Author: Stephen, Shiny; Park, Yeungâ€Ae; Chrysostomou, Anastasia
Title: Clinical benefits of Tocilizumab in COVIDâ€19â€related cytokine release syndrome in a patient with endâ€stage kidney disease on haemodialysis in Australia Cord-id: 8jrqokld Document date: 2020_8_10
ID: 8jrqokld
Snippet: COVIDâ€19 remains a global pandemic with more than ten million cases and half a million deaths worldwide. The disease manifestations in patients with chronic kidney disease and especially those on haemodialysis are still being understood, with only a few overseas case series, and small observational trials thus far. It appears the disease is more severe in this patient cohort. (1) (1) (1 1) Part of the pathophysiology of severe COVIDâ€19 is related to accompanying cytokine release syndrome. To
Document: COVIDâ€19 remains a global pandemic with more than ten million cases and half a million deaths worldwide. The disease manifestations in patients with chronic kidney disease and especially those on haemodialysis are still being understood, with only a few overseas case series, and small observational trials thus far. It appears the disease is more severe in this patient cohort. (1) (1) (1 1) Part of the pathophysiology of severe COVIDâ€19 is related to accompanying cytokine release syndrome. Tocilizumab, an interleukinâ€6 inhibitor, has been trialled for treatment of cytokine release syndrome in COVIDâ€19, but not yet approved. We present a case of an Australian patient on longâ€term haemodialysis with severe COVIDâ€19 who was successfully treated with Tocilizumab. The peak of her illness was on day 7, with a Câ€reactive protein of 624 mg/L (reference <5 mg/L), ferritin of 5293 ng/mL (reference 30â€500 ng/mL), and interleukinâ€6 level 1959.7 pg/mL, consistent with cytokine release syndrome. She was severely hypoxic on a ventilator, with rising inotropic requirements. With the use of Tocilizumab there was a significant and immediate response in her inflammatory markers, and she made a steady recovery. The patient was discharged home six weeks after presentation.
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