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A new positive-pressure device for nasal foreign body removal
Manuel de la O-Cavazos1, Josué Ríos-Solís, Fernando Montes-Tapia
1From the *Department of Pediatrics, Hospital Universitario "Dr. José E. González," and †Facultad de Medicina, Universidad Autónoma de Nuevo León, Monterrey, Nuevo León, México.
Insights
A new nasal occlusion device effectively removed foreign bodies (FBs) in 94.4% of pediatric patients. This safe and easy tool offers a promising solution for emergency room nasal FB removal.
Area of Science:
- Pediatric Emergency Medicine
- Otolaryngology
- Medical Device Technology
Background:
- Nasal foreign bodies (FBs) are a frequent reason for pediatric emergency department visits.
- Current FB removal methods have variable success rates and potential for complications.
Purpose of the Study:
- To assess the safety and efficacy of a novel nasal occlusion device for removing FBs in children.
- To evaluate a new tool designed for pediatric nasal FB extraction.
Main Methods:
- A prospective study involving 18 pediatric patients (ages 1-8) with nasal FBs.
- Utilized a nasal occlusion device employing modulated positive pressure for FB removal.
Main Results:
- Successful FB removal in 17 out of 18 patients (94.4%).
- The device achieved removal on the first attempt in 66.7% of cases.
- No complications or adverse events were reported during or after the procedure.
Conclusions:
- The nasal occlusion device demonstrated high efficacy and safety in pediatric FB removal.
- The device is a promising, user-friendly option for emergency room settings.
- This tool simplifies the management of nasal foreign bodies in children.
Objectives:
Nasal foreign bodies (FBs) are common causes of pediatric emergency consultations. The different methods for removing nasal FBs have varying levels of efficacy. The aim of this study was to evaluate the safety and efficacy of a new device for nasal FB removal in children.
Methods:
A nasal occlusion device that uses modulated positive pressure to remove FBs was evaluated in a series of 18 patients ranging in age from 1 to 8 years diagnosed with a nasal FB during a period of 7 months.
Results:
The device successfully removed FBs in 17 (94.4%) of the 18 patients. In 12 of the cases (66.7%), the FB was removed during the first attempt. None of the patients had complications or sequelae at the time of removal or at the follow-up visit.
Conclusions:
The nasal occlusion device used in this study was found to be a promising, safe, effective, and easy to use tool for FB removal in a pediatric emergency room setting.
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