改进对疑似败血症患者的护理点 (POC) 检测:宿主生物标志物和可能微生物病原体的 POC 检测。

IF 3.9 3区 医学 Q1 PATHOLOGY
Maria-Evangelia Adami, Evangelos J Giamarellos-Bourboulis, Effie Polyzogopoulou
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引用次数: 0

摘要

导言败血症是一种异质性综合征,经常被误诊。护理点(POC)诊断测试通常用于指导决策,包括宿主生物标志物和分子诊断:本综述分析了脓毒症既有和新兴生物标志物的诊断和预后准确性,包括降钙素原(PCT)、可溶性尿激酶纤溶酶原激活物受体(suPAR)、前胰蛋白酶、TRAIL/IP-10/CRP、MxA 和 MxA-CRP。此外,还介绍了使用聚合酶链反应(PCR)检测法鉴定病原体的两种流行分子技术的临床实用性:FILMARRAY 和 QIAstat-Dx RP:专家意见:在日常临床工作中结合使用 POC 生物标记物和分子诊断技术所带来的益处不断增加,在缩短周转时间、及时诊断和迅速给予适当治疗方面似乎优于传统做法。然而,这还需要在未来的研究中进一步证实。然而,POC 检测的成本效益以及假阳性和假阴性结果的高发生率表明,有必要进行全面的临床评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Towards improved point-of-care (POC) testing for patients with suspected sepsis: POC tests for host biomarkers and possible microbial pathogens.

Introduction: Sepsis is a heterogeneous syndrome often misdiagnosed. Point-of-care (POC) diagnostic tests are commonly used to guide decision and include host biomarkers and molecular diagnostics.

Areas covered: The diagnostic and prognostic accuracy of established and emerging biomarkers for sepsis, including procalcitonin (PCT) soluble urokinase plasminogen activator receptor (suPAR), presepsin, TRAIL/IP-10/CRP, MxA, and MxA-CRP, are analyzed in this review. The clinical utility of the two prevalent molecular techniques for pathogens identification using polymerase chain reaction (PCR) assays is also presented: FILMARRAY and QIAstat-Dx RP.

Expert opinion: The rising benefits of the combined use of POC biomarkers with molecular diagnostics in daily clinical routine appear to outperform conventional practices in terms of reduced turnaround time, timely diagnosis, and prompt administration of the appropriate treatment. Yet, this must be further demonstrated in future investigations. However, the cost-effectiveness of POC tests and the high rate of false positive and negative results, indicate the need for a comprehensive clinical evaluation.

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来源期刊
CiteScore
6.60
自引率
0.00%
发文量
71
审稿时长
1 months
期刊介绍: Expert Review of Molecular Diagnostics (ISSN 1473-7159) publishes expert reviews of the latest advancements in the field of molecular diagnostics including the detection and monitoring of the molecular causes of disease that are being translated into groundbreaking diagnostic and prognostic technologies to be used in the clinical diagnostic setting. Each issue of Expert Review of Molecular Diagnostics contains leading reviews on current and emerging topics relating to molecular diagnostics, subject to a rigorous peer review process; editorials discussing contentious issues in the field; diagnostic profiles featuring independent, expert evaluations of diagnostic tests; meeting reports of recent molecular diagnostics conferences and key paper evaluations featuring assessments of significant, recently published articles from specialists in molecular diagnostic therapy. Expert Review of Molecular Diagnostics provides the forum for reporting the critical advances being made in this ever-expanding field, as well as the major challenges ahead in their clinical implementation. The journal delivers this information in concise, at-a-glance article formats: invaluable to a time-constrained community.
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