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Detecting early structural lung damage in cystic fibrosis

Tiddens, Harm A.W.M.·2002·Pediatric Pulmonology

Abstract

In cystic fibrosis (CF) patients, both severe lung inflammation and severe lung damage occur early and persist throughout life. High‐resolution computed tomography (HRCT), a more sensitive method of detecting structural abnormalities than chest X‐ray, shows that airways undergo substantial thickening in early CF lung disease. Lung function tests, which are an indirect measure of structural integrity, are insensitive to localized or early damage. Thickening of the peripheral airways causes a reduction in maximal expiratory flow at 25% of forced vital capacity (MEF 25) or other measurements of peripheral air flow. Reduced peripheral flows, even in the presence of normal forced expired volume in 1 sec (FEV 1) and forced vital capacity (FVC), should be considered an early sign of substantial lung damage and should stimulate aggressive treatment to prevent further deterioration. Pediatr Pulmonol. 2002; 34:228–231. © 2002 Wiley‐Liss, Inc.

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Metadata

Authors
Tiddens, H. A. W. M.
Venue
Pediatric Pulmonology
Publisher
Wiley
Published
2002-08-14
Volume
34
Issue
3
Pages
228-231
ISSN
  • 1099-0496 (ISSN-L)
  • 8755-6863
OpenAlex
W1986108334
Cited by
177
References
0
FWCI
10.69
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Detecting early structural lung damage in cystic fibrosis. https://app.cochat.ai/papers/10.1002/ppul.10134
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Tiddens, H. A. W. M. (2002). Detecting early structural lung damage in cystic fibrosis. Pediatric Pulmonology. https://doi.org/10.1002/ppul.10134

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