跳到正文
研踪PaperTrail

YOUR RESEARCH, IN SIGHT

让下一篇重要论文,不再错过。

覆盖计算机全学科,以 AI 为快捷入口。关注方向、作者和关键词,把发现变成持续的研究积累。

部分采集异常
正在读取账号与研究记录…

全站更新概况

+2471新增论文
+2025其中 AI 相关
+163已有论文修订
+100新增 AI 导读

arXiv 最近完成扫描:2026-11-11 03:54 · 全站最近入库:2026-11-10 15:22各信源进度 →

统计口径与数据新鲜度

统计 2026-11-10 04:17 — 2026-11-11 04:17(北京时间) · 点击数字查看对应简报;AI 相关包含在新增论文内。

最近完成检查:2026-11-11 03:54最近发现新增版本:2026-11-10 15:22库内论文最新更新时间:2026-11-10 02:59

每分钟刷新已保存的数据。空检查不代表采集异常;新收录可能包含历史论文。AI 导读按新增版本计数。

20,643 已收录论文17,531 AI 相关5,643 有修订112 HF 社区发现

浏览论文库

时间范围跟随排序:版本更新、本站收录或首次发表。最新收录可能包含历史论文。部分信源异常,查看状态 →

找到 1 篇论文 · 按版本更新时间排序上轮扫描起点 2026-11-11 03:53(北京时间)
版本更新 · v3arXiv:2602.03562

NPCNet: Navigator-Driven Pseudo Text for Deep Clustering of Early Sepsis Phenotyping

Pi-Ju Tsai, Charkkri Limbud, Kuan-Fu Chen, Yi-Ju Tseng

原文摘要

Sepsis is a heterogeneous syndrome. Identifying clinically distinct phenotypes may enable more precise treatment strategies. In recent years, many researchers have applied clustering algorithms to sepsis patients. However, many existing approaches require aggregating or imputing temporal Electronic Health Records (EHRs), which can limit the model's ability to capture disease progression. Furthermore, existing clustering processes seldom incorporate domain-driven constraints, often resulting in phenotypes that lack clear clinical distinction. We propose a novel clustering network, NPCNet, that comprises a text embedding generator, a clustering operator, and a target navigator. We first transformed EHRs into pseudo texts by discretizing continuous clinical measurements and integrated them with static variables to construct the embeddings. The target navigator then infused clinical knowledge into the embeddings through auxiliary tasks, constraining clustering results to better align sepsis phenotypes with clinical significance. Finally, the clustering operator employed an iterative refinement mechanism to jointly optimize phenotype centroids and patient representations under domain-driven constraints. Extensive experiments on public datasets demonstrated that NPCNet achieved superior performance on both internal clustering and clinical metrics. We identify four distinct sepsis phenotypes with divergent SOFA trajectories. Notably, although α and δ exhibit similarly severe conditions initially, NPCNet distinguishes patients likely to improve (α) from those at risk of deterioration (δ). Furthermore, treatment effect analysis suggests that early vasopressor administration may be associated with improved outcomes in the α, \{beta}, and δ phenotypes. These findings highlight NPCNet's potential for phenotype-specific treatment strategies.

cs.LG