In the 1890’s, scientists at Bayer developed a new
medication they called aspirin. In 1899 Bayer began selling aspirin. For many decades, aspirin was used to treat
pain, fever and inflammation. However, in the 1970’s, aspirin was found to have
properties as a blood thinner. It is the blood thinning properties which makes
it beneficial for heart disease. Despite
being in existence for more than 100 years, there are still questions about aspirin,
such as the optimal dose and who should take it for the prevention of heart
disease.
Aspirin’s ability to thin the blood centers around its
effect on platelets. Platelets are cells
which circulate in the bloodstream. If there is a tear in the wall of a blood
vessel (a cut) or if a cholesterol-laden plaque in an artery breaks open, the
platelets rush to the site of the injury and initiate the blood-clotting
cascade. The resulting clot prevents
bleeding from a cut or produces a clot within a heart artery, stopping the flow
of blood and causing a heart attack. Aspirin
inhibits the platelet’s ability to form a blood clot. This puts the person
taking aspirin at risk for bleeding (since the platelets cannot trigger a blood
clot) and the “blood is thinned”. Aspirin inhibits platelets for the life of
the platelet, about 7 to 10 days. The most serious side effect of aspirin is
bleeding. Aspirin may cause bleeding in the stomach (from an ulcer), the colon
(from polyps) or the brain.
Aspirin is the mainstay of treatment for heart disease. In patients having an acute heart attack,
aspirin is given immediately (in fact the patient is asked to chew it so it may
be absorbed more quickly than if it was swallowed) to counteract the acute
blood clot forming in the heart artery.
After a heart attack, an “adult” aspirin (325 mg) is given daily to
prevent another heart attack. This is
termed secondary prevention. In this setting, aspirin has been shown to reduce
the risk of heart attack, stroke or death by 33%. Similarly, aspirin is given
to patents with chest pain due to heart artery disease, stroke patients,
patients after heart bypass surgery and patients with a heart stent. In all of these scenarios, aspirin
effectively reduces the risk of a second event balanced by a small increase in
the risk for bleeding.
The optimal dose of aspirin is still not known. Doses below
75 mg are not effective, so the lowest dose in use now is “baby” aspirin (81 mg). Aspirin doses between 75 and 1500 mg are all
felt to be equally effective. Low dose aspirin (81 mg) is associated with less
risk for bleeding and less gastrointestinal intolerance. For patients with an acute heart attack, a
fresh stent, a recent stroke or after bypass surgery, the initial dose of
aspirin should be 325 mg daily for one month, followed by aspirin 81 mg daily
indefinitely.
Can aspirin be used to prevent heart disease in people who
have not yet had a heart attack (primary prevention)? The US Preventive Services Task Force
recommends a low dose (81 mg) aspirin for adults aged 50 to 69 years old, who
have a 10% or greater risk for cardiovascular disease (based on the American
College of Cardiology cardiovascular risk calculator- http://tools.acc.org/ascvd-risk-estimator/),
are not at increased risk for bleeding, and have a life expectancy of at least
10 years.
So, shouldn’t everyone be on an aspirin? Probably not. For
those who are at low risk for heart disease, the risk of gastrointestinal
bleeding and bleeding into the brain outweighs the benefit of even a low dose
of aspirin. For those who have heart
disease or a stroke or for those who are at high risk for heart disease, an
aspirin a day can save a life and keep you away from your local heart hospital.
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