behavioral

行为
  • 文章类型: Journal Article
    每个月,大约3800人在荷兰自杀预防求助热线的网站上完成了自杀想法的匿名自我测试。尽管70%的人在自杀念头的严重程度上得分很高,<10%导航到有关联系帮助热线的网页。
    这项研究旨在测试简短的减少障碍干预(BRI)在激励有严重自杀念头的人联系预防自杀求助热线方面的有效性,特别是男性和中年人等高危人群。
    我们进行了全自动,基于网络的,随机对照试验。有严重自杀想法和很少联系求助热线的受访者被随机分配到简短的BRI,他们收到了一个简短的,根据他们自我报告的求助热线屏障量身定制的信息(n=610),或一般咨询文本(照常护理对照组:n=612)。使用行为和态度测量来评估有效性。主要结果指标是在完成干预或控制条件后使用直接链接联系求助热线。次要结果是自我报告的联系求助热线的可能性以及对接受的自我测试的满意度。
    总共,2124名网站访问者完成了自杀意念属性量表和条目筛选问卷中的人口统计问题。其中,1222人随机分为干预组和对照组。最终,772名受访者完成了随机对照试验(干预组:n=369;对照组:n=403)。两组中选择最多的障碍是“我认为我的问题不够严重。“在审判结束时,在干预组中,有33.1%(n=122)的受访者使用了与求助热线的直接链接。这与对照组的受访者没有显着差异(144/403,35.7%;比值比0.87,95%CI0.64-1.18,P=.38)。然而,接受BRI的受访者在自我报告的稍后时间点联系求助热线的可能性(B=0.22,95%CI0.12-0.32,P≤.001)和对自我测试的满意度(B=0.27,95%CI0.01-0.53,P=.04)方面得分较高.特别是对于男性和中年受访者,结果与全组相当.
    该试验是求助热线首次能够与不愿联系求助热线的高风险网站访问者联系。尽管BRI无法确保这些受访者在审判结束时立即使用与求助热线的直接链接,令人鼓舞的是,受访者表示他们更有可能在稍后的时间点联系求助热线。此外,这种低成本的干预措施使人们对所感知的服务障碍有了更深入的了解。后续研究应侧重于确定其他组件的附加值(例如,视频或照片材料)在BRI中,并提高其有效性,尤其是男性和中年人。
    UNASSIGNED: Every month, around 3800 people complete an anonymous self-test for suicidal thoughts on the website of the Dutch suicide prevention helpline. Although 70% score high on the severity of suicidal thoughts, <10% navigate to the web page about contacting the helpline.
    UNASSIGNED: This study aimed to test the effectiveness of a brief barrier reduction intervention (BRI) in motivating people with severe suicidal thoughts to contact the suicide prevention helpline, specifically in high-risk groups such as men and middle-aged people.
    UNASSIGNED: We conducted a fully automated, web-based, randomized controlled trial. Respondents with severe suicidal thoughts and little motivation to contact the helpline were randomly allocated either to a brief BRI, in which they received a short, tailored message based on their self-reported barrier to the helpline (n=610), or a general advisory text (care as usual as the control group: n=612). Effectiveness was evaluated using both behavioral and attitudinal measurements. The primary outcome measure was the use of a direct link to contact the helpline after completing the intervention or control condition. Secondary outcomes were the self-reported likelihood of contacting the helpline and satisfaction with the received self-test.
    UNASSIGNED: In total, 2124 website visitors completed the Suicidal Ideation Attributes Scale and the demographic questions in the entry screening questionnaire. Among them, 1222 were randomized into the intervention or control group. Eventually, 772 respondents completed the randomized controlled trial (intervention group: n=369; control group: n=403). The most selected barrier in both groups was \"I don\'t think that my problems are serious enough.\" At the end of the trial, 33.1% (n=122) of the respondents in the intervention group used the direct link to the helpline. This was not significantly different from the respondents in the control group (144/403, 35.7%; odds ratio 0.87, 95% CI 0.64-1.18, P=.38). However, the respondents who received the BRI did score higher on their self-reported likelihood of contacting the helpline at a later point in time (B=0.22, 95% CI 0.12-0.32, P≤.001) and on satisfaction with the self-test (B=0.27, 95% CI 0.01-0.53, P=.04). For male and middle-aged respondents specifically, the results were comparable to that of the whole group.
    UNASSIGNED: This trial was the first time the helpline was able to connect with high-risk website visitors who were hesitant to contact the helpline. Although the BRI could not ensure that those respondents immediately used the direct link to the helpline at the end of the trial, it is encouraging that respondents indicated that they were more likely to contact the helpline at a later point in time. In addition, this low-cost intervention provided greater insight into the perceived barriers to service. Follow-up research should be focused on identifying the added value of other components (eg, video or photo material) in the BRI and increasing its effectiveness, especially for men and middle-aged people.
