Avoidance of cellular blood product transfusions in LVAD recipients does not prevent HLA allosensitization

Citation
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
Citations number
17
Categorie Soggetti
Cardiovascular & Respiratory Systems
Journal title
JOURNAL OF HEART AND LUNG TRANSPLANTATION
ISSN journal
10532498 → ACNP
Volume
18
Issue
2
Year of publication
1999
Pages
160 - 165
Database
ISI
SICI code
1053-2498(199902)18:2<160:AOCBPT>2.0.ZU;2-Y
Abstract
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.