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Aspirin to prevent a heart attack: what the evidence says about taking it daily

Low-dose aspirin is a medicine cabinet classic, but the science has gradually refined when it genuinely protects you and when the bleeding risk eats up the benefit. Here's what the trials and guidelines say, without the scaremongering.

Medically reviewed byClínica Evolution medical teamPublishedUpdated
Aspirina diaria para prevenir el infarto: qué dice la evidencia

Short answer

Daily low-dose aspirin has a clear benefit in secondary prevention, when there has already been a heart attack, a stroke or diagnosed arterial disease: there it reduced serious vascular events from 8.2% to 6.7% per year (ATT Collaboration, Lancet 2009). In healthy people the benefit is small and the increase in bleeding largely offsets it, which is why guidelines no longer recommend it routinely and the decision depends on individual cardiovascular risk.

Key points

  1. In the ASPREE trial (NEJM 2018), with 19,114 healthy older people followed for a median of 4.7 years, aspirin did not significantly reduce cardiovascular disease (10.7 versus 11.3 events per 1,000 person-years; HR 0.95) but did increase major haemorrhage (3.8% versus 2.8%; HR 1.38).
  2. The USPSTF (JAMA 2022) recommends against starting aspirin for primary prevention from the age of 60 (grade D) and advises an individual decision between 40 and 59 when 10-year cardiovascular risk is 10% or higher (grade C).
  3. The summary of product characteristics for Adiro 100 mg authorised by the AEMPS states that higher doses have not shown greater efficacy and increase the number of complications: in cardiovascular prevention, a higher dose does not mean more protection.

Low-dose aspirin: secondary versus primary prevention

Both rows come from the same individual-participant-data meta-analysis; the starting difference (high risk versus low risk) is what decides whether the benefit outweighs the bleeding.

SettingWhoSerious vascular events per year (aspirin versus control)Balance according to the authors
Secondary preventionPeople with a previous heart attack, stroke or arterial disease (16 trials, about 17,000 people)6.7% versus 8.2%Clear and substantial net benefit for many of these people
Primary preventionPeople without known vascular disease (6 trials, about 95,000 people)0.51% versus 0.57%Uncertain net value: major gastrointestinal and extracranial bleeding rose from 0.07% to 0.10% per year

For decades, taking a baby aspirin every morning was sold as something close to life insurance for your heart. Today the picture is more nuanced: taking it because you have already had a heart attack or a stroke is not the same as taking it to prevent a first event when you are healthy. That distinction, the one separating secondary from primary prevention, is what has changed the recommendations in recent years. Here we explain what the major trials and guidelines say, with their figures, so you understand why the answer is no longer a yes for everybody.

What aspirin does in the body

Low-dose acetylsalicylic acid is an antiplatelet drug: it reduces the ability of platelets to clump together and form clots. It does so by blocking the synthesis of substances called prostaglandins, derived from arachidonic acid, both in the endothelium lining the blood vessels and in the platelets themselves. Put simply, it makes the blood clot less easily. That same mechanism explains both the good and the bad: if it prevents clots from blocking an artery, it protects against heart attack and stroke, but if it makes clotting harder in general, it also makes bleeding more likely.

Secondary prevention: when an event has already happened

Here the evidence is solid and in favour. In people who have already had a heart attack or a stroke, or who have established arterial disease, the large ATT Collaboration meta-analysis showed that aspirin reduced serious vascular events from 8.2% to 6.7% per year (p<0.0001), with reductions of around one fifth in total stroke (2.08% versus 2.54% per year, p=0.002). Coronary events fell by a similar proportion, also around one fifth (4.3% versus 5.3% per year, p<0.0001).

That is why the European guidelines continue to support its use in this setting. The 2021 ESC guideline recommends, for secondary prevention, treatment with aspirin at 75-100 mg a day or, in cases of intolerance, clopidogrel at 75 mg a day. The key point is that in these patients the risk of a new event is high, and that benefit outweighs the bleeding risk.

Primary prevention: here the balance shifts

The debate concerns healthy people who have never had an event. In primary prevention, the ATT Collaboration meta-analysis of 95,000 patients across six trials found a 12% proportional reduction in serious vascular events (0.51% with aspirin versus 0.57% in the control group per year, p=0.0001). It sounds good, but the caveat matters: bleeding risk was around 50% higher, and that offset much of the benefit. When your baseline risk of a heart attack is low, the absolute protection you gain is small and the danger of a haemorrhage stops being acceptable collateral damage.

