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Social determinants and vulnerable populations最新文献

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“If they’re going to ask the questions, they need to address concerns”: Clinical screening for social determinants of health “如果他们要提出问题,他们就需要解决问题”:对健康的社会决定因素进行临床筛查
Pub Date : 2022-03-01 DOI: 10.1370/afm.20.s1.2784
S. Veldheer, K. Houser, Brianna Hoglen, A. Hobkirk, Michael Hayes, William A Curry, S. Allen
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引用次数: 1
What do self-reported social risk and community-level social contextual factors tell us about diabetes self-management? 自我报告的社会风险和社区水平的社会背景因素告诉我们关于糖尿病自我管理的什么信息?
Pub Date : 2022-03-01 DOI: 10.1370/afm.20.s1.2854
Sarah Alowdi, D. Jones, J. Parra
Context: Higher exposure to social risks, such as food and housing insecurity are linked to worse outcomes for people with type 2 diabetes (T2DM). Social risks can be assessed at the individual-level (self-report of personal experience) and in aggregate at the community level (e.g. census data). What is less understood is how self-reported vs. community level information compare to one another, and which is most relevant for understanding individuals’ T2DM management. Objective: To exam ine the degree of overlap between self-reported social risk (SRSR) and community social contextual factors (CSCF), and document to what extent each is associated with T2DM management. Study Design: Cross-sectional survey geocoded and linked to publicly available data on CSCF. Setting: 12 community health centers in the San Francisco Bay Area. Population: 668 adults with T2DM. Measures: SRSR was assessed through four binary (yes/no) items related to housing instability, food insecurity, access to transportation, and difficulties paying bills. CSCF was assessed by the California Healthy Places Index (HPI), a measure that combines 25 community characteristics from five domains (neighborhood and built environment, health/health care, social/community context, education, economic stability) into a single indexed percentile score (0-100%). T2DM management outcomes included HbA1c from medical records, self-reported missed medication days and depression symptoms (PHQ8). Results: 38.2% (n=252) of our sample endorsed ≥ 1 SRSR. HPI quartiles yielded the following distribution: Q1=31.7% (n=211); Q2=30.3% (n=202); Q3=24.0% (n=160); Q4=14.0% (n=93). 10.4% of individuals in Q4 endorsed ≥1 SRSR (vs. 34.7% in Q1).
背景:面临更高的社会风险,如食物和住房不安全,与2型糖尿病(T2DM)患者的预后更差有关。社会风险可以在个人层面进行评估(个人经验的自我报告),也可以在社区层面进行总体评估(例如人口普查数据)。人们不太了解的是,自我报告和社区水平的信息如何相互比较,以及哪一点与了解个人的T2DM管理最相关。目的:检查自我报告的社会风险(SRSR)和社区社会背景因素(CSCF)之间的重叠程度,并记录它们与T2DM管理的关联程度。研究设计:横断面调查,地理编码,并链接到CSCF的公开数据。环境:旧金山湾区的12个社区卫生中心。人群:668名成年T2DM患者。测量方法:SRSR通过四个二元(是/否)项目进行评估,这些项目与住房不稳定、食品不安全、交通便利和支付账单困难有关。CSCF由加州健康场所指数(HPI)进行评估,该指数将来自五个领域(邻里和建筑环境、健康/医疗保健、社会/社区背景、教育、经济稳定性)的25个社区特征结合为一个单一的指数百分位数分数(0-100%)。T2DM管理结果包括医疗记录中的HbA1c、自我报告的未服药天数和抑郁症状(PHQ8)。结果:38.2% (n=252)的样本的SRSR≥1。HPI四分位数的分布如下:Q1=31.7% (n=211);Q2 = 30.3% (n = 202);第三季度= 24.0% (n = 160);第四季度= 14.0% (n = 93)。第四季度10.4%的个体认可SRSR≥1(第一季度为34.7%)。
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引用次数: 0
Using a QR code to register voters in a family medicine residency clinic 使用QR码在家庭医学住院医师诊所登记选民
Pub Date : 2022-03-01 DOI: 10.1370/afm.20.s1.3213
Yumiko Nakamura, Bich-May Nguyen, Vishnu Muppala
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引用次数: 0
A quasi-experimental evaluation of a clinic-based referral program to address food insecurity 以临床为基础的转介计划的准实验性评估,以解决粮食不安全问题
Pub Date : 2022-03-01 DOI: 10.1370/afm.20.s1.2869
Daniel Walker, Gennaro Di Tosto
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引用次数: 1
