric Sequential Organ Failure Assessment (pSOFA). This was a single-center retrospective cohort study. The primary outcome was pSOFA score and ISST sensitivity for severe sepsis. Secondary outcomes included clinical outcome measures. In this severe sepsis cohort (N = 491), pSOFA and ISST sensitivity were 57.6 and 61.1%, respectively. In regression analysis for a positive pSOFA, positive blood culture (odds ratio [OR] 2.2, 95% confidence interval [CI] 1.1–4.3, p = 0.025), older age (OR 1.006, 95% CI 1.003–1.009, p < 0.001), and pulmonary infectious source (OR 3.3, 95% CI 1.6–6.5, p = 0.001) demonstrated independent association. In regression analysis for a positive ISST, older age (OR 1.003, 95% CI 1–1.006, p = 0.031) and intra-abdominal infectious source (OR 0.3, 95% CI 0.1–0.8, p = 0.014) demonstrated independent association. A negative ISST was associated with higher intensive care unit (ICU) admission prevalence (p = 0.01) and fewer ICU-free days (p = 0.018). A positive pSOFA score was associated with higher ICU admission prevalence, vasopressor requirement, and vasopressor days as well as fewer ICU, hospital, and mechanical ventilation-free days (all p < 0.001). Exploratory analysis combining the ISST and pSOFA into a hybrid screen demonstrated superior sensitivity (84.3%) and outcome discrimination. The pSOFA demonstrated noninferior sensitivity to a Goldstein-based institutional sepsis screening model. Further, pSOFA was a better discriminator of poor clinical outcomes. An exploratory hybrid screening model shows superior performance but will require prospective study.","PeriodicalId":44426,"journal":{"name":"Journal of Pediatric Intensive Care","volume":"13 1","pages":""},"PeriodicalIF":0.5000,"publicationDate":"2022-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pediatric Intensive Care","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1055/s-0042-1753536","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PEDIATRICS","Score":null,"Total":0}
引用次数: 0
Abstract
Pediatric sepsis screening is recommended. The 2005 Goldstein criteria, the basis of our institutional sepsis screening tool (ISST), correlate poorly with clinically diagnosed sepsis. The study objective was to retrospectively evaluate the ISST sensitivity compared with the Pediatric Sequential Organ Failure Assessment (pSOFA). This was a single-center retrospective cohort study. The primary outcome was pSOFA score and ISST sensitivity for severe sepsis. Secondary outcomes included clinical outcome measures. In this severe sepsis cohort (N = 491), pSOFA and ISST sensitivity were 57.6 and 61.1%, respectively. In regression analysis for a positive pSOFA, positive blood culture (odds ratio [OR] 2.2, 95% confidence interval [CI] 1.1–4.3, p = 0.025), older age (OR 1.006, 95% CI 1.003–1.009, p < 0.001), and pulmonary infectious source (OR 3.3, 95% CI 1.6–6.5, p = 0.001) demonstrated independent association. In regression analysis for a positive ISST, older age (OR 1.003, 95% CI 1–1.006, p = 0.031) and intra-abdominal infectious source (OR 0.3, 95% CI 0.1–0.8, p = 0.014) demonstrated independent association. A negative ISST was associated with higher intensive care unit (ICU) admission prevalence (p = 0.01) and fewer ICU-free days (p = 0.018). A positive pSOFA score was associated with higher ICU admission prevalence, vasopressor requirement, and vasopressor days as well as fewer ICU, hospital, and mechanical ventilation-free days (all p < 0.001). Exploratory analysis combining the ISST and pSOFA into a hybrid screen demonstrated superior sensitivity (84.3%) and outcome discrimination. The pSOFA demonstrated noninferior sensitivity to a Goldstein-based institutional sepsis screening model. Further, pSOFA was a better discriminator of poor clinical outcomes. An exploratory hybrid screening model shows superior performance but will require prospective study.
建议进行儿童败血症筛查。2005年Goldstein标准,我们机构脓毒症筛查工具(ISST)的基础,与临床诊断的脓毒症相关性很差。研究目的是回顾性评价ISST与儿童序贯器官衰竭评估(pSOFA)的敏感性。这是一项单中心回顾性队列研究。主要终点是pSOFA评分和ISST对严重脓毒症的敏感性。次要结果包括临床结果测量。在这个严重脓毒症队列中(N = 491), pSOFA和ISST的敏感性分别为57.6%和61.1%。在pSOFA阳性的回归分析中,血培养阳性(比值比[OR] 2.2, 95%可信区间[CI] 1.1-4.3, p = 0.025)、年龄(比值比[OR] 1.006, 95% CI 1.003-1.009, p < 0.001)和肺部传染源(比值比[OR] 3.3, 95% CI 1.6-6.5, p = 0.001)显示出独立的相关性。在ISST阳性的回归分析中,年龄(OR 1.003, 95% CI 1-1.006, p = 0.031)和腹腔内传染源(OR 0.3, 95% CI 0.1-0.8, p = 0.014)表现出独立的相关性。ISST阴性与较高的重症监护病房(ICU)入院率(p = 0.01)和较少的无ICU天数(p = 0.018)相关。pSOFA评分阳性与较高的ICU入院率、血管加压素需求、血管加压素天数以及较少的ICU、住院和无机械通气天数相关(均p < 0.001)。探索性分析将ISST和pSOFA结合到一个混合筛选中,显示出更高的灵敏度(84.3%)和结果辨别能力。pSOFA对基于goldstein的机构脓毒症筛查模型表现出良好的敏感性。此外,pSOFA是较好的鉴别不良临床结果的指标。探索性混合筛选模型表现出优越的性能,但需要前瞻性研究。