Development of a New Analytical Method for Estimation of Trifluoperazine-HCl in Pharmaceutical Formulation

Mohammed Elhabil, Atef Elhout, Elhout Elhout, Doaa Shurrab, Eman ALhawajri, Shaimaa Alakkad, Rema Elderbi, Khaled Almghari, A. Eldalo
{"title":"Development of a New Analytical Method for Estimation of Trifluoperazine-HCl in Pharmaceutical Formulation","authors":"Mohammed Elhabil, Atef Elhout, Elhout Elhout, Doaa Shurrab, Eman ALhawajri, Shaimaa Alakkad, Rema Elderbi, Khaled Almghari, A. Eldalo","doi":"10.52865/ttqe8776","DOIUrl":null,"url":null,"abstract":"Background: Coronavirus disease 2019 (COVID-19) has spread worldwide and poses a serious public health-threat. High IL-6 levels were associated with the severity of COVID-19 and del to the use of anti-IL-6 Tocilizumab during the pandemic. Therefore, this case-control study was conducted to evaluate the role of Tocilizumab on the mortality rate among severe and critically ill COVID-19 patients. Method: A case-control study relied on the use of an electronic data collection sheet; the data were collected from February to May 2022. The study was performed on adult patients with critical COVID-19 at three major hospitals in the Gaza Strip, Palestine where patients were treated in the intensive care units (ICUs). Patients from the hospitals were included and divided into two groups by simple random sampling technique. Results: Of the 202 patients with critical COVID-19 admitted to ICUs of three hospitals, 102 (50.5%) were treated with Tocilizumab. A total of 58 (56.9%) patients in the Tocilizumab group were cured, and 44 (43.1%) died. In the control group, only 26 (26.0%) were cured and 72.0% died. There was no statistically significant effect of Tocilizumab on total hospital stay and ventilation periods. Patients treated with Tocilizumab had a longer stay in the ICU (14.02 ±8.796 days compared to 10.52 ± 9.596 days in the control group, P = 0.027), but shorter incubation periods were observed in the same group (3.25 ±1.137 days in Tocilizumab group compared to 7.38 ±3.376 days in the control group P = 0.036). Conclusion: This study found that administration of Tocilizumab can improve clinical outcomes, reduce risk of mortality, and frequency of intubation in patients severely infected with COVID-19. However, there was no significant difference between the two groups in terms of hospitalization times and mechanical ventilation needs. Based on the current report, healthcare specialists should consider Tocilizumab with the updated treatment guidelines for critically ill COVID-19 patients.","PeriodicalId":223912,"journal":{"name":"Israa University Journal for Applied Science","volume":"51 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Israa University Journal for Applied Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.52865/ttqe8776","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

Background: Coronavirus disease 2019 (COVID-19) has spread worldwide and poses a serious public health-threat. High IL-6 levels were associated with the severity of COVID-19 and del to the use of anti-IL-6 Tocilizumab during the pandemic. Therefore, this case-control study was conducted to evaluate the role of Tocilizumab on the mortality rate among severe and critically ill COVID-19 patients. Method: A case-control study relied on the use of an electronic data collection sheet; the data were collected from February to May 2022. The study was performed on adult patients with critical COVID-19 at three major hospitals in the Gaza Strip, Palestine where patients were treated in the intensive care units (ICUs). Patients from the hospitals were included and divided into two groups by simple random sampling technique. Results: Of the 202 patients with critical COVID-19 admitted to ICUs of three hospitals, 102 (50.5%) were treated with Tocilizumab. A total of 58 (56.9%) patients in the Tocilizumab group were cured, and 44 (43.1%) died. In the control group, only 26 (26.0%) were cured and 72.0% died. There was no statistically significant effect of Tocilizumab on total hospital stay and ventilation periods. Patients treated with Tocilizumab had a longer stay in the ICU (14.02 ±8.796 days compared to 10.52 ± 9.596 days in the control group, P = 0.027), but shorter incubation periods were observed in the same group (3.25 ±1.137 days in Tocilizumab group compared to 7.38 ±3.376 days in the control group P = 0.036). Conclusion: This study found that administration of Tocilizumab can improve clinical outcomes, reduce risk of mortality, and frequency of intubation in patients severely infected with COVID-19. However, there was no significant difference between the two groups in terms of hospitalization times and mechanical ventilation needs. Based on the current report, healthcare specialists should consider Tocilizumab with the updated treatment guidelines for critically ill COVID-19 patients.
制剂中盐酸三氟拉嗪含量测定新方法的建立
背景:2019冠状病毒病(COVID-19)已在全球蔓延,对公共卫生构成严重威胁。高IL-6水平与COVID-19的严重程度有关,并与大流行期间抗IL-6 Tocilizumab的使用有关。因此,本病例对照研究旨在评估托珠单抗对COVID-19重症、危重症患者死亡率的影响。方法:病例对照研究,采用电子数据收集表;数据收集于2022年2月至5月。该研究是在巴勒斯坦加沙地带三家主要医院的COVID-19重症成人患者中进行的,患者在重症监护室(icu)接受治疗。采用简单随机抽样的方法将住院患者分为两组。结果:在3家医院icu收治的202例COVID-19危重患者中,102例(50.5%)接受了托珠单抗治疗。Tocilizumab组共治愈58例(56.9%),死亡44例(43.1%)。对照组26例(26.0%)治愈,72.0%死亡。托珠单抗对总住院时间和通气时间的影响无统计学意义。托珠单抗组患者在ICU的住院时间较长(14.02±8.796天,对照组为10.52±9.596天,P = 0.027),但同一组患者的潜伏期较短(托珠单抗组为3.25±1.137天,对照组为7.38±3.376天,P = 0.036)。结论:本研究发现,托珠单抗可以改善COVID-19严重感染患者的临床结局,降低死亡风险,减少插管次数。然而,两组在住院时间和机械通气需求方面无显著差异。根据目前的报告,医疗保健专家应根据最新的COVID-19危重患者治疗指南考虑使用托珠单抗。
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 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信