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Murine Corneal Transplantation: A Model to Study the Most Common Form of Solid Organ Transplantation
Published on: November 17, 2014
Coronavirus Disease 2019 (COVID-19) in Solid Organ Transplant Recipients: A Case-Control Study
Alejandro Muñoz Serrano1, Ana Arias2, Víctor Moreno-Torres1
1Department of Internal Medicine, Hospital Universitario Puerta de Hierro-Majadahonda, Majadahonda, Spain.
Insights
Solid organ transplant (SOT) recipients with COVID-19 had higher in-hospital mortality than non-SOT patients. This increased risk was likely due to greater underlying comorbidities, not immunosuppression.
Area of Science:
- Immunology
- Infectious Diseases
- Transplant Medicine
Background:
- The clinical outcomes of coronavirus disease 2019 (COVID-19) in solid organ transplant (SOT) recipients compared to the general population remain unclear.
- Understanding COVID-19 severity and mortality in SOT patients is crucial for clinical management and public health strategies.
Purpose of the Study:
- To compare the severity and in-hospital mortality rates of COVID-19 between SOT recipients and non-SOT individuals.
- To identify factors contributing to adverse outcomes in SOT patients hospitalized with COVID-19.
Main Methods:
- A case-control study involving 32 SOT recipients and 84 matched non-SOT controls admitted with confirmed COVID-19.
- Primary endpoint: in-hospital all-cause mortality. Secondary endpoints included severe acute respiratory distress syndrome (ARDS), oxygen therapy needs, and hospital stay duration.
- Charlson Comorbidity Index (CCI) was used to assess baseline health status.
Main Results:
- SOT recipients exhibited a significantly higher median Charlson Comorbidity Index (CCI) at admission (6 vs 3, P<0.01).
- In-hospital all-cause mortality was significantly higher in SOT recipients (21.9% vs 4.7%, P<0.01).
- Despite higher mortality, rates of severe ARDS and length of hospital stay were similar between groups.
Conclusions:
- Hospitalized SOT recipients with COVID-19 experienced higher in-hospital mortality compared to non-SOT patients.
- The increased mortality risk in SOT patients appears primarily associated with a greater burden of underlying comorbidities, rather than chronic immunosuppression.
- Further research is needed to elucidate specific management strategies for COVID-19 in immunocompromised transplant populations.
Abstract:
BACKGROUND It is unclear whether solid organ transplant (SOT) patients have more severe coronavirus disease 2019 (COVID-19) and worse outcome than the general population. MATERIAL AND METHODS We conducted a case-control study on 32 SOT recipients and 84 non-SOT controls matched for age and sex admitted for confirmed COVID-19. The primary endpoint was in-hospital all-cause mortality rate. Secondary endpoints included severe acute respiratory distress syndrome (ARDS), use of high-flow oxygen therapy, and length of hospital stay. RESULTS The median (IQR) Charlson comorbidity index (CCI) at admission was significantly higher in SOT recipients (6 (3-8) vs 3 (2-4); P<0.01). Fever was less frequent in SOT recipients (78% vs 94%, P=0.01). SOT recipients had a higher median SaO2/FiO2 at admission (452 [443-462] vs 443 [419-452], P<0.01) and reached the worst SaO2/FiO2 value later during hospitalization 15 (10-21) vs 11 (9-14) days, P=0.01). Both groups had a similar severe ARDS rate during hospitalization (33% vs 28%) (p=0.59). There were no significant differences during hospitalization in terms of highest level of respiratory support needed, or length of hospital stay: 8.5 (5.5-21) vs 11.5 (6.5-16.5) days; P=0.34) in SOT recipients when compared to controls. In-hospital all-cause mortality rates were significantly higher in SOT recipients (21.9% vs 4.7%, P<0.01; OR 1.08; 95% CI 0.10-10.98), but among patients who died, median CCI was similar between groups (8 [6-8] vs 7 [6-8]). CONCLUSIONS In our experience, hospitalized SOT recipients for COVID-19 had higher in-hospital mortality compared to non-SOT patients, probably due to the greater number of underlying comorbidities, and not directly related to chronic immunosuppression.
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