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In premature infants there is no decrease in 24-hour posttransfusion allogeneic red blood cell recovery after 42 days
Demet Nalbant1, José A Cancelas2, Donald M Mock3
1Department of Pediatrics.
Insights
Red blood cell (RBC) transfusions for preterm newborns show no decrease in 24-hour recovery (PTR24) with storage duration. This supports using up to 42-day stored RBCs for neonatal transfusions, unlike in adults.
Area of Science:
- Neonatal Medicine
- Transfusion Medicine
- Hematology
Background:
- Critically ill preterm very-low-birthweight (VLBW) neonates often require red blood cell (RBC) transfusions due to anemia.
- Current understanding suggests RBC recovery decreases with storage duration in adults, but data in infants is limited.
Purpose of the Study:
- To investigate if posttransfusion 24-hour RBC recovery (PTR24) of allogeneic RBCs in VLBW newborns decreases with storage duration.
- To compare PTR24 in VLBW newborns with that in healthy adults receiving autologous RBCs.
Main Methods:
- Compared PTR24 of biotin-labeled RBCs in 46 VLBW neonates with 51Cr-labeled RBCs in 76 healthy adults.
- RBCs were stored for up to 42 days at 4°C in AS-3 or AS-5.
- Linear mixed-model analysis assessed PTR24 versus RBC storage duration.
Main Results:
- PTR24 in VLBW newborns did not significantly decrease with storage duration (p=0.18), unlike in adults (p<0.0001).
- The slopes of PTR24 versus storage duration differed significantly between newborns and adults (p=0.04).
- Projected mean PTR24 at 42 days of storage was 95.9% for newborns versus 83.8% for adults (p=0.0002).
Conclusions:
- Storage duration of allogeneic RBCs for neonates can be extended up to 42 days without impacting PTR24.
- Findings support current practices of using up to 42-day stored RBCs for small-volume neonatal transfusions.
- This practice helps minimize donor exposure for VLBW infants.
Background:
Critically ill preterm very-low-birthweight (VLBW) neonates (birthweight ≤ 1.5 kg) frequently develop anemia that is treated with red blood cell (RBC) transfusions. Although RBCs transfused to adults demonstrate progressive decreases in posttransfusion 24-hour RBC recovery (PTR24 ) during storage-to a mean of approximately 85% of the Food and Drug Administration-allowed 42-day storage-limited data in infants indicate no decrease in PTR24 with storage.
Study Design And Methods:
We hypothesized that PTR24 of allogeneic RBCs transfused to anemic VLBW newborns: 1) will be greater than PTR24 of autologous RBCs transfused into healthy adults and 2) will not decrease with increasing storage duration. RBCs were stored at 4°C for not more than 42 days in AS-3 or AS-5. PTR24 was determined in 46 VLBW neonates using biotin-labeled RBCs and in 76 healthy adults using 51 Cr-labeled RBCs. Linear mixed-model analysis was used to estimate slopes and intercepts of PTR24 versus duration of RBC storage.
Results:
For VLBW newborns, the estimated slope of PTR24 versus storage did not decrease with the duration of storage (p = 0.18) while for adults it did (p < 0.0001). These estimated slopes differed significantly in adults compared to newborns (p = 0.04). At the allowed 42-day storage limit, projected mean neonatal PTR24 was 95.9%; for adults, it was 83.8% (p = 0.0002).
Conclusions:
These data provide evidence that storage duration of allogeneic RBCs intended for neonates can be increased without affecting PTR24 . This conclusion supports the practice of transfusing RBCs stored up to 42 days for small-volume neonatal transfusions to limit donor exposure.
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