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Postconditioning with Lactate-enriched Blood for Cardioprotection in ST-segment Elevation Myocardial Infarction
Published on: May 28, 2019
The functional effect of atorvastatin dose-dependent via inflammation factors on acute ST segment elevation
Qian Liu1, Yuanyuan Wang1, Xiucui Cheng2
1Department of Cardiology, People's Hospital of Dongying.
Insights
High-dose atorvastatin significantly reduced major adverse cardiovascular events (MACE) and spontaneous myocardial infarction (MI) in patients after emergency percutaneous coronary intervention (PCI). This high-dose regimen proved more effective than moderate-dose atorvastatin over one year.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Acute ST-segment elevation myocardial infarction (MI) is a critical cardiovascular event.
- Emergency percutaneous coronary intervention (PCI) is a standard treatment for acute MI.
- Statins, like atorvastatin, are crucial for managing cardiovascular risk post-MI.
Purpose of the Study:
- To compare the efficacy of high-dose (40 mg/day) versus moderate-dose (20 mg/day) atorvastatin.
- To evaluate the impact of different atorvastatin doses on major adverse cardiovascular events (MACE) in patients with acute ST-segment elevation MI post-PCI.
Main Methods:
- A prospective study involving 265 patients with acute ST-segment elevation MI undergoing emergency PCI.
- Patients were randomized to receive either high-dose (133 patients) or moderate-dose (132 patients) atorvastatin for 1 year.
- Primary endpoints included cardiovascular death, spontaneous MI, and unplanned revascularization.
Main Results:
- High-dose atorvastatin resulted in lower LDL cholesterol levels compared to moderate-dose (1.6 ± 0.6 vs. 1.8 ± 0.6, P=0.041).
- MACE significantly decreased in the high-dose group (9.8% vs. 18.2%, P=0.03), driven by reductions in spontaneous MI (6.8% vs. 12.8%, P=0.03) and unplanned revascularization (5.2% vs. 8.3%, P=0.03).
- No significant difference in adverse event rates was observed between the two groups.
Conclusions:
- High-dose atorvastatin demonstrates superior long-term clinical performance compared to moderate-dose in patients with acute ST-segment elevation MI following emergency PCI.
- The findings support the use of high-dose atorvastatin for improved outcomes in this patient population.
Objective:
To investigate the effect of different doses of atorvastatin on patients with acute ST segment elevation myocardial infarction (MI) after emergency percutaneous coronary intervention (PCI).
Methods:
A total of 265 patients with acute ST segment elevation MI who underwent emergency PCI were enrolled, 133 in high-dose atorvastatin administration (40 mg/day) and 132 in moderate-dose atorvastatin administration (20 mg/day). All the patients continued treatment for 1 year. The incidences of major adverse cardiovascular events (MACE) were recorded, including cardiovascular death, spontaneous MI, and unplanned revascularization. The association between clinical incidences and different doses of atorvastatin treatment was studied.
Results:
Through tracking 1 year's treatment, the level of low-density lipoprotein cholesterol was lower in high-dose atorvastatin administration than in moderate treatment (1.6 ± 0.6 vs. 1.8 ± 0.6, P = 0.041). MACE significantly decreased in high-dose atorvastatin administration than in moderate treatment (9.8 vs. 18.2%, P = 0.03). Spontaneous MI was significantly more attenuated in high-dose treatment than in moderate treatment (6.8 vs. 12.8%, P = 0.03). Unplanned revascularization robustly decreased in patients with high-dose administration than those with moderate-dose treatment (5.2 vs. 8.3%, P = 0.03). There was no difference in the rate of adverse events between the two groups.
Conclusion:
For patients with acute ST segment elevation MI who underwent emergency PCI, high-dose atorvastatin could provide better performance than moderate-dose in our long-term tracking.
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