The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Progressive damage on high resolution computed tomography despite stable lung function in cystic fibrosis
Open accessAbstract
For effective clinical management of cystic fibrosis (CF) lung disease it is important to closely monitor the start and progression of lung damage. The aim of this study was to investigate the ability of high-resolution computed tomography (HRCT) scoring systems and pulmonary function tests (PFT) to detect changes in lung disease. CF children (n=48) had two HRCT scans in combination with two PFT 2 yrs apart. Their scans were scored using five scoring systems (Castile, Brody, Helbich, Santamaria and Bhalla). “Sensitivity” was defined as the ability to detect disease progression. In this group of children, HRCT scores worsened. PFT remained unchanged or improved. Of the HRCT parameters, mucous plugging and the severity, extent and peripheral extension of bronchiectasis worsened significantly. Relationships between changes in HRCT scores and PFT were weak. Substantial structural lung damage was evident in some children who had normal lung function. These data show that high-resolution computed tomography is more sensitive than pulmonary function tests in the detection of early and progressive lung disease, and suggest that high-resolution computed tomography may be useful in the follow up of cystic fibrosis children and as an outcome measure in studies that aim to reduce lung damage.
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Cites
Estimated Risks of Radiation-Induced Fatal Cancer from Pediatric CT
Brenner, D. J., Elliston, C. D., Hall, E. J., & Berdon, W. E. (2001) · American Journal of Roentgenology · doi:10.2214/ajr.176.2.1760289 · Cited by 3,222
Cited by
Konstan, M. W., Morgan, W. J., Butler, S. M., Pasta, D. J., Craib, M. L., Silva, S. J., Stokes, D. C., Wohl, M. E. B., Wagener, J. S., Regelmann, W. E., et al. (2007) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2007.03.006 · Cited by 438
Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis
Gustafsson, P. M., De Jong, P. A., Tiddens, H. A. W. M., & Lindblad, A. (2007) · Thorax · doi:10.1136/thx.2007.077784 · Cited by 364
Self-citationComputed tomographic imaging of the airways: relationship to structure and function
de Jong, P. A., Müller, N. L., Paré, P. D., & Coxson, H. O. (2005) · European Respiratory Journal · doi:10.1183/09031936.05.00007105 · Cited by 171
Self-citationRecurrent exacerbations affect FEV1 decline in adult patients with cystic fibrosis
Amadori, A., Antonelli, A., Balteri, I., Schreiber, A., Bugiani, M., & De Rose, V. (2009) · Respiratory Medicine · doi:10.1016/j.rmed.2008.09.024 · Cited by 64
Metadata
- Authors
- de Jong, P. A., Nakano, Y., Lequin, M. H., Mayo, J. R., Woods, R., Paré, P. D., & Tiddens, H. A. W. M.
- Venue
- European Respiratory Journal
- Publisher
- European Respiratory Society (ERS)
- Published
- 2003-01-01
- Volume
- 23
- Issue
- 1
- Pages
- 93-97
- ISSN
- 0903-1936 (ISSN-L)
- 1399-3003
- OpenAlex
- W2144102711
- Cited by
- 318
- References
- 1
- FWCI
- 12.26
- Type
- journal article
- Language
- en
- Open access
- bronze
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- de Jong, P. A., Nakano, Y., Lequin, M. H., Mayo, J. R., Woods, R., Paré, P. D., & Tiddens, H. A. W. M. (2004). Progressive damage on high resolution computed tomography despite stable lung function in cystic fibrosis. European Respiratory Journal. https://doi.org/10.1183/09031936.03.00006603
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