Best practices

最佳做法
  • 文章类型: Journal Article
    背景:国际神经调节学会(INS)已经认识到有必要建立最佳实践,以优化可植入设备并在未实现理想结果时进行救助。该小组成立了神经刺激适当性共识委员会(NACC)®,为我们的成员和受神经调节设备影响的更广泛的社区所需的事项提供指导。
    方法:INS执行委员会根据专业知识提名了该NACC®出版物的教师,出版物,和职业工作在这个问题上。此外,选择教师是考虑到多样性和不同的职业道路和人口类别的包容性。一旦被选中,教师被要求对当前证据进行评分,并与专家意见一起制定共识建议,以解决有关该主题的信息中的失误。
    结果:NACC®小组为使用留置装置的患者提供了有关抢救和优化护理的信息和权威建议。这些建议基于证据和专家意见,随着每个主题的新数据生成,预计将不断发展。
    结论:NACC®指导应考虑植入刺激装置治疗慢性疼痛的任何患者。应考虑这些共识点,以在外植体之前挽救可能发生故障的设备。
    BACKGROUND: The International Neuromodulation Society (INS) has recognized a need to establish best practices for optimizing implantable devices and salvage when ideal outcomes are not realized. This group has established the Neurostimulation Appropriateness Consensus Committee (NACC)® to offer guidance on matters needed for both our members and the broader community of those affected by neuromodulation devices.
    METHODS: The executive committee of the INS nominated faculty for this NACC® publication on the basis of expertise, publications, and career work on the issue. In addition, the faculty was chosen in consideration of diversity and inclusion of different career paths and demographic categories. Once chosen, the faculty was asked to grade current evidence and along with expert opinion create consensus recommendations to address the lapses in information on this topic.
    RESULTS: The NACC® group established informative and authoritative recommendations on the salvage and optimization of care for those with indwelling devices. The recommendations are based on evidence and expert opinion and will be expected to evolve as new data are generated for each topic.
    CONCLUSIONS: NACC® guidance should be considered for any patient with less-than-optimal outcomes with a stimulation device implanted for treating chronic pain. Consideration should be given to these consensus points to salvage a potentially failed device before explant.
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  • 文章类型: Journal Article
    背景:国际神经调节学会召集了一个基于专业知识和国际代表的多专业医师小组,以建立缓解神经调节并发症的循证指导。该神经刺激适当性共识委员会(NACC)®项目旨在更新循证指南,并提供专家意见,以提高疗效和安全性。
    方法:根据作者的临床专业知识选择作者,熟悉同行评审的文献,研究生产力,以及对神经调节文献的贡献。科领导监督MEDLINE的文献检索,BioMedCentral,当前内容连接,Embase,国际医药文摘,WebofScience,谷歌学者,和PubMed从2017年(NACC上次发布指南时)到2023年10月。使用美国预防服务工作组标准对确定的研究进行了分级,以证明净收益的证据和确定性。建议基于证据的强度或证据不足时的共识。
    结果:NACC审查了已发表的文献,并建立了基于证据和共识的建议,以指导最佳实践。在此过程的未来迭代中,随着新证据的发展,将出现其他指导。
    结论:NACC推荐关于缓解与神经刺激相关的并发症的最佳实践,以提高安全性和疗效。基于证据和共识的建议应用作指导,以在临床上适当时协助决策。
    BACKGROUND: The International Neuromodulation Society convened a multispecialty group of physicians based on expertise and international representation to establish evidence-based guidance on the mitigation of neuromodulation complications. This Neurostimulation Appropriateness Consensus Committee (NACC)® project intends to update evidence-based guidance and offer expert opinion that will improve efficacy and safety.
    METHODS: Authors were chosen on the basis of their clinical expertise, familiarity with the peer-reviewed literature, research productivity, and contributions to the neuromodulation literature. Section leaders supervised literature searches of MEDLINE, BioMed Central, Current Contents Connect, Embase, International Pharmaceutical Abstracts, Web of Science, Google Scholar, and PubMed from 2017 (when NACC last published guidelines) to October 2023. Identified studies were graded using the United States Preventive Services Task Force criteria for evidence and certainty of net benefit. Recommendations are based on the strength of evidence or consensus when evidence was scant.
    RESULTS: The NACC examined the published literature and established evidence- and consensus-based recommendations to guide best practices. Additional guidance will occur as new evidence is developed in future iterations of this process.
