<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>28(12)</volume><submitter>Oberkofler CE</submitter><pubmed_abstract>This study investigated the effect of low-dose aspirin in primary adult liver transplantation (LT) on acute cellular rejection (ACR) as well as arterial patency rates. The use of low-dose aspirin after LT is practiced by many transplant centers to minimize the risk of hepatic artery thrombosis (HAT), although solid recommendations do not exist. However, aspirin also possesses potent anti-inflammatory properties and might mitigate inflammatory processes after LT, such as rejection. Therefore, we hypothesized that the use of aspirin after LT has a protective effect against ACR. This is an international, multicenter cohort study of primary adult deceased donor LT. The study included 17 high-volume LT centers and covered the 3-year period from 2013 to 2015 to allow a minimum 5-year follow-up. </pubmed_abstract><journal>Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society</journal><pagination>1888-1898</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9804747</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Low-dose aspirin confers protection against acute cellular allograft rejection after primary liver transplantation.</pubmed_title><pmcid>PMC9804747</pmcid><pubmed_authors>Busuttil RW</pubmed_authors><pubmed_authors>Kirchner V</pubmed_authors><pubmed_authors>Ito T</pubmed_authors><pubmed_authors>Mehrabi A</pubmed_authors><pubmed_authors>Schlegel A</pubmed_authors><pubmed_authors>Clavien PA</pubmed_authors><pubmed_authors>Petrowsky H</pubmed_authors><pubmed_authors>Paladini J</pubmed_authors><pubmed_authors>Oberkofler CE</pubmed_authors><pubmed_authors>Marques HP</pubmed_authors><pubmed_authors>Bauldrick F</pubmed_authors><pubmed_authors>Muller PC</pubmed_authors><pubmed_authors>Tabrizian P</pubmed_authors><pubmed_authors>Lehmann K</pubmed_authors><pubmed_authors>Alford S</pubmed_authors><pubmed_authors>Rana A</pubmed_authors><pubmed_authors>Ghamarnedjad O</pubmed_authors><pubmed_authors>Contreras A</pubmed_authors><pubmed_authors>Maglione M</pubmed_authors><pubmed_authors>Johnson B</pubmed_authors><pubmed_authors>Lodge P</pubmed_authors><pubmed_authors>Florman S</pubmed_authors><pubmed_authors>Selzner M</pubmed_authors><pubmed_authors>Kron P</pubmed_authors><pubmed_authors>Parente A</pubmed_authors><pubmed_authors>Fernandes ESM</pubmed_authors><pubmed_authors>Raptis DA</pubmed_authors><pubmed_authors>Peralta P</pubmed_authors><pubmed_authors>Chavez-Villa M</pubmed_authors><pubmed_authors>Kaldas FM</pubmed_authors><pubmed_authors>Dutkowski P</pubmed_authors><pubmed_authors>Owen T</pubmed_authors><pubmed_authors>Jaklitsch M</pubmed_authors><pubmed_authors>Basto ST</pubmed_authors><pubmed_authors>Winter E</pubmed_authors><pubmed_authors>Di Benedetto F</pubmed_authors><pubmed_authors>Pollok JM</pubmed_authors><pubmed_authors>Fodor M</pubmed_authors><pubmed_authors>Halazun KJ</pubmed_authors><pubmed_authors>Sousa da Silva RX</pubmed_authors><pubmed_authors>de Santibanes M</pubmed_authors><pubmed_authors>Magistri P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Low-dose aspirin confers protection against acute cellular allograft rejection after primary liver transplantation.</name><description>This study investigated the effect of low-dose aspirin in primary adult liver transplantation (LT) on acute cellular rejection (ACR) as well as arterial patency rates. The use of low-dose aspirin after LT is practiced by many transplant centers to minimize the risk of hepatic artery thrombosis (HAT), although solid recommendations do not exist. However, aspirin also possesses potent anti-inflammatory properties and might mitigate inflammatory processes after LT, such as rejection. Therefore, we hypothesized that the use of aspirin after LT has a protective effect against ACR. This is an international, multicenter cohort study of primary adult deceased donor LT. The study included 17 high-volume LT centers and covered the 3-year period from 2013 to 2015 to allow a minimum 5-year follow-up. </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2026-05-28T03:41:36.098Z</modification><creation>2025-04-04T20:21:06.367Z</creation></dates><accession>S-EPMC9804747</accession><cross_references><pubmed>35735232</pubmed><doi>10.1002/lt.26534</doi></cross_references></HashMap>