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Presepsin as a Potential Prognostic Marker for Sepsis According to Actual Practice Guidelines

机译:根据实际实践指南寄生作为败血症的潜在预后标志物

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摘要

The 2016 Surviving Sepsis Campaign guidelines define sepsis as life-threatening organ dysfunction caused by a dysregulated host response to infection. This study had the objective of assessing the efficacy of presepsin in the prognosis of sepsis. This was a single-center prospective study, performed in Craiova Emergency Hospital, that included 114 patients admitted in the Intensive Care Unit (ICU) department between 2018 and 2019 fulfilling the sepsis criteria. Including criteria were: age ≥ 18, sepsis diagnosed by the Sequential Organ Failure Assessment (SOFA) score of pulmonary, abdominal, urinary, surgical or unknown origin, as well as lactate levels ≥ 2 mmol/l and need of vasopressors for mean arterial pressure (MAP) ≥ 65 mmHg, despite adequate volume resuscitations for patients with septic shock. Patients younger than 18, pregnant, immunocompromised, or with terminal illnesses were excluded. Based on disease severity, patients were distributed into two study groups: sepsis—76 patients and septic shock—38 patients. As expected, SOFA score and most of its components (PaO2/FiO2, platelets, and Glasgow Coma Score (GCS)) were significantly modified for patients with septic shock compared to those in the sepsis group and for survivors versus non-survivors. Overall death rate was 34.2%, with a significantly higher value for patients with septic shock (55.3% vs. 23.7%, p = 0.035). Sepsis marker presepsin was significantly elevated in all patients (2047 ng/mL) and significantly increased for the septic shock patients (2538 ng/mL, p < 0.001) and non-survivors (3138 ng/mL, p < 0.001). A significant correlation was identified between the SOFA score and presepsin (r = 0.883, p < 0.001). The receiver operating characteristics (ROC)-Area Under Curve (AUC) analysis showed significant prognostic values for presepsin regarding both sepsis severity (AUC = 0.726, 95% confidence interval CI = 0.635–0.806) and mortality risk (AUC = 0.861, 95%CI = 0.784–0.919). In conclusion, under the revised definition of sepsis, presepsin could be a useful marker for prognosis of sepsis severity and mortality risk. Additional data are required to confirm the value of presepsin in sepsis prognosis.
机译:2016年幸存的败血症竞选指南将败血症定义为威胁危及生命的器官功能障碍,由失调的宿主对感染响应引起的。本研究具有评估PREPSIN在败血症预后的疗效的目标。这是在克莱诺瓦急诊医院进行的单中心前瞻性研究,其中包括114名患者在2018年至2019年期间,在2018年至2019年期间达到了瑞士欲绝标准。包括标准是:年龄≥18,败血症被顺序器官衰竭评估(沙发)评分肺,腹部,泌尿,外科或未知来源的评分,以及乳酸水平≥2mmol/ L,并且需要血管加压剂的平均动脉压力(地图)≥65mmHg,尽管脓液休克患者的体积复苏足够的体积复苏。患者比18岁,怀孕,免疫染色,或终末疾病被排除在外。基于疾病严重程度,患者分为两项研究组:SEPSIS-76患者和脓毒症休克38例。与败血症组中的患者相比,如预期的,沙发得分和其大部分组分(Pao2 / FiO2,血小板和格拉斯哥昏迷(GCS))被显着修饰了脓毒休克和幸存者与非幸存者的患者。整体死亡率为34.2%,脓毒症休克患者的价值显着更高(55.3%,5.7%,P = 0.035)。所有患者(2047 Ng / ml)脓毒症疫苗疫苗疫苗明显升高,脓毒休克患者(2538 Ng / ml,P <0.001)和非幸存者(3138ng / ml,p <0.001)显着增加。在沙发评分和PREPSIN之间确定了显着的相关性(R = 0.883,P <0.001)。在曲线(AUC)分析下的接收器操作特性(ROC)area对脓毒症严重程度(AUC = 0.726,95%置信区间CI = 0.635-0.806)和死亡率风险(AUC = 0.861,95%)显示出显着的预后值CI = 0.784-0.919)。总之,根据败血症的修订定义,PREPSIN可能是脓毒症严重程度和死亡率风险预后的有用标志物。需要额外的数据来确认脓毒症预后PREPSIN的价值。

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