Literature DB >> 26435647

Use of lung clearance index to assess the response to intravenous treatment in cystic fibrosis.

E Hatziagorou1, V Avramidou1, F Kirvassilis1, J Tsanakas1.   

Abstract

BACKGROUND: Progressive lung disease is the main cause of clinical deterioration and mortality in cystic fibrosis (CF) patients. Being able to assess the effectiveness of interventions is very significant.
OBJECTIVES: To assess the response to intravenous (IV) treatment among CF patients, using forced expired volume in 1(st) second (FEV1) and Lung Clearance Index (LCI) as outcome measures and to compare the effect of IV treatment on lung function and LCI between CF children being treated on a regular basis, or in case of a pulmonary exacerbation. SUBJECTS AND METHODS: Thirty-two CF patients (15 males) with mean age 9.90 (range: 2-23) years, performed spirometry and multiple breath washout (MBW) before and one month after IV antibiotic treatment. Nineteen patients received a course of elective treatment (group A) and 13 received IV antibiotic regimens for an acute exacerbation (group B).
RESULTS: Statistically significant differences after treatment were seen in LCI (p≤0.001), and Forced Expiratory Flow (FEF) z-scores (p<0.05). FEV1 did not change significantly after drug intervention. Dividing patients into two groups, only LCI showed significant change (p<0.05), when treatment was administered on a regular basis. Patients being treated for an acute pulmonary exacerbation showed significant improvement in most of the lung function parameters: LCI (p=0.0001), FEV1% (p=0.05), FEV1 z-score (p=0.033) and FEF25-75 (p=0.046). The mean LCI difference was significantly greater in group B compared to group A (p=0.001).
CONCLUSION: LCI is more sensitive marker than FEV1 to assess the effect of IV antibiotic treatment among CF children. IV antibiotics are more effective on lung function parameters, when they are administered for an acute exacerbation, than when they are given on a regular basis. Hippokratia 2015, 19 (1): 47-52.

Entities:  

Keywords:  cystic fibrosis; evaluation of intervention; intravenous treatment; lung clearance index; pulmonary exacerbation

Year:  2015        PMID: 26435647      PMCID: PMC4574587     

Source DB:  PubMed          Journal:  Hippokratia        ISSN: 1108-4189            Impact factor:   0.471


  40 in total

1.  Spirometric pulmonary function in healthy preschool children.

Authors:  H Eigen; H Bieler; D Grant; K Christoph; D Terrill; D K Heilman; W T Ambrosius; R S Tepper
Journal:  Am J Respir Crit Care Med       Date:  2001-03       Impact factor: 21.405

2.  Consensus statement for inert gas washout measurement using multiple- and single- breath tests.

Authors:  Paul D Robinson; Philipp Latzin; Sylvia Verbanck; Graham L Hall; Alexander Horsley; Monika Gappa; Cindy Thamrin; Hubertus G M Arets; Paul Aurora; Susanne I Fuchs; Gregory G King; Sooky Lum; Kenneth Macleod; Manuel Paiva; Jane J Pillow; Sarath Ranganathan; Sarah Ranganathan; Felix Ratjen; Florian Singer; Samatha Sonnappa; Janet Stocks; Padmaja Subbarao; Bruce R Thompson; Per M Gustafsson
Journal:  Eur Respir J       Date:  2013-02-08       Impact factor: 16.671

Review 3.  Gas mixing efficiency from birth to adulthood measured by multiple-breath washout.

Authors:  Paul Aurora; Wanda Kozlowska; Janet Stocks
Journal:  Respir Physiol Neurobiol       Date:  2005-08-25       Impact factor: 1.931

4.  Elective versus symptomatic antibiotic treatment in cystic fibrosis patients with chronic Pseudomonas infection of the lungs.

Authors:  J S Elborn; R J Prescott; B H Stack; M C Goodchild; J Bates; C Pantin; N Ali; D J Shale; M Crane
Journal:  Thorax       Date:  2000-05       Impact factor: 9.139

5.  Changes in airway dimensions on computed tomography scans of children with cystic fibrosis.

Authors:  Pim A de Jong; Yasutaka Nakano; Wim C Hop; Frederick R Long; Harvey O Coxson; Peter D Paré; Harm A Tiddens
Journal:  Am J Respir Crit Care Med       Date:  2005-04-14       Impact factor: 21.405

6.  Ventilation inhomogeneities in relation to standard lung function in patients with cystic fibrosis.

Authors:  Richard Kraemer; Andrea Blum; Andreas Schibler; Roland A Ammann; Sabina Gallati
Journal:  Am J Respir Crit Care Med       Date:  2004-11-05       Impact factor: 21.405

Review 7.  Elective versus symptomatic intravenous antibiotic therapy for cystic fibrosis.

Authors:  Lil Breen; Nivedita Aswani
Journal:  Cochrane Database Syst Rev       Date:  2012-07-11

8.  The effect of dornase alfa on ventilation inhomogeneity in patients with cystic fibrosis.

Authors:  R Amin; P Subbarao; W Lou; A Jabar; S Balkovec; R Jensen; S Kerrigan; P Gustafsson; F Ratjen
Journal:  Eur Respir J       Date:  2010-08-06       Impact factor: 16.671

9.  Assessment of clinical response to ivacaftor with lung clearance index in cystic fibrosis patients with a G551D-CFTR mutation and preserved spirometry: a randomised controlled trial.

Authors:  Jane Davies; Helen Sheridan; Nicholas Bell; Steve Cunningham; Stephanie D Davis; J Stuart Elborn; Carlos E Milla; Timothy D Starner; Daniel J Weiner; Po-Shun Lee; Felix Ratjen
Journal:  Lancet Respir Med       Date:  2013-09-10       Impact factor: 30.700

10.  Lung function from infancy to the preschool years after clinical diagnosis of cystic fibrosis.

Authors:  Wanda J Kozlowska; Andrew Bush; Angela Wade; Paul Aurora; Siobhán B Carr; Rosie A Castle; Ah-Fong Hoo; Sooky Lum; John Price; Sarath Ranganathan; Clare Saunders; Sanja Stanojevic; John Stroobant; Colin Wallis; Janet Stocks
Journal:  Am J Respir Crit Care Med       Date:  2008-04-10       Impact factor: 21.405

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  2 in total

Review 1.  Toward the Establishment of New Clinical Endpoints for Cystic Fibrosis: The Role of Lung Clearance Index and Cardiopulmonary Exercise Testing.

Authors:  Elpis Hatziagorou; Asterios Kampouras; Vasiliki Avramidou; Ilektra Toulia; Elisavet-Anna Chrysochoou; Maria Galogavrou; Fotios Kirvassilis; John Tsanakas
Journal:  Front Pediatr       Date:  2021-02-25       Impact factor: 3.418

2.  An 8 week open-label interventional multicenter study to explore the lung clearance index as endpoint for clinical trials in cystic fibrosis patients ≥8 years of age, chronically infected with Pseudomonas aeruginosa.

Authors:  Sivagurunathan Sutharsan; Susanne Naehrig; Uwe Mellies; Christian Sieder; Jörg Ziegler
Journal:  BMC Pulm Med       Date:  2020-06-12       Impact factor: 3.317

  2 in total

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