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Can a high reloading dose of atorvastatin prior to percutaneous coronary intervention reduce periprocedural
Latifeh Nafasi1, Reza Rahmani, Akbar Shafiee
1Imam Khomeini Hospital, Tehran University of Medical Sciences , Tehran , Iran.
Insights
A high dose of atorvastatin given before percutaneous coronary intervention (PCI) significantly reduced periprocedural myocardial infarction (MI) in patients already on statins. This intervention offers a promising strategy to prevent heart attacks during PCI procedures.
Area of Science:
- Cardiology
- Interventional Cardiology
- Pharmacology
Background:
- Periprocedural myocardial infarction (MI) is a frequent complication after percutaneous coronary intervention (PCI).
- Statins are known to reduce MI in statin-naïve patients undergoing PCI.
- The efficacy of high-dose atorvastatin reloading in patients already on statin therapy remains to be fully elucidated.
Purpose of the Study:
- To determine if a high reloading dose of atorvastatin can prevent periprocedural MI in patients already receiving statin therapy.
- To evaluate the impact of atorvastatin on cardiac biomarkers and inflammatory markers post-PCI.
Main Methods:
- A triple-blind, controlled, randomized clinical trial involving 190 patients undergoing elective PCI.
- Participants, already on statins or other lipid-lowering agents, were randomized to receive either 80 mg atorvastatin or placebo within 24 hours before PCI.
- Serum levels of CK-MB, cTNI, and hs-CRP were measured at baseline and at 6 and 12 hours post-PCI. MI was defined by specific troponin elevation criteria.
Main Results:
- The frequency of MI was significantly lower in the atorvastatin group (3.1%) compared to the placebo group (10.5%) (p=0.04).
- Atorvastatin significantly reduced the rise in CK-MB within 6 hours and cTNI levels at 6 and 12 hours post-PCI.
- High-sensitive C-reactive protein (hs-CRP) levels were significantly lower in the atorvastatin group 12 hours after PCI (p=0.004).
Conclusions:
- Administering a high reloading dose of atorvastatin within 24 hours before PCI significantly reduces the incidence of periprocedural MI.
- This strategy is effective in mitigating myocardial injury and inflammation in patients already on statin therapy undergoing PCI.
- Clinical Trial Registration Code: IRCT201205209768N1.
Background:
Periprocedural myocardial infarction (MI) is a common complication following percutaneous coronary intervention (PCI) and statins have been shown to reduce MI in statin-naïve patients. We aimed to identify whether a high reloading dose of atorvastatin can prevent MI following PCI in patients who were already being treated with statins.
Material And Methods:
In this triple-blind controlled randomized clinical trial, 190 candidates for elective PCI, who were already using statins and/or other lipid lowering agents such as fibrates, were randomly assigned to two equal groups to receive either atorvastatin (80 mg) or placebo within 24 hours before the procedure. Serum levels of creatinine kinase myocardial isoenzyme (CK-MB), cardiac troponin I (cTNI) and high-sensitive C-reactive protein (hs-CRP) were measured at baseline and then 6 and 12 hours following PCI. Post-procedural MI was defined as troponin elevation>5-fold in patients with normal baseline or >20% in those with elevated baseline measurements with or without chest pain or ST segment or T wave abnormalities.
Results:
Frequency of MI in the atorvastatin group was 3 (3.1%) vs. 10 (10.5%) in the placebo group (p=0.04). The CK-MB rise within 6 hours following PCI was 0.6±0.3 mg/dl in the intervention group versus 3.0±1.6 mg/dl in the placebo group. Also, the levels of cTNI within 6 and 12 hours in the intervention group was significantly lower than the placebo group (p=0.01 and 0.008, respectively). hs-CRP was significantly lower in the intervention group after 12 hours (p=0.004).
Conclusion:
Administration of a high reloading dose of atorvastatin within 24 hours before PCI could significantly reduce the frequency of periprocedural MI. CLINICAL TRIAL REGISTRATION CODE: IRCT201205209768N1.
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