Department of Epidemiology and Public Health, University of Maryland, Baltimore.
RAND Corporation, Santa Monica, California.
JAMA Intern Med. 2020 May 1;180(5):707-716. doi: 10.1001/jamainternmed.2020.0183.
The Early Management Bundle for Severe Sepsis/Septic Shock (SEP-1) is a quality metric based on a care bundle for early sepsis management. Published evidence on the association of SEP-1 with mortality is mixed and largely excludes cases of hospital-onset sepsis.
To assess the association of the SEP-1 bundle with mortality and organ dysfunction in cohorts with hospital-onset or community-onset sepsis.
DESIGN, SETTING, AND PARTICIPANTS: This retrospective cohort study used data from 4 University of California hospitals from October 1, 2014, to October 1, 2017. Adult inpatients with a diagnosis consistent with sepsis or disseminated infection and laboratory or vital signs meeting the Sepsis-3 (Third International Consensus Definitions for Sepsis and Septic Shock) criteria were divided into community-onset sepsis and hospital-onset sepsis cohorts based on whether time 0 of sepsis occurred after arrival in the emergency department or an inpatient area. Data were analyzed from April to October 2019. Additional analyses were performed from December 2019 to January 2020.
Administration of SEP-1 and 4 individual bundle components (serum lactate level testing, blood culture, broad-spectrum intravenous antibiotic treatment, and intravenous fluid treatment).
The primary outcome was in-hospital mortality. The secondary outcome was days requiring vasopressor support, measured as vasopressor days.
Among the 6404 patient encounters identified (3535 men [55.2%]; mean [SD] age, 64.0 [18.2] years), 2296 patients (35.9%) had hospital-onset sepsis. Among 4108 patients (64.1%) with community-onset sepsis, serum lactate level testing within 3 hours of time 0 was associated with reduced mortality (absolute difference, -7.61%; 95% CI, -14.70% to -0.54%). Blood culture (absolute difference, -1.10 days; 95% CI, -1.85 to -0.34 days) and broad-spectrum intravenous antibiotic treatment (absolute difference, -0.62 days; 95% CI, -1.02 to -0.22 days) were associated with fewer vasopressor days. Among patients with hospital-onset sepsis, broad-spectrum intravenous antibiotic treatment was the only bundle component significantly associated with any improved outcome (mortality difference, -5.20%; 95% CI, -9.84% to -0.56%). Care that was adherent to the complete SEP-1 bundle was associated with increased vasopressor days in patients with community-onset sepsis (absolute difference, 0.31 days; 95% CI, 0.11-0.51 days) but was not significantly associated with reduced mortality in either cohort (absolute difference, -0.07%; 95% CI, -3.02% to 2.88% in community-onset; absolute difference, -0.42%; 95% CI, -6.77% to 5.93% in hospital-onset).
SEP-1-adherent care was not associated with improved outcomes of sepsis. Although multiple components of SEP-1 were associated with reduced mortality or decreased days of vasopressor therapy for patients who presented with sepsis in the emergency department, only broad-spectrum intravenous antibiotic treatment was associated with reduced mortality when time 0 occurred in an inpatient unit. Current sepsis quality metrics may need refinement.
早期管理严重脓毒症/脓毒症休克(SEP-1)包是基于早期脓毒症管理护理包的质量指标。关于 SEP-1 与死亡率之间的关联的已发表证据参差不齐,并且在很大程度上排除了医院获得性脓毒症的病例。
评估 SEP-1 捆绑包与医院获得性或社区获得性脓毒症患者的死亡率和器官功能障碍之间的关联。
设计、地点和参与者:本回顾性队列研究使用了 2014 年 10 月 1 日至 2017 年 10 月 1 日来自加利福尼亚大学 4 家医院的数据。符合脓毒症或播散性感染诊断标准且实验室或生命体征符合 Sepsis-3(第三代国际脓毒症和脓毒症休克定义共识)标准的成年住院患者根据时间 0 是否在急诊科或住院区发生来分为社区获得性脓毒症和医院获得性脓毒症队列。数据于 2019 年 4 月至 10 月进行分析。2019 年 12 月至 2020 年 1 月进行了额外的分析。
SEP-1 和 4 个单独捆绑包组件(血清乳酸水平检测、血液培养、广谱静脉内抗生素治疗和静脉补液治疗)的使用。
主要结果是住院死亡率。次要结果是需要血管加压支持的天数,以血管加压天数衡量。
在确定的 6404 例患者就诊中(3535 名男性[55.2%];平均[标准差]年龄,64.0[18.2]岁),2296 例(35.9%)患有医院获得性脓毒症。在 4108 例(64.1%)社区获得性脓毒症患者中,时间 0 后 3 小时内进行血清乳酸水平检测与死亡率降低相关(绝对差异,-7.61%;95%CI,-14.70%至-0.54%)。血液培养(绝对差异,-1.10 天;95%CI,-1.85 天至-0.34 天)和广谱静脉内抗生素治疗(绝对差异,-0.62 天;95%CI,-1.02 天至-0.22 天)与较少的血管加压天数相关。在医院获得性脓毒症患者中,广谱静脉内抗生素治疗是唯一与任何改善结果显著相关的捆绑包组件(死亡率差异,-5.20%;95%CI,-9.84%至-0.56%)。在社区获得性脓毒症患者中,符合完整 SEP-1 捆绑包的护理与血管加压天数的增加相关(绝对差异,0.31 天;95%CI,0.11-0.51 天),但与两个队列的死亡率降低均无显著相关性(绝对差异,-0.07%;95%CI,-3.02%至 2.88%;绝对差异,-0.42%;95%CI,-6.77%至 5.93%)。
SEP-1 一致的护理与脓毒症的改善结果无关。尽管 SEP-1 的多个组件与急诊科出现脓毒症的患者的死亡率降低或血管加压治疗天数减少相关,但只有当时间 0 发生在住院病房时,广谱静脉内抗生素治疗才与死亡率降低相关。目前的脓毒症质量指标可能需要改进。