Affiliation:
1. Research Center for Medical Genetic; Russian Medical Academy of Continuous Professional Education
2. Research Center for Medical Genetic
3. Children's Clinical Multidisciplinary Center of the Moscow Region
Abstract
Introduction. The issues of choosing the optimal product for enteral nutrition in children with cystic fibrosis in combination with comorbid conditions require a special clinical approach and cause difficulties for practitioners.Aim. To evaluate the effectiveness of correcting the nutritional status in children with cystic fibrosis against the background of concomitant conditions using a semi-element product for enteral nutrition.Materials and methods. 20 children (boys – 9, girls – 11) aged from 1 year to 3 years (average age 2.9±0.7 years) with a diagnosis of cystic fibrosis and concomitant comorbid conditions - uncupable intestinal syndrome, post-resection syndrome against the background of meconial ileus, food allergy (the semi-element formula was prescribed according to indications, the evaluation of effectiveness according to the SCORAD index was not included in the objectives of the study). The state of actual nutrition, pancreatin doses, intestinal syndrome, nutritional status (anthropometric indicators) were evaluated at baseline (before) and 3 months (after) the use of Peptamen Junior in the study group.Design:prospective, observational, without comparison group.Results and discussion. The analysis showed that the anthropometric indicators significantly increased against the background of the correction of the diet and the use of “Peptamen Junior” as an additional food. BMI increased from 34.5 percentiles to 57.0 (p < 0.05).Correction of nutrition using a semi-element formula with an altered fat composition, including SCT, and correction of the dose of pancreatic enzymes by calculating the fat content in food, led to a decrease in the manifestations of intestinal syndrome.Conclusion.The results obtained indicate the clinical effectiveness of the semi-element formula for enteral nutrition for the correction of nutritional deficiency (BMI less than 50 percentile) in young children with cystic fibrosis and concomitant pathology that requires a special approach.
Reference11 articles.
1. Kapranov N.I., Kashirskaya N.Yu. (ed.). Cystic Fibrosis. Moscow: Medpraktika-M; 2014. 672 p. (In Russ.)
2. Baranov A.A., Namazova-Baranova L.S., Kutsev S.I., Avdeev S.N., Polevichenko E.V. et al. Cystic fibrosis: clinical guidelines. Moscow; 2020. (In Russ.)
3. Kondrateva E.I., Kashirskaya N.Yu., Kapranov N.I. (ed.). National consensus. Cystic fibrosis: definition, diagnostic criteria, therapy.Moscow; 2016. 205 p. (In Russ.) Available at: http://ostrovaru.com/biblioteka/Chiesi_consensus_new_A4.pdf.
4. Turck D., Braegger C.P., Colombo C., Declercq D., Morton A., Pancheva R. et al. ESPEN-ESPGHAN-ECFS guidelines on nutrition care for infants, children, and adults with cystic fibrosis. Clin Nutr. 2016;35(3):557–577.doi: 10.1016/j.clnu.2016.03.004.
5. Corey M., McLaughlin F.J., Williams M., Levison H. A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto. J Clin Epidemiol. 1988;41(6):583–591. doi: 10.1016/0895-4356(88)90063-7.
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献