Pub Date : 2026-02-04DOI: 10.1007/s40615-025-02806-x
Michelle K Nakphong, Maria-Elena De Trinidad Young, Kevin F Lee, May Sudhinaraset
Background: Immigrants' employment is linked with health care access in the US, but we lack a thorough understanding of how immigrants' experiences of employment exclusions influence their health care access in the context of immigrant racialization. We aimed to assess employment exclusions (i.e., exclusions from jobs and violations at work) across Asian and Latine foreign-born adults, the two largest immigrant racial groups, and their associations with health care access. We also sought to understand variations by race, and current or past legal status.
Methods: We used 2018-2020 Research on Immigrant Health and State Policy survey data from 2,010 Latine and Asian foreign-born adults in California. We measured seven indicators of employment exclusions and used weighted logistic regression to estimate associations between employment exclusions and health care access: usual source of care and delaying care in the past 12 months. We tested race, current legal status and past legal status as moderators.
Results: Nearly one-quarter (23.8%) of respondents reported ≥1 employment exclusion. Latine racial identity, current status as a non-citizen without permanent residency, and being previously undocumented was associated with greater employment exclusions. Employment exclusions were associated with 1.47 times (95% CI: 1.27, 1.69) greater odds of delaying care. Previous undocumented status, but not race or current legal status, moderated associations between violations at work and delay in care.
Conclusions: Latine immigrants face a greater number of barriers to employment opportunities and protections of worker rights compared to Asians, while employment exclusions and past legal status drives poorer health care utilization.
{"title":"Employment Exclusions and Health Care Access among Latine and Asian Immigrants in the Context of Racialization.","authors":"Michelle K Nakphong, Maria-Elena De Trinidad Young, Kevin F Lee, May Sudhinaraset","doi":"10.1007/s40615-025-02806-x","DOIUrl":"https://doi.org/10.1007/s40615-025-02806-x","url":null,"abstract":"<p><strong>Background: </strong>Immigrants' employment is linked with health care access in the US, but we lack a thorough understanding of how immigrants' experiences of employment exclusions influence their health care access in the context of immigrant racialization. We aimed to assess employment exclusions (i.e., exclusions from jobs and violations at work) across Asian and Latine foreign-born adults, the two largest immigrant racial groups, and their associations with health care access. We also sought to understand variations by race, and current or past legal status.</p><p><strong>Methods: </strong>We used 2018-2020 Research on Immigrant Health and State Policy survey data from 2,010 Latine and Asian foreign-born adults in California. We measured seven indicators of employment exclusions and used weighted logistic regression to estimate associations between employment exclusions and health care access: usual source of care and delaying care in the past 12 months. We tested race, current legal status and past legal status as moderators.</p><p><strong>Results: </strong>Nearly one-quarter (23.8%) of respondents reported ≥1 employment exclusion. Latine racial identity, current status as a non-citizen without permanent residency, and being previously undocumented was associated with greater employment exclusions. Employment exclusions were associated with 1.47 times (95% CI: 1.27, 1.69) greater odds of delaying care. Previous undocumented status, but not race or current legal status, moderated associations between violations at work and delay in care.</p><p><strong>Conclusions: </strong>Latine immigrants face a greater number of barriers to employment opportunities and protections of worker rights compared to Asians, while employment exclusions and past legal status drives poorer health care utilization.</p>","PeriodicalId":16921,"journal":{"name":"Journal of Racial and Ethnic Health Disparities","volume":" ","pages":""},"PeriodicalIF":2.4,"publicationDate":"2026-02-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146119006","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-04DOI: 10.1007/s40615-026-02850-1
Kryss Shane, Anthony D Slonim
Medical gaslighting, defined as the minimization or dismissal of a patient's symptoms by healthcare providers, has gained increasing visibility, particularly among marginalized populations. This phenomenon disproportionately impacts individuals facing systemic inequities related to race, gender and class, effects that are compounded at the intersection of these identities. Medical gaslighting contributes to misdiagnosis, delayed care, emotional distress, and long-term mistrust in healthcare systems. Through an intersectional framework and illustrative case studies, this paper examines how implicit bias, structural racism, and the historical mistreatment of marginalized groups contribute to the erasure of patient experiences. The emotional and psychological toll of medical gaslighting further exacerbates existing health disparities. To address this issue, we explore strategies including provider education on implicit bias, expanded patient advocacy, and policy reforms aimed at promoting health equity. These interventions are critical for restoring trust and improving health outcomes, particularly for those most vulnerable to systemic healthcare neglect.
