作者
Pratik Sinha,V. Eric Kerchberger,Andrew Willmore,Julia Chambers,Hanjing Zhuo,Jason Abbott,Chayse Jones,Nancy Wickersham,Nelson Wu,Lucile Neyton,Charles Langelier,Eran Mick,June He,Alejandra Jáuregui,Matthew M. Churpek,A.D. Gomez,Carolyn M. Hendrickson,Kirsten N. Kangelaris,Aartik Sarma,Aleksandra Leligdowicz,Kevin Delucchi,Kathleen D. Liu,James A. Russell,Michael A. Matthay,Keith R. Walley,Lorraine B. Ware,Carolyn S. Calfee
摘要
In sepsis and acute respiratory distress syndrome (ARDS), heterogeneity has contributed to difficulty identifying effective pharmacotherapies. In ARDS, two molecular phenotypes (hypoinflammatory and hyperinflammatory) have consistently been identified, with divergent outcomes and treatment responses. In this study, we sought to derive molecular phenotypes in critically ill adults with sepsis, determine their overlap with previous ARDS phenotypes, and evaluate whether they respond differently to treatment in completed sepsis trials.