Nebulized magnesium for moderate and severe pediatric asthma: A randomized trial

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Abstract

7. Blinded active therapy significantly increased blood magnesium level 2 hr post-treatment completion compared to placebo, 0.85 vs 0.82 mmol/L, P = 0.001. There were no important adverse effects. Accelerated failure time analysis showed a non-significantly shortened time to medical readiness for discharge of 14% favoring the magnesium sulfate group, OR = 1.14, 95% CI 0.93 to 1.40, P = 0.20. Mean times until readiness for discharge were 14.7 hr [SD 9.7] versuss 15.6 hr [SD 11.3] for the investigational and placebo groups, respectively, P = 0.41. Conclusions Adding nebulized magnesium to combined nebulized bronchodilator and systemic steroid therapy failed to significantly shorten time to discharge of pediatric patients with moderate or severe asthma. Pediatr Pulmonol. 2015; 50:1191-1199.

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Alansari, K., Ahmed, W., Davidson, B. L., Alamri, M., Zakaria, I., & Alrifaai, M. (2015). Nebulized magnesium for moderate and severe pediatric asthma: A randomized trial. Pediatric Pulmonology, 50(12), 1191–1199. https://doi.org/10.1002/ppul.23158

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