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An Engineering Alternative to Lockdown During COVID-19 and Other Airborne Infectious Disease Pandemics: Feasibility Study. COVID-19 和其他空气传播传染病大流行期间封锁的工程替代方案:可行性研究。
Pub Date : 2024-05-14 DOI: 10.2196/54666
Yusaku Fujii

Background: Now and in the future, airborne diseases such as COVID-19 could become uncontrollable and lead the world into lockdowns. Finding alternatives to lockdowns, which limit individual freedoms and cause enormous economic losses, is critical.

Objective: The purpose of this study was to assess the feasibility of achieving a society or a nation that does not require lockdown during a pandemic due to airborne infectious diseases through the mass production and distribution of high-performance, low-cost, and comfortable powered air purifying respirators (PAPRs).

Methods: The feasibility of a social system using PAPR as an alternative to lockdown was examined from the following perspectives: first, what PAPRs can do as an alternative to lockdown; second, how to operate a social system utilizing PAPR; third, directions of improvement of PAPR as an alternative to lockdown; and finally, balancing between efficiency of infection control and personal freedom through the use of Internet of Things (IoT).

Results: PAPR was shown to be a possible alternative to lockdown through the reduction of airborne and droplet transmissions and through a temporary reduction of infection probability per contact. A social system in which individual constraints imposed by lockdown are replaced by PAPRs was proposed, and an example of its operation is presented in this paper. For example, the government determines the type and intensity of the lockdown and activates it. At that time, the government will also indicate how PAPR can be substituted for the different activity and movement restrictions imposed during a lockdown, for example, a curfew order may be replaced with the permission to go outside if wearing a PAPR. The following 7 points were raised as directions for improvement of PAPR as an alternative method to lockdown: flow optimization, precise differential pressure control, design improvement, maintenance method, variation development such as booth type, information terminal function, and performance evaluation method. In order to achieve the effectiveness and efficiency in controlling the spread of infection and the individual freedom at a high level in a social system that uses PAPRs as an alternative to lockdown, it was considered effective to develop a PAPR wearing rate network management system utilizing IoT.

Conclusions: This study shows that using PAPR with infection control ability and with less economic and social damage as an alternative to nationwide lockdown is possible during a pandemic due to airborne infectious diseases. Further, the efficiency of the government's infection control and each citizen's freedom can be balanced by using the PAPR wearing rate network management system utilizing an IoT system.

背景:现在和将来,COVID-19 等空气传播疾病可能变得无法控制,并导致世界陷入封锁。封锁会限制个人自由并造成巨大的经济损失,因此寻找封锁的替代方案至关重要:本研究的目的是评估通过大规模生产和分发高性能、低成本和舒适的动力空气净化呼吸器(PAPRs),实现社会或国家在空气传播传染病大流行期间无需封锁的可行性:方法:从以下几个方面研究了使用 PAPR 替代封锁的社会系统的可行性:首先,PAPR 作为封锁的替代品能做什么;其次,如何操作使用 PAPR 的社会系统;第三,PAPR 作为封锁的替代品的改进方向;最后,通过使用物联网(IoT)在感染控制的效率和个人自由之间取得平衡:结果表明,通过减少空气传播和飞沫传播,并通过暂时降低每次接触的感染概率,PAPR 可以替代封锁。本文提出了一个社会系统,在该系统中,PAPR 取代了封锁所施加的个人限制,并介绍了该系统的一个运行实例。例如,政府决定封锁的类型和强度并启动封锁。政府届时还将说明如何用 PAPR 代替封锁期间实施的不同活动和行动限制,例如,如果佩戴 PAPR,宵禁令可能会被允许外出所取代。作为封锁的替代方法,PAPR 的改进方向有以下 7 点:流量优化、精确压差控制、设计改进、维护方法、岗亭类型等差异化开发、信息终端功能和性能评估方法。为了在使用 PAPR 作为封锁替代方法的社会系统中实现控制感染传播的有效性和高效性以及个人的高度自由,利用物联网开发 PAPR 穿戴率网络管理系统被认为是有效的:本研究表明,在空气传播传染病大流行期间,使用具有感染控制能力且经济和社会损失较小的空气呼吸器替代全国范围的封锁是可行的。此外,通过利用物联网系统的 PAPR 佩戴率网络管理系统,可以平衡政府的感染控制效率和每个公民的自由。
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引用次数: 0
Preliminary Assessment of an Ambulatory Device Dedicated to Upper Airway Muscle Training in Patients With Sleep Apnea: Proof-of-Concept Study. 睡眠呼吸暂停患者上气道肌肉训练专用可移动设备的初步评估:概念验证研究
Pub Date : 2024-04-15 DOI: 10.2196/51901
Patrice Roberge, Jean Ruel, André Bégin-Drolet, Jean Lemay, Simon Gakwaya, Jean-François Masse, Frédéric Sériès

Background: Obstructive sleep apnea/hypopnea syndrome (OSAHS) is a prevalent condition affecting a substantial portion of the global population, with its prevalence increasing over the past 2 decades. OSAHS is characterized by recurrent upper airway (UA) closure during sleep, leading to significant impacts on quality of life and heightened cardiovascular and metabolic morbidity. Despite continuous positive airway pressure (CPAP) being the gold standard treatment, patient adherence remains suboptimal due to various factors, such as discomfort, side effects, and treatment unacceptability.

