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A Randomized, Controlled, Double-Blind Trial Comparing Two Loading Doses of Aminophylline

Abstract

OBJECTIVE: To compare 8 mg/kg and 6 mg/kg loading doses of aminophylline.

STUDY DESIGN: Sixty-one preterm infants weighing <1500 g were enrolled once a decision to administer intravenous aminophylline was made. A standard maintenance dose was used. Serum levels of theophylline were drawn 8 hours after the loading dose and before the fifth maintenance dose.

RESULTS: After the initial loading dose, the 8 mg/kg group achieved recommended serum theophylline levels (7–12 μg/ml) more frequently than the 6mg/kg group (39% vs 3%, p=0.002). Subsequent levels were similar between the groups. There were no increases in side effects with the higher loading dose.

CONCLUSION: If a clinical decision to start intravenous aminophylline therapy in preterm infants has been made, the use of an 8 mg/kg loading dose appears to be a better and safe way to quickly achieve serum theophylline levels within the recommended range.

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Reprints: Department of Pharmacy Services, Memorial Hermann Hospital, 6411 Fannin Street, Houston, TX 77030, USA

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Hochwald, C., Kennedy, K., Chang, J. et al. A Randomized, Controlled, Double-Blind Trial Comparing Two Loading Doses of Aminophylline. J Perinatol 22, 275–278 (2002). https://doi.org/10.1038/sj.jp.7210737

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