Breath sound analysis and wheezing in cystic fibrosis
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Keywords

Cystic Fibrosis
Spectral Analysis
Wheeze
Salbutamol Response
Pneumonology
Genetic
Pulmonary Semiology
Auscultation

How to Cite

1.
Sánchez D. I, Vizcaya A. C, García P. D. Breath sound analysis and wheezing in cystic fibrosis. Andes pediatr [Internet]. 2003 Jun. 19 [cited 2025 Oct. 21];74(6):590-4. Available from: https://andespediatrica.cl/index.php/rchped/article/view/2008

Abstract

Wheezes are musical sounds caused by obstructed airways and depend on airflow, a critical pressure and a geometrical airway distortion.

Objective: to characterize wheezing and the lung sound spectra in cystic fibrosis (CF).

Patient and Methods: 14 patients (8 boys), aged 14.2 ± 2 years, 6 children had DF508/DF508 mutation. Subjects peathed through a pneumotachograph at flows of 0.5 ± 0.05 l/s. Respiratory sounds were recorded using contact sensors on the supra-sternal notch and on the thoracic region corresponding to the right lower lobe. Sound signals were low-pass filtered, amplified and Fourier analisis was applied to sounds within the target flow range. From averaged spectra, power at low (100-200 Hz = P1) and high frequencies (400-2 000Hz = P2) were calculated. We measured the frequencies below in which 50% (F50) and 99% (SEF99) of the spectral power between 100-2 000 Hz were contained. After baseline recording, patients received inhaled salbutamol (200 mcg) and 15 minutes later the measurements were repeated. 

Results: Baseline spirometry was FVC 56 ± 15%, FEV144 ± 12%, FEF25-75: 40 ± 14% and SaO293.4 ± 2%. Only in 6/14 patients we obtained a sinusoidal waveform of a typical wheeze, the others had complex waveforms. There was a significant increase in P1and decrease in P2during inspiration after salbutamol (p < 0.001) with a significant correlation between FEV1vs F50 and SEF99 (p < 0.01). 

Conclusion: Our results show that CF patients have both complex and classical wheezes and that the sound spectral analysis correlates with lung function. Lung sounds analysis is a useful method to study ponchial obstruction mechanisms in CF patients.

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