Objective: Considering the challenges associated with CPAP adherence, an alternative approach targeting the UA muscles through myofunctional therapy was explored. This noninvasive intervention involves exercises of the lips, tongue, or both to improve oropharyngeal functions and mitigate the severity of OSAHS. With the goal of developing a portable device for home-based myofunctional therapy with continuous monitoring of exercise performance and adherence, the primary outcome of this study was the degree of completion and adherence to a 4-week training session.

Methods: This proof-of-concept study focused on a portable device that was designed to facilitate tongue and lip myofunctional therapy and enable precise monitoring of exercise performance and adherence. A clinical study was conducted to assess the effectiveness of this program in improving sleep-disordered breathing. Participants were instructed to perform tongue protrusion, lip pressure, and controlled breathing as part of various tasks 6 times a week for 4 weeks, with each session lasting approximately 35 minutes.

Results: Ten participants were enrolled in the study (n=8 male; mean age 48, SD 22 years; mean BMI 29.3, SD 3.5 kg/m2; mean apnea-hypopnea index [AHI] 20.7, SD 17.8/hour). Among the 8 participants who completed the 4-week program, the overall compliance rate was 91% (175/192 sessions). For the tongue exercise, the success rate increased from 66% (211/320 exercises; SD 18%) on the first day to 85% (272/320 exercises; SD 17%) on the last day (P=.05). AHI did not change significantly after completion of training but a noteworthy correlation between successful lip exercise improvement and AHI reduction in the supine position was observed (Rs=-0.76; P=.03). These findings demonstrate the potential of the device for accurately monitoring participants' performance in lip and tongue pressure exercises during myofunctional therapy. The diversity of the training program (it mixed exercises mixed training games), its ability to provide direct feedback for each exercise to the participants, and the easy measurement of treatment adherence are major strengths of our training program.

Conclusions: The study's portable device for home-based myofunctional therapy shows promise as

