Why the study?
Aspirin is indicated in the emergency management of acute coronary syndrome, but oral aspirin has erratic bioavailability compared to the intravenous formulation.
Does intravenous aspirin improve platelet aggregability and clinical outcomes compared to oral aspirin in patients with acute coronary syndrome?
Does intravenous aspirin improve platelet aggregability and clinical outcomes compared to oral aspirin in patients with acute coronary syndrome?
Intravenous aspirin provides faster platelet inhibition than oral aspirin in acute coronary syndrome, but current evidence shows no significant difference in short-term clinical outcomes or bleeding risk.
IV aspirin may achieve greater platelet inhibition than oral in ACS; extends limited RCT data but needs larger trials before changing practice.
BACKGROUND: Aspirin is indicated in the emergency management of acute coronary syndrome. However, oral aspirin has erratic bioavailability compared to i.v. formulation. OBJECTIVE: The objective of this study was to evaluate the comparative efficacy and safety of intravenous (IV) and oral aspirin in acute coronary syndrome. STUDY DESIGN: This was a systematic review and meta-analysis. RESULTS: Two randomized controlled trials were included. Compared to oral aspirin, lower platelet aggregability was seen with IV aspirin at 5 min and 20 min. Lower thromboxane B2 and lower platelet CD-62p levels were noted in the IV group; however, no significant difference was observed in terms of "composite cardiovascular death, stroke, and myocardial infarction (MI) at 4-6 weeks," "any cause mortality," "cardiovascular mortality," "occurrence of stroke," and "occurrence of MI/reinfarction." However, no difference was noted in terms of the occurrence of serious adverse events. CONCLUSION: IV aspirin showed some advantages in terms of platelet aggregability biomarkers at 20 min and 1 week with comparable safety to oral aspirin. No difference was seen in terms of clinical outcomes (at 24 h, 7, and 30 days) and the occurrence of serious adverse events.
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Kaur et al. (2023) studied this question.
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