The administration of intravenous immunoglobulin (IVIG) in immune and
autoimmune diseases led us to use this agent to ameliorate or prevent
the consequences of non-ABO incompatible transfusions in patients who
need this form of therapy. IVIG (400 mg/kg/day) was infused within 24
h of transfusion in 5 patients with: (1) intestinal angiodysplasia, ga
strointestinal bleeding, and anti-Kp(b); (2) paroxysmal nocturnal hemo
globinuria, anti-c, anti E, Anti Fy(b), anti-K and autoantibodies; (3)
lymphoma and autoimmune hemolytic anemia (AIHA); (4) systemic lupus e
rythematosus (SLE), AIHA, and anti-D, and (5) SLE and AHIA. A sustaine
d increase in hematocrit was noted and no transfusion reaction develop
ed in any of the cases. A single dose of pretransfusion IVIG may there
fore be a useful therapeutic alternative in patients for whom no compa
tible blood is available. Patients with severe anemia, allo- and autoa
ntibodies, either showing hemolysis in their pathophysiology or not, c
ause a serious problem in any transfusion center, especially when deal
ing with emergencies. In order to reduce the risks of incompatible tra
nsfusions, different modalities have previously been attempted, all wi
th poor results. In 1989 we reported the successful use of pretransfus
ional high-dose intravenous immunoglobulin (IVIG) in a patient with ga
strointestinal bleeding and anti-Kp(b) [19]. The transfusion of incomp
atible red blood cells improved the anemia and allowed the exploratory
laparotomy to take place. A protocol was then developed based on this
case administering pretransfusion IVIG in high doses for patients for
whom no compatible blood (non-ABO) is available.