Literature DB >> 28455785

Hypertonic Saline as a Useful Tool for Sputum Induction and Pathogen Detection in Cystic Fibrosis.

Adriana Carolina Marques Ferreira1, Fernando Augusto Lima Marson2,3, Milena Antonelli Cohen1, Carmen Silvia Bertuzzo4, Carlos Emilio Levy1,5, Antonio Fernando Ribeiro1, Jose Dirceu Ribeiro1.   

Abstract

PURPOSE: The aim of this study was to compare the qualitative and semi-quantitative detection of pathogens in the airway secretions of patients with cystic fibrosis (CF) and the sputum induction capacity before and after inhalation of 7% hypertonic saline solution (HSS).
METHODS: The study enrolled 64 patients with CF. Airway secretions were collected from all enrolled patients with CF before and after inhalation of 7% HSS, and the samples were screened for pathogens.
RESULTS: Inhalation of 7% HSS increased the probability of producing sputum from 36 to 52% (p = 0.002) in children with CF. The effect was most in children under 11 years. Inhalation of 7% HSS improved qualitative pathogen identification (p = 0.008). Inhalation of 7% HSS increased the mucoid Pseudomonas aeruginosa (p = 0.002) and non-mucoid P. aeruginosa in the semi-quantitative analysis (p = 0.035). Four new pathogens (Aspergillus fumigatus, Achromobacter xylosoxidans, Ochrobactrum anthropi, and Elizabethkingia meningoseptica) were identified in the sputum samples collected from the airways of patients with CF following 7% HSS.
CONCLUSIONS: Inhalation of 7% HSS increased sputum production and pathogen identification in children with CF. The inhalation of 7% HSS was feasible and should be implemented for routine pathogen detection in the airways of patients with CF, particularly in those patients who do not produce sputum.

Entities:  

Keywords:  CFTR; Cystic fibrosis; Diagnosis; Hypertonic saline; Lung disease; Microorganisms

Mesh:

Substances:

Year:  2017        PMID: 28455785     DOI: 10.1007/s00408-017-0008-3

Source DB:  PubMed          Journal:  Lung        ISSN: 0341-2040            Impact factor:   2.584


  34 in total

1.  Bronchial hyperresponsiveness to hypertonic saline challenge in children and adolescents.

Authors:  Paulo Kussek; Nelson Augusto Rosario Filho; Mônica Cat
Journal:  J Bras Pneumol       Date:  2006 May-Jun       Impact factor: 2.624

2.  Sputum induction as a research tool for sampling the airways of subjects with cystic fibrosis.

Authors:  N R Henig; M R Tonelli; M V Pier; J L Burns; M L Aitken
Journal:  Thorax       Date:  2001-04       Impact factor: 9.139

3.  Evaluating the "Leeds criteria" for Pseudomonas aeruginosa infection in a cystic fibrosis centre.

Authors:  M Proesmans; W Balinska-Miskiewicz; L Dupont; X Bossuyt; J Verhaegen; N Høiby; K de Boeck
Journal:  Eur Respir J       Date:  2006-05       Impact factor: 16.671

Review 4.  Culture-based diagnostic microbiology in cystic fibrosis: can we simplify the complexity?

Authors:  Jane L Burns; Jean-Marc Rolain
Journal:  J Cyst Fibros       Date:  2013-10-03       Impact factor: 5.482

5.  P. aeruginosa in the paranasal sinuses and transplanted lungs have similar adaptive mutations as isolates from chronically infected CF lungs.

Authors:  Oana Ciofu; Helle Krogh Johansen; Kasper Aanaes; Tina Wassermann; Morten Alhede; Christian von Buchwald; Niels Høiby
Journal:  J Cyst Fibros       Date:  2013-03-09       Impact factor: 5.482

6.  IL8 gene as modifier of cystic fibrosis: unraveling the factors which influence clinical variability.

Authors:  Larissa Lazzarini Furlan; Fernando Augusto Lima Marson; José Dirceu Ribeiro; Carmen Sílvia Bertuzzo; João Batista Salomão Junior; Dorotéia Rossi Silva Souza
Journal:  Hum Genet       Date:  2016-05-21       Impact factor: 4.132

7.  Clinical value of obtaining sputum and cough swab samples following inhaled hypertonic saline in children with cystic fibrosis.

Authors:  S A Ho; R Ball; L J Morrison; K G Brownlee; S P Conway
Journal:  Pediatr Pulmonol       Date:  2004-07

Review 8.  Nebulised hypertonic saline for cystic fibrosis.

Authors:  Peter Wark; Vanessa M McDonald
Journal:  Cochrane Database Syst Rev       Date:  2009-04-15

Review 9.  Cystic Fibrosis: A Review of Associated Phenotypes, Use of Molecular Diagnostic Approaches, Genetic Characteristics, Progress, and Dilemmas.

Authors:  Marie-Luise Brennan; Iris Schrijver
Journal:  J Mol Diagn       Date:  2015-11-26       Impact factor: 5.568

Review 10.  Origins of cystic fibrosis lung disease.

Authors:  David A Stoltz; David K Meyerholz; Michael J Welsh
Journal:  N Engl J Med       Date:  2015-01-22       Impact factor: 91.245

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  3 in total

Review 1.  The future of cystic fibrosis care: a global perspective.

Authors:  Scott C Bell; Marcus A Mall; Hector Gutierrez; Milan Macek; Susan Madge; Jane C Davies; Pierre-Régis Burgel; Elizabeth Tullis; Claudio Castaños; Carlo Castellani; Catherine A Byrnes; Fiona Cathcart; Sanjay H Chotirmall; Rebecca Cosgriff; Irmgard Eichler; Isabelle Fajac; Christopher H Goss; Pavel Drevinek; Philip M Farrell; Anna M Gravelle; Trudy Havermans; Nicole Mayer-Hamblett; Nataliya Kashirskaya; Eitan Kerem; Joseph L Mathew; Edward F McKone; Lutz Naehrlich; Samya Z Nasr; Gabriela R Oates; Ciaran O'Neill; Ulrike Pypops; Karen S Raraigh; Steven M Rowe; Kevin W Southern; Sheila Sivam; Anne L Stephenson; Marco Zampoli; Felix Ratjen
Journal:  Lancet Respir Med       Date:  2019-09-27       Impact factor: 30.700

2.  Challenges in the identification of Chryseobacterium indologenes and Elizabethkingia meningoseptica in cases of nosocomial infections and patients with cystic fibrosis.

Authors:  É B de Carvalho Filho; F A L Marson; C E Levy
Journal:  New Microbes New Infect       Date:  2017-09-13

3.  Hypertonic saline in people with cystic fibrosis: review of comparative studies and clinical practice.

Authors:  Vito Terlizzi; Eleonora Masi; Michela Francalanci; Giovanni Taccetti; Diletta Innocenti
Journal:  Ital J Pediatr       Date:  2021-08-06       Impact factor: 2.638

  3 in total

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