Perspectives on the scientific approach to cystic fibrosis in paediatrics [Perspectivas en el abordaje científico de la fibrosis quística en la etapa pediátrica]

Authors

DOI:

https://doi.org/10.5281/zenodo.10619665

Keywords:

respiratory tract diseases, cystic fibrosis, lung diseases

Abstract

Objective: to analyse the perspectives on the scientific approach to cystic fibrosis in the paediatric stage. Method: descriptive documentary type, the search covered specialised databases, including 15 articles distributed in PubMed, Scielo, Scopus and Web of Science (Wos). Results and conclusion: The detection of the bacterium Segniliparus rugosus in a patient with CF raises questions about the microbiology associated with the disease in this context. This finding, together with the difficulties identified in the identification of this bacterium, underscores the need for further exploration of the microbiota in CF patients in Ecuador.

Downloads

Download data is not yet available.

References

Rubin BK. Cystic Fibrosis 2017 The Year in Review. Respiratory Care. 2018; 63(2): p. 238-241.

Sánchez Infante C, Razón Behar R, Ramos Carpenter LT, Barreiro Paredes B, Reyes López C, Cantillo Gámez H, et al. Fibrosis quística en niños y su seguimiento durante 40 años (1977-2017) [Cystic fibrosis in children and its follow-up for 40 years (1977-2017)]. Revista Cubana de Pediatría. 2019; 91(3): p. e882.

Aspiazu Hinostroza KA, Solano X, Suqui E, Suquilanda E, Tuquiñagua L. Revisión bibliográfica sobre la fibrosis quística [Literature review on cystic fibrosis]. Revista Estudiantil CEUS. 2019; 1(1): p. 19-24.

Wood J, Jenkins S, Putrino D, Mulrennan S, Morey S, Cecins N, et al. A smartphone application for reporting symptoms in adults with cystic fibrosis improves the detection of exacerbations: Results of a randomized controlled trial. Journal of Cystic Fibrosis. 2020; 19(2): p. 271-276

Silva Filho LV, Castaños C, Ruíz HH. Cystic fibrosis in Latin America-Improving the awareness. J Cyst Fibros. 2016;15(6):791-793. doi:10.1016/j.jcf.2016.05.007

Patricio Valle E, Burgos RI, Valle JR, Egas Bénar D, Ruiz Cabezas JC. Analysis of CFTR gene mutations and cystic fibrosis incidence in the Ecuadorian population. Invest Clin. 2007 marzo; 48(1): p. 91-98

Lascano-Vaca Y, Ortiz-Prado E, Gomez-Barreno L, Simbaña-Rivera K, Eduardo Vasconez AL, Arteaga-Espinosa ME, et al. Clinical, genetic and microbiological characterization of pediatric patients with cystic fibrosis in a public Hospital in Ecuador. BMC Pediatrics. 2020; 20(111)

Zurita J, Sevillano G, González C, Lascano Y. Segniliparus rugosus from the sputum of a child with cystic fibrosis in Ecuador: challenges in bacterial identification. New Microbes New Infect. 2020;35:100668. doi:10.1016/j.nmni.2020.100668

Paz-Y-Miño C, Zambrano AK, Ruiz-Cabezas JC, et al. Characterization of Ancestral Origin of Cystic Fibrosis of Patients with New Reported Mutations in CFTR. Biomed Res Int. 2020;2020:9074760. doi:10.1155/2020/9074760

Moya-Quiles MR, Glover G, Mondéjar-López P, Pastor-Vivero MD, Fernández-Sánchez A, Sánchez-Solís M. CFTR H609R mutation in Ecuadorian patients with cystic fibrosis. J Cyst Fibros. 2009;8(4):280-281. doi:10.1016/j.jcf.2009.05.001

Valle EP, Burgos RI, Valle JR, Egas Béjar D, Ruiz-Cabezas JC. Analysis of CFTR gene mutations and cystic fibrosis incidence in the Ecuadorian population. Invest Clin. 2007;48(1):91-98.

Ortiz SC, Aguirre SJ, Flores S, Maldonado C, Mejía J, Salinas L. Spectrum of CFTR gene mutations in Ecuadorian cystic fibrosis patients: the second report of the p.H609R mutation. Mol Genet Genomic Med. 2017;5(6):751-757. doi:10.1002/mgg3.337

Ruiz-Cabezas JC, Barros F, Sobrino B, et al. Mutational analysis of CFTR in the Ecuadorian population using next-generation sequencing. Gene. 2019;696:28-32. doi:10.1016/j.gene.2019.02.015

González-Andrade F. Standardized clinical criteria and sweat test combined as a tool to diagnose Cystic Fibrosis. Heliyon. 2018;4(12):e01050. doi:10.1016/j.heliyon.2018.e01050

Paz-y-Miño C, Pérez JC, Burgos R, Dávalos MV, Leone PE. The DeltaF508 mutation in Ecuador, South America. Hum Mutat. 1999;14(4):348-350. doi:10.1002/(SICI)1098-1004(199910)14:4<348::AID-HUMU11>3.0.CO;2-8

Published

2024-02-05

Issue

Section

Short originals

How to Cite

1.
Philco-Toaza PE. Perspectives on the scientific approach to cystic fibrosis in paediatrics [Perspectivas en el abordaje científico de la fibrosis quística en la etapa pediátrica]. SRS [Internet]. 2024 Feb. 5 [cited 2024 Dec. 26];3(1):32-8. Available from: https://revistasinstitutoperspectivasglobales.org/index.php/sanitas/article/view/32

Similar Articles

1-10 of 27

You may also start an advanced similarity search for this article.