{"title":"Medical Gaslighting and its Impact on Vulnerable Populations.","authors":"Kryss Shane, Anthony D Slonim","doi":"10.1007/s40615-026-02850-1","DOIUrl":"https://doi.org/10.1007/s40615-026-02850-1","url":null,"abstract":"<p><p>Medical gaslighting, defined as the minimization or dismissal of a patient's symptoms by healthcare providers, has gained increasing visibility, particularly among marginalized populations. This phenomenon disproportionately impacts individuals facing systemic inequities related to race, gender and class, effects that are compounded at the intersection of these identities. Medical gaslighting contributes to misdiagnosis, delayed care, emotional distress, and long-term mistrust in healthcare systems. Through an intersectional framework and illustrative case studies, this paper examines how implicit bias, structural racism, and the historical mistreatment of marginalized groups contribute to the erasure of patient experiences. The emotional and psychological toll of medical gaslighting further exacerbates existing health disparities. To address this issue, we explore strategies including provider education on implicit bias, expanded patient advocacy, and policy reforms aimed at promoting health equity. These interventions are critical for restoring trust and improving health outcomes, particularly for those most vulnerable to systemic healthcare neglect.</p>","PeriodicalId":16921,"journal":{"name":"Journal of Racial and Ethnic Health Disparities","volume":" ","pages":""},"PeriodicalIF":2.4,"publicationDate":"2026-02-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146119162","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-04DOI: 10.1007/s40615-025-02711-3
Rachel Anderson, Kate Killion, Christie I Idiong, Curtis Antrum, Summaya Abdul-Razak, Sajal Raja, Kritee Niroula, Snehaa Ray, Michael Puglisi, Jolaade Kalinowski, Loneke T Blackman Carr, Kristen Cooksey Stowers
Interventions addressing racial and ethnic obesity inequities have lower effectiveness in Black adults. Previous literature linking the neighborhood environment to obesity inequities relies on limited food environment measures. Thus, we conducted semi-structured interviews to assess neighborhood-level barriers and facilitators to health behaviors among ethnically diverse Black adults (n = 24). Interviews were analyzed using thematic analysis (kappa = 0.70- 0.93; IRR = 83%). Participants reported barriers in the food (cost, transportation, high unhealthy food access) and physical activity environment (safety concerns). Facilitators included community food resources and access to safe areas for physical activity. These results may inform future research and weight loss programs for diverse Black adults.
{"title":"Perceived Neighborhood-level Assets and Barriers to Weight-related Behaviors among Ethnically Diverse Black Adults.","authors":"Rachel Anderson, Kate Killion, Christie I Idiong, Curtis Antrum, Summaya Abdul-Razak, Sajal Raja, Kritee Niroula, Snehaa Ray, Michael Puglisi, Jolaade Kalinowski, Loneke T Blackman Carr, Kristen Cooksey Stowers","doi":"10.1007/s40615-025-02711-3","DOIUrl":"https://doi.org/10.1007/s40615-025-02711-3","url":null,"abstract":"<p><p>Interventions addressing racial and ethnic obesity inequities have lower effectiveness in Black adults. Previous literature linking the neighborhood environment to obesity inequities relies on limited food environment measures. Thus, we conducted semi-structured interviews to assess neighborhood-level barriers and facilitators to health behaviors among ethnically diverse Black adults (n = 24). Interviews were analyzed using thematic analysis (kappa = 0.70- 0.93; IRR = 83%). Participants reported barriers in the food (cost, transportation, high unhealthy food access) and physical activity environment (safety concerns). Facilitators included community food resources and access to safe areas for physical activity. These results may inform future research and weight loss programs for diverse Black adults.</p>","PeriodicalId":16921,"journal":{"name":"Journal of Racial and Ethnic Health Disparities","volume":" ","pages":""},"PeriodicalIF":2.4,"publicationDate":"2026-02-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146119179","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-02DOI: 10.1007/s40615-026-02859-6