背景:阻塞性睡眠呼吸暂停/低通气综合征(OSAHS)是一种影响全球大部分人口的普遍病症,其发病率在过去 20 年中不断上升。OSAHS 的特点是睡眠时反复出现上气道(UA)关闭,严重影响生活质量,并增加心血管和代谢疾病的发病率。尽管持续气道正压(CPAP)是金标准治疗方法,但由于不适、副作用和治疗不可接受性等各种因素,患者的依从性仍不理想:考虑到坚持使用 CPAP 所面临的挑战,我们探索了一种通过肌肉功能疗法来治疗 UA 肌肉的替代方法。这种非侵入性干预包括嘴唇、舌头或两者的锻炼,以改善口咽功能,减轻 OSAHS 的严重程度。本研究的目标是开发一种用于家庭肌肉功能治疗的便携式设备,并对锻炼效果和坚持情况进行持续监测,研究的主要结果是完成和坚持4周训练课程的程度:这项概念验证研究的重点是一种便携式设备,该设备旨在促进舌唇肌功能治疗,并能精确监测运动表现和坚持情况。我们进行了一项临床研究,以评估该项目在改善睡眠呼吸障碍方面的效果。研究人员指导参与者进行伸舌、压唇和控制呼吸等各种训练,每周 6 次,持续 4 周,每次训练约 35 分钟:10 名参与者参加了研究(男性 8 人;平均年龄 48 岁,标准差 22 岁;平均体重指数 29.3,标准差 3.5 千克/平方米;平均呼吸暂停-低通气指数 [AHI] 20.7,标准差 17.8/小时)。8 名参与者完成了为期 4 周的计划,总体达标率为 91%(175/192 次)。舌部运动的成功率从第一天的 66%(211/320 次运动;SD 18%)上升到最后一天的 85%(272/320 次运动;SD 17%)(P=.05)。训练完成后,AHI 没有明显变化,但在成功改善唇部运动和仰卧位 AHI 降低之间观察到显著的相关性(Rs=-0.76;P=.03)。这些研究结果表明,在肌肉功能治疗过程中,该设备具有准确监测参与者唇压和舌压练习表现的潜力。训练项目的多样性(混合练习混合训练游戏)、为参与者的每次练习提供直接反馈的能力以及易于测量治疗依从性是我们训练项目的主要优势:本研究的便携式家用肌功能治疗设备有望成为降低 OSAHS 严重程度的非侵入性替代方法,成功改善唇部运动与降低 AHI 之间存在显著相关性,值得进一步开发和研究。
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引用次数: 0
Finite Element Analysis for Degenerative Cervical Myelopathy: Scoping Review of the Current Findings and Design Approaches, Including Recommendations on the Choice of Material Properties. 颈椎退行性病变的有限元分析:当前研究结果和设计方法的范围审查,包括材料特性选择建议。
Pub Date : 2024-03-28 DOI: 10.2196/48146
Benjamin Davies, Samuel Schaefer, Amir Rafati Fard, Virginia Newcombe, Michael Sutcliffe
<p><strong>Background: </strong>Degenerative cervical myelopathy (DCM) is a slow-motion spinal cord injury caused via chronic mechanical loading by spinal degenerative changes. A range of different degenerative changes can occur. Finite element analysis (FEA) can predict the distribution of mechanical stress and strain on the spinal cord to help understand the implications of any mechanical loading. One of the critical assumptions for FEA is the behavior of each anatomical element under loading (ie, its material properties).</p><p><strong>Objective: </strong>This scoping review aims to undertake a structured process to select the most appropriate material properties for use in DCM FEA. In doing so, it also provides an overview of existing modeling approaches in spinal cord disease and clinical insights into DCM.</p><p><strong>Methods: </strong>We conducted a scoping review using qualitative synthesis. Observational studies that discussed the use of FEA models involving the spinal cord in either health or disease (including DCM) were eligible for inclusion in the review. We followed the PRISMA-ScR (Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews) guidelines. The MEDLINE and Embase databases were searched to September 1, 2021. This was supplemented with citation searching to retrieve the literature used to define material properties. Duplicate title and abstract screening and data extraction were performed. The quality of evidence was appraised using the quality assessment tool we developed, adapted from the Newcastle-Ottawa Scale, and shortlisted with respect to DCM material properties, with a final recommendation provided. A qualitative synthesis of the literature is presented according to the Synthesis Without Meta-Analysis reporting guidelines.</p><p><strong>Results: </strong>A total of 60 papers were included: 41 (68%) "FEA articles" and 19 (32%) "source articles." Most FEA articles (33/41, 80%) modeled the gray matter and white matter separately, with models typically based on tabulated data or, less frequently, a hyperelastic Ogden variant or linear elastic function. Of the 19 source articles, 14 (74%) were identified as describing the material properties of the spinal cord, of which 3 (21%) were considered most relevant to DCM. Of the 41 FEA articles, 15 (37%) focused on DCM, of which 9 (60%) focused on ossification of the posterior longitudinal ligament. Our aggregated results of DCM FEA indicate that spinal cord loading is influenced by the pattern of degenerative changes, with decompression alone (eg, laminectomy) sufficient to address this as opposed to decompression combined with other procedures (eg, laminectomy and fusion).</p><p><strong>Conclusions: </strong>FEA is a promising technique for exploring the pathobiology of DCM and informing clinical care. This review describes a structured approach to help future investigators deploy FEA for DCM. However, there are limitations to these r
背景:颈椎退行性脊髓病(DCM)是一种慢动作脊髓损伤,由脊髓退行性病变造成的慢性机械负荷引起。可发生一系列不同的退行性病变。有限元分析(FEA)可以预测脊髓上机械应力和应变的分布,帮助了解任何机械负荷的影响。有限元分析的关键假设之一是每个解剖元素在负荷下的行为(即其材料特性):本范围审查旨在采用结构化流程来选择最适合用于 DCM 有限元分析的材料特性。在此过程中,它还概述了脊髓疾病的现有建模方法以及对 DCM 的临床见解:我们采用定性综述的方法进行了范围界定综述。讨论脊髓在健康或疾病(包括 DCM)中使用有限元分析模型的观察性研究均可纳入综述。我们遵循了 PRISMA-ScR(系统综述和荟萃分析的首选报告项目扩展至范围综述)指南。我们对 MEDLINE 和 Embase 数据库进行了检索,检索期至 2021 年 9 月 1 日。此外,还进行了引文检索,以检索用于定义材料特性的文献。对重复的标题和摘要进行筛选并提取数据。使用我们开发的质量评估工具(改编自纽卡斯尔-渥太华量表)对证据质量进行评估,并针对 DCM 材料特性进行筛选,最后提出建议。根据无元分析综合报告指南,对文献进行了定性综合:结果:共收录了 60 篇论文:41篇(68%)为 "有限元分析文章",19篇(32%)为 "资料来源文章"。大多数有限元分析文章(33/41,80%)分别对灰质和白质进行了建模,模型通常基于表格数据或较少见的高弹性奥格登变体或线性弹性函数。在 19 篇来源文章中,有 14 篇(74%)被确定为描述脊髓的材料特性,其中 3 篇(21%)被认为与 DCM 最为相关。在 41 篇有限元分析文章中,15 篇(37%)侧重于 DCM,其中 9 篇(60%)侧重于后纵韧带骨化。我们对 DCM FEA 的汇总结果表明,脊髓负荷受退行性病变模式的影响,单纯减压(如椎板切除术)足以解决这一问题,而减压结合其他手术(如椎板切除术和融合术)则无法解决这一问题:结论:FEA 是一种很有前途的技术,可用于探索 DCM 的病理生物学并为临床治疗提供依据。本综述介绍了一种结构化方法,可帮助未来的研究人员将 FEA 用于 DCM。然而,这些建议还存在局限性和更广泛的不确定性。要将 FEA 应用于 DCM 的临床治疗,很可能需要克服这些限制因素。
