CERTAIN ASPECTS OF RESPIRATORY AND DIGESTIVE TRACT INVOLVEMENT IN CYSTIC FIBROSIS IN CHILDREN
https://doi.org/10.15690/vsp.v12i1.574
Abstract
Cystic fibrosis is one of the severe childhood disorders with early manifestation of multiple organ involvement. The respiratory and digestive tracts are suffered the most, the prognosis of disease course depends on the degree of the impairment of these systems. The results of the analysis of cystic fibrosis prevalence in Primorsky Krai according to the neonatal immunoreactive trypsin screening in 102 251 newborn are shown in the article. The age, sex, clinical and severity structure of cystic fibrosis was studied in 71 children. The prevalence of 13 mutations of transmembrane regulator conductance gene in 41 patients was determined. Correlations between time of pulmonary complications manifestation, P. Aeruginosa infection development, chronic hypoxemia degree, malnutrition, genetic status and severity of the disease were found.
About the Authors
T. G. Vasil’evaRussian Federation
S. N. Shishatskaya
Russian Federation
A. N. Ni
Russian Federation
References
1. Krasovskiy S. A., Chernyak A. V., Amelina Ye. L., V. S. Nikonova, A.Yu. Voron kova, N.Yu. Kashirskaya, N. I. Kapranov. Survival rate of patients with cystic fibrosis in Moscow and Moscow Region during 2000–2010. Cystic fibrosis in children and adolescents: collection of articles and theses, X Anniversary National Congress. Yaroslavl. 2011. 49 pp.
2. Vasilyeva T. G., Shishatskaya S. N. Risk factors of unfavorable outcome of cystic fibrosis in children. Collection of materials of 15th Congress of Pediatricians of Russia with International Participation “Actual problems of pediatrics”. Moscow. 2011. 117 pp.
3. Kapranov N. I., Kashirskaya N.Yu, Tolstova V. D. Cystic fibrosis. Early diagnostics and treatment. Moscow: GEOTAR-Media. 2008.
4. Modern classification of clinical forms of bronchopulmonary diseases in children. Pediatriya. Zhurnal imeni G. N. Speranskogo — Pediatrics. 2010; 89 (4): 6–15.
5. Rebrova O.Yu. Statistical analysis of medical data. Use of a package of applied programs STATISTICA. Moscow: MediaSphera. 2006.
6. Radionovich A. M., Kashirskaya N.Yu., Kapranov N. I. Clinical significance of prolonged treatment with sub therapeutic doses of macrolides in patients with cystic fibrosis and chronic Pseudomonas aeruginosa infection. Pulmonology: appendix on cystic fibrosis. 2006; 40–46.
7. Tsyvkina G. I., Vasilyeva T. G., Grishchenko D.Zh. Immunotropic therapy in patients with cystic fibrosis. Collection of materials of XVI Russian National Congress “Human and Medication”. Moscow. 2009. Pp. 466–467.
8. Pavlova Ya.Ye. Endoscopic and functional evaluation of mucous tunic of gastrointestinal tract in syndrome of intestinal malabsorption in children. Author’s abstract of a doctoral dissertation. Irkutsk. 2005. Pp. 52–58. 9. Gastroenterology of children’s health. Edited by Belmer S. V., Khavkin A. I. Moscow: Medpractice. 2003.
Review
For citations:
Vasil’eva T.G., Shishatskaya S.N., Ni A.N. CERTAIN ASPECTS OF RESPIRATORY AND DIGESTIVE TRACT INVOLVEMENT IN CYSTIC FIBROSIS IN CHILDREN. Current Pediatrics. 2013;12(1):162-165. (In Russ.) https://doi.org/10.15690/vsp.v12i1.574