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All Studies   Meta Analysis    Recent:   
0 0.5 1 1.5 2+ Mortality 73% Improvement Relative Risk Discharge 73% Colchicine  Brunetti et al.  LATE TREATMENT Is late treatment with colchicine beneficial for COVID-19? PSM retrospective 66 patients in the USA Lower mortality (p=0.033) and higher discharge (p=0.033) c19early.org Brunetti et al., J. Clin. Med., 2961, Sep 2020 Favors colchicine Favors control

Colchicine to Weather the Cytokine Storm in Hospitalized Patients with COVID-19

Brunetti et al., J. Clin. Med., 9:9, 2961, doi:10.3390/jcm9092961
Sep 2020  
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Colchicine for COVID-19
5th treatment shown to reduce risk in September 2020
 
*, now known with p = 0.0000001 from 54 studies.
No treatment is 100% effective. Protocols combine complementary and synergistic treatments. * >10% efficacy in meta analysis with ≥3 clinical studies.
4,100+ studies for 60+ treatments. c19early.org
PSM matched analysis from consecutive hospitalized patients, with 33 colchicine and 33 control matched patients, showing lower mortality with treatment.
risk of death, 72.7% lower, RR 0.27, p = 0.03, treatment 3 of 33 (9.1%), control 11 of 33 (33.3%), NNT 4.1, PSM.
risk of no hospital discharge, 72.7% lower, RR 0.27, p = 0.03, treatment 3 of 33 (9.1%), control 11 of 33 (33.3%), NNT 4.1, PSM.
Effect extraction follows pre-specified rules prioritizing more serious outcomes. Submit updates
Brunetti et al., 14 Sep 2020, retrospective, propensity score matching, USA, peer-reviewed, baseline oxygen required 86.4%, 7 authors, dosage 1.2mg daily.
This PaperColchicineAll
Colchicine to Weather the Cytokine Storm in Hospitalized Patients with COVID-19
Luigi Brunetti, Oumou Diawara, Andrew Tsai, Bonnie L Firestein, Ronald G Nahass, George Poiani, Naomi Schlesinger
Journal of Clinical Medicine, doi:10.3390/jcm9092961
The repurposing of colchicine for the treatment of COVID-19 was suggested based in its immunomodulatory, anti-inflammatory, and anti-viral properties. We performed a single-center propensity score matched cohort study, including all consecutive COVID-19 patients admitted to a community hospital between 1 March 2020 and 30 May 2020. Patients were stratified according to the receipt of colchicine. The primary endpoint was defined as in-hospital death within 28-days follow-up. Secondary endpoints included favorable change in the Ordinal Scale for Clinical Improvement on days 14 and 28 versus baseline, proportion of patients not requiring supplemental oxygen on days 14 and 28, and proportion of patients discharged by day 28. In total data for 303 PCR positive COVID-19 patients were extracted and 66 patients were included in the 1:1 matched cohort study. At the end of the 28 day follow-up, patients receiving colchicine were approximately five times more likely to be discharged (odds ratio, 5.0; 95% confidence interval, 1.25-20.1; p = 0.023) and when comparing mortality, there were 3 deaths (9.1%) in patients receiving colchicine versus 11 deaths (33.3%) in the groups receiving standard of care (odds ratio, 0.20; 95% confidence interval, 0.05-0.80; p = 0.023). These observations warrant further investigation in large controlled clinical trials.
Conflicts of Interest: The authors declare no conflict of interest.
References
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Late treatment
is less effective
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