TY - JOUR
T1 - Anakinra treatment in critically ill COVID-19 patients: a prospective cohort study
AU - Kooistra, Emma J.
AU - Waalders, Nicole J. B.
AU - Grondman, Inge
AU - Janssen, Nico A. F.
AU - de Nooijer, Aline H.
AU - Netea, Mihai G.
AU - van de Veerdonk, Frank L.
AU - the RCI-COVID-19 Study Group
AU - Ewalds, Esther
AU - van der Hoeven, Johannes G.
AU - Kox, Matthijs
AU - Pickkers, Peter
AU - Kooistra, Emma J.
AU - Waalders, Nicole J. B.
AU - Grondman, Inge
AU - Janssen, Nico A. F.
AU - de Nooijer, Aline H.
AU - Netea, Mihai G.
AU - van de Veerdonk, Frank L.
AU - Ewalds, Esther
AU - van der Hoeven, Johannes G.
AU - Kox, Matthijs
AU - Pickkers, Peter
AU - Hemelaar, Pleun
AU - Beunders, Remi
AU - Bruse, Niklas
AU - Frenzel, Tim
AU - Schouten, Jeroen
AU - Touw, Hugo
AU - van der Velde, Sjef
AU - van der Eng, Hetty
AU - Roovers, Noortje
AU - Klop-Riehl, Margreet
AU - Gerretsen, Jelle
AU - Claassen, Wout
AU - Heesakkers, Hidde
AU - van Schaik, Tirsa
AU - Buijsse, Leonie
AU - Joosten, Leo
AU - de Mast, Quirijn
AU - Jaeger, Martin
AU - Kouijzer, Ilse
AU - Dijkstra, Helga
AU - Lemmers, Heidi
AU - van Crevel, Reinout
AU - van de Maat, Josephine
AU - Nijman, Gerine
AU - Moorlag, Simone
AU - Taks, Esther
AU - Debisarun, Priya
AU - Wertheim, Heiman
AU - Hopman, Joost
AU - Rahamat-Langendoen, Janette
AU - Bleeker-Rovers, Chantal
AU - Koenen, Hans
AU - Fasse, Esther
AU - van Rijssen, Esther
AU - Kolkman, Manon
AU - van Cranenbroek, Bram
AU - Smeets, Ruben
AU - Joosten, Irma
PY - 2020/12/1
Y1 - 2020/12/1
N2 - Background: A subset of critically ill COVID-19 patients develop a hyperinflammatory state. Anakinra, a recombinant interleukin-1 receptor antagonist, is known to be effective in several hyperinflammatory diseases. We investigated the effects of anakinra on inflammatory parameters and clinical outcomes in critically ill, mechanically ventilated COVID-19 patients with clinical features of hyperinflammation. Methods: In this prospective cohort study, 21 critically ill COVID-19 patients treated with anakinra were compared to a group of standard care. Serial data of clinical inflammatory parameters and concentrations of multiple circulating cytokines were determined and aligned on start day of anakinra in the treatment group, and median start day of anakinra in the control group. Analysis was performed for day − 10 to + 10 relative to alignment day. Clinical outcomes were analyzed during 28 days. Additionally, three sensitivity analyses were performed: (1) using propensity score-matched groups, (2) selecting patients who did not receive corticosteroids, and (3) using a subset of the control group aimed to match the criteria (fever, elevated ferritin) for starting anakinra treatment. Results: Baseline patient characteristics and clinical parameters on ICU admission were similar between groups. As a consequence of bias by indication, plasma levels of aspartate aminotransferase (ASAT) (p = 0.0002), ferritin (p = 0.009), and temperature (p = 0.001) were significantly higher in the anakinra group on alignment day. Following treatment, no relevant differences in kinetics of circulating cytokines were observed between both groups. Decreases of clinical parameters, including temperature (p = 0.03), white blood cell counts (p = 0.02), and plasma levels of ferritin (p = 0.003), procalcitonin (p = 0.001), creatinine (p = 0.01), and bilirubin (p = 0.007), were more pronounced in the anakinra group. No differences in duration of mechanical ventilation or ICU length of stay were observed between groups. Sensitivity analyses confirmed these results. Conclusions: Anakinra is effective in reducing clinical signs of hyperinflammation in critically ill COVID-19 patients. A randomized controlled trial is warranted to draw conclusion about the effects of anakinra on clinical outcomes.
AB - Background: A subset of critically ill COVID-19 patients develop a hyperinflammatory state. Anakinra, a recombinant interleukin-1 receptor antagonist, is known to be effective in several hyperinflammatory diseases. We investigated the effects of anakinra on inflammatory parameters and clinical outcomes in critically ill, mechanically ventilated COVID-19 patients with clinical features of hyperinflammation. Methods: In this prospective cohort study, 21 critically ill COVID-19 patients treated with anakinra were compared to a group of standard care. Serial data of clinical inflammatory parameters and concentrations of multiple circulating cytokines were determined and aligned on start day of anakinra in the treatment group, and median start day of anakinra in the control group. Analysis was performed for day − 10 to + 10 relative to alignment day. Clinical outcomes were analyzed during 28 days. Additionally, three sensitivity analyses were performed: (1) using propensity score-matched groups, (2) selecting patients who did not receive corticosteroids, and (3) using a subset of the control group aimed to match the criteria (fever, elevated ferritin) for starting anakinra treatment. Results: Baseline patient characteristics and clinical parameters on ICU admission were similar between groups. As a consequence of bias by indication, plasma levels of aspartate aminotransferase (ASAT) (p = 0.0002), ferritin (p = 0.009), and temperature (p = 0.001) were significantly higher in the anakinra group on alignment day. Following treatment, no relevant differences in kinetics of circulating cytokines were observed between both groups. Decreases of clinical parameters, including temperature (p = 0.03), white blood cell counts (p = 0.02), and plasma levels of ferritin (p = 0.003), procalcitonin (p = 0.001), creatinine (p = 0.01), and bilirubin (p = 0.007), were more pronounced in the anakinra group. No differences in duration of mechanical ventilation or ICU length of stay were observed between groups. Sensitivity analyses confirmed these results. Conclusions: Anakinra is effective in reducing clinical signs of hyperinflammation in critically ill COVID-19 patients. A randomized controlled trial is warranted to draw conclusion about the effects of anakinra on clinical outcomes.
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85097436692&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/33302991
U2 - 10.1186/s13054-020-03364-w
DO - 10.1186/s13054-020-03364-w
M3 - Article
C2 - 33302991
VL - 24
JO - Critical Care
JF - Critical Care
SN - 1466-609X
IS - 1
M1 - 688
ER -