| Literature DB >> 31911172 |
Zhenxing Xu1, Jingyuan Chou1, Xi Sheryl Zhang1, Yuan Luo2, Tamara Isakova2, Prakash Adekkanattu1, Jessica S Ancker1, Guoqian Jiang3, Richard C Kiefer3, Jennifer A Pacheco2, Luke V Rasmussen2, Jyotishman Pathak1, Fei Wang4.
Abstract
Acute Kidney Injury (AKI) is a common clinical syndrome characterized by the rapid loss of kidney excretory function, which aggravates the clinical severity of other diseases in a large number of hospitalized patients. Accurate early prediction of AKI can enable in-time interventions and treatments. However, AKI is highly heterogeneous, thus identification of AKI sub-phenotypes can lead to an improved understanding of the disease pathophysiology and development of more targeted clinical interventions. This study used a memory network-based deep learning approach to discover AKI sub-phenotypes using structured and unstructured electronic health record (EHR) data of patients before AKI diagnosis. We leveraged a real world critical care EHR corpus including 37,486 ICU stays. Our approach identified three distinct sub-phenotypes: sub-phenotype I is with an average age of 63.03±17.25 years, and is characterized by mild loss of kidney excretory function (Serum Creatinine (SCr) 1.55±0.34 mg/dL, estimated Glomerular Filtration Rate Test (eGFR) 107.65±54.98 mL/min/1.73 m2). These patients are more likely to develop stage I AKI. Sub-phenotype II is with average age 66.81±10.43 years, and was characterized by severe loss of kidney excretory function (SCr 1.96±0.49 mg/dL, eGFR 82.19±55.92 mL/min/1.73 m2). These patients are more likely to develop stage III AKI. Sub-phenotype III is with average age 65.07±11.32 years, and was characterized moderate loss of kidney excretory function and thus more likely to develop stage II AKI (SCr 1.69±0.32 mg/dL, eGFR 93.97±56.53 mL/min/1.73 m2). Both SCr and eGFR are significantly different across the three sub-phenotypes with statistical testing plus postdoc analysis, and the conclusion still holds after age adjustment.Entities:
Keywords: Acute Kidney Injury; Electronic health record; Memory networks; Phenotyping
Mesh:
Substances:
Year: 2020 PMID: 31911172 DOI: 10.1016/j.jbi.2019.103361
Source DB: PubMed Journal: J Biomed Inform ISSN: 1532-0464 Impact factor: 6.317