    CONCLUSIONS: The NACC recommends best practices regarding the mitigation of complications associated with neurostimulation to improve safety and efficacy. The evidence- and consensus-based recommendations should be used as a guide to assist decision-making when clinically appropriate.
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  • 文章类型: Journal Article
    输精管结扎术是美国最常见的泌尿外科手术,是一种非常有效的男性避孕方式。泌尿外科学会引入的指南已经标准化了输精管切除术护理。供应商应该意识到这些指导方针背后的理由,以及它们之间的主要差异。虽然在过去的40年中,输精管切除术技术几乎没有重大变化,新,可逆血管闭塞技术可能会影响未来男性避孕护理的实施。这里,我们对来自全球6个泌尿外科学会的输精管结扎术指南进行了比较回顾.此外,我们报告了在未来十年内可能出现的几种实验性血管闭塞方法的现状.
    Vasectomy is the most commonly performed urologic procedure in the United States and is a highly effective form of male contraception. The introduction of guidelines by urological societies has standardized vasectomy care. Providers should be awadre of the rationale behind these guidelines, as well as key differences among them. While few major changes to vasectomy technique have been adopted over the past 40 years, new, reversible vasal occlusive technologies may affect delivery of male contraceptive care in the future. Here, we perform a comparative review of vasectomy guidelines from six urological societies worldwide. In addition, we report on the status of several experimental vasal occlusion methods that may be available in the next decade.
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  • 文章类型: Journal Article
    背景:国际神经调节学会召集了一个由医生和科学家组成的多专业小组,以具有国际代表性的专业知识为基础,建立了鞘内给药治疗慢性疼痛的循证指导。这个多重镇痛共识会议(PACC)®项目,创建于二十多年前,旨在为鞘内给药的重要安全性和有效性问题及其对神经调节实践的影响提供循证指导。
    方法:根据作者的临床专业知识选择作者,熟悉同行评审的文献,研究生产力,以及对神经调节文献的贡献。科领导监督MEDLINE的文献检索,BioMedCentral,当前内容连接,Embase,国际医药文摘,WebofScience,谷歌学者,和PubMed从2017年(PACC®上次发布指南时)到现在。使用美国预防服务工作组标准对确定的研究进行了分级,以证明净收益的证据和确定性。建议基于证据的强度或在证据不足时的共识。
    结果:PACC®审查了已发表的文献,并建立了基于证据和共识的建议,以指导最佳实践。在此过程的未来迭代中,随着新证据的发展,将出现其他指导。
    结论:PACC®建议鞘内给药的最佳实践,以提高安全性和有效性。基于证据和共识的建议应用作指导,以在临床上适当时协助决策。
    BACKGROUND: The International Neuromodulation Society convened a multispecialty group of physicians and scientists based on expertise with international representation to establish evidence-based guidance on intrathecal drug delivery in treating chronic pain. This Polyanalgesic Consensus Conference (PACC)® project, created more than two decades ago, intends to provide evidence-based guidance for important safety and efficacy issues surrounding intrathecal drug delivery and its impact on the practice of neuromodulation.
    METHODS: Authors were chosen on the basis of their clinical expertise, familiarity with the peer-reviewed literature, research productivity, and contributions to the neuromodulation literature. Section leaders supervised literature searches of MEDLINE, BioMed Central, Current Contents Connect, Embase, International Pharmaceutical Abstracts, Web of Science, Google Scholar, and PubMed from 2017 (when PACC® last published guidelines) to the present. Identified studies were graded using the United States Preventive Services Task Force criteria for evidence and certainty of net benefit. Recommendations are based on the strength of evidence or consensus when evidence is scant.
    RESULTS: The PACC® examined the published literature and established evidence- and consensus-based recommendations to guide best practices. Additional guidance will occur as new evidence is developed in future iterations of this process.
    CONCLUSIONS: The PACC® recommends best practices regarding intrathecal drug delivery to improve safety and efficacy. The evidence- and consensus-based recommendations should be used as a guide to assist decision-making when clinically appropriate.
