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Microfluidic Flow Chambers Using Reconstituted Blood to Model Hemostasis and Platelet Transfusion In Vitro
Published on: March 19, 2016
The contribution of red blood cell transfusion to neonatal morbidity and mortality
Tara M Crawford1, Chad C Andersen1,2, Nicolette A Hodyl1
1Robinson Research Institute, School of Medicine, University of Adelaide, Adelaide, South Australia, Australia.
Insights
Very preterm infants often need red blood cell (RBC) transfusions due to anemia. Transfusion-related immunomodulation (TRIM) may link RBC transfusions to adverse outcomes in newborns, necessitating safer transfusion strategies.
Area of Science:
- Neonatal Medicine
- Transfusion Medicine
- Immunology
Background:
- Anemia of prematurity affects 90% of very preterm infants, often requiring red blood cell (RBC) transfusions.
- Multiple transfusions are common in preterm infants, raising concerns about transfusion-associated risks.
- While severe transfusion reactions are rare in newborns, the link between transfusions and adverse outcomes needs further investigation.
Purpose of the Study:
- To explore the potential mechanisms linking RBC transfusions to adverse neonatal outcomes.
- To discuss the role of transfusion-related immunomodulation (TRIM) in neonatal transfusion medicine.
- To identify emerging research areas for improving transfusion safety in preterm infants.
Main Methods:
- Review of preclinical studies demonstrating RBCs' immunomodulatory effects.
- Analysis of existing literature on transfusion-associated morbidities in neonates.
- Discussion of current transfusion practices and future research directions.
Main Results:
- Preclinical evidence suggests RBCs can modulate immune cell function, a process termed TRIM.
- TRIM offers a potential pathway explaining the association between RBC transfusions and neonatal morbidities.
- Established transfusion reactions in adults are seldom recognized in newborns, highlighting a knowledge gap.
Conclusions:
- TRIM is a critical pathway to consider in neonatal transfusion medicine.
- Addressing TRIM requires innovative strategies to mitigate risks associated with RBC transfusions in preterm infants.
- Further research is essential to enhance the safety and efficacy of transfusions for vulnerable neonatal populations.
Abstract:
Anaemia of prematurity will affect 90% of all very preterm infants, resulting in at least one red blood cell (RBC) transfusion. A significant proportion of preterm infants require multiple transfusions over the course of hospital admission. Growing evidence supports an association between transfusion exposure and adverse neonatal outcomes. In adults, transfusion-associated sepsis, transfusion-related acute lung injury and haemolytic reactions are the leading causes of transfusion-related morbidity and mortality; however, these are seldom recognised in newborns. The association between transfusion and adverse outcomes remains inconclusive. However, the evidence from preclinical studies demonstrates that RBC products can directly modulate immune cell function, a pathway termed transfusion-related immunomodulation (TRIM), which may provide a mechanism linking transfusion exposure with neonatal morbidities. Finally, we discuss the impact of TRIM on transfusion medicine, how we may address these issues and the emerging areas of research aimed at improving the safety of transfusions in this vulnerable population.
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