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Agreement Between Apple Watch and Actical Step Counts in a Community Setting: Cross-Sectional Investigation From the Framingham Heart Study. 社区环境中 Apple Watch 和 Actical 步数的一致性:来自弗雷明汉心脏研究的横断面调查
Pub Date : 2024-07-24 DOI: 10.2196/54631
Nicole L Spartano, Yuankai Zhang, Chunyu Liu, Ariel Chernofsky, Honghuang Lin, Ludovic Trinquart, Belinda Borrelli, Chathurangi H Pathiravasan, Vik Kheterpal, Christopher Nowak, Ramachandran S Vasan, Emelia J Benjamin, David D McManus, Joanne M Murabito

Background: Step counting is comparable among many research-grade and consumer-grade accelerometers in laboratory settings.

Objective: The purpose of this study was to compare the agreement between Actical and Apple Watch step-counting in a community setting.

Methods: Among Third Generation Framingham Heart Study participants (N=3486), we examined the agreement of step-counting between those who wore a consumer-grade accelerometer (Apple Watch Series 0) and a research-grade accelerometer (Actical) on the same days. Secondarily, we examined the agreement during each hour when both devices were worn to account for differences in wear time between devices.

Results: We studied 523 participants (n=3223 person-days, mean age 51.7, SD 8.9 years; women: n=298, 57.0%). Between devices, we observed modest correlation (intraclass correlation [ICC] 0.56, 95% CI 0.54-0.59), poor continuous agreement (29.7%, n=957 of days having steps counts with ≤15% difference), a mean difference of 499 steps per day higher count by Actical, and wide limits of agreement, roughly ±9000 steps per day. However, devices showed stronger agreement in identifying who meets various steps per day thresholds (eg, at 8000 steps per day, kappa coefficient=0.49), for which devices were concordant for 74.8% (n=391) of participants. In secondary analyses, in the hours during which both devices were worn (n=456 participants, n=18,760 person-hours), the correlation was much stronger (ICC 0.86, 95% CI 0.85-0.86), but continuous agreement remained poor (27.3%, n=5115 of hours having step counts with ≤15% difference) between devices and was slightly worse for those with mobility limitations or obesity.

Conclusions: Our investigation suggests poor overall agreement between steps counted by the Actical device and those counted by the Apple Watch device, with stronger agreement in discriminating who meets certain step thresholds. The impact of these challenges may be minimized if accelerometers are used by individuals to determine whether they are meeting physical activity guidelines or tracking step counts. It is also possible that some of the limitations of these older accelerometers may be improved in newer devices.

背景:在实验室环境中,许多研究级和消费级加速度计的计步性能相当:在实验室环境中,许多研究级和消费级加速度计的计步结果具有可比性:本研究旨在比较 Actical 和 Apple Watch 在社区环境中计步的一致性:在第三代弗雷明汉心脏研究参与者(N=3486)中,我们检查了在同一天佩戴消费级加速度计(Apple Watch Series 0)和研究级加速度计(Actical)的参与者的计步一致性。其次,我们还考察了在佩戴两种设备的每个小时内的一致性,以考虑设备之间佩戴时间的差异:我们研究了 523 名参与者(n=3223 人天,平均年龄 51.7 岁,SD 8.9 岁;女性:n=298,57.0%)。在不同设备之间,我们观察到了适度的相关性(类内相关性 [ICC] 0.56,95% CI 0.54-0.59)、较差的连续一致性(29.7%,n=957 天的步数差异≤15%)、Actical 每天平均高出 499 步的差异以及较宽的一致性范围(大约为每天 ±9000 步)。不过,设备在识别哪些人达到了不同的日步数阈值(例如,在日步数为 8000 步时,卡帕系数=0.49)时表现出了更强的一致性,在这一点上,74.8% 的参与者(人数=391)的设备是一致的。在二次分析中,在佩戴两种设备的小时数中(456 名参与者,18760 人时),设备间的相关性更强(ICC 0.86,95% CI 0.85-0.86),但设备间的连续一致性仍然较差(27.3%,5115 个小时的步数差异≤15%),对于行动不便或肥胖者,设备间的一致性略差:我们的调查表明,Actical 设备计算的步数与 Apple Watch 设备计算的步数之间的整体一致性较差,而在区分哪些人达到特定步数阈值方面的一致性较强。如果个人使用加速度计来确定自己是否符合体育锻炼指南或跟踪步数,这些挑战的影响可能会降到最低。此外,这些老式加速度计的一些局限性也有可能在更新的设备中得到改善。
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引用次数: 0
Stroke Survivors' Interaction With Hand Rehabilitation Devices: Observational Study. 中风幸存者与手部康复设备的互动:观察研究。
Pub Date : 2024-06-26 DOI: 10.2196/54159
Chioma Obinuchi Wodu, Gillian Sweeney, Milena Slachetka, Andrew Kerr

Background: The hand is crucial for carrying out activities of daily living as well as social interaction. Functional use of the upper limb is affected in up to 55% to 75% of stroke survivors 3 to 6 months after stroke. Rehabilitation can help restore function, and several rehabilitation devices have been designed to improve hand function. However, access to these devices is compromised in people with more severe loss of function.

Objective: In this study, we aimed to observe stroke survivors with poor hand function interacting with a range of commonly used hand rehabilitation devices.

Methods: Participants were engaged in an 8-week rehabilitation intervention at a technology-enriched rehabilitation gym. The participants spent 50-60 minutes of the 2-hour session in the upper limb section at least twice a week. Each participant communicated their rehabilitation goals, and an Action Research Arm Test (ARAT) was used to measure and categorize hand function as poor (scores of 0-9), moderate (scores of 10-56), or good (score of 57). Participants were observed during their interactions with 3 hand-based rehabilitation devices that focused on hand rehabilitation: the GripAble, NeuroBall, and Semi-Circular Peg Board. Observations of device interactions were recorded for each session.

