The purpose of this study is to compare the immediate effects of retrograde rhinopharyngeal clearance with nasopharyngeal aspiration in children admitted with acute viral bronchiolitis. The investigators selected children, up to 12 months old, admitted for acute viral bronchiolitis. Patients were divided in aspiration group (AG), submitted to nasopharyngeal aspiration, and clearance group (CG), submitted to retrograde rhinopharyngeal clearance with physiological solution (0.9%) instillation (RRC) technique. In both groups children were evaluated three times in the same day in order to verify cardiorespiratory parameters, clinical score of respiratory dysfunction and adverse effects.
Children up to 12 months old, admitted for acute viral acute viral bronchiolitis were selected. All children participating in the study should be in the first 48 hours of hospitalization. Patients were divided in aspiration group (AG), submitted to nasopharyngeal aspiration, and clearance group (CG), submitted to retrograde rhinopharyngeal clearance (RRC) technique with physiological solution (0.9%) instillation. In both groups children were evaluated three times in the same day (data collection 1 (C1) - performed early in the morning; data collecting 2 (C2) - performed in the early afternoon; and data collecting 3 (C3) - performed in the evening). In each data collection, cardiorespiratory parameters and clinical score of respiratory dysfunction were evaluated before procedures (T0), 10 minutes after (T1) and 30 minutes after (T2). Adverse effects were evaluated during the whole day of the study.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
100
At the end of the expiratory time, the child's mouth was closed by the hand of the researcher (raising the lower jaw), leading the child to perform a nasal aspiration maneuver.
A sterile aspiration catheter was connected to an extension and carefully introduced into the nasal cavity of the patient.
0.9% saline consists of physiological solution and was instilled in both experimental groups.
Occurrence of chest retractions as a measure of respiratory distress
Time frame: 30 minutes
Occurrence of wheezing as a measure of respiratory distress
Time frame: 30 minutes
Number of nasal bleeding events as a measure of adverse effects
Time frame: 1 day
Number of vomit episodes as a measure of adverse effects
Time frame: 1 day
Measurement of the heart rate using an oximeter
Time frame: 30 minutes
Measurement of the respiratory rate
Time frame: 30 minutes
Measurement of the oxygen saturation using an oximeter
Time frame: 30 minutes
Severity scores on the Wood clinical score
Time frame: 30 minutes
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