TY - JOUR
T1 - Influence of patient characteristics and immunosuppressant management on mortality in kidney transplant recipients hospitalized with coronavirus disease 2019 (COVID-19)
AU - Santeusanio, Andrew D.
AU - Menon, Madhav C.
AU - Liu, Caroline
AU - Bhansali, Arjun
AU - Patel, Niralee
AU - Mahir, Fahima
AU - Rana, Meenakshi
AU - Tedla, Fasika
AU - Mahamid, Ahmad
AU - Fenig, Yaniv
AU - Zendel, Alexey
AU - Delaney, Veronica
AU - De Boccardo, Graciela
AU - Farouk, Samira S.
AU - Sehgal, Vinita
AU - Khaim, Rafael
AU - Jacobs, Samantha E.
AU - Dunn, Dallas
AU - Sullivan, Timothy
AU - Taimur, Sarah
AU - Baneman, Emily
AU - Florman, Sander
AU - Shapiro, Ron
N1 - Funding Information:
The authors of this manuscript have no conflicts of interest to disclose. The authors did not receive any funding to assist with the completion of this research. MCM acknowledges research and salary support from NIH‐NIDDK: RO1‐DK122164.
Funding Information:
The authors of this manuscript have no conflicts of interest to disclose. The authors did not receive any funding to assist with the completion of this research. MCM acknowledges research and salary support from NIH-NIDDK: RO1-DK122164.
Publisher Copyright:
© 2021 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
PY - 2021/4
Y1 - 2021/4
N2 - The influence of patient characteristics and immunosuppression management on COVID-19 outcomes in kidney transplant recipients (KTRs) remains uncertain. We performed a single-center, retrospective review of all adult KTRs admitted to the hospital with confirmed COVID-19 between 03/15/2020 and 05/15/2020. Patients were followed from the date of admission up to 1 month following hospital discharge or study conclusion (06/15/2020). Baseline characteristics, laboratory parameters, and immunosuppression were compared between survivors and patients who died to identify predictors of mortality. 38 KTRs with a mean baseline eGFR of 52.5 ml/min/1.73 m2 were hospitalized during the review period. Maintenance immunosuppression included tacrolimus (84.2%), mycophenolate (89.5%), and corticosteroids (81.6%) in the majority of patients. Eleven patients (28.9%) died during the hospitalization. Older age (OR = 2.05; 1.04-4.04), peak D-dimer (OR = 1.20; 1.04-1.39), and peak white blood cell count (OR = 1.11; 1.02-1.21) were all associated with mortality among KTRs hospitalized for COVID-19. Increased mortality was also observed among KTRs with concomitant HIV infection (87.5% vs. 36.1%; p <.01). Conversely, immunosuppression intensity and degree of reduction following COVID-19 diagnosis were not associated with either survival or acute allograft rejection. Our findings potentially support a strategy of individualization of immunosuppression targets based on patient-specific risk factors, rather than universal immunosuppression reduction for KTRs at risk from COVID-19.
AB - The influence of patient characteristics and immunosuppression management on COVID-19 outcomes in kidney transplant recipients (KTRs) remains uncertain. We performed a single-center, retrospective review of all adult KTRs admitted to the hospital with confirmed COVID-19 between 03/15/2020 and 05/15/2020. Patients were followed from the date of admission up to 1 month following hospital discharge or study conclusion (06/15/2020). Baseline characteristics, laboratory parameters, and immunosuppression were compared between survivors and patients who died to identify predictors of mortality. 38 KTRs with a mean baseline eGFR of 52.5 ml/min/1.73 m2 were hospitalized during the review period. Maintenance immunosuppression included tacrolimus (84.2%), mycophenolate (89.5%), and corticosteroids (81.6%) in the majority of patients. Eleven patients (28.9%) died during the hospitalization. Older age (OR = 2.05; 1.04-4.04), peak D-dimer (OR = 1.20; 1.04-1.39), and peak white blood cell count (OR = 1.11; 1.02-1.21) were all associated with mortality among KTRs hospitalized for COVID-19. Increased mortality was also observed among KTRs with concomitant HIV infection (87.5% vs. 36.1%; p <.01). Conversely, immunosuppression intensity and degree of reduction following COVID-19 diagnosis were not associated with either survival or acute allograft rejection. Our findings potentially support a strategy of individualization of immunosuppression targets based on patient-specific risk factors, rather than universal immunosuppression reduction for KTRs at risk from COVID-19.
KW - COVID-19
KW - immunosuppressive agents
KW - kidney transplantation
KW - transplant recipients
UR - http://www.scopus.com/inward/record.url?scp=85100107503&partnerID=8YFLogxK
U2 - 10.1111/ctr.14221
DO - 10.1111/ctr.14221
M3 - Article
C2 - 33421213
AN - SCOPUS:85100107503
SN - 0902-0063
VL - 35
JO - Clinical Transplantation
JF - Clinical Transplantation
IS - 4
M1 - e14221
ER -