Results: A total of 29 participants were included in this study, of whom 10 (34%) had poor hand function, 17 (59%) had moderate hand function, and 2 (7%) had good hand function. There were no differences in the age and years after stroke among participants with poor hand function and those with moderate (P=.06 and P=.09, respectively) and good (P=.37 and P=.99, respectively) hand function. Regarding the ability of the 10 participants with poor hand function to interact with the 3 hand-based rehabilitation devices, 2 (20%) participants with an ARAT score greater than 0 were able to interact with the devices, whereas the other 8 (80%) who had an ARAT score of 0 could not. Their inability to interact with these devices was clinically examined, and the reason was determined to be a result of either the presence of (1) muscle tone or stiffness or (2) muscle weakness.

Conclusions: Not all stroke survivors with impairments in their hands can make use of currently available rehabilitation technologies. Those with an ARAT score of 0 cannot actively interact with hand rehabilitation devices, as they cannot carry out the hand movement necessary for such interaction. The design of devices for hand rehabilitation should consider the accessibility needs of those with poor hand function.

背景:手对于日常生活活动和社会交往至关重要。多达 55% 至 75% 的中风幸存者在中风 3 至 6 个月后上肢功能会受到影响。康复训练可以帮助恢复手部功能,目前已设计出多种康复设备来改善手部功能。然而,对于功能丧失较严重的人来说,使用这些设备的机会受到了影响:在这项研究中,我们旨在观察手部功能较差的中风幸存者与一系列常用手部康复设备的互动情况:方法:参与者在一家科技含量较高的康复健身房进行为期 8 周的康复干预。每周至少两次,每次 2 小时,每次 50-60 分钟。每位参与者都会告知自己的康复目标,并使用行动研究手臂测试(ARAT)来测量手部功能并将其分为较差(0-9 分)、中等(10-56 分)或良好(57 分)。在参与者与三种手部康复设备(GripAble、NeuroBall 和 Semi-Circular Peg Board)互动的过程中,对他们进行了观察。每节课都对设备互动情况进行了观察记录:本研究共纳入 29 名参与者,其中 10 人(34%)手部功能较差,17 人(59%)手部功能中等,2 人(7%)手部功能良好。手部功能差的参与者与手部功能中等(分别为 P=.06 和 P=.09)和手部功能良好(分别为 P=.37 和 P=.99)的参与者在年龄和卒中后年数上没有差异。关于 10 名手部功能较差的参与者与 3 种手部康复设备的互动能力,2 名(20%)ARAT 得分大于 0 的参与者能够与设备互动,而其他 8 名(80%)ARAT 得分为 0 的参与者则不能。经临床检查,他们无法与这些设备互动的原因是:(1)肌肉张力或僵硬或(2)肌肉无力:结论:并非所有手部受损的中风幸存者都能使用现有的康复技术。ARAT评分为0分的患者无法与手部康复设备积极互动,因为他们无法进行互动所需的手部运动。手部康复设备的设计应考虑手部功能不良者的无障碍需求。
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引用次数: 0
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。
{"title":"Preliminary Assessment of an Ambulatory Device Dedicated to Upper Airway Muscle Training in Patients With Sleep Apnea: Proof-of-Concept Study.","authors":"Patrice Roberge, Jean Ruel, André Bégin-Drolet, Jean Lemay, Simon Gakwaya, Jean-François Masse, Frédéric Sériès","doi":"10.2196/51901","DOIUrl":"10.2196/51901","url":null,"abstract":"<p><strong>Background: </strong>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.</p><p><strong>Objective: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>Ten participants were enrolled in the study (n=8 male; mean age 48, SD 22 years; mean BMI 29.3, SD 3.5 kg/m<sup>2</sup>; 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 (R<sub>s</sub>=-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.</p><p><strong>Conclusions: </strong>The study's portable device for home-based myofunctional therapy shows promise as","PeriodicalId":87288,"journal":{"name":"JMIR biomedical engineering","volume":"9 ","pages":"e51901"},"PeriodicalIF":0.0,"publicationDate":"2024-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11058550/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141322167","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
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。
{"title":"Finite Element Analysis for Degenerative Cervical Myelopathy: Scoping Review of the Current Findings and Design Approaches, Including Recommendations on the Choice of Material Properties.","authors":"Benjamin Davies, Samuel Schaefer, Amir Rafati Fard, Virginia Newcombe, Michael Sutcliffe","doi":"10.2196/48146","DOIUrl":"10.2196/48146","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;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).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;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.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;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.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;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).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;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","PeriodicalId":87288,"journal":{"name":"JMIR biomedical engineering","volume":"9 ","pages":"e48146"},"PeriodicalIF":0.0,"publicationDate":"2024-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11041437/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141322166","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
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。
{"title":"Validation of a Novel Noninvasive Technology to Estimate Blood Oxygen Saturation Using Green Light: Observational Study","authors":"Sanjay Gokhale, V. Daggubati, Georgios Alexandrakis","doi":"10.2196/46974","DOIUrl":"https://doi.org/10.2196/46974","url":null,"abstract":"\u0000 \u0000 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.\u0000 \u0000 \u0000 \u0000 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.\u0000 \u0000 \u0000 \u0000 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.\u0000 \u0000 \u0000 \u0000 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.\u0000 \u0000 \u0000 \u0000 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","PeriodicalId":87288,"journal":{"name":"JMIR biomedical engineering","volume":"30 24","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140373716","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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。
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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
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JMIR biomedical engineering
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