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  • 文章类型: Journal Article
    背景:抗菌素耐药性(AMR)代表了公众健康日益关注的问题。
    目的:我们试图探索与开发和实施旨在改善医院AMS的复杂干预措施相关的挑战。
    方法:我们对复杂的AMS干预进行了定性评估,行为,以及英国医院5个病房的技术组件。在开始干预后2周和7周,我们采访了25位干预用户,包括高级和初级开药者,一位高级护士,药剂师,和微生物学家。讨论的主题包括干预措施和促进者的不同要素的影响以及有效使用的障碍。访谈得到了2次病房观察的补充,以了解AMS实践。数据是音频记录的,转录,并使用NVivo12进行归纳和演绎分析。
    结果:追踪干预措施的各个组成部分的采用和影响是困难的,因为它被引入了一个充满竞争压力的环境。这些特别受影响的行为和教育成分(例如,培训,提高认识活动),通常是临时交付的。我们发现,参与式干预设计已经解决了典型的用例,但没有满足边缘案例,只有在现实世界的环境中进行干预时才变得可见(例如,不同专业和条件下处方工作流程的差异)。
    结论:以用户为中心的复杂干预措施的有效设计可以促进AMS的接受和使用。然而,并非所有的要求和潜在的使用障碍都可以在现实环境中全面实施之前完全预期或测试。
    BACKGROUND: Antimicrobial resistance (AMR) represents a growing concern for public health.
    OBJECTIVE: We sought to explore the challenges associated with development and implementation of a complex intervention designed to improve AMS in hospitals.
    METHODS: We conducted a qualitative evaluation of a complex AMS intervention with educational, behavioral, and technological components in 5 wards of an English hospital. At 2 weeks and 7 weeks after initiating the intervention, we interviewed 25 users of the intervention, including senior and junior prescribers, a senior nurse, a pharmacist, and a microbiologist. Topics discussed included perceived impacts of different elements of the intervention and facilitators and barriers to effective use. Interviews were supplemented by 2 observations of ward rounds to gain insights into AMS practices. Data were audio-recorded, transcribed, and inductively and deductively analyzed thematically using NVivo12.
    RESULTS: Tracing the adoption and impact of the various components of the intervention was difficult, as it had been introduced into a setting with competing pressures. These particularly affected behavioral and educational components (eg, training, awareness-building activities), which were often delivered ad hoc. We found that the participatory intervention design had addressed typical use cases but had not catered for edge cases that only became visible when the intervention was delivered in real-world settings (eg, variations in prescribing workflows across different specialties and conditions).
    CONCLUSIONS: Effective user-focused design of complex interventions to promote AMS can support acceptance and use. However, not all requirements and potential barriers to use can be fully anticipated or tested in advance of full implementation in real-world settings.
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  • 文章类型: Journal Article
    男男性行为者(MSM)之间的性传播已成为主要的HIV传播途径。然而,在中国,已经进行了有限的研究来调查交易性行为(TS)与HIV发病率之间的关系。
    本研究旨在调查在中国从事TS(MSM-TS)的MSM中的HIV发病率,并区分与HIV发病率相关的社会人口统计学和性行为危险因素。
    我们使用基于微信的平台进行了一项前瞻性队列研究,以评估中国MSM的HIV发病率。包括宁波的MSM-TS,从2019年7月至2022年6月招募。每次访问,参与者在接受线下HIV检测之前,在微信平台上完成了一份问卷并预约了HIV咨询和检测.HIV发病率密度计算为HIV血清转化数除以随访的人年(PYs),进行单因素和多因素Cox比例风险回归,以确定与HIV发病率相关的因素.
    共有932名参与者贡献了630.9个PYs的随访,在研究期间观察到25例HIV血清转化,导致每100个PYs的HIV发病率估计为4.0(95%CI2.7-5.8)。MSM-TS中的HIV发病率为每100个PYs18.4(95%CI8.7-34.7),显着高于不从事TS的MSM中每100个PYs3.2(95%CI2.1-5.0)的发生率。在调整了社会人口统计学特征后,与HIV感染相关的因素是MSM-TS(调整后的风险比[AHR]3.93,95%CI1.29-11.93),与男性发生无保护性行为(aHR10.35,95%CI2.25-47.69),并且在过去6个月中有多个男性性伴侣(aHR3.43,95%CI1.22-9.64)。
    这项研究发现,宁波的MSM-TS中HIV的发病率很高,中国。与艾滋病毒发病率相关的危险因素包括TS,与男人发生无保护的性行为,有多个男性性伴侣.这些发现强调需要制定有针对性的干预措施,并提供全面的医疗服务,艾滋病毒检测,和MSM的暴露前预防,特别是那些从事TS的人。
    UNASSIGNED: Sexual transmission among men who have sex with men (MSM) has become the major HIV transmission route. However, limited research has been conducted to investigate the association between transactional sex (TS) and HIV incidence in China.
    UNASSIGNED: This study aims to investigate HIV incidence and distinguish sociodemographic and sexual behavioral risk factors associated with HIV incidence among MSM who engage in TS (MSM-TS) in China.
