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10.1136/rmdopen-2020-001455

http://scihub22266oqcxt.onion/10.1136/rmdopen-2020-001455
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33542047!7868202!33542047
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suck abstract from ncbi


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pmid33542047      RMD+Open 2021 ; 7 (1): ä
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  • Beneficial effects of colchicine for moderate to severe COVID-19: a randomised, double-blinded, placebo-controlled clinical trial #MMPMID33542047
  • Lopes MI; Bonjorno LP; Giannini MC; Amaral NB; Menezes PI; Dib SM; Gigante SL; Benatti MN; Rezek UC; Emrich-Filho LL; Sousa BAA; Almeida SCL; Luppino Assad R; Veras FP; Schneider A; Rodrigues TS; Leiria LOS; Cunha LD; Alves-Filho JC; Cunha TM; Arruda E; Miranda CH; Pazin-Filho A; Auxiliadora-Martins M; Borges MC; Fonseca BAL; Bollela VR; Del-Ben CM; Cunha FQ; Zamboni DS; Santana RC; Vilar FC; Louzada-Junior P; Oliveira RDR
  • RMD Open 2021[Feb]; 7 (1): ä PMID33542047show ga
  • OBJECTIVE: To evaluate whether the addition of colchicine to standard treatment for COVID-19 results in better outcomes. DESIGN: We present the results of a randomised, double-blinded, placebo-controlled clinical trial of colchicine for the treatment of moderate to severe COVID-19, with 75 patients allocated 1:1 from 11 April to 30 August 2020. Colchicine regimen was 0.5 mg thrice daily for 5 days, then 0.5 mg twice daily for 5 days. The primary endpoints were the need for supplemental oxygen, time of hospitalisation, need for admission and length of stay in intensive care unit and death rate. RESULTS: Seventy-two patients (36 for placebo and 36 for colchicine) completed the study. Median (and IQR) time of need for supplemental oxygen was 4.0 (2.0-6.0) days for the colchicine group and 6.5 (4.0-9.0) days for the placebo group (p<0.001). Median (IQR) time of hospitalisation was 7.0 (5.0-9.0) days for the colchicine group and 9.0 (7.0-12.0) days for the placebo group (p=0.003). At day 2, 67% versus 86% of patients maintained the need for supplemental oxygen, while at day 7, the values were 9% versus 42%, in the colchicine and the placebo groups, respectively (log rank; p=0.001). Two patients died, both in placebo group. Diarrhoea was more frequent in the colchicine group (p=0.26). CONCLUSION: Colchicine reduced the length of both, supplemental oxygen therapy and hospitalisation. The drug was safe and well tolerated. Once death was an uncommon event, it is not possible to ensure that colchicine reduced mortality of COVID-19. TRIAL REGISTRATION NUMBER: RBR-8jyhxh.
  • |*COVID-19 Drug Treatment[MESH]
  • |*Length of Stay[MESH]
  • |*Oxygen Inhalation Therapy[MESH]
  • |*Severity of Illness Index[MESH]
  • |Adult[MESH]
  • |Aged[MESH]
  • |COVID-19/mortality/virology[MESH]
  • |Colchicine/*administration & dosage/adverse effects[MESH]
  • |Diarrhea/chemically induced[MESH]
  • |Double-Blind Method[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Intensive Care Units[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Reverse Transcriptase Polymerase Chain Reaction[MESH]
  • |SARS-CoV-2/*genetics[MESH]
  • |Time Factors[MESH]


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