TY - JOUR
T1 - Quantifying infection risks in incompatible living donor kidney transplant recipients
AU - Avery, Robin K.
AU - Motter, Jennifer D.
AU - Jackson, Kyle R.
AU - Montgomery, Robert A.
AU - Massie, Allan B.
AU - Kraus, Edward S.
AU - Marr, Kieren A.
AU - Lonze, Bonnie E.
AU - Alachkar, Nada
AU - Holechek, Mary J.
AU - Ostrander, Darin
AU - Desai, Niraj
AU - Waldram, Madeleine M.
AU - Shoham, Shmuel
AU - Steinke, Seema Mehta
AU - Subramanian, Aruna
AU - Hiller, Janet M.
AU - Langlee, Julie
AU - Young, Sheila
AU - Segev, Dorry L.
AU - Garonzik Wang, Jacqueline M.
N1 - Publisher Copyright:
© 2020 The Authors. American Journal of Transplantation published by Wiley Periodicals LLC on behalf of The American Society of Transplantation and the American Society of Transplant Surgeons
PY - 2021/4
Y1 - 2021/4
N2 - Desensitization has enabled incompatible living donor kidney transplantation (ILDKT) across HLA/ABO barriers, but added immunomodulation might put patients at increased risk of infections. We studied 475 recipients from our center from 2010 to 2015, categorized by desensitization intensity: none/compatible (n = 260), low (0-4 plasmaphereses, n = 47), moderate (5-9, n = 74), and high (≥10, n = 94). The 1-year cumulative incidence of infection was 50.1%, 49.8%, 66.0%, and 73.5% for recipients who received none, low, moderate, and high-intensity desensitization (P <.001). The most common infections were UTI (33.5% of ILDKT vs. 21.5% compatible), opportunistic (21.9% vs. 10.8%), and bloodstream (19.1% vs. 5.4%) (P <.001). In weighted models, a trend toward increased risk was seen in low (wIRR = 0.771.402.56,P =.3) and moderately (wIRR = 0.881.352.06,P =.2) desensitized recipients, with a statistically significant 2.22-fold (wIRR = 1.332.223.72,P =.002) increased risk in highly desensitized recipients. Recipients with ≥4 infections were at higher risk of prolonged hospitalization (wIRR = 2.623.574.88, P <.001) and death-censored graft loss (wHR = 1.154.0113.95,P =.03). Post–KT infections are more common in desensitized ILDKT recipients. A subset of highly desensitized patients is at ultra-high risk for infections. Strategies should be designed to protect patients from the morbidity of recurrent infections, and to extend the survival benefit of ILDKT across the spectrum of recipients.
AB - Desensitization has enabled incompatible living donor kidney transplantation (ILDKT) across HLA/ABO barriers, but added immunomodulation might put patients at increased risk of infections. We studied 475 recipients from our center from 2010 to 2015, categorized by desensitization intensity: none/compatible (n = 260), low (0-4 plasmaphereses, n = 47), moderate (5-9, n = 74), and high (≥10, n = 94). The 1-year cumulative incidence of infection was 50.1%, 49.8%, 66.0%, and 73.5% for recipients who received none, low, moderate, and high-intensity desensitization (P <.001). The most common infections were UTI (33.5% of ILDKT vs. 21.5% compatible), opportunistic (21.9% vs. 10.8%), and bloodstream (19.1% vs. 5.4%) (P <.001). In weighted models, a trend toward increased risk was seen in low (wIRR = 0.771.402.56,P =.3) and moderately (wIRR = 0.881.352.06,P =.2) desensitized recipients, with a statistically significant 2.22-fold (wIRR = 1.332.223.72,P =.002) increased risk in highly desensitized recipients. Recipients with ≥4 infections were at higher risk of prolonged hospitalization (wIRR = 2.623.574.88, P <.001) and death-censored graft loss (wHR = 1.154.0113.95,P =.03). Post–KT infections are more common in desensitized ILDKT recipients. A subset of highly desensitized patients is at ultra-high risk for infections. Strategies should be designed to protect patients from the morbidity of recurrent infections, and to extend the survival benefit of ILDKT across the spectrum of recipients.
KW - clinical research / practice
KW - desensitization
KW - infection and infectious agents
KW - infectious disease
KW - kidney transplantation / nephrology
KW - kidney transplantation: living donor
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U2 - 10.1111/ajt.16316
DO - 10.1111/ajt.16316
M3 - Article
C2 - 32949093
AN - SCOPUS:85093671362
SN - 1600-6135
VL - 21
SP - 1564
EP - 1575
JO - American Journal of Transplantation
JF - American Journal of Transplantation
IS - 4
ER -