online forum

在线论坛
  • 文章类型: Journal Article
    背景:自杀死亡率一直在上升,让理解风险因素变得越来越重要。在接触明确的自杀相关媒体时,例如新闻报道中的手段描述或耸人听闻的虚构写照,已知会增加人口自杀率,不知道自杀网站论坛,经常宣传或促进有关致命自杀手段的信息,与自杀死亡的总体变化或特定方式有关。
    目的:这项研究旨在估计在美国,随着时间的推移,谷歌搜索已知自杀网络论坛的频率和内容与自杀死亡的关联。按年龄,性别,和死亡的手段。
    方法:2010年1月至2021年12月期间,针对常见自杀网站名称的全国每月Google搜索数据是从GoogleHealthTrendsAPI(应用程序编程接口)中提取的。自杀死亡是使用CDC(疾病控制和预防中心)国家生命统计系统(NVSS)确定的。并确定了3种主要死亡方式(中毒,窒息,和枪支)。然后使用分布式滞后非线性模型(DLNMs)来估计Google搜索次数与自杀死亡率之间的滞后关联,按年龄分层,性别,和手段,并调整了一个月。敏感性分析,包括使用自回归综合移动平均(ARIMA)建模方法,也进行了。
    结果:在美国,自杀网站搜索率增加的几个月中,有更多记录的青少年和成年人因故意中毒和窒息而死亡。例如,青少年和青少年(10~24岁)的中毒自杀风险为1.79倍(95%CI1.06~3.03),与0次搜索相比,每10百万人中有22次搜索.在25-64岁的成年人中,中毒自杀的风险是1.10(95%CI1.03-1.16)倍,在搜索达到9/10万后1个月,而0搜索。我们还观察到,搜索率的增加与青少年枪支自杀死亡人数减少有关,青少年的时间滞后3个月。这些模型对敏感性测试是稳健的。
    结论:虽然需要更多的分析,这些发现暗示了自杀网站访问量增加与自杀死亡人数增加之间的关联,特别是中毒和窒息死亡。这些发现强调需要进一步调查包含潜在危险信息的地点及其与自杀死亡的关联,因为它们可能会影响弱势群体。
    BACKGROUND:  The rate of suicide death has been increasing, making understanding risk factors of growing importance. While exposure to explicit suicide-related media, such as description of means in news reports or sensationalized fictional portrayal, is known to increase population suicide rates, it is not known whether prosuicide website forums, which often promote or facilitate information about fatal suicide means, are related to change in suicide deaths overall or by specific means.
    OBJECTIVE:  This study aimed to estimate the association of the frequency of Google searches of known prosuicide web forums and content with death by suicide over time in the United States, by age, sex, and means of death.
    METHODS:  National monthly Google search data for names of common prosuicide websites between January 2010 and December 2021 were extracted from Google Health Trends API (application programming interface). Suicide deaths were identified using the CDC (Centers for Disease Control and Prevention) National Vital Statistics System (NVSS), and 3 primary means of death were identified (poisoning, suffocation, and firearm). Distributed lag nonlinear models (DLNMs) were then used to estimate the lagged association between the number of Google searches on suicide mortality, stratified by age, sex, and means, and adjusted for month. Sensitivity analyses, including using autoregressive integrated moving average (ARIMA) modeling approaches, were also conducted.
    RESULTS:  Months in the United States in which search rates for prosuicide websites increased had more documented deaths by intentional poisoning and suffocation among both adolescents and adults. For example, the risk of poisoning suicide among youth and young adults (age 10-24 years) was 1.79 (95% CI 1.06-3.03) times higher in months with 22 searches per 10 million as compared to 0 searches. The risk of poisoning suicide among adults aged 25-64 was 1.10 (95% CI 1.03-1.16) times higher 1 month after searches reached 9 per 10 million compared with 0 searches. We also observed that increased search rates were associated with fewer youth suicide deaths by firearms with a 3-month time lag for adolescents. These models were robust to sensitivity tests.
    CONCLUSIONS:  Although more analysis is needed, the findings are suggestive of an association between increased prosuicide website access and increased suicide deaths, specifically deaths by poisoning and suffocation. These findings emphasize the need to further investigate sites containing potentially dangerous information and their associations with deaths by suicide, as they may affect vulnerable individuals.
