Literature DB >> 9530060

Cystic fibrosis: a system for assessing and predicting progression.

R H Cleveland1, A S Neish, D Zurakowski, D P Nichols, M E Wohl, A A Colin.   

Abstract

OBJECTIVE: This study presents a radiography-based database scoring changes over time in a large population of patients with cystic fibrosis. The purpose of this database is to provide comparison for groups of patients undergoing experimental treatment to assess effect of the treatment. The data may also be used to compare individuals with their age-matched cohorts with cystic fibrosis.
MATERIALS AND METHODS: From 230 patients, 3038 chest radiographs were scored using the Brasfield system. The scores from radiographs from all the patients were individually plotted for age, and a single age-based severity curve was created. The age-based severity curve was compared with similar curves derived from pulmonary function studies of a subset of the same patient population.
RESULTS: We found high inter- and intraobserver reliability. The difference between the observers averaged 1.3 Brasfield points, the scale of which ranges up to 25 points. The age-based severity curve was presented as mean Brasfield scores versus age (birth to > 30 years) plotted with 95% confidence limits; the curve was also plotted in percentiles. The rate of decline of this curve was similar to the decline of pulmonary function studies in this patient population.
CONCLUSION: The age-based curve, a structural anatomic parameter, differs from pulmonary function studies, which are functional. Thus the age-based severity curve provides an additional, independent basis for comparison between groups and individuals. It may be used for the initial assessment of lung disease and for gauging and predicting the rate of decline. The curve may be used as a long-range outcome criterion to evaluate new treatments in groups of patients with cystic fibrosis.

Entities:  

Mesh:

Year:  1998        PMID: 9530060     DOI: 10.2214/ajr.170.4.9530060

Source DB:  PubMed          Journal:  AJR Am J Roentgenol        ISSN: 0361-803X            Impact factor:   3.959


  12 in total

Review 1.  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

2.  Pulmonary radiographic findings in young children with cystic fibrosis.

Authors:  Jesiana Ferreira Pedrosa; Cássio da Cunha Ibiapina; Cristina Gonçalves Alvim; Paulo Augusto Moreira Camargos; Fabiana Paiva Martins; Elizabet Vilar Guimarães; Renata Marcos Bedran
Journal:  Pediatr Radiol       Date:  2014-07-22

3.  Similar performance of Brasfield and Wisconsin scoring systems in young children with cystic fibrosis.

Authors:  Robert H Cleveland; Gregory S Sawicki; Catherine Stamoulis
Journal:  Pediatr Radiol       Date:  2015-05-29

4.  Computed tomography in children with cystic fibrosis: a new way to reduce radiation dose.

Authors:  S Jiménez; J R Jiménez; M Crespo; E Santamarta; C Bousoño; J Rodríguez
Journal:  Arch Dis Child       Date:  2006-01-31       Impact factor: 3.791

5.  Description and validation of a scoring system for tomosynthesis in pulmonary cystic fibrosis.

Authors:  Kristina Vult von Steyern; Isabella M Björkman-Burtscher; Peter Höglund; Gracijela Bozovic; Marie Wiklund; Mats Geijer
Journal:  Eur Radiol       Date:  2012-06-30       Impact factor: 5.315

6.  Pulmonary outcome prediction (POP) tools for cystic fibrosis patients.

Authors:  Donald R VanDevanter; Jeffrey S Wagener; David J Pasta; Eric Elkin; Joan R Jacobs; Wayne J Morgan; Michael W Konstan
Journal:  Pediatr Pulmonol       Date:  2010-08-17

7.  Lack of correlation between pulmonary disease and cystic fibrosis transmembrane conductance regulator dysfunction in cystic fibrosis: a case report.

Authors:  Hara Levy; Carolynn L Cannon; Daniel Asher; Christopher García; Robert H Cleveland; Gerald B Pier; Michael R Knowles; Andrew A Colin
Journal:  J Med Case Rep       Date:  2010-04-26

8.  Brasfield and Wisconsin scoring systems have equal value as outcome assessment tools of cystic fibrosis lung disease.

Authors:  Robert H Cleveland; Catherine Stamoulis; Gregory Sawicki; Emma Kelliher; Evan J Zucker; Christopher Wood; David Zurakowski; Edward Lee
Journal:  Pediatr Radiol       Date:  2013-12-27

9.  Sleep-disordered breathing in cystic fibrosis.

Authors:  Aarti Shakkottai; Samya Z Nasr; Fauziya Hassan; Sanaya Irani; Louise M O'Brien; Ronald D Chervin
Journal:  Sleep Med       Date:  2020-06-05       Impact factor: 3.492

10.  The correlation of brody high resolution computed tomography scoring system with clinical status and pulmonary function test in patients with cystic fibrosis.

Authors:  Soheila Khalilzadeh; Shahram Kahkouee; Maryam Hassanzad; Nazanin Parsanejad; Nooshin Baghaie; Mohammad Reza Bloorsa
Journal:  Iran J Med Sci       Date:  2011-03
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