Objectives Determining the rupture risk of large abdominal aortic aneurysms (AAA) through clinical studies remains elusive. We sought to employ computational methods on existing literature data and briefly report on stratified rupture risk of large AAAs.
Methods We reviewed published English-language literature reporting on rupture risk of large AAAs. Analysis of rupture risk was performed on Microsoft Excel and Visual Basic scripting. Outcome of interest was annual rupture probabilities stratified by aneurysm size (range 5.0/5.5 – 10.0 cm in women/men) and patient sex. Uncertainty in rupture probabilities was considered through probability distributions.
Results For aneurysms sized 5.5 – 7.0 cm, estimated annual rupture probabilities in women were much higher than literature-reported estimates in men, ranging from 6.4% (95% confidence interval: 3.5% – 10.1%) to 54.5% (95% confidence interval: 39.3% – 69.3%). For aneurysms sized 7.5 cm, estimated annual rupture probabilities were 32.4% (95% confidence interval: 26.1% – 39.0%) in men and 64.8% (95% confidence interval: 51.3% – 77.1%) in women. For aneurysms sized 10.0 cm, estimated rupture probabilities increased to near-certainty at 96.6% (95% confidence interval: 94.0% – 98.5%) in men and 98.8% (95% confidence interval: 96.8% – 99.9%) in women.
Conclusion Computational analysis of existing data is feasible to estimate stratified rupture probabilities of large AAAs, based on aneurysm size and patient sex. Further clinical studies are needed to obtain more precise estimates of rupture probabilities.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementThis study did not receive any funding.
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I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
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Data AvailabilityAll data produced in the present study are available upon reasonable request to the authors.
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