Jc. Stringham et al., Avoidance of cellular blood product transfusions in LVAD recipients does not prevent HLA allosensitization, J HEART LUN, 18(2), 1999, pp. 160-165
Background: Transfusion of cellular blood products during left ventricular
assist device (LVAD) implantation has been associated with HLA allosensitiz
ation, resulting in the need for a negative prospective cross-match and pro
longed transplant waiting times. In order to prevent this risk, we develope
d a protocol to avoid transfusion of cellular blood products.
Methods: The protocol included preoperative patient stabilization, perioper
ative recombinant erythropoietin and blood conservation strategies, and pos
toperative monitoring of mixed venous oxygen saturation (SVO2) to assure ad
equate peripheral oxygen delivery. Panel reactive antibody (PRA) was measur
ed in all patients pre and post LVAD placement to assess KLA sensitization.
Results: Seven consecutive patients underwent LVAD implantation without tra
nsfusion of blood or platelets, one of-whom expired perioperatively. Mean h
ematocrit was 35.2% preoperatively, and 21.8% postoperatively, reaching a n
adir of 20.2%. postoperative SVO2 was >60% in all patients. In the six surv
ivors, mean hematocrit reach 24.3%, 27.3%, and 33.0% by postoperative day s
even, fourteen, and thirty, respectively. PRA in three patients was 0% preo
peratively and remained 0% until transplantation after 33, 34, and 50 days
of support. In two patients, preoperative PRA was 7% and 17%, dropped to 3%
and 0% after thirty days, then progressively rose to 96% and 100% after 60
and 90 days, respectively. In one other patient, preoperative PRA was 0%,
remained at 0% after thirty days, then rose to 96%, by 60 days.
Conclusions: Avoiding transfusion of cellular blood products in LVAD recipi
ents is safe and well tolerated, but does not universally protect from HLA
allosensitization. Other factors may also produce sensitization, such as im
munogenic components of the LVAD, soluble antigen in fresh frozen plasma, o
r latent sensitization which is not initially evident in critically ill and
possibly anergic patients.