Author: Koschmieder, Steffen; Jost, Edgar; Cornelissen, Christian; Müller, Tobias; Schulzeâ€Hagen, Maximilian; Bickenbach, Johannes; Marx, Gernot; Kleines, Michael; Marx, Nikolaus; Brümmendorf, Tim H.; Dreher, Michael
Title: Favorable COVIDâ€19 course despite significant comorbidities in a ruxolitinibâ€treated patient with primary myelofibrosis Cord-id: udyfm2bn Document date: 2020_6_27
ID: udyfm2bn
Snippet: COVIDâ€19 carries a high risk of severe disease course, particularly in patients with comorbidities. Therapy of severe COVIDâ€19 infection has relied on supportive intensive care measures. More specific approaches including drugs that limit the detrimental “cytokine stormâ€, such as Janusâ€activated kinase (JAK) inhibitors, are being discussed. Here, we report a compelling case of a 55â€yo patient with proven COVIDâ€19 pneumonia, who was taking the JAK1/2 inhibitor ruxolitinib inâ€label
Document: COVIDâ€19 carries a high risk of severe disease course, particularly in patients with comorbidities. Therapy of severe COVIDâ€19 infection has relied on supportive intensive care measures. More specific approaches including drugs that limit the detrimental “cytokine stormâ€, such as Janusâ€activated kinase (JAK) inhibitors, are being discussed. Here, we report a compelling case of a 55â€yo patient with proven COVIDâ€19 pneumonia, who was taking the JAK1/2 inhibitor ruxolitinib inâ€label for coâ€existing primary myelofibrosis for 15 months prior to coronavirus infection. The patient had significant comorbidities, including chronic kidney disease, arterial hypertension, and obesity, and our previous cohort suggested that he was thus at high risk for acute respiratory distress syndrome (ARDS) and death from COVIDâ€19. Since abrupt discontinuation of ruxolitinib may cause fatal cytokine storm and ARDS, ruxolitinib treatment was continued and was well tolerated, and the patient´s condition remained stable, without the need for mechanical ventilation or vasopressors. The patient became negative for SARSâ€CoVâ€2 and was discharged home after 15 days. In conclusion, our report provides clinical evidence that ruxolitinib treatment is feasible and can be beneficial in patients with COVIDâ€19 pneumonia, preventing cytokine storm and ARDS.
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