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  • 文章类型: Journal Article
    从诊断和治疗的角度来看,骶髂疾病的临床管理已被证明具有挑战性。尽管它被广泛认为是下腰痛的常见来源,关于骶髂关节疼痛和功能障碍的适当临床管理几乎没有共识。了解生物力学,神经支配,这种复杂的承载关节的功能对于制定针对SI关节疾病的适当治疗算法至关重要。ASPN制定了这一综合实践指南,以利用现有的最佳证据作为SI关节疾病适当管理的基础参考,并作为美国和全球成人患者治疗的基础指南。
    Clinical management of sacroiliac disease has proven challenging from both diagnostic and therapeutic perspectives. Although it is widely regarded as a common source of low back pain, little consensus exists on the appropriate clinical management of sacroiliac joint pain and dysfunction. Understanding the biomechanics, innervation, and function of this complex load bearing joint is critical to formulating appropriate treatment algorithms for SI joint disorders. ASPN has developed this comprehensive practice guideline to serve as a foundational reference on the appropriate management of SI joint disorders utilizing the best available evidence and serve as a foundational guide for the treatment of adult patients in the United States and globally.
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  • 文章类型: Journal Article
    目的:现有的银屑病关节炎(PsA)指南涵盖了许多方面的管理。在常规实践应用方面仍然存在一些差距。专家组旨在加强当前的指导并为临床实践提供建议,以补充现有指南。
    方法:由经验丰富的指导委员会组成,风湿病学研究活跃的临床医生,皮肤科和初级保健就主题和相关问题达成一致。根据PICO框架对PubMed和Embase进行了有针对性的文献综述。在第二次会议上,起草了建议,随后由风湿病学家组成的扩展学院,皮肤科医生,初级保健临床医生,专科护士,专职医疗人员,非临床学术参与者和Brit-PACT患者组的成员,被招募。当75%的受访者在9分制的7-9范围内达成共识时,通过在线投票平台达成共识。
    结果:指南包括34个陈述,涵盖了四个PsA主题。诊断侧重于早期识别PsA并适当转诊的策略,诊断指标的评估,使用筛查工具和使用成像。疾病评估以疾病活动的整体考虑为中心,从患者的角度来看,身体功能和影响,以及如何实施共同决策。对于合并症,建议包括针对抑郁症和肥胖症等高影响力疾病的具体指导.管理声明(不包括现有的药物治疗指南)涵盖了多学科团队工作,实施生活方式改变和目标治疗策略。建议在可行的情况下尽量减少使用皮质类固醇。
    结论:共识小组提出了基于证据的最佳实践建议,以加强现有指南。
    OBJECTIVE: Existing guidelines for psoriatic arthritis (PsA) cover many aspects of management. Some gaps remain relating to routine practice application. An expert group aimed to enhance current guidance and develop recommendations for clinical practice that are complementary to existing guidelines.
    METHODS: A steering committee comprising experienced, research-active clinicians in rheumatology, dermatology and primary care agreed on themes and relevant questions. A targeted literature review of PubMed and Embase following a PICO framework was conducted. At a second meeting, recommendations were drafted and subsequently an extended faculty comprising rheumatologists, dermatologists, primary care clinicians, specialist nurses, allied health professionals, non-clinical academic participants and members of the Brit-PACT patient group, was recruited. Consensus was achieved via an online voting platform when 75% of respondents agreed in the range of 7-9 on a 9-point scale.
    RESULTS: The guidance comprised 34 statements covering four PsA themes. Diagnosis focused on strategies to identify PsA early and refer appropriately, assessment of diagnostic indicators, use of screening tools and use of imaging. Disease assessment centred on holistic consideration of disease activity, physical functioning and impact from a patient perspective, and on how to implement shared decision-making. For comorbidities, recommendations included specific guidance for high-impact conditions such as depression and obesity. Management statements (which excluded extant guidance on pharmacological therapies) covered multidisciplinary team working, implementation of lifestyle modifications and treat-to-target strategies. Minimising corticosteroid use was recommended where feasible.
    CONCLUSIONS: The consensus group have made evidence-based best practice recommendations for the management of PsA to enhance the existing guidelines.
