Current clinical and microbiological peculiarities of cystic fibrosis in children and adolescents

Authors

  • S. I. Ilchenko

DOI:

https://doi.org/10.14739/2310-1237.2014.3.36980

Keywords:

Сystic Fibrosis, Child, Adolescent, Prognosis, Antibiotic Resistance

Abstract

Aim. Statistical dataabout the prevalence of cystic fibrosis in children and adolescents in Dnipropetrovskfor last 5 years were analyzed to determine the clinical and microbiological peculiarities of cystic fibrosis.

Methods and results.Analysis of the clinical and microbiological data of 35 patients using clinical and medical history, an assessment of physical development, radiological, sonographic, spirometric, microbiological examinationswas studied.  The structure of the disease according to the clinical forms and respiratory tract microbiotawas specified. Factors reducing the quality of life of patients and causing unfavorable prognosis of the disease, including violations of nutritional status and the presence of sputum gram negative pathogens with high resistance to antibacterial agentswere studied.

Conclusion.This demonstrates the necessity of more careful selection of therapy because children with identified resistant respiratory tract microbiota are at increased risk of severe and complicated course of CF.

References

Asherova, I. K. & Kapranov, N. I. ( 2013). Mukoviscidoz [Cysticfibrosis]. Moscow. [in Russian].

Ginter, E. K., Kapranov, N. I, Petrova, N. V., &. Kashirskaya, N. Yu. (2010) Genetika bronkholegochnykh zabolevanij [Genetics of bronchopulmonary diseases]. Moscow: Atmosfera. [in Russian].

Timkovskaya, E. E., Petrova, N. V., Kashirskaya, N. Yu, Voronkova, A. Y., & Radionovich, A. M. (2008). Issledovanie vzaimosvyazi MVTR-ganotipa i klinicheskikh proyavlenij u bol'nykh mukoviscidozom [Study the relationship of CFTR-genotip and clinical manifestations in patients with cystic fibrosis]. Detskaya bol'nica, 1, 8–14. [in Russian].

Kapranov, N. I.., & Kashirskaya, N. Y.(2008). Mukoviscidoz: sovremennye dostizheniya i aktual'nye problemy [Cystic fibrosis: recent advances and current problems]. Moscow. [in Russian].

Bush, A.,. & Gotz, M. (2006) Cystic fibrosis. Eur. Resp. Mon.,15,.234–289.

Hodson, M., Duncan, G., & Bush, A. (2007) Cystic fibrosis. Cystic fibrosis. Third edition London: Edward Arnold (Publishers).Ltd., 477.

Nissim-Rafinia, M., Kerem, B., &Kerem, E. (2007) Molecular biology of cystic fibrosis:MBTP processing and functions, and classes of mutations. Cystic fibrosis. Third edition, London: Edward Arnold (Publishers) Ltd.

Wang, S. S., O’Leary, L. A., Simmons, S. C. & Khoury, M. J. (2002) The impact of early cystic fibrosis diagnosis on pulmonary function in children. J.Pediatr., 141, 804-810. doi: http://dx.doi.org/10.1067/mpd.2002.129845

How to Cite

1.
Ilchenko SI. Current clinical and microbiological peculiarities of cystic fibrosis in children and adolescents. Pathologia [Internet]. 2014Dec.23 [cited 2024Apr.24];(3). Available from: http://pat.zsmu.edu.ua/article/view/36980

Issue

Section

Original research