A practical guide to reducing/eliminating red blood cell transfusions in the neonatal intensive care unit.

Semin Fetal Neonatal Med

Division of Neonatology, Department of Pediatrics, University of Utah, 295 Chipeta Way, Salt Lake City, UT, 84108, USA; Women and Newborns Research, Intermountain Health, Murray, UT, USA.

Published: October 2024

AI Article Synopsis

  • * Common risks include worsening inflammatory issues and potential long-term effects like retinopathy of prematurity and neurodevelopmental delays, which are sometimes not fully addressed during the informed consent process.
  • * Implementing non-drug methods to avoid transfusions, alongside erythropoietic stimulating agents, can significantly reduce the need for transfusions in NICU patients, making care both more effective and cost-efficient.

Article Abstract

Red blood cell transfusions can be lifesaving for neonates with severe anemia or acute massive hemorrhage. However, it is imperative to understand that red cell transfusions convey unique and significant risks for neonates. The extremely rare risks of transmitting a viral, bacterial, or other microbial infection, or causing circulatory overload are well known and are part of blood transfusion informed consent. Less well known, and not always part of the consent process, are more common risks of transfusing the smallest and most immature NICU patients; specifically, multiple transfusions may worsen inflammatory conditions (particularly pulmonary inflammation), and in certain subsets are associated with retinopathy of prematurity and neurodevelopmental delay. Instituting non-pharmacological transfusion-avoidance techniques reduces transfusion rates. Pharmacological transfusion-avoidance, specifically erythropoietic stimulating agents, further reduces the risk of needing a transfusion. The protocols described herein constitute an efficient and cost-effective transfusion-avoidance program. Using these protocols, many NICU patients can remain transfusion-free.

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Source
http://dx.doi.org/10.1016/j.siny.2024.101545DOI Listing

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