Pub Date : 2026-01-17DOI: 10.1016/j.socscimed.2026.118982
Mark D. Fleming , Dani MacVicar , Aoife M. McDermott , Amanda L. Brewster
Demands for alternatives to police responses to mental health crises have driven significant transformations in the frontlines of emergency care. This ethnographic study (2022-2025) analyzes how the boundaries between policing and behavioral health have been negotiated, contested, and reconstructed during the implementation of a large-scale crisis response initiative in California, USA. Taking an ethnographic approach, we demonstrate how boundary work among law enforcement, behavioral health professionals, and organizational leaders unfolds through intertwined dynamics of competition, collaboration, and reconfiguration. Our findings highlight how boundary work is embedded within broader socio-political contexts shaped by advocacy for racial justice, critiques of police violence, and demands for systemic reform. Specifically, we reveal how the frontline enactment of crisis response is characterized by ongoing negotiations around authority, legitimacy, safety, and care, reflecting and reshaping political and ethical debates on criminalization and police reform. This paper contributes to boundary work theory by illustrating how professional and institutional boundaries are dynamic sites of dialectical engagement that both respond to and actively shape contemporary struggles around race, violence, mental health, and justice.
{"title":"Policing and care in mental health crisis response: Boundary work and the politics of safety and authority","authors":"Mark D. Fleming , Dani MacVicar , Aoife M. McDermott , Amanda L. Brewster","doi":"10.1016/j.socscimed.2026.118982","DOIUrl":"10.1016/j.socscimed.2026.118982","url":null,"abstract":"<div><div>Demands for alternatives to police responses to mental health crises have driven significant transformations in the frontlines of emergency care. This ethnographic study (2022-2025) analyzes how the boundaries between policing and behavioral health have been negotiated, contested, and reconstructed during the implementation of a large-scale crisis response initiative in California, USA. Taking an ethnographic approach, we demonstrate how boundary work among law enforcement, behavioral health professionals, and organizational leaders unfolds through intertwined dynamics of competition, collaboration, and reconfiguration. Our findings highlight how boundary work is embedded within broader socio-political contexts shaped by advocacy for racial justice, critiques of police violence, and demands for systemic reform. Specifically, we reveal how the frontline enactment of crisis response is characterized by ongoing negotiations around authority, legitimacy, safety, and care, reflecting and reshaping political and ethical debates on criminalization and police reform. This paper contributes to boundary work theory by illustrating how professional and institutional boundaries are dynamic sites of dialectical engagement that both respond to and actively shape contemporary struggles around race, violence, mental health, and justice.</div></div>","PeriodicalId":49122,"journal":{"name":"Social Science & Medicine","volume":"393 ","pages":"Article 118982"},"PeriodicalIF":5.0,"publicationDate":"2026-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146081015","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-17DOI: 10.1016/j.socscimed.2026.118999
Kathleen Broussard , Laura D. Lindberg , Emily S. Mann
A growing body of research describes coercive experiences in contraceptive care in the clinic setting, a phenomenon that disproportionately constrains the contraceptive autonomy of women who are young, low-income, Black, or Latinx. Less research has examined how other social influences may constrain contraceptive use and decision-making. We examine contraceptive autonomy across three domains of interpersonal influence (healthcare providers, sexual partners, and parents) and by race (Black vs. White). Between July–September 2023, we surveyed 1207 Black and White adolescents and young adults (AYAs) assigned female at birth living in five southern states. Over half of all respondents reported feeling social pressure related to their contraceptive use. More respondents spoke with a sexual partner or healthcare provider than with a parent about contraception, but those who did speak with a parent were most likely to report contraceptive pressure. Furthermore, respondents who reported social pressure were less likely to be using their preferred method of contraception. Black (vs. White) AYAs were less likely to have conversations with healthcare providers and sexual partners about contraception; more likely to report social pressure across all interpersonal domains; and less likely to be using their preferred method. By examining social pressures beyond the clinic setting, findings reveal the multifaceted and socially patterned ways that bodily autonomy is constrained for AYAs assigned female at birth and how this is magnified for Black AYAs.
