Use and Outcome of Remdesivir in patients with COVID 19 presenting to Mayo Hospital Lahore

Hina Latif, N. Butt, Rabia Rathore, F. A. Randhawa, Adil M. Iqbal, Tayyab Latif
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Abstract

Aim: To assess the usage of Remdesivir in COVID 19 patients admitted to Mayo hospital Lahore Methods: This Quasi experimental study was carried out in COVID-19 ward from July 2020 to September 2020 on patients presenting to Mayo Hospital with COVID-19.The sample size (n=150) was calculated through non-probability convenient sampling technique. We gave intravenous Remdesivir to hospitalized COVID-19 patients with proven SARS-CoV-2 infection with an oxygen saturation of ≤94% who were breathing ambient air or needed oxygen support and had an oxygen saturation of less than 94%. Remdesivir was administered to patients over the course of a 10-day course, starting with 200 mg intravenously (I/V) on day 1 and continuing with 100 mg per day for the following nine days. Results: Among 150 participants in our study, 103 (69%) were male and 47(31.3%) were females. Mean age was 57.37±13.42years. Selected parameters were evaluated at day 1, 5 and 10. Significant improvement in fever, dyspnea score, serum C- Reactive proteins (CRP) and lactate dehydrogenase (LDH) was found on day 1 and 10 with a p value of 0.01 to 0.000 for CRP and 0.48 to 0.000 for LDH respectively. Serum ferritin also showed a statistical difference with a significant p value of 0.038 at day 10 as compared to day 1 and 5. Conclusion: Among patients presenting with severe Covid-19, clinical improvement was noticed earlier in those who received Remdesivir than those who didn’t receive this drug. Measurement of effectiveness will require ongoing randomized controlled trials of Remdesivir drug therapy. Keywords: COVID-19, intravenous Remdesivir, earlier clinical improvement, outcome, oxygen support, breathlessness
在拉合尔梅奥医院就诊的COVID - 19患者中瑞德西韦的使用和疗效
目的:评估在拉合尔梅奥医院收治的COVID-19患者中瑞德西韦的使用情况方法:本研究于2020年7月至2020年9月在梅奥医院的COVID-19病房进行准实验研究。通过非概率方便抽样技术计算样本量(n=150)。对血氧饱和度≤94%、呼吸环境空气或需要氧气支持且血氧饱和度低于94%的住院COVID-19患者静脉给予瑞德西韦。Remdesivir在10天的疗程中给予患者,从第1天开始静脉注射200mg (I/V),然后在接下来的9天内继续每天100mg。结果:150名受试者中,男性103人(69%),女性47人(31.3%)。平均年龄57.37±13.42岁。选择的参数在第1、5和10天进行评估。第1天和第10天患者发热、呼吸困难评分、血清C-反应蛋白(CRP)和乳酸脱氢酶(LDH)均有显著改善,CRP和LDH的p值分别为0.01 ~ 0.000和0.48 ~ 0.000。与第1、5天相比,第10天血清铁蛋白含量也有统计学差异,p值为0.038。结论:在重症Covid-19患者中,接受瑞德西韦治疗的患者比未接受该药物治疗的患者更早发现临床改善。有效性的测量需要对瑞德西韦药物治疗进行持续的随机对照试验。关键词:COVID-19,静脉注射瑞德西韦,早期临床改善,结局,氧支持,呼吸困难
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