Analysis of aspirin-associated risks in healthy individuals

Chin Hur1, Lee S Simon, G Scott Gazelle

  • 1Harvard Medical School, Institute for Technology Assessment and Gastrointestinal Unit, Massachusetts General Hospital, Boston, MA 02114-4719, USA. chur@mgh-ita.org

Insights

For healthy individuals, daily aspirin use without proven benefit reduces quality-adjusted life-years (QALYs) and life expectancy. Complications occur in about 1 in 15, with a 1 in 556 mortality risk.

Area of Science:

  • Pharmacology and Preventive Medicine
  • Health Economics and Outcomes Research

Background:

  • Aspirin is standard for secondary cardiovascular prevention.
  • Growing trend of aspirin use for primary prevention in healthy individuals for cardiovascular disease and cancer.
  • Lack of data on the impact of aspirin complications on quality of life in healthy populations.

Purpose of the Study:

  • To evaluate the impact of aspirin therapy complications on quality-adjusted life-years (QALYs) in healthy individuals.
  • To assess the net effect of aspirin use, considering only its adverse events.

Main Methods:

  • A decision-analytic model simulating daily 325 mg enteric-coated aspirin use in healthy individuals from age 50.
  • Analysis conducted from a societal perspective, incorporating complication risks and discontinuation of therapy upon adverse events.
  • Extensive sensitivity analyses performed to test parameter variations (age, gender, follow-up duration).

Main Results:

  • Aspirin therapy, assuming no benefits, reduced QALYs by 0.03 per individual.
  • Life expectancy decreased by 0.04 years (2 weeks) per person.
  • Lifetime complication rate was 6.79% (1 in 15), with a mortality rate of 0.18% (1 in 556).

Conclusions:

  • In healthy individuals without proven benefit, aspirin therapy leads to a small reduction in QALYs.
  • The risk of aspirin-induced complications is significant, affecting approximately 1 in 15 individuals.
  • Aspirin therapy in this population carries a small but definite risk of mortality (1 in 556).
Abstract

Related Concept Videos

Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors01:20

Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors

Antiplatelet drugs emerge as frontline defenders against the insidious threat of thromboembolic diseases, where abnormal clots obstruct vital blood vessels. These drugs stand as bulwarks, inhibiting platelet aggregation and clot formation, thereby mitigating the risk of life-threatening conditions like myocardial infarction, coronary artery disease, and thrombotic strokes.
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
Drug Toxicity: Risk factors01:24

Drug Toxicity: Risk factors

Adverse Drug Reactions (ADRs) are potential complications that arise during pharmacotherapy, influenced by multiple risk factors. Age plays a significant role; both neonates and the elderly are at heightened risk due to their respective immature and diminished metabolic and elimination processes. Gender also impacts ADRs, with females experiencing a 1.5 to 1.7-fold greater risk than males, which may be linked to pharmacokinetic, pharmacodynamic, and hormonal differences. Notably, neonates, the...
Bioavailability Study Design: Healthy Subjects Versus Patients01:15

Bioavailability Study Design: Healthy Subjects Versus Patients

Bioavailability studies are essential for evaluating a drug's therapeutic efficacy and understanding its absorption patterns under various physiological conditions. Conducting such studies on target patient populations provides more relevant data by simulating real-world disease states. However, practical challenges often necessitate the use of young, healthy adult volunteers as study subjects.Patients may exhibit altered drug absorption patterns due to the effects of the disease itself,...
Drug toxicity: Drug–Drug Interaction01:30

Drug toxicity: Drug–Drug Interaction

Drug–drug interactions can precipitate toxicity through multiple mechanisms. Absorption interactions alter how drugs enter the body, exemplified when ranitidine increases the absorption of basic drugs, while cholestyramine decreases the levels of propranolol. Protein binding interactions occur when drugs share the same binding sites on plasma proteins. Drugs like aspirin and warfarin, when bound in excess, can lead to increased free drug concentrations, enhancing the potential for...
Pharmacodynamics in Geriatric Patients: Effects of Age01:27

Pharmacodynamics in Geriatric Patients: Effects of Age

Age-related pharmacokinetic changes are extensively documented, but understanding age-related pharmacodynamic alterations is relatively limited. This knowledge gap can be partly attributed to the complexity of developing appropriate measures of drug responses compared to bioanalytical methods for determining drug concentrations.Most information regarding age-related differences in human pharmacodynamics originates from cross-sectional studies. However, these studies assume that observed mean...
Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...