{"title":"Contraceptive autonomy of adolescents and young adults in the U.S. South: The influence of healthcare providers, partners, and parents","authors":"Kathleen Broussard , Laura D. Lindberg , Emily S. Mann","doi":"10.1016/j.socscimed.2026.118999","DOIUrl":"10.1016/j.socscimed.2026.118999","url":null,"abstract":"<div><div>A growing body of research describes coercive experiences in contraceptive care in the clinic setting, a phenomenon that disproportionately constrains the contraceptive autonomy of women who are young, low-income, Black, or Latinx. Less research has examined how other social influences may constrain contraceptive use and decision-making. We examine contraceptive autonomy across three domains of interpersonal influence (healthcare providers, sexual partners, and parents) and by race (Black vs. White). Between July–September 2023, we surveyed 1207 Black and White adolescents and young adults (AYAs) assigned female at birth living in five southern states. Over half of all respondents reported feeling social pressure related to their contraceptive use. More respondents spoke with a sexual partner or healthcare provider than with a parent about contraception, but those who did speak with a parent were most likely to report contraceptive pressure. Furthermore, respondents who reported social pressure were less likely to be using their preferred method of contraception. Black (vs. White) AYAs were less likely to have conversations with healthcare providers and sexual partners about contraception; more likely to report social pressure across all interpersonal domains; and less likely to be using their preferred method. By examining social pressures beyond the clinic setting, findings reveal the multifaceted and socially patterned ways that bodily autonomy is constrained for AYAs assigned female at birth and how this is magnified for Black AYAs.</div></div>","PeriodicalId":49122,"journal":{"name":"Social Science & Medicine","volume":"392 ","pages":"Article 118999"},"PeriodicalIF":5.0,"publicationDate":"2026-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146020307","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-17DOI: 10.1016/j.socscimed.2026.119002
MohammadHossein Hadi , Dennis Petrie , Umair Khalil
This paper presents the first empirical evidence linking tobacco tax policies to unintended social consequences in the form of increased energy poverty. We focus on Australia, where smokers face some of the world's highest cigarette prices. We analyse an unanticipated aggressive tax regime implemented in 2010 using a difference-in-differences approach with a nationally representative panel dataset covering 14 years. Our findings indicate significant increases in the incidence of energy poverty among smoking households. Relative to the smoking cohort's pre-policy mean, subjective reports of heating difficulties rose by 24 %, while objective measures increased by 38 % (10 % energy-burden threshold), 15 % (twice-median burden), and 26 % under the Low-Income High Costs (LIHC) measure. Mechanism analyses indicate that reduced energy expenditures and compromised financial stability exacerbate the observed energy poverty. The impacts were particularly pronounced among lower-income families, heavy smokers, and individuals who find quitting hard. This research highlights the complex trade-offs involved in aggressive tobacco taxation and emphasises the need for targeted measures to mitigate the negative consequences on the energy well-being of vulnerable smokers and their families.
{"title":"Energy poverty consequences of aggressive tobacco tax policies","authors":"MohammadHossein Hadi , Dennis Petrie , Umair Khalil","doi":"10.1016/j.socscimed.2026.119002","DOIUrl":"10.1016/j.socscimed.2026.119002","url":null,"abstract":"<div><div>This paper presents the first empirical evidence linking tobacco tax policies to unintended social consequences in the form of increased energy poverty. We focus on Australia, where smokers face some of the world's highest cigarette prices. We analyse an unanticipated aggressive tax regime implemented in 2010 using a difference-in-differences approach with a nationally representative panel dataset covering 14 years. Our findings indicate significant increases in the incidence of energy poverty among smoking households. Relative to the smoking cohort's pre-policy mean, subjective reports of heating difficulties rose by 24 %, while objective measures increased by 38 % (10 % energy-burden threshold), 15 % (twice-median burden), and 26 % under the Low-Income High Costs (LIHC) measure. Mechanism analyses indicate that reduced energy expenditures and compromised financial stability exacerbate the observed energy poverty. The impacts were particularly pronounced among lower-income families, heavy smokers, and individuals who find quitting hard. This research highlights the complex trade-offs involved in aggressive tobacco taxation and emphasises the need for targeted measures to mitigate the negative consequences on the energy well-being of vulnerable smokers and their families.</div></div>","PeriodicalId":49122,"journal":{"name":"Social Science & Medicine","volume":"395 ","pages":"Article 119002"},"PeriodicalIF":5.0,"publicationDate":"2026-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146193050","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-16DOI: 10.1016/j.socscimed.2026.118997
Umair Majid , Quinn Grundy , Stephanie Kelly , Kelly Holloway
Background
Plasma-derived medical products (PDMPs) can represent life-saving treatments for immunodeficiencies, autoimmune diseases, and other health conditions. Immunogloublin (Ig) is a PDMP used to treat a large number of inherited or acquired diseases. As the beneficiaries of a highly complex supply chain, recipients of Ig can illuminate the practical implications of supply challenges and policy initiatives on their health and well-being. This study explores the perspectives of Ig recipients.
