THE RECENT publication of The American Association for Thoracic Surgery consensus guidelines on bicuspid aortic valve-related aortopathy by Borger et al. 1 is the most comprehensive to date after several other publications. 2-5 We aim to provide a short synopsis of these guidelines with a particular focus on the potential implications for cardiothoracic anesthesiologists and the perioperative echocardiographers. Epidemiology Bicuspid aortic valve (BAV) is a common valve pathology with a prevalence of 1% to 2% in the general population; and a male to female predominance of 3:1. 6 It is the most common congenital cardiac lesion worldwide and causes more morbidity and mortality than all other congenital lesions combined. Despite this, appropriately managed patients diagnosed with BAV have a similar life expectancy to the normal population cohort. Valve dysfunction, aortopathy, or aortic dissection may complicate BAV. In addition, other coreported findings with BAV include Turner's and Williams syndromes, abnormal coronary anatomy (nondominant right coronaries adjacent to commissures), aortic coarctation, patent ductus arteriosus, and prolapse of the anterior leaflet of the mitral valve. Aortic valve function may be normal or generally deteriorates over time causing aortic stenosis (AS), aortic insufficiency (AI), or mixed lesions. BAV-AS is the commonest pathology presenting typically in older patients aged 50 to 70 years old, and BAV-AI occurs less often and predominantly in a younger patient cohort. The clinical findings in the BAV patient depend on native valve function and the presence or absence of associated lesions. The initial presentation of BAV varies, as patients may have asymptomatic auscultatory findings, or symptoms of valve dysfunction, bacterial endocarditis, or evidence of an aortic root or ascending aortic aneurysm, or be in extremis with acute aortic dissection. Patients with BAV-AS continue to be asymptomatic for a prolonged period. Those with severe AS may progress to the classic symptoms of dyspnea, decreased exercise tolerance, exertional dizziness, angina, and syncope. Patients with BAV-AI also may remain asymptomatic, though those with severe AI may present with atypical chest pain, palpitations, or dyspnea. Diagnosis The morphology of BAV varies resulting in different phenotypes that relate to the (1) orientation of the open cusps, (2) position of the commissures, and (3) the presence or absence of a raphe. Though several classification systems describe the BAV, the most frequently used is the Sievers' classification (Fig 1). 8 This classification system categorizes BAV into 3 subtypes based on the number of raphe present: Type 0, no raphe (6%), Type 1, one raphe (89%), and Type 2, 2 raphes (5%). Type 1 is the commonest and is further divided by the spatial position of the cusps into left-and right-coronary cusp fusion (71%), right-and noncoronary cusp fusion (15%), and non-and left-coronary cusp fusion (3%). 8 The resulting 2 functional cusps are usually asymmetric in size, and the nonfuse...