13 results match your criteria: "Sanquin-LUMC Jon J. Van Rood Center for Clinical Transfusion Research[Affiliation]"
Intensive Care Med Exp
July 2024
Department of Intensive Care Medicine, Leiden University Medical Center, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
Haematologica
August 2024
Department of Clinical Epidemiology, Leiden University Medical Center, Leiden.
Previous studies found exposure to red blood cell transfusions from female donors who have been pregnant reduces survival in male patients compared to exposure to male donor products, but evidence is not consistent. We postulate the previously observed association is modified by offspring sex, with an expected increased mortality risk for male patients receiving units from female donors with sons. Here, marginal structural models were used to assess the association between exposure to units from ever-pregnant donors, ever-pregnant donors with sons and ever-pregnant donors with daughters, and mortality.
View Article and Find Full Text PDFVox Sang
January 2024
Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands.
Background And Objectives: Donor characteristics have been implicated in transfusion-related adverse events. Uncertainty remains about whether sex, and specifically pregnancy history of the blood donor, could affect patient outcomes. Whether storage duration of the blood product could be important for patient outcomes has also been investigated, and a small detrimental effect of fresh products remains a possibility.
View Article and Find Full Text PDFArq Bras Cardiol
September 2023
Department of Clinical Epidemiology, Leiden University Medical Center, Leiden - Países Baixos.
Background: The mortality rate of Brazilian people with haemophilia (PwH) is decreasing, but the relative incidence of deaths associated with cardiovascular disease (CVD) is increasing.
Objectives: We aimed to describe the CVD risk score of PwH according to Pooled Cohort Equations Risk (PCER) Calculator tool and its treatment recommendations. We also compared the PCER estimates with the respective Framingham Risk Score (FRS).
Transfusion
September 2021
Jon J van Rood Center for Clinical Transfusion Research, Sanquin/LUMC, Leiden, The Netherlands.
Background: Prophylactic platelet transfusions prevent bleeding in hemato-oncology patients, but it is unclear how any benefit varies between patients. Our aim was to assess if patients with different baseline risks for bleeding benefit differently from a prophylactic platelet transfusion strategy.
Study Design And Methods: Using the data from the randomized controlled TOPPS trial (Trial of Platelet Prophylaxis), we developed a prediction model for World Health Organization grades 2, 3, and 4 bleeding risk (defined as at least one bleeding episode in a 30 days period) and grouped patients in four risk-quartiles based on this predicted baseline risk.
BMJ Open
June 2020
Jon J van Rood Center for Clinical Transfusion Research, Sanquin/LUMC, Leiden, The Netherlands
Introduction: Haemato-oncological patients often receive platelet count driven prophylactic platelet transfusions to prevent bleeding. However, many prophylactically transfused patients still bleed. More knowledge on risk factors for bleeding is therefore needed.
View Article and Find Full Text PDFVox Sang
July 2017
Department of Hemotherapy and Hemostasis, University Clinic Hospital, Villaroel 170, Barcelona, 08036, Spain.
Background: More women than men are encountered with red blood cell (RBC) antibodies. It is not clear whether this difference is explained by more immunizing events in women or by a different acting immune system. To assess whether there is a difference in the posttransfusion RBC alloimmunization rate between women and men, a study on RBC alloimmunization during a 5-year period was conducted in patients with at least one antibody follow-up more than 14 days after transfusion.
View Article and Find Full Text PDFBlood Transfus
January 2014
Donor Services Unit, Sanquin Blood Supply, Rotterdam, The Netherlands Department Donor Studies, Sanquin Blood Supply, Nijmegen, The Netherlands.
Background: First-time donation is among recognised risk factors for vasovagal reactions to blood donation and reactions are known to reduce donor return. We assessed associations between potential risk factors and vasovagal reactions and needle-related complications in first-time whole blood donation in comparison to repeat donation and analysed the impact of complications on donor return.
Materials And Methods: We performed a cohort study on whole blood donations in The Netherlands from 1/1/2010 to 31/12/2010 using data extracted from the blood service information system.
Transfusion
December 2013
Sanquin-LUMC Jon J. van Rood Center for Clinical Transfusion Research, Leiden, the Netherlands; Sanquin Blood Supply Foundation, Amsterdam, the Netherlands; Department of Pediatrics, Division of Neonatology, Beatrix Children's Hospital, University Medical Center, Groningen, the Netherlands; Department of Pediatrics, Division of Neonatology, Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, the Netherlands; Department of Pediatrics, Division of Neonatology, Sophia Children's Hospital, Erasmus Medical Center, Rotterdam, the Netherlands.
Background: In the Netherlands different platelet (PLT) products are used for neonatal transfusions: volume-reduced PLTs, PLT additive solution (PAS) II PLTs, and plasma PLTs. These are standard products at three different neonatal intensive care units where local transfusion guidelines apply. Here we assess the posttransfusion count increments with these products.
View Article and Find Full Text PDFTransfusion
May 2013
Sanquin-LUMC Jon J. van Rood Center for Clinical Transfusion Research and the Department of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, the Netherlands.
Background: Women whose fetuses were treated with intrauterine transfusions (IUTs) for alloimmune hemolytic disease are high responders to red blood cell (RBC) antigens. We investigated the risk for HLA alloimmunization.
Study Design And Methods: Women and their children treated with IUT between 1987 and 2008 were included.
Introduction: Individuals exposed to red blood cell alloantigens through transfusion, pregnancy or transplantation may produce antibodies against the alloantigens. Alloantibodies can pose serious clinical problems such as delayed haemolytic reactions and logistic problems, for example, to obtain timely and properly matched transfusion blood for patients in which new alloantibodies are detected.
Objective: The authors hypothesise that the particular clinical conditions (eg, used medication, concomitant infection, cellular immunity) during which transfusions are given may contribute to the risk of immunisation.
Transfus Med Rev
October 2012
Sanquin-LUMC, Jon J van Rood Center for Clinical Transfusion Research, Leiden, The Netherlands.