首页> 外文期刊>Therapeutic Drug Monitoring >Severe side effects and drug plasma concentrations in preterm infants treated with doxapram.
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Severe side effects and drug plasma concentrations in preterm infants treated with doxapram.

机译:用多沙普仑治疗的早产儿的严重副作用和药物血浆浓度。

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A high-performance liquid chromatography method has been developed for simultaneous determination of doxapram and its metabolites including ketodoxapram, the main and only active metabolite. The aim of the study was to evaluate this microtechnique and to report the cases involving severe adverse effects to determine toxic plasma levels in neonates. The method was found to be selective, and showed a good baseline separation of doxapram and metabolites. Recovery, linearity, intraday/interday precision, and limit of detection determined in aqueous solutions and in spiked plasma were satisfactory. The assay is simple, rapid, and plasma-sparing, which represents a true advantage in managing neonates. Case analysis was performed in two consecutive periods: 124 preterm infants in the first period and 173 in the second period. Severe toxic effects were observed in 4 cases in the first period, with doxapram plus keto-doxapram levels 9 mg/L. In the second period, only one case was observed. High-range plasma concentrations were significantly less frequent in the second period than in the first one. The authors conclude that measuring doxapram plus keto-doxapram in plasma may be of interest to avoid severe toxic effects in preterm neonates treated with doxapram.
机译:已开发出一种高效液相色谱方法,用于同时测定多沙普仑及其代谢物,包括主要和唯一的活性代谢物酮多沙普仑。该研究的目的是评估这种微技术并报告涉及严重不良反应的病例,以确定新生儿的毒性血浆水平。发现该方法具有选择性,并且显示了多沙普兰和代谢物的良好基线分离。在水溶液和加标血浆中测定的回收率,线性,日间/日间精度和检测极限均令人满意。该测定方法简单,快速且可保留血浆,这代表了在管理新生儿方面的真正优势。病例分析连续两个时期进行:第一期124例早产儿,第二期173例。在第一阶段中有4例患者观察到严重的毒性作用,多沙普仑加酮-多沙普仑的水平为9 mg / L。在第二阶段,仅观察到一个案例。在第二阶段,高范围血浆浓度的发生频率明显低于第一阶段。作者得出结论,在血浆中测量多沙普仑加酮-多沙普仑可能对避免用多沙普仑治疗的早产儿产生严重的毒性作用感兴趣。

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