Prognosis of patients with a history of organ transplantation during active COVID-19 infection.

Prognosis of patients with a history of organ transplantation during active COVID-19 infection.

Publication date: Dec 12, 2025

Solid organ transplant recipients were among the most vulnerable groups during the COVID-19 pandemic. Chronic immunosuppression and multiple comorbidities greatly increase the risk of severe illness and death. Despite global advances in vaccination and treatment, practical tools for early risk assessment in this group are still limited. This study aims to address this gap by identifying simple, widely available laboratory markers that can be used upon hospital admission to predict short-term outcomes in COVID-19 patients with a history of organ transplantation. We retrospectively analyzed a cohort of solid organ transplant recipients hospitalized with confirmed COVID-19 infection at the University Clinical Center in Gdańsk, Poland, between 2020 and 2022. Patients were admitted to either a general COVID-19 ward or an intensive care unit based on disease severity. Data were collected from electronic medical records and included demographic characteristics, chest imaging, and routine laboratory tests: lymphocyte count, serum creatinine, aspartate aminotransferase, C-reactive protein, and procalcitonin. Statistical analyses were performed to evaluate the association of these variables with in-hospital mortality. Our analysis identified that elevated levels of serum creatinine, aspartate aminotransferase, C-reactive protein, and procalcitonin were significantly associated with increased risk of in-hospital mortality. Conversely, a higher lymphocyte count at admission was associated with better survival. These markers are widely available, inexpensive, and can be assessed during the initial diagnostic workup. This study offers a practical, evidence-based approach to early risk stratification in transplant recipients with COVID-19. The identified laboratory markers are not only simple and accessible but also clinically meaningful, providing frontline clinicians with actionable information during the early stages of care. In light of the continued presence of COVID-19 and the likelihood of future viral outbreaks, these findings have broad implications for the management of immunosuppressed patients. The study provides valuable insights into a currently underserved area of transplant medicine and has strong potential to inform clinical practice across diverse healthcare settings. Not applicable.

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Concepts Keywords
Death Biochemical markers
Early COVID-19 pandemic
Immunosuppression Immunosuppression
Laboratory Morphological markers
Organ Mortality
Organ transplant recipients
Prognostic markers

Semantics

Type Source Name
disease MESH COVID-19
disease MESH infection
disease MESH death
disease MESH included
drug DRUGBANK Creatinine
drug DRUGBANK Tropicamide
disease MESH Infectious Diseases
disease MESH Dis
pathway REACTOME Reproduction
disease MESH Hypertension
disease MESH Viral infections
disease MESH Middle East Respiratory Syndrome
disease MESH Severe Acute Respiratory Syndrome
disease MESH respiratory failure
disease MESH obesity
disease MESH metabolic syndrome
disease MESH diabetes mellitus
disease MESH chronic kidney disease
disease MESH lung diseases
pathway REACTOME Immune System
disease MESH acute respiratory distress syndrome
disease MESH inflammation
drug DRUGBANK Oxygen
drug DRUGBANK Aspartame
disease MESH cough
disease MESH syncope
disease MESH fatigue
disease MESH diarrhea
drug DRUGBANK Methionine
disease MESH injury
disease MESH myocardial infarction
disease MESH ischemic stroke
disease MESH gastrointestinal hemorrhage
disease MESH PCT
drug DRUGBANK Nesiritide
disease MESH CRB
disease MESH confusion
disease MESH pneumonia
disease MESH pulmonary embolism
disease MESH embolism
disease MESH lymphopenia
disease MESH kidney diseases
disease MESH Coronary heart disease
disease MESH Heart failure
disease MESH Arrhythmia
disease MESH Venous thromboembolism
disease MESH Cerebral infarction
drug DRUGBANK Hyaluronic acid

Original Article

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