Coronavirus disease 2019 (COVID-19) is currently a major public health problem. The development of pulmonary fibrosis secondary to acute respiratory distress syndrome (ARDS) is one of the expected sequelae. In this case series, we describe five instances of the use of anakinra in late-phase COVID-19 pneumonia in hospitalized patients with pulmonary fibrosis and refractory respiratory failure fulfilling ARDS criteria. The study demonstrates that anakinra has promising efficacy and safety in late-phase COVID-19 infection in patients with ARDS and refractory hypoxaemia, and suggests its potential application as antifibrotic therapy in these patients. Learning points: Up to one third of patients with severe COVID-19 pneumonia progress to acu...
SARS-CoV-2 leads to an inflammatory and fibrotic state in the lungs which can be the cause of death ...
Summary: Background: The SAVE-MORE trial demonstrated that anakinra treatment in COVID-19 pneumonia...
Background At the end of 2021, the European Medicines Agency (EMA) expanded its approval for the r...
Coronavirus disease 2019 (COVID-19) is currently a major public health problem. The development of p...
The current COVID-19 pandemic has spread like wildfire worldwide and has affected millions of people...
International audienceBackground: Patients with COVID-19 pneumonia have an excess of inflammation an...
Early increase of soluble urokinase plasminogen activator receptor (suPAR) serum levels is indicativ...
More than 220 countries and territories are globally affected by the recent pandemic COVID-19 which ...
Little evidence appears to exist for the use of anakinra, a recombinant interleukin-1 receptor antag...
Coronavirus has affected more than 128 million humans worldwide with invasionsin 129 countries acros...
ObjectiveWe aimed to investigate whether anakinra, an interleukin-1receptor inhibitor, could improve...
Coronavirus Disease-2019 (COVID-19), caused by the novel coronavirus, remains a largely unsolved mys...
A subgroup of patients with SARS-CoV-2 infection was thought to have developed cytokine release synd...
Introduction: Severe COVID-19 cases have a detrimental hyper-inflammatory host response and differen...
International audienceObjective: we aimed to investigate whether anakinra, an interleukin-1receptor ...
SARS-CoV-2 leads to an inflammatory and fibrotic state in the lungs which can be the cause of death ...
Summary: Background: The SAVE-MORE trial demonstrated that anakinra treatment in COVID-19 pneumonia...
Background At the end of 2021, the European Medicines Agency (EMA) expanded its approval for the r...
Coronavirus disease 2019 (COVID-19) is currently a major public health problem. The development of p...
The current COVID-19 pandemic has spread like wildfire worldwide and has affected millions of people...
International audienceBackground: Patients with COVID-19 pneumonia have an excess of inflammation an...
Early increase of soluble urokinase plasminogen activator receptor (suPAR) serum levels is indicativ...
More than 220 countries and territories are globally affected by the recent pandemic COVID-19 which ...
Little evidence appears to exist for the use of anakinra, a recombinant interleukin-1 receptor antag...
Coronavirus has affected more than 128 million humans worldwide with invasionsin 129 countries acros...
ObjectiveWe aimed to investigate whether anakinra, an interleukin-1receptor inhibitor, could improve...
Coronavirus Disease-2019 (COVID-19), caused by the novel coronavirus, remains a largely unsolved mys...
A subgroup of patients with SARS-CoV-2 infection was thought to have developed cytokine release synd...
Introduction: Severe COVID-19 cases have a detrimental hyper-inflammatory host response and differen...
International audienceObjective: we aimed to investigate whether anakinra, an interleukin-1receptor ...
SARS-CoV-2 leads to an inflammatory and fibrotic state in the lungs which can be the cause of death ...
Summary: Background: The SAVE-MORE trial demonstrated that anakinra treatment in COVID-19 pneumonia...
Background At the end of 2021, the European Medicines Agency (EMA) expanded its approval for the r...