相关实验视频

Updated: Jun 7, 2025

A Semi-automated Approach to Preparing Antibody Cocktails for Immunophenotypic Analysis of Human Peripheral Blood

A Semi-automated Approach to Preparing Antibody Cocktails for Immunophenotypic Analysis of Human Peripheral Blood

Published on: February 8, 2016

对液体药物剂量的条形码辅助药物制备技术的评估

Niaz Deyhim¹, Mobolaji Adeola¹, Sunny B Bhakta¹

¹Department of Pharmacy Services, Houston Methodist Hospital, Houston, TX, USA.

American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists

|November 9, 2024

概括

卫生系统药房的条形码辅助药物制备 (BCMP) 技术改善了口服注射器剂量制备的安全性,并减少了药物浪费. 这个系统在两年内实现了高合规性,并提高了近乎失误的检测率.

科学领域:

药房实践在药房实践.
医疗信息学医疗信息学
患者安全患者安全

背景情况:

口服注射器剂量制备是卫生系统药房的关键过程.
在这个过程中确保准确性和安全性对于患者的福祉至关重要.
现有的工作流可能会出现错误的机会,需要技术集成.

研究的目的:

评估实施条码辅助药物制备 (BCMP) 技术和口服注射器剂量制备工作流程的结果.
评估BCMP对医药制剂安全性和效率在卫生系统药房中的影响.
通过BCMP集成来确定运营改进和潜在的废物减少.

主要方法:

一个集成电子医疗记录 (EMR) 的BCMP工作流程在一个中央药房中实施.
该研究评估了两年来对BCMP工作流程的遵守情况.
主要终点包括BCMP实施合规性和近乎失误检测率;次要终点集中在操作标记,IT需求和浪费避免上.

主要成果:

在两年内,实现了95%的BCMP工作流程合规率.
接近失误的检测率有所改善,受BCMP合规性增加的影响.
错误的成分警告有效地防止了错误,96.1%的警报导致取消了制剂.

结论:

集成EMR的BCMP技术显著提高了口服注射器剂量制备的安全性.
对BCMP的实施为运营绩效和数量指标提供了有价值的见解.
该技术有助于减少药房环境中的潜在药物浪费.

关键词:

条形码技术条形码技术数字医疗保健数字医疗保健开支准备开支准备准备液体药物液体药物液体药物药房药房药房药房技术技术的技术技术的技术.

更多相关视频

Automated Acoustic Dispensing for the Serial Dilution of Peptide Agonists in Potency Determination Assays

Automated Acoustic Dispensing for the Serial Dilution of Peptide Agonists in Potency Determination Assays

Published on: November 10, 2016

Automated Robotic Liquid Handling Assembly of Modular DNA Devices

Automated Robotic Liquid Handling Assembly of Modular DNA Devices

Published on: December 1, 2017

相关概念视频

Factors Influencing Drug Absorption: Pharmaceutical Parameters

Factors Influencing Drug Absorption: Pharmaceutical Parameters

Solid dosage forms such as tablets and capsules undergo rigorous manufacturing processes to ensure stability and effectiveness. Their dissolution and absorption properties are influenced significantly by the choice of excipients (inactive ingredients that serve various roles in the formulation), and the methodology applied during production. The manufacturing parameters, such as compression force and granulation techniques, significantly affect dissolution rates. Elevated compression forces...