Your browser doesn't support javascript.
loading
Bronchodilator response to albuterol nebulized with hypertonic saline in asthmatic children.
Teper, Alejandro; Kofman, Carlos; Alchundia Moreira, Jessica; Köhler, Teresa; García Bournissen, Facundo.
Afiliação
  • Teper A; Centro Respiratorio Dr Alberto Alvarez, Hospital de Niños Dr Ricardo Gutiérrez, Ciudad Autónoma de Buenos Aires, Argentina.
  • Kofman C; Centro Respiratorio Dr Alberto Alvarez, Hospital de Niños Dr Ricardo Gutiérrez, Ciudad Autónoma de Buenos Aires, Argentina.
  • Alchundia Moreira J; Centro Respiratorio Dr Alberto Alvarez, Hospital de Niños Dr Ricardo Gutiérrez, Ciudad Autónoma de Buenos Aires, Argentina.
  • Köhler T; Centro Respiratorio Dr Alberto Alvarez, Hospital de Niños Dr Ricardo Gutiérrez, Ciudad Autónoma de Buenos Aires, Argentina.
  • García Bournissen F; Centro Respiratorio Dr Alberto Alvarez, Hospital de Niños Dr Ricardo Gutiérrez, Ciudad Autónoma de Buenos Aires, Argentina.
Pediatr Pulmonol ; 56(12): 3714-3719, 2021 12.
Article em En | MEDLINE | ID: mdl-34499820
INTRODUCTION: Asthma is distinguished by bronchial obstruction reversible by bronchodilators. The first-line treatment for asthmatic exacerbations is the use of inhaled beta-agonists, by pressurized metered-dose inhalers or nebulized with normal saline solution (NSS). There are no reports of nebulized beta agonists' efficacy in asthmatic children when administered with hypertonic saline solution (HSS). OBJECTIVE: To evaluate bronchodilator responses (BDR) to albuterol nebulized with 3%-HSS in asthmatic children, compared to albuterol nebulized with NSS. POPULATION AND METHODS: In a prospective, experimental, double-blind, randomized clinical study, children with a confirmed diagnosis of asthma with mild or moderate bronchial obstruction (FEV1 40%-79% of predicted) were randomized to receive a nebulization with 2.5 mg of albuterol diluted in 3 cc of 3%-HSS or NSS (0.9%), by means of a jet nebulizer. After 30 min, the BDR was assessed. RESULTS: Fifty patients (mean age 12.0 ± 3 years, 29 males) were enrolled; 25 were randomized to the 3%-HSS group (FEV1 65.2% ± 10) and 25 to the NSS group (FEV1 69.1% ± 7.1). The BDR of FEV1 was 41.2% (SD: ±20.1; 95% confidence interval [CI]: 35.1-50.4) and 17.3% (SD: ±19.4; 95% CI: 9.7-24.9) (p < .0001) and of maximum mid-expiratory flow was 130% (SD: ±90.8; 95% CI: 94.6-166) and 69.8% (SD: ±72.5; 95% CI: 41.4-98.2) (p < .01), for the 3%-HSS and NSS groups, respectively. CONCLUSION: Albuterol produces a greater BDR when nebulized with 3%-HSS compared to NSS in asthmatic children with mild or moderate bronchial obstruction.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Asma / Broncodilatadores Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Adolescent / Child / Humans / Male Idioma: En Revista: Pediatr Pulmonol Assunto da revista: PEDIATRIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Argentina País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Asma / Broncodilatadores Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Adolescent / Child / Humans / Male Idioma: En Revista: Pediatr Pulmonol Assunto da revista: PEDIATRIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Argentina País de publicação: Estados Unidos