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Variation in Early Anakinra Use and Short-Term Outcomes in Multisystem Inflammatory Syndrome in Children.
Chang, Joyce C; Young, Cameron C; Muscal, Eyal; Sexson Tejtel, Sara K; Newhams, Margaret M; Kucukak, Suden; Crandall, Hillary; Maddux, Aline B; Rowan, Courtney M; Halasa, Natasha B; Harvey, Helen A; Hobbs, Charlotte V; Hall, Mark W; Kong, Michele; Aguiar, Cassyanne L; Schuster, Jennifer E; Fitzgerald, Julie C; Singh, Aalok R; Wellnitz, Kari; Nofziger, Ryan A; Cvijanovich, Natalie Z; Mack, Elizabeth H; Schwarz, Adam J; Heidemann, Sabrina M; Newburger, Jane W; Zambrano, Laura D; Campbell, Angela P; Patel, Manish M; Randolph, Adrienne G; Son, Mary Beth F.
Affiliation
  • Chang JC; Division of Immunology, Boston Children's Hospital, and Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.
  • Young CC; Department of Anesthesiology, Critical Care, and Pain Medicine, Boston Children's Hospital, Boston, Massachusetts.
  • Muscal E; Division of Rheumatology, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.
  • Sexson Tejtel SK; Division of Pediatric Cardiology, Department of Pediatrics, Baylor College of Medicine and Texas Children's Fetal Center, Houston, Texas.
  • Newhams MM; Department of Anesthesiology, Critical Care, and Pain Medicine, Boston Children's Hospital, Boston, Massachusetts.
  • Kucukak S; Department of Anesthesiology, Critical Care, and Pain Medicine, Boston Children's Hospital, Boston, Massachusetts.
  • Crandall H; Division of Pediatric Critical Care, Department of Pediatrics, University of Utah and Primary Children's Hospital, Salt Lake City, Utah.
  • Maddux AB; Department of Pediatrics, Section of Critical Care Medicine, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora.
  • Rowan CM; Division of Pediatric Critical Care Medicine and Department of Pediatrics, Indiana University School of Medicine, Riley Hospital for Children, Indianapolis.
  • Halasa NB; Division of Pediatric Infectious Diseases, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Harvey HA; Department of Critical Care Medicine, Rady Children's Hospital-San Diego, San Diego, California.
  • Hobbs CV; Division of Infectious Disease, Department of Pediatrics, University of Mississippi Medical Center, Jackson.
  • Hall MW; Division of Critical Care Medicine, Department of Pediatrics, Nationwide Children's Hospital, Columbus, Ohio.
  • Kong M; Division of Pediatric Critical Care Medicine, Department of Pediatrics, University of Alabama at Birmingham.
  • Aguiar CL; Department of Pediatric Rheumatology, Children's Hospital of The King's Daughters, Eastern Virginia Medical School, Norfolk.
  • Schuster JE; Division of Pediatric Infectious Disease, Department of Pediatrics, Children's Mercy Kansas City, Kansas City, Missouri.
  • Fitzgerald JC; Department of Anesthesiology and Critical Care, Children's Hospital of Philadelphia, University of Pennsylvania Perelman School of Medicine, Philadelphia.
  • Singh AR; Pediatric Critical Care Division, Maria Fareri Children's Hospital at Westchester Medical Center and New York Medical College, Valhalla, New York.
  • Wellnitz K; Division of Pediatric Critical Care, Department of Pediatrics, University of Iowa Carver College of Medicine, Iowa City.
  • Nofziger RA; Division of Critical Care Medicine, Akron Children's Hospital, Akron, Ohio.
  • Cvijanovich NZ; Division of Critical Care Medicine, UCSF Benioff Children's Hospital Oakland, Oakland, California.
  • Mack EH; Division of Pediatric Critical Care Medicine, Medical University of South Carolina, Charleston.
  • Schwarz AJ; Division of Critical Care Medicine, Children's Hospital Orange County, Orange, California.
  • Heidemann SM; Division of Pediatric Critical Care Medicine, Children's Hospital of Michigan, Central Michigan University, Detroit.
  • Newburger JW; Department of Cardiology, Boston Children's Hospital, and Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.
  • Zambrano LD; CDC COVID-19 Response Team, Atlanta, Georgia.
  • Campbell AP; CDC COVID-19 Response Team, Atlanta, Georgia.
  • Patel MM; CDC COVID-19 Response Team, Atlanta, Georgia.
  • Randolph AG; Department of Anesthesiology, Critical Care, and Pain Medicine, Boston Children's Hospital, and Departments of Pediatrics and Anaesthesia, Harvard Medical School, Boston, Massachusetts.
  • Son MBF; Division of Immunology, Boston Children's Hospital, and Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.
Arthritis Rheumatol ; 75(8): 1466-1476, 2023 08.
Article in En | MEDLINE | ID: mdl-36908050
ABSTRACT

OBJECTIVE:

Evidence 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.

METHODS:

We 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.

RESULTS:

Among 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.

CONCLUSION:

We 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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Connective Tissue Diseases / Interleukin 1 Receptor Antagonist Protein Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Humans Language: En Journal: Arthritis Rheumatol Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Connective Tissue Diseases / Interleukin 1 Receptor Antagonist Protein Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Humans Language: En Journal: Arthritis Rheumatol Year: 2023 Document type: Article