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Published on: February 9, 2022
Relative ability of full and partial forced expiratory maneuvers to identify diminished airway function in infants
Sarath C Ranganathan1, Andrew Bush, Carol Dezateux
1Portex Anaesthesia, Intensive Therapy and Respiratory Medicine Unit, Institute of Child Health, London, United Kingdom. drsarath@clara.net
Insights
The raised volume technique better detects diminished airway function in infants with cystic fibrosis (CF) compared to the tidal technique. This is crucial for early diagnosis, even in infants with normal clinical respiratory status.
Area of Science:
- Pediatric Pulmonology
- Respiratory Physiology
- Infant Health
Background:
- Infant airway function assessment is critical for early disease detection.
- Tidal and raised volume rapid thoracoabdominal compression are emerging techniques.
- Cystic Fibrosis (CF) diagnosis in infancy necessitates sensitive airway function evaluation.
Purpose of the Study:
- To compare the efficacy of tidal and raised volume techniques in identifying diminished airway function in infants with CF.
- To assess airway function in CF infants with and without prior lower respiratory illness.
- To correlate objective lung function measurements with clinical respiratory assessments.
Main Methods:
- Cross-sectional, prospective study involving 47 infants with CF and 187 healthy controls.
- Measurement of VmaxFRC (tidal technique) and FVC, FEV0.5, FEF75, FEF25-75 (raised volume technique).
- Statistical analysis using multiple linear regression and comparison with clinical assessments.
Main Results:
- FEV0.5 was significantly diminished in 13 infants with CF, including 4 considered clinically normal.
- Only one CF infant had reduced VmaxFRC, indicating lower sensitivity of the tidal technique.
- The raised volume technique identified diminished airway function more frequently in CF infants.
Conclusions:
- Airway function is compromised in infants with CF, regardless of clinical status or prior respiratory infections.
- The raised volume technique is more sensitive for detecting early airway dysfunction in infants with CF.
- Early detection of airway dysfunction in CF infants is possible even with normal clinical findings.
Abstract:
The tidal and raised volume rapid thoracoabdominal compression techniques are increasingly used to detect diminished airway function in infancy. The aim of this study was to assess the relative ability of parameters measured by these techniques to identify diminished airway function in infants newly diagnosed with cystic fibrosis (CF) with and without clinical evidence of prior lower respiratory illness. A cross-sectional, prospective study design was used in which maximal flow at functional residual capacity (VmaxFRC) from the tidal technique and FVC, FEV0.5, FEF75, and FEF25-75 from the raised volume technique were measured in 47 infants with CF and 187 healthy infants of similar body size, sex distribution, ethnic group, and exposure to maternal smoking. Multiple linear regression was used to assess group differences and to calculate SD scores for each parameter for the infants with CF. Airway function was also compared with clinical assessments of respiratory status made by pediatric pulmonologists. FEV0.5 was significantly diminished in 13 infants with CF, of whom 4 had been identified by clinicians as having normal respiratory status. Only one infant with CF had a VmaxFRC below the estimated normal range. Airway function is diminished in infants with CF irrespective of prior lower respiratory illness and in those whose respiratory status is considered normal by pediatric pulmonologists. In infants with CF, the raised volume technique identified diminished airway function more frequently than the tidal technique.
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