Epsilon aminocaproic acid is associated with acute kidney injury after life‐threatening hemorrhage in children

Author:

Kolodziej Julia H.1ORCID,Leeper Christine M.2ORCID,Leonard Julie C.3,Josephson Cassandra D.4ORCID,Zenati Mazen S.5,Spinella Philip C.26ORCID

Affiliation:

1. Division of Pediatric Critical Care Medicine, Washington University in St. Louis School of Medicine St. Louis Children's Hospital St. Louis Missouri USA

2. Trauma and Transfusion Medicine Center, Department of Surgery, University of Pittsburgh School of Medicine Children's Hospital of Pittsburgh Pittsburgh Pennsylvania USA

3. Division of Emergency Medicine, Department of Pediatrics, Nationwide Children's Hospital The Ohio State University College of Medicine Columbus Ohio USA

4. Cancer and Blood Disorders Institute, Blood Bank and Transfusion Medicine Johns Hopkin All Children's Hospital Florida USA

5. Departments of Surgery, Epidemiology, and Clinical and Translational Science University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA

6. Department of Critical Care Medicine University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA

Abstract

AbstractBackgroundAntifibrinolytic medications have been associated with reduced mortality in pediatric hemorrhage but may contribute to adverse events such as acute kidney injury (AKI).Study Design and MethodsWe conducted a secondary analysis of the MAssive Transfusion in Children (MATIC), a prospectively collected database of children with life‐threatening hemorrhage (LTH), and evaluated for risk of adverse events with either antifibrinolytic treatment, epsilon aminocaproic acid (EACA) or tranexamic acid (TXA). The primary outcome was AKI and secondary outcomes were acute respiratory distress syndrome (ARDS) and sepsis.ResultsOf 448 children included, median (interquartile range) age was 7 (2–15) years, 55% were male, and LTH etiology was 46% trauma, 34% operative, and 20% medical. Three hundred and ninety‐three patients did not receive an antifibrinolytic (88%); 37 (8%) received TXA and 18 (4%) received EACA. Sixty‐seven (17.1%) patients in the no antifibrinolytic group developed AKI, 6 (16.2%) patients in the TXA group, and 9 (50%) patients in the EACA group (p = .002). After adjusting for cardiothoracic surgery, cyanotic heart disease, preexisting renal disease, lowest hemoglobin pre‐LTH, and total weight‐adjusted transfusion volume during the LTH, the EACA group had increased risk of AKI (adjusted odds ratio 3.3 [95% CI: 1.0–10.3]) compared to no antifibrinolytic. TXA was not associated with AKI. Neither antifibrinolytic treatment was associated with ARDS or sepsis.ConclusionAdministration of EACA during LTH may increase the risk of AKI. Additional studies are needed to compare the risk of AKI between EACA and TXA in pediatric patients.

Funder

National Heart, Lung, and Blood Institute

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

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