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Published on: November 30, 2010
Congenital nasal pyriform aperture stenosis: feeding evaluation and management
Babar Sultan1, Maureen A Lefton-Greif, David J Brown
1Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA.
Insights
Feeding difficulties are common in infants with congenital nasal pyriform aperture stenosis (CNPAS). Supplemental feeding may be necessary, and comprehensive swallowing evaluations are recommended for optimal outcomes.
Area of Science:
- Pediatric Otolaryngology
- Pediatric Gastroenterology
- Speech-Language Pathology
Background:
- Congenital nasal pyriform aperture stenosis (CNPAS) can cause significant feeding and respiratory issues in infants.
- Feeding difficulties in CNPAS are under-recognized compared to other nasal obstructions like choanal atresia.
Purpose of the Study:
- To investigate the prevalence and characteristics of feeding difficulties in infants diagnosed with CNPAS.
- To evaluate the effectiveness of interventions and the long-term feeding prognosis for infants with CNPAS.
Main Methods:
- Case series of four infants with CNPAS presenting with feeding and respiratory challenges.
- Utilized nasal steroids, nasal saline, and surgical repair as treatments.
- Conducted upper gastrointestinal tract contrast studies, bedside swallow evaluations, and videofluoroscopic swallow studies (VFSS).
Main Results:
- Three out of four infants experienced feeding difficulties, including nasal congestion and desaturations during oral feeding.
- One infant showed trace aspiration; three required supplemental feeding in the first year.
- Successful oral feeding was achieved by 16 months in three patients with normal brain MRIs.
Conclusions:
- Feeding problems are a significant concern in infants with CNPAS, often requiring supplemental support beyond airway management.
- Comprehensive feeding and swallowing assessments, including VFSS, are crucial for infants with CNPAS.
- Prognosis for oral feeding is generally good, influenced by airway obstruction severity and comorbidities.
Purpose:
We identified four patients with congenital nasal pyriform aperture stenosis (CNPAS) with feeding and respiratory difficulties. While feeding difficulties have been described in infants with other causes of nasal obstruction (e.g., choanal atresia), little attention has been focused on feeding in infants with CNPAS.
Findings:
All four patients were treated with nasal steroids and nasal saline and two underwent surgical repair of the CNPAS at 2 months of age. Except for gastroesophageal reflux in one patient, upper gastrointestinal tract (UGI) contrast studies were normal in all patients. Three patients underwent bedside swallow evaluations, two of whom participated in videoflouroscopic swallow studies (VFSS) because of limited oral intake or respiratory problems during feeding. These three patients presented with intact oral-motor coordination at rest and during non-nutritive sucking, and nasal whistling, nasal congestion, or breathing difficulties/desaturations with oral feeding. On VFSS, one infant had trace aspiration with thin and thick liquids. Three patients required supplemental feeding during the first year of life. All three patients with normal brain MRIs were successful oral feeders by 16 months of age, the fourth is undergoing feeding therapy at 24 months of age.
Summary:
Feeding problems are common in infants with CNPAS and supplemental feedings may be needed even after management of airway difficulties. Infants with CNPAS should undergo comprehensive feeding/swallowing evaluations which may include bedside swallow evaluations and VFSSs. The prognosis for transitioning to total oral feedings is good and related to the extent of the airway obstruction and presence of other comorbidities.
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