Chronic struggle: A new framework for understanding chronic pain and marginalization 慢性斗争:理解慢性疼痛和边缘化的新框架
Pub Date : 2022-03-01 DOI: 10.1370/afm.20.s1.2965
F. Webster, Laura Connoy, K. Rice, J. Katz, Abhimanyu Sud, C. Dale
Medicine often ignores the social aspects of health experience. Applying the lens of social determinants of health has not fully mitigated the tendency of Western medicine to focus on biological causes and pharmaceutical solutions. Objective: We present the stories of 26 people living with chronic pain who have been rendered socially, economically, and politically marginal by existing systems and structures of inequity in ways that exacerbate suffering. We argue that their diverse and multi-faceted experiences are better understood by the term “chronic struggle” rather than “chronic pain”, thus de -centering the medical aspects of people's experiences. Study Design: Institutional ethnography (IE) is a sociological approach increasingly used in health studies. IE begins in the standpoint of people with lived experience and considers them as experts of that experience. IE analysis follows sequences of action, with one informant’s interview leading the way to the next or to a text for analysis. Through this process, we linked participants’ micro level experiences to macro level systems and structures. Setting or Dataset: Participants were recruited for in-depth telephone interviews in online spaces (e.g. Twitter and Kijiji) and through existing networks of our multi-disciplinary research team across several provinces in Canada. Population Studied: Our study focuses on people who are over the age of 18, speak fluent English and who self-identify as living with chronic pain and marginalization. Results: Our findings call attention to the complexities and ‘everyday emergencies’ (Millar, 2014; Mitchell, 2020) that come to shape and d efine one’s experiences with chronic pain. Our themes capture the cascading and inter - related experiences of illness, mental illness, addiction and poverty as they are described and understood by people with lived experience. Combined, we are made aware of how chronic pain is not the key defining difficulty of one’s life— a biographical disruption — but rather one additional difficulty in a life that is always already defined by health and social complexities. Conclusions: As
医学常常忽视健康经验的社会方面。应用健康的社会决定因素的镜头并没有完全减轻西方医学侧重于生物原因和药物解决方案的倾向。目的:我们呈现了26名慢性疼痛患者的故事,他们被现有的不平等制度和结构以加剧痛苦的方式在社会、经济和政治上边缘化。我们认为,他们的多样化和多方面的经验是更好地理解术语“慢性斗争”,而不是“慢性疼痛”,从而去中心的医疗方面的人的经验。研究设计:制度人种学(IE)是一种越来越多地用于健康研究的社会学方法。IE从有生活经验的人的角度出发,把他们看作是经验方面的专家。IE分析遵循一系列的行动,由一个信息提供者的采访引导到下一个或一个文本进行分析。通过这个过程,我们将参与者的微观体验与宏观系统和结构联系起来。设置或数据集:参与者通过在线空间(如Twitter和Kijiji)和我们在加拿大几个省的多学科研究团队的现有网络进行深度电话采访。研究人群:我们的研究重点是18岁以上、英语流利、自我认同患有慢性疼痛和边缘化的人群。结果:我们的研究结果呼吁人们关注复杂性和“日常紧急情况”(Millar, 2014;Mitchell, 2020)来塑造和定义一个人的慢性疼痛经历。我们的主题捕捉了疾病、精神疾病、成瘾和贫困的层叠和相互关联的经历,因为它们是由有生活经验的人描述和理解的。综上所述,我们意识到慢性疼痛并不是定义一个人生活的关键困难——一种传记性的破坏——而是生活中一个额外的困难,而这个困难总是由健康和社会复杂性所定义的。结论:
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引用次数: 0
Hospital team perspectives on social care activities at an urban safety-net hospital during the COVID-19 pandemic 2019冠状病毒病大流行期间城市安全网医院社会护理活动的医院团队视角
Pub Date : 2022-03-01 DOI: 10.1370/afm.20.s1.2873
E. D. De Marchis, O. Nguyễn, Laura Gottlieb, N. Razon, E. Brown
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引用次数: 0
Examining a clinic-based referral program to address food insecurity: A multi-stakeholder qualitative study of implementation 检查以诊所为基础的转诊计划,以解决粮食不安全问题:实施的多利益相关者定性研究
Pub Date : 2022-03-01 DOI: 10.1370/afm.20.s1.2868
D. Walker, Matthew J. Depuccio, Aaron D Clark, Jennifer Garner, Nicolette Coovert, Jennifer L. Hefner
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引用次数: 0