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引用次数: 0
Validation of a Novel Noninvasive Technology to Estimate Blood Oxygen Saturation Using Green Light: Observational Study 利用绿光估算血氧饱和度的新型无创技术的验证:观察研究
Pub Date : 2024-03-27 DOI: 10.2196/46974
Sanjay Gokhale, V. Daggubati, Georgios Alexandrakis
Pulse oximeters work within the red-infrared wavelengths. Therefore, these oximeters produce erratic results in dark-skinned subjects and in subjects with cold extremities. Pulse oximetry is routinely performed in patients with fever; however, an elevation in body temperature decreases the affinity of hemoglobin for oxygen, causing a drop in oxygen saturation or oxyhemoglobin concentrations. We aimed to determine whether our new investigational device, the Shani device or SH1 (US Patent 11191460), detects a drop in oxygen saturation or a decrease in oxyhemoglobin concentrations. An observational study (phase 1) was performed in two separate groups to validate measurements of hemoglobin and oxygen concentrations, including 39 participants recruited among current university students and staff aged 20-40 years. All volunteers completed baseline readings using the SH1 device and the commercially available Food and Drug Administration–approved pulse oximeter Masimo. SH1 uses two light-emitting diodes in which the emitted wavelengths match with absorption peaks of oxyhemoglobin (hemoglobin combined with oxygen) and deoxyhemoglobin (hemoglobin without oxygen or reduced hemoglobin). Total hemoglobin was calculated as the sum of oxyhemoglobin and deoxyhemoglobin. Subsequently, 16 subjects completed the “heat jacket study” and the others completed the “blood donation study.” Masimo was consistently used on the finger for comparison. The melanin level was accounted for using the von Luschan skin color scale (VLS) and a specifically designed algorithm. We here focus on the results of the heat jacket study, in which the subject wore a double-layered heated jacket and pair of trousers including a network of polythene tubules along with an inlet and outlet. Warm water was circulated to increase the body temperature by 0.5-0.8 °C above the baseline body temperature. We expected a slight drop in oxyhemoglobin concentrations in the heating phase at the tissue level. The mean age of the participants was 24.1 (SD 0.8) years. The skin tone varied from 12 to 36 on the VLS, representing a uniform distribution with one-third of the participants having fair skin, brown skin, and dark skin, respectively. Using a specific algorithm and software, the reflection ratio for oxyhemoglobin was displayed on the screen of the device along with direct hemoglobin values. The SH1 device picked up more minor changes in oxyhemoglobin levels after a change in body temperature compared to the pulse oximeter, with a maximum drop in oxyhemoglobin concentration detected of 6.5% and 2.54%, respectively. Our new investigational device SH1 measures oxygen saturation at the tissue level by reflectance spectroscopy using green wavelengths. This device fared well regardless of skin color. This device can thus eliminate racial disparity in these key biomarker assessments. Moreover, since the light is shone on the wrist, SH1 can be readily miniaturized into a wearabl
脉冲血氧仪的工作波长为红外线。因此,这些血氧仪对深肤色受试者和四肢冰冷的受试者产生的结果不稳定。脉搏血氧仪是发热患者的常规检测仪器,但体温升高会降低血红蛋白对氧气的亲和力,导致血氧饱和度或氧血红蛋白浓度下降。 我们的目的是确定我们的新型研究设备--Shani 设备或 SH1(美国专利 11191460)是否能检测到血氧饱和度下降或氧血红蛋白浓度降低。 为了验证血红蛋白和氧浓度的测量结果,我们在两个不同的小组中分别进行了观察研究(第 1 阶段),其中包括从 20-40 岁的在校大学生和教职员工中招募的 39 名参与者。所有志愿者都使用 SH1 设备和经美国食品和药物管理局批准的商用脉搏血氧仪 Masimo 完成了基线读数。SH1 使用两个发光二极管,其发射波长与氧合血红蛋白(含氧血红蛋白)和脱氧血红蛋白(不含氧血红蛋白或还原血红蛋白)的吸收峰相匹配。总血红蛋白的计算是氧合血红蛋白和脱氧血红蛋白之和。随后,16 名受试者完成了 "热夹克研究",其他受试者完成了 "献血研究"。始终使用 Masimo 对手指进行比较。黑色素水平是通过 von Luschan 皮肤色标(VLS)和专门设计的算法计算得出的。在这项研究中,受试者穿着双层加热夹克和裤子,其中包括一个聚乙烯管网和一个进出口。通过循环温水,使体温比基准体温高出 0.5-0.8 °C。我们预计在加热阶段,氧合血红蛋白在组织水平的浓度会略有下降。 参与者的平均年龄为 24.1 岁(标准差为 0.8 岁)。在 VLS 上,肤色从 12 到 36 不等,分布均匀,三分之一的参与者分别为白皙皮肤、棕色皮肤和深色皮肤。通过特定的算法和软件,氧合血红蛋白的反射比值与直接血红蛋白值一起显示在设备屏幕上。与脉搏血氧仪相比,SH1 设备在体温变化后能捕捉到更多的氧合血红蛋白水平的微小变化,检测到的氧合血红蛋白浓度的最大降幅分别为 6.5% 和 2.54%。 我们的新型研究设备 SH1 通过使用绿色波长的反射光谱法测量组织水平的血氧饱和度。无论肤色如何,该设备都表现良好。因此,该设备可以消除这些关键生物标志物评估中的种族差异。此外,由于光照在手腕上,SH1 可以很容易地微型化,成为一种可穿戴设备。
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引用次数: 0
Enhancing Energy Efficiency in Telehealth Internet of Things Systems Through Fog and Cloud Computing Integration: Simulation Study. 通过雾和云计算集成提高远程医疗物联网系统的能效:模拟研究。
Pub Date : 2024-03-06 DOI: 10.2196/50175
Yunyong Guo, Sudhakar Ganti, Yi Wu

