Show simple item record

dc.contributor.authorAljuhani, O.
dc.contributor.authorAl Sulaiman, K.
dc.contributor.authorAlshabasy, A.
dc.contributor.authorEljaaly, K.
dc.contributor.authorAl Shaya, A.I.
dc.contributor.authorNoureldeen, H.
dc.contributor.authorAboudeif, M.
dc.contributor.authorAl Dosari, B.
dc.contributor.authorAlkhalaf, A.
dc.contributor.authorKorayem, G.B.
dc.contributor.authorAleissa, M.M.
dc.contributor.authorBadreldin, H.A.
dc.contributor.authorAl Harbi, S.
dc.contributor.authorAlhammad, A.
dc.contributor.authorVishwakarma, R.
dc.date.accessioned2021-12-13T23:23:20Z
dc.date.available2021-12-13T23:23:20Z
dc.date.issued2021
dc.identifier.citationAljuhani, O., Al Sulaiman, K., Alshabasy, A., Eljaaly, K., Al Shaya, A. I., Noureldeen, H., Aboudeif, M., Al Dosari, B., Alkhalaf, A., Korayem, G. B., Aleissa, M. M., Badreldin, H. A., Al Harbi, S., Alhammad, A., & Vishwakarma, R. (2021). Association between tocilizumab and emerging multidrug-resistant organisms in critically ill patients with COVID-19: A multicenter, retrospective cohort study. BMC Infectious Diseases.
dc.identifier.issn1471-2334
dc.identifier.doi10.1186/s12879-021-06813-1
dc.identifier.urihttp://hdl.handle.net/10150/662516
dc.description.abstractBackground: Tocilizumab is an IgG1 class recombinant humanized monoclonal antibody that directly inhibits the IL-6 receptor. Several randomized clinical trials have evaluated its safety and efficacy in patients with coronavirus disease 2019 (COVID-19), and these studies demonstrate conflicting results. Our study aimed to determine the association between tocilizumab treatment and microbial isolation and emergence of multidrug-resistant bacteria in critically ill patients with COVID-19. Methods: A multicenter retrospective cohort study was conducted at two tertiary government hospitals in Saudi Arabia. All critically ill patients admitted to intensive care units with a positive COVID-19 PCR test between March 1 and December 31, 2020, who met study criteria were included. Patients who received tocilizumab were compared to those who did not receive it. Results: A total of 738 patients who met our inclusion criteria were included in the analysis. Of these, 262 (35.5%) received tocilizumab, and 476 (64.5%) were included in the control group. Patients who received tocilizumab had higher odds for microbial isolation (OR 1.34; 95% CI 0.91–1.94, p = 0.13); however, the difference was not statistically significant. Development of resistant organisms (OR 1.00; 95% CI 0.51–1.98, p = 0.99) or detection of carbapenem-resistant Enterobacteriaceae (CRE) (OR 0.67; 95% CI 0.29–1.54, p = 0.34) was not statistically significant between the two groups. Conclusions: Tocilizumab use in critically ill patients with COVID-19 is not associated with higher microbial isolation, the emergence of resistant organisms, or the detection of CRE organisms. © 2021, The Author(s).
dc.language.isoen
dc.publisherBioMed Central Ltd
dc.rightsCopyright © The Author(s) 2021. This article is licensed under a Creative Commons Attribution 4.0 International License.
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectCOVID-19
dc.subjectCRE
dc.subjectCritically ill
dc.subjectImmunomodulatory drugs
dc.subjectIntensive care units (ICUs)
dc.subjectSARS-Cov-2
dc.subjectSecondary infection
dc.subjectTocilizumab
dc.titleAssociation between tocilizumab and emerging multidrug-resistant organisms in critically ill patients with COVID-19: A multicenter, retrospective cohort study
dc.typeArticle
dc.typetext
dc.contributor.departmentCollege of Pharmacy, University of Arizona
dc.identifier.journalBMC Infectious Diseases
dc.description.noteOpen access journal
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
dc.eprint.versionFinal published version
dc.source.journaltitleBMC Infectious Diseases
refterms.dateFOA2021-12-13T23:23:20Z


Files in this item

Thumbnail
Name:
s12879-021-06813-1.pdf
Size:
1017.Kb
Format:
PDF
Description:
Final Published Version

This item appears in the following Collection(s)

Show simple item record

Copyright © The Author(s) 2021. This article is licensed under a Creative Commons Attribution 4.0 International License.
Except where otherwise noted, this item's license is described as Copyright © The Author(s) 2021. This article is licensed under a Creative Commons Attribution 4.0 International License.