Knowledge of the distribution of velocities across the ascending aorta is important for measurements of cardiac output; for understanding the function of normal and diseased valves and for the evaluation of prosthetic valves. The aim of this study was to investigate, in detail, the spatial distribution of axial velocities in the human ascending aorta, covering a nearly complete cross-section of the lumen in a time continuous modus. During open-heart surgery, blood velocities in the ascending aorta were mapped in 10 patients. All patients had aortic valves with no significant clinical evidence of disease. Pulsed Doppler ultrasound technique was used to measure blood velocity using an intraluminal probe with a 1 mm, 10 MHz crystal connected to a position-sensitive device. The distribution of blood velocity in the aorta 6-8 cm above the valve was characterized by a skewed and irregular peak systolic flow, with maximum velocity posteriorly. There was a positive correlation (r=0.854, P<0.002) between the maximum skewness slope and the stroke volume. Significant retrograde flow was recorded in all patients in the left posterior part of aorta in late systole and early diastole. The rotation of the point of maximal velocity was anticlockwise in six patients, clockwise in three and alternating in one. The present study shows that there is a considerable individual variation in the velocity distribution in the ascending aorta, with no plane symmetric features, and that large sampling volumes are required for reliable estimates of mean velocity.
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http://dx.doi.org/10.1111/j.1475-097x.1996.tb00572.x | DOI Listing |
Cureus
December 2024
Internal Medicine, Hospital de Braga, Braga, PRT.
Aortic dissection is a life-threatening vascular emergency associated with high morbidity and mortality. Clinical manifestations might include severe chest pain to neurological deficits, depending on the arterial segments involved. Extensive dissections involving multiple aortic segments and branch vessel occlusions, such as the carotid arteries, are rare and pose unique diagnostic and therapeutic challenges.
View Article and Find Full Text PDFJACC Case Rep
January 2025
Heart, Vascular, and Thoracic Institute, Cleveland Clinic London, London, United Kingdom.
We describe the case of a 52-year-old man with radiation-induced severe mixed aortic and mitral valve disease, thickening of the aortomitral continuity, mitral annular calcification, and porcelain aorta with limited transcatheter treatment options. By replacing the aorta during circulatory arrest, we demonstrate that it is possible to clamp the ascending aorta to facilitate prosthetic aortic and mitral valve replacement.
View Article and Find Full Text PDFTrials
January 2025
Department of Vascular Surgery, The Fourth Affiliated Hospital, Zhejiang University School of Medicine, Yiwu, Zhejiang, China.
Background: Thoracic aortic pathologies involving the aortic arch are a great challenge for vascular surgeons. Maintaining the patency of supra-aortic branches while excluding the aortic lesion remains difficult. Thoracic EndoVascular Aortic Repair (TEVAR) with fenestrations provides a feasible and effective approach for this type of disease.
View Article and Find Full Text PDFJ Vasc Surg
January 2025
Division of Vascular and Endovascular Surgery, Mayo Clinic, Rochester MN, USA. Electronic address:
Objectives: Celiac artery (CA) incorporation during FB-EVAR for complex abdominal aortic aneurysms (cAAA) is typically performed with fenestrations. Double-wide scallops (DWS) can be used when appropriate. We aimed to assess outcomes of patients treated with DWS for the CA during FB-EVAR for cAAA.
View Article and Find Full Text PDFArterioscler Thromb Vasc Biol
January 2025
Department of Cardiovascular Medicine, The University of Tokyo, Bunkyo-ku, Japan. (H. Yagi, H.A., Q.L., A.S.-K., M.U., H.K., R.M., A.S., S.O., H.T., Norifumi Takeda, I.K.).
Background: Marfan syndrome (MFS) is an inherited disorder caused by mutations in the gene encoding fibrillin-1, a matrix component of extracellular microfibrils. The main cause of morbidity and mortality in MFS is thoracic aortic aneurysm and dissection, but the underlying mechanisms remain undetermined.
Methods: To elucidate the role of endothelial XOR (xanthine oxidoreductase)-derived reactive oxygen species in aortic aneurysm progression, we inhibited in vivo function of XOR either by endothelial cell (EC)-specific disruption of the gene or by systemic administration of an XOR inhibitor febuxostat in MFS mice harboring the missense mutation p.
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