Sepsis, Management & Advances in Metabolomics.

Q1 Pharmacology, Toxicology and Pharmaceutics
Nanotheranostics Pub Date : 2024-02-25 eCollection Date: 2024-01-01 DOI:10.7150/ntno.94071
Swarnima Pandey
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引用次数: 0

Abstract

Though there have been developments in clinical care and management, early and accurate diagnosis and risk stratification are still bottlenecks in septic shock patients. Since septic shock is multifactorial with patient-specific underlying co-morbid conditions, early assessment of sepsis becomes challenging due to variable symptoms and clinical manifestations. Moreover, the treatment strategies are traditionally based on their progression and corresponding clinical symptoms, not personalized. The complex pathophysiology assures that a single biomarker cannot identify, stratify, and describe patients affected by septic shock. Traditional biomarkers like CRP, PCT, and cytokines are not sensitive and specific enough to be used entirely for a patient's diagnosis and prognosis. Thus, the need of the hour is a sensitive and specific biomarker after comprehensive analysis that may facilitate an early diagnosis, prognosis, and drug development. Integration of clinical data with metabolomics would provide means to understand the patient's condition, stratify patients better, and predict the clinical outcome.

败血症、管理和代谢组学进展。
尽管临床护理和管理有所发展,但早期准确诊断和风险分层仍是脓毒性休克患者的瓶颈。由于脓毒性休克是一种多因素疾病,患者的基础并发症各不相同,脓毒症的早期评估因症状和临床表现多变而变得具有挑战性。此外,传统的治疗策略是根据其进展情况和相应的临床症状,而非个性化治疗。复杂的病理生理学确保了单一生物标志物无法识别、分层和描述脓毒性休克患者。CRP、PCT 和细胞因子等传统生物标志物不够敏感和特异,不能完全用于患者的诊断和预后。因此,当务之急是在综合分析后找到一种灵敏而特异的生物标志物,以促进早期诊断、预后和药物开发。临床数据与代谢组学的整合将为了解患者病情、更好地对患者进行分层以及预测临床结果提供手段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nanotheranostics
Nanotheranostics Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
10.40
自引率
0.00%
发文量
37
审稿时长
12 weeks
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