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  • 文章类型: Journal Article
    背景:有证据表明,社会互动与神经退行性疾病的发展呈负相关。PREDICT-帕金森病(PREDICT-PD)是一项在线英国队列研究,对参与者的未来帕金森病(PD)风险进行分层。
    目的:本研究旨在探索在PREDICT-PD平台中评估有发展PD风险的人的数字社会特征及其社会资本的方法和可行性,对基于网络的社交参与与PD的潜在预测风险指标之间的关系进行假设。
    方法:构建了一个基于Web的应用程序,以通过PREDICT-PD门户进行社交互动。从该队列的现有成员那里寻求反馈,并告知飞行员的设计。敬业的员工使用每周的参与活动,由PD相关研究组成,事实,和查询,激发讨论。数据由托管平台收集。我们使用社交网络分析,通过帖子和回复的累积数量以及自我网络来检查随着时间的推移产生的联系模式。我们使用网络度量来描述这种联系,桥接,以及平台上参与者之间的社会资本联系。使用描述性统计学分析相关的人口统计学数据和帕金森风险评分(表示为奇数1:x)。进行回归分析以估计风险评分(经过对数转换)与网络度量之间的关系。
    结果:总体而言,219名参与者参加了嵌入研究网站的为期4个月的试点论坛。在它,200人(n=80,40%的男性和n=113,57%的女性)连接在一个大的群体,大多数用户可以通过其他用户直接或间接地联系到对方。共有59%(20/34)的讨论是由参与者自发开始的。参与是异步的,一些人充当讨论小组之间的“经纪人”。随着越来越多的参与者加入论坛并通过在线帖子相互联系,不同的连接用户群开始出现。该试点表明,队列网络平台中的论坛应用程序是可行且可接受的,并促进了数字社交互动。在PREDICT-PD研究中,将参与者基于网络的社交参与与先前收集的个人数据进行匹配是可行的,显示出未来分析的潜力,将在线网络特征与随着时间的推移的PD风险相关联,以及测试数字社交参与作为一种干预措施,以改变患神经退行性疾病的风险。
    结论:试点结果表明,在线论坛可以作为一种干预措施,以增强社交联系,并调查在线参与模式是否会通过长期随访影响发展为PD的风险。这凸显了利用在线平台研究社会资本在调节PD风险中的作用的潜力,并强调了此类方法在未来研究或干预中的可行性。
    BACKGROUND: There is evidence that social interaction has an inverse association with the development of neurodegenerative diseases. PREDICT-Parkinson Disease (PREDICT-PD) is an online UK cohort study that stratifies participants for risk of future Parkinson disease (PD).
    OBJECTIVE: This study aims to explore the methodological approach and feasibility of assessing the digital social characteristics of people at risk of developing PD and their social capital within the PREDICT-PD platform, making hypotheses about the relationship between web-based social engagement and potential predictive risk indicators of PD.
    METHODS: A web-based application was built to enable social interaction through the PREDICT-PD portal. Feedback from existing members of the cohort was sought and informed the design of the pilot. Dedicated staff used weekly engagement activities, consisting of PD-related research, facts, and queries, to stimulate discussion. Data were collected by the hosting platform. We examined the pattern of connections generated over time through the cumulative number of posts and replies and ego networks using social network analysis. We used network metrics to describe the bonding, bridging, and linking of social capital among participants on the platform. Relevant demographic data and Parkinson risk scores (expressed as an odd 1:x) were analyzed using descriptive statistics. Regression analysis was conducted to estimate the relationship between risk scores (after log transformation) and network measures.
    RESULTS: Overall, 219 participants took part in a 4-month pilot forum embedded in the study website. In it, 200 people (n=80, 40% male and n=113, 57% female) connected in a large group, where most pairs of users could reach one another either directly or indirectly through other users. A total of 59% (20/34) of discussions were spontaneously started by participants. Participation was asynchronous, with some individuals acting as \"brokers\" between groups of discussions. As more participants joined the forum and connected to one another through online posts, distinct groups of connected users started to emerge. This pilot showed that a forum application within the cohort web platform was feasible and acceptable and fostered digital social interaction. Matching participants\' web-based social engagement with previously collected data at individual level in the PREDICT-PD study was feasible, showing potential for future analyses correlating online network characteristics with the risk of PD over time, as well as testing digital social engagement as an intervention to modify the risk of developing neurodegenerative diseases.