Oyintoun-Emi Ozobokeme, Morgan Snell
{"title":"A Systematic Review and Narrative Synthesis of Associations Between Education and Use of and Knowledge About Skin Bleaching and Skin Lightening Products.","authors":"Oyintoun-Emi Ozobokeme, Morgan Snell","doi":"10.1007/s40615-026-02859-6","DOIUrl":"https://doi.org/10.1007/s40615-026-02859-6","url":null,"abstract":"","PeriodicalId":16921,"journal":{"name":"Journal of Racial and Ethnic Health Disparities","volume":" ","pages":""},"PeriodicalIF":2.4,"publicationDate":"2026-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146105662","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-02DOI: 10.1007/s40615-026-02853-y
Subin Na, Phyllis Solomon, Nari Yoo
This study examined whether the presence of Asian language-speaking mental health providers increases patient volume among Asian Americans in mental health facilities and whether this relationship is moderated by state-level Medicaid spending per capita. Data were drawn from national facility-level surveys conducted by SAMHSA between 2019 and 2023 (N = 265,395), supplemented with state-level Medicaid spending data from the Kaiser Family Foundation and demographic estimates from the American Community Survey. An instrumental variable approach was used to estimate the effect of Asian language-speaking staff on the number of Asian patients served, addressing potential endogeneity. To assess moderation by Medicaid spending, multilevel modeling with a cross-level interaction was conducted, accounting for clustering of facilities within states. Instrumental variable regression showed facilities with Asian language-speaking staff served significantly more Asian patients (B = 2.92, p < .001). The Hausman test supported IV estimation, and the Anderson-Rubin test confirmed robustness. Multilevel modeling revealed a significant interaction between Medicaid spending per capita and the presence of Asian language-speaking staff (B = 0.028, SE = 0.010, p < .01). Asian language-speaking providers play a significant role in increasing patient volume among Asian American patients. These findings underscore the importance of language-accessible mental health care in improving access for populations with limited English language proficiency. Moreover, results from the moderation analysis suggest this effect is amplified in states with greater Medicaid investment, highlighting the combined importance of workforce diversity and structural funding in reducing racial and linguistic disparities in behavioral health care for Asian American communities.
本研究考察了说亚洲语言的精神卫生服务提供者的存在是否增加了亚裔美国人在精神卫生设施中的患者数量,以及这种关系是否受到州一级人均医疗补助支出的调节。数据来自SAMHSA在2019年至2023年期间进行的全国设施级调查(N = 265,395),并辅以凯撒家庭基金会的州级医疗补助支出数据和美国社区调查的人口统计数据。使用工具变量方法来估计说亚洲语言的工作人员对亚洲患者服务数量的影响,解决潜在的内生性问题。为了评估医疗补助支出的适度性,进行了具有跨层次互动的多层次建模,考虑了州内设施的聚集性。工具变量回归显示,拥有亚洲语言工作人员的医疗机构为更多的亚洲患者提供服务(B = 2.92, p < 0.001)。Hausman检验支持IV估计,Anderson-Rubin检验证实稳健性。多水平模型显示,人均医疗补助支出与使用亚洲语言的工作人员之间存在显著的相互作用(B = 0.028, SE = 0.010, p < 0.01)。说亚洲语言的医生在增加亚裔美国患者数量方面发挥了重要作用。这些发现强调了语言无障碍精神卫生保健在改善英语水平有限的人群获得服务方面的重要性。此外,适度分析的结果表明,在医疗补助投资较多的州,这种影响被放大了,这突出了劳动力多样性和结构性资金在减少亚裔美国人社区行为卫生保健中的种族和语言差异方面的综合重要性。
{"title":"Impact of Asian Language-Speaking Mental Health Providers on Asian American Patient Volume in Mental Health Treatment Facilities: Moderating Role of Medicaid Spending.","authors":"Subin Na, Phyllis Solomon, Nari Yoo","doi":"10.1007/s40615-026-02853-y","DOIUrl":"https://doi.org/10.1007/s40615-026-02853-y","url":null,"abstract":"<p><p>This study examined whether the presence of Asian language-speaking mental health providers increases patient volume among Asian Americans in mental health facilities and whether this relationship is moderated by state-level Medicaid spending per capita. Data were drawn from national facility-level surveys conducted by SAMHSA between 2019 and 2023 (N = 265,395), supplemented with state-level Medicaid spending data from the Kaiser Family Foundation and demographic estimates from the American Community Survey. An instrumental variable approach was used to estimate the effect of Asian language-speaking staff