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Prospective Observational Study of Clinical Outcomes After Intravenous Magnesium for Moderate and Severe Acute Asthma Exacerbations in Children.
Arnold, Donald H; Gong, Wu; Antoon, James W; Bacharier, Leonard B; Stewart, Thomas G; Johnson, David P; Akers, Wendell S; Hartert, Tina V.
Afiliación
  • Arnold DH; Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tenn. Electronic address: don.arnold@vumc.org.
  • Gong W; Department of Biostatistics, Vanderbilt University School of Medicine, Nashville, Tenn.
  • Antoon JW; Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tenn.
  • Bacharier LB; Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tenn.
  • Stewart TG; Department of Biostatistics, Vanderbilt University School of Medicine, Nashville, Tenn.
  • Johnson DP; Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tenn.
  • Akers WS; Department of Pharmaceutical Sciences, Lipscomb University College of Pharmacy, Nashville, Tenn.
  • Hartert TV; Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tenn.
J Allergy Clin Immunol Pract ; 10(5): 1238-1246, 2022 05.
Article en En | MEDLINE | ID: mdl-34915226
ABSTRACT

BACKGROUND:

There is limited knowledge regarding whether intravenous magnesium (IV-Mg) improves outcomes in children with acute asthma exacerbations.

OBJECTIVE:

To examine whether IV-Mg improves outcomes in children with moderate and severe exacerbations.

METHODS:

We performed a secondary analysis using data from a prospective observational cohort of children aged 5 to 17 years with moderate and severe exacerbations. Standardized treatment included systemic corticosteroid and inhaled albuterol, with consideration of IV-Mg (75 mg/kg) for patients with insufficient response after 20 minutes. Propensity score (PS) models were used to examine associations of IV-Mg treatment with change in the validated Acute Asthma Intensity Research Score, hospitalization rate, and time to spacing of inhaled albuterol of 4 hours or more among hospitalized participants.

RESULTS:

Among 301 children, median (interquartile range) age was 8.1 (6.4-10.2) years, 170 were Black (57%), 201 were male (67%), and 84 received IV-Mg (28%). In a PS covariate-adjusted multivariable linear regression model, IV-Mg treatment was associated with a 2-hour increase in the Acute Asthma Intensity Research Score (ß-coefficient = 0.98; 95% confidence interval [CI], 0.20-1.77), indicating increased exacerbation severity. Three additional PS-based models yielded similar results. Participants receiving IV-Mg had 5.8-fold (95% CI, 2.8-11.9) and 6.8-fold (95% CI, 3.6-12.9) greater odds of hospitalization in PS-based multivariable regression models. Among hospitalized participants, there was no difference in time to albuterol of every 4 hours or more in a PS covariate-adjusted Cox proportional hazards model (hazard ratio = 1.2; 95% CI, 0.8-1.8).

CONCLUSIONS:

Among children with moderate and severe exacerbations, IV-Mg is associated with increased exacerbation severity, increased risk for hospitalization, and no acceleration in exacerbation resolution among hospitalized participants.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Asma / Antiasmáticos Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Female / Humans / Male Idioma: En Revista: J Allergy Clin Immunol Pract Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Asma / Antiasmáticos Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Female / Humans / Male Idioma: En Revista: J Allergy Clin Immunol Pract Año: 2022 Tipo del documento: Article