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  • 文章类型: Journal Article
    NCAA-DoD心智问题挑战赛提出了“有用且可行”的共识建议,以改善大学运动员和军事学员的脑震荡护理寻求行为。鉴于运动教练(AT)作为脑震荡教育和医疗保健提供者的角色,重要的是要了解他们是否同意专家小组的建议是有用和可行的。
    描述和比较中学(SS)和大学设置ATs对NCAA-DoDMindMatters挑战建议的实用性和可行性的看法,以改善脑震荡教育。
    横断面研究。
    电子测量。
    在SS(60.6%)或大学(38.4%)设置中练习的五百十五(515)AT(年龄40.7±12.4,女性占53.1%)。
    一项在线调查向参与者询问了他们对声明的认识,然后询问了17对有关每个建议的实用性和可行性的Likert项目问题,回答范围从No(1)到Yes(9)。模仿共识过程,我们将共识定义为平均评分≥7.00.我们使用Mann-WhitneyU检验与i=.05比较了SS和大学设置参与者之间的效用和可行性评级响应。
    三分之二(66.6%)的参与者不知道共识声明。参与者认为所有建议都是有用的(所有手段≥7.0);然而,与利益相关者合作的4项建议未达到可行性界限(平均范围=6.66-6.84)。与教育内容相关的SSAT评级较低的可行性(p值范围=.001-.014),在整个恢复过程中提供患者教育(p=0.002),并促进同伴干预(p=.019),但与大学ATs相比,提供家长教育的效用更高(p=.007)和可行性(p=.002)。
    NCAA-DoD心智问题挑战建议需要进一步传播。ATs将与利益相关者的合作视为可行性障碍。SSAT需要更多的教育内容资源,消息传递,促进同伴干预,但发现教育运动员的父母比大学ATS更有用、更可行。
    BACKGROUND: The National Collegiate Athletic Association and Department of Defense (NCAA-DoD) Mind Matters Challenge created \"useful and feasible\" consensus recommendations to improve concussion care-seeking behavior in collegiate athletes and military cadets. Given athletic trainers\' (ATs\') role as providers of concussion education and medical care, it is important to understand if they agree with the expert panel that the recommendations are useful and feasible.
    OBJECTIVE: To describe and compare the perceptions of ATs in the secondary school (SS) and collegiate settings of the utility and feasibility of the NCAA-DoD Mind Matters Challenge recommendations on improving concussion education.
    METHODS: Cross-sectional study.
    METHODS: Electronic survey.
    METHODS: Five hundred fifteen (515) ATs (age = 40.7 ± 12.4 years, 53.1% female gender) practicing in the SS (60.6%) or collegiate (38.4%) setting.
    METHODS: An online survey asked participants about their awareness of the statement followed by 17 pairs of Likert-item questions regarding each recommendation\'s utility and feasibility with responses ranging from no (1) to yes (9). Mimicking the consensus process, we defined consensus as a mean rating of ≥7.00. We compared utility and feasibility rating responses between SS and collegiate setting participants using Mann-Whitney U tests with α = .05.
    RESULTS: Two-thirds (66.6%) of participants were unaware of the consensus statement. Participants felt all recommendations were useful (all means ≥ 7.0); however, 4 recommendations related to collaborating with stakeholders did not meet the feasibility cutoff (mean range = 6.66-6.84). Secondary school ATs rated lower feasibility related to educational content (P value range = .001-.014), providing patient education throughout recovery (P = .002), and promoting peer intervention (P = .019) but higher utility (P = .007) and feasibility (P = .002) for providing parent education than collegiate ATs.
    CONCLUSIONS: The NCAA-DoD Mind Matters Challenge recommendations require further dissemination. Athletic trainers rated collaboration with stakeholders as a feasibility barrier. Secondary school ATs require more resources for educational content, messaging, and promoting peer intervention but find educating athletes\' parents more useful and feasible than collegiate ATs.
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  • 文章类型: Journal Article
    背景:哮喘是一种慢性呼吸系统疾病,需要长期药物治疗和明智的患者自我管理。很少有研究系统地评估哮喘移动健康(mHealth)应用程序的质量和功能;然而,没有人系统地评估这些应用程序的内容是否与国际最佳实践指南保持一致。
    目的:本综述旨在对澳大利亚市场上当前的mHealth应用程序的功能进行系统的搜索和评估,质量,并与最佳实践指南保持一致。
    方法:对最新的全球哮喘倡议(GINA)指南进行了审查,以确定可以可行地纳入mHealth应用程序的关键建议。我们根据这些建议和以前开发的框架的修改版本开发了一份清单。对应用程序商店进行了审查,以根据预定义的标准识别潜在的mHealth应用程序。评估合适的应用程序包括评估技术信息,使用经过验证的移动应用评分量表(MARS)框架进行应用质量评估,以及使用洲际医学统计健康信息学研究所(IMS)功能评分系统的应用程序功能评估。最后,使用我们制定的检查表,对mHealth应用程序的内容与GINA指南的一致性进行了评估.
