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. 2024 Aug 21;24:847. doi: 10.1186/s12879-024-09581-w

Table 1.

Characteristics of included studies

Author Year Country Study Design Study Population Total participants Mean (SD) or median (IQR) age MIS diagnosis criteria Number of patients with anakinra treatment Dose and frequency of anakinra Key findings
Akkoyun 2023 [24] 2023 USA Retrospective cohort study Children hospitalized for MIS-C 138 9.9 (8.1–13.9) years CDC criteria 32 IV anakinra was started at 8–10 mg/kg/day divided every 6 h in critically ill patients and 6–8 mg/kg/day divided every 6 h in non-critically ill patients Anakinra use showed no differences in median duration of vasoactive support, fever resolution, CRP reduction, or Vasopressor-Inotrope Score
Chang 2023 [25] 2023 USA Retrospective cohort study MIS-C cases in a US surveillance registry 1516 10.1 (4.1) years CDC criteria 121 4 mg/kg/day (range 0.2–20 mg/kg/day) No short-term cardiovascular benefits observed with the early addition of anakinra to IVIG and glucocorticoids compared to using IVIG and glucocorticoids alone.
Dizon 2023 [26] 2023 USA Observational clinical cohort study Children hospitalized for MIS-C 46 8 (4–10) years CDC criteria 32 8–10 mg/kg/day divided every 6 h in critically ill patients and 6–8 mg/kg/day divided every 6 h in non-critically ill patients Anakinra treatment, primarily used alongside IVIG in patients with severe MIS-C, was linked to enhanced cardiac function and fever reduction
Dusser 2024 [27] 2024 France Prospective study Children Hospitalized for MIS-C 470 10.06 (3.9) years CDC criteria 18 2.53 ± 1.3 mg/kg/day for a median duration of 3 days Subcutaneous anakinra is a safe and effective option for treating heart failure or MAS in MIS-C.
Taddio 2024 [28] 2024 Italy Retrospective cohort study Children with MIS-C 239 8 (I4–11) years RCPCH criteria 21 NA Early treatment with anakinra is both safe and highly effective in patients with severe MIS-C.
Yang 2023 [29] 2023 USA Retrospective cohort study Hospitalized pediatric patients (age ≤ 21 years) for MIS-C 14 6 (4.0-10.5) years NA 14 Initial median dose of 2.3 mg/kg with a median dosing interval of 12 h for a median initial treatment duration of 3.5 days Clinicians should assess patient history and previous therapy responses before starting IV anakinra. Further extensive studies are needed to confirm its off-label safety and efficacy.

Abbreviations: CDC: Centers for Disease Control and Prevention, CRP: C-reactive protein, IV: Intravenous, IVIG: Intravenous Immunoglobulin, IQR: Interquartile Range, MAS: Macrophage Activation Syndrome, MIS-C: Multisystem Inflammatory Syndrome in Children, RCPCH: Royal College of Paediatrics and Child Health, SD: Standard Deviation, VIS: Vasopressor-Inotrope Score