A Mobile Application to Reduce Time to Calculate Medication Dosage and Medication Administration Errors in Simulated Pediatric and Neonatal Settings: A Research Protocol for a Cross-Over, Randomized Controlled Trial

IF 2.1 Q2 MEDICINE, GENERAL & INTERNAL
Somaye Norouzi, Zahra Sarkohi, Leila Alizadeh, Leila Ahmadian
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引用次数: 0

Abstract

Background

Pediatric and neonate medication safety is a major issue. Children are at a higher risk of adverse drug events and medication errors than adults. As the mediation administration is the final stage of protection to impede potential unintentional adverse effects on patients. Thus, there is a strong need for research to explore new ways of reducing medication administration errors and time to calculate medication dosage in the pediatric and neonatal context. The objective is to assess the effectiveness of the Medication Administration Clinical Decision Support Systems (MACDSS) compared to the traditional method in a simulated environment for pediatric and neonatal care.

Methods

An open-label (unmasked), two-treatment, two-period, cross-over randomized controlled trial will be conducted in pediatric and neonatal settings with simulated scenarios to assess time to calculate medication dosage and medication administration errors with the MACDSS application compared to the traditional method. This study will recruit 16 participants randomly (1:1) from the Afzali-poor hospital in Kerman. The participants are supposed to perform nine highly realistic scenarios, three at a high level of complexity, three at a medium level, and three simple scenarios. For the cross-over stage, different scenarios at the same level of complexity will be presented. The main outcome will be the time spent to calculate the drug dosage by the nurse.

Conclusion

Developing a MACDSS as a mobile application may significantly improve the time needed to calculate dosage or amount and lower medication administration errors. If this application proves to be effective, it can be a very cost-effective means of improving outcomes in the medication administration process, positively affecting many pediatrics and neonates' patients.

Trial Registration

Irct.behdasht.gov.ir, ID: IRCT20240409061457N1 registered on June 22, 2024.

Abstract Image

在模拟儿科和新生儿环境中减少计算药物剂量和给药错误时间的移动应用程序:一项交叉、随机对照试验的研究方案
儿童和新生儿用药安全是一个重大问题。儿童发生药物不良事件和用药错误的风险高于成人。由于调解给药是防止对患者潜在的意外不良影响的最后保护阶段。因此,迫切需要研究探索减少儿科和新生儿用药错误和计算用药剂量时间的新方法。目的是评估药物管理临床决策支持系统(MACDSS)在儿科和新生儿护理模拟环境中与传统方法相比的有效性。方法采用开放标签(无遮盖)、两治疗、两期、交叉随机对照试验,在儿童和新生儿环境中模拟情景,评估MACDSS应用与传统方法相比计算给药剂量的时间和给药误差。本研究将从克尔曼的阿夫扎利贫困医院随机(1:1)招募16名参与者。参与者需要完成9个高度真实的场景,3个高度复杂的场景,3个中等复杂的场景,3个简单的场景。在交叉阶段,将呈现相同复杂程度的不同场景。主要结果将是护士计算药物剂量所花费的时间。结论将MACDSS开发为移动应用程序可显著缩短计算剂量或用量的时间,减少给药错误。如果这种应用被证明是有效的,它可以是一种非常经济有效的手段,可以改善药物管理过程的结果,对许多儿科和新生儿患者产生积极影响。试验注册号:IRCT20240409061457N1,注册日期为2024年6月22日。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Health Science Reports
Health Science Reports Medicine-Medicine (all)
CiteScore
1.80
自引率
0.00%
发文量
458
审稿时长
20 weeks
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