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The aspirin cardiovascular/gastrointestinal risk calculator--a tool to aid clinicians in practice
A Lanas1, M Polo-Tomás, R Casado-Arroyo
1Service of Digestive Diseases, University Hospital Lozano Blesa, University of Zaragoza, IIS Aragón, Spain. alanas@unizar.es
Insights
Balancing the benefits and risks of low-dose aspirin is challenging. A new calculator helps estimate cardiovascular (CV) and gastrointestinal (GI) risks to guide clinical decisions for aspirin therapy.
Area of Science:
- Cardiology
- Gastroenterology
- Clinical Decision Support
Background:
- Assessing the balance between gastrointestinal (GI) and cardiovascular (CV) risks versus the benefits of low-dose aspirin presents clinical challenges.
- Individual patient risk stratification for low-dose aspirin therapy requires careful consideration of potential adverse events.
Purpose of the Study:
- To develop a clinical decision support tool for estimating individual patient CV and GI risks associated with low-dose aspirin.
- Facilitate informed decision-making regarding the initiation and management of low-dose aspirin therapy.
Main Methods:
- Constructed risk-ratio estimations based on incidence data for CV events and upper GI complications.
- Incorporated risk factors, including low-dose aspirin use, proton pump inhibitor (PPI) co-therapy, and H. pylori eradication.
- Assumed baseline GI complication incidence, aspirin-induced risk increase, and risk reduction with PPIs and H. pylori eradication.
Main Results:
- A web-based calculator (http://www.asariskcalculator.com) was developed to estimate CV and GI risks.
- In low CV risk patients, GI complications from aspirin may outweigh prevented CV events.
- Even in high CV risk patients, GI complications can offset the benefits of aspirin; PPIs can mitigate but may not eliminate this risk in high GI risk individuals.
Conclusions:
- Clinical scenarios exist where aspirin-induced upper GI complications may exceed prevented CV events.
- A risk calculator is essential for guiding physicians in optimizing aspirin therapy and maximizing patient benefit while minimizing harm.
Background:
Assessment of both GI and CV risks vs. the benefits of low-dose aspirin for individual patients can be difficult in clinical practice.
Aim:
To develop a tool to estimate CV and GI risks to facilitate the clinical decision-making process.
Methods:
We constructed risk-ratio estimations and determined the incidence of CV events and upper GI complications according to the presence of different risk factors. For upper GI complications we assumed a baseline incidence of 1 case/1000-persons-year, a twofold increased risk with low-dose aspirin, and estimated a 60% GI risk reduction with proton pump inhibitors (PPI) co-therapy and a 60% risk reduction with H. pylori eradication in patients with a history of peptic ulcer.
Results:
The calculator can be found at http://www.asariskcalculator.com. In patients with low CV risk the number of GI complications induced by low-dose aspirin may be greater than the number of CV events prevented. In patients with high CV risk, low-dose aspirin is recommended, but the number of GI complications induced may still overcome the CV events saved. The use of PPI reduces the number of complication events induced by low-dose aspirin, but the number of CV events saved may still be offset by the number of GI complications induced in patients at very high GI risk.
Conclusions:
There are many clinical situations where the number of potential upper GI complications induced by low-dose aspirin may exceed the number of potentially prevented CV events. A risk calculator should guide physicians in choosing appropriate therapy and maximise the aspirin benefit.
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