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Sepsis Physiomarkers for Appropriate Risk Knowledge of monitored patients in the ICU (SPARK-ICU)

Sepsis Physiomarkers for Appropriate Risk Knowledge of monitored patients in the ICU (SPARK-ICU)
用于对 ICU 中受监测患者进行适当风险了解的脓毒症生理标志物 (SPARK-ICU)
批准号:
10295735
负责人:
Rishikesan Kamaleswaran
金额:
$55.41万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
未结题
起止时间:
2021-09-10 至 2026-06-30

项目摘要

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中文摘要
翻译
项目摘要 住进ICU的危重病人如果出现继发性感染和败血症,可能会面临高达五倍的 与非脓毒症患者相比,死亡风险增加。大多数患者出现了 继发性感染在入院时病情更为危重,因此需要更多的资源。 用于预测脓毒症的传统机器学习算法在很大程度上被关注和依赖于使用 来自电子病历(EMR)的结构化数据,然而,电子病历主要是作为一种帐单来开发的 机制和临床工作流程的审核日志。因此,许多数据的结构和可用性通常是 时间延迟,容易因手工输入而出错,因各种机构、个人和培训偏见而产生偏差, 并最终包含大量丢失的数据。在这个提议中,我们试图发现新的 从从非人类衍生数据生成的连续生理数据流中提取的“生理标记物” 预测这一关键人群中脓毒症发病的来源。使用这种例行收集的数据,以及 从电子病历中提取的常见临床指标,我们提出了生成健壮的机器学习算法 这可以更通用、更可重复,并消除手动数据输入的偏见和陷阱。我们 建议这类模型不仅可以提醒临床医生注意急危重症患者有可能患上 实时发展脓毒症,但也调查干预效果,如容量反应性 并支持脓毒症新亚型的发现。其次,现有的许多关于预测的文献 脓毒症的模型主要集中在普通病房的住院患者,然而,预测感染发病的模型 住进ICU后继发感染的患者的脓毒症是有限的。在我们之前的 我们已经证明,从连续的数字数据流中发现的标记可以更早地告知 儿童和成人脓毒症的预测。然而,这些分析没有使用来自 波形,封装了丰富的生理学特征。因此,通过强调发现 这种新颖的标记和通过应用数据驱动的学习算法,我们期待着发展 算法和工具,以提高我们对重症脓毒症生理动力学变化的理解 病人生病了。在这个拟议的计划中,我们将整合一些独特的专业知识,这些专业知识 横跨信号处理、数学、计算机科学和医学,开发能够 分析这些数据以揭示有意义的洞察力。简而言之,我们将提供有关该角色的重要知识 以及目前在临床实践中大量可用的复杂生理相互作用的应用 很少用于临床决策。
英文摘要
Project Summary Critically ill patients admitted to the ICU who develop secondary infection and sepsis, can face up to a five-fold increase in the risk for death when compared to non-sepsis patients. The majority of patients who developed secondary infections are more critically ill at admission and therefore require significantly greater resources. Traditional machine learning algorithms for predicting sepsis has been largely focused and relied on the use of structured data from the electronic medical record (EMR), however the EMR was developed largely as a billing mechanism and an audit log for clinical workflow. Hence, much of the structure and availability of data are often time-delayed, prone to errors from manual entry, biases from various institutional, personal and training biases, and finally contain a significant amount of missing data. In this proposal, we seek to discover novel `physiomarkers' extracted from continuous physiological data streams, generated from non-human derived data sources, that predict the onset of sepsis in this critical population. Using such routinely collected data, along with common clinical indicators extracted from the EMR, we propose to generate robust machine learning algorithms that can be more generalized, reproducible and removed from the biases and pitfalls of manual data entry. We propose that such classes of models not only may alert clinicians to acute and critically ill patients at risk for developing sepsis in real-time, but also investigate intervention effectiveness, such as volume responsiveness and support the discovery of novel sub-types of sepsis. Secondly, much of the existing literature on predictive models for sepsis focus on hospitalized patients in the general ward, however, models that predict the onset of sepsis among patients who developed secondary infections after admission to the ICU is limited. In our previous work, we have demonstrated that markers discovered from continuous numeric data streams can inform earlier prediction of sepsis in children and adults. However, those analysis did not use high-fidelity data from the waveforms, which encapsulate rich characteristics of physiology. Therefore, by emphasizing the discovery of such novel markers and through the application of data-driven learning algorithms, we expect to develop algorithms and tools that improve our understanding of the changing physiologic dynamics of sepsis in critically ill patient. In this proposed program, we will integrate knowledge across a number of distinctive expertise that spans signal processing, mathematics, computer science and medicine to develop sophisticated tools that can analyze such data to reveal meaningful insight. In short, we will contribute significant knowledge about the role and utility of complex physiological interactions that are at present abundantly available in clinical practice but seldom used for clinical decision making.
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EQuitable, Uniform and Intelligent Time-based conformal Inference (EQUITI) Framework
  • 批准号:
    10599622
  • 项目类别:
  • 资助金额:
    $23.22万
  • 财政年份:
    2021
  • 负责人:
    Rishikesan Kamaleswaran
  • 依托单位:
Sepsis Physiomarkers for Appropriate Risk Knowledge of monitored patients in the ICU (SPARK-ICU)
  • 批准号:
    10655628
  • 项目类别:
  • 资助金额:
    $51.84万
  • 财政年份:
    2021
  • 负责人:
    Rishikesan Kamaleswaran
  • 依托单位: