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Tocilizumab for Treatment of Mechanically Ventilated Patients With COVID-19.
Somers, Emily C; Eschenauer, Gregory A; Troost, Jonathan P; Golob, Jonathan L; Gandhi, Tejal N; Wang, Lu; Zhou, Nina; Petty, Lindsay A; Baang, Ji Hoon; Dillman, Nicholas O; Frame, David; Gregg, Kevin S; Kaul, Dan R; Nagel, Jerod; Patel, Twisha S; Zhou, Shiwei; Lauring, Adam S; Hanauer, David A; Martin, Emily; Sharma, Pratima; Fung, Christopher M; Pogue, Jason M.
  • Somers EC; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Eschenauer GA; Department of Environmental Health Sciences, University of Michigan, Ann Arbor, Michigan, USA.
  • Troost JP; Department of Obstetrics & Gynecology, University of Michigan, Ann Arbor, Michigan, USA.
  • Golob JL; Department of Clinical Pharmacy, College of Pharmacy, University of Michigan, Ann Arbor, Michigan, USA.
  • Gandhi TN; Michigan Institute for Clinical & Health Research, University of Michigan, Ann Arbor, Michigan, USA.
  • Wang L; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Zhou N; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Petty LA; Department of Biostatistics, University of Michigan, Ann Arbor, Michigan, USA.
  • Baang JH; Department of Biostatistics, University of Michigan, Ann Arbor, Michigan, USA.
  • Dillman NO; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Frame D; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Gregg KS; Department of Pharmacy, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Kaul DR; Department of Clinical Pharmacy, College of Pharmacy, University of Michigan, Ann Arbor, Michigan, USA.
  • Nagel J; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Patel TS; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Zhou S; Department of Pharmacy, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Lauring AS; Department of Pharmacy, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Hanauer DA; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Martin E; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Sharma P; Department of Learning Health Sciences, University of Michigan, Ann Arbor, Michigan, USA.
  • Fung CM; Department of Epidemiology, University of Michigan, Ann Arbor, Michigan, USA.
  • Pogue JM; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Clin Infect Dis ; 73(2): e445-e454, 2021 07 15.
Article in English | MEDLINE | ID: covidwho-640452
Preprint
This scientific journal article is probably based on a previously available preprint. It has been identified through a machine matching algorithm, human confirmation is still pending.
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ABSTRACT

BACKGROUND:

Severe coronavirus disease 2019 (COVID-19) can manifest in rapid decompensation and respiratory failure with elevated inflammatory markers, consistent with cytokine release syndrome for which IL-6 blockade is an approved treatment.

METHODS:

We assessed effectiveness and safety of IL-6 blockade with tocilizumab in a single-center cohort of patients with COVID-19 requiring mechanical ventilation. The primary endpoint was survival probability postintubation; secondary analyses included an ordinal illness severity scale integrating superinfections. Outcomes in patients who received tocilizumab compared with tocilizumab-untreated controls were evaluated using multivariable Cox regression with propensity score inverse probability of treatment weighting (IPTW).

RESULTS:

154 patients were included, of whom 78 received tocilizumab and 76 did not. Median follow-up was 47 days (range, 28-67). Baseline characteristics were similar between groups, although tocilizumab-treated patients were younger (mean 55 vs 60 years), less likely to have chronic pulmonary disease (10% vs 28%), and had lower D-dimer values at time of intubation (median 2.4 vs 6.5 mg/dL). In IPTW-adjusted models, tocilizumab was associated with a 45% reduction in hazard of death (HR, .55; 95% CI, .33-.90) and improved status on the ordinal outcome scale [OR per 1-level increase, .58; .36-.94). Although tocilizumab was associated with an increased proportion of patients with superinfections (54% vs 26%; P < .001), there was no difference in 28-day case fatality rate among tocilizumab-treated patients with versus without superinfection (22% vs 15%; P = .42). Staphylococcus aureus accounted for ~50% of bacterial pneumonia.

CONCLUSIONS:

In this cohort of mechanically ventilated COVID-19 patients, tocilizumab was associated with lower mortality despite higher superinfection occurrence.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Respiration, Artificial / COVID-19 Drug Treatment Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Limits: Humans Language: English Journal: Clin Infect Dis Journal subject: Communicable Diseases Year: 2021 Document Type: Article Affiliation country: Cid

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Respiration, Artificial / COVID-19 Drug Treatment Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Limits: Humans Language: English Journal: Clin Infect Dis Journal subject: Communicable Diseases Year: 2021 Document Type: Article Affiliation country: Cid