Department of Infectious Diseases of Hospital Geral De Roraima. Universidade Federal De Roraima. Boa Vista Brazil.
Post Graduate Program in Health Science of Universidade Federal De Roraima, Health Science Center, Boa Vista, Brazil.
Pathog Glob Health. 2021 Jun;115(4):235-242. doi: 10.1080/20477724.2021.1890887. Epub 2021 Mar 8.
: Given the urgent need for strategies to minimize the damage caused by this pandemic, this study performed a randomized, double-blind phase 2 study to assess the safety of the effectiveness of chloroquine (CQ), hydroxychloroquine (HCQ) or ivermectin in severe forms of COVID-19, in addition to identifying predictors of mortality in this group of patients.: Phase 2, double-blind, randomized study to assess the safety and efficacy of enteral CQ, HCQ or ivermectin in patients hospitalized for SARS-CoV-2 infection, admitted to a Reference Hospital in Roraima (Brazil) in may 2020. Patients were randomized in a 1:1:1 ratio. The endpoints were need of supplemental O, invasive ventilation, admission in ICU and death. The study was approved by an independent IRB.: 168 patients were randomized. The mean age was 53.4 years (±15.6), most participants were male ( = 95; 58.2%). Therapy with corticosteroid, anticoagulant or antibiotics was a decision of the attending physicians, and there was no difference between the groups. The mortality was similar in three groups (22.2%; 21.3% and 23.0%) suggesting ineffectiveness of the drugs. No difference in the incidence of serious adverse events were observed. To be older than 60 years of age, obesity, diabetes, extensive pulmonary involvement and low SaO at hospital admission due to independent risk factors for mortality.: Although CQ, HCQ or ivermectin revealed a favorable safety profile, the tested drugs do not reduce the need for supplemental oxygen, ICU admission, invasive ventilation or death, in patients hospitalized with a severe form of COVID-19.
鉴于迫切需要制定策略来减轻这种大流行造成的损害,本研究进行了一项随机、双盲的 2 期研究,以评估氯喹(CQ)、羟氯喹(HCQ)或伊维菌素在 COVID-19 严重形式中的安全性,此外还确定了这组患者死亡的预测因素。
2 期、双盲、随机研究,评估 2020 年 5 月在巴西罗赖马的一家参考医院住院的因 SARS-CoV-2 感染住院的患者中肠内 CQ、HCQ 或伊维菌素的安全性和疗效。患者以 1:1:1 的比例随机分组。终点是需要补充氧气、有创通气、入住 ICU 和死亡。该研究得到了一个独立的 IRB 的批准。
168 名患者被随机分组。平均年龄为 53.4 岁(±15.6),大多数参与者为男性(=95;58.2%)。皮质类固醇、抗凝剂或抗生素的治疗是主治医生的决定,各组之间没有差异。三组的死亡率相似(22.2%、21.3%和 23.0%),表明药物无效。未观察到严重不良事件的发生率存在差异。年龄大于 60 岁、肥胖、糖尿病、广泛的肺部受累和入院时低 SaO2 是死亡的独立危险因素。
尽管 CQ、HCQ 或伊维菌素显示出良好的安全性,但在住院治疗 COVID-19 严重形式的患者中,测试药物并不能减少对补充氧气、入住 ICU、有创通气或死亡的需求。