Comparative Efficacy of Atorvastatin and Placebo in Intensive Care Unit Patients with Coronavirus Disease 2019: A Randomized Controlled Trial.

IF 0.7 Q4 PHARMACOLOGY & PHARMACY
Journal of Research in Pharmacy Practice Pub Date : 2025-04-24 eCollection Date: 2024-10-01 DOI:10.4103/jrpp.jrpp_10_25
Fatemeh Taghavi, Saeed Abbasi, Malihe Nejati, Shadi Farsaei
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引用次数: 0

Abstract

Objective: Statins, recognized for their lipid-lowering properties, are being studied in clinical studies for potential benefits in treating coronavirus disease 2019 (COVID-19). This clinical trial evaluated the efficacy of a moderate dose of atorvastatin in influencing the clinical response among critically ill COVID-19 patients.

Methods: This investigation involved adult individuals diagnosed with laboratory-confirmed COVID-19 and experiencing critical illness. Patients meeting the eligibility criteria and receiving atorvastatin were allocated to continue treatment at a daily dosage of 20 mg (PHA). In contrast, the remaining eligible patients were randomly assigned to the atorvastatin intervention (AIN: administration of 20 mg atorvastatin daily) and control groups. Patients followed up for 14 days for the primary endpoints of the COVID-19 severity and APACHE II scores. The secondary endpoints and different biochemical parameters were also assessed.

Findings: Finally, 116 people completed the study. The studied groups had no significant differences regarding the demographic and basic clinical data. C-reactive protein on the 7th and 14th days in the AIN and PHA groups was significantly lower than in the control group (P = 0.008 and P = 0.018). IL6 on the 7th day (P = 0.04) showed a significant decrease in AIN compared to PHA and control groups. However, no significant differences in APACHE-II score and disease severity were detected between the groups.

Conclusion: Atorvastatin could effectively reduce inflammation in intensive care unit (ICU) patients admitted for COVID-19 management, but it could not influence the clinical outcomes. We suggested investigating its effect on COVID-19 in larger sample sizes, nonICU patients, and from the beginning of the diagnosis for a longer duration.

阿托伐他汀与安慰剂在2019冠状病毒病重症监护病房患者中的比较疗效:一项随机对照试验。
目的:他汀类药物以其降脂特性而闻名,目前正在临床研究中研究其治疗冠状病毒病2019 (COVID-19)的潜在益处。本临床试验评估了中等剂量阿托伐他汀对COVID-19危重患者临床反应的影响。方法:本调查涉及实验室确诊的COVID-19成人危重患者。符合资格标准并接受阿托伐他汀治疗的患者被分配以每日20mg (PHA)的剂量继续治疗。相比之下,其余符合条件的患者被随机分配到阿托伐他汀干预组(AIN:每天给药20mg阿托伐他汀)和对照组。患者随访14天,主要终点为COVID-19严重程度和APACHE II评分。次要终点和不同生化参数也进行了评估。结果:最终,116人完成了这项研究。两组在人口学和基本临床资料方面无显著差异。AIN组和PHA组第7天和第14天的c反应蛋白含量显著低于对照组(P = 0.008和P = 0.018)。与PHA组和对照组相比,AIN组第7天的IL6明显降低(P = 0.04)。然而,两组之间在APACHE-II评分和疾病严重程度上没有显著差异。结论:阿托伐他汀可有效减轻新冠肺炎重症监护病房(ICU)患者的炎症反应,但不影响临床结局。我们建议在更大的样本量、非icu患者中调查其对COVID-19的影响,并从诊断开始持续更长的时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Research in Pharmacy Practice
Journal of Research in Pharmacy Practice PHARMACOLOGY & PHARMACY-
自引率
0.00%
发文量
8
审稿时长
21 weeks
期刊介绍: The main focus of the journal will be on evidence-based drug-related medical researches (with clinical pharmacists’ intervention or documentation), particularly in the Eastern Mediterranean region. However, a wide range of closely related issues will be also covered. These will include clinical studies in the field of pharmaceutical care, reporting adverse drug reactions and human medical toxicology, pharmaco-epidemiology and toxico-epidemiology (poisoning epidemiology), social aspects of pharmacy practice, pharmacy education and economic evaluations of treatment protocols (e.g. cost-effectiveness studies). Local reports of medication utilization studies at hospital or pharmacy levels will only be considered for peer-review process only if they have a new and useful message for the international pharmacy practice professionals and readers.
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