Department of Clinical Pharmacology, JIPMER, Puducherry, India.
Department of Biostatistics, JIPMER, Puducherry, India.
Br J Clin Pharmacol. 2022 Sep;88(9):4080-4091. doi: 10.1111/bcp.15338. Epub 2022 Apr 13.
To perform network meta-analysis for a head-to-head comparison of various interventions used in coronavirus disease 2019 (COVID-19) on mortality, clinical recovery, time to clinical improvement and the occurrence of serious adverse events.
Systematic search was performed using online databases with suitable MeSH terms including coronavirus, COVID-19, randomized controlled trial, hydroxychloroquine, lopinavir/ritonavir, tocilizumab, remdesivir, favipiravir, dexamethasone and interferon-β. Data were independently extracted by 2 study investigators and analysed.
Out of 1225 studies screened, 23 were included for qualitative and quantitative analysis. Among the drugs studied, dexamethasone reduces mortality by 10%, with a relative risk of 0.90 (95% confidence interval [0.82-0.97]) and increases clinical recovery by 6% (relative risk 1.06, 95% confidence interval [1.02-1.10]) compared to standard of care. Similarly, remdesivir administered for 10 days increased clinical recovery by 10%, reduced time to clinical improvement by 4 days and lowered the occurrence of serious adverse events by 27% as compared to standard of care.
In comparison to standard of care, dexamethasone was found to increase clinical recovery and lower mortality; remdesivir was significantly associated with a lower risk of mortality as compared to tocilizumab and higher clinical recovery and shorter time to clinical improvement as compared to hydroxychloroquine and tocilizumab; remdesivir followed by tocilizumab were found to have lesser occurrence of serious adverse events in patients with moderate to severe COVID-19.
针对 2019 年冠状病毒病(COVID-19)中使用的各种干预措施进行头对头比较的网络荟萃分析,以评估死亡率、临床康复、临床改善时间和严重不良事件的发生情况。
使用在线数据库进行系统搜索,使用合适的 MeSH 术语包括冠状病毒、COVID-19、随机对照试验、羟氯喹、洛匹那韦/利托那韦、托珠单抗、瑞德西韦、法匹拉韦、地塞米松和干扰素-β。由 2 名研究人员独立提取和分析数据。
在筛选出的 1225 项研究中,有 23 项研究被纳入定性和定量分析。在所研究的药物中,与标准治疗相比,地塞米松可降低 10%的死亡率,相对风险为 0.90(95%置信区间[0.82-0.97]),并增加 6%的临床康复率(相对风险 1.06,95%置信区间[1.02-1.10])。同样,与标准治疗相比,瑞德西韦治疗 10 天可使临床康复率提高 10%,临床改善时间缩短 4 天,严重不良事件发生率降低 27%。
与标准治疗相比,地塞米松可增加临床康复率并降低死亡率;与托珠单抗相比,瑞德西韦与死亡率降低显著相关,与羟氯喹和托珠单抗相比,临床康复率更高,临床改善时间更短;与单独使用瑞德西韦相比,瑞德西韦序贯托珠单抗治疗中度至重度 COVID-19 患者的严重不良事件发生率更低。