Clinical Characteristics and Outcomes of Immunocompromised Patients With Coronavirus Disease 2019 Caused by the Omicron Variant: A Prospective, Observational Study

Abstract Background Illness after infection with the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant is less severe compared with previous variants. Data on the disease burden in immunocompromised patients are lacking. We investigated the clinical characteristics and out...

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Veröffentlicht in:Clinical infectious diseases 2023-02, Vol.76 (3), p.e172-e178
Hauptverfasser: Malahe, S Reshwan K, Hoek, Rogier A S, Dalm, Virgil A S H, Broers, Annoek E C, den Hoed, Caroline M, Manintveld, Olivier C, Baan, Carla C, van Deuzen, Charlotte M, Papageorgiou, Grigorios, Bax, Hannelore I, Van Kampen, Jeroen J, Hellemons, Merel E, Kho, Marcia M L, de Vries, Rory D, Molenkamp, Richard, Reinders, Marlies E J, Rijnders, Bart J A
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Sprache:eng
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Zusammenfassung:Abstract Background Illness after infection with the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant is less severe compared with previous variants. Data on the disease burden in immunocompromised patients are lacking. We investigated the clinical characteristics and outcomes of immunocompromised patients with coronavirus disease 2019 (COVID-19) caused by Omicron. Methods Organ transplant recipients, patients on anti-CD20 therapy, and allogenic hematopoietic stem cell transplantation recipients infected with the Omicron variant were included. Characteristics of consenting patients were collected and patients were contacted regularly until symptom resolution. To identify possible risk factors for hospitalization, a univariate logistic analysis was performed. Results 114 consecutive immunocompromised patients were enrolled. Eighty-nine percent had previously received 3 mRNA vaccinations. While only 1 patient died, 23 (20%) were hospitalized for a median of 11 days. A low SARS-CoV-2 immunoglobulin G (IgG) antibody response (
ISSN:1058-4838
1537-6591
DOI:10.1093/cid/ciac571