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What about tocilizumab? A retrospective study from a NYC Hospital during the COVID-19 outbreak.
Mehta, Monica; Purpura, Lawrence J; McConville, Thomas H; Neidell, Matthew J; Anderson, Michaela R; Bernstein, Elana J; Dietz, Donald E; Laracy, Justin; Gunaratne, Shauna H; Miller, Emily Happy; Cheng, Jennifer; Zucker, Jason; Shah, Shivang S; Chaudhuri, Shaoli; Gordillo, Christian A; Patel, Shreena R; Guo, Tai Wei; Karaaslan, Lara E; Reshef, Ran; Miko, Benjamin A; Bathon, Joan M; Pereira, Marcus R; Uhlemann, Anne-Catrin; Yin, Michael T; Sobieszczyk, Magdalena E.
  • Mehta M; Department of Pharmacy, NewYork-Presbyterian Hospital, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Purpura LJ; Division of Infectious Diseases, Department of Medicine, Columbia University Irving Medical Center, New York, New York, United States of America.
  • McConville TH; ICAP, Mailman School of Public Health, Columbia University, New York, New York, United States of America.
  • Neidell MJ; Division of Infectious Diseases, Department of Medicine, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Anderson MR; Department of Health Policy and Management, Mailman School of Public Health, Columbia University, New York, New York, United States of America.
  • Bernstein EJ; Division of Pulmonary Critical Care, Department of Medicine, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Dietz DE; Division of Rheumatology, Department of Medicine, NewYork-Presbyterian Hospital, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Laracy J; Division of Infectious Diseases, Department of Medicine, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Gunaratne SH; Division of Infectious Diseases, Department of Medicine, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Miller EH; Division of Infectious Diseases, Department of Medicine, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Cheng J; Division of Infectious Diseases, Department of Medicine, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Zucker J; Department of Pharmacy, NewYork-Presbyterian Hospital, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Shah SS; Division of Infectious Diseases, Department of Medicine, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Chaudhuri S; Division of Infectious Diseases, Department of Pediatrics, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Gordillo CA; Department of Medicine, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Patel SR; Blood and Marrow Transplantation Program, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Guo TW; Division of Pulmonary Critical Care, Department of Medicine, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Karaaslan LE; Vagelos College of Physicians and Surgeons, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Reshef R; Vagelos College of Physicians and Surgeons, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Miko BA; Blood and Marrow Transplantation Program, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Bathon JM; Division of Infectious Diseases, Department of Medicine, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Pereira MR; Division of Rheumatology, Department of Medicine, NewYork-Presbyterian Hospital, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Uhlemann AC; Division of Infectious Diseases, Department of Medicine, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Yin MT; Division of Infectious Diseases, Department of Medicine, Columbia University Irving Medical Center, New York, New York, United States of America.
  • Sobieszczyk ME; Division of Infectious Diseases, Department of Medicine, Columbia University Irving Medical Center, New York, New York, United States of America.
PLoS One ; 16(4): e0249349, 2021.
Article in English | MEDLINE | ID: covidwho-1172877
ABSTRACT

BACKGROUND:

Tocilizumab, an interleukin-6 receptor blocker, has been used in the inflammatory phase of COVID-19, but its impact independent of corticosteroids remains unclear in patients with severe disease.

METHODS:

In this retrospective analysis of patients with COVID-19 admitted between March 2 and April 14, 2020 to a large academic medical center in New York City, we describe outcomes associated with tocilizumab 400 mg (without methylprednisolone) compared to a propensity-matched control. The primary endpoints were change in a 7-point ordinal scale of oxygenation and ventilator free survival, both at days 14 and 28. Secondary endpoints include incidence of bacterial superinfections and gastrointestinal perforation. Primary outcomes were evaluated using t-test.

RESULTS:

We identified 33 patients who received tocilizumab and matched 74 controls based on demographics and health measures upon admission. After adjusting for illness severity and baseline ordinal scale, we failed to find evidence of an improvement in hypoxemia based on an ordinal scale at hospital day 14 in the tocilizumab group (OR 2.2; 95% CI, 0.7-6.5; p = 0.157) or day 28 (OR 1.1; 95% CI, 0.4-3.6; p = 0.82). There also was no evidence of an improvement in ventilator-free survival at day 14 (OR 0.8; 95% CI, 0.18-3.5; p = 0.75) or day 28 (OR 1.1; 95% CI, 0.1-1.8; p = 0.23). There was no increase in secondary bacterial infection rates in the tocilizumab group compared to controls (OR 0.37; 95% CI, 0.09-1.53; p = 0.168).

CONCLUSIONS:

There was no evidence to support an improvement in hypoxemia or ventilator-free survival with use of tocilizumab 400 mg in the absence of corticosteroids. No increase in secondary bacterial infections was observed in the group receiving tocilizumab.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: Bacterial Infections / Disease Outbreaks / Antibodies, Monoclonal, Humanized / SARS-CoV-2 / COVID-19 / COVID-19 Drug Treatment / Hospitals, Teaching Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Limits: Female / Humans / Male / Middle aged Country/Region as subject: North America Language: English Journal: PLoS One Journal subject: Science / Medicine Year: 2021 Document Type: Article Affiliation country: Journal.pone.0249349

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Bacterial Infections / Disease Outbreaks / Antibodies, Monoclonal, Humanized / SARS-CoV-2 / COVID-19 / COVID-19 Drug Treatment / Hospitals, Teaching Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Limits: Female / Humans / Male / Middle aged Country/Region as subject: North America Language: English Journal: PLoS One Journal subject: Science / Medicine Year: 2021 Document Type: Article Affiliation country: Journal.pone.0249349