    UNASSIGNED: We conducted a prospective cohort study using a WeChat-based platform to evaluate HIV incidence among Chinese MSM, including MSM-TS in Ningbo, recruited from July 2019 until June 2022. At each visit, participants completed a questionnaire and scheduled an appointment for HIV counseling and testing on the WeChat-based platform before undergoing offline HIV tests. HIV incidence density was calculated as the number of HIV seroconversions divided by person-years (PYs) of follow-up, and univariate and multivariate Cox proportional hazards regression was conducted to identify factors associated with HIV incidence.
    UNASSIGNED: A total of 932 participants contributed 630.9 PYs of follow-up, and 25 HIV seroconversions were observed during the study period, resulting in an estimated HIV incidence of 4.0 (95% CI 2.7-5.8) per 100 PYs. The HIV incidence among MSM-TS was 18.4 (95% CI 8.7-34.7) per 100 PYs, which was significantly higher than the incidence of 3.2 (95% CI 2.1-5.0) per 100 PYs among MSM who do not engage in TS. After adjusting for sociodemographic characteristics, factors associated with HIV acquisition were MSM-TS (adjusted hazard ratio [aHR] 3.93, 95% CI 1.29-11.93), having unprotected sex with men (aHR 10.35, 95% CI 2.25-47.69), and having multiple male sex partners (aHR 3.43, 95% CI 1.22-9.64) in the past 6 months.
    UNASSIGNED: This study found a high incidence of HIV among MSM-TS in Ningbo, China. The risk factors associated with HIV incidence include TS, having unprotected sex with men, and having multiple male sex partners. These findings emphasize the need for developing targeted interventions and providing comprehensive medical care, HIV testing, and preexposure prophylaxis for MSM, particularly those who engage in TS.
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  • 文章类型: Journal Article
    背景:在慢性肝病患者中,缺乏与酒精减少相关的行为干预和过程级研究的随机对照试验(例如,丙型肝炎病毒(HCV)感染。我们进行了一个过程级别,对丙型肝炎-酒精减少治疗(HepART)试验进行二次分析,以研究综合行为模型(IBM)提出的心理过程变化与世界卫生组织(WHO)饮酒风险水平变化之间的关系。
    方法:从肝病诊所招募饮酒的HCV患者,并接受提供者提供的SBIRT(筛查,简短干预,转诊治疗)或SBIRT+6个月的共定位酒精咨询。由于没有发现组间差异,因此将治疗组合并进行此分析。在基线和6个月时,根据2000年WHO风险类别(基于平均每日酒精克数),使用时间线跟随法确定酒精风险水平.对饮酒和WHO风险水平的变化进行了量化,并根据个体心理过程的变化进行了回归(例如,准备就绪,自我效能感,动机,态度,和策略)从基线到6个月。
    结果:在基线评估时,162名参与者被归类为禁欲(5%),低(47%),中等(16%),高(19%),或非常高(13%)的世卫组织风险水平。6个月时,38%保持在相同的风险水平,48%下降至少一个水平。在单变量分析中,12个心理过程中有7个的变化与风险水平的变化相关.调整后的多变量分析表明,四个过程的变化与风险水平的变化显着相关,包括苏格拉底采取步骤,矛盾,识别分数和酒精减少策略。
    结论:这些研究结果表明,在HCV患者的机会性酒精干预后,饮酒的定量指标显着降低。然而,结果为IBM心理过程的变化与饮酒之间的关联提供了混合支持。
    BACKGROUND: There is a lack of randomized controlled trials of behavioral interventions and process-level research related to alcohol reduction among patients with chronic liver disease (e.g., hepatitis C viral (HCV) infection). We conducted a process-level, secondary analysis of the Hepatitis C-Alcohol Reduction Treatment (HepART) trial to investigate the association between change in psychological processes posited by the Integrated Behavioral Model (IBM) and change in World Health Organization (WHO) drinking risk levels.
    METHODS: Patients with HCV who consume alcohol were recruited from hepatology clinics and received provider-delivered SBIRT (Screening, Brief Intervention, Referral to Treatment) or SBIRT+ 6 months of co-located alcohol counseling. Treatment arms were combined for this analysis because no between-group differences were found. At baseline and 6 months, the timeline followback method was used to determine alcohol risk levels according to the 2000 WHO risk categories (based on average grams of alcohol per day). Changes in alcohol consumption and WHO risk levels were quantified and regressed on change in individual psychological processes (e.g., readiness, self-efficacy, motives, attitudes, and strategies) from baseline to 6 months.
    RESULTS: At the baseline assessment, 162 participants were classified as abstinent (5%), low (47%), moderate (16%), high (19%), or very high (13%) WHO risk levels. At 6 months, 38% remained at the same risk level and 48% decreased by at least one level. In univariate analyses, changes in 7 of 12 psychological processes were associated with change in risk levels. Adjusted multivariate analyses demonstrated that change in four processes were significantly associated with change in risk levels, including SOCRATES Taking Steps, Ambivalence, and Recognition scores and alcohol reduction strategies.
