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用于指导脓毒症管理的生物标志物。

Biomarkers to guide sepsis management.

作者信息

Bourika Vasiliki, Rekoumi Evangelia-Areti, Giamarellos-Bourboulis Evangelos J

机构信息

Hellenic Institute for the Study of Sepsis, Athens, Greece.

4th Department of Internal Medicine, National and Kapodistrian University of Athens, Athens, Greece.

出版信息

Ann Intensive Care. 2025 Jul 21;15(1):103. doi: 10.1186/s13613-025-01524-1.

Abstract

BACKGROUND

Sepsis remains a major cause of morbidity and mortality. Precision therapeutics are now regarded as a novel prospective to improve outcome. This approach relies on biomarkers to identify a pathway of pathogenesis which prevails and directs the best available therapeutic option to modulate this pathway. This review provides the most recent findings on biomarkers for bacterial or viral sepsis. These biomarkers provide guidance for prompt diagnosis and management tailored to specific needs.

MAIN BODY

Keywords relative to sepsis management (early recognition, antibiotic administration, selection of fluids, vasopressors and immunotherapy) were searched across PubMed database. Published evidence the last five years exists for heparin-binding protein (HBP), monocyte distribution width (MDW), interleukin-10 (IL-10), presepsin, procalcitonin and C-reactive protein (CRP) for early sepsis diagnosis; procalcitonin is the most well-studied biomarker for antibiotic guidance. Endothelial and cardiac biomarkers have been explored as tools to tailor circulatory support in sepsis, including fluid therapy, and the targeted use of vasopressors for vascular tone optimization.

CONCLUSION

This review explored how biomarkers can optimize immunomodulatory therapies, guide vasopressor initiation, inform antibiotic stewardship, and aid in fluid resuscitation decisions, ultimately improving patient outcomes.

摘要

背景

脓毒症仍然是发病和死亡的主要原因。精准治疗目前被视为改善预后的一种新的前景。这种方法依赖生物标志物来识别占主导地位的发病机制途径,并指导最佳可用治疗方案来调节该途径。本综述提供了关于细菌性或病毒性脓毒症生物标志物的最新研究结果。这些生物标志物为根据特定需求进行的快速诊断和管理提供指导。

主体

在PubMed数据库中搜索了与脓毒症管理相关的关键词(早期识别、抗生素给药、液体选择、血管加压药和免疫治疗)。过去五年有关于肝素结合蛋白(HBP)、单核细胞分布宽度(MDW)、白细胞介素-10(IL-10)、可溶性髓系细胞触发受体-1(presepsin)、降钙素原和C反应蛋白(CRP)用于早期脓毒症诊断的已发表证据;降钙素原是用于抗生素指导研究最多的生物标志物。内皮和心脏生物标志物已被探索作为调整脓毒症循环支持的工具,包括液体治疗,以及针对性使用血管加压药以优化血管张力。

结论

本综述探讨了生物标志物如何优化免疫调节治疗、指导血管加压药的起始使用、为抗生素管理提供信息以及辅助液体复苏决策,最终改善患者预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c520/12277237/3a2d2038e727/13613_2025_1524_Fig1_HTML.jpg

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