Synopsis
Recognise thoracic aortic dilatation, identify heritable and valve-associated disease, plan imaging surveillance and know when urgent or surgical review is needed.
- Thoracic aortic aneurysm is usually silent and found on echocardiography, CT or MRI; symptoms may reflect compression, valve disease or impending complication.
- Confirm the involved segment and obtain reproducible orthogonal measurements; echocardiography assesses the root/ascending aorta and valve, while CT or MRI maps the whole thoracic aorta.
- At diagnosis, look for bicuspid aortic valve, coarctation, syndromic features and a family history of thoracic aneurysm, dissection or sudden unexplained death.
- The 2024 ESC guideline recommends surgery for an ascending aortic aneurysm at a maximal diameter of at least 55 mm in the usual non-heritable setting.
- Lower intervention thresholds may apply in heritable aortopathy, bicuspid valve with additional risk factors, rapid growth, pregnancy planning, small body size or when valve surgery is already planned.
- A symptomatic aneurysm or rapid enlargement needs expedited aortic-team review regardless of a routine surveillance date.
- Control blood pressure, stop smoking and avoid extreme isometric strain; the specific drug and target must reflect comorbidity and any genetic syndrome.
- Acute dissection is a time-critical separate pathway: do not label sudden pain as a stable aneurysm symptom.
Key red flags
Abrupt maximal-at-onset chest/back pain, migrating pain, pulse deficit, focal neurology, syncope, shock or new diastolic murmur requires emergency assessment.
New symptoms or credible interval enlargement beyond expected measurement variability should trigger earlier cross-sectional imaging and aortic-team review.