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1.
Transplantation proceedings ; 2023.
Article in English | EuropePMC | ID: covidwho-2254004

ABSTRACT

Background During the COVID-19 pandemic, efforts to maintain solid-organ transplantation have continued, including the use of SARS-CoV-2 positive heart donors. Methods We present our institution's initial experience with SARS-CoV-2 positive heart donors. All donors met our institution's Transplant Center criteria, including a negative bronchoalveolar lavage (BAL) PCR result. All but one patient received postexposure prophylaxis (PEP) with anti-spike monoclonal antibody therapy, remdesivir, or both. Results A total of 6 patients received a heart transplant from a SARS-CoV-2 positive donor. One heart transplant was complicated by catastrophic secondary graft dysfunction requiring venoarterial extracorporeal membrane oxygenation and retransplant. The remaining five patients did well postoperatively and were discharged home. None of the patients had evidence of COVID-19 infection after surgery. Conclusion Heart transplants from SARS-CoV-2 PCR positive donors are feasible and safe with adequate screening and PEP.

2.
Transplant Proc ; 55(3): 533-539, 2023 Apr.
Article in English | MEDLINE | ID: covidwho-2254005

ABSTRACT

BACKGROUND: During the COVID-19 pandemic, efforts to maintain solid-organ transplantation have continued, including the use of SARS-CoV-2-positive heart donors. METHODS: We present our institution's initial experience with SARS-CoV-2-positive heart donors. All donors met our institution's Transplant Center criteria, including a negative bronchoalveolar lavage polymerase chain reaction result. All but 1 patient received postexposure prophylaxis with anti-spike monoclonal antibody therapy, remdesivir, or both. RESULTS: A total of 6 patients received a heart transplant from a SARS-CoV-2-positive donor. One heart transplant was complicated by catastrophic secondary graft dysfunction requiring venoarterial extracorporeal membrane oxygenation and retransplant. The remaining 5 patients did well postoperatively and were discharged from the hospital. None of the patients had evidence of COVID-19 infection after surgery. CONCLUSION: Heart transplants from SARS-CoV-2 polymerase chain reaction-positive donors are feasible and safe with adequate screening and postexposure prophylaxis.


Subject(s)
COVID-19 , Heart Transplantation , Humans , COVID-19/diagnosis , SARS-CoV-2 , Pandemics , Heart Transplantation/adverse effects , Tissue Donors
3.
Curr Opin Organ Transplant ; 27(4): 269-276, 2022 Aug 01.
Article in English | MEDLINE | ID: covidwho-2118071

ABSTRACT

PURPOSE OF REVIEW: Coronavirus disease-2019 (COVID-19) disproportionately causes severe outcomes in solid organ transplant recipients (SOTR). Antispike monoclonal antibodies have been authorized for therapy and prophylaxis for COVID-19. Here, we review the current state of antispike monoclonal antibodies and their role for SOTRs. RECENT FINDINGS: Bamlanivimab with or without etesevimab, casirivimab-imdevimab and sotrovimab have reduced the rates of hospitalization and severe disease in high-risk patients with mild-to-moderate COVID-19. Multiple retrospective studies have also demonstrated monoclonal antibodies are effective in SOTR populations. However, the evolution of resistant severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants of concerns has resulted in revocation of the authorization of bamlanivimab with or without etesevimab, and casirivimab-imdevimab as treatment and postexposure prophylaxis (PEP). Sotrovimab and bebtelovimab are currently authorized for treatment of the predominant circulating SARS-CoV-2 B.1.1.529 (Omicron), but not as pre or PEP. Tixagevimab-cilgavimab, a long-acting antibody combination preparation, is authorized for preexposure prophylaxis in high-risk immunocompromised populations, including SOTRs, who are less likely to mount an effective immune response following vaccination series and booster. SUMMARY: Antispike monoclonal antibodies are useful for the prevention and treatment of mild-to-moderate COVID-19 in SOTRs. However, their clinical use should be determined by the evolving epidemiology of SARS-CoV-2 variants in the community.


Subject(s)
COVID-19 , Organ Transplantation , Humans , SARS-CoV-2 , COVID-19/prevention & control , Retrospective Studies , Antibodies, Monoclonal/adverse effects , Organ Transplantation/adverse effects , Transplant Recipients
4.
Transpl Infect Dis ; 24(2): e13779, 2022 Apr.
Article in English | MEDLINE | ID: covidwho-1583253

ABSTRACT

BACKGROUND: Solid organ transplant (SOT) recipients are at increased risk for complications from SARS-CoV-2 infection. Little is known regarding clinical course and outcomes of breakthrough COVID-19 in the fully vaccinated SOT population. We sought to describe our cohort of SOT recipients who developed symptomatic breakthrough COVID-19 after full vaccination. METHODS: We conducted a retrospective review of SOT recipients diagnosed with COVID-19 at least 14 days after completing SARS-CoV-2 vaccination. Patients were analyzed according to those presenting with mild-to-moderate and severe COVID-19, respectively. We described presenting characteristics, COVID-19 therapy, and analyzed outcomes including emergency department (ED) visits, hospitalization, and intensive care unit (ICU) admission. RESULTS: Thirty-five patients met inclusion criteria. These had a mean age of 60.8 years and kidney transplant was the most common SOT type. Five patients presented with severe COVID-19 at diagnosis, all requiring hospitalization without ICU admission. From the 30 patients who presented with mild-to-moderate infection, 28 received casirivimab-imdevimab. Four of these 28 (14.3%) had an ED visit, with one requiring hospital admission (3.4%). No patients required ICU admission. CONCLUSION: Breakthrough COVID-19 may occur in SOT recipients after full vaccination, though they appear to have acceptable outcomes. Anti-spike monoclonal antibody therapy for eligible SOT patients may have mitigated clinical progression and improved the outcomes. Further study with large cohorts is warranted.


Subject(s)
COVID-19 , Organ Transplantation , Antibodies, Monoclonal , Antibodies, Monoclonal, Humanized , COVID-19 Vaccines , Humans , Middle Aged , Organ Transplantation/adverse effects , SARS-CoV-2 , Transplant Recipients , Vaccination
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