Article
Identifying Hemophagocytic Lymphohistiocytosis and Describing Outcomes Using Computable Phenotypes: Retrospective Cohort Study.
JMIR cancer - 26 Mar 2026
Ocak Suheyla, Yi Martin, Wolochacz Agata, Mehrdadi Ida, Naqvi Ahmed, Gupta Sumit, Sung Lillian, Yan Adam P
Abstract excerpt
Background: Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening hyperinflammatory syndrome that requires rapid diagnosis and intervention. However, identifying these patients is difficult because the HLH-2004 diagnostic criteria are complex and not always captured systematically in electronic health records (EHRs). Furthermore, it is unclear how clinicians use these criteria to diagnose HLH and make...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