on the number of Asian patients served, addressing potential endogeneity. To assess moderation by Medicaid spending, multilevel modeling with a cross-level interaction was conducted, accounting for clustering of facilities within states. Instrumental variable regression showed facilities with Asian language-speaking staff served significantly more Asian patients (B = 2.92, p < .001). The Hausman test supported IV estimation, and the Anderson-Rubin test confirmed robustness. Multilevel modeling revealed a significant interaction between Medicaid spending per capita and the presence of Asian language-speaking staff (B = 0.028, SE = 0.010, p < .01). Asian language-speaking providers play a significant role in increasing patient volume among Asian American patients. These findings underscore the importance of language-accessible mental health care in improving access for populations with limited English language proficiency. Moreover, results from the moderation analysis suggest this effect is amplified in states with greater Medicaid investment, highlighting the combined importance of workforce diversity and structural funding in reducing racial and linguistic disparities in behavioral health care for Asian American communities.</p>","PeriodicalId":16921,"journal":{"name":"Journal of Racial and Ethnic Health Disparities","volume":" ","pages":""},"PeriodicalIF":2.4,"publicationDate":"2026-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146105835","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-02DOI: 10.1007/s40615-025-02819-6
Eunji Kim, HeeSoon Juon, Giyoung Lee, Katherine C Smith, Mimi Chang, Ann C Klassen
Chronic Hepatitis B (CHB), a serious disease requiring lifelong management, disproportionately affects Asian Americans, including Korean Americans. Many Korean Americans experience linguistic and sociocultural barriers, potentially worsening health challenges. While social ties and social support are well-recognized determinants of health, their role within unique populations merits exploration. Using longitudinal survey data, we identified patterns of social ties and social support among Korean Americans living with CHB, and how these related to self-assessed physical and mental health over time. Patients in Los Angeles and Philadelphia (n = 309) completed surveys at two timepoints between 2021 and 2024. We measured social ties with the Lubben Social Network Scale (LSNS-6), social support with the eight-item Medical Outcomes Study Social Support Survey (mMOS-SS), and self-assessed health using SF-12 Physical and Mental Component Summary Scores (PCS, MCS). Greater baseline social ties were higher among married, college-educated, and bicultural- or Western-identifying participants. Social support scores were higher among married, English-fluent, and currently working participants. Greater social ties were associated with better baseline physical health (β = 0.134, p = 0.009), and greater social support with better mental well-being (β = 0.206, p < 0.001). Controlling on baseline health, social ties predicted better follow-up PCS (β = 0.108, p = 0.012), and social support predicted better follow-up MCS (β = 0.136, p = 0.007), suggesting that social ties and social support independently and differentially influence physical and mental health over time. Strengthening both structural connections through social ties and perceived social support may delay health decline among immigrant populations managing chronic conditions.
慢性乙型肝炎(CHB)是一种需要终生治疗的严重疾病,对亚裔美国人(包括韩裔美国人)的影响尤为严重。许多韩裔美国人经历了语言和社会文化障碍,这可能会加剧健康问题。虽然社会关系和社会支持是公认的健康决定因素,但它们在特殊人群中的作用值得探讨。利用纵向调查数据,我们确定了美籍韩裔慢性乙型肝炎患者的社会关系和社会支持模式,以及这些模式与长期自我评估的身心健康之间的关系。洛杉矶和费城的患者(n = 309)在2021年至2024年之间的两个时间点完成了调查。我们使用Lubben社会网络量表(LSNS-6)测量社会联系,使用八项医疗结果研究社会支持调查(mMOS-SS)测量社会支持,并使用SF-12身心成分总结分数(PCS, MCS)自我评估健康。在已婚、受过大学教育、双文化或西方认同的参与者中,基线社会关系更高。社会支持得分在已婚、英语流利、在职的参与者中较高。更大的社会关系与更好的基线身体健康相关(β = 0.134, p = 0.009),更大的社会支持与更好的心理健康相关(β = 0.206, p
