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SM ISO690:2012 CEPRAGA, Victoria, PALEGA, Daniela, MUNTEANU, Ana, LUPU, Victoria, SELEVESTRU, Rodica, PALII, Ina, ŞCIUCA, Svetlana. Evaluation of ecocardiographical indicators in pulmonary hypertension in children with bronchiectasis. In: Cercetarea în biomedicină și sănătate: calitate, excelență și performanță, Ed. 1, 20-22 octombrie 2021, Chişinău. Chișinău, Republica Moldova: 2021, p. 363. ISBN 978-9975-82-223-7 (PDF).. |
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Cercetarea în biomedicină și sănătate: calitate, excelență și performanță 2021 | ||||||
Conferința "Cercetarea în biomedicină și sănătate: calitate, excelență și performanță" 1, Chişinău, Moldova, 20-22 octombrie 2021 | ||||||
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Background. Arterial hypoxemia is the leading cause of secondary pulmonary hypertension (HP) in patients with bronchopulmonary disease, especially in those with cystic fibrosis (CF). Objective of the study. Evaluation of secondary pulmonary hypertension in children with bronchiectasis from chronic bronchopulmonary diseases Material and Methods. The study included 37 children with chronic bronchopulmonary disease:22 children (59.5%:95%CI 42.1-75.2) with CF and 15(40.5%: 95% CI 24.8-57.9 ) with other bronchopulmonarydiseases.Patients were evaluated by M 2D color Doppler EcoCG with assessment of pulmonary arterial systolic pressure (PSAP), tricuspid valve insufficiency (IVT) and chest computed tomography (CT). Results. The average age of children with CF-7.72±0.92 years(variations 0.5–15.5 years) and 9.69±1.42 years (1.5–17 years)-control group; F state 1.57,P>0.05. The PSAP value is increased in children with FC-33.5±1.6 mmHg(minimum-22 mmHg, maximum-50 mmHg), compared to children in the control group-28.8±1.7 mmHg(variations 22–47 mmHg);F state 3.9,P>0.05.IVT in CF was found in 19 children(95%:95%CI 75.1-99.9) and in all children of the control group, χ2=0.6, p>0.05.Children with CF had varicose(36.4%) and cylindrical(40.9%) bronchiectasis, compared to those in the control group in which traction(46.7%), cylindrical(33.3%) and more rarely predominated varicose bronchiectasis. Conclusion. PSAP is increased in children with CF, who have more severe lung damage due to the presence of extensive bronchiectasis compared to patients with non-CF bronchiectasis. |
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Cuvinte-cheie pulmonaryhypertension, cysticfibrosis, children, hipertensiunea pulmonară, Fibroza chistică, copii |
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