Department of Emergency Medicine, University of Ottawa, Ottawa, Ontario, Canada
Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Emerg Med J. 2022 Jul;39(7):501-507. doi: 10.1136/emermed-2020-211095. Epub 2021 Nov 5.
Published risk tools do not provide possible management options for syncope in the emergency department (ED). Using the 30-day observed risk estimates based on the Canadian Syncope Risk Score (CSRS), we developed personalised risk prediction to guide management decisions.
We pooled previously reported data from two large cohort studies, the CSRS derivation and validation cohorts, that prospectively enrolled adults (≥16 years) with syncope at 11 Canadian EDs between 2010 and 2018. Using this larger cohort, we calculated the CSRS calibration and discrimination, and determined with greater precision than in previous studies the 30-day risk of adjudicated serious outcomes not identified during the index ED evaluation depending on the CSRS and the risk category. Based on these findings, we developed an on-line calculator and pictorial decision aids.
8233 patients were included of whom 295 (3.6%, 95% CI 3.2% to 4.0%) experienced 30-day serious outcomes. The calibration slope was 1.0, and the area under the curve was 0.88 (95% CI 0.87 to 0.91). The observed risk increased from 0.3% (95% CI 0.2% to 0.5%) in the very-low-risk group (CSRS -3 to -2) to 42.7% (95% CI 35.0% to 50.7%), in the very-high-risk (CSRS≥+6) group (Cochrane-Armitage trend test p<0.001). Among the very-low and low-risk patients (score -3 to 0), ≤1.0% had any serious outcome, there was one death due to sepsis and none suffered a ventricular arrhythmia. Among the medium-risk patients (score +1 to+3), 7.8% had serious outcomes, with <1% death, and a serious outcome was present in >20% of high/very-high-risk patients (score +4 to+11) including 4%-6% deaths. The online calculator and the pictorial aids can be found at: https://teamvenk.com/csrs CONCLUSIONS: 30-day observed risk estimates from a large cohort of patients can be obtained for management decision-making. Our work suggests very-low-risk and low-risk patients may be discharged, discussion with patients regarding investigations and disposition are needed for medium-risk patients, and high-risk patients should be hospitalised. The online calculator, accompanied by pictorial decision aids for the CSRS, may assist in discussion with patients.
已发表的风险工具并未为急诊科(ED)中的晕厥提供可能的管理选择。使用基于加拿大晕厥风险评分(CSRS)的 30 天观察风险估计值,我们进行了个性化风险预测,以指导管理决策。
我们汇集了先前在两个大型队列研究中的报告数据,即 CSRS 推导和验证队列,这些队列前瞻性地纳入了 2010 年至 2018 年期间在加拿大 11 个 ED 就诊的成年(≥16 岁)晕厥患者。使用这个更大的队列,我们计算了 CSRS 的校准和区分度,并以前瞻性研究中更精确的方式确定了 30 天内根据 CSRS 和风险类别确定的未在指数 ED 评估期间确定的经裁决的严重结局的风险。基于这些发现,我们开发了一个在线计算器和图形决策辅助工具。
共纳入 8233 例患者,其中 295 例(3.6%,95%CI 3.2%至 4.0%)在 30 天内发生严重结局。校准斜率为 1.0,曲线下面积为 0.88(95%CI 0.87 至 0.91)。观察到的风险从极低风险组(CSRS-3 至-2)的 0.3%(95%CI 0.2%至 0.5%)增加到极高风险组(CSRS≥+6)的 42.7%(95%CI 35.0%至 50.7%)(Cochrane-Armitage 趋势检验,p<0.001)。在极低和低风险患者(评分-3 至 0)中,≤1.0%发生任何严重结局,有 1 例因败血症死亡,无室性心律失常。在中风险患者(评分+1 至+3)中,7.8%发生严重结局,<1%死亡,高/极高风险患者(评分+4 至+11)中有>20%发生严重结局,包括 4%-6%的死亡率。在线计算器和图形辅助工具可在以下网址获得:https://teamvenk.com/csrs。
可根据大量患者的队列获得 30 天观察风险估计值,以进行管理决策。我们的工作表明,极低风险和低风险患者可能需要出院,中风险患者需要与患者讨论检查和处置,高风险患者需要住院。在线计算器与 CSRS 的图形决策辅助工具一起,可帮助与患者进行讨论。