Department of Infectious Diseases, Namik Kemal University School of Medicine, Tekirdag, Turkiye
Department of Cardiology, Istanbul University School of Medicine, Istanbul, Turkiye
J Coll Physicians Surg Pak. 2024 Jun;34(6):659-666. doi: 10.29271/jcpsp.2024.06.659.
To evaluate the effect of favipiravir administered to diabetic and non-diabetic COVID-19 patients on the QT/QTc interval.
Analytical study. Place and Duration of the Study: Republic of Turkey, Ministry of Health, State Hospital, Corlu, Tekirdag, Turkiye, from March to September 2021.
Electrocardiogram (ECG) analysis was performed on all participants (n=180) divided into four groups. Group 1 included only healthy volunteers. Group 2 included only cases diagnosed with T2DM. Group 3 included only severe acute respiratory syndrome coronavirus-2 (SARS-Cov-2) cases. Group 4 included cases diagnosed with both SARS and T2DM. Favipiravir was administered only to the cases in Group 3 and Group 4. In the cases that were administered favipiravir, the QT/QTc interval was calculated and recorded at different time intervals on the first and fifth days of the therapy. The difference between groups was determined by Tukeye's test after ANOVA. Pearson's correlation test was used to determine whether there was a linear relationship between two numericals. The alpha significance value was determined to be <0.05 in all statistical analyses.
When all groups were compared, it was seen that both QT and QTc values increased in Groups 3 and 4, which were administered favipiravir (p <0.05). Favipiravir may cause an increased risk of ventricular and atrial arrhythmias.
Favipiravir may cause QT interval prolongation, particularly in SARS-Cov-2 patients diagnosed with T2DM.
COVID-19, Drug-induced long QT syndrome, Intra-infarct haemorrhage; Favipiravir, Type 2 diabetes mellitus.
评估给予糖尿病和非糖尿病 COVID-19 患者法维拉韦对 QT/QTc 间期的影响。
分析性研究。研究地点和时间:土耳其共和国,卫生部,科尔卢州,泰基尔达,土耳其,2021 年 3 月至 9 月。
对所有参与者(n=180)进行心电图(ECG)分析,参与者分为四组。第 1 组仅包括健康志愿者。第 2 组仅包括诊断为 T2DM 的病例。第 3 组仅包括严重急性呼吸综合征冠状病毒-2(SARS-Cov-2)病例。第 4 组包括同时诊断出 SARS 和 T2DM 的病例。仅向第 3 组和第 4 组的病例给予法维拉韦。在给予法维拉韦的病例中,在治疗的第 1 天和第 5 天的不同时间间隔计算并记录 QT/QTc 间期。在方差分析后,通过 Tukeye 检验确定组间差异。采用 Pearson 相关检验确定两个数值之间是否存在线性关系。在所有统计分析中,alpha 显著性值均确定为<0.05。
当比较所有组时,发现给予法维拉韦的第 3 组和第 4 组的 QT 和 QTc 值均升高(p<0.05)。法维拉韦可能会增加室性和房性心律失常的风险。
法维拉韦可能会导致 QT 间期延长,尤其是在诊断出 T2DM 的 SARS-Cov-2 患者中。
COVID-19,药物引起的长 QT 综合征,梗死内出血;法维拉韦,2 型糖尿病。