Background: The increasing adoption of telehealth Internet of Things (IoT) devices in health care informatics has led to concerns about energy use and data processing efficiency.

Objective: This paper introduces an innovative model that integrates telehealth IoT devices with a fog and cloud computing-based platform, aiming to enhance energy efficiency in telehealth IoT systems.

Methods: The proposed model incorporates adaptive energy-saving strategies, localized fog nodes, and a hybrid cloud infrastructure. Simulation analyses were conducted to assess the model's effectiveness in reducing energy consumption and enhancing data processing efficiency.

Results: Simulation results demonstrated significant energy savings, with a 2% reduction in energy consumption achieved through adaptive energy-saving strategies. The sample size for the simulation was 10-40, providing statistical robustness to the findings.

Conclusions: The proposed model successfully addresses energy and data processing challenges in telehealth IoT scenarios. By integrating fog computing for local processing and a hybrid cloud infrastructure, substantial energy savings are achieved. Ongoing research will focus on refining the energy conservation model and exploring additional functional enhancements for broader applicability in health care and industrial contexts.

背景随着远程医疗物联网(IoT)设备在医疗信息学中的应用日益广泛,人们开始关注能源使用和数据处理效率问题:本文介绍了一种将远程医疗物联网设备与基于雾和云计算的平台相结合的创新模式,旨在提高远程医疗物联网系统的能效:所提出的模型结合了自适应节能策略、本地化雾节点和混合云基础设施。我们进行了仿真分析,以评估该模型在降低能耗和提高数据处理效率方面的有效性:仿真结果表明节能效果显著,通过自适应节能策略,能耗降低了 2%。模拟的样本量为 10-40 个,为研究结果提供了统计稳健性:所提出的模型成功地解决了远程医疗物联网场景中的能源和数据处理难题。通过整合用于本地处理的雾计算和混合云基础设施,实现了大幅节能。正在进行的研究将侧重于完善节能模型,并探索更多的功能改进,以便在医疗保健和工业环境中更广泛地应用。
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引用次数: 0
A Deep Learning Framework for Predicting Patient Decannulation on Extracorporeal Membrane Oxygenation Devices: Development and Model Analysis Study. 用于预测体外膜氧合设备上病人拔管情况的深度学习框架:开发和模型分析研究。
Pub Date : 2024-02-02 DOI: 10.2196/48497
Joshua Fuller, Alexey Abramov, Dana Mullin, James Beck, Philippe Lemaitre, Elham Azizi

Background: Venovenous extracorporeal membrane oxygenation (VV-ECMO) is a therapy for patients with refractory respiratory failure. The decision to decannulate someone from extracorporeal membrane oxygenation (ECMO) often involves weaning trials and clinical intuition. To date, there are limited prognostication metrics to guide clinical decision-making to determine which patients will be successfully weaned and decannulated.

Objective: This study aims to assist clinicians with the decision to decannulate a patient from ECMO, using Continuous Evaluation of VV-ECMO Outcomes (CEVVO), a deep learning-based model for predicting success of decannulation in patients supported on VV-ECMO. The running metric may be applied daily to categorize patients into high-risk and low-risk groups. Using these data, providers may consider initiating a weaning trial based on their expertise and CEVVO.

Methods: Data were collected from 118 patients supported with VV-ECMO at the Columbia University Irving Medical Center. Using a long short-term memory-based network, CEVVO is the first model capable of integrating discrete clinical information with continuous data collected from an ECMO device. A total of 12 sets of 5-fold cross validations were conducted to assess the performance, which was measured using the area under the receiver operating characteristic curve (AUROC) and average precision (AP). To translate the predicted values into a clinically useful metric, the model results were calibrated and stratified into risk groups, ranging from 0 (high risk) to 3 (low risk). To further investigate the performance edge of CEVVO, 2 synthetic data sets were generated using Gaussian process regression. The first data set preserved the long-term dependency of the patient data set, whereas the second did not.

Results: CEVVO demonstrated consistently superior classification performance compared with contemporary models (P<.001 and P=.04 compared with the next highest AUROC and AP). Although the model's patient-by-patient predictive power may be too low to be integrated into a clinical setting (AUROC 95% CI 0.6822-0.7055; AP 95% CI 0.8515-0.8682), the patient risk classification system displayed greater potential. When measured at 72 hours, the high-risk group had a successful decannulation rate of 58% (7/12), whereas the low-risk group had a successful decannulation rate of 92% (11/12; P=.04). When measured at 96 hours, the high- and low-risk groups had a successful decannulation rate of 54% (6/11) and 100% (9/9), respectively (P=.01). We hypothesized that the improved performance of CEVVO was owing to its ability to efficiently capture transient temporal patterns. Indeed, CEVVO exhibited improved performance on synthetic data with inherent temporal dependencies (P<.001) compared with logistic regression and a dense neural network.