    CONCLUSIONS: The results from the pilot suggest that an online forum can serve as an intervention to enhance social connectedness and investigate whether patterns of online engagement can impact the risk of developing PD through long-term follow-up. This highlights the potential of leveraging online platforms to study the role of social capital in moderating PD risk and underscores the feasibility of such approaches in future research or interventions.
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  • 文章类型: Journal Article
    人们越来越关注使用亚硝酸钠(SN)作为一种新兴的自杀手段,尤其是年轻人。鉴于传统公共卫生监测来源关于该主题的信息有限,我们研究了一个网上自杀论坛的帖子,\"被制裁的自杀,“这是有关SN使用和采购的主要信息来源。
    本研究旨在确定SN购买和使用的趋势,通过数据挖掘从论坛上的订阅者帖子获得。我们还旨在确定与SN共同出现的物质和主题,以及SN的用户和来源的地理分布。
    我们收集了该网站于2018年3月成立至2022年10月的所有公开可用信息。使用数据驱动方法,包括自然语言处理和机器学习,我们分析了SN提及随着时间的推移,包括SN消费者的位置和采购SN的来源。我们开发了基于变压器的源和位置分类器,以确定SN源的地理分布。
    与SN有关的帖子显示受欢迎程度上升,与疾病控制和预防中心(CDC)广泛的流行病学研究在线数据(=0.727;P<.001)和国家毒物数据系统(=0.866;P=.001)的数据相比,SN的实际使用与自杀意图之间存在统计学上的显着相关性。我们观察到止吐药的频繁出现,苯二氮卓类药物,和具有SN的酸调节剂。我们提出的基于机器学习的源和位置分类器可以检测到潜在的SN源,准确率为72.92%,并显示在美国和其他地方的消费。
    可以从在线论坛获得有关SN和其他新兴自杀机制的重要信息。
    UNASSIGNED: There is growing concern around the use of sodium nitrite (SN) as an emerging means of suicide, particularly among younger people. Given the limited information on the topic from traditional public health surveillance sources, we studied posts made to an online suicide discussion forum, \"Sanctioned Suicide,\" which is a primary source of information on the use and procurement of SN.
    UNASSIGNED: This study aims to determine the trends in SN purchase and use, as obtained via data mining from subscriber posts on the forum. We also aim to determine the substances and topics commonly co-occurring with SN, as well as the geographical distribution of users and sources of SN.
    UNASSIGNED: We collected all publicly available from the site\'s inception in March 2018 to October 2022. Using data-driven methods, including natural language processing and machine learning, we analyzed the trends in SN mentions over time, including the locations of SN consumers and the sources from which SN is procured. We developed a transformer-based source and location classifier to determine the geographical distribution of the sources of SN.
    UNASSIGNED: Posts pertaining to SN show a rise in popularity, and there were statistically significant correlations between real-life use of SN and suicidal intent when compared to data from the Centers for Disease Control and Prevention (CDC) Wide-Ranging Online Data for Epidemiologic Research (⍴=0.727; P<.001) and the National Poison Data System (⍴=0.866; P=.001). We observed frequent co-mentions of antiemetics, benzodiazepines, and acid regulators with SN. Our proposed machine learning-based source and location classifier can detect potential sources of SN with an accuracy of 72.92% and showed consumption in the United States and elsewhere.
    UNASSIGNED: Vital information about SN and other emerging mechanisms of suicide can be obtained from online forums.