    结果:在最初确定的422个应用程序中,53例适用于基于纳入和排除标准的进一步分析。单个应用程序的行为改变技术的平均数量为3.26(SD2.27)。所有审查的应用程序的平均MARS评分为3.05(SD0.54)。在53个应用程序中,27人(51%)的MARS总分≥3。平均而言,审查的应用程序在11点IMS功能量表上实现了5.1(SD2.79)功能。鉴定的功能性的中位值为5(IQR2-7)。总的来说,45个应用程序中有10个(22%)在该领域获得了审阅者的共识,提供了有关哮喘的一般知识。在53个应用程序中,峰值流量计的技能培训,吸入器装置,识别或应对恶化,8例(17%)中发现了非药物哮喘管理,12(25%),11(28%),和14个(31%)应用程序,分别有19个(37%)应用程序可以跟踪或记录“哮喘症状”,“这是最常记录的指标。最常见的提示是服用预防性药物,在9个(20%)应用程序中可用。五个(10%)应用程序为患者提供了存储或输入其哮喘行动计划的区域。
    结论:本研究使用根据GINA指南开发的独特清单来评估哮喘应用程序的内容一致性。缺乏与国际最佳实践哮喘指南相一致的高质量哮喘应用程序。未来的应用程序开发应针对本研究中确定的当前缺乏的关键功能,包括使用哮喘行动计划和部署行为改变技术来吸引和重新吸引用户。这项研究对临床医生导航不断扩大的慢性病mHealthapp市场具有重要意义。
    背景:PROSPEROCRD42021269894;https://www.crd.约克。AC.uk/prospro/display_record.php?RecordID=269894。
    RR2-10.2196/33103。
    BACKGROUND: Asthma is a chronic respiratory disorder requiring long-term pharmacotherapy and judicious patient self-management. Few studies have systematically evaluated asthma mobile health (mHealth) apps for quality and functionality; however, none have systematically assessed these apps for their content alignment with international best practice guidelines.
    OBJECTIVE: This review aims to conduct a systematic search and evaluation of current mHealth apps in the Australian marketplace for their functionality, quality, and consistency with best practice guidelines.
    METHODS: The most recent Global Initiative for Asthma (GINA) guidelines were reviewed to identify key recommendations that could be feasibly incorporated into an mHealth app. We developed a checklist based on these recommendations and a modified version of a previously developed framework. App stores were reviewed to identify potential mHealth apps based on predefined criteria. Evaluation of suitable apps included the assessment of technical information, an app quality assessment using the validated Mobile App Rating Scale (MARS) framework, and an app functionality assessment using the Intercontinental Medical Statistics Institute for Health Informatics (IMS) Functionality Scoring System. Finally, the mHealth apps were assessed for their content alignment with the GINA guidelines using the checklist we developed.
    RESULTS: Of the 422 apps initially identified, 53 were suitable for further analysis based on inclusion and exclusion criteria. The mean number of behavioral change techniques for a single app was 3.26 (SD 2.27). The mean MARS score for all the reviewed apps was 3.05 (SD 0.54). Of 53 apps, 27 (51%) achieved a total MARS score of ≥3. On average, the reviewed apps achieved 5.1 (SD 2.79) functionalities on the 11-point IMS functionality scale. The median number of functionalities identified was 5 (IQR 2-7). Overall, 10 (22%) of the 45 apps with reviewer consensus in this domain provided general knowledge regarding asthma. Of 53 apps, skill training in peak flow meters, inhaler devices, recognizing or responding to exacerbations, and nonpharmacological asthma management were identified in 8 (17%), 12 (25%), 11 (28%), and 14 (31%) apps, respectively; 19 (37%) apps could track or record \"asthma symptoms,\" which was the most commonly recorded metric. The most frequently identified prompt was for taking preventive medications, available in 9 (20%) apps. Five (10%) apps provided an area for patients to store or enter their asthma action plan.
