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      Late Onset Infectious Complications and Safety of Tocilizumab in the Management of COVID‐19

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          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 March 1 st and April 25 th, 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. Seven‐teen infections in the TCZ group (23%) and 6 (8%) infections in the control group occurred >48 hours after admission (p=0.013). 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=0.03).

          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.

          This article is protected by copyright. All rights reserved.

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          Author and article information

          Contributors
          natasha.pettit@uchospitals.edu
          Journal
          J Med Virol
          J. Med. Virol
          10.1002/(ISSN)1096-9071
          JMV
          Journal of Medical Virology
          John Wiley and Sons Inc. (Hoboken )
          0146-6615
          1096-9071
          13 August 2020
          : 10.1002/jmv.26429
          Affiliations
          [ 1 ] Department of Pharmacy University of Chicago Medicine Chicago IL
          [ 2 ] Department of Medicine Section of Infectious Diseases and Global Health, University of Chicago Medicine Chicago IL
          [ 3 ] Department of Medicine Section of Pulmonary and Critical Care Medicine, University of Chicago Medicine Chicago IL
          Author notes
          [*] [* ] Correspondence Natasha N. Pettit, Department of Pharmacy, University of Chicago Medicine, Chicago, IL.

          Email: natasha.pettit@ 123456uchospitals.edu

          Author information
          http://orcid.org/0000-0002-8937-8039
          Article
          JMV26429
          10.1002/jmv.26429
          7436682
          32790075
          e142be11-c620-4e6f-baa2-46f0de98200d
          This article is protected by copyright. All rights reserved.

          This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.

          History
          Page count
          Figures: 0, Tables: 0, Pages: 22, Words: 363
          Categories
          Research Article
          Research Articles
          Custom metadata
          2.0
          accepted-manuscript
          Converter:WILEY_ML3GV2_TO_JATSPMC version:5.8.7 mode:remove_FC converted:19.08.2020

          Microbiology & Virology
          coronavirus < virus classification,cytokine/chemokine < immune responses,sars coronavirus < virus classification

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