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  • 文章类型: Journal Article
    这项研究通过提供有关在线健康社区中医疗保健的作用和价值的宝贵见解,为理论和实践做出了重要贡献。这项研究强调了患者及其家人对健康信息在线来源的依赖日益增加,以及技术支持有健康信息需求的个人的潜力。本研究通过使用偏最小二乘结构方程模型以及多组和重要性性能图分析来分析横截面调查的数据,从而建立了理论框架。这项研究的结果确定了最有益的技术相关问题,如易于网站导航和与其他在线成员的互动,这对在线健康社区的发展和管理具有重要意义。医疗保健专业人员还可以使用此信息有效地向患有慢性疾病的人传播相关信息。本研究建议论坛管理员和参与者之间的主动参与,以改善技术使用和互动,强调有效技术使用准则的好处,以增强用户的信息寻求过程。总的来说,这项研究的重要贡献在于它确定了在信息寻求过程中帮助在线健康社区参与者的因素,向专业人士提供有价值的信息,使用技术传播与COPD等慢性疾病相关的信息。
    This study significantly contributes to both theory and practice by providing valuable insights into the role and value of healthcare in the context of online health communities. This study highlights the increasing dependence of patients and their families on online sources for health information and the potential of technology to support individuals with health information needs. This study develops a theoretical framework by analyzing data from a cross-sectional survey using partial least squares structural equation modeling and multi-group and importance-performance map analysis. The findings of this study identify the most beneficial technology-related issues, like ease of site navigation and interaction with other online members, which have important implications for the development and management of online health communities. Healthcare professionals can also use this information to disseminate relevant information to those with chronic illnesses effectively. This study recommends proactive engagement between forum admins and participants to improve technology use and interaction, highlighting the benefits of guidelines for effective technology use to enhance users\' information-seeking processes. Overall, this study\'s significant contribution lies in its identification of factors that aid online health community participants in the information-seeking process, providing valuable information to professionals on using technology to disseminate information relevant to chronic illnesses like COPD.
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  • 文章类型: Journal Article
    由于涉及自我识别的乱伦的暴力事件,全球学术注意力已转移到乱伦(非自愿独身)现象。推动这些意识形态扩散的平台越来越多,暴力事件日益严重。这项研究构成了意大利背景下有限的实证研究之一。这项研究旨在检查被识别为incels的个体之间的心理健康及其与自尊和时间观点的关联。58名年龄在18至45岁之间的男性受试者参与了该研究。参与者,通过在线交流渠道招募,完成了三份侧重于评估心理健康的问卷,自尊,和时间取向。结果表明,incel受试者的自尊心较低,并且倾向于以享乐主义的当下为中心的观点,旨在立即满足而不是未来的计划。值得注意的是与未来时间视角相关的数据,这对incel受试者的幸福感没有任何预测价值。他们有长期计划的能力,推迟立即满足,而控制行为通过对可能的后果的预期和评价出现减弱。这项研究讨论了制定有针对性的干预计划的意义,鉴于incel现象越来越普遍。是的,因此,至关重要的是,不要低估了乱伦在未来可能构成的潜在威胁。
    The global scholarly attention has shifted toward the phenomenon of inceldom (involuntary celibacy) due to violent incidents involving self-identified incels. There is a growing number of platforms promoting the proliferation of these ideologies, and cases of violence are becoming increasingly severe. This research constitutes one of the limited empirical investigations within an Italian context. This study aims to examine the mental well-being and its associations with self-esteem and temporal perspectives among individuals identifying as incels. Fifty-eighth male subjects aged between 18 and 45 years old participated in the study. Participants, recruited through online communication channels, completed three questionnaires focused on assessing mental well-being, self-esteem, and temporal orientation. The results reveal that incel subjects exhibit low self-esteem and are inclined toward a hedonistic present-focused perspective aimed at immediate gratification rather than future planning. Of note are the data related to the future temporal perspective, which does not show any predictive value on the well-being of incel subjects. Their ability to plan for the long term, defer immediate gratification, and control behavior through the anticipation and evaluation of possible consequences appears diminished. This study discusses the implications of developing targeted intervention programs, given that the incel phenomenon is becoming increasingly widespread. It is, therefore, crucial not to underestimate the potential threat that inceldom could pose in the future.
