Role of aspirin in primary prevention of cardiovascular disease

The benefits of aspirin therapy for the secondary prevention of cardiovascular disease clearly outweigh the risks of bleeding, and low-dose aspirin is uniformly recommended in this setting. However, no clear consensus exists about whether, and if so in whom, aspirin therapy is appropriate for the pr...

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Veröffentlicht in:Nature reviews cardiology 2019-11, Vol.16 (11), p.675-686
Hauptverfasser: Patrono, Carlo, Baigent, Colin
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description The benefits of aspirin therapy for the secondary prevention of cardiovascular disease clearly outweigh the risks of bleeding, and low-dose aspirin is uniformly recommended in this setting. However, no clear consensus exists about whether, and if so in whom, aspirin therapy is appropriate for the primary prevention of cardiovascular disease. Three trials of low-dose aspirin versus placebo in three populations at increased risk of myocardial infarction or ischaemic stroke in the absence of established cardiovascular disease were reported in 2018. The ASPREE trial in elderly people was terminated early for futility because aspirin had no effect on disability-free survival but significantly increased the risk of major haemorrhage and, unexpectedly, all-cause mortality. In the ASCEND trial in patients with diabetes mellitus and no evidence of vascular disease, aspirin significantly reduced serious vascular events but increased major bleeding. In the ARRIVE trial in people with multiple risk factors for cardiovascular disease, aspirin had no effect on major cardiovascular events but increased gastrointestinal bleeding. The aim of this Review is to place these new results in the context of previous evidence on aspirin for the primary prevention of cardiovascular disease and to appraise whether the new evidence is likely to enable the more targeted use of aspirin in particular individuals for whom the net benefit is both clinically worthwhile and statistically definite. The role of aspirin for the primary prevention of cardiovascular disease is controversial. In this Review, Patrono and Baigent discuss the new randomized trials on aspirin for the primary prevention of cardiovascular disease in the context of previous evidence, and appraise whether the new evidence is likely to enable a more targeted use of aspirin Key points The benefits of aspirin therapy for the secondary prevention of cardiovascular disease (CVD) clearly outweigh the risks of bleeding, but whether to recommend low-dose aspirin for primary prevention of CVD is controversial. Use of risk scores for vascular events and major extracranial bleeds to classify individual participant data from a meta-analysis shows that individuals at the highest risk of vascular events are also at the highest risk of bleeding. In 2018, results from three trials of low-dose aspirin in three populations at increased risk of myocardial infarction or ischaemic stroke in the absence of established CVD added to the evidenc
doi_str_mv 10.1038/s41569-019-0225-y
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However, no clear consensus exists about whether, and if so in whom, aspirin therapy is appropriate for the primary prevention of cardiovascular disease. Three trials of low-dose aspirin versus placebo in three populations at increased risk of myocardial infarction or ischaemic stroke in the absence of established cardiovascular disease were reported in 2018. The ASPREE trial in elderly people was terminated early for futility because aspirin had no effect on disability-free survival but significantly increased the risk of major haemorrhage and, unexpectedly, all-cause mortality. In the ASCEND trial in patients with diabetes mellitus and no evidence of vascular disease, aspirin significantly reduced serious vascular events but increased major bleeding. In the ARRIVE trial in people with multiple risk factors for cardiovascular disease, aspirin had no effect on major cardiovascular events but increased gastrointestinal bleeding. The aim of this Review is to place these new results in the context of previous evidence on aspirin for the primary prevention of cardiovascular disease and to appraise whether the new evidence is likely to enable the more targeted use of aspirin in particular individuals for whom the net benefit is both clinically worthwhile and statistically definite. The role of aspirin for the primary prevention of cardiovascular disease is controversial. In