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Aspirin I.V. Loading during Elective Percutaneous Coronary Intervention
David Naguib1,2, Carolin Helten1,2, Saif Zako1,2
1Department of Cardiology, Pulmonology, and Vascular Medicine, University Hospital Düsseldorf, Düsseldorf, Germany.
Insights
An additional loading dose of acetylsalicylic acid (ASA) during percutaneous coronary interventions (PCI) did not reduce high on-treatment platelet reactivity (HTPR) to aspirin. This pilot study found no significant increase in adverse events or bleeding complications.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- Percutaneous coronary interventions (PCI) often involve additional acetylsalicylic acid (ASA) loading doses despite ongoing oral ASA therapy.
- The clinical impact of this practice on platelet reactivity and patient outcomes remains unclear.
Purpose of the Study:
- To investigate high on-treatment platelet reactivity (HTPR) to aspirin in patients undergoing elective PCI.
- To compare platelet reactivity and clinical events between patients receiving a peri-procedural ASA loading dose versus those not receiving it.
Main Methods:
- A pilot study involving 100 patients on chronic low-dose ASA medication undergoing elective PCI.
- Platelet reactivity was assessed using light-transmission aggregometry, measuring arachidonic acid-induced maximum aggregation (MoA).
- Patients were divided into groups with and without an additional intravenous ASA loading dose (500 mg).
Main Results:
- The rate of HTPR (defined as MoA >20%) was similar between the loading dose and control groups (6% vs. 16%).
- No significant differences in in-hospital major adverse cerebro- and cardiovascular events (MACCEs) were observed between the groups.
- Thrombolysis in Myocardial Infarction (TIMI) minimal bleeding events were numerically higher in the control group (without ASA loading).
Conclusions:
- Peri-procedural ASA loading did not effectively reduce HTPR in patients on chronic low-dose ASA undergoing PCI.
- The additional ASA loading dose did not increase in-hospital MACCEs or bleeding complications in this pilot study.
Abstract:
Additional loading dose of acetylsalicylic acid (ASA) during percutaneous coronary interventions (PCIs) despite permanent oral ASA medication is frequently applicated. The impact on platelet reactivity and clinical events is not known. In this pilot study, we aimed to analyze high on-treatment platelet reactivity (HTPR) to aspirin in patients undergoing elective PCI. Platelet reactivity was measured using light-transmission aggregometry in 100 patients on permanent low-dose ASA medication undergoing elective PCI. Platelet reactivity measured by arachidonic acid-induced maximum of aggregation (MoA) in patients with versus without additional peri-procedural ASA loading (500 mg i.v.) was compared. HTPR was defined as MoA >20% for ASA. Major adverse cerebro- and cardiovascular events (MACCEs) and bleeding events were evaluated during hospital course. HTPR rate was similar in both groups (HTPR to ASA: loading vs. control 6% vs. 16%, odds ratio [OR] = 0.33, 95% confidence interval [CI] 0.08-1.35, p = 0.12). In-hospital MACCEs were not different between groups (MACCE: loading vs. control: 0 vs. 0 patient, OR = 1.32, 95% CI 0.03-67.95, p = 0.89). Thrombolysis in myocardial infarction minimal bleedings were numerically higher in patients without ASA loading dose. In this pharmacodynamic pilot study, additional ASA loading did not reduce HTPR to ASA. Furthermore, ASA loading did not increase in-hospital MACCE and bleeding complications.
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