Transfusion targets and adverse events in pediatric perioperative acute Anemia

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Abstract

Study objective: To evaluate the association between pretransfusion and posttransfusion hemoglobin concentrations and the outcomes of children undergoing noncardiac surgery. Design: Retrospective review of patient records. We focused on initial postoperative hemoglobin concentrations, which may provide a more useful representation of transfusion adequacy than pretransfusion hemoglobin triggers (the latter often cannot be obtained during acute surgical hemorrhage). Setting: Single-center, observational cohort study. Patients: We evaluated all pediatric patients undergoing noncardiac surgery who received intraoperative red blood cell transfusions from January 1, 2008, through December 31, 2018. Interventions: None. Measurements: Associations between pre- and posttransfusion hemoglobin concentrations (g/dL), hospital-free days, intensive care unit admission, postoperative mechanical ventilation, and infectious complications were evaluated with multivariable regression modeling. Main results: In total, 113,713 unique noncardiac surgical procedures in pediatric patients were evaluated, and 741 procedures met inclusion criteria (median [range] age, 7 [1–14] years). Four hundred ninety-eight patients (68%) with a known preoperative hemoglobin level had anemia; of these, 14% had a preexisting diagnosis of anemia in their health record. Median (IQR) pretransfusion hemoglobin concentration was 8.1 (7.4–9.2) g/dL and median (IQR) initial postoperative hemoglobin concentration was 10.4 (9.3–11.6) g/dL. Each decrease of 1 g/dL in the initial postoperative hemoglobin concentration was associated with increased odds of transfusion within the first 24 postoperative hours (odds ratio [95% CI], 1.62 [1.37–1.93]; P

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Warner, L. L., Thalji, L., Hunter Guevara, L. R., Warner, M. A., Kor, D. J., Warner, D. O., … Nemergut, M. E. (2024). Transfusion targets and adverse events in pediatric perioperative acute Anemia. Journal of Clinical Anesthesia, 94. https://doi.org/10.1016/j.jclinane.2024.111405

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