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Updated: Sep 15, 2025

Conducting Respiratory Oscillometry in an Outpatient Setting
Published on: April 8, 2022
Impulse oscillometry for evaluating pulmonary function in pediatric pectus deformities: a prospective controlled
Ece Ocak1, Ece Halis2, Gökçen Kartal Öztürk2
1Department of Pediatric Pulmonology, Faculty of Medicine, Ege University, Izmir, Turkey. ecesakizli@gmail.com.
Impulse oscillometry (IOS) detects subtle respiratory issues in children with pectus deformities (PDs) missed by spirometry. This suggests IOS is valuable for early diagnosis and management of PD-related pulmonary function changes.
Area of Science:
- Pediatric Pulmonology
- Respiratory Physiology
Background:
- Pectus deformities (PDs) can impact pulmonary mechanics, but spirometry often fails to identify subtle abnormalities.
- Impulse oscillometry (IOS) is a sensitive, effort-independent method for assessing respiratory mechanics.
Purpose of the Study:
- To evaluate pulmonary function in children with PDs using both spirometry and IOS.
- To identify potential markers for respiratory impairment in this population.
Main Methods:
- Prospective cross-sectional study involving 73 children with PDs and 80 healthy controls.
- Spirometry and IOS testing were performed, with z-scores calculated for all parameters.
- A possible restrictive ventilatory defect was defined using z-scores for forced vital capacity (zFVC) and forced expiratory volume in 1 second (zFEV1).
Main Results:
- Children with PDs showed significantly lower zFVC and zFEV1, and higher reactance at 5 cmH2O (zAX) and reactance at 15 Hz (zX15) compared to controls.
- No obstructive pattern was observed, but 61.6% of children with PDs had a possible restrictive ventilatory defect.
- Lower body mass index (zBMI) and higher zAX independently predicted restriction.
Conclusions:
- IOS offers added value in detecting respiratory impairment in children with PDs.
- The combination of IOS and spirometry can facilitate earlier identification of functional limitations.
- zAX may serve as a useful marker for clinical decision-making and follow-up in children with PDs.
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