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评估一种数字化液体平衡监测技术的真实临床应用体验。

Evaluation of a real-life experience with a digital fluid balance monitoring technology.

机构信息

Department of Urology, Zealand University Hospital, Køge, Denmark.

Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

出版信息

Technol Health Care. 2024;32(6):3913-3924. doi: 10.3233/THC-231303.

Abstract

BACKGROUND

Innovations in healthcare technologies have the potential to address challenges, including the monitoring of fluid balance.

OBJECTIVE

This study aims to evaluate the functionality and accuracy of a digital technology compared to standard manual documentation in a real-life setting.

METHODS

The digital technology, LICENSE, was designed to calculate fluid balance using data collected from devices measuring urine, oral and intravenous fluids. Participating patients were connected to the LICENSE system, which transmitted data wirelessly to a database. These data were compared to the nursing staff's manual measurements documented in the electronic patient record according to their usual practice.

RESULTS

We included 55 patients in the Urology Department needing fluid balance charting and observed them for an average of 22.9 hours. We found a mean difference of -44.2 ml in total fluid balance between the two methods. Differences ranged from -2230 ml to 2695 ml, with a divergence exceeding 500 ml in 57.4% of cases. The primary source of error was inaccurate or omitted manual documentation. However, errors were also identified in the oral LICENSE device.

CONCLUSIONS

When used correctly, the LICENSE system performs satisfactorily in measuring urine and intravenous fluids, although the oral device requires revision due to identified errors.

摘要

背景

医疗技术的创新有潜力解决各种挑战,包括液体平衡的监测。

目的

本研究旨在评估数字技术在实际环境中的功能和准确性,并与标准的手动文档记录进行比较。

方法

数字技术 LICENSE 旨在使用从测量尿液、口服和静脉液体的设备中收集的数据来计算液体平衡。参与的患者被连接到 LICENSE 系统,该系统通过无线传输将数据传输到数据库。这些数据与护理人员根据其常规做法在电子病历中记录的手动测量值进行了比较。

结果

我们在泌尿科纳入了 55 名需要进行液体平衡图表记录的患者,平均观察时间为 22.9 小时。我们发现两种方法之间的总液体平衡差异为-44.2 毫升。差异范围从-2230 毫升到 2695 毫升,57.4%的情况下差异超过 500 毫升。主要误差源是不准确或遗漏的手动文档记录。然而,在口服 LICENSE 设备中也发现了误差。

结论

当正确使用时,LICENSE 系统在测量尿液和静脉液体方面表现良好,尽管由于已识别的误差,口服设备需要修订。

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