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Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Aspirin and cardiovascular primary prevention in non-endstage chronic kidney disease: A meta-analysis
Rupert W Major1, Issaam Oozeerally2, Simon Dawson2
1Department of Health Sciences, University of Leicester, UK; John Walls Renal Unit, University Hospitals of Leicester, UK.
Insights
Aspirin does not clearly prevent cardiovascular events or reduce mortality in chronic kidney disease (CKD) patients. It may increase bleeding risk, and more data is needed to guide its use in CKD primary prevention.
Area of Science:
- Nephrology
- Cardiology
- Clinical Trials
Background:
- Chronic kidney disease (CKD) is a significant risk factor for cardiovascular disease (CVD).
- No prior meta-analyses have evaluated aspirin for primary CVD prevention in CKD patients.
Purpose of the Study:
- To systematically review and meta-analyze the efficacy and safety of aspirin for primary CVD prevention in individuals with non-endstage CKD.
Main Methods:
- Systematic review and meta-analysis of randomized controlled trials (RCTs) using a pre-defined protocol.
- Searched Medline and Embase (1996-2015) for adult subjects with non-endstage CKD and no prior CVD.
- Co-primary outcomes: major cardiovascular events and all-cause mortality; secondary outcome: bleeding events.
Main Results:
- Included 3 trials with 4468 participants; 2 provided new data.
- Aspirin showed no significant reduction in major cardiovascular events (RR 0.92) or mortality (RR 0.74).
- Aspirin significantly increased major bleeding events (RR 1.98).
Conclusions:
- Aspirin offers no clear benefit for primary CVD prevention in CKD.
- Aspirin use is associated with an increased risk of major bleeding.
- Insufficient RCT data currently exists to recommend aspirin for primary CVD prevention in CKD.
Background And Aims:
Chronic kidney disease is a strong independent predictor of cardiovascular disease. No published meta-analyses on the use of aspirin for the primary prevention of cardiovascular disease in chronic kidney disease exist. We therefore performed a systematic review and meta-analysis of this subject.
Methods:
We used a pre-defined and registered protocol (PROSPERO identification CRD42014008860). We searched Medline and Embase between 1996 and July 2015. Inclusion criteria were adult subjects with non-endstage chronic kidney disease (CKD) and no history of cardiovascular disease. The co-primary outcomes were major cardiovascular events and all-cause mortality. Secondary outcomes included bleeding-related events. We used a random effects model to pool data.
Results:
Three trials were identified and two of these provided previously unpublished data. The studies included 4468 participants and 16,740 person-years of follow-up. There were no statistically significant reductions in the risk of major cardiovascular events (RR 0.92, 95% CI 0.49 to 1.73, p = 0.79, I(2) 71%) or mortality (RR 0.74, 95% CI 0.55 to 1.00, p = 0.05, I(2) 0%) with aspirin compared to the control group. Major bleeding events were increased with aspirin though (RR 1.98, 95% CI 1.11 to 3.52, p = 0.02, I(2) 0%).
Conclusions:
There is no clear benefit of aspirin for the primary prevention of cardiovascular events in CKD and no statistically significant reduction in mortality. Aspirin is likely to increase the risk of major bleeding events. Currently, insufficient randomised control trial data exists to recommend universal use or avoidance of aspirin for primary prevention of cardiovascular events in CKD.
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