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Late onset infectious complications and safety of tocilizumab in the management of COVID-19.
Pettit, Natasha N; Nguyen, Cynthia T; Mutlu, Gökhan M; Wu, David; Kimmig, Lucas; Pitrak, David; Pursell, Kenneth.
Affiliation
  • Pettit NN; Department of Pharmacy, University of Chicago Medicine, Chicago, Illinois.
  • Nguyen CT; Department of Pharmacy, University of Chicago Medicine, Chicago, Illinois.
  • Mutlu GM; Department of Medicine, Section of Pulmonary and Critical Care Medicine, University of Chicago Medicine, Chicago, Illinois.
  • Wu D; Department of Medicine, Section of Pulmonary and Critical Care Medicine, University of Chicago Medicine, Chicago, Illinois.
  • Kimmig L; Department of Medicine, Section of Pulmonary and Critical Care Medicine, University of Chicago Medicine, Chicago, Illinois.
  • Pitrak D; Department of Medicine, Section of Infectious Diseases and Global Health, University of Chicago Medicine, Chicago, Illinois.
  • Pursell K; Department of Medicine, Section of Infectious Diseases and Global Health, University of Chicago Medicine, Chicago, Illinois.
J Med Virol ; 93(3): 1459-1464, 2021 03.
Article in En | MEDLINE | ID: mdl-32790075
ABSTRACT

BACKGROUND:

Tocilizumab (TCZ) has been used in the management of COVID-19-related cytokine release syndrome (CRS). Concerns exist regarding the risk of infections and drug-related toxicities. We sought to evaluate the incidence of these TCZ complications among COVID-19 patients.

METHODS:

All adult inpatients with COVID-19 between 1 March and 25 April 2020 that received TCZ were included. We compared the rate of late-onset infections (>48 hours following admission) to a control group matched according to intensive care unit admission and mechanical ventilation requirement. Post-TCZ toxicities evaluated included elevated liver function tests (LFTs), GI perforation, diverticulitis, neutropenia, hypertension, allergic reactions, and infusion-related reactions.

RESULTS:

Seventy-four patients were included in each group. Seventeen infections in the TCZ group (23%) and 6 (8%) infections in the control group occurred >48 hours after admission (P = .013). Most infections were bacterial with pneumonia being the most common manifestation. Among patients receiving TCZ, LFT elevations were observed in 51%, neutropenia in 1.4%, and hypertension in 8%. The mortality rate among those that received TCZ was greater than the control (39% versus 23%, P = .03).

CONCLUSION:

Late onset infections were significantly more common among those receiving TCZ. Combining infections and TCZ-related toxicities, 61% of patients had a possible post-TCZ complication. While awaiting clinical trial results to establish the efficacy of TCZ for COVID-19 related CRS, the potential for infections and TCZ related toxicities should be carefully weighed when considering use.
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bacterial Infections / Antibodies, Monoclonal, Humanized / Cytokine Release Syndrome / COVID-19 / COVID-19 Drug Treatment / Mycoses Type of study: Observational_studies / Risk_factors_studies Limits: Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: J Med Virol Year: 2021 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bacterial Infections / Antibodies, Monoclonal, Humanized / Cytokine Release Syndrome / COVID-19 / COVID-19 Drug Treatment / Mycoses Type of study: Observational_studies / Risk_factors_studies Limits: Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: J Med Virol Year: 2021 Type: Article