“… 1 , 2 , 3 However, due to their rarity, there are limited data available on PAA treatment practices and outcomes, with the largest patient cohorts typically coming from population‐based data, national insurance claim data sets, or vascular registries. 4 , 5 , 6 , 7 , 8 , 9 While demographic descriptions of larger collectives of patients with PAAs have been conducted before, including subgroup analyses stratified by sex, 5 , 10 symptoms, 6 , 8 or treatment modalities, 11 , 12 the complexity of aneurysm pathophysiology, the heterogeneity, and interactions among patient characteristics make a solely hypothetico‐deductive approach challenging, and many questions remain unanswered. For instance, risk patterns for symptomatic presentation and perioperative complications have not been conclusively clarified yet.…”