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Articolul urmator |
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Ultima descărcare din IBN: 2023-08-02 18:54 |
SM ISO690:2012 GAVRILIUC, Natalia, PALII, Ina, REVENCO, Ninel, EŞANU, Valeriu, CIUHRII, Olga. Depășirea diametrului: când să cercetăm aorta la copiii cu aortopatii congenitale. In: Congresul consacrat aniversării a 75-a de la fondarea Universității de Stat de Medicină şi Farmacie „Nicolae Testemiţanu”, 21-23 octombrie 2020, Chişinău. Chişinău: USMF, 2020, p. 536. |
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Congresul consacrat aniversării a 75-a de la fondarea Universității de Stat de Medicină şi Farmacie „Nicolae Testemiţanu” 2020 | ||||||
Congresul "Congresul consacrat aniversării a 75-a de la fondarea Universității de Stat de Medicină şi Farmacie „Nicolae Testemiţanu”" Chişinău, Moldova, 21-23 octombrie 2020 | ||||||
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Pag. 536-536 | ||||||
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Rezumat | ||||||
Background. The importance of early diagnosis of a complication in congenital/ genetic aortopathies (C/GAo) in children was demonstrated by the results of our study. Objective of the study. Appreciation of the Z score of diameters at different segments of the thoracic aorta. Material and Method. Analytical, observational, cohort study. 150 children were admitted. Statistical program used - SPSS version 20. Results. As a result of the research of children with C/GAo, the presence of aortic dilation was confirmed (Z score>2 SD), in aortic coarctation: at the level of the diameter of the valve ring (22.9%), of the Valsalva sinus (25.0%), of the sino-tubular jonction (8.3%) and aortic arch (20.8%); in aortic stenosis and bicuspid aortic valve: at the diameter of the ascending (36.8%) and descending aorta (31.6%); in genetic syndromes: at the diameter of the valve ring (33.3%) and the ascending aorta (50.0%). The analysis of the correlation coefficient between the 6 diameters certifies the hypothesis according to which a dilation at at least one aortic segment becomes a risk factor for its develop Conclusion. The results of the study indicated that aortic morphometry and Z-score calculation of aortic diameters are useful and practical in preventing an C/G Ao complication in children. |
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Cuvinte-cheie complications, congenital / genetic aortopathies, children, aortopatii congenitale / genetice, copii, complicaţii |
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