Articles producció científicaMedicina i Cirurgia

Airway surface liquid pH in paediatric patients with cystic fibrosis

  • Datos identificativos

    Identificador:  imarina:9370410
    Autores:  Vasquez-Perez A; Bosque-García M; Rudi-Sola N; Parada-Ricart E; Closa-Monasterolo R
    Resumen:
    Background: Cystic fibrosis (CF) patients have more acidic airway surface liquid (ASL), which can denature antimicrobial defensins. Induced sputum is non-invasive and is as representative as bronchoalveolar lavage. Objectives: The objectives of this study were to analyse the ASL pH obtained by induced sputum and assess the relationship between clinical features in paediatric CF patients. Methods: This is a prospective observational study in CF paediatric patients. Sputum was induced in a patient by inhaling 4.5% hypertonic saline, the sputum was collected into a sterile container for pathological analysis, and the pH was measured from the liquid part (ASL) in a gas machine. Results: A total of 27 patients were included in the study: mean age (11.96 ± 3.9) years, mean sweat test (99.38 ± 17.76) ng/L, common mutation Del508F (N24, 88.8%), mean FEV1% 91.94% ± –12.6%, Staphylococcus colonization 14 (51.9%), normal chest CT 8 (29.6%), air trapping 12 (44.4%), bronchiectasis 6 (22.2%), and mean ASL pH 6.72 ± 0.06 (n = 15). A significant correlation was found between a higher sweat test and lower ASL pH (R = 0.683, p = 0.005). There were no differences between altered chest CT (p = 0.199) and positive Staphylococcus aureus (p = 0.17). Conclusion: This is the first publication that use induced sputum to obtain the ASL pH in CF patients. The ASL pH in CF patients is usually acidic and correlated with altered transmembrane function conductance.
  • Otros:

    Enlace a la fuente original: https://www.revistadepatologiarespiratoria.org/frame_eng.php?id=68
    Referencia de l'ítem segons les normes APA: Vasquez-Perez A; Bosque-García M; Rudi-Sola N; Parada-Ricart E; Closa-Monasterolo R (2023). Airway surface liquid pH in paediatric patients with cystic fibrosis. Revista De Patologia Respiratoria, 26(4), 105-112. DOI: 10.24875/RPR.23000033
    Referencia al articulo segun fuente origial: Revista De Patologia Respiratoria. 26 (4): 105-112
    DOI del artículo: 10.24875/RPR.23000033
    Año de publicación de la revista: 2023
    Entidad: Universitat Rovira i Virgili
    Versión del articulo depositado: info:eu-repo/semantics/publishedVersion
    Fecha de alta del registro: 2024-10-12
    Autor/es de la URV: Closa Monasterolo, Ricardo / Parada Ricart, Esther / Vásquez Pérez, Amalui Vanecsa
    Departamento: Medicina i Cirurgia
    URL Documento de licencia: https://repositori.urv.cat/ca/proteccio-de-dades/
    Tipo de publicación: Journal Publications
    Autor según el artículo: Vasquez-Perez A; Bosque-García M; Rudi-Sola N; Parada-Ricart E; Closa-Monasterolo R
    Áreas temáticas: Pulmonary and respiratory medicine
    Direcció de correo del autor: amalui.vasquez@urv.cat, esther.parada@urv.cat, amalui.vasquez@urv.cat, ricardo.closa@urv.cat
  • Palabras clave:

    Sweat test
    Infections
    Cystic fibrosis
    Children
    Cftr
    Airway surface liquid ph
    Pulmonary and Respiratory Medicine
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