The ASPREE trial made this fairly clear in healthy older adults. After a median of 4.7 years, cardiovascular disease was only slightly lower with aspirin (10.7 versus 11.3 events per 1,000 person-years; HR 0.95; 95% CI 0.83-1.08), a non-significant difference. Major bleeding, on the other hand, was higher: 3.8% versus 2.8% (HR 1.38; 95% CI 1.18-1.62; p<0.001). Nor did aspirin prolong disability-free survival over 5 years.

There was also a signal that should be interpreted cautiously: in ASPREE, all-cause mortality was 12.7 per 1,000 person-years with aspirin versus 11.1 with placebo (HR 1.14; 95% CI 1.01-1.29), and cancer was the main contributor, with 1.6 excess deaths per 1,000 person-years. The authors themselves called for caution: this is a signal, not an established causal relationship, and it should not be read as aspirin causing cancer.

What the guidelines say today

The recommendations have followed the evidence. The US Preventive Services Task Force (USPSTF) recommends that the decision to start low-dose aspirin for primary prevention in adults aged 40 to 59 with a 10-year cardiovascular risk of 10% or higher be taken on an individual basis (grade C), and recommends against starting it in adults aged 60 or over (grade D). In Europe, the 2021 ESC guideline advises against antiplatelet drugs in people at low or moderate cardiovascular risk, precisely because of the bleeding risk.

Even so, inertia carries weight. It has been estimated that between 23% and 46% of older adults in the United States are still taking low-dose aspirin for primary prevention despite the change in recommendations. That is a US population figure and cannot be extrapolated to Spain, but it illustrates how hard it is to unlearn a habit that for years was considered prudent.

Available products and authorised uses in Spain

In Spain, low-dose aspirin is marketed under brands including Adiro 100 mg, as gastro-resistant tablets authorised by the AEMPS (the Spanish Agency for Medicines and Medical Devices; the 300 mg presentation is authorised but not currently marketed), and as A.A.S. 100 mg. The authorised indications for A.A.S. 100 mg include prophylaxis of myocardial infarction and reinfarction in unstable angina and a history of infarction, prevention of aortocoronary bypass occlusion, and treatment of transient ischaemic attacks in men to reduce the risk of stroke.

There is one important practical detail: because of its delayed-release formulation, Adiro is not indicated in acute myocardial infarction; in an emergency it is recommended that the tablet be crushed or chewed to speed up absorption. And here is a myth worth dismantling with data: higher doses of aspirin have not shown greater efficacy and do increase the number of complications. More is not better.

When it is not appropriate, and precautions

A.A.S. 100 mg is contraindicated in patients with active or recurrent peptic ulcer, a history of gastric bleeding or perforation after taking aspirin or other NSAIDs, a bleeding disorder or bleeding risk, and in those with asthma or nasal polyps induced or worsened by acetylsalicylic acid. In addition, aspirin should not be given to under-16s with feverish illnesses, influenza (flu) or chickenpox, because of its association with Reye's syndrome, a rare but serious condition.

In summary, and what you can do today

What to take away: aspirin remains valuable when there has already been a heart attack, a stroke or established vascular disease, but in healthy people its role has narrowed because the bleeding outweighs the benefit. The decision depends on your real cardiovascular risk, and that calls for individual assessment, not an inherited habit. If you are also going through the menopause and want a doctor to look at your situation as a whole, what does exist in Spain today is menopause treatment with a prior assessment, prescription when appropriate by a registered doctor, and ongoing follow-up. The first step is to check whether you are eligible.

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Frequently asked questions

Should I take an aspirin a day to avoid a heart attack if I'm healthy?

Not automatically. The USPSTF advises against starting it to prevent a first event from the age of 60 and only considers it, case by case, between 40 and 59 with high cardiovascular risk. In healthy people the absolute benefit is small and the extra bleeding eats up much of it, so it is a decision to make with your doctor based on your real risk.

If I've already had a heart attack or a stroke, does aspirin still help?

Yes, this is the setting where the evidence is strongest: in people who already have vascular disease, the risk of a new event is high and the benefit outweighs the risk of bleeding. The regimen is set and reviewed by the doctor who prescribed it; any change is decided with them.

Does taking more aspirin protect the heart more?

No. The summary of product characteristics for Adiro states that higher doses have not shown greater efficacy and increase complications. That is why low doses are used in cardiovascular prevention.

What should I do if I think I'm having a heart attack and I have Adiro at home?

The first thing is to call the emergency services (112). The summary of product characteristics states that Adiro, because of its delayed release, is not indicated in acute myocardial infarction and that, if it had to be used in an emergency, it should be crushed or chewed to speed up absorption; this is a decision guided by the emergency services, not something to manage alone at home.