在我的医院注射了适当的意图混合

Chairun Wiedyaningsih, Shalahuddin Al Madury, Rina Mutiara
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引用次数: 0

摘要

背景:静脉内混合制剂的制备过程是需要特别注意的阶段之一,以免影响所得制剂的质量。为了保持所生产产品的无菌性和确保其安全性,需要无菌技术。目的:根据指南和其他相关标准,确定静脉制剂实施的适宜性。方法:选取2022年10 - 11月在北京大学Muhammadiyah Wonosari医院进行的静脉注射制剂样品100份,采用检查表进行直接观察,并进行定量分析。结果:准备阶段的适宜性百分比为89%。制备阶段最适宜使用的是一次性口罩,占97%。本研究中静脉制剂的适宜性为54%。在工作台上准备所有设备和材料阶段(100%)和使用相容溶剂混合所有药物阶段(100%),每个评估项目的最高适宜性最高。结论:制剂过程中多数符合参考标准,但在静脉掺合阶段,均匀度仍较低,需改进无菌工艺
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kesesuaian Pencampuran Sediaan Injeksi Intravena di Rumah Sakit PKU Muhammadiyah Wonosari
Background: The process of intravenous admixture preparations is one of the stages that require special attention to not affect the quality of the resulting preparations. An aseptic technique is required to maintain the sterility of the product produced and ensure its safety.Objective: To identify the appropriateness of the implementation of intravenous admixture based on guidelines and other standard relevant.Methods: This research was conducted at PKU Muhammadiyah Wonosari Hospital in the October-November 2022 period with 100 samples of intravenous injection preparations, which were directly observed using a checklist sheet which was then analyzed quantitativelyResults: The percentage of suitability for the preparatory stage was 89% in the appropriate category. Most suitability in the preparation stage is the use of disposable masks, which is 97%. The suitability of the IV admixture preparations in this study was 54%. The highest suitability of each assessment item is the highest at the stage of preparing all equipment and materials on the workbench (100%) and All drugs mixed using a compatible solvent (100%). Conclusion: In the preparation process, most of them are in accordance with the referenced standards, but at the intravenous admixture stage, the evenness is still low, so improvements are needed to improve aseptic techniques
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