危重病护理人员非医学授权用血培训试验。

Hazel Smith, Heidi Doughty
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引用次数: 0

摘要

空中救护人员院前输血的使用正在增加。输血传统上是由医生“授权”的,而不是处方。然而,越来越多的人有兴趣将授权能力扩展到其他从业者-即非医疗授权(NMA)。自2007年以来,英国的护士和助产士框架已经存在,但对重症护理护理人员(CCPs)的培训一直有限。院前血液制品复苏(RePHILL)试验于2016年启动,需要院前给药红细胞和LyoPlas。最初的授权仅限于医生,导致医护人员错过了招聘。试验方案于2019年进行了修订,允许在适当的培训和利益相关者咨询后进行NMA。我们提出了一个有针对性的培训方案,旨在支持院前试验框架内护理人员主导的输血。我们考虑了NMA所需的知识和技能,并将其与护理人员培训的基线知识进行比较,以确定培训差距。我们研究了现有的军事和民用NMA培训的例子,以制定一个针对单一空中救护车的目标方案。我们的培训计划包括四项内容:课程前的在线培训、之前的试用参与、面对面培训和能力评估。培训对象为3名中心控制人员,他们将培训扩展到14名同事。培训时间是一个上午,包括面对面的培训和评估。新颖的主题包括输血的生理触发和院前环境中的输血风险。鼓励护理人员识别和报告不良事件的新模式。反思性反馈表明,该项目为中央医院提供了自主招募试验患者和批准输血的知识。
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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Training trial of critical care paramedics for non-medical authorisation of blood.

The use of pre-hospital blood transfusion by air ambulance crews is increasing. Blood transfusion is traditionally 'authorised' by doctors, not prescribed. However, there is an increasing interest in extending the capability of authorisation to other practitioners - that is, non-medical authorisation (NMA). A UK framework for nurses and midwives has existed since 2007, but training for critical care paramedics (CCPs) has been limited. The Resuscitation with Pre-Hospital Blood Products (RePHILL) trial was launched in 2016, requiring pre-hospital administration of red cells and LyoPlas. Authorisation was initially restricted to doctors, leading to missed recruitment by paramedic-only crews. The trial protocol was amended in 2019 to permit NMA following suitable training and stakeholder consultation. We present a targeted training programme designed to support paramedic-led transfusion within the framework of the pre-hospital trial. We considered the knowledge and skills required for NMA and compared this with baseline knowledge from paramedic training to identify the training gap. We examined examples of existing military and civilian NMA training to develop a targeted programme for a single air ambulance. The four elements of our training programme were pre-course online training, previous trial participation, face-to-face training and competency assessment. Training was delivered to three CCPs, who cascaded the training to 14 colleagues. The training time was one morning, including a face-to-face session and assessment. Novel topics included physiological triggers for transfusion and transfusion risks in the pre-hospital environment. Paramedics were encouraged to recognise and report new patterns of adverse events. Reflective feedback suggests the programme provided CCPs the knowledge to autonomously recruit trial patients and authorise transfusion.

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