Conclusions: The ability to interpret

背景:静脉体外膜氧合(VV-ECMO)是治疗难治性呼吸衰竭患者的一种疗法。决定是否让患者脱离体外膜肺氧合(ECMO)常常涉及断流试验和临床直觉。迄今为止,用于指导临床决策以确定哪些患者将成功断奶并脱离监护的预后指标非常有限:本研究旨在使用 "VV-ECMO 结果持续评估"(CEVVO)协助临床医生做出决定,该模型基于深度学习,可预测 VV-ECMO 支持患者的断血成功率。该运行指标每天都可用于将患者分为高风险组和低风险组。利用这些数据,医疗服务提供者可根据其专业知识和 CEVVO 考虑启动断流试验:收集了哥伦比亚大学欧文医疗中心 118 名接受 VV-ECMO 支持的患者的数据。CEVVO 使用基于长短期记忆的网络,是首个能够将离散临床信息与从 ECMO 设备收集的连续数据相结合的模型。该模型共进行了 12 组 5 倍交叉验证来评估其性能,并使用接收者操作特征曲线下面积(AUROC)和平均精度(AP)来衡量。为了将预测值转化为临床有用的指标,对模型结果进行了校准,并将其分为 0(高风险)至 3(低风险)的风险组。为进一步研究 CEVVO 的性能优势,使用高斯过程回归生成了两个合成数据集。第一个数据集保留了患者数据集的长期依赖性,而第二个数据集则没有:结果:CEVVO 的分类性能始终优于当代模型(PC 结论:CEVVO 的分类性能始终优于当代模型:解释和整合大型数据集的能力对于创建准确的模型至关重要,这些模型能够帮助临床医生对接受 VV-ECMO 支持的患者进行风险分层。我们的框架可为将来将 CEVVO 纳入更全面的重症监护系统提供指导。
{"title":"A Deep Learning Framework for Predicting Patient Decannulation on Extracorporeal Membrane Oxygenation Devices: Development and Model Analysis Study.","authors":"Joshua Fuller, Alexey Abramov, Dana Mullin, James Beck, Philippe Lemaitre, Elham Azizi","doi":"10.2196/48497","DOIUrl":"10.2196/48497","url":null,"abstract":"<p><strong>Background: </strong>Venovenous extracorporeal membrane oxygenation (VV-ECMO) is a therapy for patients with refractory respiratory failure. The decision to decannulate someone from extracorporeal membrane oxygenation (ECMO) often involves weaning trials and clinical intuition. To date, there are limited prognostication metrics to guide clinical decision-making to determine which patients will be successfully weaned and decannulated.</p><p><strong>Objective: </strong>This study aims to assist clinicians with the decision to decannulate a patient from ECMO, using Continuous Evaluation of VV-ECMO Outcomes (CEVVO), a deep learning-based model for predicting success of decannulation in patients supported on VV-ECMO. The running metric may be applied daily to categorize patients into high-risk and low-risk groups. Using these data, providers may consider initiating a weaning trial based on their expertise and CEVVO.</p><p><strong>Methods: </strong>Data were collected from 118 patients supported with VV-ECMO at the Columbia University Irving Medical Center. Using a long short-term memory-based network, CEVVO is the first model capable of integrating discrete clinical information with continuous data collected from an ECMO device. A total of 12 sets of 5-fold cross validations were conducted to assess the performance, which was measured using the area under the receiver operating characteristic curve (AUROC) and average precision (AP). To translate the predicted values into a clinically useful metric, the model results were calibrated and stratified into risk groups, ranging from 0 (high risk) to 3 (low risk). To further investigate the performance edge of CEVVO, 2 synthetic data sets were generated using Gaussian process regression. The first data set preserved the long-term dependency of the patient data set, whereas the second did not.</p><p><strong>Results: </strong>CEVVO demonstrated consistently superior classification performance compared with contemporary models (P<.001 and P=.04 compared with the next highest AUROC and AP). Although the model's patient-by-patient predictive power may be too low to be integrated into a clinical setting (AUROC 95% CI 0.6822-0.7055; AP 95% CI 0.8515-0.8682), the patient risk classification system displayed greater potential. When measured at 72 hours, the high-risk group had a successful decannulation rate of 58% (7/12), whereas the low-risk group had a successful decannulation rate of 92% (11/12; P=.04). When measured at 96 hours, the high- and low-risk groups had a successful decannulation rate of 54% (6/11) and 100% (9/9), respectively (P=.01). We hypothesized that the improved performance of CEVVO was owing to its ability to efficiently capture transient temporal patterns. Indeed, CEVVO exhibited improved performance on synthetic data with inherent temporal dependencies (P<.001) compared with logistic regression and a dense neural network.</p><p><strong>Conclusions: </strong>The ability to interpret","PeriodicalId":87288,"journal":{"name":"JMIR biomedical engineering","volume":"9 ","pages":"e48497"},"PeriodicalIF":0.0,"publicationDate":"2024-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11041448/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141322163","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
An Investigation of Deepfake Voice Detection using Speech Pause Patterns: Pilot Study (Preprint) 利用语音停顿模式进行深度伪语音检测的研究:试点研究(预印本)
Pub Date : 2024-01-16 DOI: 10.2196/56245