    CONCLUSIONS: These findings demonstrate significant reductions in quantitative indices of alcohol consumption following opportunistic alcohol interventions in patients with HCV. However, results provided mixed support for associations between change in IBM psychological processes and alcohol consumption.
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  • 文章类型: Journal Article
    氧化石墨烯(GO)纳米颗粒在各个领域引起了越来越多的兴趣,尤其是因为它们独特的特征和可能的用途。然而,关于它们对神经健康影响的担忧正在出现,强调需要深入研究以评估其神经毒性。本研究考察了GO暴露对中枢神经系统(CNS)的神经行为和生化影响。为此,我们在46天的治疗期内向小鼠施用两种剂量的GO(2和5mg/kgGO)。我们对老鼠进行了一系列行为测试,包括评估运动活动的开放场地,迷宫加上测量焦虑,极点测试评估平衡和旋转杆测量电机协调。并行,我们分析了暴露于GO纳米颗粒的小鼠大脑中的丙二醛(MDA)水平和过氧化氢酶活性。此外,进行X射线能量色散(EDX)分析以确定脑的分子组成。我们的观察结果揭示了通过腹膜内注射暴露于GO的小鼠的大脑改变,显示剂量依赖性关系。我们确定了暴露于GO的小鼠的行为改变,比如焦虑加剧,运动协调性下降,减少的运动活动和平衡障碍。这些变化是剂量依赖性的,提示GO给药量与行为改变程度之间存在相关性。同时,观察到丙二醛和过氧化氢酶活性的剂量依赖性增加,加强暴露强度和相关生化反应之间的相关性。
    Graphene oxide (GO) nanoparticles are attracting growing interest in various fields, not least because of their distinct characteristics and possible uses. However, concerns about their impact on neurological health are emerging, underlining the need for in-depth studies to assess their neurotoxicity. This study examines GO exposure\'s neurobehavioral and biochemical effects on the central nervous system (CNS). To this end, we administered two doses of GO (2 and 5 mg/kg GO) to mice over a 46-day treatment period. We performed a battery of behavioral tests on the mice, including the open field to assess locomotor activity, the maze plus to measure anxiety, the pole test to assess balance and the rotarod to measure motor coordination. In parallel, we analyzed malondialdehyde (MDA) levels and catalase activity in the brains of mice exposed to GO nanoparticles. In addition, X-ray energy dispersive (EDX) analysis was performed to determine the molecular composition of the brain. Our observations reveal brain alterations in mice exposed to GO by intraperitoneal injection, demonstrating a dose-dependent relationship. We identified behavioral alterations in mice exposed to GO, such as increased anxiety, decreased motor coordination, reduced locomotor activity and balance disorders. These changes were dose-dependent, suggesting a correlation between the amount of GO administered and the extent of behavioral alterations. At the same time, a dose-dependent increase in malondialdehyde and catalase activity was observed, reinforcing the correlation between exposure intensity and associated biochemical responses.
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  • 文章类型: Journal Article
    背景:2型糖尿病(T2D)极大地影响了全球患者的健康和医疗保健。改变生活方式可以帮助抑制T2D的负担。然而,健康行为改变是医学的复杂相互作用,行为,和心理因素。个性化的生活方式建议和促进自我管理可以帮助患者改变健康行为,改善血糖调节。数字工具在自我管理领域是有效的,并且由于低成本而具有支持患者自我管理的巨大潜力,24/7可用性,以及动态自动反馈的选项。为了开发成功的eHealth解决方案,重要的是在整个开发过程中包括利益相关者,并使用结构化方法来指导开发团队进行规划,协调,并执行开发过程。
    目的:本研究的目的是开发一种综合,eHealth支持,T2D患者的教育护理路径。
    方法:教育护理途径是使用电子健康和福祉研究中心路线图的前3个阶段开发的:情境调查,价值规范,和设计阶段。按照这个路线图,我们使用了关于糖尿病自我管理教育和电子健康的范围审查,我们医院过去的电子健康实践经验,与医疗保健专业人员(HCP)的焦点小组,和一个病人小组来开发一个教育护理途径的原型。这种护理途径被称为糖尿病箱(莱顿大学医学中心),包括个性化教育,数字教育材料,葡萄糖的自我测量,血压,活动,和睡眠,和智能手机应用程序,把它结合在一起。
    结果:范围审查强调了自我管理教育的重要性以及远程监测和移动应用程序对T2D患者血糖调节的潜力。有HCP的焦点小组揭示了纳入所有相关生活方式因素的重要性,使用量身定制的方法,并使用数字咨询。上下文调查导致了一系列价值观,利益相关者认为这些价值观很重要,必须包括在教育护理途径中。所有值都是在与关键利益相关者的双周会议上指定的,并设计了一个原型。该原型在患者小组中进行了评估,该小组显示了对护理途径的总体积极印象,但强调应用程序的数量应限于一个,葡萄糖值可视化不应该有延迟,胰岛素的使用应该被纳入应用程序。患者和HCP都强调了糖尿病盒子中直接自动反馈的重要性。
    结论:在使用电子健康与健康研究中心路线图开发糖尿病盒原型后,所有利益相关者都认为糖尿病箱的概念是有用和可行的,并且对压力和睡眠的直接自动反馈和教育至关重要。计划进行一项试点研究,以评估可行性,可接受性,更详细的有用性。
    BACKGROUND: Type 2 diabetes (T2D) tremendously affects patient health and health care globally. Changing lifestyle behaviors can help curb the burden of T2D. However, health behavior change is a complex interplay of medical, behavioral, and psychological factors. Personalized lifestyle advice and promotion of self-management can help patients change their health behavior and improve glucose regulation. Digital tools are effective in areas of self-management and have great potential to support patient self-management due to low costs, 24/7 availability, and the option of dynamic automated feedback. To develop successful eHealth solutions, it is important to include stakeholders throughout the development and use a structured approach to guide the development team in planning, coordinating, and executing the development process.