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  • 文章类型: Journal Article
    背景:现有的医疗保健研究,包括重病研究,往往低估了历史上被边缘化社区的个人。很难捕捉个人围绕其医疗保健交流经历的细微差别观点。需要新的研究策略,以增加来自不同背景的个人的参与。
    目的:本研究的目的是通过定性在线论坛开发一种混合方法方法,以更好地了解个人的健康交流经验,包括来自历史上被边缘化的群体的人,如黑人和拉丁裔人;老年人;和低收入人群,残疾,或严重的疾病。
    方法:我们使用了多相混合方法,社区知情的研究方法来设计研究工具和参与参与者。我们聘请了一群不同的合作者,他们有丰富的医疗保健系统导航经验,他们提供了关于仪器的反馈,添加了测试概念,并为参与者提供了创建安全体验的指导(第一阶段)。我们在2021年4月至5月之间进行了一项全国性的定量调查,人际关系,和系统级域,特别关注患者和临床医生之间的人际沟通(第二阶段)。我们进行了两个异步,定性在线论坛,一种用于市场研究的技术,在2021年6月至8月之间,这使我们能够将学习和测试概念和消息的背景化(第3阶段)。使用在线论坛使我们能够更深入地调查调查结果和假设,以更好地了解浮出水面的“为什么”和“什么”,并测试公共信息以鼓励围绕健康采取行动。
    结果:我们邀请了46个社区合作伙伴,包括来自联邦合格健康中心的患者和临床医生,为研究仪器设计提供信息。在定量调查中,1854名成年人回答说:包括50.5%的女性,65岁以上的人占25.2%,51.9%的低收入人群。近三分之二的人被认定为非西班牙裔白人(65.7%),10.4%被确定为非西班牙裔黑人,15.5%的人被认定为西班牙裔/拉丁裔。另有580人参加网上论坛,包括60.7%的女性,17.4%65岁以上的人,和49.0%的低收入个人。在参与者中,70.3%被认定为非西班牙裔白人,16.0%为非西班牙裔黑人,9.5%为西班牙裔/拉丁裔。我们收到了富人,来自我们在线论坛参与者的不同输入,他们强调了对参与论坛的满意度和更多的知识。
    结论:我们在65岁以上的人群中取得了适度的代表性,被认定为非西班牙裔黑人,在我们的在线论坛上收入很低。在线论坛的规模(N=580)反映了93名黑人和55名西班牙裔/拉丁裔参与者的声音。被认定为西班牙裔/拉丁美洲人的个人人数仍然不足,可能是因为在线论坛仅以英语提供。总的来说,我们的研究结果表明,在混合方法研究中使用在线论坛定性方法的可行性,澄清,并阐述了设计公共卫生和临床沟通干预措施时的定量结果。
    Existing health care research, including serious illness research, often underrepresents individuals from historically marginalized communities. Capturing the nuanced perspectives of individuals around their health care communication experiences is difficult. New research strategies are needed that increase engagement of individuals from diverse backgrounds.
    The aim of this study was to develop a mixed methods approach with qualitative online forums to better understand health communication experiences of individuals, including people from groups historically marginalized such as Black and Latino individuals; older adults; and people with low income, disability, or serious illness.
    We used a multiphase mixed methods, community-informed research approach to design study instruments and engage participants. We engaged a diverse group of collaborators with lived experience of navigating the health care system who provided feedback on instruments, added concepts for testing, and offered guidance on creating a safe experience for participants (phase 1). We conducted a national quantitative survey between April and May 2021 across intrapersonal, interpersonal, and systems-level domains, with particular focus on interpersonal communication between patients and clinicians (phase 2). We conducted two asynchronous, qualitative online forums, a technique used in market research, between June and August 2021, which allowed us to contextualize the learnings and test concepts and messages (phase 3). Using online forums allowed us to probe more deeply into results and hypotheses from the survey to better understand the \"whys\" and \"whats\" that surfaced and to test public messages to encourage action around health.
    We engaged 46 community partners, including patients and clinicians from a Federally Qualified Health Center, to inform study instrument design. In the quantitative survey, 1854 adults responded, including 50.5% women, 25.2% individuals over 65 years old, and 51.9% individuals with low income. Nearly two-thirds identified as non-Hispanic white (65.7%), 10.4% identified as non-Hispanic Black, and 15.5% identified as Hispanic/Latino. An additional 580 individuals participated in online forums, including 60.7% women, 17.4% individuals over 65 years old, and 49.0% individuals with low income. Among the participants, 70.3% identified as non-Hispanic white, 16.0% as non-Hispanic Black, and 9.5% as Hispanic/Latino. We received rich, diverse input from our online forum participants, and they highlighted satisfaction and increased knowledge with engagement in the forums.
