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Maribeth Friend a Department
of Medical and Research Technology and Medicine, University of Maryland
Medical Center, Baltimore, MD 21201, USA, b Division of Cardiology,
University of Maryland Medical Center Correspondence to: M Miller mmiller@heart.umaryland.edu
| The first 150 words of the full text of this article appear below. |
Aspirin 325 mg/day reduces the rate of events associated
with coronary heart disease. In most people, aspirin produces
irreversible inhibition of platelet aggregation, but in a sizeable
minority of patients, the degree of platelet aggregation needed to
prevent events according to in vitro assessments is not
achieved.1 Risk factors for coronary heart disease may
contribute to aspirin resistance (the inability of aspirin to protect
individuals from thrombotic complications), so aspirin may not be
cardioprotective in patients with hyperlipidaemia.2 We
evaluated patients with a range of cholesterol concentrations to
determine the impact of hypercholesterolaemia on platelet
responsiveness in patients treated with aspirin.
| |
Participants, methods, and results |
|---|
Consecutive patients (n=56) were recruited from the University
of Maryland Preventive Cardiology Outpatient Center. The mean (SD) age
was 54.3 (11.1) years, and 40 (72%) of the patients were men. Patients
were eligible if they were taking aspirin 325 mg/day and presented with
a history of coronary heart disease or at least two
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