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Updated: Aug 26, 2026

Assessment and Evaluation of the High Risk Neonate: The NICU Network Neurobehavioral Scale
Published on: August 25, 2014
Rational approach to the wheezy infant
1Department of Pediatrics, University of Louisville School of Medicine, Louisville, Kentucky 40202-3830, USA. nseid@louisville.edu
Insights
Diagnosing persistent wheezing in infants requires a thorough history and diagnostic tests. Pulmonary function testing helps identify airflow obstruction, guiding further evaluation for conditions like infantile asthma or cystic fibrosis (CF).
Area of Science:
- Pediatrics
- Pulmonology
- Diagnostic Medicine
Background:
- Infantile wheezing presents a diagnostic challenge in children under two years old.
- Key risk factors include maternal smoking, feeding, environmental exposures, and family history of asthma or cystic fibrosis (CF).
- A systematic diagnostic approach is crucial for accurate identification of wheezing causes.
Purpose of the Study:
- To outline a diagnostic strategy for persistent or recurrent wheezing in infants.
- To differentiate between various causes of airflow obstruction in young children.
- To guide clinical decision-making for effective management of infantile respiratory symptoms.
Main Methods:
- Comprehensive medical history focusing on risk factors.
- Diagnostic imaging including chest radiography and upper gastrointestinal (UGI) series.
- Infant pulmonary function testing (IPFT) to assess airflow obstruction (central vs. peripheral).
- Flexible fiberoptic bronchoscopy for specific airway abnormalities.
- Therapeutic trials with anti-inflammatory agents and bronchodilators.
Main Results:
- Chest radiography is non-specific but can suggest airway anomalies.
- IPFT differentiates central from peripheral airflow obstruction, guiding further investigations like bronchoscopy or UGI series.
- Response to anti-inflammatory therapy suggests inflammatory conditions (asthma, CF).
- Infantile asthma is diagnosed with peripheral obstruction and significant bronchodilator response (>25%).
- Lack of bronchodilator response in peripheral obstruction warrants evaluation for GERD and other causes.
Conclusions:
- A structured diagnostic pathway utilizing history, IPFT, and targeted investigations is effective for infantile wheezing.
- Differentiating airflow obstruction types guides appropriate interventions, including bronchoscopy, UGI series, or medical management.
- Identifying specific causes like infantile asthma or GERD is essential for optimal patient outcomes.
Abstract:
The infant or child presenting to the physician's office with persistent or recurrent wheezing during the first two year's of life poses a diagnostic dilemma. A careful medical history should document risk factors for persistent wheezing, including maternal smoking, feeding practices, environmental history, and family history of asthma or cystic fibrosis (CF). A suggested diagnostic approach to the causes of infantile wheezing is outlined. A chest radiograph is non-specific, but may suggest a congenital airway anomaly. Infant pulmonary function testing (IPFT) can help differentiate between central airflow (intrathoracic, extrathoracic, or fixed) and peripheral airflow obstruction. The infant with either intrathoracic, extrathoracic, or fixed airflow obstruction on the PFT may benefit from flexible fiberoptic bronchoscopy. The infant with either an intrathoracic or fixed airway obstruction should undergo an upper gastrointestinal (UGI) series to evaluate the anatomy for extrinsic tracheal compression. The response to treatment with anti-inflammatory therapy may suggest an inflammatory disease such as asthma or CF. The infant with peripheral airflow obstruction and a good response to bronchodilators (> or =25%) using the forced exhalation technique is given the diagnosis of infantile asthma. The infant with peripheral airflow obstruction and no response to bronchodilators should be evaluated further for possible gastroesophageal reflux disease (GERD), and for other causes, which are associated with wheezing symptoms.
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