    We achieved modest overrepresentation of people who were over 65 years old, identified as non-Hispanic Black, and had low income in our online forums. The size of the online forums (N=580) reflected the voices of 93 Black and 55 Hispanic/Latino participants. Individuals who identify as Hispanic/Latino remained underrepresented, likely because the online forums were offered only in English. Overall, our findings demonstrate the feasibility of using the online forum qualitative approach in a mixed methods study to contextualize, clarify, and expound on quantitative findings when designing public health and clinical communications interventions.
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  • 文章类型: Journal Article
    自杀思想和行为(STB)的社会吸引力和污名化性质使其特别容易受到大多数现代数字通信平台的审查。技术与日常生活的无处不在的集成为利用前所未有的大量数据来研究STB提供了宝贵的机会,然而,主流在线社区中研究审查制度的复杂病因和后果使STB表现不完整。在减轻对责备的恐惧的环境中针对自杀用户的在线书面内容的分析可以提供对STB表达的现代趋势和信号的新颖见解。
    N=192个用户的完整书面内容,包括被确定为潜在自杀完成者/最高风险用户(HRU)的n=48,在支持选择自杀论坛上,制裁自杀,使用基于词典的主题建模(EMPATH)和探索性网络分析技术进行建模,以表征和突出无审查自杀话语的突出方面。
    在37,136个论坛帖子中对超过200万个令牌进行建模,发现HRU中积极情绪和乐观情绪的频率更高,强调寻求和分享行为的方法,突出以前没有记载的行话,以及与孤独和生活逆境有关的语义。
    这种自然语言处理(NLP)和网络驱动的在线STB亚文化暴露揭示了趋势,值得在自杀学中进一步关注,因为它们可能能够支持检测,干预,以及预防自杀结果和暴露。
    UNASSIGNED: The socially unattractive and stigmatizing nature of suicidal thought and behavior (STB) makes it especially susceptible to censorship across most modern digital communication platforms. The ubiquitous integration of technology with day-to-day life has presented an invaluable opportunity to leverage unprecedented amounts of data to study STB, yet the complex etiologies and consequences of censorship for research within mainstream online communities render an incomplete picture of STB manifestation. Analyses targeting online written content of suicidal users in environments where fear of reproach is mitigated may provide novel insight into modern trends and signals of STB expression.
    UNASSIGNED: Complete written content of N = 192 users, including n = 48 identified as potential suicide completers/highest-risk users (HRUs), on the pro-choice suicide forum, Sanctioned Suicide, was modeled using a combination of lexicon-based topic modeling (EMPATH) and exploratory network analysis techniques to characterize and highlight prominent aspects of censorship-free suicidal discourse.
    UNASSIGNED: Modeling of over 2 million tokens across 37,136 forum posts found higher frequency of positive emotion and optimism among HRUs, emphasis on methods seeking and sharing behaviors, prominence of previously undocumented jargon, and semantics related to loneliness and life adversity.
    UNASSIGNED: This natural language processing (NLP)- and network-driven exposé of online STB subculture uncovered trends that deserve further attention within suicidology as they may be able to bolster detection, intervention, and prevention of suicidal outcomes and exposures.
