Literature DB >> 21511313

[Tolerance of two inhaled hypertonic saline solutions in patients with cystic fibrosis].

Luis Máiz Carro1, Adelaida Lamas Ferreiro, Marta Ruiz de Valbuena Maiz, Carolin Wagner Struwing, Gustavo Gabilondo Álvarez, Lucrecia Suárez Cortina.   

Abstract

BACKGROUND AND
OBJECTIVE: The aim of our study was to evaluate the tolerance of two inhaled hypertonic saline solutions (HS) in patients with cystic fibrosis. PATIENTS AND
METHOD: Eighty one cystic fibrosis (CF) patients (44 males; mean age 23.63 years) inhaled 5 ml of 7% inhaled HS solution and, in those patients who did not tolerate HS, we evaluated the tolerance of a 7% HS (at dose of 5 ml) added to 0.1% hyaluronic acid at least twenty-four hours later.
RESULTS: Twenty one (26%) patients did not tolerate the HS solution immediately after its inhalation. Cough was the most common symptom. Patients over 18 years of age showed worse tolerance to HS than patients younger than 18 years of age. Those patients that did not tolerate HS had a worse lung function that the ones that showed good tolerance. Eighty-one percent of patients who did not tolerate the HS alone tolerated well the HS with hyaluronic acid.
CONCLUSIONS: CF patients cannot tolerate inhaled HS immediately after nebulisation. Patients over 18 years and those with worse lung function tolerate HS worst. Hyaluronate acid added to 7% HS solution improves the tolerability.
Copyright © 2010 Elsevier España, S.L. All rights reserved.

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Year:  2011        PMID: 21511313     DOI: 10.1016/j.medcli.2011.02.022

Source DB:  PubMed          Journal:  Med Clin (Barc)        ISSN: 0025-7753            Impact factor:   1.725


  7 in total

1.  Pathological Hyaluronan Matrices in Cystic Fibrosis Airways and Secretions.

Authors:  Brittany Matuska; Suzy Comhair; Carol Farver; James Chmiel; Ronald J Midura; Tracey Bonfield; Mark E Lauer
Journal:  Am J Respir Cell Mol Biol       Date:  2016-10       Impact factor: 6.914

Review 2.  Targeting of Glycosaminoglycans in Genetic and Inflammatory Airway Disease.

Authors:  Robin Caird; Michael Williamson; Azeez Yusuf; Debananda Gogoi; Michelle Casey; Noel G McElvaney; Emer P Reeves
Journal:  Int J Mol Sci       Date:  2022-06-08       Impact factor: 6.208

Review 3.  The role of hyaluronan in the pathobiology and treatment of respiratory disease.

Authors:  Stavros Garantziotis; Martin Brezina; Paolo Castelnuovo; Lorenzo Drago
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2016-01-08       Impact factor: 5.464

Review 4.  Nebulized hypertonic saline in noncystic fibrosis bronchiectasis: a comprehensive review.

Authors:  Luis Máiz Carro; Miguel A Martínez-García
Journal:  Ther Adv Respir Dis       Date:  2019 Jan-Dec       Impact factor: 4.031

Review 5.  The Rise and Fall of Hyaluronan in Respiratory Diseases.

Authors:  Mark E Lauer; Raed A Dweik; Stavros Garantziotis; Mark A Aronica
Journal:  Int J Cell Biol       Date:  2015-09-10

6.  Addition of hyaluronic acid improves tolerance to 7% hypertonic saline solution in bronchiectasis patients.

Authors:  Luis Máiz; Rosa M Girón; Eva Prats; Marta G Clemente; Eva Polverino; Silvia Caño; Rosa Cordovilla; Jordi Dorca; Carlos Peñalver; Félix Baranda; Miguel A Martínez-García
Journal:  Ther Adv Respir Dis       Date:  2018 Jan-Dec       Impact factor: 4.031

Review 7.  Use of Hyaluronic Acid (HA) in Chronic Airway Diseases.

Authors:  Luis Máiz Carro; Miguel A Martínez-García
Journal:  Cells       Date:  2020-09-29       Impact factor: 6.600

  7 in total

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