scholarly journals Soluble factors from packed red blood cells augmented LPS Induced monocyte production of IL-1Β and caspase-1

Pathology ◽  
2020 ◽  
Vol 52 ◽  
pp. S119
Author(s):  
Robert Flower ◽  
Fenny Chong ◽  
Kelly Rooks ◽  
Melinda Dean
2014 ◽  
Vol 186 (2) ◽  
pp. 683
Author(s):  
J.A. Yi ◽  
K. Lo ◽  
C.C. Silliman ◽  
B.H. Edil ◽  
R.D. Schulick ◽  
...  

2021 ◽  
pp. 100487
Author(s):  
Marlene C. Gerner ◽  
Andrea Bileck ◽  
Lukas Janker ◽  
Liesa S. Ziegler ◽  
Thomas Öhlinger ◽  
...  

PEDIATRICS ◽  
1981 ◽  
Vol 68 (6) ◽  
pp. 770-774 ◽  
Author(s):  
Linda M. Sacks ◽  
David B. Schaffer ◽  
Endla K. Anday ◽  
George J. Peckham ◽  
Maria Delivoria-Papadopoulos

The relative contribution of transfusions of adult blood to the development of retrolental fibroplasia (RLF) in very low-birth-weight infants was examined. Five years of experience with the expanded use of replacement and exchange transfusions in 90 infants with birth weight ≤1,250 gm was reviewed. Twenty percent of the infants developed cicatricial RLF. Exchange transfusion was not related to development of cicatricial RLF. The incidence of RLF in infants receiving ≥130 ml of packed red blood cells per kilogram of birth weight as replacement blood transfusion (RBT) was significantly higher (42.9%) than that in infants receiving 61 to 131 ml of packed red blood cells per kilogram (15.4%) and infants receiving ≤60 ml of packed red blood cells per kilogram (0%), P < .001. The need for RBT, however, was strongly correlated (r = .85, P < .001) with increasing duration of O2 therapy. When O2 therapy was controlled for, the association between RBT and RLF did not achieve statistical significance (P = .07). The association between RBT and RLF remained significant when adjusted for duration of therapy in fractional inspired oxygen (FIO2) >0.4. Further detailed studies of large numbers of susceptible infants are warranted to assess the magnitude of the contribution of transfusions of adult blood to development of RLF.


JAMA ◽  
1976 ◽  
Vol 235 (24) ◽  
pp. 2586
Author(s):  
Alfred J. Grindon

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