Establishing prescription drug affordability as a new vital sign in primary care: Findings from a community health center 建立处方药可负担性作为初级保健的新生命体征:来自社区卫生中心的调查结果
Pub Date : 2022-03-01 DOI: 10.1370/afm.20.s1.3256
Rita K. Kuwahara
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引用次数: 0
Social determinants of health: More is more. Results from a CERA survey of program directors 健康的社会决定因素:多多益善。CERA对项目主管的调查结果
Pub Date : 2022-03-01 DOI: 10.1370/afm.20.s1.2612
Katherine Wright, P. Cronholm, S. Wheat, Carla M. Villarreal, Deborah S Clements, P. Ravenna
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引用次数: 0
Chronic pain and marginalization in a time of pandemic 大流行时期的慢性疼痛和边缘化
Pub Date : 2022-03-01 DOI: 10.1370/afm.20.s1.2971
F. Webster, Laura Connoy, K. Rice, J. Katz, Abhimanyu Sud, C. Dale
Context: The current pandemic has drawn attention to the importance, failings and weaknesses of the public health system in promoting and maintaining health for all and especially vulnerable groups and those living with serious chronic conditions; this includes those living with chronic pain. COVID-19 response measures are creating barriers to accessing services for those living with pain, such as pain management services and supervised injection sites, which is contributing to a spike in overdoses. Objective: Our project examines how people living with chronic pain and marginalization persevere during COVID-19. Our overa rching research question is “how do participants with chronic pain, who also live with poverty, addictions and mental illness, manage their lives in the time of this pandemic?”. Study Design: Our research is conducted using applied qualitative methods, drawing on an approach known as institutional ethnography, which uses people’s everyday experiences as the starting point for an exploration of the often invisible social relations that orient those experiences. Setting or Dataset: Given the pandemic restrictions, participants were recruited in online spaces (e.g. Twitter and Kijiji) and through the existing networks of our multi-disciplinary study team and interviewed by telephone. Interviews were approximately 60-90 minutes in length depending on how much information the participants wanted to share. Population Studied: Our study focused on people living in Canada over the age of 18, who speak fluent English and who self-identify as living with chronic pain, and marginalization. Results: Our findings highlight the complex ways in which people have been impacted by policies, both negatively and positively. For some people, the pandemic was an equalizer, insofar as they already lived lives marked by isolation and believed that others now knew "how that felt". Others described their mistrust of or inability to adhere to public health recommendations as causing additional stress. Conclusions: By identifying the strategies people use to persevere we are able to provide information for targeted interventions to address structural vulnerabilities
背景:当前的大流行使人们注意到公共卫生系统在促进和维护所有人,特别是弱势群体和严重慢性病患者的健康方面的重要性、缺陷和弱点;这包括那些患有慢性疼痛的人。COVID-19应对措施正在为疼痛患者获得服务(例如疼痛管理服务和受监督的注射场所)制造障碍,从而导致过量用药激增。目的:我们的项目研究慢性疼痛和边缘化患者如何在2019冠状病毒病期间坚持下去。我们最重要的研究问题是“患有慢性疼痛的参与者,他们也生活在贫困、成瘾和精神疾病中,在这场大流行期间如何管理自己的生活?”研究设计:我们的研究采用了应用定性方法,借鉴了一种被称为制度人种学的方法,该方法以人们的日常经历为起点,探索那些往往是无形的社会关系。设置或数据集:考虑到大流行的限制,参与者是在在线空间(例如Twitter和Kijiji)以及通过我们多学科研究团队的现有网络招募的,并通过电话采访。访谈时长约为60-90分钟,取决于参与者想要分享多少信息。人口研究:我们的研究重点是居住在加拿大的18岁以上的人,他们说流利的英语,并自认为患有慢性疼痛和边缘化。结果:我们的研究结果突出了人们受到政策影响的复杂方式,既有消极的,也有积极的。对一些人来说,大流行是一种平衡,因为他们已经过着与世隔绝的生活,并相信其他人现在知道“那种感觉”。另一些人则表示,他们对公共卫生建议的不信任或无法遵守,造成了额外的压力。结论:通过确定人们用于坚持的策略,我们能够为有针对性的干预措施提供信息,以解决结构性脆弱性
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Social determinants and vulnerable populations
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