Literature DB >> 11340684

Use of computerized tomography and chest x-rays in evaluating efficacy of aerosolized recombinant human DNase in cystic fibrosis patients younger than age 5 years: a preliminary study.

S Z Nasr1, L R Kuhns, R W Brown, M E Hurwitz, G M Sanders, P J Strouse.   

Abstract

The aim of this study was to evaluate the ability of high-resolution computerized tomography (HRCT) of the chest and chest x-rays (CXR) to determine efficacy of inhaled recombinant human DNase (rhDNase) in cystic fibrosis (CF) patients younger than 5 years of age. A randomized, double-blind, placebo-controlled pilot study of 12 patients with CF younger than 5 years of age, attending the University of Michigan Cystic Fibrosis Center (Ann Arbor, MI) was conducted. The changes in the HRCT and CXR score from baseline to day 100 of therapy were assessed using a previously validated scoring system. The mean changes of HRCT scores between the rhDNase and placebo groups were found to be significant at the 95% level, with mean change +/- SE mean of - 1.00 +/- 0.53 and 0.58 +/- 0.24 for rhDNase and placebo groups, respectively (P = 0.02). The difference in CXR score was not significant between the two groups. An analysis was performed to relate HRCT subscores to CXR score; only thickening of the intra-interlobular septae was significantly correlated with the total CXR score (r = - 0.7, P < 0.01). There was improvement in the parents' assessments of the patients' well-being, with improvement in physical activity, decreased cough, sleep quality, and appetite in those subjects receiving rhDNase. We conclude that the administration of rhDNase was associated with improvement in the HRCT scan in CF patients younger than 5 years of age. Findings indicate that HRCT of the chest is useful and sensitive in studying responses to therapy in patients with CF lung disease. To our knowledge, this is the first report of the use of HRCT to assess the effectiveness of a therapeutic modality in so young a CF patient population. Copyright 2001 Wiley-Liss, Inc.

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Year:  2001        PMID: 11340684     DOI: 10.1002/ppul.1061

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  23 in total

1.  Is limited computed tomography the future for imaging the lungs of children with cystic fibrosis?

Authors:  S C Langton Hewer
Journal:  Arch Dis Child       Date:  2006-05       Impact factor: 3.791

2.  Comparison of quiet breathing and controlled ventilation in the high-resolution CT assessment of airway disease in infants with cystic fibrosis.

Authors:  Frederick R Long; Roger S Williams; Brent H Adler; Robert G Castile
Journal:  Pediatr Radiol       Date:  2005-07-23

Review 3.  Cystic fibrosis lung disease: genetic influences, microbial interactions, and radiological assessment.

Authors:  Samuel M Moskowitz; Ronald L Gibson; Eric L Effmann
Journal:  Pediatr Radiol       Date:  2005-05-03

Review 4.  Timing of dornase alfa inhalation for cystic fibrosis.

Authors:  Ruth Dentice; Mark Elkins
Journal:  Cochrane Database Syst Rev       Date:  2016-07-26

Review 5.  Computed tomography and cystic fibrosis: promises and problems.

Authors:  Z A Aziz; J C Davies; E W Alton; A U Wells; D M Geddes; D M Hansell
Journal:  Thorax       Date:  2007-02       Impact factor: 9.139

6.  Development and validation of automated 2D-3D bronchial airway matching to track changes in regional bronchial morphology using serial low-dose chest CT scans in children with chronic lung disease.

Authors:  Pavithra Raman; Raghav Raman; Beverley Newman; Raman Venkatraman; Bhargav Raman; Terry E Robinson
Journal:  J Digit Imaging       Date:  2009-09-15       Impact factor: 4.056

Review 7.  Endpoints for clinical trials in young children with cystic fibrosis.

Authors:  Stephanie D Davis; Alan S Brody; Mary J Emond; Lyndia C Brumback; Margaret Rosenfeld
Journal:  Proc Am Thorac Soc       Date:  2007-08-01

Review 8.  Scoring of chest CT in children with cystic fibrosis: state of the art.

Authors:  Alistair D Calder; Andrew Bush; Alan S Brody; Catherine M Owens
Journal:  Pediatr Radiol       Date:  2014-08-28

Review 9.  Use of lung imaging studies as outcome measures for development of new therapies in cystic fibrosis.

Authors:  Bonnie W Ramsey
Journal:  Proc Am Thorac Soc       Date:  2007-08-01

10.  Review of recombinant human deoxyribonuclease (rhDNase) in the management of patients with cystic fibrosis.

Authors:  Tacjana Pressler
Journal:  Biologics       Date:  2008-12
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