Key result
Low-dose aspirin exposure was not associated with a reduced risk of the primary composite outcome in patients with AAA/TAAA (HR 1.000; 95% CI 0.994-1.005) or TAA (HR 1.010; 95% CI 0.994-1.026).
Why the study?
Does low-dose aspirin reduce the composite outcome of death, aortic dissection, rupture, unruptured event, or surgical repair in patients with aortic aneurysms?
Cohort (n=287)
Yes
Does low-dose aspirin reduce the composite outcome of death, aortic dissection, rupture, unruptured event, or surgical repair in patients with aortic aneurysms?
Low-dose aspirin use is not associated with a reduction in mortality or exacerbation events in patients with aortic aneurysms.
Low-dose aspirin shows no benefit in aortic aneurysms; leaves open need for randomized confirmation.
BACKGROUND: Limited studies evaluated the association between low-dose aspirin use and abdominal aortic aneurysm (AAA), thoracoabdominal aortic aneurysm (TAAA), and thoracic aortic aneurysm (TAA) treatment. We conducted this study to investigative the association of low-dose aspirin in terms of preventing death and exacerbation of different aortic aneurysms. METHODS: This retrospective study identified aortic aneurysm cases between 1999 and 2006 from the National Health Insurance Research Database and used time-dependent methods to determine whether the use of low-dose aspirin reduced the risk of outcomes. Primary outcomes, including a composite outcome of death, aortic dissection, a rupture event, an unruptured event, or surgical repair, and secondary outcomes, the composite end point of death and readmission for aortic aneurysm events, were estimated separately. RESULTS: Two hundred eighty-seven cases were identified. The hazard ratio for the primary outcome in patients taking low-dose aspirin in AAA/TAAA patients at each 90-day interval based on the time-dependent analysis was 1.000 (95% confidence interval [CI], 0.994-1.005), and in TAA patients 1.010 (95% CI, 0.994-1.026) compared with those with no exposure. In terms of the secondary outcomes, the hazard ratio for all-cause mortality was 0.995 (95% CI, 0.988-1.003) for AAA/TAAA patients and 1.008 (95% CI, 0.991-1.026) for TAA patients. CONCLUSIONS: From a national population database, we did not find an association between low-dose aspirin exposure and mortality or exacerbation in different aortic aneurysms by using time-dependent analysis. However, adjustments for aneurysms size and smoking status could not be made, which may limit the validity of the study.
No takes yet. Share an insight, caveat, or question.
Chen et al. (2013) conducted a cohort in Aortic aneurysms (AAA, TAAA, and TAA) (n=287). Low-dose aspirin vs. No exposure was evaluated on Composite outcome of death, aortic dissection, a rupture event, an unruptured event, or surgical repair (HR 1.000, 95% CI 0.994-1.005). Low-dose aspirin exposure was not associated with a reduced risk of the primary composite outcome in patients with AAA/TAAA (HR 1.000; 95% CI 0.994-1.005) or TAA (HR 1.010; 95% CI 0.994-1.026).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: