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临床试验/NCT03921346
NCT03921346已完成不适用

A Mobile Device App to Reduce Prehospital Medication Errors and Time to Drug Preparation and Delivery by EMS During Simulated Pediatric Cardiopulmonary Resuscitation: a Multicenter, Prospective, Randomized, Controlled Trial

Pediatric Clinical Research Platform1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2019年9月3日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
150
试验地点
1
主要终点
Medication Dosage Errors

研究概览

简要总结

The study investigators will recruit paramedics in many Emergency Medical Services (EMS) in Switzerland to prepare direct intravenous (IV) emergency drugs during a standardized simulation-based pediatric out-of-hospital cardiac arrest scenario. According to randomization, each paramedic will be asked to prepare sequentially 4 IV emergency drugs (epinephrine, midazolam, dextrose 10%, sodium bicarbonate 4.2%) following either their current conventional methods or by the aim of a mobile device app. This app is designed to support drug preparation at pediatric dosages. In a previous multicenter randomized trial with nurses, the investigators reported the ability of this app to significantly reduce in-hospital continuous infusion medication error rates and drug preparation time compared to conventional preparation methods during simulation-based resuscitations. In this trial, the aim was to assess this app during pediatric out-of-hospital cardiopulmonary resuscitation with paramedics.

详细描述

Children represent a vulnerable population with specific medical needs compared to adults. Fast, accurate, and safe preparation and administration of IV drugs is both complex and time consuming in pediatric critical situations, such as cardiopulmonary resuscitation (CPR). Most drugs given IV to children are provided in vials originally prepared for the adult population, which leads to the need for a specific individual, weight-based drug dose calculation and preparation for each child that varies widely across age groups. This error-prone process and the lower dosing error tolerance of children place them at a high risk for life-threatening medication errors. Despite well equipped and staffed environments with numerous available safeguards, direct IV medication errors have been reported in up to 41% of cases during simulated in-hospital pediatric resuscitations, 65% of which were incorrect medication dosage, making it the most common error. The rate of errors is also important in the prehospital setting, occurring in more than 30% of all pediatric drugs administered. As paramedics have little exposure to critically ill children, they have limited opportunities to administer resuscitation drugs at pediatric doses and to train this skill.

Moreover, in resuscitation, time is inversely correlated to survival. During the first 15 min of in-hospital pediatric CPR, survival and favorable neurological outcome decrease linearly by 2,1% and 1,2% per min, respectively, and rely in part on drug preparation time either in- or out-of-hospital. Among non-shockable pediatric out-of-hospital cardiac arrests, each minute delay to epinephrine delivery is associated with 9% decrease in the odds of survival. Regrettably, in the prehospital setting, the majority of patients receive epinephrine more than 10 minutes after EMS arrival. The chain of survival therefore critically relies on early out-of-hospital CPR by EMS, and onsite administration of IV emergency drugs without delay before a rapid transfer to pediatric emergency departments and advanced care.

In a previous multicenter, randomized crossover trial, medication errors, time to drug preparation, and time to drug delivery for continuous infusions during simulation-based pediatric in-hospital postcardiac arrest scenarios were significantly reduced by using a mobile device app - the pediatric accurate medication in emergency situations (PedAMINES™) app - designed to help pediatric drug preparation.

The present multicenter trial aims to compare the impact of this app with conventional calculation methods for the preparation of direct IV drugs during standardized, simulation-based, pediatric out-of-hospital cardiac arrest scenarios. The investigators hypothesized that use of the app might extend and scale up the previous multicenter in-hospital observations by similarly reducing occurrence of medication errors and time to drug preparation and delivery when used by paramedics in out-of-hospital settings.

In this trial, the investigators will recruit paramedics in many EMS in Switzerland to prepare direct IV emergency drugs during a standardized simulation-based pediatric out-of-hospital cardiac arrest scenario with a high-fidelity WiFi manikin (Laerdal SimBaby). The scenario will take place out-of-hospital in a simulated children's room to increase realism.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

盲法说明

Blinding to the direct IV drugs and doses intended for use will be maintained during recruitment to minimize preparation bias. Allocation concealment will be ensured with an allocation software and not released until the paramedics start the scenario. Study team members will be revealed to the participants just before the scenario starts. Paramedics will be unblinded when the simulated scenario starts. Although the intervention could not be masked, all investigators will remain unaware of the outcomes until all data will be unlocked for analysis at the end of the trial. All scenarios will be video-recorded for later analysis. Post-scenario video review will be done without blinding by two reviewers, but undertaken independently and blinded to each other's reviews. In case of disagreement, a third independent evaluator will help reach a consensus. The data analyst will be blinded to treatment allocation.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •To be paramedic certified
  • •To know how to prepare direct IV drugs
  • •To have previously completed the 5-minute introductory course to the use of the app PedAMINES™ dispensed by the study investigators
  • •Participation agreement

排除标准

  • •To have at any time previously used the app PedAMINES™
  • •To have not undergone the 5-minute introductory course to the use of the app PedAMINES™

研究组 & 干预措施

Arm A (mobile device app)

Experimental

Paramedics preparing drugs with the help of the mobile device app PedAMINES™.

