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Reports indicate an increased mortality risk for solid organ transplant recipients with COVID-19 [1, 2], which may have been influenced by clinical decision making (triage) during the early phase of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic. In Germany, relatively few transplant recipients were infected, and the capacity of the healthcare system was at no point in time overwhelmed. Hereby, high capacity PCR testing including all potential organ donors, symptomatic organ recipients or other patients, as well as a relatively high number of hospitals with intensive care units (1248) and transplant centers (40) with high capacities allowed a completely unimpaired organ procurement and transplantation situation throughout the first wave of the pandemic despite having SARS-CoV-2 infection rates of app. 2200 per million persons at the end of May 2020. Our data lead to a different assessment of the risk associated with COVID-19 after organ transplantation. In organ recipients, transplantation was performed more than 1 year ago in over 80%. Calcineurin inhibitor-based immunosuppression was administered in 71.7%, mycophenolate acid/mofetil was given in 63.4%, mTOR inhibitors were given in 10.9%, and corticosteroid maintenance therapy was given in 63%. No transplant recipient received a T-cell depleting treatment, and B-cell depleting agents were administered in one patient. Two patients received a steroid bolus within the last six months before COVID-19 diagnosis. None of the patients were treated with remdesivir or with reconvalescent patient plasma. A matched-pair analysis (1:30) of 46 transplant recipients with 1380 controls without transplantation within one registry (LEOSS) was performed. With the exception of chronic kidney disease, which was more frequent in the transplant patient group, known COVID-19 risk factors such as age, gender and comorbidities [3-5] were closely matched with controls (Table 1). Multivariable conditional logistic regression failed to identify organ transplantation as a risk factor for mortality (OR 0.27, 95% CI 0.12–1.25); the proportion of people who survived was comparable in transplant recipients (91.3%) and the control population (82.5%). Similarly, immunosuppressant administration was also not associated with an increased mortality risk in this combined cohort of transplant and control patients with COVID-19. To expand on this observation, sensitivity analyses were performed on 153 immunosuppressed patients, excluding individuals with organ transplantation, and compared to a cohort matched at a ratio of 1:10 characterized by the identical risk factors. Mortality was found to be independent of the chronic use of immunosuppressive therapy at the time of COVID-19 diagnosis. While the relatively small number of transplant patients is a limitation of this study, the major result appeared to be robust also with other matching ratios (1:10 or 1:20). Expectedly, the overall need for mechanical ventilation, late presentation in complicated or critical clinical phase, and lymphocyte counts below 500/µl were identified as risk factors for increased mortality. In conclusion, while clinical condition and severe lymphopenia at the time of COVID-19 diagnosis were confirmed as relevant risk factors for an unfavorable outcome, prior solid organ transplantation was not shown to have an adverse effect on mortality in comparison with a matched COVID-19 reference population.
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Hugo et al. (2020) studied this question.
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