Machine Learning Prediction of Early In-Hospital Mortality in Lung Cancer Patients Using Administrative Data.

Ali Nemati, Amirreza Bakhshi, Keith Dookeran, Lu He, Jake Luo, Rohit Kate
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Abstract

This study develops and validates an interpretable machine learning model for predicting early in-hospital mortality (death within 7 days of admission) among lung cancer patients using diagnosis codes available at admission. We analyzed the 2016-2019 Maryland State Inpatient Database (HCUP SID), with patient history captured from 2014, identifying 57,625 adult lung cancer patients who died during hospitalization. Of these, 40,651 (70.5%) experienced early death. One hundred binary clinical features were derived from ICD-10-CM codes mapped to AHRQ Clinical Classifications Software Refined categories. XGBoost achieved an AUC of 0.787 (95% CI: 0.782- 0.792) at baseline, improving to 0.791 with engineered features, outperforming logistic regression (0.783), random forest (0.769), and traditional comorbidity indices (Charlson: 0.367; Elixhauser: 0.325). Notably, comorbidity indices performed worse than chance, suggesting chronic disease burden is inversely associated with rapid deterioration. Interpretability analyses using gain importance, permutation importance, and SHAP consistently identified acute metabolic derangements, electrolyte imbalances, malnutrition, and severe infections as dominant predictors. Risk stratification showed monotonic separation with observed early mortality ranging from 31.5% (lowest quintile) to 95.6% (highest quintile). These findings demonstrate that administrative data can support real-time risk stratification for palliative care and intensity-of-care decisions in acute oncology settings.

使用管理数据的机器学习预测肺癌患者早期住院死亡率。
本研究开发并验证了一个可解释的机器学习模型,该模型使用入院时可用的诊断代码预测肺癌患者的早期住院死亡率(入院后7天内死亡)。我们分析了2016-2019年马里兰州住院患者数据库(HCUP SID),其中包括2014年的患者病史,确定了57,625名在住院期间死亡的成年肺癌患者。其中,40,651人(70.5%)经历了早期死亡。100个二进制临床特征来源于ICD-10-CM代码,映射到AHRQ临床分类软件精细分类。XGBoost在基线时的AUC为0.787 (95% CI: 0.782- 0.792),采用工程特征后提高到0.791,优于逻辑回归(0.783)、随机森林(0.769)和传统的合并症指数(Charlson: 0.367; Elixhauser: 0.325)。值得注意的是,合并症指数的表现比偶然性差,表明慢性疾病负担与快速恶化呈负相关。可解释性分析使用增益重要性、排列重要性和SHAP一致确定急性代谢紊乱、电解质失衡、营养不良和严重感染是主要的预测因素。风险分层显示单调分离,观察到的早期死亡率从31.5%(最低五分位数)到95.6%(最高五分位数)不等。这些发现表明,管理数据可以支持急性肿瘤环境中姑息治疗和护理强度决策的实时风险分层。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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