Duration of infectious virus shedding of SARS-CoV-2 Omicron variant among immunocompromised patients.

Publication date: Jan 21, 2025

The duration of viral shedding and criteria for de-isolation in the hospital among immunocompromised patients with coronavirus disease 2019 (COVID-19) remain unclear. This study aimed to evaluate viral shedding duration in immunocompromised patients infected with the Omicron variant of severe acute respiratory syndrome coronavirus 2. A prospective cohort study was performed at 2 tertiary medical centers in Japan during the Omicron epidemic waves from July 2022 to January 2023. Nasopharyngeal swabs were serially collected from immunocompromised patients with COVID-19, including those with hematological malignancies, solid tumors, autoimmune diseases, and human immunodeficiency virus infection. Patients were classified as severely or moderately immunocompromised according to the Japanese national guidelines for tixagevimab-cilgavimab. The relationship between patient characteristics, immune status, duration of viral RNA presence, and infectious virus shedding were assessed using Mann-Whitney U and Fisher’s exact tests. Among 41 patients (163 samples), 9 (47 samples) were severely and 32 (116 samples) were moderately immunocompromised. In the severely and moderately immunocompromised groups, 87. 2% and 75. 0% of the samples were viral RNA-positive, while 36. 2% and 35. 3% were culture-positive, respectively. Five culture-positive samples after day 20 were from 2 severely immunocompromised patients on B cell depletion therapy. No culture-positive samples were found for the moderately immunocompromised patients after day 10. Long-term viral shedding should be closely monitored in severely immunocompromised patients with COVID-19.

Concepts Keywords
Coronavirus De-isolation
January Immunocompromised
Japanese Infectivity
July SARS-CoV-2
Therapy

Semantics

Type Source Name
disease MESH virus shedding
disease MESH immunocompromised patients
disease MESH coronavirus disease 2019
disease MESH hematological malignancies
disease MESH tumors
disease MESH autoimmune diseases
disease IDO immunodeficiency
disease MESH virus infection
disease IDO cell
disease IDO infectivity

Original Article

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