Document Detail


Changes in lung function measured by spirometry and the forced oscillation technique in cystic fibrosis patients undergoing treatment for respiratory tract exacerbation.
MedLine Citation:
PMID:  16496336     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Objective measures of lung function are critical for the treatment and study of lung diseases such as cystic fibrosis (CF). Spirometry is the most widely used and accepted method of pulmonary function testing in CF, but not all patients can perform the maneuvers required to obtain valid results from spirometry. The forced oscillation technique (FOT) requires less cooperation than spirometry. The goals of this study were to determine if FOT could detect changes in lung function in CF patients receiving inpatient treatment of respiratory tract exacerbations (RTEs), and to gather preliminary data on the magnitude of these changes and the variability of FOT data in such patients. We performed a retrospective chart review of CF patients admitted to the hospital for RTEs. We identified 14 patients who had both spirometry and FOT performed at the beginning and end of their treatment course. Their mean age was 15.9 years (range, 8-18). The mean forced expiratory volume in 1 sec (FEV1) on admission was 62.57% predicted. FEV1 increased by 27.1 +/- 33.15% (mean +/- SD, P = 0.008). The absolute value of reactance at 5 Hz (X5) decreased by 22.3 +/- 25.1% (P = 0.005), while resistance at 5 Hz decreased by 11.6 +/- 17.3% (P = 0.025). There was a significant relationship between changes in FEV1 and X5 (P = 0.003, r2 = 0.54). Our study demonstrates that FOT can detect significant changes in lung function in CF patients receiving treatment for RTEs. We speculate that FOT can serve as an alternative method to measure lung function in CF patients unable to perform spirometry, such as young children.
Authors:
Clement L Ren; Justin L Brucker; Amy K Rovitelli; Kimberly A Bordeaux
Related Documents :
8730646 - Mmpi profiles of patients with chronic fatigue syndrome.
3164496 - Sclerosing cholangitis in cystic fibrosis.
16328636 - Serologic and histologic findings in patients with capsular contracture after breast au...
6723186 - Kyphosis and pulmonary function in cystic fibrosis.
2538676 - Different therapeutic efficacy of ketoconazole in patients with cushing's syndrome.
15047946 - Transmission of tuberculosis from smear negative patients: a molecular epidemiology study.
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Pediatric pulmonology     Volume:  41     ISSN:  8755-6863     ISO Abbreviation:  Pediatr. Pulmonol.     Publication Date:  2006 Apr 
Date Detail:
Created Date:  2006-03-06     Completed Date:  2006-08-31     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  8510590     Medline TA:  Pediatr Pulmonol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  345-9     Citation Subset:  IM    
Copyright Information:
2006 Wiley-Liss, Inc.
Affiliation:
Division of Pediatric Pulmonology, University of Rochester, Rochester, New York 14642, USA. clement_ren@urmc.rochester.edu
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adolescent
Anti-Bacterial Agents / therapeutic use
Child
Cystic Fibrosis / physiopathology*
Female
Humans
Male
Respiratory Function Tests / methods*
Respiratory Tract Infections / drug therapy*,  physiopathology
Retrospective Studies
Spirometry*
Chemical
Reg. No./Substance:
0/Anti-Bacterial Agents

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Prolonged dark adaptation changes connexin expression in the mouse retina.
Next Document:  HuC:Kaede, a useful tool to label neural morphologies in networks in vivo.