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Opinion paper on innovative approach of biomarkers for infectious diseases and sepsis management in the emergency department

机译:关于急诊科传染病和败血症管理生物标志物创新方法的意见书

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Sepsis is a leading healthcare problem, accounting for the vast majority of fatal events in critically ill patients. Beyond early diagnosis and appropriate treatment, this condition requires a multifaceted approach for monitoring the severity, the potential organ failure as well as the risk of death. Monitoring of the efficacy of treatment is also a major issue in the emergency department (ED). The assessment of critically ill conditions and the prognosis of patients with sepsis is currently based on some scoring systems, which are, however, inefficient to provide definite clues about organ failure and prognosis in general. The discretionary and appropriate use of some selected biomarkers such as procalcitonin, inducible protein 10(IP10), Group IV phospholipase A2 type II (PLA2 II), neutrophil gelatinase-associated lipocalin (NGAL), natriuretic peptides, mature adrenomedullin (ADM), mid-regional pro-adrenomedullin (MR-proADM), copeptin, thrombopoietin, Mer receptor and even red blood cell distribution width (RDW) represent thereby an appealing perspective in the diagnosis and management of patients with sepsis. Nevertheless, at the moment, it is not still clear if it is better to use a multimarkers approach or if a single, most appropriate, biomarker exists. This collective opinion paper is aimed at providing an overview about the potential clinical usefulness of some innovative biomarkers of sepsis in its diagnosis and prognosis, but also in the treatment management of the disease. This manuscript represents a synopsis of the lectures of Third Italian GREAT Network Congress, that was hold in Rome, 15-19 October 2012.
机译:脓毒症是一个主要的医疗保健问题,占危重患者致命事件的绝大部分。除了早期诊断和适当的治疗之外,这种情况还需要采取多方面的方法来监测严重程度,潜在的器官衰竭以及死亡风险。监测治疗效果也是急诊科(ED)的主要问题。当前对重症病情和败血症患者的预后的评估是基于一些评分系统,但是这些评分系统通常无法提供有关器官衰竭和预后的确切线索。可酌情酌情使用某些选定的生物标志物,例如降钙素,诱导型蛋白质10(IP10),IV组II型磷脂酶A2(PLA2 II),中性粒细胞明胶酶相关脂质运载蛋白(NGAL),利钠肽,成熟肾上腺髓质素(ADM),中期区域性肾上腺髓质素(MR-proADM),肽素,血小板生成素,Mer受体,甚至红细胞分布宽度(RDW)代表了败血症患者的诊断和治疗方面的诱人观点。然而,目前尚不清楚使用多标记方法是否更好,或者是否存在单个,最合适的生物标记。这份集体意见文件旨在概述败血症的一些创新生物标志物在其诊断和预后以及在疾病的治疗管理方面的潜在临床实用性。该手稿代表了2012年10月15日至19日在罗马举行的第三届意大利GREAT网络大会演讲的摘要。

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