Efficacy and Outcome of Remdesivir and Tocilizumab Combination Against Dexamethasone for the Treatment of Severe COVID-19: A Randomized Controlled Trial

被引:12
作者
Chowdhury, Abu Taiub Mohammed Mohiuddin [1 ,2 ]
Kamal, Aktar [3 ]
Abbas, Kafil Uddin [4 ]
Talukder, Shubhashis [5 ]
Karim, Md Rezaul [6 ,7 ]
Ali, Md. Ahsan [8 ]
Nuruzzaman, Md. [9 ]
Li, Yarui [1 ]
He, Shuixiang [1 ]
机构
[1] Xi An Jiao Tong Univ, Dept Gastroenterol, Affiliated Hosp 1, Xi'an, Peoples R China
[2] Minist Hlth & Family Welf, OSD DGHS, Dhaka, Bangladesh
[3] M Abdur Rahim Med Coll Hosp, Dept Crit Care, Dinajpur, Bangladesh
[4] Coxs Bazar 250 Bed Dist Sadar Hosp, Dept Crit Care, Cox's Bazar, Bangladesh
[5] 250 Bed Chattogram Gen Hosp, Dept Crit Care, Chattogram, Bangladesh
[6] Hubei Univ Med, Inst Neurosci, Hubei Key Lab Embryon Stem Cell Res, Shiyan, Peoples R China
[7] Univ Hosp Limerick, Acute Med Unit, Limerick, Ireland
[8] Xi An Jiao Tong Univ, Dept Histol, Xi'an, Peoples R China
[9] M Abdur Rahim Med Coll Hosp, Dept Internal Med, Dinajpur, Bangladesh
关键词
COVID-19; SARS-Cov-2; remdecivir; tocilizumab; dexamethasone; ARDS; Bangladesh; MANAGEMENT; THERAPY;
D O I
10.3389/fphar.2022.690726
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: In this study, we investigated the efficacy and safety of remdesivir and tocilizumab combination therapy against dexamethasone for the management of severe COVID-19 patients.Methods: This was a multicenter study. Cases were randomly chosen and divided into two groups using an odd-even ratio of 1:1 applied to the hospital registration number. Group A received remdesivir [5 mg/kg (< 40 kg) or 200 mg (> 40 kg) on day 1 and then 2.5 mg/kg (< 40 kg) or 100 mg (> 40 kg) daily] + tocilizumab [8 mg/kg up to 800 mg highest 12 h apart], and group B was the control and received dexamethasone 6 mg/day. In addition, a broad-spectrum antibiotic and other essential treatments were received by all patients. To evaluate the mortality risk, the sequential organ failure assessment (SOFA) score was calculated on day-1. Treatment outcomes were measured as time to clinical improvement; mortality rate; duration of ICU stay; total period of hospitalization; the rate of (Supplementary Material) oxygen use; time to clinical failure; National Early Warning Score-2 (NEWS), and the percentage of lung recovery on CT of chest on discharge. Clinical trial registration ID: .Results: Remdesivir-Tocilizumab group had a lower mortality rate (25.49%) than the control (30.77%). The time to clinical improvement (Group A-9.41; B-14.21 days), NEWS-2 on discharge (Group A-0.89; B-1.2), duration of ICU stay (Group A-7.68; B-10.58), and duration of hospitalization (Group A-9.91; B-14.68) were less in the treatment group. Group A had a better percentage of lung recovery on chest CT than the control (Group A-22.13; B-11.74). All these differences were statistically significant (p= < 0.05) in a t-test. However, no significant survival benefit was found among the study groups in Kaplan-Meier survival analysis, p = 0.739.Conclusion: The remdesivir-tocilizumab combination had preferable outcomes compared to the dexamethasone therapy for the treatment of severe COVID-19 concerning mortality rate and clinical and pulmonary improvement, although it did not demonstrate a significant survival benefit.& nbsp;
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页数:10
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