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Articolul urmator |
811 21 |
Ultima descărcare din IBN: 2023-11-05 19:57 |
Căutarea după subiecte similare conform CZU |
616.37-003.4-004.1-06:616.24-053.2 (2) |
Patologia sistemului digestiv. Tulburări ale tubului alimentar (1732) |
Patologia sistemului respirator. Tulburări ale organelor de respiraţie (757) |
SM ISO690:2012 SELEVESTRU, Rodica, PLAHOTNIUC, Ana, NEAMŢU, Irina, CERNACOVSCHI, A., BALANEŢCHI, Ludmila, BELÎI, Olga, CEBAN, Ana, ADAM, Ianoş, ŞCIUCA, Svetlana. Statusul nutriţional şi funcţia respiratorie la copiii cu fibroză chistică. In: Buletin de Perinatologie, 2018, nr. 5(81), pp. 21-25. ISSN 1810-5289. |
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Buletin de Perinatologie | |||
Numărul 5(81) / 2018 / ISSN 1810-5289 | |||
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CZU: 616.37-003.4-004.1-06:616.24-053.2 | |||
Pag. 21-25 | |||
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Introduction. The cystic fi brosis (CF) is estimated to occur in as many as 1:2000-1:3000 birth in the Republic of Moldova. Major risks of fatal prognosis are explained by a multitude of complications (pulmonar, gastrointestinal, nutritional and others) in these children. Objective of the study. To evaluate nutritional status and lung function in children with cystic fi brosis Material and methods. An observational clinical study. Were evaluated 8 children with FC hospitalized in the Pneumology Department of the Mother and Child Health Care Center . Statistical calculations were made in the EpiInfo. Results. The average age of children with CF is 9,07±1,0 years. There were fi ve girls (62,5%: 95CI 24,5-91,5) and three boys (37,5%: 95 CI 8,5-75,5) who were participated in the study. One child (12,5%: 95 CI 0,3-52,7) was confi rmed with the pulmonary form of FC, 7 children (87,5%: 95 CI 47,3-99,7) were with mixed form (pulmonary and intestinal). Children had mean FVC concentrations equal to 58,2 ± 15,1%, with minimum variations of 34%, maximum 99%. The bronchiectasis were found in 87,5%: 95 CI 47,3-99,7 cases, three children presented the grade 1 exocrine pancreatic insuffi ciency (37,5%: 95 CI 8,5-45,5), 2 children - grade 2 (25%: 95CI 3,2-65,1), 1 child - grade 3 (12,5%: 95 CI 0,3-52,7), and only 2 children (25%: 95CI 3,2-65,1) were identifi ed with no weight defi cit. There is a direct correlation between weight loss and respiratory distress in these children χ2 = 12,9; (P <0,04). Conclusions: Alteration of nutritional status is directly proportional to lung function impairment in children with cystic fi brosis, χ2 = 12,9; (P <0,04). |
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Cuvinte-cheie cystic fi brosis, children, nutritional status, pulmonary function, муковисцидоз, дети, статус питания, лёгочная функция |
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