• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

了解药物配制问题。

Understanding medication compounding issues.

作者信息

Hicks Rodney W

出版信息

AORN J. 2014 Apr;99(4):466-76; quiz 477-9. doi: 10.1016/j.aorn.2013.07.021.

DOI:10.1016/j.aorn.2013.07.021
PMID:24674793
Abstract

The potential for contamination of compounded products and the resulting infections are a serious threat to patient safety. Immediate use products are used frequently in the perioperative department, and perioperative nurses should be familiar with the guidelines and practices that aim to reduce the contamination that can occur during the sterile compounding process. Four common themes lead to successful compounding: quality (eg, product identification, purity, stability, compatibility, risk level assessment), the environment (eg, using a segregated compounding area with specialized airflow capabilities, reducing particulate matter, practicing proper hand hygiene, performing gloved fingertip sampling, properly cleaning equipment and work areas), personnel activities (eg, familiarity with types of containers used and how often they can be accessed, following expiration dates and the number of times containers can be accessed), and the control process (eg, process monitoring, quality improvement). If a third-party vendor is contracted to handle compounding for a facility, perioperative personnel should be aware of the responsibilities for the facility and the vendor to ensure a quality compounding program.

摘要

复方制剂受污染的可能性以及由此引发的感染对患者安全构成严重威胁。即配即用产品在围手术期科室经常使用,围手术期护士应熟悉旨在减少无菌配制过程中可能发生污染的指南和操作规范。成功配制有四个共同主题:质量(如产品识别、纯度、稳定性、兼容性、风险水平评估)、环境(如使用具有专门气流能力的隔离配制区域、减少颗粒物、正确进行手部卫生、进行戴手套指尖采样、正确清洁设备和工作区域)、人员活动(如熟悉所用容器的类型及其可取用的频率、遵循有效期以及容器可取用的次数)以及控制过程(如过程监测、质量改进)。如果与第三方供应商签约为医疗机构处理配制工作,围手术期人员应了解医疗机构和供应商的职责,以确保有一个高质量的配制计划。

相似文献

1
Understanding medication compounding issues.了解药物配制问题。
AORN J. 2014 Apr;99(4):466-76; quiz 477-9. doi: 10.1016/j.aorn.2013.07.021.
2
Survey of sterile product compounding practices in Canadian hospital pharmacies.加拿大医院药房无菌产品配制实践调查。
Can J Hosp Pharm. 1993 Dec;46(6):249-60.
3
National survey of quality assurance activities for pharmacy-prepared sterile products in hospitals.医院药房配制无菌产品质量保证活动的全国性调查。
Am J Hosp Pharm. 1991 Nov;48(11):2398-413.
4
Compounding parenteral nutrition: reducing the risks.肠外营养配制:降低风险
Nutr Clin Pract. 2009 Aug-Sep;24(4):441-6. doi: 10.1177/0884533609339070.
5
Equipment, supplies, and facilites required for hospital compounding.医院配制所需的设备、耗材和设施。
Int J Pharm Compd. 2006 Nov-Dec;10(6):436-41.
6
Potential for airborne contamination in turbulent- and unidirectional-airflow compounding aseptic isolators.紊流和单向气流复合无菌隔离器中空气传播污染的可能性。
Am J Health Syst Pharm. 2007 Mar 15;64(6):622-31. doi: 10.2146/ajhp060067.
7
Compounding pharmacy conundrum: "we cannot live without them but we cannot live with them" according to the present paradigm.根据目前的模式,药剂师面临着一个难题:“没有他们我们无法生存,但我们又不能与他们共存”。
Chest. 2013 Apr;143(4):896-900. doi: 10.1378/chest.13-0212.
8
End-preparation assessments and tests for compounded sterile preparations.复方无菌制剂的终末配制评估与测试
Int J Pharm Compd. 2013 Jul-Aug;17(4):307-11.
9
Establishing powder-handling workflow practices and standard operating procedures: compounding pharmacy and safety.
Int J Pharm Compd. 2014 May-Jun;18(3):222-6.
10
The standardization of nonsterile compounding: a study in quality control and assessment for hormone compounding.非无菌配制的标准化:激素配制的质量控制与评估研究
Int J Pharm Compd. 2014 Mar-Apr;18(2):162-8.