    OBJECTIVE: The aim of this study is to develop an integrated, eHealth-supported, educational care pathway for patients with T2D.
    METHODS: The educational care pathway was developed using the first 3 phases of the Center for eHealth and Wellbeing Research roadmap: the contextual inquiry, the value specification, and the design phase. Following this roadmap, we used a scoping review about diabetes self-management education and eHealth, past experiences of eHealth practices in our hospital, focus groups with health care professionals (HCPs), and a patient panel to develop a prototype of an educational care pathway. This care pathway is called the Diabetes Box (Leiden University Medical Center) and consists of personalized education, digital educational material, self-measurements of glucose, blood pressure, activity, and sleep, and a smartphone app to bring it all together.
    RESULTS: The scoping review highlights the importance of self-management education and the potential of telemonitoring and mobile apps for blood glucose regulation in patients with T2D. Focus groups with HCPs revealed the importance of including all relevant lifestyle factors, using a tailored approach, and using digital consultations. The contextual inquiry led to a set of values that stakeholders found important to include in the educational care pathway. All values were specified in biweekly meetings with key stakeholders, and a prototype was designed. This prototype was evaluated in a patient panel that revealed an overall positive impression of the care pathway but stressed that the number of apps should be restricted to one, that there should be no delay in glucose value visualization, and that insulin use should be incorporated into the app. Both patients and HCPs stressed the importance of direct automated feedback in the Diabetes Box.
    CONCLUSIONS: After developing the Diabetes Box prototype using the Center for eHealth and Wellbeing Research roadmap, all stakeholders believe that the concept of the Diabetes Box is useful and feasible and that direct automated feedback and education on stress and sleep are essential. A pilot study is planned to assess feasibility, acceptability, and usefulness in more detail.
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  • 文章类型: Journal Article
    心理,情感,行为障碍是慢性儿科疾病,近几十年来,它们的患病率一直在上升。受影响的儿童有长期健康后遗症,与健康相关的生活质量下降。由于缺乏经过验证的药物流行病学研究数据库,情感,和行为障碍,文献中报道的患病率存在不确定性.
    我们旨在评估与儿科精神相关的编码的准确性,情感,和行为障碍的大型综合卫生保健系统的电子健康记录(EHR),并比较编码质量前后的国际疾病分类,第十次修订,临床修改(ICD-10-CM)编码以及COVID-19大流行之前和之后。
    在COVID-19大流行之前(2012年1月1日至2014年12月31日,ICD-9-CM编码期;以及2017年1月1日至2019年12月31日,ICD-10-CM编码期)和COVID-19大流行之后(从2021年1月1日至2022年12月31日进行分层审查),对1200名2-17岁成员儿童两名训练有素的研究人员审查了自闭症谱系障碍(ASD)所有潜在病例的EHR,注意缺陷多动障碍(ADHD),重度抑郁症(MDD),焦虑症(AD),研究期间儿童的破坏性行为障碍(DBD)。只有在相应时间段内电子图表中提到任何一种情况(诊断是),儿童才被视为病例。诊断代码的有效性是通过直接将其与使用灵敏度的图表抽象的黄金标准进行比较来评估的。特异性,正预测值,负预测值,F分数的汇总统计,和尤登·J统计。计算了2个抽象者之间的评分者间可靠性的κ统计量。
    精神识别之间的总体协议,行为,在ICD-9-CM和ICD-10-CM编码期间以及在流行前和大流行时间段内,使用诊断代码与医疗记录摘要相比,使用诊断代码的情绪状况很强且相似。AD编码的性能,虽然坚强,与其他条件相比相对较低。加权灵敏度,特异性,正预测值,5个条件中的每一个的阴性预测值如下:100%,100%,99.2%,100%,分别,对于ASD;100%,99.9%,99.2%,100%,分别,对于ADHD;100%,100%,100%,100%,分别为DBD;87.7%,100%,100%,99.2%,分别,对于AD;和100%,100%,99.2%,100%,分别,MDD。F分数和YoudenJ统计量在87.7%和100%之间。摘要者之间的总体一致性几乎是完美的(κ=95%)。
    诊断代码对于识别选定的儿童精神非常可靠,行为,和情绪状况。在大流行期间和在EHR系统中实施ICD-10-CM编码后,发现仍然相似。
    UNASSIGNED: Mental, emotional, and behavioral disorders are chronic pediatric conditions, and their prevalence has been on the rise over recent decades. Affected children have long-term health sequelae and a decline in health-related quality of life. Due to the lack of a validated database for pharmacoepidemiological research on selected mental, emotional, and behavioral disorders, there is uncertainty in their reported prevalence in the literature.
