A randomized, controlled, double-blind trial comparing two loading doses of aminophylline

被引:8
作者
Hochwald C. [1 ]
Kennedy K. [2 ]
Chang J. [1 ]
Moya F. [2 ]
机构
[1] Memorial Hermann Children's Hospital, Houston, TX
[2] Department of Pediatrics, UT Houston School of Medicine, Houston, TX
关键词
D O I
10.1038/sj.jp.7210737
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学科分类号
摘要
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 6 mg/kg groups (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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页码:275 / 278
页数:3
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