The effect of auxiliary admixture equipment on the hygiene conditions and quality of Pharmacy Intravenous Admixture Services

Li, Guochun; Hong, Xu; Zhao, Huaibi; Deng, Gulin; Huang, Xinwu

doi:10.1007/s13204-022-02369-x

Cited by 2 publications

(2 citation statements)

References 4 publications

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“…To ensure the safe and e cient operation of PIVAS, various intelligent machines, and systems have been implemented, including labeling systems, infusion sequence annotation systems, review prescription databases, intelligent dispensing robots, and automatic infusion sorting devices (12)(13)(14) . However, the utilization of this equipment only addresses workload challenges and helps mitigate human errors in speci c aspects of the work ow.…”

Section: Constructionmentioning

confidence: 99%

Research on Capability Maturity Evaluation of Pharmacy Intravenous Admixture Services using Pharmacy Intravenous Admixture Services Data Reporting and Analysis Platform

Tian

Xie

Xu³

et al. 2023

Preprint

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Purpose: To enhance the capabilities of Pharmacy Intravenous Admixture Services (PIVAS) in ensuring the safety and appropriate utilization of intravenous medications in medical institutions. Methods: The Regional Pharmacy Intravenous Admixture Services Data Reporting and Analysis Platform (RPDRAP) was established in 2018. This platform comprises a data collection system and a data analysis system. The data collection system consists of 67 data items and utilizes network-based data collection. The collected data were analyzed using a model with 20 indicators within the data analysis system. Fifteen PIVAS participated in the platform's application evaluation. Results: The study revealed significant differences in PIVAS total score, supervisors, and workload between 2020 and 2022. The platform's application results demonstrated improvements in personnel management, work efficiency, and infection control within these PIVAS. Although statistical significance was observed in only 8 out of the 25 items, most of the scores showed an increase, with a small portion remaining unchanged and no decline in scores. Conclusions: This platform can be recommended for PIVAS homogeneous and regional efficient management. The use of this platform not only improves the quality control ability of PIVAS but also enables the management department to quickly grasp the current situation and characteristics of each PIVAS through standardized data collection and analysis.

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Section: Constructionmentioning

confidence: 99%

Research on Capability Maturity Evaluation of Pharmacy Intravenous Admixture Services using Pharmacy Intravenous Admixture Services Data Reporting and Analysis Platform

Tian

Xie

Xu³

et al. 2023

Preprint

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show abstract

“…[5][6][7][8] The goal of the PIVAS is to centrally and precisely dispense finished infusions using standard operating procedures. 9 However, at present, the PIVAS's inability to reasonably use drugs is mainly focused on the review of prescriptions [10][11][12] despite the lack of standardized management of the process from configuration to delivery of medication to the patient, which results in the placement time for finished infusion solutions being overlooked. The finished infusion solution that is configured at the PIVAS must undergo mixed dosing and preparation, pharmacist scanning and verification, dispensing, special distribution, handover, nurse verification, and finally, patient infusion.…”

Section: Introductionmentioning

confidence: 99%

Statistical analysis of the storage time of finished product infusion

Yuhan,

Qingqing,

Zhihui

et al. 2024

J Int Med Res

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Objective This retrospective study determined the storage time of finished infusion in each hospital ward and assessed whether the storage time of finished infusion was within an acceptable range. Methods The research object was the finished infusion (one bag of infusion with only one drug) that is centrally dosed at the Pharmacy Intravenous Admixture Service (PIVAS) of Jiading District Central Hospital Affiliated Shanghai University of Medicine & Health Sciences. We used an automatic scanner to assess the placement time of finished infusion products in various wards of the hospital. We classified the drugs used in various wards, analyzed whether their placement times were reasonable, assessed the reasons for unreasonable placement times, and took intervention measures. Similarly, the storage time of finished infusion was deemed reasonable or unreasonable, the reasons for unreasonable storage times were analyzed, and intervention measures were taken. Results In September 2021, the proportion of infusions stored for an unreasonable time was 12.69%, a decrease of 5.37% compared with August 2021, indicating the effectiveness of intervention measures. Conclusion By using statistical analysis and intervention measures, our PIVAS improved the standardized use of finished infusion products and ensured the safety of medication for patients.

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The effect of auxiliary admixture equipment on the hygiene conditions and quality of Pharmacy Intravenous Admixture Services

Cited by 2 publications

References 4 publications

Research on Capability Maturity Evaluation of Pharmacy Intravenous Admixture Services using Pharmacy Intravenous Admixture Services Data Reporting and Analysis Platform

Research on Capability Maturity Evaluation of Pharmacy Intravenous Admixture Services using Pharmacy Intravenous Admixture Services Data Reporting and Analysis Platform

Statistical analysis of the storage time of finished product infusion

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