Department of Pneumology, Hospital Clinic of Barcelona, Barcelona, Spain; August Pi i Sunyer Biomedical Research Institute (IDIBAPS), University of Barcelona, Barcelona, Spain; Biomedical Research Networking Centers in Respiratory Diseases (CIBERES), Barcelona, Spain; Faculty of Health Sciences, Continental University, Huancayo, Peru.
Treat Systems, Aalborg, Denmark.
Chest. 2023 Jan;163(1):77-88. doi: 10.1016/j.chest.2022.07.005. Epub 2022 Jul 16.
Artificial intelligence tools and techniques such as machine learning (ML) are increasingly seen as a suitable manner in which to increase the prediction capacity of currently available clinical tools, including prognostic scores. However, studies evaluating the efficacy of ML methods in enhancing the predictive capacity of existing scores for community-acquired pneumonia (CAP) are limited. We aimed to apply and validate a causal probabilistic network (CPN) model to predict mortality in patients with CAP.
Is a CPN model able to predict mortality in patients with CAP better than the commonly used severity scores?
This was a derivation-validation retrospective study conducted in two Spanish university hospitals. The ability of a CPN designed to predict mortality in sepsis (SepsisFinder [SeF]), and adapted for CAP (SeF-ML), to predict 30-day mortality was assessed and compared with other scoring systems (Pneumonia Severity Index [PSI], Sequential Organ Failure Assessment [SOFA], quick Sequential Organ Failure Assessment [qSOFA], and CURB-65 criteria [confusion, urea, respiratory rate, BP, age ≥ 65 years]). The SeF models are proprietary software. Differences between receiver operating characteristic curves were assessed by the DeLong method for correlated receiver operating characteristic curves.
The derivation cohort comprised 4,531 patients, and the validation cohort consisted of 1,034 patients. In the derivation cohort, the areas under the curve (AUCs) of SeF-ML, CURB-65, SOFA, PSI, and qSOFA were 0.801, 0.759, 0.671, 0.799, and 0.642, respectively, for 30-day mortality prediction. In the validation study, the AUC of SeF-ML was 0.826, concordant with the AUC (0.801) in the derivation data (P = .51). The AUC of SeF-ML was significantly higher than those of CURB-65 (0.764; P = .03) and qSOFA (0.729, P = .005). However, it did not differ significantly from those of PSI (0.830; P = .92) and SOFA (0.771; P = .14).
SeF-ML shows potential for improving mortality prediction among patients with CAP, using structured health data. Additional external validation studies should be conducted to support generalizability.
人工智能工具和技术,如机器学习(ML),被越来越多地视为提高现有临床工具预测能力的合适方式,包括预后评分。然而,评估 ML 方法在增强社区获得性肺炎(CAP)现有评分预测能力方面的疗效的研究是有限的。我们旨在应用和验证因果概率网络(CPN)模型来预测 CAP 患者的死亡率。
CPN 模型是否能够比常用的严重程度评分更好地预测 CAP 患者的死亡率?
这是一项在西班牙两所大学医院进行的推导-验证回顾性研究。评估并比较了为预测败血症死亡率而设计的 CPN(SepsisFinder [SeF])和为预测 CAP 死亡率而改编的 CPN(SeF-ML)预测 30 天死亡率的能力,以及其他评分系统(肺炎严重指数 [PSI]、序贯器官衰竭评估 [SOFA]、快速序贯器官衰竭评估 [qSOFA]和 CURB-65 标准 [意识障碍、尿素、呼吸频率、血压、年龄≥65 岁])。SeF 模型是专有的软件。通过相关接受者操作特征曲线的 DeLong 方法评估接受者操作特征曲线之间的差异。
推导队列包括 4531 名患者,验证队列包括 1034 名患者。在推导队列中,SeF-ML、CURB-65、SOFA、PSI 和 qSOFA 的曲线下面积(AUCs)分别为 0.801、0.759、0.671、0.799 和 0.642,用于预测 30 天死亡率。在验证研究中,SeF-ML 的 AUC 为 0.826,与推导数据中的 AUC(0.801)一致(P=0.51)。SeF-ML 的 AUC 显著高于 CURB-65(0.764;P=0.03)和 qSOFA(0.729,P=0.005)。然而,它与 PSI(0.830;P=0.92)和 SOFA(0.771;P=0.14)的 AUC 没有显著差异。
使用结构化健康数据,SeF-ML 显示出改善 CAP 患者死亡率预测的潜力。应进行额外的外部验证研究以支持其普遍性。