Experience of using specialized mixture of enteral nutrition in children with nutritive deficiency in cystic fibrosis
https://doi.org/10.33667/2078-5631-2019-2-21(396)-47-52
Abstract
Сystic fibrosis is an autosomal recessive hereditary multisystem disease which is characterized by severe exocrine pancreatic insufficiency, chronic lung disease, and protein-energy malnutrition. Some studies have indicated that the body mass index is an independent factor which adversely affected survival of patients with cystic fibrosis. There is a direct correlation between body mass index, lung function and life expectancy. Objective. To determine the effectiveness and tolerability of the product for children’s dietary nutrition ‘NUTRINIdrink with dietary fibre (neutral taste)’ for children over one year of age for enteral nutrition in cystic fibrosis complicated by protein-energy deficiency.
About the Authors
E. I. Kondratieva
Medical and Genetic Research Centre n. a. academician N. P. Bochkov; Moscow Regional Consultative and Diagnostic Centre for Children
Russian Federation
Russian Federation
Moscow
T. Yu. Maksimycheva
Medical and Genetic Research Centre n. a. academician N. P. Bochkov; Moscow Regional Consultative and Diagnostic Centre for Children
Russian Federation
Russian Federation
Moscow
A. Yu. Voronkova
Medical and Genetic Research Centre n. a. academician N. P. Bochkov; Moscow Regional Consultative and Diagnostic Centre for Children
Russian Federation
Russian Federation
Moscow
V. D. Sherman
Medical and Genetic Research Centre n. a. academician N. P. Bochkov; Moscow Regional Consultative and Diagnostic Centre for Children
Russian Federation
Russian Federation
Moscow
References
1. Koletzko B. et al. (ed.). Pediatric nutrition in practice. — Karger Medical and Scientific Publishers, 2015.
2. Koletzko B., Dokoupil K., Koletzko S. Gedeihstörung und Untergewicht bei kindlichen Erkrankungen // Monatsschrift Kinderheilkunde. — 2016. — Т. 164. — N 1. — С. 19–30.
3. Koletzko B., Goulet O. Nutritional support in infants, children and adolescents // Basics in Clinical Nutrition, ed. — 2011. — Т. 4. — С. 625–653.
4. Hecht C. et al. Disease associated malnutrition correlates with length of hospital stay in children // Clinical nutrition. — 2015. — Т. 34. — N 1. — С. 53–59.
5. Капранов Н. И. и др. Муковисцидоз // Современные достижения и актуальные проблемы): Метод. рекомендации. — 2014. — Т. 3.
6. Medical Position Paper The Need for Nutrition Support Teams in Pediatric Units: A Commentary by the ESPGHAN Committee on Nutrition Journal of Pediatric Gastroenterology and Nutrition. 41: 8–11 July 2005 Lippincott Williams & Wilkins, Philadelphia.
7. Tsiountsioura M. et al. Detailed assessment of nutritional status and eating patterns in children with gastrointestinal diseases attending an outpatients clinic and contemporary healthy controls //European journal of clinical nutrition. — 2014. — Т. 68. — N 6. — С. 700.
8. Клинические рекомендации. Кистозный фиброз (муковисцидоз) у детей МКБ 10: Е84 Год утверждения (частота пересмотра): 2016 (пересмотр каждые 3 года).
9. Национальный консенсус (1-е издание) «Муковисцидоз: определение, диагностические критерии, терапия» 2016. Под редакцией Е. И. Кондратьевой, Н. Ю. Каширской, Н. И. Капранова — М.: ООО «Компания БОРГЕС». 2016, 214.
10. Steinkamp G., Wiedemann B. Relationship between nutritional status and lung function in cystic fibrosis: cross sectional and longitudinal analyses from the German CF quality assurance (CFQA) project // Thorax. — 2002. — Т. 57. — N 7. — С. 596–601.
11. Ruzafa E. L. et al. Fórmulas de nutrición enteral pediátrica.¿ Cómo elegir la adecuada? // Acta Pediátrica Española. — 2011. — Т. 69. — N 9. — С. 393.
12. Costa C. M. Valoración del estado de nutrición del niño // manual básico de nutrición clínica y dietética. — с. 198.
13. Haack A., Aragão G. G., Novaes M. R.C.G. Pathophysiology of cystic fibrosis and drugs used in associated digestive tract diseases // World journal of gastroenterology: WJG. — 2013. — Т. 19. — N 46. — С. 8552.
14. Culhane S. Malnutrition in cystic fibrosis: a review. / S. Culhane, С. George, В. Pearo, Е. Spoede // Nutr Clin Pract. — 2013. — N 28 (6). — р. 676–83.
15. An Pediatr Contin. 2011; 9(4): 209–23 A.S.P.E.N. recommendations for enteral nutrition: practice is the result of potential benefits, harms, clinical judgment, and ethical issues. JPEN J Parenter Enteral Nutr. 2015.
16. Culhane S. Malnutrition in cystic fibrosis: a review. / S. Culhane, С. George, В. Pearo, Е. Spoede // Nutr Clin Pract. — 2013. — № 28 (6). — р. 676–83.
17. den Broeder E, Lippens RJ, van´t Hof MA, Tolboom JJM, Sengers RCA, van den Berg AMK, et al. Nasogastric tube fee-ding in children with cancer: the effect of two different formulas on weight, body composition and serum protein concentrations. JPEN J Parenteral Enteral Nutr. 2000; 24: 351–60.
18. Tenius L. et al. Oral nutritional supplement for children with cancer: 7 different high-energy drinks compared to cacao, a double-blinded feeding trial // Aktuelle Ernährungsmedizin. — 2018. — Т. 43. — N 3. — С. P65.18.
19. nutricia-medical.ru.
Review
For citations:
Kondratieva E.I., Maksimycheva T.Yu., Voronkova A.Yu., Sherman V.D. Experience of using specialized mixture of enteral nutrition in children with nutritive deficiency in cystic fibrosis. Medical alphabet. 2019;2(21):47-52. (In Russ.) https://doi.org/10.33667/2078-5631-2019-2-21(396)-47-52
Views:
459
Email this article 