Outcomes Associated With COVID-19 Hospitalization in Heart Transplantation Patients.


Journal

Transplantation proceedings
ISSN: 1873-2623
Titre abrégé: Transplant Proc
Pays: United States
ID NLM: 0243532

Informations de publication

Date de publication:
Dec 2022
Historique:
received: 20 05 2022
revised: 04 06 2022
accepted: 12 06 2022
pubmed: 24 8 2022
medline: 21 12 2022
entrez: 23 8 2022
Statut: ppublish

Résumé

Heart transplantation (HT) recipients infected with COVID-19 may be at an increased risk of severe illness due to chronic immunosuppression. Adult HT patients hospitalized with COVID-19 at the Cleveland Clinic between March 2020 and March 2021 were included in this retrospective cohort analysis. Twenty-four HT cases were matched to 96 non-HT controls, similarly hospitalized with COVID-19, out of 11,481 patients based on different baseline characteristics. Primary outcome was all-cause mortality; secondary outcomes included mechanical ventilation, intensive care unit admission, vasopressor need, dialysis, pneumonia, and 90-day readmission. Subgroup analysis was performed based on the time from transplantation (within 1 year of transplantation and greater than 1 year since transplantation). Both primary and secondary outcomes were not significant. Subgroup analysis did not show a significant difference in mortality (P = .355) or 30-day readmission (P = .841) between patients who were within 1 year of transplantation and remote transplantation beyond 1 year. Univariable analysis of immunosuppressant continuation, dose-reduction, or discontinuation did not significantly affect HT mortality. Despite limited sample size, our results suggest that HT patients do not show worse outcomes after acquiring COVID-19, whether in the first year of transplantation or after a remote transplantation procedure. Future studies with multicenter data that incorporate the subsequent COVID-19 variants (eg, Delta and Omicron), the impact of long COVID-19, and assessing full vs reduced immunosuppression regimens would add insights to this patient population.

Sections du résumé

BACKGROUND BACKGROUND
Heart transplantation (HT) recipients infected with COVID-19 may be at an increased risk of severe illness due to chronic immunosuppression.
MATERIALS AND METHODS METHODS
Adult HT patients hospitalized with COVID-19 at the Cleveland Clinic between March 2020 and March 2021 were included in this retrospective cohort analysis. Twenty-four HT cases were matched to 96 non-HT controls, similarly hospitalized with COVID-19, out of 11,481 patients based on different baseline characteristics. Primary outcome was all-cause mortality; secondary outcomes included mechanical ventilation, intensive care unit admission, vasopressor need, dialysis, pneumonia, and 90-day readmission. Subgroup analysis was performed based on the time from transplantation (within 1 year of transplantation and greater than 1 year since transplantation).
RESULTS RESULTS
Both primary and secondary outcomes were not significant. Subgroup analysis did not show a significant difference in mortality (P = .355) or 30-day readmission (P = .841) between patients who were within 1 year of transplantation and remote transplantation beyond 1 year. Univariable analysis of immunosuppressant continuation, dose-reduction, or discontinuation did not significantly affect HT mortality.
CONCLUSIONS CONCLUSIONS
Despite limited sample size, our results suggest that HT patients do not show worse outcomes after acquiring COVID-19, whether in the first year of transplantation or after a remote transplantation procedure. Future studies with multicenter data that incorporate the subsequent COVID-19 variants (eg, Delta and Omicron), the impact of long COVID-19, and assessing full vs reduced immunosuppression regimens would add insights to this patient population.

Identifiants

pubmed: 35999107
pii: S0041-1345(22)00453-5
doi: 10.1016/j.transproceed.2022.06.002
pmc: PMC9212532
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2688-2691

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL141892
Pays : United States

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Références

Transpl Int. 2021 Apr;34(4):721-731
pubmed: 33539616
Am J Transplant. 2021 Mar;21(3):1285-1294
pubmed: 33252201
Am J Transplant. 2020 Nov;20(11):3051-3060
pubmed: 32654332
Transplantation. 2021 Jan 1;105(1):128-137
pubmed: 32890139
JAMA Cardiol. 2020 Oct 1;5(10):1165-1169
pubmed: 32402056
JACC Heart Fail. 2021 Jan;9(1):52-61
pubmed: 33309578
J Heart Lung Transplant. 2020 May;39(5):496-497
pubmed: 32362394

Auteurs

Christopher N Kanaan (CN)

Department of Internal Medicine, Cleveland Clinic Foundation, Cleveland, Ohio.

Jean-Pierre Iskandar (JP)

Department of Internal Medicine, Cleveland Clinic Foundation, Cleveland, Ohio.

Mohamed M Gad (MM)

Department of Internal Medicine, Cleveland Clinic Foundation, Cleveland, Ohio.

Nicholas P Kondoleon (NP)

Department of Internal Medicine, Cleveland Clinic Foundation, Cleveland, Ohio.

Saeid Mirzai (S)

Department of Internal Medicine, Cleveland Clinic Foundation, Cleveland, Ohio.

Eileen M Hsich (EM)

Kaufman Center for Heart Failure, Department of Cardiology, Cleveland Clinic, Cleveland, Ohio.

Jerry D Estep (JD)

Kaufman Center for Heart Failure, Department of Cardiology, Cleveland Clinic, Cleveland, Ohio.

Maan A Fares (MA)

Heart and Vascular Institute, Cleveland Clinic, Cleveland, Ohio. Electronic address: faresm@ccf.org.

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Classifications MeSH