From the, Department of Emergency Medicine, Washington University School of Medicine, St. Louis, MO, USA.
and the, Department of Psychiatry, Washington University School of Medicine, St. Louis, MO, USA.
Acad Emerg Med. 2020 Dec;27(12):1279-1290. doi: 10.1111/acem.14101. Epub 2020 Sep 1.
Recognized as a premier approach for adverse event (AE) detection, trigger tools have been developed for multiple clinical settings outside the emergency department (ED). We recently derived and tested an ED trigger tool (EDTT) with enhanced features for high-yield detection of harm, consisting of 30 triggers associated with AEs. In this study, we validate the EDTT in an independent sample and compare record selection approaches to optimize yield for quality improvement.
This is a retrospective observational study using data from 13 months of visits to an urban, academic ED by patients aged ≥ 18 years (92,859 records). We conducted standard two-tiered trigger tool reviews on an independent validation sample of 3,724 records with at least one of the 30 triggers found associated with AEs in our previous derivation sample (N = 1,786). We also tested three new candidate triggers and reviewed 72 records with no triggers for comparison purposes. We compare derivation and validation samples on: 1) triggers showing persistent associations with AEs, 2) AE yield (AEs detected/records reviewed), and 3) representativeness of AE types detected. We use bivariate associations of triggers with AEs as the basis for trigger selection. We then use multivariable modeling in the combined derivation and validation samples to determine AE risk scores using trigger weights. This allows us to predict occurrence of AEs and derive population prevalence estimates. Finally, we compare yield for detection of AEs under three record selection strategies (random selection, trigger counts, weighted trigger counts).
Twenty-four of the 30 triggers were confirmed to be associated with AEs on bivariate testing. Three previously marginal triggers and two of three new candidate triggers were also found to be associated with AEs. The presence of any of these 29 triggers was associated with an AE rate of 10% in our selected sample (compared to 1.1% for none, p < 0.001). The risk of an AE increased with number of triggers. Combining data from both phases, we identified 461 AEs in 429 unique visits in 5,582 records reviewed. Our multivariable model (which emphasized parsimony) retained 12 triggers with a ROC AUC of 82% in both samples. Selecting records for review based on number of triggers improves yield to 14% for 4+ triggers (top 10% of visits) and to 28% for 8+ (top 1%). A weighted trigger count has corresponding yields of 18 and 38%. The method for selecting records for review did not appear to affect event-type representativeness, with similar distributions of event types and severities detected.
In this single-site study of the EDTT we observed high levels of validity in trigger selection, yield, and representativeness of AEs, with yields that are superior to estimates for traditional approaches to AE detection. Record selection using weighted triggers outperforms a trigger count threshold approach and far outperforms random sampling from records with at least one trigger. The EDTT is a promising efficient and high-yield approach for detecting all-cause harm to guide quality improvement efforts in the ED.
作为一种检测不良事件(AE)的主要方法,触发工具已经在急诊科(ED)以外的多个临床环境中开发出来。我们最近开发并测试了一种具有增强功能的 ED 触发工具(EDTT),用于高效检测伤害,其中包括 30 个与 AE 相关的触发因素。在这项研究中,我们在一个独立的样本中验证了 EDTT,并比较了记录选择方法,以优化质量改进的效果。
这是一项回顾性观察性研究,使用了 13 个月内年龄在 18 岁及以上的患者在城市学术 ED 就诊的记录(92859 条)。我们对之前推导样本中发现与 AE 相关的 30 个触发因素中的至少一个相关的 3724 条记录进行了标准的两级触发工具审查(N=1786)。我们还测试了三个新的候选触发因素,并审查了 72 条没有触发因素的记录进行比较。我们在以下方面比较推导和验证样本:1)显示与 AE 持续相关的触发因素,2)AE 检出率(检出的 AE/审查的记录),以及 3)检出的 AE 类型的代表性。我们使用触发因素与 AE 的二元关联作为触发因素选择的基础。然后,我们在推导和验证样本中使用多变量建模来确定使用触发权重的 AE 风险评分。这使我们能够预测 AE 的发生,并得出人群患病率估计。最后,我们比较了在三种记录选择策略(随机选择、触发计数、加权触发计数)下检测 AE 的效果。
在二元检验中,30 个触发因素中有 24 个被证实与 AE 相关。三个以前边缘性的触发因素和两个新的候选触发因素也与 AE 相关。在我们选择的样本中,任何这些 29 个触发因素的存在都与 AE 发生率为 10%相关(而不存在触发因素的发生率为 1.1%,p<0.001)。AE 的风险随着触发因素的数量而增加。结合两个阶段的数据,我们在 5582 条审查记录中的 429 个独特就诊中确定了 461 例 AE。我们的多变量模型(强调简约)在两个样本中保留了 12 个触发因素,ROC AUC 为 82%。根据触发因素的数量选择记录进行审查,可以将检出率提高到 4+触发因素(前 10%就诊)的 14%和 8+触发因素(前 1%就诊)的 28%。加权触发计数的检出率分别为 18%和 38%。选择记录进行审查的方法似乎不会影响事件类型的代表性,检出的事件类型和严重程度分布相似。
在这项 EDTT 的单中心研究中,我们观察到触发因素选择、效果和 AE 代表性方面具有较高的有效性,检出率优于传统 AE 检测方法。使用加权触发因素的记录选择优于触发计数阈值方法,并且远远优于至少有一个触发因素的记录的随机抽样。EDTT 是一种很有前途的高效、高检出率的方法,可以检测所有原因的伤害,指导 ED 中的质量改进工作。