Literature DB >> 9266869

Distribution of disease in cystic fibrosis: correlation with pulmonary function.

J W Gurney1, T G Habbe, J Hicklin.   

Abstract

STUDY
OBJECTIVE: We hypothesized that the radiographic distribution of disease is important in determining pulmonary function, with the lower lung zones of more importance than the upper lung zones. To test this hypothesis, we retrospectively studied patients with cystic fibrosis, a disease with a known proclivity for the upper lung zones. SUBJECTS AND METHODS: Two hundred seventy-six chest radiographs obtained at 2- to 3-year intervals from 51 patients were scored by two radiologists using a 100-point visual severity scale. The distribution of disease was assessed by dividing the lungs into four equal horizontal zones and scoring each zone for the severity of disease. There were 146 concurrent chest radiographs and pulmonary function tests from which multiple linear regression was used to correlate these zonal scores with FEV1/FVC percent predicted.
RESULTS: There was excellent interobserver agreement, intraclass correlation coefficients >0.7. The distribution of disease became predominant in the upper lung zones as the patients aged. Although the median score in the upper lung zones was nearly twice that of the lower lung zones, the lower lung zones were nearly three times (partial F ratio; 6.9 lower zone score vs 2.4 upper lung zone score) as important in determining pulmonary function.
CONCLUSION: The regional distribution of disease is important in determining pulmonary function. Sparing of the lower lung zones is important in preserving pulmonary function.

Entities:  

Mesh:

Year:  1997        PMID: 9266869     DOI: 10.1378/chest.112.2.357

Source DB:  PubMed          Journal:  Chest        ISSN: 0012-3692            Impact factor:   9.410


  5 in total

1.  Regional Isolation Drives Bacterial Diversification within Cystic Fibrosis Lungs.

Authors:  Peter Jorth; Benjamin J Staudinger; Xia Wu; Katherine B Hisert; Hillary Hayden; Jayanthi Garudathri; Christopher L Harding; Matthew C Radey; Amir Rezayat; Gilbert Bautista; William R Berrington; Amanda F Goddard; Chunxiang Zheng; Angus Angermeyer; Mitchell J Brittnacher; Jacob Kitzman; Jay Shendure; Corinne L Fligner; John Mittler; Moira L Aitken; Colin Manoil; James E Bruce; Timothy L Yahr; Pradeep K Singh
Journal:  Cell Host Microbe       Date:  2015-08-20       Impact factor: 21.023

2.  Case studies of the spatial heterogeneity of DNA viruses in the cystic fibrosis lung.

Authors:  Dana Willner; Matthew R Haynes; Mike Furlan; Nicole Hanson; Breeann Kirby; Yan Wei Lim; Paul B Rainey; Robert Schmieder; Merry Youle; Douglas Conrad; Forest Rohwer
Journal:  Am J Respir Cell Mol Biol       Date:  2011-10-06       Impact factor: 6.914

3.  Visual score and quantitative CT indices in pulmonary fibrosis: Relationship with physiologic impairment.

Authors:  N Sverzellati; E Calabrò; A Chetta; G Concari; A R Larici; M Mereu; R Cobelli; M De Filippo; M Zompatori
Journal:  Radiol Med       Date:  2007-12-13       Impact factor: 3.469

4.  The practical application and interpretation of simple lung function tests in cystic fibrosis.

Authors:  P L Brand; C K van der Ent
Journal:  J R Soc Med       Date:  1999       Impact factor: 18.000

5.  Strain-Resolved Dynamics of the Lung Microbiome in Patients with Cystic Fibrosis.

Authors:  Marija Dmitrijeva; Christian R Kahlert; Rounak Feigelman; Rebekka L Kleiner; Oliver Nolte; Werner C Albrich; Florent Baty; Christian von Mering
Journal:  mBio       Date:  2021-03-09       Impact factor: 7.867

  5 in total

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