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Abdominal Aortic Aneurysm: Screening and Surveillance

Cardiology Clinical medicine Definition and Pathophysiology An abdominal aortic aneurysm (AAA) is diagnosed when the abdominal aortic diameter exceeds 3 cm. Most AAAs are located…

Risk Factor Modification: The Evidence Base for Primary Prevention

Cardiology Clinical medicine Definition and Scope Primary prevention aims to prevent the clinical manifestation of cardiovascular disease (CVD) in individuals without established clinical CVD. It…

Cardiovascular Risk in Inflammatory and Autoimmune Disease

Cardiology Clinical medicine Definition and scope Inflammatory and autoimmune diseases are immune mediated inflammatory diseases (IMIDs) that include rheumatoid arthritis (RA), psoriatic arthritis, spondyloarthropathies, systemic…

Lipoprotein(a): Measurement and Clinical Implications

Cardiology Clinical chemistry & laboratory medicine Definition and structure Lipoprotein(a), abbreviated Lp(a), is an LDL like circulating lipoprotein particle. It contains one molecule of…

Familial and Genetic Screening in Premature Cardiovascular Disease

…cardiovascular medicine is the systematic assessment of relatives and other individuals who may carry an inherited predisposition to cardiovascular disease. It combines a structured family…

Quiz: ECG in athletes

…to ECG interpretation 1. Which of the following ECG findings is typically considered a normal variant in asymptomatic athletes with no significant family history? A:…

🟠 Adjusted aortic root dimension

…aorta, aortic arch) All individuals 60 mm (descending aorta) All individuals Risk factors : previous dissection, family history of dissection, severe aortic regurgitation or mitral regurgitation…

Primary Aldosteronism: Screening and Management

…familial forms associated with adrenal adenoma or bilateral adrenal hyperplasia. A family history is therefore important, particularly in patients with early onset hypertension or premature…

Brugada syndrome: ECG, clinical features and management

…syndrome – appeared to be hereditary, since many patients reported a family history of the same symptoms and events. Perhaps the most distinguishing feature was the…

Dilated Cardiomyopathy (DCM): Definition, Types, Diagnostics & Treatment

…of the left ventricle . Patients with DCM typically develop heart failure early in life and a family history of heart failure, ventricular arrhythmias or sudden…

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