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"Influence of age on survival, late hypertension, and recoarctation in elective aortic coarctation repair. Including long-term results after elective aortic coarctation repair with a follow-up from 25 to 44 years". The Journal of Thoracic and Cardiovascular Surgery. 108 (3): 525– 31. doi: 10.1016/S0022-5223(94)70264-0. PMID 8078345.
There are two forms of aortic coarctation to be familiar with, an “infant” form and an “adult” form. With the infant form, which accounts for about 70% of cases, the coarctation comes after the aortic arch, which branches off to the upper extremities and to the head, and before the ductus arteriosus.
Central aortic pressure (CAP), central aortic blood pressure (CABP), or central aortic systolic pressure (CASP) is the blood pressure at the root of aorta.Studies have shown the importance of central aortic pressure, especially as compared to peripheral blood pressure, and its implications in assessing the efficacy of antihypertensive treatment with respect to cardiovascular risk factors ...
An aortic cross-clamp is a surgical instrument used in cardiac surgery to clamp the aorta and separate the systemic circulation from the outflow of the heart. [ 1 ] An aortic cross-clamping procedure serves, for example, in the repairing of coarctation of the aorta.
Post-stroke depression may involve depressed mood and decreased interest and pleasure that impairs social and occupational functioning, but does not necessarily need to meet the full criteria of a major depressive disorder. [citation needed]
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An aortic coarctation is a narrowing of the aorta, which is split into infant and adult forms. In the infant form, it's often accompanied by patent ductus arteriosus, and mixing of deoxygenated and oxygenated blood, whereas in the adult form, the ductus arteriosus has closed off.
Coarctation of the aorta is also a known risk factor, [11] as is arteriovenous malformation. [14] Genetic conditions associated with connective tissue disease may also be associated with the development of aneurysms. [11] This includes: [18] autosomal dominant polycystic kidney disease, neurofibromatosis type I, Marfan syndrome,