开发用于监测心血管疾病进展模式的队列分析工具:先进的随机建模方法

IF 3.1 3区 医学 Q2 MEDICAL INFORMATICS
Arindam Brahma, Samir Chatterjee, Kala Seal, Ben Fitzpatrick, Youyou Tao
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引用次数: 0

摘要

背景:世界卫生组织(WHO)报告称,心血管疾病(CVDs)是导致全球死亡的主要原因。心血管疾病是慢性病,其发展模式复杂,涉及并发症和多发病的发作。在处理慢性疾病时,医生往往采取 "观察等待 "策略,在获得信息之前推迟行动。将时变随机建模方法应用于队列研究中的患者纵向数据,可以揭示人群水平的转变概率和进展模式。心血管疾病从业人员提供的信息表明,生成和可视化队列过渡模式的工具在临床应用中具有很多影响力。由此产生的计算模型可嵌入临床医生的数字决策支持工具中。然而,迄今为止,还没有研究尝试为心血管疾病实现这一目标:本研究旨在应用先进的随机建模方法,从心血管疾病患者队列的纵向偶发数据中发现转归概率和进展模式,然后利用计算模型构建数字化临床队列分析工具,展示此类模型的可操作性:我们的数据来源于美国国家心肺血液研究所的 9 项流行病学队列研究,包括 1274 名患者 16 年间 4839 次心血管疾病发作的时间记录。然后,我们使用连续时间马尔可夫链方法建立了模型,该方法为慢性疾病中疾病状态之间的时变过渡提供了一种稳健的方法:我们的研究显示了心血管疾病状态变化的时变过渡概率,揭示了心血管疾病随时间发展的模式。我们发现,从心肌梗死(MI)到中风的转变速度最快(平均转变时间为 3 天,标度为 0 天,因为数据集中只有 1 名患者从心肌梗死转变为中风),而从心肌梗死到心绞痛的转变速度最慢(平均转变时间为 1457 天,标度为 1449 天)。充血性心力衰竭最有可能是首次发病(371/840,44.2%),其次是中风(216/840,25.7%)。由此产生的人工智能具有可操作性,因为它可以作为电子健康队列分析工具,帮助医生深入了解治疗和干预策略。通过专家小组访谈和调查,我们发现了模型的 9 个应用案例:过去的研究没有提供基于全面、10 状态、连续时间马尔可夫链模型的可操作队列级决策支持工具,以从真实世界的患者数据中揭示复杂的心血管疾病进展模式并支持临床决策。本文旨在解决这一关键的局限性。我们的随机模型嵌入式人工智能可以帮助临床医生在真实患者数据的客观数据驱动见解的指导下,进行高效的疾病监测和干预决策。此外,只需输入 3 个数据元素:合成患者标识符、病程名称和从基线日期算起的病程时间(以天为单位),所提出的模型就能揭示任何慢性疾病的进展模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a Cohort Analytics Tool for Monitoring Progression Patterns in Cardiovascular Diseases: Advanced Stochastic Modeling Approach.

Background: The World Health Organization (WHO) reported that cardiovascular diseases (CVDs) are the leading cause of death worldwide. CVDs are chronic, with complex progression patterns involving episodes of comorbidities and multimorbidities. When dealing with chronic diseases, physicians often adopt a "watchful waiting" strategy, and actions are postponed until information is available. Population-level transition probabilities and progression patterns can be revealed by applying time-variant stochastic modeling methods to longitudinal patient data from cohort studies. Inputs from CVD practitioners indicate that tools to generate and visualize cohort transition patterns have many impactful clinical applications. The resultant computational model can be embedded in digital decision support tools for clinicians. However, to date, no study has attempted to accomplish this for CVDs.

Objective: This study aims to apply advanced stochastic modeling methods to uncover the transition probabilities and progression patterns from longitudinal episodic data of patient cohorts with CVD and thereafter use the computational model to build a digital clinical cohort analytics artifact demonstrating the actionability of such models.

Methods: Our data were sourced from 9 epidemiological cohort studies by the National Heart Lung and Blood Institute and comprised chronological records of 1274 patients associated with 4839 CVD episodes across 16 years. We then used the continuous-time Markov chain method to develop our model, which offers a robust approach to time-variant transitions between disease states in chronic diseases.

Results: Our study presents time-variant transition probabilities of CVD state changes, revealing patterns of CVD progression against time. We found that the transition from myocardial infarction (MI) to stroke has the fastest transition rate (mean transition time 3, SD 0 days, because only 1 patient had a MI-to-stroke transition in the dataset), and the transition from MI to angina is the slowest (mean transition time 1457, SD 1449 days). Congestive heart failure is the most probable first episode (371/840, 44.2%), followed by stroke (216/840, 25.7%). The resultant artifact is actionable as it can act as an eHealth cohort analytics tool, helping physicians gain insights into treatment and intervention strategies. Through expert panel interviews and surveys, we found 9 application use cases of our model.

Conclusions: Past research does not provide actionable cohort-level decision support tools based on a comprehensive, 10-state, continuous-time Markov chain model to unveil complex CVD progression patterns from real-world patient data and support clinical decision-making. This paper aims to address this crucial limitation. Our stochastic model-embedded artifact can help clinicians in efficient disease monitoring and intervention decisions, guided by objective data-driven insights from real patient data. Furthermore, the proposed model can unveil progression patterns of any chronic disease of interest by inputting only 3 data elements: a synthetic patient identifier, episode name, and episode time in days from a baseline date.

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来源期刊
JMIR Medical Informatics
JMIR Medical Informatics Medicine-Health Informatics
CiteScore
7.90
自引率
3.10%
发文量
173
审稿时长
12 weeks
期刊介绍: JMIR Medical Informatics (JMI, ISSN 2291-9694) is a top-rated, tier A journal which focuses on clinical informatics, big data in health and health care, decision support for health professionals, electronic health records, ehealth infrastructures and implementation. It has a focus on applied, translational research, with a broad readership including clinicians, CIOs, engineers, industry and health informatics professionals. Published by JMIR Publications, publisher of the Journal of Medical Internet Research (JMIR), the leading eHealth/mHealth journal (Impact Factor 2016: 5.175), JMIR Med Inform has a slightly different scope (emphasizing more on applications for clinicians and health professionals rather than consumers/citizens, which is the focus of JMIR), publishes even faster, and also allows papers which are more technical or more formative than what would be published in the Journal of Medical Internet Research.
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