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
{"title":"Use and Outcome of Remdesivir in patients with COVID 19 presenting to Mayo Hospital Lahore","authors":"Hina Latif, N. Butt, Rabia Rathore, F. A. Randhawa, Adil M. Iqbal, Tayyab Latif","doi":"10.53350/pjmhs202317637","DOIUrl":null,"url":null,"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","PeriodicalId":19842,"journal":{"name":"Pakistan Journal of Medical and Health Sciences","volume":"30 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pakistan Journal of Medical and Health Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.53350/pjmhs202317637","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

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
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Clinical Profile and Outcomes of Primary PCI in Patients with Acute STEMI The Prevalence of BRCA1 and BRCA2 Mutations in Breast Cancer Patients Association Between Body Mass Index (BMI) and Occurrence of Esophageal Cancer Effects of Dietary Factors on Gastroesophageal Reflux Disease (GERD) Among the Student and Faculty of Public and Private Medical Universities of Karachi, Pakistan Positivity of BRCA 1 & 2 Mutations in Ovarian Cancer
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1