Methods
This paper stems from a study based on Narrative Inquiry, which delved into the experiences and perspectives of Ig recipients. A two-interview format was employed to capture 1, the recipient's diagnostic journey and challenges, reported elsewhere; and 2, their knowledge, awareness, and engagement in Ig production and distribution. The second interviews were analyzed with reflexive thematic analysis and are reported in this manuscript.
Results
Participants in this study described access to Ig as variable and uncertain. The uncertainty was shaped by the relationships that they negotiated with the other social actors in the blood system. They described feeling bound to their physician as the gatekeeper to a diagnosis, and therefore treatment, and to navigate a complex health system on their behalf. They were deeply grateful for the plasma donor, but when access felt precarious, the reliance on the donor was unsettling due to uncertainty around product availability. Finally, participants felt removed from the process in which decisions were made about treatment.
Conclusions
Our study engaged Ig recipients as important social actors in the systems responsible for collecting and distributing Ig. Participants offered specific and thorough recommendations for meaningful change. Such guidance holds the potential to foster a more integrated environment in which all interest-holders collaborate to meet patient needs more equitably and sustainably.
{"title":"Engaging patients in blood systems: A qualitative study on immune globulin recipient perspectives","authors":"Umair Majid , Quinn Grundy , Stephanie Kelly , Kelly Holloway","doi":"10.1016/j.socscimed.2026.118997","DOIUrl":"10.1016/j.socscimed.2026.118997","url":null,"abstract":"<div><h3>Background</h3><div>Plasma-derived medical products (PDMPs) can represent life-saving treatments for immunodeficiencies, autoimmune diseases, and other health conditions. Immunogloublin (Ig) is a PDMP used to treat a large number of inherited or acquired diseases. As the beneficiaries of a highly complex supply chain, recipients of Ig can illuminate the practical implications of supply challenges and policy initiatives on their health and well-being. This study explores the perspectives of Ig recipients.</div></div><div><h3>Methods</h3><div>This paper stems from a study based on Narrative Inquiry, which delved into the experiences and perspectives of Ig recipients. A two-interview format was employed to capture 1, the recipient's diagnostic journey and challenges, reported elsewhere; and 2, their knowledge, awareness, and engagement in Ig production and distribution. The second interviews were analyzed with reflexive thematic analysis and are reported in this manuscript.</div></div><div><h3>Results</h3><div>Participants in this study described access to Ig as variable and uncertain. The uncertainty was shaped by the relationships that they negotiated with the other social actors in the blood system. They described feeling bound to their physician as the gatekeeper to a diagnosis, and therefore treatment, and to navigate a complex health system on their behalf. They were deeply grateful for the plasma donor, but when access felt precarious, the reliance on the donor was unsettling due to uncertainty around product availability. Finally, participants felt removed from the process in which decisions were made about treatment.</div></div><div><h3>Conclusions</h3><div>Our study engaged Ig recipients as important social actors in the systems responsible for collecting and distributing Ig. Participants offered specific and thorough recommendations for meaningful change. Such guidance holds the potential to foster a more integrated environment in which all interest-holders collaborate to meet patient needs more equitably and sustainably.</div></div>","PeriodicalId":49122,"journal":{"name":"Social Science & Medicine","volume":"392 ","pages":"Article 118997"},"PeriodicalIF":5.0,"publicationDate":"2026-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146020383","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-16DOI: 10.1016/j.socscimed.2026.119000
Marieke van Wieringen
This paper studies how certified nursing assistants (CNAs), as members of a low-status occupational group, engage in identity reconstruction as they attempt to alter their marginalized position within long-term care organizations. Micro-level process data consist of 160 h of participant observations of a professional development programme for CNAs and 130 in-depth interviews with programme participants and their colleagues in care organizations. The findings show that the identity reconstruction process involved four micro-processes: 1) recognizing the dominance of marginalized identity, 2) seeking an upgraded identity, 3) grappling with identity validation and dissociation, 4) experiencing disillusion when struggling to sustain upgraded identity. By capturing these micro-processes, this research contributes, first, by showing that identity reconstruction in low-status occupational groups begins not from a coherent identity under threat but from a