The Immunosuppressive Aspects of Blood Transfusion

1992 ◽  
Vol 7 (4) ◽  
pp. 176-188 ◽  
Author(s):  
Thomas A. Mickler ◽  
David E. Longnecker

Blood transfusion is associated with immunosuppression, although the exact etiology of the immunosuppressive effect is not fully understood. The clinical significance of the immunosuppressive effect of blood transfusion has been examined in three situations: (1) studies of renal allograft survival after renal transplantation, (2) outcome studies in patients who have had surgical resection of solid cancer tumors, and (3) studies of infection rates in postoperative patients. In each scenario, the data support the conclusion that transfusion is associated with immunosuppression as manifested by increased renal allograft survival, increased recurrence and mortality rates in patients with cancer, and increased infection rates in postoperative patients who are transfused. Not all studies demonstrate an immunosuppressive effect of transfusion. There are several possible explanations for these discrepancies. First, prognostic variables other than transfusion itself account for the outcome results in these retrospective studies. Second, the extent of immunosuppression may be influenced by the type of blood product transfused, the amount transfused, and the timing of the transfusion; these factors have not been considered in all studies. For example, whole blood has been implicated as having a greater immunosuppressive effect than packed red blood cells, and many studies have shown that more than three units of packed red blood cells are necessary to affect outcome. Controlled animal studies have tested the hypothesis that transfusions increase solid tumor growth or the risk for infection. These studies have yielded conflicting results. Nevertheless, evidence that blood transfusion influences clinical outcome mitigates that a decision to transfuse must consider both risks and benefits of a transfusion; the possible consequences of immunosuppression must be included among the risks. Use of autologous blood, erythropoietin, and, in the future, synthetic hemoglobin may lead to improved outcome in patients with certain disease processes.

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.


Blood ◽  
2006 ◽  
Vol 108 (11) ◽  
pp. 966-966
Author(s):  
David Berz ◽  
Himani Singh ◽  
Elise McCormack ◽  
Eric Mazur

Abstract Background: Optimally the necessary laboratory evaluation for the diagnosis of the underlying causes for anemia is done before blood transfusion. However, clinical and logistical demands often mandate the transfusion of packed red blood cells before all the necessary parameters are obtained. It is poorly defined which impact transfusion has on the parameters necessary for the diagnosis of the underlying anemia cause. We conducted a prospective study to investigate the effect of the transfusion of two units packed red blood cells on lactate dehydrogenase(LDH), ferritin, transferrin, haptoglobin, total iron binding capacity(TIBC), folate, cyanocobalamine(B12), hemoglobin, MCV and hematocrit by measuring those tests before and at 6, 12, 24 and 48 hrs after transfusion. Patients and Methods: We included nineteen normovolemic, not actively bleeding consecutive patients; six of whom were diagnosed with anemia of chronic disease, one MDS and twelve iron deficiency anemias. Acutely bleeding patients, patients not able to give informed consent, prisoners under hospitalization and patients younger than 18 years old were excluded. All patients received transfusion of two units of packed red blood cells. The statistical analysis was performed using a repeated measurement ANOVA algorithm. Results: The transfusion of two units of packed red blood cells did not result in a significant change of ferritin, transferrin, haptoglobin, cyanocobalamin and lactate dehydrogenase throughout the observation period. Hemoglobin, MCV and hematocrit demonstrated an early change and equilibration without significant change after the first six hours post transfusion. Serum iron levels were transiently elevated in the severely iron deficient population, but returned back to baseline after 24hrs. Folate experienced a statistically significant, persistent change in the posttransfusion period. For the first 48 hrs post transfusion the following conclusions were made: First, the diagnosis of iron deficiency or chronic disease anemia is not confounded by blood transfusion, particularly when using ferritin as the predominant diagnostic parameter. Second, the diagnosis of hemolytic anemias, using haptoglobin and LDH is not interfered by transfusion of two units of packed red blood cells. Third, vitamin B12 deficiency can be diagnosed after transfusion, whilst folate deficiency on the base of red blood cell folate cannot.


2011 ◽  
Author(s):  
Arturo J Martí-Carvajal ◽  
Daniel Simancas ◽  
Ricardo Hidalgo

2013 ◽  
Vol 28 (2) ◽  
pp. 183-189
Author(s):  
Leonardo Leiria de Moura da Silva ◽  
Anna Júlia de Borba Andres ◽  
Roberta Senger ◽  
Ralf Stuermer ◽  
Maria Celoni de Mello de Godoy ◽  
...  

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