Variation in Early Anakinra Use and Short‐Term Outcomes in Multisystem Inflammatory Syndrome in Children

Author:

Chang Joyce C.1ORCID,Young Cameron C.2,Muscal Eyal3,Sexson Tejtel Sara K.4,Newhams Margaret M.2,Kucukak Suden2,Crandall Hillary5,Maddux Aline B.6,Rowan Courtney M.7,Halasa Natasha B.8,Harvey Helen A.9,Hobbs Charlotte V.10,Hall Mark W.11,Kong Michele12,Aguiar Cassyanne L.13,Schuster Jennifer E.14,Fitzgerald Julie C.15,Singh Aalok R.16,Wellnitz Kari17,Nofziger Ryan A.18,Cvijanovich Natalie Z.19,Mack Elizabeth H.20,Schwarz Adam J.21,Heidemann Sabrina M.22,Newburger Jane W.23,Zambrano Laura D.24,Campbell Angela P.24ORCID,Patel Manish M.24,Randolph Adrienne G.25,Son Mary Beth F.1,

Affiliation:

1. Division of Immunology, Boston Children's Hospital, and Department of Pediatrics Harvard Medical School Boston Massachusetts

2. Department of Anesthesiology, Critical Care, and Pain Medicine Boston Children's Hospital Boston Massachusetts

3. Division of Rheumatology, Department of Pediatrics Baylor College of Medicine Houston Texas

4. Division of Pediatric Cardiology, Department of Pediatrics Baylor College of Medicine and Texas Children's Fetal Center Houston Texas

5. Division of Pediatric Critical Care, Department of Pediatrics University of Utah and Primary Children's Hospital Salt Lake City Utah

6. Department of Pediatrics, Section of Critical Care Medicine University of Colorado School of Medicine and Children's Hospital Colorado Aurora

7. Division of Pediatric Critical Care Medicine and Department of Pediatrics Indiana University School of Medicine, Riley Hospital for Children Indianapolis

8. Division of Pediatric Infectious Diseases, Department of Pediatrics Vanderbilt University Medical Center Nashville Tennessee

9. Department of Critical Care Medicine Rady Children's Hospital–San Diego San Diego California

10. Division of Infectious Disease, Department of Pediatrics University of Mississippi Medical Center Jackson

11. Division of Critical Care Medicine, Department of Pediatrics Nationwide Children's Hospital Columbus Ohio

12. Division of Pediatric Critical Care Medicine, Department of Pediatrics University of Alabama at Birmingham

13. Department of Pediatric Rheumatology Children's Hospital of The King's Daughters, Eastern Virginia Medical School Norfolk

14. Division of Pediatric Infectious Disease, Department of Pediatrics Children's Mercy Kansas City Kansas City Missouri

15. Department of Anesthesiology and Critical Care Children's Hospital of Philadelphia, University of Pennsylvania Perelman School of Medicine Philadelphia

16. Pediatric Critical Care Division Maria Fareri Children's Hospital at Westchester Medical Center and New York Medical College Valhalla New York

17. Division of Pediatric Critical Care, Department of Pediatrics University of Iowa Carver College of Medicine Iowa City

18. Division of Critical Care Medicine Akron Children's Hospital Akron Ohio

19. Division of Critical Care Medicine UCSF Benioff Children's Hospital Oakland Oakland California

20. Division of Pediatric Critical Care Medicine Medical University of South Carolina Charleston

21. Division of Critical Care Medicine Children's Hospital Orange County Orange California

22. Division of Pediatric Critical Care Medicine Children's Hospital of Michigan, Central Michigan University Detroit

23. Department of Cardiology Boston Children's Hospital, and Department of Pediatrics, Harvard Medical School Boston Massachusetts

24. CDC COVID‐19 Response Team Atlanta Georgia

25. Department of Anesthesiology, Critical Care, and Pain Medicine, Boston Children's Hospital, and Departments of Pediatrics and Anaesthesia Harvard Medical School Boston Massachusetts

Abstract

ObjectiveEvidence regarding effectiveness of interleukin‐1 receptor antagonism in multisystem inflammatory syndrome in children (MIS‐C) is lacking. We characterized variation in initial treatment with anakinra and evaluated cardiovascular outcomes associated with adding anakinra to standard initial therapy.MethodsWe conducted a retrospective cohort study of MIS‐C cases in a US surveillance registry from November 2020 to December 2021. Day 0 was the first calendar day of immunomodulatory treatment. Factors associated with initial anakinra use (days 0–1) were identified. We compared cases in patients ages 2–20 years receiving intravenous immunoglobulin (IVIG) and glucocorticoids versus anakinra plus IVIG and/or glucocorticoids on days 0–1, using inverse probability weighting to balance disease severity. Primary outcomes were vasopressor requirement on day 3 and impaired left ventricular ejection fraction on days 3–4. The secondary outcome was 50% reduction in C‐reactive protein on day 3.ResultsAmong 1,516 MIS‐C cases at 44 sites, 193 (13%) patients received anakinra alone or with other immunomodulators as initial treatment (range 0–74% by site). Site accounted for 59% of residual variance in anakinra use. After balancing disease severity, initial treatment with anakinra plus IVIG and/or glucocorticoids (n = 121) versus IVIG plus glucocorticoids (n = 389) was not associated with significant differences in vasopressor requirement (25.6% versus 20.1%, respectively; risk ratio [RR] 1.27 [95% confidence interval (95% CI) 0.88–1.84]), ventricular dysfunction (33.7% versus 25.7%, respectively; RR 1.31 [95% CI 0.98–1.75]), or C‐reactive protein reduction.ConclusionWe identified substantial variation in initial anakinra use in a real‐world population of children with MIS‐C, but no average short‐term improvement in cardiovascular outcomes associated with early addition of anakinra to IVIG and/or glucocorticoids compared to IVIG and glucocorticoids alone.

Funder

National Institutes of Health

Publisher

Wiley

Subject

Immunology,Rheumatology,Immunology and Allergy

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