Publications by authors named "J A Oud"

Article Synopsis
  • The study explores the connection between red blood cell autoimmunity and alloimmunity in transfused patients, focusing on the incidence of red blood cell alloimmunisation in those with a positive direct antiglobulin test (DAT).
  • Among 47,285 patients analyzed, those with a positive DAT had a cumulative alloimmunisation incidence of 4.5% after receiving 10 transfusions, which was statistically similar to the 4.2% incidence in the control group.
  • The findings suggest that while DAT-positive patients may have a higher risk of red blood cell immune responses, their overall risk is not significantly higher than that of control patients, indicating that more extensive matching for transfusions may not be necessary in these cases.
View Article and Find Full Text PDF

Maternal alloantibodies directed against fetal red blood cell (RBC) antigens may cause potentially life-threatening haemolytic disease of the fetus and newborn (HDFN). Dutch transfusion guidelines therefore prescribe preventive cEK matching for all (pre-)fertile females. To quantify the impact of cEK matching, we compared overall and antigen-specific cumulative RBC alloimmunisation incidences in females and males aged <45 years.

View Article and Find Full Text PDF

Background: Renal failure and renal replacement therapy (RRT) affect the immune system and could therefore modulate red blood cell (RBC) alloimmunization after transfusion.

Study Design And Methods: We performed a nationwide multicenter case-control study within a source population of newly transfused patients between 2005 and 2015. Using conditional multivariate logistic regression, we compared first-time transfusion-induced RBC alloantibody formers (N = 505) with two nonalloimmunized recipients with similar transfusion burden (N = 1010).

View Article and Find Full Text PDF

Unlabelled: Essentials Substitution therapy for von Willebrand (VW) disease leaves mutant VW factor (VWF) unhindered. Presence of mutant VWF may negatively affect phenotypes despite treatment. Inhibition of VWF by allele-specific siRNAs targeting single-nucleotide polymorphisms is effective.

View Article and Find Full Text PDF