Nikhil Valsan Kulangareth, Jaycee M. Kaufman, Jessica Oreskovic, Yan Fossat
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引用次数: 0
Impact of Audio Data Compression on Feature Extraction for Vocal Biomarker Detection: Validation Study (Preprint) 音频数据压缩对声乐生物标记检测特征提取的影响:验证研究(预印本)
Pub Date : 2024-01-10 DOI: 10.2196/56246
Jessica Oreskovic, Jaycee M. Kaufman, Yan Fossat
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引用次数: 0
Assessment of Skin Maturity by LED Light at Birth and Its Association With Lung Maturity: Clinical Trial Secondary Outcomes 用 LED 光评估出生时皮肤成熟度及其与肺成熟度的关系临床试验的次要结果
Pub Date : 2023-12-25 DOI: 10.2196/52468
Gabriela Silveira Neves, Z. Reis, Roberta Romanelli, James Batchelor
Clinicians face barriers when assessing lung maturity at birth due to global inequalities. Still, strategies for testing based solely on gestational age to predict the likelihood of respiratory distress syndrome (RDS) do not offer a comprehensive approach to addressing the challenge of uncertain outcomes. We hypothesize that a noninvasive assessment of skin maturity may indicate lung maturity. This study aimed to assess the association between a newborn’s skin maturity and RDS occurrence. We conducted a case-control nested in a prospective cohort study, a secondary endpoint of a multicenter clinical trial. The study was carried out in 5 Brazilian urban reference centers for highly complex perinatal care. Of 781 newborns from the cohort study, 640 were selected for the case-control analysis. Newborns with RDS formed the case group and newborns without RDS were the controls. All newborns with other diseases exhibiting respiratory manifestations were excluded. Skin maturity was assessed from the newborn's skin over the sole by an optical device that acquired a reflection signal through an LED sensor. The device, previously validated, measured and recorded skin reflectance. Clinical data related to respiratory outcomes were gathered from medical records during the 72-hour follow-up of the newborn, or until discharge or death, whichever occurred first. The main outcome measure was the association between skin reflectance and RDS using univariate and multivariate binary logistic regression. Additionally, we assessed the connection between skin reflectance and factors such as neonatal intensive care unit (NICU) admission and the need for ventilatory support. Out of 604 newborns, 470 (73.4%) were from the RDS group and 170 (26.6%) were from the control group. According to comparisons between the groups, newborns with RDS had a younger gestational age (31.6 vs 39.1 weeks, P<.001) and birth weight (1491 vs 3121 grams, P<.001) than controls. Skin reflectance was associated with RDS (odds ratio [OR] 0.982, 95% CI 0.979-0.985, R2=0.632, P<.001). This relationship remained significant when adjusted by the cofactors antenatal corticosteroid and birth weight (OR 0.994, 95% CI 0.990-0.998, R2=0.843, P<.001). Secondary outcomes also showed differences in skin reflectance. The mean difference was 0.219 (95% CI 0.200-0.238) between newborns that required ventilatory support versus those that did not and 0.223 (95% CI 0.205-0.241) between newborns that required NICU admission versus those that did not. Skin reflectance was associated with ventilatory support (OR 0.996, 95% CI 0.992-0.999, R2=0.814, P=.01) and with NICU admission (OR 0.994, 95% CI 0.990-0.998, R2=0.867, P=.004). Our findings present a potential marker of lung immaturity at birth using the indirect method of skin assessment. Using the RDS clinical condition and a medical device, this study demonstrated the synchrony between lung and skin maturity. Registro Brasileiro
由于全球范围内的不平等,临床医生在评估婴儿出生时的肺成熟度时面临障碍。然而,仅根据胎龄来预测呼吸窘迫综合征(RDS)可能性的检测策略并不能提供一种全面的方法来应对结果不确定的挑战。我们假设,对皮肤成熟度的无创评估可能预示着肺成熟度。 本研究旨在评估新生儿皮肤成熟度与 RDS 发生率之间的关联。 我们在一项前瞻性队列研究中进行了病例对照,这是一项多中心临床试验的次要终点。这项研究在巴西 5 个城市的高度复杂围产期护理参考中心进行。在队列研究的 781 名新生儿中,有 640 名被选中进行病例对照分析。患有 RDS 的新生儿为病例组,无 RDS 的新生儿为对照组。所有患有其他呼吸系统疾病的新生儿均被排除在外。新生儿足底皮肤成熟度的评估是通过一个光学装置进行的,该装置通过 LED 传感器获取反射信号。该设备已通过验证,可测量和记录皮肤反射率。与呼吸系统结果相关的临床数据来自新生儿 72 小时随访期间的医疗记录,或直至出院或死亡,以先发生者为准。主要结果测量是使用单变量和多变量二元逻辑回归分析皮肤反射率与 RDS 之间的关系。此外,我们还评估了皮肤反光与新生儿重症监护室(NICU)入院和呼吸支持需求等因素之间的联系。 在 604 名新生儿中,470 名(73.4%)来自 RDS 组,170 名(26.6%)来自对照组。与对照组相比,RDS 组新生儿的胎龄(31.6 周对 39.1 周,P<.001)和出生体重(1491 克对 3121 克,P<.001)均小于对照组。皮肤反射率与 RDS 相关(几率比 [OR] 0.982,95% CI 0.979-0.985,R2=0.632,P<.001)。经产前皮质类固醇和出生体重等辅助因子调整后,这一关系仍很明显(OR 0.994,95% CI 0.990-0.998,R2=0.843,P<.001)。次要结果还显示了皮肤反射率的差异。需要通气支持的新生儿与不需要通气支持的新生儿之间的平均差异为 0.219(95% CI 0.200-0.238),需要入住新生儿重症监护室的新生儿与不需要入住新生儿重症监护室的新生儿之间的平均差异为 0.223(95% CI 0.205-0.241)。皮肤反射率与通气支持相关(OR 0.996,95% CI 0.992-0.999,R2=0.814,P=.01),与入住新生儿重症监护室相关(OR 0.994,95% CI 0.990-0.998,R2=0.867,P=.004)。 我们的研究结果利用皮肤评估的间接方法提出了出生时肺部不成熟的潜在标志物。本研究利用 RDS 临床条件和医疗设备证明了肺和皮肤成熟度之间的同步性。 Registro Brasileiro de Ensaios Clínicos (ReBEC) RBR-3f5bm5; https://tinyurl.com/9fb7zrdb RR2-10.1136/bmjopen-2018-027442
