TY - JOUR
T1 - Breakthrough COVID-19 after SARS-CoV-2 vaccination in solid organ transplant recipients
T2 - An analysis of symptomatic cases and monoclonal antibody therapy
AU - Yetmar, Zachary A.
AU - Bhaimia, Eric
AU - Bierle, Dennis M.
AU - Ganesh, Ravindra
AU - Razonable, Raymund R.
N1 - Funding Information:
This publication was supported by NIH/NCRR/NCATS CTSA Grant Number UL1TR002377. Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIH.
Funding Information:
This work was supported by research funding from the Mayo Clinic (to RRR).
Publisher Copyright:
© 2021 Wiley Periodicals LLC.
PY - 2022/4
Y1 - 2022/4
N2 - 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.
AB - 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.
KW - COVID-19
KW - SARS-CoV-2
KW - breakthrough infection
KW - casirivimab–imdevimab
KW - monoclonal antibody therapy
KW - organ transplantation
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U2 - 10.1111/tid.13779
DO - 10.1111/tid.13779
M3 - Article
C2 - 34932874
AN - SCOPUS:85123950033
SN - 1398-2273
VL - 24
JO - Transplant Infectious Disease
JF - Transplant Infectious Disease
IS - 2
M1 - e13779
ER -