    UNASSIGNED: We aimed to evaluate the accuracy of coding related to pediatric mental, emotional, and behavioral disorders in a large integrated health care system\'s electronic health records (EHRs) and compare the coding quality before and after the implementation of the International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) coding as well as before and after the COVID-19 pandemic.
    UNASSIGNED: Medical records of 1200 member children aged 2-17 years with at least 1 clinical visit before the COVID-19 pandemic (January 1, 2012, to December 31, 2014, the ICD-9-CM coding period; and January 1, 2017, to December 31, 2019, the ICD-10-CM coding period) and after the COVID-19 pandemic (January 1, 2021, to December 31, 2022) were selected with stratified random sampling from EHRs for chart review. Two trained research associates reviewed the EHRs for all potential cases of autism spectrum disorder (ASD), attention-deficit hyperactivity disorder (ADHD), major depression disorder (MDD), anxiety disorder (AD), and disruptive behavior disorders (DBD) in children during the study period. Children were considered cases only if there was a mention of any one of the conditions (yes for diagnosis) in the electronic chart during the corresponding time period. The validity of diagnosis codes was evaluated by directly comparing them with the gold standard of chart abstraction using sensitivity, specificity, positive predictive value, negative predictive value, the summary statistics of the F-score, and Youden J statistic. κ statistic for interrater reliability among the 2 abstractors was calculated.
    UNASSIGNED: The overall agreement between the identification of mental, behavioral, and emotional conditions using diagnosis codes compared to medical record abstraction was strong and similar across the ICD-9-CM and ICD-10-CM coding periods as well as during the prepandemic and pandemic time periods. The performance of AD coding, while strong, was relatively lower compared to the other conditions. The weighted sensitivity, specificity, positive predictive value, and negative predictive value for each of the 5 conditions were as follows: 100%, 100%, 99.2%, and 100%, respectively, for ASD; 100%, 99.9%, 99.2%, and 100%, respectively, for ADHD; 100%, 100%, 100%, and 100%, respectively for DBD; 87.7%, 100%, 100%, and 99.2%, respectively, for AD; and 100%, 100%, 99.2%, and 100%, respectively, for MDD. The F-score and Youden J statistic ranged between 87.7% and 100%. The overall agreement between abstractors was almost perfect (κ=95%).
    UNASSIGNED: Diagnostic codes are quite reliable for identifying selected childhood mental, behavioral, and emotional conditions. The findings remained similar during the pandemic and after the implementation of the ICD-10-CM coding in the EHR system.
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  • 文章类型: Journal Article
    背景:环境和行为因素每年导致1260万人死亡,占全球死亡和慢性病的25%。通过“一个健康”倡议,世界卫生组织和其他国际卫生组织计划改善这些指标,到2030年创造更健康的环境。为了迎接这一挑战,培训初级保健专业人员应该是国家政策的优先事项。全科医生(GP)已准备好参与其中,但需要进行深入的培训,以获得并将环境健康(EH)知识应用于他们的实践。作为回应,我们与法国Occitanie地区卫生局合作设计了初级保健环境与健康(PCEH)在线课程。本课程用于培训蒙彼利埃-尼姆医学院的GP居民的EH知识。该课程分为两个连续部分:(1)异步电子学习模块化课程,重点是EH知识和工具;(2)1天的面对面课程。
    目的:本研究评估了PCEH课程的电子学习部分对参与者满意度的影响,知识,和行为向EH改变。
    方法:这是一项试验前后研究。在6小时的电子学习课程中提供了四个模块:EH简介,基于人口的方法(制图工具和资源),临床病例,和通信工具。从2021年8月到9月,我们从蒙彼利埃大学(N=130)招募了第一年的GP居民。参与者的满意度,19个EH风险的知识改进,在线向卫生当局报告EH风险的程序,和行为变化(考虑环境对自身和患者健康的可能影响)使用Likert量表(1-5)的自我报告问卷进行评估。采用配对的Studentt检验和McNemarχ2检验比较定量和定性变量,分别,课程之前和之后。
    结果:共有74名GP居民完成了电子学习,并回答了测试前和测试后的问卷。5分的平均满意度评分为4.0(SD0.9)。电子学习课程后,EH风险的知识得分显着增加,所有项目的平均差为30%(P<.001)。参与者的健康行为评分显著提高了18%,患者的健康行为评分显著提高了26%(P<.001)。这些改善根据参与者的特征没有显著差异(例如,性别,孩子们,工作地点)。
    结论:电子学习课程改善了与EH相关的知识和行为。需要进一步的研究来评估PCEH课程对临床实践的影响以及对患者的潜在益处。本课程旨在作为一个知识库,每年都可以重复使用,以实现可持续性。本课程将整合新的模块,并将适应EH状态指标和目标人口需求的演变。