fractured, self-diminishing identity, making the recognition of marginality itself a pivotal catalyst for upgrading identity. Second, it conceptualizes how identity reconstruction centers on identity upgrading, surfacing and legitimizing undervalued forms of knowledge, rather than acquiring new roles or competencies. The third contribution lies in revealing that early affirmations can create a false sense of establishment, even complacency, and deter further proactive “work” in asserting and enacting a reconstructed identity within broader organizational contexts, thereby undermining previous identity work done. Taken together, this study offers a more comprehensive understanding of identity reconstruction processes by members of low-status occupational groups, showing its precariousness.
{"title":"‘They're big and I is small’: The precarious identity reconstruction process of a low-status occupational group","authors":"Marieke van Wieringen","doi":"10.1016/j.socscimed.2026.119000","DOIUrl":"10.1016/j.socscimed.2026.119000","url":null,"abstract":"<div><div>This paper studies how certified nursing assistants (CNAs), as members of a low-status occupational group, engage in identity reconstruction as they attempt to alter their marginalized position within long-term care organizations. Micro-level process data consist of 160 h of participant observations of a professional development programme for CNAs and 130 in-depth interviews with programme participants and their colleagues in care organizations. The findings show that the identity reconstruction process involved four micro-processes: 1) recognizing the dominance of marginalized identity, 2) seeking an upgraded identity, 3) grappling with identity validation and dissociation, 4) experiencing disillusion when struggling to sustain upgraded identity. By capturing these micro-processes, this research contributes, first, by showing that identity reconstruction in low-status occupational groups begins not from a coherent identity under threat but from a fractured, self-diminishing identity, making the recognition of marginality itself a pivotal catalyst for upgrading identity. Second, it conceptualizes how identity reconstruction centers on identity upgrading, surfacing and legitimizing undervalued forms of knowledge, rather than acquiring new roles or competencies. The third contribution lies in revealing that early affirmations can create a false sense of establishment, even complacency, and deter further proactive “work” in asserting and enacting a reconstructed identity within broader organizational contexts, thereby undermining previous identity work done. Taken together, this study offers a more comprehensive understanding of identity reconstruction processes by members of low-status occupational groups, showing its precariousness.</div></div>","PeriodicalId":49122,"journal":{"name":"Social Science & Medicine","volume":"392 ","pages":"Article 119000"},"PeriodicalIF":5.0,"publicationDate":"2026-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146012963","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-16DOI: 10.1016/j.socscimed.2026.118995
Lilah M. Besser , Sarah Forrester , Diana Mitsova , Pauline Maillard , Charles DeCarli , Rachel Whitmer , Oanh L. Meyer
Ethnoracial segregation has been associated with worse cognitive functioning among Black older adults, while its impact on Latinx individuals is less clear. We investigated whether Black and Latinx older adults living in segregated neighborhoods demonstrate worse magnetic resonance imaging (MRI) outcomes. We used data on participants from the University of California Davis Alzheimer's Disease Research Center. MRI outcomes included hippocampal and white matter hyperintensity (WMH) volumes. Black and Latinx segregation was defined using the Getis-Ord (Gi∗) statistic, which compares the proportion of Black or Latinx residents, respectively, in the participant's Census tract to surrounding neighborhoods and greater study region (higher Gi∗ = greater clustering/segregation). Multivariable linear regression analyses examined associations between Gi∗ segregation measures and MRI outcomes, stratified by the participants' ethnoracial group (Black, Latinx, or White). Participants (n = 269) were on average 74 ± 7 years of age and 24 % were Black, 25 % were Latinx, and 51 % were White. In adjusted analyses, Black participants in more Latinx segregated neighborhoods had lower hippocampal volumes, and Latinx participants in more Black segregated neighborhoods had lower hippocampal volumes. Latinx participants in more Latinx segregated neighborhoods had greater white matter hyperintensity volumes. Overall, Black and Latinx but not White participants living in segregated neighborhoods had worse MRI outcomes. Future studies are needed to replicate our findings in geographically diverse samples and to elucidate the potential psychosocial/social determinant and biological mechanisms that relate segregation to brain health (e.g., Latinx segregated neighborhoods may have fewer recreational and physical activity resources to promote healthy lifestyles).
