紫外-拉曼自动机对儿童化疗制剂的分析控制:实施18个月后的结果和小体积制剂的合适方法的开发

T. Chouquet, G. Benoit, K. Morand
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引用次数: 5

摘要

背景:在法国,强烈建议控制化疗制剂。分析控制是鉴别和定量药物的首选方法。儿科制剂通常含有少量药物,并且最终体积很低,直到那时才进行分析控制。在开发和验证了一种新的紫外/拉曼自检(QCPrep +)小体积化疗制剂的采样和分析方法后,对患者使用的制剂进行了为期18个月的质量控制结果分析。方法从制剂类型(小体积和大体积)、单分子、操纵器和合格率分散度等方面进行了研究。结果在此期间,进行了7,548次对照,占我们产量的87.7%。75.5%的对照涉及小体积制剂(<50mL)。总体符合率为94.4%。符合率最低的是长春花生物碱、甲氨蝶呤和一些很少操作的药物(顺铂、地西他滨、表柔比星)。结果分散的研究表明,低浓度不符合增加,特别是儿科。这些结果显示了儿科制剂分析控制的局限性。对某些浓度和药物的分析灵敏度较低,需要补充质量控制工具,如照相机或视频。然而,这种新的分析方法使我们能够提高注射化疗回路的安全性。结论年轻患者可获得与成人患者相同的安全性和质量。一些关键点可以突出:制剂的均匀性,某些药物的分析敏感性和人为因素。这些数据使我们能够将工作重点放在员工培训、改进校准范围和开发补充控制工具上。
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Analytical Control of Pediatric Chemotherapy Preparations with a UV-Raman Automaton: Results After 18 Months of Implementation and Development of A Suitable Method for Low Volume Preparations
Abstract Background In France, control of chemotherapy preparations is highly recommended. Analytical control is a method of choice for identifying and quantifying drugs. Pediatric preparations, which often contain small quantities of drugs and are made in low final volumes were until then not analytically controlled. After the development and validation of a new sampling and assaying method for low volume chemotherapy preparations with an UV/Raman automaton (QCPrep +), the quality control results of the preparations intended for the patients were analyzed over a period of eighteen months Methods The results were studied by type of preparation (low and high volume), per molecule, manipulator, and conformity rates dispersion. Results Over the period, 7,548 controls were carried out, representing 87.7% of our production. 75.5% of these controls concerned low-volume preparations (<50mL). The overall conformity rate was 94.4%. The lowest conformity rates were found for vinca alkaloids, methotrexate and some rarely manipulated drugs (cisplatin, decitabine, epirubicin). The study of the results dispersion showed non-conformities increasing with low concentrations, specific to pediatrics. These results show the limits of analytical control for pediatric preparations. The low analytical sensitivity encountered for certain concentrations and drugs requires a complementary quality control tool, like camera or video. However this new analytical method allows us to improve the safety of the injectable chemotherapy circuit. Conclusion Young patients can benefit from the same level of safety and quality as adult patients. Some critical points could be highlighted: the homogenization of the preparations, the analytical sensitivity of some drugs and human factors. This data allow us to focus our work on staff training, improving our calibration ranges and on the development of complementary control tools.
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