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Background: The new kidney allocation systems (KAS) instituted December 2014 permitted A2 to B deceased donor kidney transplantation (DDKTx) to improve access and reduce disparities in wait time for minorities. A recent United Network for Organ Sharing (UNOS) analysis, however, indicated only 4.5% of B candidates were registered for A2 kidneys. Cited barriers to A2 to B DDKTx include titer thresholds, patient eligibility, and increased costs. There are little published data on post-transplantation anti-A titers or outcomes of A2 to B DDKTx since this allocation change.
Study Design: We conducted a retrospective, single center, cohort analysis of 29 consecutive A2 to B and 50 B to B DDKTx from December 2014 to December 2017. Pre- and postoperative anti-A titers were monitored prospectively. Outcomes included post-transplant anti-A titers, patient and graft survival, renal function, and hospital costs.
Results: African Americans comprised 72% of the A2 to B and 60% of the B to B group. There was no difference in mean wait time (58.8 vs 70.8 months). Paired tests indicated that anti-A IgG titers in A2 to B DDKTx were increased at discharge (p = 0.001) and at 4 weeks (p = 0.037). There were no significant differences in patient or graft survival, serum creatinine (SCr), or estimated glomerular filtration rate (eGFR), but the trajectories of SCr and eGFR differed between groups over the follow-up period. A2 to B had significantly higher mean transplant total hospital costs ($114,638 vs $91,697, p < 0.001) and hospital costs net organ acquisition costs ($42,356 vs $20,983, p < 0.001).
Conclusions: Initial experience under KAS shows comparable outcomes for A2 to B vs B to B DDKTx. Anti-A titers increased significantly post-transplantation, but did not adversely affect outcomes. Hospital costs were significantly higher with A2 to B DDKTx. Transplant programs, regulators, and payors will need to weigh improved access for minorities with increased costs.
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http://dx.doi.org/10.1016/j.jamcollsurg.2018.12.023 | DOI Listing |
J Heart Lung Transplant
August 2025
Department of Cardiothoracic Transplantation, Great Ormond Street Hospital, London, UK. Electronic address:
Background And Aims: Pediatric heart transplantation remains hampered by the limited availability of donor organs. The introduction of ABO-incompatible (ABOi) heart transplantation for infants in the early 2000s expanded the donor pool for individual candidates. Nonetheless, concerns remain about ABOi heart transplantation in children aged over 2 years, and it has not been routinely adopted.
View Article and Find Full Text PDFAsian J Transfus Sci
December 2022
Department of Paediatrics and Neonatology, Pondicherry Institute of Medical Sciences, Puducherry, India.
Background: Hemolytic disease of the newborn (HDN) was more common due to Rh incompatibility. Its prevalence has decreased due to introduction of Immunoglobulin G (IgG) prophylaxis against RhD antigen. HDN due to ABO incompatibility has become more common.
View Article and Find Full Text PDFBackground: ABO antibodies can activate complement and cause hemolysis, sometimes with ABO minor incompatible platelet or plasma transfusions. Donor low titres of anti-ABO are used to assess transfusion safety. However, the correlation between antibody titres (measured semi-quantitatively or quantitatively) and their ability to activate complement is unclear.
View Article and Find Full Text PDFBlood Transfus
June 2025
Department of Clinical Immunology and Transfusion Medicine, Office of Medical Services, Region Skåne, Lund, Sweden.
Background: This systematic review aims to determine the loads of anti-A and anti-B in plasma-containing blood products that can safely be transfused to adults.
Materials And Methods: A comprehensive literature search was performed in PubMed, including studies dating back to 1940 until January 1, 2023. In total 1,869 articles were screened, describing 86 cases of hemolytic transfusion reactions (HTR) due to anti-A and/or anti-B in ABO incompatible products.
Transfus Apher Sci
August 2025
Department of Transfusion Medicine, Government Medical College and Hospital, Chandigarh, India.
Background: Maternal IgG anti-A and anti-B isoagglutinin titers are key predictors of neonatal outcomes in ABO incompatibility-related hemolytic disease of the fetus and new-born (HDFN). This study aimed to compare the Column Agglutination Technique (CAT) and conventional tube technique (CTT) in measuring maternal IgG anti-A and anti-B isoagglutinin titers and assess their correlation with neonatal outcomes.
Material And Methods: This prospective observational study included 125 O Rh-D positive pregnant mothers and their neonates with A, or B blood groups.