Protective test to prevent nose lesions of babies that require oxygen supplied through continuous positive airway pressure with prongs
- Conditions
- Wounds and injuriesnoseinfant, prematureA01.456.505.733M01.060.703.520.520
- Registration Number
- RBR-67zvpn
- Lead Sponsor
- niversidade Federal de Alagoas
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Newborns hospitalized in neonatal intensive or intermediary care units of the institutions chosen as place of this study; independent of city or institution of birth, which requiring positive pressure ventilatory support associated with the continuous positive airway pressure with nasal prongs interface; on admission or after initial invasive mechanical ventilation
Newborn with pre-existing nasal deformities detected during physical examination; newborn with congenital malformations of upper respiratory tract; newborn with large congenital or macrosomia anomalies; newborn with persistent physiological instability; newborn with coagulation disorder, or shock; newborn that terminates the use of positive pressure ventilatory support with continuous positive airway pressure with nasal prong before the period established for process monitoring
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Development of nasal lesion, evaluated from the daily visual inspection and systematic instrument associated with the photograph of the region of the nose during seven days of accompaniment
- Secondary Outcome Measures
Name Time Method Classification of nasal lesion, from instruments the international of the National pressure Ulcer Advisory Panel (NPUAP) and European pressure Ulcer Advisory Panel (EPUAP) in three distinct stages: I-hyperemia, II-ulcer, III-necrosis