this Review, Patrono and Baigent discuss the new randomized trials on aspirin for the primary prevention of cardiovascular disease in the context of previous evidence, and appraise whether the new evidence is likely to enable a more targeted use of aspirin Key points The benefits of aspirin therapy for the secondary prevention of cardiovascular disease (CVD) clearly outweigh the risks of bleeding, but whether to recommend low-dose aspirin for primary prevention of CVD is controversial. Use of risk scores for vascular events and major extracranial bleeds to classify individual participant data from a meta-analysis shows that individuals at the highest risk of vascular events are also at the highest risk of bleeding. In 2018, results from three trials of low-dose aspirin in three populations at increased risk of myocardial infarction or ischaemic stroke in the absence of established CVD added to the evidence base. Overall, other than for myocardial infarction, the effects of aspirin on the other major efficacy and safety outcomes seem similar in all the primary prevention trials, including the three (ASPREE, ASCEND and ARRIVE) completed in 2018. The main challenge when assessing the net benefit of aspirin is that benefits and risks are strongly correlated; therefore, identifying large numbers of people at high risk of vascular ischaemia but low risk of bleeding is difficult. New approaches are required to overcome this challenge, perhaps combining coronary imaging to identify apparently healthy people at substantially increased risk of vascular events with gastroprotectant therapy to reduce the risk of bleeding.</description><identifier>ISSN: 1759-5002</identifier><identifier>EISSN: 1759-5010</identifier><identifier>DOI: 10.1038/s41569-019-0225-y</identifier><identifier>PMID: 31243390</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject><![CDATA[692/4019/592/75 ; 692/700/459 ; 692/700/565/1436 ; Aspirin ; Aspirin - administration & dosage ; Aspirin - adverse effects ; Brain Ischemia - complications ; Brain Ischemia - prevention & control ; Cardiac Imaging ; Cardiac Surgery ; Cardiology ; Cardiovascular disease ; Cardiovascular diseases ; Cardiovascular Diseases - prevention & control ; Cardiovascular research ; Diabetes Complications - complications ; Disease prevention ; Gastrointestinal Hemorrhage - chemically induced ; Health risk assessment ; Heart attacks ; Humans ; Medicine ; Medicine & Public Health ; Myocardial Infarction - prevention & control ; Patient outcomes ; Platelet Aggregation Inhibitors - administration & dosage ; Platelet Aggregation Inhibitors - adverse effects ; Prevention ; Primary Prevention ; Randomized Controlled Trials as Topic ; Review Article ; Risk Assessment ; Risk Factors ; Stroke - etiology ; Stroke - prevention & control]]></subject><ispartof>Nature reviews cardiology, 2019-11, Vol.16 (11), p.675-686</ispartof><rights>Springer Nature Limited 2019</rights><rights>COPYRIGHT 2019 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Nov 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c579t-dfd542ee17354e73bb7c9a90196f2e92065675f1a2e2d5cbbde46d6d177cdcfc3</citedby><cites>FETCH-LOGICAL-c579t-dfd542ee17354e73bb7c9a90196f2e92065675f1a2e2d5cbbde46d6d177cdcfc3</cites><orcidid>0000-0002-6447-2424</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31243390$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Patrono, Carlo</creatorcontrib><creatorcontrib>Baigent, Colin</creatorcontrib><title>Role of aspirin in primary prevention of cardiovascular disease</title><title>Nature reviews cardiology</title><addtitle>Nat Rev Cardiol</addtitle><addtitle>Nat Rev Cardiol</addtitle><description>The benefits of aspirin therapy for the secondary prevention of cardiovascular disease clearly outweigh the risks of bleeding, and low-dose aspirin is uniformly recommended in this setting. However, no clear consensus exists about whether, and if so in whom, aspirin therapy is appropriate for the primary prevention of cardiovascular disease. Three trials of low-dose aspirin versus placebo in three populations at increased risk of myocardial infarction or ischaemic stroke in the absence of established cardiovascular disease were reported in 2018. The ASPREE trial in elderly people was terminated early for futility because aspirin had no effect on disability-free survival but significantly increased the risk of major haemorrhage and, unexpectedly, all-cause mortality. In the ASCEND trial in patients with diabetes mellitus and no evidence of vascular disease, aspirin significantly reduced serious vascular events but increased major bleeding. In the ARRIVE trial in people with multiple risk factors for cardiovascular disease, aspirin had no effect on major cardiovascular events but increased gastrointestinal bleeding. 