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Reduced fixed dose tocilizumab 400 mg IV compared to weight-based dosing in critically ill patients with COVID-19: A before-after cohort study.
Stukas, Sophie; Goshua, George; Kinkade, Angus; Grey, Rebecca; Mah, Gregory; Biggs, Catherine M; Jamal, Shahin; Thiara, Sonny; Lau, Tim T Y; Piszczek, Jolanta; Partovi, Nilu; Sweet, David D; Lee, Agnes Y Y; Wellington, Cheryl L; Sekhon, Mypinder S; Chen, Luke Y C.
  • Stukas S; Djavad Mowafaghian Centre for Brain Health, Department of Pathology and Laboratory Medicine, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.
  • Goshua G; Section of Hematology, Yale University School of Medicine, New Haven, CT, USA.
  • Kinkade A; Department of Health Policy and Management, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
  • Grey R; Lower Mainland Pharmacy Services, Vancouver, British Columbia.
  • Mah G; Division of Critical Care Medicine, Department of Medicine, University of British Columbia, Vancouver, BC, Canada.
  • Biggs CM; Department of Pharmacy, Vancouver General Hospital, Vancouver, BC, Canada.
  • Jamal S; Division of Allergy and Immunology, Department of Pediatrics, University of British Columbia, Vancouver, BC, Canada.
  • Thiara S; Division of Rheumatology, Department of Medicine, University of British Columbia, Canada.
  • Lau TTY; Division of Critical Care Medicine, Department of Medicine, University of British Columbia, Vancouver, BC, Canada.
  • Piszczek J; Faculty of Pharmaceutical Sciences, and Division of Infectious Diseases, Department of Medicine, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.
  • Partovi N; British Columbia COVID Therapeutic Committee, Victoria, BC, Canada.
  • Sweet DD; Department of Pharmacy, Vancouver General Hospital, Vancouver, BC, Canada.
  • Lee AYY; Division of Critical Care Medicine and Department of Emergency Medicine, University of British Columbia, Vancouver, BC, Canada.
  • Wellington CL; Division of Hematology, Department of Medicine, University of British Columbia, Vancouver, BC, Canada.
  • Sekhon MS; Department of Pathology and Laboratory Medicine, Djavad Mowafaghian Centre for Brain Health, International Collaboration on Repair Discoveries, University of British Columbia, Vancouver, BC, Canada.
  • Chen LYC; Division of Critical Care Medicine, Department of Medicine, University of British Columbia, Vancouver, BC, Canada.
Lancet Reg Health Am ; 11: 100228, 2022 Jul.
Article in English | MEDLINE | ID: covidwho-1921232
ABSTRACT

Background:

Interleukin-6 inhibitors reduce mortality in severe COVID-19. British Columbia began using tocilizumab 8 mg/kg (maximum 800 mg) in January 2021 in critically ill patients with COVID-19, but due to drug shortages, decreased dosing to 400 mg IV fixed dose in April 2021. The aims of this study were twofold to compare physiological responses and clinical outcomes of these two strategies, and examine the cost-effectiveness of treating all patients with 400 mg versus half the patients with 8 mg/kg and the other half without tocilizumab.

Methods:

This was a single-centre, before-after cohort study of critically ill COVID-19 patients treated with tocilizumab, and a control cohort treated with dexamethasone only. Physiological responses and clinical outcomes were compared between patients receiving both doses of tocilizumab and those receiving dexamethasone only. We built a decision tree model to examine cost-effectiveness.

Findings:

152 patients were included; 40 received tocilizumab 8 mg/kg, 59 received 400 mg and 53 received dexamethasone only. Median CRP fell from 103 mg/L to 5.2 mg/L, 96 mg/L to 6.8 mg/L and from 81.3 mg/L to 48 mg/L in the 8 mg/kg, 400 mg tocilizumab, and dexamethasone only groups, respectively. 28-day mortality was 5% (n=2) vs 8% (n=5) vs 13% (n=7), with no significant difference in all pair-wise comparison. At an assumed willingness-to-pay threshold of $50,000 Canadian per life-year, utilizing 400 mg for all patients rather than 8 mg/kg for half the patients is cost-effective in 51.6% of 10,000 Monte Carlo simulations.

Interpretation:

Both doses of tocilizumab demonstrated comparable reduction of inflammation with similar 28-day mortality. Without consideration of equity, the net monetary benefits of providing 400 mg tocilizumab to all patients are comparable to 8 mg/kg to half the patients. In the context of ongoing drug shortages, fixed-dose 400 mg tocilizumab may be a practical, feasible and economical option.

Funding:

This work was supported by a gift donation from Hsu & Taylor Family to the VGH Foundation, and the Yale Bernard G. Forget Scholarship.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Language: English Journal: Lancet Reg Health Am Year: 2022 Document Type: Article Affiliation country: J.lana.2022.100228

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Language: English Journal: Lancet Reg Health Am Year: 2022 Document Type: Article Affiliation country: J.lana.2022.100228