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Association between clopidogrel preloading time and post-procedural troponin elevation in patients with stable angina
Sungho Jo1, Jeong Tae Byoun1, Donghyeon Joo1
1Department of Cardiovascular Medicine, Regional Cardiocerebrovascular Center, Wonkwang University Hospital, Iksan, Korea.
Insights
Clopidogrel preloading within 6 hours before elective percutaneous coronary intervention (PCI) did not increase 30-day major adverse cardiovascular events (MACE). Shorter preloading times were linked to higher troponin T elevation after PCI.
Area of Science:
- Cardiology
- Pharmacology
- Interventional Cardiology
Background:
- Clopidogrel, an antiplatelet medication, requires several hours for optimal platelet inhibition.
- Elective percutaneous coronary intervention (PCI) in stable angina patients necessitates timely and effective platelet inhibition.
Purpose of the Study:
- To investigate the association between clopidogrel preloading time and 30-day clinical outcomes.
- To assess the relationship between clopidogrel preloading duration and post-procedural troponin T elevation in stable angina patients undergoing elective PCI.
Main Methods:
- A retrospective cohort study of 1,020 clopidogrel-naive stable angina patients undergoing elective PCI.
- Patients were stratified by clopidogrel preloading-to-balloon time: ≤6 hours vs. >6 hours.
- Stabilized inverse probability of treatment weighting (IPTW) was employed to analyze outcomes.
Main Results:
- No significant difference in 30-day MACE (death, MI, stroke, revascularization) between the ≤6-hour and >6-hour groups (0.5% vs. 0.4%, p=0.754).
- Higher post-procedural troponin T levels observed at 6, 24, and 48 hours in the ≤6-hour group.
- Increased frequency of troponin T elevation ≥5× and ≥25× in the ≤6-hour group, with no difference at ≥70× elevation.
Conclusions:
- Clopidogrel preloading ≤6 hours before elective PCI is not associated with increased 30-day MACE in stable angina patients.
- Shorter preloading times (≤6 hours) are associated with elevated post-procedural troponin T levels, particularly at lower thresholds.
Background:
Clopidogrel requires several hours to achieve adequate platelet inhibition. We investigated the association of clopidogrel preloading time with 30-day clinical outcomes and post-procedural troponin ,elevation in patients with stable angina undergoing elective percutaneous coronary intervention (PCI).
Methods:
This single-center retrospective cohort study included 1,020 patients with stable angina (clopidogrel-naive) who received 300 mg clopidogrel preloading within 24 hours before elective PCI between 2012 and 2020. Patients were categorized according to clopidogrel preloading-to-balloon time ≤6 hours or >6 hours. The primary endpoint was 30-day major adverse cardiovascular events (MACE), defined as a composite of all-cause death, myocardial infarction, stroke, and any revascularization. Secondary endpoints included serial troponin T changes and troponin T elevation ≥5×, ≥25×, and ≥70× the upper reference limit. Stabilized inverse probability of treatment weighting (IPTW) was used.
Results:
Thirty-day MACE occurred in five patients (0.49%) and did not differ between the ≤6-hour and >6-hour groups after IPTW (0.5% vs. 0.4%, p=0.754). Post-procedural troponin T levels at 6, 24, and 48 hours were higher in the ≤6-hour group. Patients with shorter preloading-to-balloon times showed higher peak troponin T levels, with the greatest difference at the ≤1-hour cutoff (geometric mean ratio, 2.12; 95% confidence interval, 1.53-2.95; p<0.001) and progressive attenuation at longer cutoffs. Troponin T elevation ≥5× and ≥25× was more frequent in the ≤6-hour group, whereas ≥70× elevation did not differ.
Conclusion:
Clopidogrel preloading ≤6 hours before elective PCI was not associated with increased 30-day MACE but was associated with lower-threshold post-procedural troponin T elevation.
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