{"title":"Residential segregation of Black and Latinx older adults and brain imaging outcomes","authors":"Lilah M. Besser , Sarah Forrester , Diana Mitsova , Pauline Maillard , Charles DeCarli , Rachel Whitmer , Oanh L. Meyer","doi":"10.1016/j.socscimed.2026.118995","DOIUrl":"10.1016/j.socscimed.2026.118995","url":null,"abstract":"<div><div>Ethnoracial segregation has been associated with worse cognitive functioning among Black older adults, while its impact on Latinx individuals is less clear. We investigated whether Black and Latinx older adults living in segregated neighborhoods demonstrate worse magnetic resonance imaging (MRI) outcomes. We used data on participants from the University of California Davis Alzheimer's Disease Research Center. MRI outcomes included hippocampal and white matter hyperintensity (WMH) volumes. Black and Latinx segregation was defined using the Getis-Ord (Gi∗) statistic, which compares the proportion of Black or Latinx residents, respectively, in the participant's Census tract to surrounding neighborhoods and greater study region (higher Gi∗ = greater clustering/segregation). Multivariable linear regression analyses examined associations between Gi∗ segregation measures and MRI outcomes, stratified by the participants' ethnoracial group (Black, Latinx, or White). Participants (n = 269) were on average 74 ± 7 years of age and 24 % were Black, 25 % were Latinx, and 51 % were White. In adjusted analyses, Black participants in more Latinx segregated neighborhoods had lower hippocampal volumes, and Latinx participants in more Black segregated neighborhoods had lower hippocampal volumes. Latinx participants in more Latinx segregated neighborhoods had greater white matter hyperintensity volumes. Overall, Black and Latinx but not White participants living in segregated neighborhoods had worse MRI outcomes. Future studies are needed to replicate our findings in geographically diverse samples and to elucidate the potential psychosocial/social determinant and biological mechanisms that relate segregation to brain health (e.g., Latinx segregated neighborhoods may have fewer recreational and physical activity resources to promote healthy lifestyles).</div></div>","PeriodicalId":49122,"journal":{"name":"Social Science & Medicine","volume":"393 ","pages":"Article 118995"},"PeriodicalIF":5.0,"publicationDate":"2026-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146025678","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-16DOI: 10.1016/j.socscimed.2026.118996
Susan L. Brown , I-Fen Lin , Francesca A. Marino , Kagan A. Mellencamp
Limited family ties are increasingly common among U.S. older adults. Kinless individuals lack a family of procreation, namely a spouse/partner and children. Sole family survivorship refers to lacking family of origin kin, including parents and siblings. Familial ties are linked to health across the life course and, in line with socioemotional selectivity theory, play an increasingly salient role with age. Consequently, older adults who are kinless or sole family survivors may face worse health outcomes than their counterparts with kin. However, substitution of friends or relatives nearby may mitigate some of the health burden of limited family ties. Drawing on 191,146 person-waves of data from the 1998–2018 Health and Retirement Study, we assessed how these two forms of limited family ties were associated with chronic conditions, (instrumental) activities of daily living (ADL/IADL) limitations, self-rated poor health, and depressive symptoms. Among women, kinlessness was largely unrelated to women's health, only being associated with an increased rate of ADL/IADL difficulties. In contrast, sole family survivorship was positively associated with women's ADL/IADL difficulties, self-rated poor health, and depressive symptoms. Among men, kinlessness was not associated with worse health outcomes. Sole family survivorship was associated with more ADL/IADL difficulties and depressive symptoms among men. Social ties were not uniformly protective of women's and men's health, calling into question the viability of substitutes and underscoring the unique advantages of immediate family ties in later life. Our study demonstrates the utility of examining multiple forms of limited family ties which have distinct ramifications for older adult well-being.
