Aye Than Than, Myat Kaung, Tun Hpone Pyae, Thiha Phyo, Han Tin Myo, Win Yin Yin, Han Aye Moh Moh
Dr. Med. Sc. (General Medicine), Professor Emeritus at University of Medicine 2, Yangon; Consultant Endocrinologist at Grand Hantha International Hospital, Yangon, Myanmar.
M. Med. Sc (Internal Medicine), General Physician, Lapyaewon Primary Care Clinic, Tharkaytha Township, Yangon, Myanmar.
J Family Med Prim Care. 2022 Aug;11(8):4644-4649. doi: 10.4103/jfmpc.jfmpc_2350_21. Epub 2022 Aug 30.
Although Remdesivir has been evaluated for the treatment of coronavirus disease 2019 (COVID-19), few study has yet shown effective mortality reduction. It might be because, in almost all those studies, remdesivir therapy was started beyond 7 days from the onset of symptoms when the active viral replications have already gone.
This study reviewed the effectiveness of early remdesivir therapy during viral phase of COVID-19 and safety of its administration at home or community care during the outbreak of COVID-19 from July to September 2021 in Myanmar. We retrospectively reviewed clinical records of 204 high risk COVID-19 patients who had received remdesivir therapy within 7 days from the onset of illness and before oxygen desaturation.
All patients received remdesivir therapy according to standard five days course of 200 mg loading dose on day 1, followed by 100 mg daily for up to 4 additional days. Out of 204 patients, 60.75% (124/204) were aged 60 years and above with comorbidity; 21.1% (43/204) aged under 60 years with comorbidity and 18.1% (37/204) were aged more than 60 years old without comorbidity. The patients who received RDSV therapy within 1-4 days and within 5-7 days were 50.5% (103/204) and 49.5% (101/204) respectively. All patients survived to 21 days without ICU admission or mechanical ventilation. Eighty six percent of patients had no hypoxia and only five percent had moderate to severe hypoxia, requiring oxygen. Those who received RDSV therapy within 1 to 4 days from the onset of symptoms had significantly lower rate of hypoxia compared to those who received remdesivir therapy on 5 to 7 days. After RDSV therapy, increased lymphocyte count and decreased CPR were observed in 74.5% (152/204) and 52.9% (108/204) of the patients respectively. There was no report of major adverse events.
Remdesivir, if given within first 4 days from the onset of symptoms, is the most effective strategy for prevention of oxygen desaturation, further progression of COVID-19 and death although it is still beneficial if given later, days 5 to 7. It is a safe drug to be prescribed in hospital at home care. It may be cost-benefit if high-risk group of patients with COVID-19 were selected for early remdesivir therapy in the community.
尽管瑞德西韦已被评估用于治疗2019冠状病毒病(COVID-19),但很少有研究表明其能有效降低死亡率。这可能是因为,在几乎所有这些研究中,瑞德西韦治疗都是在症状出现7天之后开始的,而此时活跃的病毒复制已经结束。
本研究回顾了2021年7月至9月缅甸COVID-19疫情期间,瑞德西韦早期治疗在COVID-19病毒感染阶段的有效性以及在家中或社区护理中使用瑞德西韦的安全性。我们回顾性分析了204例高危COVID-19患者的临床记录,这些患者在发病后7天内且在出现氧饱和度下降之前接受了瑞德西韦治疗。
所有患者均按照标准的五天疗程接受瑞德西韦治疗,第1天给予200mg负荷剂量,随后连续4天每天给予100mg。在204例患者中,60.75%(124/204)年龄在60岁及以上且患有合并症;21.1%(43/204)年龄在60岁以下且患有合并症,18.1%(37/204)年龄在60岁以上且无合并症。在症状出现1 - 4天内和5 - 7天内接受瑞德西韦治疗的患者分别为50.5%(103/204)和49.5%(101/204)。所有患者均存活至21天,未入住重症监护病房或接受机械通气。86%的患者无低氧血症,仅有5%的患者有中度至重度低氧血症,需要吸氧。与在症状出现5至7天接受瑞德西韦治疗的患者相比,在症状出现1至4天内接受瑞德西韦治疗的患者低氧血症发生率显著更低。瑞德西韦治疗后,分别有74.5%(152/204)和52.9%(108/204)的患者淋巴细胞计数增加和CPR降低。未报告重大不良事件。
瑞德西韦如果在症状出现后的前4天内给予,是预防氧饱和度下降、COVID-19进一步进展和死亡的最有效策略,尽管在第5至7天给予也仍然有益。它是一种可在医院、家庭护理中开具的安全药物。如果选择COVID-19高危患者群体在社区中进行早期瑞德西韦治疗,可能具有成本效益。