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引用次数: 0
Measuring Heart Rate Accurately in Patients With Parkinson Disease During Intense Exercise: Usability Study of Fitbit Charge 4 准确测量帕金森病患者在剧烈运动时的心率:Fitbit Charge 4 的可用性研究
Pub Date : 2023-12-08 DOI: 10.2196/51515
Giulia Colonna, Jocelyn Hoye, Bart de Laat, Gelsina Stanley, Alaaddin Ibrahimy, S. Tinaz, Evan D. Morris
Parkinson disease (PD) is the second most common neurodegenerative disease, affecting approximately 1% of the world’s population.Increasing evidence suggests that aerobic physical exercise can be beneficial in mitigating both motor and nonmotor symptoms of the disease.In a recent pilot study of the role of exercise on PD, we sought to confirm exercise intensity by monitoring heart rate (HR). For this purpose, we asked participants to wear a chest strap HR monitor (Polar Electro Oy) and the Fitbit Charge 4 (Fitbit Inc) wrist-worn HR monitor as a potential proxy due to its convenience.Polar H10 has been shown to provide highly accurate R-R interval measurements. Therefore, we treated it as the gold standard in this study. It has been shown that Fitbit Charge 4 has comparable accuracy to Polar H10 in healthy participants. It has yet to be determined if the Fitbit is as accurate as Polar H10 in patients with PD during rest and exercise. This study aimed to compare Fitbit Charge 4 to Polar H10 for monitoring HR in patients with PD at rest and during an intensive exercise program. A total of 596 exercise sessions from 11 (6 male and 5 female) participants were collected simultaneously with both devices. Patients with early-stage PD (Hoehn and Yahr ≤2) were enrolled in a 6-month exercise program designed for patients with PD. They participated in 3 one-hour exercise sessions per week. They wore both Fitbit and Polar H10 during each session. Sessions included rest, warm-up, intense exercise, and cool-down periods.We calculated the bias in the HR of the Fitbit Charge 4 at rest (5 min) and during intense exercise (20 min) by comparing the mean HR during each of the periods to the respective means measured by Polar H10 (HRFitbit – HRPolar). We also measured the sensitivity and specificity of Fitbit Charge 4 to detect average HRs that exceed the threshold for intensive exercise, defined as 70% of an individual’s theoretical maximum HR. Different types of correlations between the 2 devices were investigated. The mean bias was 1.68 beats per minute (bpm) at rest and 6.29 bpm during high-intensity exercise, with an overestimation by Fitbit Charge 4 in both conditions. The mean bias of the Fitbit across both rest and intensive exercise periods was 3.98 bpm. The device’s sensitivity in identifying high-intensity exercise sessions was 97.14%. The correlation between the 2 devices was nonlinear, suggesting Fitbit’s tendency to saturate at high values of HR. The performance of Fitbit Charge 4 is comparable to Polar H10 for assessing exercise intensity in a cohort of patients with PD (mean bias 3.98 bpm). The device could be considered a reasonable surrogate for more cumbersome chest-worn devices in future studies of clinical cohorts.
帕金森病(PD)是第二大最常见的神经退行性疾病,影响约1%的世界人口。越来越多的证据表明,有氧体育锻炼可以减轻疾病的运动和非运动症状。在最近的一项关于运动对PD的作用的初步研究中,我们试图通过监测心率(HR)来确认运动强度。为此,我们要求参与者佩戴胸带式人力资源监测器(Polar Electro Oy)和Fitbit Charge 4 (Fitbit Inc)腕带式人力资源监测器作为潜在的替代品,因为它很方便。Polar H10已被证明可以提供高度精确的R-R区间测量。因此,我们将其作为本研究的金标准。研究表明,Fitbit Charge 4在健康参与者中的准确性与Polar H10相当。在PD患者休息和运动时,Fitbit是否和Polar H10一样准确还有待确定。本研究旨在比较Fitbit Charge 4和Polar H10在PD患者休息和强化锻炼期间监测HR的效果。同时收集了11名参与者(6名男性和5名女性)的596次运动记录。早期PD患者(Hoehn和Yahr≤2)被纳入为PD患者设计的为期6个月的运动计划。他们每周参加三次一小时的锻炼。他们每次都戴着Fitbit和Polar H10。疗程包括休息、热身、剧烈运动和冷静期。通过将每个时间段的平均HR与Polar H10 (HRFitbit - HRPolar)测量的各自平均值进行比较,我们计算了Fitbit Charge 4在休息(5分钟)和剧烈运动(20分钟)时的HR偏差。我们还测量了Fitbit Charge 4的灵敏度和特异性,以检测超过高强度运动阈值的平均HR,定义为个人理论最大HR的70%。研究了两种器件之间不同类型的相关性。休息时的平均偏差为每分钟1.68次,高强度运动时的平均偏差为每分钟6.29次,在这两种情况下,Fitbit Charge 4都高估了这一偏差。Fitbit在休息和剧烈运动期间的平均偏差为每分钟3.98次。该设备识别高强度运动的灵敏度为97.14%。两种设备之间的相关性是非线性的,表明Fitbit倾向于在高HR值时饱和。Fitbit Charge 4在评估PD患者队列运动强度方面的表现与Polar H10相当(平均偏差3.98 bpm)。在未来的临床队列研究中,该设备可以被认为是更笨重的胸戴设备的合理替代品。
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