Department of Population Medicine, Harvard Medical School, Harvard Pilgrim Health Care Institute, Boston, Massachusetts.
Division of Infectious Diseases, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
JAMA Netw Open. 2021 Dec 1;4(12):e2138596. doi: 10.1001/jamanetworkopen.2021.38596.
In October 2015, the Centers for Medicare & Medicaid Services began requiring US hospitals to report adherence to the Severe Sepsis and Septic Shock Early Management Bundle (SEP-1).
To evaluate the association of SEP-1 implementation with sepsis treatment patterns and outcomes in diverse hospitals.
DESIGN, SETTING, AND PARTICIPANTS: This retrospective cohort study with interrupted time-series analysis and logistic regression models was conducted among adults admitted to 114 hospitals from October 2013 to December 2017 with suspected sepsis (blood culture orders, ≥2 systemic inflammatory response syndrome criteria, and acute organ dysfunction) within 24 hours of hospital arrival. Data analysis was conducted from September 2020 to September 2021.
SEP-1 implementation in the fourth quarter (Q4) of 2015.
The primary outcome was quarterly rates of risk-adjusted short-term mortality (in-hospital death or discharge to hospice). Secondary outcomes included lactate testing and administration of anti-methicillin-resistant Staphylococcus aureus (MRSA) or antipseudomonal β-lactam antibiotics within 24 hours of hospital arrival. Generalized estimating equations with robust sandwich variances were used to fit logistic regression models to assess for changes in level or trends in these outcomes, adjusting for baseline characteristics and severity of illness.
The cohort included 117 510 patients (median [IQR] age, 67 years [55-78] years; 60 530 [51.5%] men and 56 980 [48.5%] women) with suspected sepsis. Lactate testing rates increased from 55.1% (95% CI, 53.9%-56.2%) in Q4 of 2013 to 76.7% (95% CI, 75.4%-78.0%) in Q4 of 2017, with a significant level change following SEP-1 implementation (odds ratio [OR], 1.34; 95% CI, 1.04-1.74). There were increases in use of anti-MRSA antibiotics (19.8% [95% CI, 18.9%-20.7%] in Q4 of 2013 to 26.3% [95% CI, 24.9%-27.7%] in Q4 of 2017) and antipseudomonal antibiotics (27.7% [95% CI, 26.7%-28.8%] in Q4 of 2013 to 40.5% [95% CI, 38.9%-42.0%] in Q4 of 2017), but these trends preceded SEP-1 and did not change with SEP-1 implementation. Unadjusted short-term mortality rates were similar in the pre-SEP-1 period (Q4 of 2013 through Q3 of 2015) vs the post-SEP-1 period (Q1 of 2016 through Q4 of 2017) (20.3% [95% CI, 20.0%-20.6%] vs 20.4% [95% CI, 20.1%-20.7%]), and SEP-1 implementation was not associated with changes in level (OR, 0.94; 95% CI, 0.68-1.29) or trend (OR, 1.00; 95% CI, 0.97-1.04) for risk-adjusted short-term mortality rates.
In this cohort study, SEP-1 implementation was associated with an immediate increase in lactate testing rates, no change in already-increasing rates of broad-spectrum antibiotic use, and no change in short-term mortality rates for patients with suspected sepsis. Other approaches to decrease sepsis mortality may be warranted.
2015 年 10 月,医疗保险和医疗补助服务中心开始要求美国医院报告对严重脓毒症和脓毒症性休克早期管理包(SEP-1)的遵守情况。
评估 SEP-1 实施与不同医院脓毒症治疗模式和结局的关联。
设计、地点和参与者:这是一项回顾性队列研究,采用中断时间序列分析和逻辑回归模型,纳入了 2013 年 10 月至 2017 年 12 月期间入住 114 家医院的成年人,这些患者在到达医院的 24 小时内疑似患有败血症(血培养订单、≥2 个全身炎症反应综合征标准和急性器官功能障碍)。数据分析于 2020 年 9 月至 2021 年 9 月进行。
2015 年第四季度(Q4)SEP-1 的实施。
主要结局是风险调整后的短期死亡率(院内死亡或出院至临终关怀)的季度率。次要结局包括入住医院 24 小时内乳酸测试和使用抗耐甲氧西林金黄色葡萄球菌(MRSA)或抗假单胞菌β-内酰胺类抗生素。采用广义估计方程和稳健的夹心方差来拟合逻辑回归模型,以评估这些结局的变化水平或趋势,同时调整基线特征和疾病严重程度。
队列包括 117510 名疑似败血症患者(中位数[IQR]年龄,67 岁[55-78]岁;60530 名[51.5%]男性和 56980 名[48.5%]女性)。乳酸测试率从 2013 年第四季度的 55.1%(95%CI,53.9%-56.2%)增加到 2017 年第四季度的 76.7%(95%CI,75.4%-78.0%),在 SEP-1 实施后出现显著水平变化(比值比[OR],1.34;95%CI,1.04-1.74)。抗 MRSA 抗生素的使用率增加(2013 年第四季度为 19.8%[95%CI,18.9%-20.7%],2017 年第四季度为 26.3%[95%CI,24.9%-27.7%]),抗假单胞菌抗生素的使用率也增加(2013 年第四季度为 27.7%[95%CI,26.7%-28.8%],2017 年第四季度为 40.5%[95%CI,38.9%-42.0%]),但这些趋势先于 SEP-1 出现,并且在 SEP-1 实施后没有变化。在 SEP-1 实施前的时期(2013 年第四季度至 2015 年第三季度)与 SEP-1 实施后的时期(2016 年第一季度至 2017 年第四季度)相比,未调整的短期死亡率相似(20.3%[95%CI,20.0%-20.6%]与 20.4%[95%CI,20.1%-20.7%]),并且 SEP-1 实施与风险调整后短期死亡率的水平(OR,0.94;95%CI,0.68-1.29)或趋势(OR,1.00;95%CI,0.97-1.04)无关。
在这项队列研究中,SEP-1 的实施与乳酸测试率的立即增加有关,与广谱抗生素使用已经增加的趋势无关,也与疑似败血症患者的短期死亡率无关。可能需要采取其他方法来降低败血症死亡率。