使用综合患者特征描述算法评估肾病进展:混合聚类方法

Mohammad A. Al-Mamun, Ki Jin Jeun, Todd Brothers, Ernest Asare, Khaled Shawwa, Imtiaz Ahmed
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背景在美国 3550 万慢性肾脏病(CKD)成人患者中,超过 55.7 万人正在接受透析治疗,每位患者每年的费用从 97,373 美元到 102,206 美元不等。急性肾损伤(AKI)可导致罹患 CKD 的风险增加约九倍。在了解 AKI 到 CKD 的进展方面存在着巨大的知识差距。我们的目的是开发并测试一种混合聚类算法,以研究推动 AKI 向 CKD 进展的临床表型。方法这项回顾性观察研究利用了 2010 年至 2022 年期间 90,602 份患者电子健康记录 (EHR) 中的数据。我们将 AKI 分成三组:医院获得性 AKI(HA-AKI)、社区获得性 AKI(CA-AKI)和无 AKI。我们开发了一个定制的表型疾病和程序网络以及一个互补变量聚类来研究三组之间的风险因素。该算法确定了前三个匹配群组。结果在 58606 名慢性肾脏病患者中,AKI 组的心力衰竭(21.1%)和 2 型糖尿病(45.3%)发病率较高。与 AKI 组相比,无 AKI 组的合并症负担更重,平均合并症为 2.84 vs. 2.04; p < 0.05; 74.6% vs. 53.6%。两组 AKI 患者均存在多种危险因素,包括长期使用阿片类镇痛药、肺不张、缺血性心脏病史和乳酸酸中毒。与无 AKI 组相比,HA-AKI 患者的合并症网络更为复杂,节点数(64 对 55)和边数(645 对 520)都更高。与 CA-AKI 组相比,HA-AKI 组有几种情况的度数和度间中心性更高,包括高胆固醇(34,91.10)、慢性疼痛(33,103.38)、三尖瓣功能不全(38,113.37)、骨关节炎(34,56.14)和消化道组件切除(37,68.66)。结论我们提出的定制患者特征分析算法可根据合并症和医疗程序识别 AKI 表型,为利用大型 EHR 数据识别 CKD 早期风险因素提供了一种可行的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluating the kidney disease progression using a comprehensive patient profiling algorithm: A hybrid clustering approach
Background Among 35.5 million U.S. adults with chronic kidney disease (CKD), more than 557,000 are on dialysis with incurred cost ranges from $97,373 to $102,206 per patient per year. Acute kidney injury (AKI) can lead to an approximate ninefold increased risk for developing CKD. Significant knowledge gaps exist in understanding AKI to CKD progression. We aimed to develop and test a hybrid clustering algorithm to investigate the clinical phenotypes driving AKI to CKD progression. Methods This retrospective observational study utilized data from 90,602 patient electronic health records (EHR) from 2010 to 2022. We classified AKI into three groups: Hospital Acquired AKI (HA-AKI), Community Acquired AKI (CA-AKI), and No-AKI. We developed a custom phenotypic disease and procedure network and a complementary variable clustering to examine risk factors among three groups. The algorithm identified top three matched clusters. Results Among 58,606 CKD patients, AKI group had a higher prevalence of heart failure (21.1%) and Type 2 Diabetes (45.3%). The No-AKI group had a higher comorbidity burden compared to AKI group, with average comorbidities of 2.84 vs. 2.04; p < 0.05; 74.6% vs. 53.6%. Multiple risk factors were identified in both AKI cohorts including long-term opiate analgesic use, atelectasis, history of ischemic heart disease, and lactic acidosis. The comorbidity network in HA-AKI patients was more complex compared to the No-AKI group with higher number of nodes (64 vs. 55) and edges (645 vs. 520). The HA-AKI cohort had several conditions with higher degree and betweenness centrality including high cholesterol (34, 91.10), chronic pain (33, 103.38), tricuspid insufficiency (38, 113.37), osteoarthritis (34, 56.14), and removal of GI tract components (37, 68.66) compared to the CA-AKI cohort. Conclusion Our proposed custom patient profiling algorithm identifies AKI phenotypes based on comorbidities and medical procedures, offering a promising approach to identify early risk factors for CKD using large EHR data.
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