{"title":"Kinlessness, sole family survivorship, and the mental and physical health of U.S. older adults","authors":"Susan L. Brown , I-Fen Lin , Francesca A. Marino , Kagan A. Mellencamp","doi":"10.1016/j.socscimed.2026.118996","DOIUrl":"10.1016/j.socscimed.2026.118996","url":null,"abstract":"<div><div>Limited family ties are increasingly common among U.S. older adults. Kinless individuals lack a family of procreation, namely a spouse/partner and children. Sole family survivorship refers to lacking family of origin kin, including parents and siblings. Familial ties are linked to health across the life course and, in line with socioemotional selectivity theory, play an increasingly salient role with age. Consequently, older adults who are kinless or sole family survivors may face worse health outcomes than their counterparts with kin. However, substitution of friends or relatives nearby may mitigate some of the health burden of limited family ties. Drawing on 191,146 person-waves of data from the 1998–2018 Health and Retirement Study, we assessed how these two forms of limited family ties were associated with chronic conditions, (instrumental) activities of daily living (ADL/IADL) limitations, self-rated poor health, and depressive symptoms. Among women, kinlessness was largely unrelated to women's health, only being associated with an increased rate of ADL/IADL difficulties. In contrast, sole family survivorship was positively associated with women's ADL/IADL difficulties, self-rated poor health, and depressive symptoms. Among men, kinlessness was not associated with worse health outcomes. Sole family survivorship was associated with more ADL/IADL difficulties and depressive symptoms among men. Social ties were not uniformly protective of women's and men's health, calling into question the viability of substitutes and underscoring the unique advantages of immediate family ties in later life. Our study demonstrates the utility of examining multiple forms of limited family ties which have distinct ramifications for older adult well-being.</div></div>","PeriodicalId":49122,"journal":{"name":"Social Science & Medicine","volume":"393 ","pages":"Article 118996"},"PeriodicalIF":5.0,"publicationDate":"2026-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146100634","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-16DOI: 10.1016/j.socscimed.2026.118994
Ying-Yeh Chen , Vera Yu Men , Cheuk Yui Yeung , Kevin Chien-Chang Wu , Ying-Chen Chi , Paul SF. Yip
Media coverage of celebrity suicides can shape population-level suicidal behavior, yet most existing evidence focuses on mortality rather than non-fatal attempts. This study investigates the impact of media coverage following the suicide of Chiung Yao, an 86-year-old best-selling novelist and cultural figure in Chinese-speaking societies, on suicide mortality and suicide attempts in Taiwan.
We drew on suicide attempt data from Taiwan's National Suicide Surveillance System and mortality data from the Taiwan Death Registry. Using an interrupted time-series design with quasi-Poisson regression, we analyzed seven-day rolling counts of suicide attempts and deaths during the four weeks before and after her death (December 4th, 2024), stratified by sex, age group, and suicide method.
No significant overall changes in suicide attempts or mortality were observed. However, suicide attempts increased by 12.3 % among women aged 45–64 (IRR = 1.123; 95 % CI: 1.030–1.225), with a slight increase of the post-death trend among women aged 25–44. Suicide deaths by charcoal burning, the method used by the celebrity, increased by 47.0 % (IRR = 1.470; 95 % CI: 1.195–1.807), and mortality among men aged 25–44 and ≥65 rose by 35.5 % (IRR = 1.355; 95 % CI: 1.095–1.679) and 20.7 % (IRR = 1.207; 95 % CI: 0.992–1.468), respectively.
Media coverage of the suicide of an older celebrity was not associated with population-level increases in suicide, but associated with method- and subgroup-specific changes in suicide attempts and mortality. These findings highlight the importance of monitoring media practices with attention to differential vulnerability following highly publicized suicides.
