用自动分类模型定义诱导后血流动力学不稳定性

Eline Kho,Rogier V Immink,Bjorn J P van der Ster,Ward H van der Ven,Jimmy Schenk,Markus W Hollmann,Johan T M Tol,Lotte E Terwindt,Alexander P J Vlaar,Denise P Veelo
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Noninvasive blood pressure was continuously measured between 5 minutes before up to 15 minutes after the first induction agent had been administered. An expert panel rated whether the patient experienced clinically relevant hemodynamic instability or not. Interrater correlation coefficient and intraclass correlation were computed to check for consistency between experts. Next, an automated classification model for clinically relevant hemodynamic instability was developed using mean, maximum, minimum systolic, mean, diastolic arterial blood pressure (SAP, MAP, and DAP, respectively) and their corresponding time course of decline. The model was trained and tested based on the hemodynamic instability labels provided by the experts.\r\n\r\nRESULTS\r\nIn total 78 patients were classified as having experienced hemodynamic instability and 279 as not. 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摘要

背景诱导后低血压(PIH)可能与发病率和死亡率的增加有关。在早期的研究中,PIH 的定义仅基于不同的绝对或相对阈值。然而,时间过程(如诱导过程中血压下降的速度)很少被纳入其中,而这可能代表了患者血液动力学的不稳定性。我们提出了一个综合模型,通过将血压阈值与血压下降的幅度和速度相结合来区分血流动力学不稳定和稳定的患者。在使用第一种诱导剂前 5 分钟至使用后 15 分钟期间,连续测量无创血压。专家小组对患者是否出现临床相关的血流动力学不稳定进行评分。计算了专家间相关系数和类内相关性,以检查专家间的一致性。接下来,利用收缩压、舒张压和平均动脉压的平均值、最大值、最小值及其相应的下降时间过程,建立了临床相关血流动力学不稳定的自动分类模型。根据专家提供的血流动力学不稳定标签对模型进行了训练和测试。结果共有 78 名患者被归类为经历过血流动力学不稳定,279 名患者未经历过。血流动力学不稳定患者的年龄明显偏大(7 岁,95% 置信区间(CI),4-11,P < .001),慢性阻塞性肺病(COPD)的发病率更高(3%,95% CI,1-8,P = .036)。诱导前,血流动力学不稳定患者的 SAP 较高(中位数(第一至第三四分位数):161(145-175)):161 (145-175) mm Hg vs 150 (134-166) mm Hg,P < .001)。专家之间的内部一致性为 0.92(95% CI,0.89-0.94)。随机森林分类器模型表现优异,接收者操作曲线下面积(AUROC)为 0.96,灵敏度为 0.84,特异度为 0.94。该分类模型将为今后有关血流动力学不稳定及其预防的研究铺平道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Defining Postinduction Hemodynamic Instability With an Automated Classification Model.
BACKGROUND Postinduction hypotension (PIH) may be associated with increased morbidity and mortality. In earlier studies, the definition of PIH is solely based on different absolute or relative thresholds. However, the time-course (eg, how fast blood pressure drops during induction) is rarely incorporated, whereas it might represent the hemodynamic instability of a patient. We propose a comprehensive model to distinguish hemodynamically unstable from stable patients by combining blood pressure thresholds with the magnitude and speed of decline. METHODS This prospective study included 375 adult elective noncardiac surgery patients. Noninvasive blood pressure was continuously measured between 5 minutes before up to 15 minutes after the first induction agent had been administered. An expert panel rated whether the patient experienced clinically relevant hemodynamic instability or not. Interrater correlation coefficient and intraclass correlation were computed to check for consistency between experts. Next, an automated classification model for clinically relevant hemodynamic instability was developed using mean, maximum, minimum systolic, mean, diastolic arterial blood pressure (SAP, MAP, and DAP, respectively) and their corresponding time course of decline. The model was trained and tested based on the hemodynamic instability labels provided by the experts. RESULTS In total 78 patients were classified as having experienced hemodynamic instability and 279 as not. The hemodynamically unstable patients were significantly older (7 years, 95% confidence interval (CI), 4-11, P < .001), with a higher prevalence of chronic obstructive pulmonary disease (COPD) (3% higher, 95% CI, 1-8, P = .036). Before induction, hemodynamically unstable patients had a higher SAP (median (first-third quartile): 161 (145-175) mm Hg vs 150 (134-166) mm Hg, P < .001) compared to hemodynamic stable patients. Interrater agreement between experts was 0.92 (95% CI, 0.89-0.94). The random forest classifier model showed excellent performance with an area under the receiver operating curve (AUROC) of 0.96, a sensitivity of 0.84, and specificity of 0.94. CONCLUSIONS Based on the high sensitivity and specificity, the developed model is able to differentiate between clinically relevant hemodynamic instability and hemodynamic stable patients. This classification model will pave the way for future research concerning hemodynamic instability and its prevention.
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