Colchicine in Recently Hospitalized Patients with COVID-19: A Randomized Controlled Trial (COL-COVID)

被引:25
作者
Pascual-Figal, Domingo A. [1 ,2 ,3 ]
Roura-Piloto, Aychel E. [4 ]
Moral-Escudero, Encarnacion [4 ]
Bernal, Enrique [5 ]
Albendin-Iglesias, Helena [4 ]
Teresa Perez-Martinez, M. [1 ]
Antonio Noguera-Velasco, Jose [6 ]
Cebreiros-Lopez, Iria [6 ]
Hernandez-Vicente, Alvaro [1 ]
Vazquez-Andres, David [1 ]
Sanchez-Perez, Carmen [2 ]
Khan, Amjad [7 ]
Sanchez-Cabo, Fatima [3 ]
Garcia-Vazquez, Elisa [4 ]
机构
[1] Univ Murcia, Hosp Univ Virgen Arrixaca, Cardiol Dept, IMIB Arrixaca, Murcia, Spain
[2] CIBERCV, Ctr Invest Biomed Red Enfermedades Cardiovasc, Madrid, Spain
[3] Ctr Nacl Invest Cardiovasc CNIC, Madrid, Spain
[4] Univ Murcia, Hosp Univ Virgen Arrixaca, Infect Dis & Internal Med Dept, IMIB Arrixaca, Murcia, Spain
[5] Univ Murcia, Hosp Univ Reina Sofia, Infect Dis & Internal Med Dept, IMIB Arrixaca, Murcia, Spain
[6] Univ Murcia, Hosp Univ Virgen Arrixaca, Clin Biochem Dept, IMIB Arrixaca, Murcia, Spain
[7] Univ Oxford, Dept Chem, Oxford, England
关键词
colchicine; COVID-19; inflammation;
D O I
10.2147/IJGM.S329810
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Colchicine has been proposed as a potential therapy in coronavirus disease 2019 (COVID-19) due to their anti-inflammatory actions. Methods: The COL-COVID study was a prospective, randomized, controlled and openlabel clinical trial that compared colchicine added to standard treatment vs standard treatment in hospitalized COVID-19 patients that do not need mechanical ventilatory support. Colchicine was initiated within the first 48 hours of admission at a 1.5 mg loading dose, followed by 0.5 mg b.i.d. for one week and 0.5 mg per day for 28 days. The study endpoints were clinical status (7-points WHO ordinal scale) and inflammatory biomarkers (IL-6 and CRP). Results: A total of 103 patients (51 +/- 12 years, 52% male) were randomly allocated to colchicine arm (n=52) and control arm (n=51). At day 28, all patients in the colchicine group were alive and discharged, whereas in the control group, two patients died in-hospital and one patient remained hospitalized. Clinical improvement in terms of changes on WHO scale at day 14 and 28 and time to 1-point clinical improvement did not differ between the two groups. Clinical deterioration (increase of at least 1-point in WHO scale) was observed in a higher proportion of cases in colchicine group (13.8%) vs control group (5.8%) (p=0.303); after adjustment by baseline risk factors and concomitant therapies, colchicine therapy was associated with a lower risk of clinical deterioration (p=0.030). Inflammatory biomarkers CRP and IL-6 concentrations course did not differ between the two arms. Conclusion: In hospitalized COVID-19 patients, colchicine treatment neither improved the clinical status, nor the inflammatory response, over the standard treatment. Nevertheless, a preventive effect for further clinical deterioration might be possible.
引用
收藏
页码:5517 / 5526
页数:10
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