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  • 文章类型: Journal Article
    背景:多囊卵巢综合征(PCOS)是一种异质性疾病,影响4%至21%的卵巢患者。对PCOS的临床治疗的难以接近或不满意导致一些患有这种情况的人在专门的基于网络的论坛上讨论他们的经验。
    目的:本研究通过收集和分析在活跃的PCOS论坛上发布的实验室测试结果,探索将此类基于网络的论坛用于临床研究目的的可行性。特别是在Reddit上托管的PCOSsubreddit。
    方法:我们从PCOSsubreddit收集了大约45,000个帖子。手动读取了5000个帖子的随机子集,和实验室测试结果的存在被标记。这些标记的帖子用于训练机器学习模型,以识别其余帖子中的哪些包含实验室结果。实验室结果是从确定的帖子中手动提取的。将这些自我报告的实验室测试结果与已发表文献中的值进行比较,以评估结果是否与研究人员发表的PCOS队列的值一致。总共选择了10篇论文来代表已发表的PCOS文献,选择标准包括鹿特丹的PCOS诊断标准,过去20年内的出版日期,和至少50名PCOS参与者。
    结果:总体而言,在PCOS网络论坛的实验室检测结果中观察到的总体趋势与临床报告的PCOS一致.一些结果,如促卵泡激素,空腹胰岛素,和抗苗勒管激素,与已发表的PCOS患者的价值一致。这些结果在文献中以及与subreddit相比的高度一致性表明,卵泡刺激素,空腹胰岛素,和抗苗勒管激素在PCOS表型中比其他测试结果更一致。一些结果,比如睾丸激素,性激素结合球蛋白,和稳态模型评估-估计的胰岛素抵抗指数,介于PCOS文献值和正常值之间,由临床测试限值定义。有趣的是,其他结果,包括硫酸脱氢表雄酮,黄体生成素,和空腹血糖,似乎比文献中报道的稍微失调。
    结论:论坛发表的结果与文献中发表的结果之间的差异可能是由于临床研究中的选择过程以及论坛不成比例地描述了PCOS表型的可能性,这些表型不太可能通过医疗干预得到缓解。然而,大多数实验室检测值的一致性程度意味着PCOS网络论坛参与者是研究确定的PCOS队列的代表.PCOSsubreddit的这种验证提供了对subreddit的内容进行更多研究的可能性,以及使用其他医学互联网论坛的内容进行类似研究的想法。
    BACKGROUND: Polycystic ovary syndrome (PCOS) is a heterogeneous condition that affects 4% to 21% of people with ovaries. Inaccessibility or dissatisfaction with clinical treatment for PCOS has led to some individuals with the condition discussing their experiences in specialized web-based forums.
    OBJECTIVE: This study explores the feasibility of using such web-based forums for clinical research purposes by gathering and analyzing laboratory test results posted in an active PCOS forum, specifically the PCOS subreddit hosted on Reddit.
    METHODS: We gathered around 45,000 posts from the PCOS subreddit. A random subset of 5000 posts was manually read, and the presence of laboratory test results was labeled. These labeled posts were used to train a machine learning model to identify which of the remaining posts contained laboratory results. The laboratory results were extracted manually from the identified posts. These self-reported laboratory test results were compared with values in the published literature to assess whether the results were concordant with researcher-published values for PCOS cohorts. A total of 10 papers were chosen to represent published PCOS literature, with selection criteria including the Rotterdam diagnostic criteria for PCOS, a publication date within the last 20 years, and at least 50 participants with PCOS.
    RESULTS: Overall, the general trends observed in the laboratory test results from the PCOS web-based forum were consistent with clinically reported PCOS. A number of results, such as follicle stimulating hormone, fasting insulin, and anti-Mullerian hormone, were concordant with published values for patients with PCOS. The high consistency of these results among the literature and when compared to the subreddit suggests that follicle stimulating hormone, fasting insulin, and anti-Mullerian hormone are more consistent across PCOS phenotypes than other test results. Some results, such as testosterone, sex hormone-binding globulin, and homeostasis model assessment-estimated insulin resistance index, were between those of PCOS literature values and normal values, as defined by clinical testing limits. Interestingly, other results, including dehydroepiandrosterone sulfate, luteinizing hormone, and fasting glucose, appeared to be slightly more dysregulated than those reported in the literature.
    CONCLUSIONS: The differences between the forum-posted results and those published in the literature may be due to the selection process in clinical studies and the possibility that the forum disproportionally describes PCOS phenotypes that are less likely to be alleviated with medical intervention. However, the degree of concordance in most laboratory test values implied that the PCOS web-based forum participants were representative of research-identified PCOS cohorts. This validation of the PCOS subreddit grants the possibility for more research into the contents of the subreddit and the idea of undertaking similar research using the contents of other medical internet forums.
