Background: Kidney transplant candidates may be incompatible with their intended living donors because of the presence of antibodies against HLA and/or ABO. To increase the possibility of finding an acceptable kidney donor for these patients, the Scandiatransplant Exchange Program (STEP) program within Scandiatransplant was launched in 2019.
Methods: This is a retrospective review of our experiences from the first 4 y of the STEP program, including details about the match runs, performed transplantations, and recipient outcomes within the program.
Results: During 2019-2022, 11 match runs and 4 reruns were performed. In total, 114 pairs and 6 anonymous donors participated in these match runs. Fifty-one pairs (45%) participated in 1 match run, 31 pairs (27%) participated in 2 match runs, and 32 pairs (29%) participated in ≥3 match runs. Seventy-two individuals (63%) participated because of HLA incompatibility, 19 (17%) because of ABO incompatibility, and 7 (6%) because of both HLA and ABO incompatibility.Forty percent of the patients enrolled in the program underwent transplantation. In total, 49 transplantations have so far been performed within the program, and 46 (94%) of the recipients had a functioning kidney graft at follow-up in February 2023.
Conclusions: The STEP program offers sensitized patients an enlarged pool of living donors and a chance of a compatible international living donor, resulting in an increased number of total transplantations. Currently, STEP is one of the largest transnational kidney exchange programs and has improved the situation for patients waiting for kidney transplantation in Scandiatransplant.
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http://dx.doi.org/10.1097/TXD.0000000000001549 | DOI Listing |
Mol Cell Proteomics
December 2024
Department of Chemistry & Biochemistry, University of Maryland, College Park, MD 20742. Electronic address:
Detection of trace-sensitive signals is a current challenge in single-cell mass spectrometry (MS) proteomics. Separation prior to detection improves the fidelity and depth of proteome identification and quantification. We recently recognized capillary electrophoresis (CE) electrospray ionization (ESI) for ordering peptides into mass-to-charge (m/z)-dependent series, introducing electrophoresis-correlative (Eco) data-independent acquisition.
View Article and Find Full Text PDFEur J Sport Sci
December 2024
Department of Exercise and Sport Science, LUNEX, Differdange, Luxembourg.
Active breaks are suggested to support recovery and performance in sports. Previous research in ball and team sports focused on motor performance such as repetitive sprinting or change of direction. This does not account for the interaction between motor and cognitive task demands in sports.
View Article and Find Full Text PDFAnn Work Expo Health
November 2024
Division of Preventive Medicine, University of Alberta, 8303 112 St, Edmonton, Alberta, T6G 2T4, Canada.
Quantitative analysis of proteomics data frequently employs peptide-identity-propagation (PIP) - also known as match-between-runs (MBR) - to increase the number of peptides quantified in a given LC-MS/MS experiment. PIP can routinely account for up to 40% of all quantitative results, with that proportion rising as high as 75% in single-cell proteomics. Therefore, a significant concern for any PIP method is the possibility of false discoveries: errors that result in peptides being quantified incorrectly.
View Article and Find Full Text PDFNat Commun
November 2024
Advanced Research Centre, University of Glasgow, 11 Chapel Lane, Glasgow, UK.
Despite recent proliferation of programmable robotic chemistry hardware, current chemical programming ontologies lack essential structured programming constructs like variables, functions, and loops. Herein we present an integration of these concepts into χDL, a universal high-level chemical programming language executable in the Chemputer. To achieve this, we introduce reaction blueprints as a chemical analog to functions in computer science, allowing to apply sets of synthesis operations to different reagents and conditions.
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