Key result
A developed risk calculator demonstrates that in many clinical situations, the number of potential upper GI complications induced by low-dose aspirin may exceed the number of prevented CV events.
Why the study?
Does a risk calculator help estimate the balance of cardiovascular benefits and gastrointestinal risks of low-dose aspirin?
Does a risk calculator help estimate the balance of cardiovascular benefits and gastrointestinal risks of low-dose aspirin?
A newly developed risk calculator helps clinicians weigh the cardiovascular benefits against the gastrointestinal risks of low-dose aspirin for individual patients.
Answers are grounded in this paper and cite their sources.
May prompt individualized aspirin decisions balancing GI and CV risks; leaves open prospective validation of the calculator.
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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Lanas et al. (2013) studied Cardiovascular and gastrointestinal risk assessment. Low-dose aspirin was evaluated on Cardiovascular events and upper gastrointestinal complications. A developed risk calculator demonstrates that in many clinical situations, the number of potential upper GI complications induced by low-dose aspirin may exceed the number of prevented CV events.
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