西爪哇省X医院内科住院病房非细胞抑制剂注射药物无菌配药的实施

Novita Sari, R. Sumarny, D. Laksmitawati, W. Nurcholis
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摘要

无菌配药活动是一个程序,以尽量减少从热原和污染物的威胁的药物制剂。本研究旨在确定2022年1月至2月期间西爪哇“X”医院内科住院病房实施非细胞抑制剂注射药物的无菌配药和静脉混合制剂的无菌性。这是一项采用横断面方法的描述性观察性前瞻性研究。研究人员直接观察了配药人员、房间和设备以及无菌配药活动的过程,包括无菌配药产品的制备、混合、储存和处置阶段以及无菌检验。根据研究结果,在收集到的150种静脉混合制剂中,稀释静脉制剂的活性为40种,包装成即食制剂的活性为100种,混合静脉制剂的活性为10种,房间适宜性为74%,制剂整理程序为68%,混合程序为44%,储存程序为100%,处置程序为63%。由此可见,西哇哇“X”医院内科住院病房非细胞抑制剂注射液的无菌配药不符合指南要求,特别是在混合工序阶段(≤50)。在混合静脉制剂的过程中,需要考虑配药人员的依从性和房间的清洁度。非细胞抑制剂注射剂无菌调剂过程中的污染鉴定结果显示,150个样品中有1个(0.66%)被污染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Implementation of Aseptic Dispensing for Non-Cytostatic Injectable Drugs in the Internal Medicine Inpatient Ward of 'X' Hospital, West Java
Aseptic Dispensing activity is a procedure to minimize pharmaceutical preparations from the threats of pyrogens and contaminants. This study aims to determine the implementation of aseptic dispensing for non-cytostatic injectable drugs and the sterility of intravenous mixed preparations in the Internal Medicine Inpatient Ward of 'X' hospital, West Java for the period January - February 2022. This was a descriptive observational prospective study with a cross sectional approach. Researchers made direct observations of dispensing personnel, room and equipment as well as the process of aseptic dispensing activities including the stages of preparation, mixing, storage and disposal as well as sterility test of aseptic dispensing products. Based on the study results, it was obtained that of the 150 intravenous mixed preparations collected, there were 40 activities of diluting intravenous preparations, 100 activities of packaging into ready-to-use preparations and 10 activities of mixing intravenous preparations into infusion fluids, room suitability by 74%, preparations arrangement procedure by 68%, mixing procedure by 44%, storage procedure by 100% and disposal procedure by 63%. It can be concluded that the aseptic dispensing of non-cytostatic injection drugs in the internal medicine inpatient ward of 'X' hospital, West Java was not in accordance with the guidelines, especially at the mixing procedure stage (≤50). Compliance of dispensing personnel and room cleanliness during the process of mixing intravenous preparations need to be considered. The result of the identification of contamination during  the aseptic dispensing activity of non-cytostatic injectable drugs showed that 1 in 150 samples (0.66%) was contaminated.
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