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However, no clear consensus exists about whether, and if so in whom, aspirin therapy is appropriate for the primary prevention of cardiovascular disease. Three trials of low-dose aspirin versus placebo in three populations at increased risk of myocardial infarction or ischaemic stroke in the absence of established cardiovascular disease were reported in 2018. The ASPREE trial in elderly people was terminated early for futility because aspirin had no effect on disability-free survival but significantly increased the risk of major haemorrhage and, unexpectedly, all-cause mortality. In the ASCEND trial in patients with diabetes mellitus and no evidence of vascular disease, aspirin significantly reduced serious vascular events but increased major bleeding. In the ARRIVE trial in people with multiple risk factors for cardiovascular disease, aspirin had no effect on major cardiovascular events but increased gastrointestinal bleeding. The aim of this Review is to place these new results in the context of previous evidence on aspirin for the primary prevention of cardiovascular disease and to appraise whether the new evidence is likely to enable the more targeted use of aspirin in particular individuals for whom the net benefit is both clinically worthwhile and statistically definite. The role of aspirin for the primary prevention of cardiovascular disease is controversial. In this Review, Patrono and Baigent discuss the new randomized trials on aspirin for the primary prevention of cardiovascular disease in the context of previous evidence, and appraise whether the new evidence is likely to enable a more targeted use of aspirin Key points The benefits of aspirin therapy for the secondary prevention of cardiovascular disease (CVD) clearly outweigh the risks of bleeding, but whether to recommend low-dose aspirin for primary prevention of CVD is controversial. Use of risk scores for vascular events and major extracranial bleeds to classify individual participant data from a meta-analysis shows that individuals at the highest risk of vascular events are also at the highest risk of bleeding. In 2018, results from three trials of low-dose aspirin in three populations at increased risk of myocardial infarction or ischaemic stroke in the absence of established CVD added to the evidence base. Overall, other than for myocardial infarction, the effects of aspirin on the other major efficacy and safety outcomes seem similar in all the primary prevention trials, including the three (ASPREE, ASCEND and ARRIVE) completed in 2018. The main challenge when assessing the net benefit of aspirin is that benefits and risks are strongly correlated; therefore, identifying large numbers of people at high risk of vascular ischaemia but low risk of bleeding is difficult. New approaches are required to overcome this challenge, perhaps combining coronary imaging to identify apparently healthy people at substantially increased risk of vascular events with gastroprotectant therapy to reduce the risk of bleeding.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>31243390</pmid><doi>10.1038/s41569-019-0225-y</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-6447-2424</orcidid><oa>free_for_read</oa></addata></record>
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subjects 692/4019/592/75
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Aspirin
Aspirin - administration & dosage
Aspirin - adverse effects
Brain Ischemia - complications
Brain Ischemia - prevention & control
Cardiac Imaging
Cardiac Surgery
Cardiology
Cardiovascular disease
Cardiovascular diseases
Cardiovascular Diseases - prevention & control
Cardiovascular research
Diabetes Complications - complications
Disease prevention
Gastrointestinal Hemorrhage - chemically induced
Health risk assessment
Heart attacks
Humans
Medicine
Medicine & Public Health
Myocardial Infarction - prevention & control
Patient outcomes
Platelet Aggregation Inhibitors - administration & dosage
Platelet Aggregation Inhibitors - adverse effects
Prevention
Primary Prevention
Randomized Controlled Trials as Topic
Review Article
Risk Assessment
Risk Factors
Stroke - etiology
Stroke - prevention & control
title Role of aspirin in primary prevention of cardiovascular disease
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