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  • 文章类型: Journal Article
    通过分析健康论坛上的讨论,我们研究了在新冠肺炎大流行期间戴卫生口罩如何改变人们的生活,以及需要进行哪些调整。在我们的审查中,我们遇到了被与会者称为“阴谋论”的理论,这些理论导致了论坛上的激烈交流。令人惊讶的是,这些互动促进了,而不是阻止,集体探索,并导致了与戴口罩有关的问题的丰富讨论。采用定量和定性相结合的方法,我们首先分析讨论的动态,其进展,以及它随着时间的推移而保持的条件,甚至给出了不可调和立场的激进表达。第二,我们从描述面具引发的问题和这些描述所基于的不同权威的角度来研究讨论的结果。我们得出的结论是,由于科学权威的动摇和与大流行有关的问题的不确定性,科学与非科学之间的界限有时会模糊,而不是因为对科学的普遍不信任。我们自相矛盾地认识到,“阴谋家”理论有助于知识的产生,对这些理论的坚持可能更多地来自自称的个人的个人经历,而不是来自阴谋论的污染力。
    By analyzing the discussion on a health forum, we examine how wearing sanitary masks during the Covid-19 pandemic changed people\'s lives and what adjustments were required. During our review, we encountered theories referred to by participants as \"conspiracy theories\" that led to heated exchanges on the forum. Surprisingly, these interactions promoted, rather than prevented, collective exploration and resulted in a rich discussion of the issues related to wearing masks. Using a combination of quantitative and qualitative methods, we first analyze the dynamics of the discussion, its progression, and the conditions under which it was maintained over time, even given the radical expression of irreconcilable positions. Second, we examine the results of the discussion in terms of describing the problems triggered by the mask and the different authorities on which these descriptions were based. We conclude that the boundaries between science and non-science were occasionally blurred because of the wavering of scientific authorities and the uncertainty of the questions related to the pandemic, rather than because of a generalized distrust of science. We recognize that paradoxically, \"conspiracist\" theories contribute to the production of knowledge and that the adherence to these theories may stem more from the personal experiences of the individuals who profess them, rather than from the contaminating power of conspiracy theories.
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  • 文章类型: Journal Article
    在COVID-19大流行期间,新父母不成比例地受到公共卫生限制改变服务可及性和增加压力源的影响。然而,最少的研究已经调查了自然匿名环境中与大流行相关的压力源和围产期父亲的经历。父母寻求联系和信息的一种重要而新颖的方式是通过在线论坛,在COVID-19期间增加。本研究通过框架分析方法对2020年9月至12月围产期父亲的经历进行了定性分析,以使用reddit上的在线论坛predaddit识别COVID-19期间未满足的支持需求。专题框架中的五个主要主题包括论坛的使用,COVID-19,社会心理困扰,家庭功能,儿童健康和发展,每个都有相关的子主题。调查结果强调了predaddit作为信息来源的效用,和相互作用,父亲告知心理健康服务。总的来说,在社会孤立的时期,父亲们利用这个论坛与其他父亲接触,并在过渡到为人父母的过程中获得支持。该手稿强调了围产期父亲未满足的支持需求,以及将父亲纳入围产期护理的重要性,对父母双方实施常规围产期情绪筛查,并制定计划,在这一过渡期间支持父亲,以促进家庭幸福。
    During the COVID-19 pandemic, new parents were disproportionately affected by public health restrictions changing service accessibility and increasing stressors. However, minimal research has examined pandemic-related stressors and experiences of perinatal fathers in naturalistic anonymous settings. An important and novel way parents seek connection and information is through online forums, which increased during COVID-19. The current study qualitatively analyzed the experiences of perinatal fathers from September to December 2020 through the Framework Analytic Approach to identify unmet support needs during COVID-19 using the online forum predaddit on reddit. Five main themes in the thematic framework included forum use, COVID-19, psychosocial distress, family functioning, and child health and development, each with related subthemes. Findings highlight the utility of predaddit as a source of information for, and interactions of, fathers to inform mental health services. Overall, fathers used the forum to engage with other fathers during a time of social isolation and for support during the transition to parenthood. This manuscript highlights the unmet support needs of fathers during the perinatal period and the importance of including fathers in perinatal care, implementing routine perinatal mood screening for both parents, and developing programs to support fathers during this transition to promote family wellbeing.
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