    BACKGROUND: Environmental and behavioral factors are responsible for 12.6 million deaths annually and contribute to 25% of deaths and chronic diseases worldwide. Through the One Health initiative, the World Health Organization and other international health organizations plan to improve these indicators to create healthier environments by 2030. To meet this challenge, training primary care professionals should be the priority of national policies. General practitioners (GPs) are ready to become involved but need in-depth training to gain and apply environmental health (EH) knowledge to their practice. In response, we designed the Primary Care Environment and Health (PCEH) online course in partnership with the Occitanie Regional Health Agency in France. This course was used to train GP residents from the Montpelier-Nimes Faculty of Medicine in EH knowledge. The course was organized in 2 successive parts: (1) an asynchronous e-learning modular course focusing on EH knowledge and tools and (2) 1 day of face-to-face sessions.
    OBJECTIVE: This study assessed the impact of the e-learning component of the PCEH course on participants\' satisfaction, knowledge, and behavior changes toward EH.
    METHODS: This was a pilot before-and-after study. Four modules were available in the 6-hour e-learning course: introduction to EH, population-based approach (mapping tools and resources), clinical cases, and communication tools. From August to September 2021, we recruited first-year GP residents from the University of Montpellier (N=130). Participants\' satisfaction, knowledge improvements for 19 EH risks, procedure to report EH risks to health authorities online, and behavior change (to consider the possible effects of the environment on their own and their patients\' health) were assessed using self-reported questionnaires on a Likert scale (1-5). Paired Student t tests and the McNemar χ2 test were used to compare quantitative and qualitative variables, respectively, before and after the course.
    RESULTS: A total of 74 GP residents completed the e-learning and answered the pre- and posttest questionnaires. The mean satisfaction score was 4.0 (SD 0.9) out of 5. Knowledge scores of EH risks increased significantly after the e-learning course, with a mean difference of 30% (P<.001) for all items. Behavioral scores improved significantly by 18% for the participant\'s health and by 26% for patients\' health (P<.001). These improvements did not vary significantly according to participant characteristics (eg, sex, children, place of work).
    CONCLUSIONS: The e-learning course improved knowledge and behavior related to EH. Further studies are needed to assess the impact of the PCEH course on clinical practice and potential benefits for patients. This course was designed to serve as a knowledge base that could be reused each year with a view toward sustainability. This course will integrate new modules and will be adapted to the evolution of EH status indicators and target population needs.
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  • 文章类型: Journal Article
    背景:社交媒体正迅速成为向公众传播邀请以考虑参与研究的主要来源。有,然而,关于如何传达广告内容以促进参与并随后促进参与研究的意图的信息很少。
    目的:本文描述了一项实验研究,该研究测试了招募现实生活中观察性病例对照研究的研究参与者的不同行为信息。
    方法:我们在基于网络的实验中纳入了1060名女性,并将其随机分配到3个实验条件中的1个:标准广告(n=360),患者代言广告(n=345),和社会规范广告(n=355)。看到3个广告中的1个后,参与者被要求说明(1)他们打算参加宣传的病例对照研究,(2)易于理解的信息和学习目的,(3)他们在完成调查后愿意重定向到病例对照研究的网站。进一步要求个人提出改进信息的方法。使用序数逻辑回归比较各组之间的意图,以百分比报告,调整后的赔率比(AOR),和95%CIs。
    结果:与标准广告组相比,参加患者认可和基于社会规范的广告组的参加广告研究的意愿明显较低(aOR0.73,95%CI0.55-0.97;P=.03和aOR0.69,95%CI0.52-0.92;P=.009)。患者代言广告被认为更难以理解(aOR0.65,95%CI0.48-0.87;P=.004),并且不太清楚地传达研究目标(aOR0.72,95%CI0.55-0.95;P=.01)。虽然患者代言广告对访问主要研究网站的意向没有影响,与标准广告组相比,社会规范广告意愿下降(157/355,44.2%vs191/360,53.1%;aOR0.74,95%CI0.54-0.99;P=.02)。大多数参与者(395/609,64.8%)表示,这些消息不需要更改,但有些人更喜欢更清晰(75/609,12.3%)和更短(59/609,9.7%)的信息。
    结论:这项研究的结果表明,在模拟推文中添加规范的行为信息会降低参与者参与我们基于网络的病例对照研究的意愿,因为这使得这条推文更难理解。这表明,简单的消息应用于通过Twitter招募参与者(随后更名为X)。
    BACKGROUND: Social media is rapidly becoming the primary source to disseminate invitations to the public to consider taking part in research studies. There is, however, little information on how the contents of the advertisement can be communicated to facilitate engagement and subsequently promote intentions to participate in research.
