2001
DOI: 10.1002/ppul.1061
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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*

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 basel… Show more

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Cited by 89 publications
(57 citation statements)
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“…Anteroposterior and lateral chest radiographs were obtained at the time of hospital admission and 3 days afterwards. The radiograph assessment score described by Nasr et al 19,30 was utilized.…”
Section: Methodsmentioning
confidence: 99%
“…Anteroposterior and lateral chest radiographs were obtained at the time of hospital admission and 3 days afterwards. The radiograph assessment score described by Nasr et al 19,30 was utilized.…”
Section: Methodsmentioning
confidence: 99%
“…[75][76][77][78][79][80][81] Dornase alfa has been shown to have positive effects on CT changes and LCI [82][83][84] and improved health-related quality-of-life scores in children >6 years. 85 Safety and tolerability of dornase alfa has been demonstrated in children ages 3 months to 5 years.…”
Section: Dornase Alfamentioning
confidence: 99%
“…This is not an unexpected result, since HRCT can detect regional abnormalities such as small areas of atelectasis and bronchiectasis that may be functionally silent. A few, small clinical trials have been performed using HRCT score as an end-point, some of which failed to demonstrate a significant treatment effect; however, the time period between repeat scans was short [132,137,140,153,154].…”
Section: Airway Imaging In Cystic Fibrosismentioning
confidence: 99%