Treatment variables associated with outcome in emergency department patients with suspected sepsis.

IF 5.5 1区 医学 Q1 CRITICAL CARE MEDICINE Annals of Intensive Care Pub Date : 2020-10-14 DOI:10.1186/s13613-020-00747-8
Narani Sivayoham, Lesley A Blake, Shafi E Tharimoopantavida, Saad Chughtai, Adil N Hussain, Andrew Rhodes
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引用次数: 6

Abstract

Background: Early treatment is advocated in the management of patients with suspected sepsis in the emergency department (ED). We sought to understand the association between the ED treatments and outcome in patients admitted with suspected sepsis. The treatments studied were: (i) the time to antibiotics, where time zero is the time the patient was booked in which is also the triage time; (ii) the volume of intravenous fluid (IVF); (iii) mean arterial pressure (MAP) after 2000 ml of IVF and (iv) the final MAP in the ED.

Methods: We performed a retrospective analysis of the ED database of patients aged ≥ 18 year who met two SIRS criteria or one red flag sepsis criteria on arrival, received intravenous antibiotics for a suspected infection and admitted between 8th February 2016 and 31st August 2017. The primary outcome measure was all-cause in-hospital mortality. The four treatments stated above were controlled for severity of illness and subject to multivariate logistic regression and Cox proportional-hazard regression to identify independent predictors of mortality.

Results: Of the 2,066 patients studied 272 (13.2%) died in hospital. The median time to antibiotics was 48 (interquartile range 30-82) minutes. The time to antibiotics was an independent predictor of mortality only in those who developed refractory hypotension (RH); antibiotics administered more than 55 mins after arrival was associated with an odds ratio (OR) for mortality of 2.75 [95% confidence interval (CI) 1.22-6.14]. The number-needed-to-treat was 4. IVF > 2000 ml (95% CI > 500- > 2100), except in RH, and a MAP ≤ 66 mmHg after 2000 ml of IVF were also independent predictors of mortality. The OR for mortality of IVF > 2,000 ml in non-RH was 1.80 (95% CI 1.15-2.82); Number-needed-to-harm was 14. The OR for morality for a MAP ≤ 66 mmHg after 2000 ml of IVF was 3.42 (95% CI 2.10-5.57). A final MAP < 75 mmHg in the ED was associated with, but not an independent predictor of mortality. An initial systolic blood pressure of < 100 mmHg has a sensitivity of 63.3% and specificity of 88.4% for the development of RH.

Conclusion: In this study, antibiotics were found to be time-critical in RH. Intravenous fluids > 2000 ml (except in RH) and a MAP ≤ 66 mmHg after 2000 ml of IVF were also independent predictors of mortality.

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急诊疑似脓毒症患者治疗变量与预后相关
背景:急诊部门提倡对疑似脓毒症患者进行早期治疗。我们试图了解ED治疗与疑似脓毒症患者预后之间的关系。研究的治疗方法是:(i)使用抗生素的时间,其中时间零是病人被预约的时间,也是分诊时间;(ii)静脉注射液量(体外受精);(iii) 2000 ml试管婴儿(IVF)后的平均动脉压(MAP)和(iv) ED中的最终MAP。方法:我们对年龄≥18岁的ED数据库进行回顾性分析,这些患者在到达时符合两个SIRS标准或一个红旗败血症标准,因疑似感染接受静脉注射抗生素,并在2016年2月8日至2017年8月31日期间入院。主要结局指标为全因住院死亡率。对上述四种治疗方法进行疾病严重程度控制,并进行多因素logistic回归和Cox比例风险回归,以确定死亡率的独立预测因子。结果:在研究的2066例患者中,272例(13.2%)在医院死亡。抗生素治疗的中位时间为48分钟(四分位数范围30-82分钟)。抗生素治疗时间仅是难治性低血压(RH)患者死亡率的独立预测因子;到达后超过55分钟使用抗生素与死亡率的比值比(OR)为2.75相关[95%可信区间(CI) 1.22-6.14]。需要招待的数量是4。IVF > 2000 ml (95% CI > 500- > 2100) (RH除外)和IVF 2000 ml后MAP≤66 mmHg也是死亡率的独立预测因子。非rh患者IVF > 2,000 ml的死亡率OR为1.80 (95% CI 1.15-2.82);需要伤害的人数是14人。2000 ml体外受精后MAP≤66 mmHg的道德OR为3.42 (95% CI 2.10-5.57)。最后的MAP结论:在本研究中,抗生素在RH中被发现是时间关键的。静脉输液> 2000 ml (RH除外)和体外受精2000 ml后MAP≤66 mmHg也是死亡率的独立预测因子。
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来源期刊
Annals of Intensive Care
Annals of Intensive Care CRITICAL CARE MEDICINE-
CiteScore
14.20
自引率
3.70%
发文量
107
审稿时长
13 weeks
期刊介绍: Annals of Intensive Care is an online peer-reviewed journal that publishes high-quality review articles and original research papers in the field of intensive care medicine. It targets critical care providers including attending physicians, fellows, residents, nurses, and physiotherapists, who aim to enhance their knowledge and provide optimal care for their patients. The journal's articles are included in various prestigious databases such as CAS, Current contents, DOAJ, Embase, Journal Citation Reports/Science Edition, OCLC, PubMed, PubMed Central, Science Citation Index Expanded, SCOPUS, and Summon by Serial Solutions.
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