    OBJECTIVE: This paper describes an experimental study that tested different behavioral messages for recruiting study participants for a real-life observational case-control study.
    METHODS: We included 1060 women in a web-based experiment and randomized them to 1 of 3 experimental conditions: standard advertisement (n=360), patient endorsement advertisement (n=345), and social norms advertisement (n=355). After seeing 1 of the 3 advertisements, participants were asked to state (1) their intention to take part in the advertised case-control study, (2) the ease of understanding the message and study aims, and (3) their willingness to be redirected to the website of the case-control study after completing the survey. Individuals were further asked to suggest ways to improve the messages. Intentions were compared between groups using ordinal logistic regression, reported in percentages, adjusted odds ratio (aOR), and 95% CIs.
    RESULTS: Those who were in the patient endorsement and social norms-based advertisement groups had significantly lower intentions to take part in the advertised study compared with those in the standard advertisement group (aOR 0.73, 95% CI 0.55-0.97; P=.03 and aOR 0.69, 95% CI 0.52-0.92; P=.009, respectively). The patient endorsement advertisement was perceived to be more difficult to understand (aOR 0.65, 95% CI 0.48-0.87; P=.004) and to communicate the study aims less clearly (aOR 0.72, 95% CI 0.55-0.95; P=.01). While the patient endorsement advertisement had no impact on intention to visit the main study website, the social norms advertisement decreased willingness compared with the standard advertisement group (157/355, 44.2% vs 191/360, 53.1%; aOR 0.74, 95% CI 0.54-0.99; P=.02). The majority of participants (395/609, 64.8%) stated that the messages did not require changes, but some preferred clearer (75/609, 12.3%) and shorter (59/609, 9.7%) messages.
    CONCLUSIONS: The results of this study indicate that adding normative behavioral messages to simulated tweets decreased participant intention to take part in our web-based case-control study, as this made the tweet harder to understand. This suggests that simple messages should be used for participant recruitment through Twitter (subsequently rebranded X).
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  • 文章类型: Journal Article
    我们先前进行了一项三臂随机试验(263名患有慢性下腰痛的成年人),该试验比较了基于小组的(1)单次疼痛缓解技能干预(EmpoweredRelief;ER);(2)慢性背痛的8次认知行为疗法(CBT);(3)单次健康和背痛教育课程(HE)。结果表明ER与ER的非劣效性CBT在治疗后3个月对一系列结果。
    这里,我们测试了治疗后6个月治疗效果的持久性.我们检查了6个月时主要和次要结局的组间差异,以及每个治疗组中从3个月到6个月的结局侵蚀或改善的程度。
    授权救济在大多数结果上都不劣于CBT,而ER和CBT在大多数结局上仍然优于HE。ER内的结果改善从3个月到6个月没有显着下降,事实上,ER在疼痛灾难方面显示出额外的3到6个月的改善,痛苦烦恼,和焦虑。治疗后6个月ER的影响(中期结果)与接受8次CBT的参与者报告的影响保持同步。
    这些绝对水平的维持意味着ER效应的强烈稳定性。结果延伸至治疗后6个月,以前的发现证明ER和CBT对结果表现出类似的有效影响。
    UNASSIGNED: We previously conducted a 3-arm randomized trial (263 adults with chronic low back pain) which compared group-based (1) single-session pain relief skills intervention (Empowered Relief; ER); (2) 8-session cognitive behavioral therapy (CBT) for chronic back pain; and (3) single-session health and back pain education class (HE). Results suggested non-inferiority of ER vs. CBT at 3 months post-treatment on an array of outcomes.
    UNASSIGNED: Here, we tested the durability of treatment effects at 6 months post-treatment. We examined group differences in primary and secondary outcomes at 6 months and the degree to which outcomes eroded or improved from 3-month to 6-month within each treatment group.
    UNASSIGNED: Empowered Relief remained non-inferior to CBT on most outcomes, whereas both ER and CBT remained superior to HE on most outcomes. Outcome improvements within ER did not decrease significantly from 3-month to 6-month, and indeed ER showed additional 3- to 6-month improvements on pain catastrophizing, pain bothersomeness, and anxiety. Effects of ER at 6 months post-treatment (moderate term outcomes) kept pace with effects reported by participants who underwent 8-session CBT.
    UNASSIGNED: The maintenance of these absolute levels implies strong stability of ER effects. Results extend to 6 months post-treatment previous findings documenting that ER and CBT exhibit similarly potent effects on outcomes.
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