胸片在学术急诊科评估非外伤性胸痛的应用评估

Rucker Garrett, Kalayanamitra Ricci, Gopaul Ravindra
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引用次数: 2

摘要

背景:过度使用胸部x光片(CXR)成本高,效率低,并导致辐射暴露增加。一些研究提出了临床决策规则(CDR),用于胸片在非创伤性胸痛患者到急诊科(ED)的应用。然而,cdr往往不是放之四海而皆准的,可能会根据人口的变化而有所不同。本研究的目的是:1)评估以非创伤性胸痛为表现的疑似急性冠状动脉综合征(ACS)的ED患者的CXR使用情况;2)使用先前开发的cdr标准评估与患者群体中异常CXR相关的因素。方法:我们从先前导出的cdr中确定了14个可能预测异常CXR的临床标准。我们回顾性地确定了500名在2016年1月至2017年12月期间出现非创伤性胸痛的18岁以上患者。对图表进行筛选:1)是否进行了CXR, 2) CXR结果,以及3)14项临床标准中的任何一项的存在。结果:487例(97%)非外伤性胸痛患者行了胸腔镜检查。266例(54.6%)14个危险因素均为零的患者进行了CXR。11例(4.1%)患者的CXR表现异常,其中3例(1.1%)患者改变了临床处理方法。14项临床标准的缺失导致99%的阴性预测值(NPV)。进一步的分析显示,14个危险因素中的9个可以在我们的人群中消除,而NPV没有变化。结论:使用先前开发的cdr中的6个危险因素将使CXR利用率降低55%,NPV为99%。没有单一的CDR完全适合我们的ED人群,因此显示了可变性,需要为每个患者群体量身定制标准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of Chest X-Ray Utilization for the Evaluation of Non-Traumatic Chest Pain in an Academic Emergency Department
Background: Overutilization of chest X-rays (CXR) is costly, inefficient and results in increased radiation exposure. Several studies have proposed clinical decision rules (CDR) for chest X-ray utilization in non-traumatic chest pain patients presenting to the Emergency Department (ED). However, CDRs are often not one size fits all and may differ based on population variability. The purpose of this study is to 1) Evaluate CXR utilization among ED patients suspected of acute coronary syndrome (ACS) presenting with non-traumatic chest pain and 2) Assess for factors associated with an abnormal CXR in our patient population using criteria from previously developed CDRs. Methods: We identified 14 clinical criteria from previously derived CDRs that may be predictive of an abnormal CXR. We retrospectively identified 500 patients over age 18 who presented with non-traumatic chest pain between January 2016 and December 2017. Charts were screened for 1) Whether a CXR was performed, 2) CXR results, and 3) The presence of any of the 14 clinical criteria. Results: 487 (97%) non-traumatic chest pain patients had a CXR performed. 266 (54.6%) patients with zero of the 14 risk factors had a CXR performed. Of those patients, 11 (4.1%) had an abnormality on CXR, 3 (1.1%) of which led to a change in clinical management. Absence of all 14 clinical criteria resulted in a negative predictive value (NPV) of 99%. Further analysis revealed that 9 of the 14 risk factors could be removed in our population with no change in the NPV. Conclusion: The use of the 6 risk factors from the previously developed CDRs would have reduced CXR utilization by 55% with a NPV of 99%. No single CDR perfectly fit our ED population thus demonstrating variability and need to tailor criteria to each patient population.
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