There’s little controversy surrounding the use of
aspirin for the prevention of cardiovascular events in patients with
established disease. By contrast, there’s far more smoke than light
regarding the issue of aspirin for primary prevention. We all commonly
face the proverbial “handle-on-the-doorknob” question, “Should I be
taking aspirin?” from patients without established cardiovascular
disease. Such interactions tax us to recall our most recently-attended
CME meeting to try and remember what the general mood of clinicians was
on this issue.
A recent large meta-analysis (Arch Intern Med.2012;Jan 9 [doi:10.1001/archinternmed.2011.626])
will inform these conversations in the year ahead. In this study,
investigators conducted a meta-analysis of studies that had at least one
year of follow-up and at least 1,000 participants. Nine trials
involving a total of more than 100,000 patients were included. Aspirin
was associated with a reduction in cardiovascular (CVD) events
attributable primarily to the nonfatal MI. No effect of aspirin was
observed on fatal MI, stroke, CVD death or cancer mortality. A 70%
increase in bleeding events was observed with a 30% increase in the risk
of clinically significant bleeding events, defined as fatal bleeding
from any site, cerebrovascular or retinal bleeding, bleeding from hollow
viscus, bleeding requiring hospitalization and/or transfusion, or
study-defined major bleeding regardless of source. The number needed to
treat for nonfatal MI was 162 compared to the number needed to harm for
nontrivial bleed of 73.
The data suggest that for every two patients to whom
we recommend aspirin to prevent a nonfatal MI we will have two
clinically significant bleeding events. Perhaps the authors are correct
in suggesting that aspirin may add little extra value to CVD risk
reduction efforts that aggressively target lipid levels, blood pressure,
and tobacco use behaviors. But we can’t ignore the aspirin question
because patients want to know what to do and, commonly, the
justification for it. In patients at low risk for CVD events, aspirin
prophylaxis may make them bleed. But let us not throw the baby out with
the bathwater because among higher risk patients, the data are strong
that aspirin may prevent a heart attack and some patients may place high
value on this prevention. For those in the middle, perhaps creative
aspirin dosing, such as every-other-day, could be explored.
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