Toward Standardization and High Reliability: Improved Sepsis Screening in Emergency Department Triage Across an Academic Health System

IF 2.3 Q2 HEALTH CARE SCIENCES & SERVICES
Stephen Biederman MD (is Assistant Professor, Division of Hospital Medicine, Virginia Commonwealth University (VCU).), Aashish Batheja MPH (is Medical Student, VCU.), Sharon Bednar MSN, RN, CEN, CPHQ, CLSS (is Process Engineer/Project Manager, Senior, VCU Health, Richmond, Virginia.), Chris Orange (is IT Professional, VCU Health.), Amy Hicks (is Training and Development Coordinator, VCU Health.), Stephen Miller DO (is Assistant Professor, Department of Emergency Medicine, VCU.), Patrice Forsen MS, RN, CEN (is Registered Nurse, VCU Health.), Amanda Stark MSN, RN (is Registered Nurse, VCU Health.), Gonzalo Bearman MD, MPH, FACP, FSHEA, FIDSA (is Professor, Department of Internal Medicine, VCU. Please address correspondence to Stephen Biederman)
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引用次数: 0

Abstract

Background

Sepsis is a life-threatening emergency, and early recognition and treatment in the emergency department (ED) is critical to improving outcomes.

Methods

The authors implemented an interdisciplinary quality improvement (QI) project to standardize sepsis screening workflow across an academic health system consisting of a large tertiary care urban hospital, one freestanding ED, and two small rural affiliate hospitals (RA-1 and RA-2). The research team used the Institute for Healthcare Improvement Model for Improvement framework, consisting of iterative Plan-Do-Study-Act (PDSA) cycles. The primary outcome was rates of screening for sepsis at each site. Secondary outcomes included sepsis mortality and Centers for Medicare & Medicaid Services (CMS) sepsis bundle (SEP-1) compliance at our main medical center. Primary outcome was assessed using electronic dashboards extracting the ratio of ED encounters with electronic health record (EHR)–documented sepsis screening per total ED encounters. The SEP-1 bundle was assessed as percent compliance, and mortality was calculated as average observed to expected (O:E). Averages were compared from preintervention to after initiating improvements using two-tailed t-tests.

Results

This QI project took place from December 2022 to December 2023 across four EDs that experience around 138,000 visits annually. A standardized workflow was established at ED triage with an EHR–based question and an associated nurse and physician defined response. Preintervention (October 2022 to November 2022) triage rates for sepsis were 1.7% (163/9,560), 25.3% (523/2,068), 11.0% (360/3,272), and 36.5% (915/2,506) at our main hospital, freestanding ED, RA-1, and RA-2, respectively. After four PDSA cycles, triage rates rose to 91.9% (4,927/5,360), 97.5% (1,032/1,059), 99.0% (1,845/1,863), and 97.4% (1,328/1,363), respectively (p < 0.005). Sepsis triage rates rose most slowly at the large academic medical center, where progressive PDSA cycles were needed to achieve > 90% screening for sepsis. Mean O:E mortality was 0.99 for the 9 months of available data preintervention and 0.83 in the 17 months postintervention (p = 0.07). CMS sepsis bundle compliance was 28.4% for the 15 months preintervention and 40.5% in the 17 months postintervention, (p = 0.14).

Conclusion

An interdisciplinary QI project leveraged EHR optimization to integrate with human workflows over four PDSA cycles to achieve standardized and improved screening for sepsis in the ED. This resulted in lower sepsis mortality and increased sepsis bundle compliance, though results were not statistically significant.
实现标准化和高可靠性:改进学术医疗系统急诊科分诊中的败血症筛查
背景败血症是一种危及生命的急症,急诊科(ED)的早期识别和治疗对改善预后至关重要。方法作者实施了一个跨学科质量改进(QI)项目,以规范一个学术医疗系统的败血症筛查工作流程,该系统由一家大型三级医疗城市医院、一家独立的急诊科和两家小型农村附属医院(RA-1 和 RA-2)组成。研究小组采用了美国医疗保健改进研究所的改进模式框架,包括 "计划-实施-研究-行动"(PDSA)迭代循环。主要结果是各医疗机构的败血症筛查率。次要结果包括脓毒症死亡率和我们主要医疗中心的医疗保险和医疗补助服务中心(CMS)脓毒症捆绑治疗(SEP-1)达标率。主要结果是通过电子仪表盘提取有电子健康记录(EHR)记录的脓毒症筛查的急诊室就诊人次与急诊室就诊总人次的比率来评估的。SEP-1 套件的合规性以百分比进行评估,死亡率则以平均观察值与预期值 (O:E) 进行计算。结果该 QI 项目于 2022 年 12 月至 2023 年 12 月在四家急诊室开展,这四家急诊室每年的就诊量约为 138,000 人次。在急诊室分流时建立了标准化工作流程,其中包括一个基于电子病历的问题以及相关护士和医生定义的回复。干预前(2022 年 10 月至 2022 年 11 月),主医院、独立急诊室、RA-1 和 RA-2 的败血症分诊率分别为 1.7%(163/9,560)、25.3%(523/2,068)、11.0%(360/3,272)和 36.5%(915/2,506)。经过四个 PDSA 循环后,分流率分别上升到 91.9%(4,927/5,360)、97.5%(1,032/1,059)、99.0%(1,845/1,863)和 97.4%(1,328/1,363)(p <0.005)。大型学术医疗中心的败血症分流率上升最慢,该中心需要逐步推进 PDSA 循环,以达到 90% 的败血症筛查率。干预前 9 个月的平均 O:E 死亡率为 0.99,干预后 17 个月的平均 O:E 死亡率为 0.83(p = 0.07)。在干预前的 15 个月和干预后的 17 个月中,CMS 败血症捆绑包合规率分别为 28.4% 和 40.5%(p = 0.14)。结论一个跨学科 QI 项目利用 EHR 优化与人类工作流程的整合,通过四个 PDSA 循环,实现了 ED 败血症筛查的标准化和改进。这降低了脓毒症死亡率,提高了脓毒症捆绑治疗的依从性,但结果并无统计学意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.80
自引率
4.30%
发文量
116
审稿时长
49 days
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