Abdominal aortic aneurysm (AAA) rupture is a local event in the aneurysm wall that naturally demands tools to assess the risk for local wall rupture. Consequently, global parameters like the maximum diameter and its expansion over time can only give very rough risk indications; therefore, they frequently fail to predict individual risk for AAA rupture. In contrast, the Biomechanical Rupture Risk Assessment (BRRA) method investigates the wall's risk for local rupture by quantitatively integrating many known AAA rupture risk factors like female sex, large relative expansion, intraluminal thrombus-related wall weakening, and high blood pressure. The BRRA method is almost 20 years old and has progressed considerably in recent years, it can now potentially enrich the diameter indication for AAA repair. The present paper reviews the current state of the BRRA method by summarizing its key underlying concepts (i.e., geometry modeling, biomechanical simulation, and result interpretation). Specifically, the validity of the underlying model assumptions is critically disused in relation to the intended simulation objective (i.e., a clinical AAA rupture risk assessment). Next, reported clinical BRRA validation studies are summarized, and their clinical relevance is reviewed. The BRRA method is a generic, biomecha nics-based approach that provides several interfaces to incorporate information from different research disciplines. As an example, the final section of this review suggests integrating growth aspects to (potentially) further improve BRRA sensitivity and specificity. Despite the fact that no prospective validation studies are reported, a significant and still growing body of validation evidence suggests integrating the BRRA method into the clinical decision-making process (i.e., enriching diameterbased decision-making in AAA patient treatment).
Problem DefinitionAbdominal aortic aneurysm (AAA) disease is a serious condition and causes many deaths, especially in males over 65 years. Progressive treatment (i.e., surgical or endovascular AAA repair) cannot be offered to all patients, and according to the best clinical practice, AAA repair is indicated if rupture risk exceeds the interventional risks. While center-specific treatment risks are reasonably predictable, assessing AAA rupture risk for individual patients remains the bottleneck in clinical decision making. However, an accurate rupture risk assessment is critical to reduce aneurysm-related mortality without substantially increasing the rate of AAA repair.According to the current clinical practice, AAA rupture risk is assessed by the aneurysm's largest