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Poor performance of quick-SOFA (qSOFA) score in predicting severe sepsis and mortality: a prospective study of patients admitted with infection to the emergency department

机译:快速sOFa(qsOFa)评分在预测严重脓毒症和死亡率方面表现不佳:对急诊室感染患者的前瞻性研究

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摘要

BackgroundWe aimed to evaluate the clinical usefulness of qSOFA as a risk stratification tool for patients admitted with infection compared to traditional SIRS criteria or our triage system; the Rapid Emergency Triage and Treatment System (RETTS).MethodsThe study was an observational cohort study performed at one Emergency Department (ED) in an urban university teaching hospital in Norway, with approximately 20,000 visits per year. All patients >16 years presenting with symptoms or clinical signs suggesting an infection (n = 1535) were prospectively included in the study from January 1 to December 31, 2012. At arrival in the ED, vital signs were recorded and all patients were triaged according to RETTS vital signs, presenting infection, and sepsis symptoms. These admission data were also used to calculate qSOFA and SIRS. Treatment outcome was later retrieved from the patients’ electronic records (EPR) and mortality data from the Norwegian population registry.ResultsOf the 1535 admitted patients, 108 (7.0%) fulfilled the Sepsis2 criteria for severe sepsis. The qSOFA score ≥2 identified only 33 (sensitivity 0.32, specificity 0.98) of the patients with severe sepsis, whilst the RETTS-alert ≥ orange identified 92 patients (sensitivity 0.85, specificity 0.55). Twenty-six patients died within 7 days of admission; four (15.4%) of them had a qSOFA ≥2, and 16 (61.5%) had RETTS ≥ orange alert. Of the 68 patients that died within 30 days, only eight (11.9%) scored ≥2 on the qSOFA, and 45 (66.1%) had a RETTS ≥ orange alert.DiscussionIn order to achieve timely treatment for sepsis, a sensitive screening tool is more important than a specific one. Our study is the fourth study were qSOFA finds few of the sepsis cases in prehospital or at arrival to the ED. We add information on the RETTS triage system, the two highest acuity levels together had a high sensitivity (85%) for identifying sepsis at arrival to the ED - and thus, RETTS should not be replaced by qSOFA as a screening and trigger tool for sepsis at arrival.ConclusionIn this observational cohort study, qSOFA failed to identify two thirds of the patients admitted to an ED with severe sepsis. Further, qSOFA failed to be a risk stratification tool as the sensitivity to predict 7-day and 30-day mortality was low. The sensitivity was poorer than the other warning scores already in use at the study site, RETTS-triage and the SIRS criteria.
机译:背景我们旨在评估与传统的SIRS标准或我们的分类系统相比,qSOFA作为被感染患者的风险分层工具的临床实用性;方法本研究是一项观察性队列研究,在挪威城市大学教学医院的一个急诊科(ED)进行,每年约20,000次就诊。从2012年1月1日至2012年12月31日前瞻性地纳入了所有> 16岁且症状或临床体征提示感染(n = 1535)的患者。在到达急诊室时,记录了生命体征,并对所有患者进行了分类。 RETTS生命体征,出现感染和败血症症状。这些入学数据还用于计算qSOFA和SIRS。随后,从患者的电子记录(EPR)和挪威人口登记处的死亡率数据中检索治疗结果。结果在1535名入院患者中,有108名(7.0%)符合严重脓毒症的Sepsis2标准。 qSOFA得分≥2仅能识别出33名严重脓毒症患者(敏感性0.32,特异性0.98),而RETTS-alert≥橙色的患者可识别92例患者(敏感性0.85,特异性0.55)。入院7天内有26例患者死亡。其中有4名(15.4%)的qSOFA≥2,有16名(61.5%)的RETTS≥≥橙色。在30天之内死亡的68例患者中,qSOFA评分≥2的只有8例(11.9%),并且有RETTS≥橙色警报的45例(66.1%)。讨论为了及时治疗败血症,需要使用敏感的筛查工具比特定的重要。我们的研究是qSOFA在院前或到达ED时很少发现败血症病例的第四项研究。我们添加了有关RETTS分诊系统的信息,两个最高敏锐度一起对识别到达ED的败血症具有很高的敏感性(85%)-因此,不应将qTSFA代替RETTS作为脓毒症的筛查和触发工具结论在这项观察性队列研究中,qSOFA未能识别出患有严重脓毒症的ED患者中的三分之二。此外,由于预测7天和30天死亡率的敏感性较低,因此qSOFA不能作为风险分层工具。敏感性低于研究地点已经使用的其他警告评分,RETTS-triage和SIRS标准。

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