Conţinutul numărului revistei |
Articolul precedent |
Articolul urmator |
795 12 |
Ultima descărcare din IBN: 2023-02-07 00:13 |
Căutarea după subiecte similare conform CZU |
616.12-007.2-089-053.31 (1) |
Patologia sistemului circulator, a vaselor sanguine. Tulburări cardiovasculare (975) |
SM ISO690:2012 ŞOITU, Marcela, PANFIL, Ana. Coarctaţia de aortă la nou-născut – prezentare de caz. In: Buletin de Perinatologie, 2018, nr. 2(78-S), pp. 80-83. ISSN 1810-5289. |
EXPORT metadate: Google Scholar Crossref CERIF DataCite Dublin Core |
Buletin de Perinatologie | ||||||
Numărul 2(78-S) / 2018 / ISSN 1810-5289 | ||||||
|
||||||
CZU: 616.12-007.2-089-053.31 | ||||||
Pag. 80-83 | ||||||
|
||||||
Descarcă PDF | ||||||
Rezumat | ||||||
Aortic coarctation in the baby accounts for approximately 6-8% of all congenital heart malformations, being the fourth most common lesion requiring surgery or catheterization during childhood. It is estimated that 60-80% of isolated newborns with CoAo exit the hospital as healthy babies, then develop hemodynamic complications that are abruptly or gradually installed with arterial canal closure (AC). Therefore, cardiac screening of all newborns before discharge is required, consisting of pre- and post-ductal pulsoximetry and blood pressure (BP) measurement in all four limbs. Prenatal diagnosis improves and reduces morbidity by allowing planning in a tertiary level center and the initiation of prostaglandin (PGE) treatment to prevent AC constriction. The most common defects associated with aortic coarctation are arterial canal persistence, VSD and aortic stenosis. Thus, aortic bicuspidia can be observed in nearly two-thirds of children with aortic coarctation. If surgical intervention is performed early (up to 14 years), survival up to 20 years after surgery is 91%, and in the case of correction of the late abnormality, survival decreases to 79%. Treatment options include surgery, balloon angioplasty and endovascular stenting. The authors present the case of a child with CoAo, aortic arch and isthmus hypoplasia, VSD and bicuspidia, with surgery performed on the 5th day of life with the purpose of correcting the muscular septal defect and the aortic arch. |
||||||
Cuvinte-cheie newborn, aortic coarctation, surgical treatment, permeable arterial duct, prostaglandine |
||||||
|