    CONCLUSIONS: This study used a unique checklist developed based on the GINA guidelines to evaluate the content alignment of asthma apps. Good-quality asthma apps aligned with international best practice asthma guidelines are lacking. Future app development should target the currently lacking key features identified in this study, including the use of asthma action plans and the deployment of behavioral change techniques to engage and re-engage with users. This study has implications for clinicians navigating the ever-expanding mHealth app market for chronic diseases.
    BACKGROUND: PROSPERO CRD42021269894; https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=269894.
    UNASSIGNED: RR2-10.2196/33103.
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  • 文章类型: Journal Article
    链接的加速度计和全球定位系统数据的热点分析通常用于识别校园中的高/低活动区域。我们说明了一系列方法决策的潜在影响(i)加速度计度量;(ii)监测时期;(iii)休会期/天数和聚集水平;(iv)样本量;(v)距离带;(vi)空间与时空加权方案;(vii)时间带。加速度计度量导致不同的聚类模式。更长的时期导致对校园行为的详细了解。由于跨期和日之间的差异,数据聚合水平影响了集群模式,但是聚类与样本量的增加是一致的。使用时空权重矩阵可以更好地分离热点和冷点,并揭示出潜在的重要时间聚类模式。增加距离或时间带导致将小簇重新分配给较大簇。热点分析决策应在未来的研究中明确报告。
    Hot spot analysis of linked accelerometer and Global Positioning System data is often used to identify areas of high/low activity in the schoolyard. We illustrate the potential impact of a suite of methodological decisions (i) accelerometer metric; (ii) monitor epoch; (iii) number of recess periods/days and level of aggregation; (iv) sample size; (v) distance band; (vi) spatial versus spatiotemporal weighting scheme; and (vii) time band. Accelerometer metrics resulted in different clustering patterns. Longer epochs resulted in a less detailed picture of schoolyard behavior. Level of data aggregation impacted cluster patterns due to inter-period and inter-day differences, but clusters were consistent with increasing sample size. Use of spatiotemporal weight matrices resulted in better separation of hot and cold spots and revealed potentially important temporal clustering patterns. Increasing distance or time band resulted in reallocation of small clusters to larger clusters. Hot spot analysis decisions should be clearly reported in future studies.
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  • 文章类型: Journal Article
    可穿戴设备越来越多地用于测量真实世界的头部撞击和研究脑损伤机制。这些设备必须经过验证测试,以确保它们为头部碰撞感应提供可靠和准确的信息,和受控实验室测试应该是验证的第一步。过去的验证研究采用了不同的方法,和一些设备已部署在现场使用未经验证。本文提出了在实验室中验证可穿戴式头部运动设备的最佳实践建议,以标准化验证测试方法和数据报告为目标。关键考虑因素,推荐的方法,并针对实验室验证的四个主要方面制定了具体考虑因素,包括选择代理人,试验条件,数据收集,和数据分析。建议由具有头部运动学传感和实验室验证方法专业知识的小组生成,并由更大的小组进行审查,以就最佳实践达成共识。我们建议制造商遵循这些最佳实践,用户,和审稿人进行和/或审查可穿戴设备的实验室验证,这是现场验证和部署之前的最低初始步骤。我们预计,最佳实践建议将导致对可穿戴式头部运动设备的更严格验证和头部撞击数据的更高准确性。这可以随后推进脑损伤的研究和管理。
    Wearable devices are increasingly used to measure real-world head impacts and study brain injury mechanisms. These devices must undergo validation testing to ensure they provide reliable and accurate information for head impact sensing, and controlled laboratory testing should be the first step of validation. Past validation studies have applied varying methodologies, and some devices have been deployed for on-field use without validation. This paper presents best practices recommendations for validating wearable head kinematic devices in the laboratory, with the goal of standardizing validation test methods and data reporting. Key considerations, recommended approaches, and specific considerations were developed for four main aspects of laboratory validation, including surrogate selection, test conditions, data collection, and data analysis. Recommendations were generated by a group with expertise in head kinematic sensing and laboratory validation methods and reviewed by a larger group to achieve consensus on best practices. We recommend that these best practices are followed by manufacturers, users, and reviewers to conduct and/or review laboratory validation of wearable devices, which is a minimum initial step prior to on-field validation and deployment. We anticipate that the best practices recommendations will lead to more rigorous validation of wearable head kinematic devices and higher accuracy in head impact data, which can subsequently advance brain injury research and management.
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