OBJECTIVE: The use of aspirin for primary prevention of cardiovascular even
ts in the general population is controversial. The purpose of this study wa
s to create a versatile model to evaluate the effects of aspirin in the pri
mary prevention of cardiovascular events in patients with different risk pr
ofiles.
DESIGN:A Markov decision-analytic model evaluated the expected length and q
uality of life for the cohort's next 10 years as measured by quality-adjust
ed survival for the options of taking or not taking aspirin.
SETTING: Hypothetical model of patients in a primary care setting.
PATIENTS: Several cohorts of patients with a range of risk profiles typical
ly seen in a primary care setting were considered. Risk factors considered
included gender, age, cholesterol levels, systolic blood pressure, smoking
status, diabetes, and presence of left ventricular hypertrophy. The cohorts
were followed for 10 years. Outcomes were myocardial infarction, stroke, g
astrointestinal bleed, ulcer, and death.
MAIN RESULTS: For the cases considered, the effects of aspirin varied accor
ding to the cohort's risk profile. By taking aspirin, the lowest-risk cohor
t would be the most harmed with a loss of 1.8 quality-adjusted life days by
taking aspirin; the highest risk cohort would achieve the most benefit wit
h a gain of 11.3 quality-adjusted life days. Results without quality adjust
ment favored taking aspirin in all the cohorts, with a gain of 0.73 to 8.04
days. The decision was extremely sensitive to variations in the utility of
taking aspirin and to aspirin's effects on cardiovascular mortality. The m
odel was robust to other probability and utility changes within reasonable
parameters.
CONCLUSIONS: The decision of whether to take aspirin as primary prevention
for cardiovascular events depends on patient risk. It is a harmful interven
tion for patients with no risk factors, and it is beneficial in moderate an
d high-risk patients. The benefits of aspirin in this population are compar
able to those of other widely accepted preventive strategies. It is especia
lly dependent on the patient's risk profile, patient preferences for the ad
verse effects of aspirin, and on the level of beneficial effects of aspirin
on cardiovascular-related mortality.