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Reduced Complications after Arterial Reconnection in a Rat Model of Orthotopic Liver Transplantation
Published on: November 7, 2020
Coronavirus disease 2019 in liver transplant patients: Clinical and therapeutic aspects
Carmelo Loinaz-Segurola1, Alberto Marcacuzco-Quinto2, Mario Fernández-Ruiz3
1HBP and Transplant Surgery Unit. Department of General Surgery, Digestive Tract and Abdominal Organ Transplantation, Hospital Universitario "12 de Octubre", Instituto de Investigación Sanitaria Hospital "12 de Octubre" (imas12), Universidad Complutense, Madrid 28041, Spain. cloinaz@ucm.es.
Insights
The COVID-19 pandemic reduced liver transplants globally. While infection rates are similar to the general population, liver transplant recipients face higher mortality risks, possibly due to age and comorbidities, not transplant status.
Area of Science:
- Hepatology
- Transplant Surgery
- Infectious Diseases
Background:
- The COVID-19 pandemic significantly disrupted liver transplant (LT) activity worldwide, decreasing donations and procedures.
- Liver transplant recipients (LTRs) experience COVID-19 incidence comparable to the general population, with similar clinical presentations.
- LTRs hospitalized with COVID-19 have a high mortality risk (12-19%), potentially linked to age and comorbidities.
Purpose of the Study:
- To review the impact of COVID-19 on liver transplant activity and outcomes.
- To analyze COVID-19 incidence, clinical features, and mortality in LTRs.
- To discuss management strategies, immunosuppression, vaccination response, and future challenges in LTRs.
Main Methods:
- Literature review and synthesis of existing data on COVID-19 in LTRs.
- Analysis of reported incidence, clinical characteristics, and mortality rates.
- Discussion of immunosuppressive strategies, vaccine efficacy, and emerging variants.
Main Results:
- LT activity decreased significantly during the pandemic.
- COVID-19 incidence in LTRs is comparable to the general population, but mortality is high.
- Immunosuppression, particularly tacrolimus, may offer protection; vaccine response is impaired.
Conclusions:
- While LTRs face high mortality from COVID-19, immunosuppression might be protective.
- Optimal management of COVID-19 in LTRs requires further research, with guidelines suggesting reduced anti-proliferative agents.
- Impaired vaccine response and emerging variants pose ongoing challenges for LTRs.
Abstract:
The coronavirus disease 2019 (COVID-19) pandemic has profoundly impacted liver transplant (LT) activity across the world, with notable decreases in the number of donations and procedures in most Western countries, in particular throughout the first wave. The cumulative incidence of COVID-19 in LT recipients (with estimates ranging from 0.34% to 1.56%) appears to be at least comparable to that observed for the general population. Clinical and radiological features at presentation are also similar to non-transplant patients. The risk of death among LT recipients requiring hospital admission is high (from 12% to 19%), although some authors have suggested that overall mortality may be actually lower compared to the general non-transplant population. It is likely that these poor outcomes may be mainly influenced by the older age and higher comorbidity burden of LT recipients, rather than by the transplant status itself. In fact, it has been hypothesized that post-transplant immunosuppression would exert a protective role, with special focus on tacrolimus-containing regimens. There is scarce evidence to guide the optimal management of post-transplant COVID-19 and the use of antiviral or immunomodulatory therapies, although both clinical practice and guidelines support the dose reduction or withdrawal of anti-proliferative agents such as mofetil mycophenolate. Preliminary reports suggest that the antibody response to messenger RNA vaccines is significantly impaired as compared to non-immunocompromised individuals, in line with other transplant populations. Finally, it is foreseeable that the future will be conditioned by the emerging variants of severe acute respiratory syndrome coronavirus 2 with increased transmissibility among LT recipients.
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