Systematic Reviews
Copyright ©The Author(s) 2022.
World J Crit Care Med. Jul 9, 2022; 11(4): 269-297
Published online Jul 9, 2022. doi: 10.5492/wjccm.v11.i4.269
Table 1 Summary of studies addressing interleukin-1 blockers on coronavirus disease 2019
Ref.
Patients
Intervention
Comparison
Outcome
CORIMUNO-19 Collaborative group[74], RCTHospitalized patient with mild-to-moderate pneumonia, non-ICU admittedAnakinra (200 mg twice a day on days 1-3, 100 mg twice on day 4, 100 mg once on day 5) (n = 59)Standard care (n = 55)No difference in NIV/MV/death at day 4. Stopped early following the recommendation of the data and safety monitoring board
Cavalli et al[75], observationalPneumonia with moderate-to-severe ARDS and hyperinflammation (non-MV, non-ICU admitted)Anakinra (high dose: 5 mg/kg twice a day intravenously, n = 29; or low dose: 100 mg twice a day subcutaneously, n = 7)Standard care (retrospective cohort) (n = 16)Survival. High-dose anakinra: 72%, SC: 56%, P = 0.009
Huet et al[76], observationalBilateral pneumonia (non-ICU admitted)Anakinra (100 mg twice daily for 72 h, followed by 100 mg daily for 7 d) (n = 52)Standard care (historical group) (n = 44)Death/MV. Anakinra: HR = 0.22 (95%CI: 0.11-0.41), P < 0.0001. Death. Anakinra: HR = 0.30 (95%CI: 0.12-0.71), P = 0.0063. MV: Anakinra: HR = 0.22 (95%CI: 0.09-0.56), P = 0.0015
Kooistra et al[77], observationalICU admitted pneumonia (MV: 100%)Anakinra (300 mg iv, followed by 100 mg iv/6 h) (n = 21)Standard care (n = 39)No differences in duration of MV, ICU length of stay, or mortality