败血症
医学
精密医学
重症监护医学
鉴定(生物学)
同种类的
主机响应
梅德林
生物信息学
计算生物学
临床实习
数据科学
临床判断
寄主(生物学)
病人护理
作者
Elizabeth A. Gay,Nuala J. Meyer,Pratik Sinha
标识
DOI:10.1097/ccm.0000000000007043
摘要
Due to its nonspecific clinical criteria, sepsis is clinically, microbiologically, pathophysiologically and immunologically highly heterogeneous. Consequently, despite hundreds of clinical trials, no host-targeted therapy has been shown to be ubiquitously efficacious, leading investigators to pursue more precision-based approaches for enriching sepsis populations through the identification of subgroups or phenotypes. Here, we review the myriad domains in which heterogeneity is observed in sepsis and the challenges and opportunities they offer to improve outcomes. We review current strategies used by investigators leveraging novel biological measurements and/or computational algorithms to identify more homogeneous subgroups either based on pathogen or host characteristics or both. Finally, we review some of the most promising recent advances that seek to bring these complex and innovative discoveries to the bedside to facilitate precision medicine in sepsis.
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