Each paramedic will have to prepare sequentially 4 direct IV emergency drugs with the help of the mobile device app PedAMINES™.

干预措施: Mobile device app (PedAMINES™) 1st drug (Device)

Arm A (mobile device app)

Experimental

Paramedics preparing drugs with the help of the mobile device app PedAMINES™.

Each paramedic will have to prepare sequentially 4 direct IV emergency drugs with the help of the mobile device app PedAMINES™.

干预措施: Mobile device app (PedAMINES™) 2nd drug (Device)

Arm A (mobile device app)

Experimental

Paramedics preparing drugs with the help of the mobile device app PedAMINES™.

Each paramedic will have to prepare sequentially 4 direct IV emergency drugs with the help of the mobile device app PedAMINES™.

干预措施: Mobile device app (PedAMINES™) 3rd drug (Device)

Arm A (mobile device app)

Experimental

Paramedics preparing drugs with the help of the mobile device app PedAMINES™.

Each paramedic will have to prepare sequentially 4 direct IV emergency drugs with the help of the mobile device app PedAMINES™.

干预措施: Mobile device app (PedAMINES™) 4th drug (Device)

Arm B (conventional preparation method)

Active Comparator

Paramedics preparing drugs with the help of conventional method.

Each paramedic will have to prepare sequentially 4 direct IV emergency drugs with the help of conventional method

干预措施: Conventional method 1st drug (Device)

Arm B (conventional preparation method)

Active Comparator

Paramedics preparing drugs with the help of conventional method.

Each paramedic will have to prepare sequentially 4 direct IV emergency drugs with the help of conventional method

干预措施: Conventional method 2nd drug (Device)

Arm B (conventional preparation method)

Active Comparator

Paramedics preparing drugs with the help of conventional method.

Each paramedic will have to prepare sequentially 4 direct IV emergency drugs with the help of conventional method

干预措施: Conventional method 3rd drug (Device)

Arm B (conventional preparation method)

Active Comparator

Paramedics preparing drugs with the help of conventional method.

Each paramedic will have to prepare sequentially 4 direct IV emergency drugs with the help of conventional method

干预措施: Conventional method 4th drug (Device)

结局指标

主要结局

Medication Dosage Errors

时间窗: 20 minutes

To measure in each allocation group the number and percentage of medication dosage containing errors that occur during the sequence from drug preparation to drug injection. We define an emergency medication dose administration error as a failure in drug preparation if at least one of the following errors is committed: a deviation in drug dose of more than 10% from the correct weight dose; inability to calculate drug dosage without guidance help from the paramedic investigator (LB) leading the resuscitation in the room; and/or (because of its clinical relevance) a deviation of more than 10% of the final administered concentration of sodium bicarbonate from the prescribed 4.2% concentration. These errors will be measured both as the percentage deviation from the amount of delivered drug compared with the correct weight dose as prescribed by the physician and the absolute deviations from that dose.

次要结局

  • Time to Drug Preparation and Time to Drug Delivery(20 minutes)
  • Type of Medication Errors(During each of the 4 drug preparations, an average of 20 minutes per drug preparation.)
  • Perceived Stress(At preintervention and postintervention, a total of 20 minutes will be used to complete the STAI questionnaire.)
  • Stress Level Measured by Heart Rate Monitoring (Smartwatch).(Baseline, recovery, and during each of the 4 drug preparations, a total of 20 minutes per participant will be used to continuously record heart rates on the smartwatch. Maximal HRpeak is the maximum HR across all preparations)
  • Unified Theory of Acceptance and Use of Technology (UTAUT) Questionnaire and System Usability Score (SUS)(60 minutes)

研究者

发起方
Pediatric Clinical Research Platform
申办方类型
Other
责任方
Principal Investigator
主要研究者

Johan Siebert, MD

MD: Deputy Head

University Hospital, Geneva

研究点 (1)

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