{"title":"The impact of media coverage of a celebrity suicide on suicide and attempted suicide rates in Taiwan","authors":"Ying-Yeh Chen , Vera Yu Men , Cheuk Yui Yeung , Kevin Chien-Chang Wu , Ying-Chen Chi , Paul SF. Yip","doi":"10.1016/j.socscimed.2026.118994","DOIUrl":"10.1016/j.socscimed.2026.118994","url":null,"abstract":"<div><div>Media coverage of celebrity suicides can shape population-level suicidal behavior, yet most existing evidence focuses on mortality rather than non-fatal attempts. This study investigates the impact of media coverage following the suicide of Chiung Yao, an 86-year-old best-selling novelist and cultural figure in Chinese-speaking societies, on suicide mortality and suicide attempts in Taiwan.</div><div>We drew on suicide attempt data from Taiwan's National Suicide Surveillance System and mortality data from the Taiwan Death Registry. Using an interrupted time-series design with quasi-Poisson regression, we analyzed seven-day rolling counts of suicide attempts and deaths during the four weeks before and after her death (December 4th, 2024), stratified by sex, age group, and suicide method.</div><div>No significant overall changes in suicide attempts or mortality were observed. However, suicide attempts increased by 12.3 % among women aged 45–64 (IRR = 1.123; 95 % CI: 1.030–1.225), with a slight increase of the post-death trend among women aged 25–44. Suicide deaths by charcoal burning, the method used by the celebrity, increased by 47.0 % (IRR = 1.470; 95 % CI: 1.195–1.807), and mortality among men aged 25–44 and ≥65 rose by 35.5 % (IRR = 1.355; 95 % CI: 1.095–1.679) and 20.7 % (IRR = 1.207; 95 % CI: 0.992–1.468), respectively.</div><div>Media coverage of the suicide of an older celebrity was not associated with population-level increases in suicide, but associated with method- and subgroup-specific changes in suicide attempts and mortality. These findings highlight the importance of monitoring media practices with attention to differential vulnerability following highly publicized suicides.</div></div>","PeriodicalId":49122,"journal":{"name":"Social Science & Medicine","volume":"392 ","pages":"Article 118994"},"PeriodicalIF":5.0,"publicationDate":"2026-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146020341","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-16DOI: 10.1016/j.socscimed.2026.118998
Nicole Miriam Daniels
Contributing to critical health scholarship, this multi-sited ethnography into private sector obstetrics in Cape Town, South Africa generated comparative public sector data through observation and interviews with seven obstetricians and fourteen pregnant women between 2017 and 2019. Entrenched inequalities in the provision and access to quality obstetric care, provoked in the politics of birth, are significant for broader societal movements and governance approaches towards universal healthcare in Africa. With near universal maternity care, South Africa is an important case study for understanding possible private sector contributions to National Health Insurance reforms aiming to consolidate health services for all. Drawing on feminist new materialist theory and socio-material analysis, I outline a care continuum, which I use to interrogate the logics of care that articulate an interdependent yet dichotomized health system. Dichotomized as poles either end of the care continuum is a generalised public sector and individualised private sector. A continuum helps demonstrate that material, experiential and discursive differences in care are not pre-existing but intra-actively related, meaning their differences are produced and maintained through relatedness. I illustrate this looking at movements of obstetric practices, patients, and providers, spatialities of services, and temporalities in care to propose that that public-private maternity care boundaries are co-produced through their mutual entanglement.
