院前现场分诊的安全指数(SINEPOST)研究:风险预测模型的开发和验证,以支持救护车临床转运决策现场-a协议。

Jamie Miles, Richard Jacques, Janette Turner, Suzanne Mason
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引用次数: 2

摘要

背景:对救护车服务和急诊科(ED)的需求每年都在上升,当这两个系统的需求都过高时,救护人员在急诊室排队等待将病人交给病人。一些救护车运送的病人是“低敏锐度”,不需要急诊科治疗。然而,护理人员发现准确识别这些病人是一项挑战。决策支持工具已经开发利用专家意见来帮助识别这些低敏锐度患者,但未能显示出超出常规决策的好处。预测算法可能能够建立准确的模型,这些模型可以在现场使用,以支持不将低视力患者送往急诊室的决定。方法和分析:2019年7月至2020年2月期间,约克郡所有被救护车送往急诊室的患者都将被纳入其中。救护车电子病人护理记录(ePCR)临床数据将被用作模型的候选预测因子。然后这些将被链接到相应的ED记录,该记录记录了“非紧急出勤”的结果。估计样本量为52,958,有4767个事件,EPP为7.48。XGBoost算法将用于模型开发。首先,将使用所有数据导出一个模型,并评估表观性能。然后,内部-外部验证将使用非随机嵌套交叉验证(CV),并为每个ED(空间验证)提供测试集。所有模型建立后,将进行随机效应荟萃分析。这将汇集诸如拟合优度、鉴别和校准等性能度量。它还将生成预测区间并度量集群之间的异质性。完整模型的性能将使用合并的结果进行更新。讨论:在这一领域创建风险预测模型将导致临床决策支持工具的进一步发展,以确保每个救护车患者都能在第一时间到达正确的护理地点。如果这项研究成功,它可以帮助护理人员在病人离开现场之前评估将他们送到急诊科的好处。它还可以减少紧急护理系统的拥堵。试验注册:本研究在ISRCTN上回顾性注册:12121281。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Safety INdEx of Prehospital On Scene Triage (SINEPOST) study: the development and validation of a risk prediction model to support ambulance clinical transport decisions on-scene-a protocol.

The Safety INdEx of Prehospital On Scene Triage (SINEPOST) study: the development and validation of a risk prediction model to support ambulance clinical transport decisions on-scene-a protocol.

Background: Demand for both the ambulance service and the emergency department (ED) is rising every year and when this demand is excessive in both systems, ambulance crews queue at the ED waiting to hand patients over. Some transported ambulance patients are 'low-acuity' and do not require the treatment of the ED. However, paramedics can find it challenging to identify these patients accurately. Decision support tools have been developed using expert opinion to help identify these low acuity patients but have failed to show a benefit beyond regular decision-making. Predictive algorithms may be able to build accurate models, which can be used in the field to support the decision not to take a low-acuity patient to an ED.

Methods and analysis: All patients in Yorkshire who were transported to the ED by ambulance between July 2019 and February 2020 will be included. Ambulance electronic patient care record (ePCR) clinical data will be used as candidate predictors for the model. These will then be linked to the corresponding ED record, which holds the outcome of a 'non-urgent attendance'. The estimated sample size is 52,958, with 4767 events and an EPP of 7.48. An XGBoost algorithm will be used for model development. Initially, a model will be derived using all the data and the apparent performance will be assessed. Then internal-external validation will use non-random nested cross-validation (CV) with test sets held out for each ED (spatial validation). After all models are created, a random-effects meta-analysis will be undertaken. This will pool performance measures such as goodness of fit, discrimination and calibration. It will also generate a prediction interval and measure heterogeneity between clusters. The performance of the full model will be updated with the pooled results.

Discussion: Creating a risk prediction model in this area will lead to further development of a clinical decision support tool that ensures every ambulance patient can get to the right place of care, first time. If this study is successful, it could help paramedics evaluate the benefit of transporting a patient to the ED before they leave the scene. It could also reduce congestion in the urgent and emergency care system.

Trial registration: This study was retrospectively registered with the ISRCTN: 12121281.

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