Wong Ambrose H, Sapre Atharva V, Wang Kaicheng, Nath Bidisha, Shah Dhruvil, Kumar Anusha, Faustino Isaac V, Desai Riddhi, Hu Yue, Robinson Leah, Meng Can, Tong Guangyu, Bernstein Steven L, Yonkers Kimberly A, Melnick Edward R, Dziura James D, Taylor R Andrew
Department of Emergency Medicine, Yale School of Medicine, New Haven, Connecticut.
Department of Biostatistics, Yale School of Public Health, New Haven, Connecticut.
JAMA Netw Open. 2025 May 1;8(5):e258927. doi: 10.1001/jamanetworkopen.2025.8927.
Agitation events are increasing in emergency departments (EDs), exacerbating safety risks for patients and clinicians. A wide range of clinical etiologies and behavioral patterns in the emergency setting make agitation prediction difficult in this setting.
To develop, train, and validate an agitation-specific prediction model based on a large, diverse set of past ED visit data.
DESIGN, SETTING, AND PARTICIPANTS: This cohort study included electronic health record data collected from 9 ED sites within a large, urban health system in the Northeast US. All ED visits featuring patients aged 18 years or older from January 1, 2015, to December 31, 2022, were included in the analysis and modeling. Data analysis occurred between May 2023 and September 2024.
Variables that served as potential exposures of interest, encompassing demographic information, patient history, initial vital signs, visit information, mode of arrival, and health services utilization.
The primary outcome of agitation was defined as the presence of an intramuscular chemical sedation and/or violent physical restraint order during an ED visit. A clinical model was developed to identify risk factors that predict agitation development during an ED visit prior to symptom onset. Model performance was measured using area under the receiver operating characteristic curve (AUROC) and area under the precision recall curve (PR-AUC).
The final cohort comprised 3 048 780 visits. The cohort had a mean (SD) age of 50.2 (20.4) years, with 54.7% visits among female patients. The final artificial intelligence model used 50 predictors for the primary outcome of predicting agitation events. The model achieved an AUROC of 0.94 (95% CI, 0.93-0.94) and a PR-AUC of 0.41 (95% CI, 0.40-0.42) in cross-validation, indicating good discriminative ability. Calibration of the model was evaluated and demonstrated robustness across the range of predicted probabilities. The top predictors in the final model included factors such as number of past ED visits, initial vital signs, medical history, chief concern, and number of previous sedation and restraint events.
Using a cross-sectional cohort of ED visits across 9 hospitals, the prediction model included factors for detecting risk of agitation that demonstrated high accuracy and applicability across diverse patient populations. These results suggest that clinical application of the model may enhance patient-centered care through preemptive deescalation and prevention of agitation.
急诊科的躁动事件不断增加,加剧了患者和临床医生面临的安全风险。急诊环境中广泛的临床病因和行为模式使得在此环境下进行躁动预测变得困难。
基于大量多样的既往急诊就诊数据,开发、训练并验证一个特定于躁动的预测模型。
设计、地点和参与者:这项队列研究纳入了从美国东北部一个大型城市卫生系统内的9个急诊科收集的电子健康记录数据。分析和建模纳入了2015年1月1日至2022年12月31日期间所有18岁及以上患者的急诊就诊情况。数据分析于2023年5月至2024年9月进行。
作为潜在感兴趣暴露因素的变量,包括人口统计学信息、患者病史、初始生命体征、就诊信息、到达方式和医疗服务利用情况。
躁动的主要结局定义为急诊就诊期间存在肌内注射化学镇静和/或暴力身体约束医嘱。开发了一个临床模型,以识别在症状出现前预测急诊就诊期间躁动发生的危险因素。使用受试者操作特征曲线下面积(AUROC)和精确召回率曲线下面积(PR-AUC)来衡量模型性能。
最终队列包括3048780次就诊。该队列的平均(标准差)年龄为50.2(20.4)岁,女性患者就诊占54.7%。最终的人工智能模型使用50个预测因素来预测躁动事件的主要结局。该模型在交叉验证中AUROC为0.94(95%CI,0.93 - 0.94),PR-AUC为0.41(95%CI,0.40 - 0.42),表明具有良好的判别能力。对模型的校准进行了评估,并证明在预测概率范围内具有稳健性。最终模型中的顶级预测因素包括既往急诊就诊次数、初始生命体征、病史、主要关注点以及既往镇静和约束事件的次数等因素。
利用9家医院急诊就诊的横断面队列,该预测模型纳入了用于检测躁动风险的因素,在不同患者群体中显示出高准确性和适用性。这些结果表明,该模型的临床应用可能通过先发制人的降级处理和预防躁动来加强以患者为中心的护理。