Comparison Between Nebulized 0.9% Normal Saline and 3% Hypertonic Saline in the Management of Acute Bronchiolitis in the Emergency Department
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Background: Acute bronchiolitis is an acute viral infection of the lower respiratory tract that primarily affects infants and young children, usually under two years of age. It is characterized by inflammation, edema, and necrosis of the epithelial cells lining the small airways, resulting in increased mucus production, airway obstruction, wheezing, and respiratory distress. Respiratory syncytial virus is the most common causative agent. Nebulized 3% hypertonic saline is a sterile sodium chloride solution administered as a fine mist directly into the airways. It functions as a mucolytic and airway-hydrating agent by drawing water into the mucus and airway surface, thereby thinning secretions, improving mucus rheology, and enhancing mucociliary clearance through osmotic mechanisms. Nebulized 0.9% normal saline is an isotonic sterile sodium chloride solution commonly used to hydrate the airways, facilitate mucus clearance, and dilute inhaled medications. Although normal saline provides a gentle and soothing effect in respiratory infections, some studies suggest that 3% hypertonic saline may be more effective in reducing the duration of hospitalization among infants with bronchiolitis. Aim of the Study: This study aimed to compare the clinical effectiveness of nebulized 0.9% normal saline and nebulized 3% hypertonic saline in the management of acute bronchiolitis in the emergency department. Patients and Methods: This prospective comparative study was conducted at Babil Teaching Hospital for Maternity and Children, Babil City, Iraq, from November 1, 2025, to March 15, 2026. A total of 200 consecutive infants diagnosed with acute bronchiolitis were included. The participants were divided into two groups. Group H consisted of 100 infants who received 4 mL of nebulized 3% hypertonic saline at each treatment session, whereas Group N consisted of 100 infants who received 4 mL of nebulized 0.9% normal saline. Clinical responses were assessed using the Modified Tal Score. Statistical significance was set at p < 0.05. Results: The mean age was 5.095 ± 4.13 months in Group H and 6.03 ± 3.90 months in Group N, with no statistically significant difference between the groups (p = 0.1181). A statistically significant difference was observed in body weight between Group H (6.16 ± 2.12 kg) and Group N (6.86 ± 2.28 kg; p < 0.001). The initial Modified Tal Score was slightly higher in Group N (5.12 ± 1.49) than in Group H (4.98 ± 1.64), although the difference was not statistically significant (p = 0.110). One hour after nebulization, Group H had a lower mean Modified Tal Score (3.91 ± 0.99) than Group N (4.14 ± 0.99), but the difference remained statistically non-significant (p = 0.149). After the second nebulization session, Group H continued to demonstrate a lower mean score (3.20 ± 1.23) than Group N (3.50 ± 1.26), with no statistically significant difference (p = 0.103). Following the third nebulization session, the mean Modified Tal Score was 2.70 ± 1.09 in Group H and 2.95 ± 1.16 in Group N, with no statistically significant difference between the groups (p = 0.976). Conclusion: Nebulized 3% hypertonic saline produced slightly greater clinical improvement than nebulized 0.9% normal saline in infants with acute bronchiolitis. However, the differences in Modified Tal Scores between the two treatment groups were not statistically significant.
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