{"title":"Towards a care continuum: A socio-material analysis of intra-acting public-private maternity care in South Africa","authors":"Nicole Miriam Daniels","doi":"10.1016/j.socscimed.2026.118998","DOIUrl":"10.1016/j.socscimed.2026.118998","url":null,"abstract":"<div><div>Contributing to critical health scholarship, this multi-sited ethnography into private sector obstetrics in Cape Town, South Africa generated comparative public sector data through observation and interviews with seven obstetricians and fourteen pregnant women between 2017 and 2019. Entrenched inequalities in the provision and access to quality obstetric care, provoked in the politics of birth, are significant for broader societal movements and governance approaches towards universal healthcare in Africa. With near universal maternity care, South Africa is an important case study for understanding possible private sector contributions to National Health Insurance reforms aiming to consolidate health services for all. Drawing on feminist new materialist theory and socio-material analysis, I outline a <em>care continuum</em>, which I use to interrogate the logics of care that articulate an interdependent yet dichotomized health system. Dichotomized as poles either end of the care continuum is a generalised public sector and individualised private sector. A continuum helps demonstrate that material, experiential and discursive differences in care are not pre-existing but intra-actively related, meaning their differences are produced and maintained through relatedness. I illustrate this looking at movements of obstetric practices, patients, and providers, spatialities of services, and temporalities in care to propose that that public-private maternity care boundaries are co-produced through their mutual entanglement.</div></div>","PeriodicalId":49122,"journal":{"name":"Social Science & Medicine","volume":"393 ","pages":"Article 118998"},"PeriodicalIF":5.0,"publicationDate":"2026-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146025873","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-14DOI: 10.1016/j.socscimed.2026.118987
Xiaqing Jiang , Yuying Zhang , Jiamin Gao
Objectives
This study examines how city-level socioeconomic status (SES) is associated with cognitive function among older adults in China, and explores the mediating role of healthcare resources and the moderating role of individual SES in this context.
Methods
We relied on data from the 2018 wave of the China Health and Retirement Longitudinal Study, which provided individual cognitive function and demographic characteristics. Area-level SES and healthcare resource indicators were obtained from national statistical sources. A total of 9520 individuals aged 60 years or older from 123 cities were included in the analysis. A multilevel moderated mediation model was applied, and subgroup analyses by gender were conducted.
Results
Both individual- and area-level SES were positively associated with cognitive function. Multilevel mediation models of healthcare resources showed that only physician density (i.e., not hospital or bed supply) partially mediated the association between area-level SES and cognitive function. After individual SES was introduced as a moderator, the cognitive benefits of healthcare human resources were greater for low-SES individuals than for high-SES individuals. However, evidence for this moderating effect was not consistently supported across variations in sample composition and cognitive measurement. Gender-stratified analyses further showed no clear evidence supporting an individual-SES-based moderating effect in either men or women.
Conclusion
Our findings emphasize the fact that area-level SES and healthcare human resources shape late-life cognition, suggesting equity-focused policies that address structural disadvantage to reduce disparities in cognitive aging.
{"title":"Area-socioeconomic disadvantage and cognitive function among Chinese older adults: the mediating role of healthcare resources and the moderating role of individual socioeconomic status","authors":"Xiaqing Jiang , Yuying Zhang , Jiamin Gao","doi":"10.1016/j.socscimed.2026.118987","DOIUrl":"10.1016/j.socscimed.2026.118987","url":null,"abstract":"<div><h3>Objectives</h3><div>This study examines how city-level socioeconomic status (SES) is associated with cognitive function among older adults in China, and explores the mediating role of healthcare resources and the moderating role of individual SES in this context.</div></div><div><h3>Methods</h3><div>We relied on data from the 2018 wave of the China Health and Retirement Longitudinal Study, which provided individual cognitive function and demographic characteristics. Area-level SES and healthcare resource indicators were obtained from national statistical sources. A total of 9520 individuals aged 60 years or older from 123 cities were included in the analysis. A multilevel moderated mediation model was applied, and subgroup analyses by gender were conducted.</div></div><div><h3>Results</h3><div>Both individual- and area-level SES were positively associated with cognitive function. Multilevel mediation models of healthcare resources showed that only physician density (i.e., not hospital or bed supply) partially mediated the association between area-level SES and cognitive function. After individual SES was introduced as a moderator, the cognitive benefits of healthcare human resources were greater for low-SES individuals than for high-SES individuals. However, evidence for this moderating effect was not consistently supported across variations in sample composition and cognitive measurement. Gender-stratified analyses further showed no clear evidence supporting an individual-SES-based moderating effect in either men or women.</div></div><div><h3>Conclusion</h3><div>Our findings emphasize the fact that area-level SES and healthcare human resources shape late-life cognition, suggesting equity-focused policies that address structural disadvantage to reduce disparities in cognitive aging.</div></div>","PeriodicalId":49122,"journal":{"name":"Social Science & Medicine","volume":"392 ","pages":"Article 118987"},"PeriodicalIF":5.0,"publicationDate":"2026-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145979836","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}