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了解多巴胺和多巴酚丁胺在模拟新生儿病房条件下24小时内的稳定性。

Understanding the Stability of Dopamine and Dobutamine Over 24 h in Simulated Neonatal Ward Conditions.

作者信息

Kirupakaran Katherine, Mahoney Liam, Rabe Heike, Patel Bhavik A

机构信息

Brighton and Sussex Medical School, Brighton, UK.

Department of Neonatology, Brighton and Sussex University Hospital NHS Trust, Brighton, UK.

出版信息

Paediatr Drugs. 2017 Oct;19(5):487-495. doi: 10.1007/s40272-017-0234-4.

Abstract

OBJECTIVES

Our objectives were to investigate the possible effects of temperature and light on the stability of dopamine and dobutamine continuous infusions over 24 h when prepared in a variety of dilution vehicles.

METHODS

Syringe-driver infusion apparatuses were set up for dopamine and dobutamine diluted with either 0.9% sodium chloride (NaCl) or 5% glucose delivering 3 and 5 μg/kg/min, respectively, via 206-cm extension sets. All infusions were prepared for a neonate weight of 1 kg. Infusions were run over 24 h with approximately half the tubing within an incubator set at 35 °C. Cyclic voltammetry was used to monitor the concentration of the inotrope within the syringe and at the end of the extension set, both initially and after 24 h.

RESULTS

The variation in the concentration of dopamine and dobutamine in the vials (n = 6) was 3.58 and 1.22%, respectively. This variation increased to 10.88% for dopamine and 5.76% for dobutamine in the syringe. After 24 h, a significant reduction in the concentration of dopamine was observed at the end of the extension set when prepared in 0.9% NaCl versus 5% glucose (p < 0.001; n = 6-7) and in dobutamine when prepared in 0.9% NaCl (p < 0.001; n = 6-7). No differences in the concentration of dopamine prepared in 0.9% NaCl were observed after 24 h in light-exposed and light-protected extension sets (n = 6-7).

CONCLUSIONS

Dobutamine is more stable in dilution vehicles than dopamine, and inotropes are more stable in the 5% glucose dilution vehicle than in 0.9% NaCl. Such findings will provide guidance on the choice of inotropes.

摘要

目的

我们的目的是研究在多种稀释溶媒中配制时,温度和光照对多巴胺和多巴酚丁胺持续输注24小时稳定性的可能影响。

方法

设置注射器驱动输注装置,用于分别用0.9%氯化钠(NaCl)或5%葡萄糖稀释的多巴胺和多巴酚丁胺,通过206厘米延长管分别以3和5μg/kg/分钟的速度输注。所有输注液均针对体重1kg的新生儿配制。输注持续24小时,约一半的延长管置于温度设定为35°C的培养箱内。采用循环伏安法监测注射器内及延长管末端在初始时和24小时后的血管活性药物浓度。

结果

小瓶(n = 6)中多巴胺和多巴酚丁胺浓度的变化分别为3.58%和1.22%。注射器中多巴胺的这种变化增加到10.88%,多巴酚丁胺增加到5.76%。24小时后,当用0.9% NaCl与5%葡萄糖配制时,在延长管末端观察到多巴胺浓度显著降低(p < 0.001;n = 6 - 7),用0.9% NaCl配制的多巴酚丁胺也出现这种情况(p < 0.001;n = 6 - 7)。在光照和避光的延长管中,24小时后用0.9% NaCl配制的多巴胺浓度未观察到差异(n = 6 - 7)。

结论

多巴酚丁胺在稀释溶媒中比多巴胺更稳定,血管活性药物在5%葡萄糖稀释溶媒中比在0.9% NaCl中更稳定。这些发现将为血管活性药物的选择提供指导。

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