Related Experiment Video
Updated: Jul 2, 2025

Live Imaging and Quantification of Viral Infection in K18 hACE2 Transgenic Mice Using Reporter-Expressing Recombinant SARS-CoV-2
Published on: November 5, 2021
Atorvastatin for reduction of 28-day mortality in severe and critical COVID-19 patients: a randomized controlled
Naglaa Hamdi Eltahan1, Neamat Hamdy Elsawy2,3, Kholoud M Abdelaaty4
1Sherbin Central Hospital, Ministry of Health and Population, Sherbin, Egypt.
Atorvastatin did not significantly reduce mortality in severe COVID-19 patients. This study found no benefit in 28-day or 6-month survival rates for atorvastatin users compared to placebo.
Area of Science:
- Cardiology
- Infectious Diseases
- Critical Care Medicine
Background:
- COVID-19 involves abnormal host response, endothelial dysfunction, and multi-organ failure.
- Atorvastatin, a statin, has been investigated for its potential to mitigate COVID-19 severity.
- Previous hypotheses suggested atorvastatin might reduce COVID-19 severity and mortality.
Purpose of the Study:
- To evaluate the efficacy of atorvastatin in reducing mortality among severe COVID-19 patients.
- To assess the impact of atorvastatin on clinical improvement and hospital stay duration.
- To investigate the effect of atorvastatin on secondary outcomes like acute kidney injury and need for mechanical ventilation.
Main Methods:
- A randomized, double-blind, placebo-controlled trial involving 220 COVID-19 patients.
- Patients received either 40 mg of atorvastatin daily or a placebo for 28 days.
- Primary outcome was 28-day all-cause mortality; secondary outcomes included 6-month mortality, clinical improvement, and length of stay.
Main Results:
- No statistically significant difference in 28-day all-cause mortality between atorvastatin (50%) and placebo (52.4%) groups (P=0.727).
- Six-month mortality also showed no significant difference (52% vs. 60.8%, P=0.208).
- Atorvastatin did not shorten time to clinical improvement or reduce hospital stay duration.
Conclusions:
- Atorvastatin did not demonstrate a significant benefit in reducing mortality for severe or critical COVID-19 patients.
- The drug did not improve clinical recovery times or reduce hospital length of stay.
- Further research may be needed to explore potential benefits in specific patient subgroups or at different stages of the disease.
More Related Videos
05:41Left Anterior Descending Coronary Artery Ligation for Ischemia-Reperfusion Research: Model Improvement via Technical Modifications and Quality Control
Published on: December 16, 2022
08:45LDL Cholesterol Uptake Assay Using Live Cell Imaging Analysis with Cell Health Monitoring
Published on: November 17, 2018
Related Concept Videos
Lipid-Lowering Drugs: Statins and Miscellaneous Agents
Time Course of Drug Effect
Antianginal Drugs: Calcium Channel Blockers and Ranolazine
CCBs, a diverse class that includes dihydropyridines (nifedipine) and diphenylalkylamines (verapamil and diltiazem), exert their effect by blocking calcium channels in cardiac and smooth muscle cells. This...
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
Heart Failure Drugs: β-Blockers