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The Use of Aspirin for Primary Prevention of Cardiovascular Diseases

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Presentation on theme: "The Use of Aspirin for Primary Prevention of Cardiovascular Diseases"— Presentation transcript:

1 The Use of Aspirin for Primary Prevention of Cardiovascular Diseases
Naama Hermann Pnimit B, Tel Hashomer

2 Aspirin Hippocrates described salicylic acid as a bitter willow bark extract that eases pains and reduces fever. Synthetic salicylate first manufactured in 1897 Mechanism discovered in 1971 The modern derivative named after St Aspirinius, the patron saint protecting from headaches. ערבה

3 Aspirin Analgesic, antipyretic, anti-inflammatory and antiaggregant agent Irreversibly inhibits cyclo-oxygenase (COX-1 and 2) Decrease formation of precursors of prostaglandins from arachidonic acid Affects platelet function by preventing formation of the aggregating agent thromboxane A2

4 Aspirin for All!

5 Aspirin for All! The guidelines
U.S. Preventive Services Task Force Grade A recommendation chemoprevention for adults at increased risk (10-year CHD risk ≥ 6%) American Heart Association Low-dose aspirin primary prevention in adults at higher risk of coronary heart disease (especially those with a 10-year CHD risk ≥ 10%) Joint British Society (British Cardiac Society, British Hypertension Society, Diabetes UK, HEART UK, Primary Care Cardiovascular Society, The Stroke Association) Aspirin 75 mg daily recommended for all people over the age of 50 with total CVD risk > 20%, and in selected people with diabetes (> 50 years, had the disease for over 10 years, or receiving treatment for hypertension)

6 Aspirin for Primary Prevention of CVS Diseases
Do the benefits outweigh the harms? Is there a benefit??

7 Aspirin in the primary and secondary prevention of vascular disease: collaborative meta-analysis of individual participant data from randomised trials Antithrombotic Trialists' (ATT) Collaboration Lancet May 30; 373(9678): 1849–1860 Meta-analyses of six primary prevention trials (95,000 individuals) comparing serious vascular events (MI, stroke, or vascular death) Increased major gastrointestinal and other extracranial bleeds (0·10% vs 0·07% per year) Allocation to aspirin had no significant effect on fatal stroke, coronary heart disease or other vascular causes of death

8 Antithrombotic Trialists' (ATT) Collaboration
the same group that wrote the original 2002 aspirin primary-prevention meta-analysis, published in the BMJ Credited by many to have been the paper that cemented the role of low-dose aspirin in primary prevention Claim critical typo in the original paper: the final sentence reads: "For most healthy individuals, however, for whom the risk of a vascular event is likely to be substantially less than 1% a year, daily aspirin may well be appropriate." A correction swiftly issued by the BMJ noted that final word should, in fact, be inappropriate.

9 Aspirin for Asymptomatic Atherosclerosis (AAA) study European Society of Cardiology (ESC), August 2009 3350 participants allocated randomly to enteric coated aspirin 100 mg once daily or placebo Mean age 62 No history of vascular disease Asymptomatic atherosclerosis indicated by ABI ≤0.95 mean follow-up 8.2 years

10 Primary end-point results for aspirin vs placebo
Aspirin (n=1675), n (%) Placebo (n=1675), n (%) Fatal coronary event 28 (1.7) 18 (1.1) Fatal stroke 7 (0.4) 12 (0.7) Nonfatal coronary event 62 (3.7) 68 (4.1) Nonfatal stroke 37 (2.2) 38 (2.3) Coronary revascularization 24 (1.4) 20 (1.2) Peripheral revascularization 23 (1.4) Adverse events with aspirin vs placebo Adverse event Aspirin (n=1675), n (%) Placebo (n=1675), n (%) Major hemorrhage 34 (2.0) 20 (1.2) Gastrointestinal ulcer 14 (0.8) 8 (0.5) Fowkes G. European Society of Cardiology 2009 Congress; August 30, 2009; Barcelona, Spain.

11 Aspirin for Asymptomatic Atherosclerosis (AAA) study European Society of Cardiology (ESC), 2009
No difference in number of primary and secondary endpoint events Primary endpoint: an initial fatal / nonfatal coronary event, stroke or revascularization secondary endpoint - All-cause mortality fatal coronary events more likely with aspirin than with placebo treatment (1.7% vs. 1.1%) Gastric ulcers more frequent with aspirin use (0.8% vs. 0.5%). Interestingly, cancer mortality was higher in the placebo group than in the aspirin group, Fowkes noted No support for the routine use of aspirin for the prevention of vascular events in the context of ABI screening of the general population

12 Current evidence does not identify a worthwhile net benefit
Don’t use aspirin for primary prevention of cardiovascular disease Helen Barnett et al, BMJ 2010;340:c1805 Current evidence does not identify a worthwhile net benefit No justification even in specific subgroups with high predicted risk, HTN or DM The routine practice of Aspirin prophylaxis should be abandoned Review patients currently receiving treatment

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