Open AccessDecreased incidence of acute rejection without increased incidence of cytomegalovirus (CMV) infection in kidney transplant recipients receiving rabbit anti‐thymocyte globulin without CMV prophylaxis – a cohort single‐center study
Author(s) -
Paula Mayara Ivani,
Bowring Mary Grace,
Shaffer Ashton A.,
GaronzikWang Jacqueline,
Bessa Adrieli Barros,
Felipe Claudia Rosso,
Cristelli Marina Pontello,
Massie Allan B.,
MedinaPestana Jose,
Segev Dorry L.,
TedescoSilva Helio
Publication year - 2021
Publication title -
transplant international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.998
H-Index - 82
eISSN - 1432-2277
pISSN - 0934-0874
DOI - 10.1111/tri.13800
Subject(s) - medicine , anti thymocyte globulin , incidence (geometry) , serostatus , cytomegalovirus , gastroenterology , single center , relative risk , proportional hazards model , cohort , immunology , transplantation , confidence interval , viral load , virus , viral disease , physics , herpesviridae , optics
Summary Induction therapy with rabbit anti‐thymocyte globulin (rATG) in low‐risk kidney transplant recipients (KTR) remains controversial, given the associated increased risk of cytomegalovirus (CMV) infection. This natural experiment compared 12‐month clinical outcomes in low‐risk KTR without CMV prophylaxis (January/3/13–September/16/15) receiving no induction or a single 3 mg/kg dose of rATG. We used logistic regression to characterize delayed graft function (DGF), negative binomial to characterize length of hospital stay (LOS), and Cox regression to characterize acute rejection (AR), CMV infection, graft loss, death, and hospital readmissions. Recipients receiving 3 mg/kg rATG had an 81% lower risk of AR (aHR 0.14 0.19 0.25 , P < 0.001) but no increased rate of hospital readmissions because of infections ( 0.68 0.91 1.21 , P = 0.5). There was no association between 3 mg/kg rATG and CMV infection/disease (aHR 0.86 1.10 1.40 , P = 0.5), even when the analysis was stratified according to recipient CMV serostatus positive (aHR 0.94 1.25 1.65 , P = 0.1) and negative (aHR 0.28 0.57 1.16 , P = 0.1). There was no association between 3 mg/kg rATG and mortality (aHR 0.51 1.25 3.08 , P = 0.6), and graft loss (aHR 0.34 0.73 1.55 , P = 0.4). Among low‐risk KTR receiving no CMV pharmacological prophylaxis, 3 mg/kg rATG induction was associated with a significant reduction in the incidence of AR without an increased risk of CMV infection, regardless of recipient pretransplant CMV serostatus.