» Articles » PMID: 32809173

The Use of Aspirin in Contemporary Primary Prevention of Atherosclerotic Cardiovascular Diseases Revisited: The Increasing Need and Call for a Personalized Therapeutic Approach

Overview
Date 2020 Aug 19
PMID 32809173
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

The use of aspirin has been widely accepted for the secondary prevention of atherosclerotic cardiovascular disease (ASCVD) in all patient populations, as the benefits linked to the reduction of clinical events outweigh the risk of major bleeding. However, despite the undisputable, though modest, potential of aspirin to reduce atherothrombotic events, its overall efficacy and safety in primary ASCVD prevention remains debatable, despite being used for this purpose for decades. The net clinical benefit of aspirin was brought into question by three recent large contemporary randomized controlled trials evaluating its role in various primary prevention populations (individuals with diabetes [ASCEND], an elderly population [ASPREE], and middle-aged adults at high estimated cardiovascular risk [ARRIVE]) and numerous large meta-analyses published during the past year. As a result, the usual generalized recommendations for the use of aspirin in patients with estimated intermediate to high ASCVD risk but without overt ASCVD have already been removed from most international guidelines. Since the primary prevention framework encompasses heterogenous groups of subjects with variable absolute ASCVD risk, a more individualized approach based on the best possible estimated ratio between the potential health benefits from fewer atherothrombotic events and harms because of potential increases in major bleeding is warranted in clinical practice. With this compromise, clinicians can better decide on the personalized use of aspirin in patients at high risk of major adverse cardiovascular events.

Citing Articles

Long-Term Effects of Low-Dose Aspirin on Gastrointestinal Symptoms and Bleeding Complications in Patients with Type 2 Diabetes.

Masutani N, Ogawa H, Soejima H, Okada S, Masuda I, Waki M Am J Cardiovasc Drugs. 2024; 25(1):95-112.

PMID: 39340686 DOI: 10.1007/s40256-024-00679-9.


Comprehensive effect of Naoxintong capsule combined with Western medicine on coronary heart disease after percutaneous coronary intervention: a meta-analysis.

Yu L, Huang P, Wang M, Li Z, Cai H, Feng Y Front Pharmacol. 2024; 15:1274000.

PMID: 38590642 PMC: 11000174. DOI: 10.3389/fphar.2024.1274000.


Factors Associated with Aspirin Resistance in Hong Kong Chinese Patients with Stable Coronary Heart Disease Using the Multiplate Analyzer and Serum Thromboxane B.

Zeng W, Chu T, Chow E, Hu M, Fok B, Chan J Pharmaceutics. 2022; 14(10).

PMID: 36297534 PMC: 9609623. DOI: 10.3390/pharmaceutics14102099.


Synthesis of Ti-Al-xNb Ternary Alloys via Laser-Engineered Net Shaping for Biomedical Application: Densification, Electrochemical and Mechanical Properties Studies.

Kanyane L, Popoola A, Pityana S, Tlotleng M Materials (Basel). 2022; 15(2).

PMID: 35057262 PMC: 8781035. DOI: 10.3390/ma15020544.


Impact of Antecedent Aspirin Use on Infarct Size, Bleeding and Composite Endpoint in Patients with de Novo Acute Myocardial Infarction.

Enhos A, Karacop E Ther Clin Risk Manag. 2021; 17:441-452.

PMID: 34054296 PMC: 8149313. DOI: 10.2147/TCRM.S307768.

References
1.
Sneader W . The discovery of aspirin: a reappraisal. BMJ. 2000; 321(7276):1591-4. PMC: 1119266. DOI: 10.1136/bmj.321.7276.1591. View

2.
Raber I, McCarthy C, Vaduganathan M, Bhatt D, Wood D, Cleland J . The rise and fall of aspirin in the primary prevention of cardiovascular disease. Lancet. 2019; 393(10186):2155-2167. DOI: 10.1016/S0140-6736(19)30541-0. View

3.
Kolte D, Aronow W, Banach M . Polypills for the prevention of Cardiovascular diseases. Expert Opin Investig Drugs. 2016; 25(11):1255-1264. DOI: 10.1080/13543784.2016.1236912. View

4.
CRAVEN L . Coronary thrombosis can be prevented. J Insur Med (1946). 1950; 5(4):47-8. View

5.
Patrono C, Baigent C . Low-dose aspirin, coxibs, and other NSAIDS: a clinical mosaic emerges. Mol Interv. 2009; 9(1):31-9. DOI: 10.1124/mi.9.1.8. View