2023
DOI: 10.1016/s0140-6736(23)00510-x
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Higher dose corticosteroids in patients admitted to hospital with COVID-19 who are hypoxic but not requiring ventilatory support (RECOVERY): a randomised, controlled, open-label, platform trial

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Cited by 37 publications
(4 citation statements)
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“…Several studies have found a negative impact of long-term high-dose corticosteroid therapy during COVID-19 on the occurrence of, among others, myocardial infarction, bacterial sepsis, cerebrovascular and ophthalmological diseases. [44][45][46][47] Similarly, Remdesivir potentially affects cardiac repolarisation. 48 Several studies have reported cardiovascular side effects of Remdesivir, including bradycardia, hypotension, QTc prolongation, nonspecific T wave changes, and cardiac arrest.…”
Section: Discussionmentioning
confidence: 99%
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“…Several studies have found a negative impact of long-term high-dose corticosteroid therapy during COVID-19 on the occurrence of, among others, myocardial infarction, bacterial sepsis, cerebrovascular and ophthalmological diseases. [44][45][46][47] Similarly, Remdesivir potentially affects cardiac repolarisation. 48 Several studies have reported cardiovascular side effects of Remdesivir, including bradycardia, hypotension, QTc prolongation, nonspecific T wave changes, and cardiac arrest.…”
Section: Discussionmentioning
confidence: 99%
“…The authors did not consider the effect of drugs intake chronically or during and after infection, which may affect the occurrence and persistence of disorders in long-COVID. The examined patients were not hospitalized and did not take steroids or Remdesivir; this is particularly important due to the influence of corticosteroids [44][45][46][47] or Remdesivir 48 on heart muscle function. Another limitation is the lack of knowledge about whether patients had myocardial dysfunction before contracting COVID-19, as it had not been previously diagnosed.…”
Section: Strengths and Limitations Of The Studymentioning
confidence: 99%
“…In this issue of The Lancet, the RECOVERY Collaborative Group 7 reports the results of a multicentre, multicountry, randomised, open-label platform trial evaluating a higher dose of dexamethasone (20 mg once daily for 5 days followed by 10 mg once daily for 5 days) compared with usual care (6 mg dexamethasone once daily for 10 days) in 1272 patients with COVID-19 receiving no oxygen (n=8) or simple oxygen supplementation (n=1264). 769 (60%) participants were male and 503 (40%) were female, with a mean age of 61·1 (SD 17·5) years; 688 (54%) were Asian, 454 (36%) were White, 14 (1%) were Black, and 116 (9%) were of other or unknown ethnicity.…”
mentioning
confidence: 99%
“…The occurrence of non-COVID-19 pneumonia and hyperglycaemia was also higher in the higher-dose group. 7 …”
mentioning
confidence: 99%