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Severe COVID‐19 in a renal transplant recipient: A focus on pharmacokinetics
Author(s) -
Meziyerh Soufian,
Zwart Tom C.,
Etten Ronald W.,
Janson Jeroen A.,
Gelder Teun,
Alwayn Ian P. J.,
Fijter Johan W.,
Reinders Marlies E. J.,
Moes Dirk J. A. R.,
Vries Aiko P. J.
Publication year - 2020
Publication title -
american journal of transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.89
H-Index - 188
eISSN - 1600-6143
pISSN - 1600-6135
DOI - 10.1111/ajt.15943
Subject(s) - medicine , lopinavir , ritonavir , intensive care medicine , pneumonia , transplantation , everolimus , viral pneumonia , lopinavir/ritonavir , transplant rejection , pharmacotherapy , kidney transplantation , covid-19 , disease , immunology , viral load , infectious disease (medical specialty) , antiretroviral therapy , human immunodeficiency virus (hiv)
The current coronavirus disease 2019 (COVID‐19) pandemic requires extra attention for immunocompromised patients, including solid organ transplant recipients. We report on a case of a 35‐year‐old renal transplant recipient who suffered from a severe COVID‐19 pneumonia. The clinical course was complicated by extreme overexposure to the mammalian target of rapamycin inhibitor everolimus, following coadministration of chloroquine and lopinavir/ritonavir therapy. The case is illustrative for dilemmas that transplant professionals may face in the absence of evidence‐based COVID‐19 therapy and concurrent pressure for exploration of experimental pharmacological treatment options. However, the risk‐benefit balance of experimental or off‐label therapy may be weighed differently in organ transplant recipients than in otherwise healthy COVID‐19 patients, owing to their immunocompromised status and potential drug interactions with immunosuppressive therapy. With this case report, we aimed to achieve increased awareness and improved management of drug‐drug interactions associated with the various treatment options for COVID‐19 in renal transplant patients.