{"title":"The Role of Social Ties and Social Support in Maintaining Physical and Mental Well-Being Among Korean Americans Living with Chronic Hepatitis B.","authors":"Eunji Kim, HeeSoon Juon, Giyoung Lee, Katherine C Smith, Mimi Chang, Ann C Klassen","doi":"10.1007/s40615-025-02819-6","DOIUrl":"https://doi.org/10.1007/s40615-025-02819-6","url":null,"abstract":"<p><p>Chronic Hepatitis B (CHB), a serious disease requiring lifelong management, disproportionately affects Asian Americans, including Korean Americans. Many Korean Americans experience linguistic and sociocultural barriers, potentially worsening health challenges. While social ties and social support are well-recognized determinants of health, their role within unique populations merits exploration. Using longitudinal survey data, we identified patterns of social ties and social support among Korean Americans living with CHB, and how these related to self-assessed physical and mental health over time. Patients in Los Angeles and Philadelphia (n = 309) completed surveys at two timepoints between 2021 and 2024. We measured social ties with the Lubben Social Network Scale (LSNS-6), social support with the eight-item Medical Outcomes Study Social Support Survey (mMOS-SS), and self-assessed health using SF-12 Physical and Mental Component Summary Scores (PCS, MCS). Greater baseline social ties were higher among married, college-educated, and bicultural- or Western-identifying participants. Social support scores were higher among married, English-fluent, and currently working participants. Greater social ties were associated with better baseline physical health (β = 0.134, p = 0.009), and greater social support with better mental well-being (β = 0.206, p < 0.001). Controlling on baseline health, social ties predicted better follow-up PCS (β = 0.108, p = 0.012), and social support predicted better follow-up MCS (β = 0.136, p = 0.007), suggesting that social ties and social support independently and differentially influence physical and mental health over time. Strengthening both structural connections through social ties and perceived social support may delay health decline among immigrant populations managing chronic conditions.</p>","PeriodicalId":16921,"journal":{"name":"Journal of Racial and Ethnic Health Disparities","volume":" ","pages":""},"PeriodicalIF":2.4,"publicationDate":"2026-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146105924","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2024-11-27DOI: 10.1007/s40615-024-02230-7
Jocelyn T Vaughn, Caryn E Peterson, Jana L Hirschtick, Lawrence J Ouellet, Ronald C Hershow, Sage J Kim
Women and racial/ethnic minorities living with HIV are less likely than White men to be engaged in HIV treatment when entering US jails. Few studies have examined the intersection of gender and race/ethnicity among incarcerated populations. The "Enhancing Linkages to HIV Primary Care and Services in Jail Settings Initiative" (EnhanceLink) was a 10-site prospective cohort study of 1,270 people living with HIV in correctional facilities between 2008 and 2011. Using data from this study (N = 1,096), we assessed the likelihood of having a usual source of HIV care, utilizing ART, and viral suppression (HIV-1 RNA < 200 copies/ml) within 30 days of incarceration among the following groups, stratified by current gender and race/ethnicity, relative to non-Hispanic White men: Non-Hispanic Black women, non-Hispanic Black men, Hispanic/Latina (Hispanic) women, Hispanic men, and non-Hispanic White women. Compared to non-Hispanic White men, non-Hispanic Black women were 20% less likely to report that they had access to HIV care before incarceration after adjusting for age, sexual orientation, incarceration history, and medical comorbidities (prevalence ratio (PR) = 0.8, 95% CI: 0.7-0.9, p = 0.0002). Non-Hispanic Black, Hispanic, and Non-Hispanic White women were 30% less likely to utilize ART (respectively) than White men after adjusting for the same potential confounders (PR = 0.7, 95% CI: 0.6-0.9, p = 0.002; PR = 0.7, 95% CI: 0.5-0.9, p = 0.02; PR = 0.7, 95% CI: 0.5-1.0, p = 0.03). Our findings underscore the importance of culturally informed, community-based HIV interventions that promote equitable access to HIV care.
与白人男性相比,感染艾滋病毒的女性和少数种族/族裔在进入美国监狱时接受艾滋病毒治疗的可能性较低。很少有研究对被监禁人群中性别与种族/民族的交叉点进行研究。2008年至2011年期间,"在监狱环境中加强艾滋病初级医疗和服务的联系倡议"(EnhanceLink)是一项针对惩教机构中1270名艾滋病感染者的10个地点前瞻性队列研究。利用这项研究的数据(N = 1,096),我们评估了拥有 HIV 护理常规来源、使用抗逆转录病毒疗法和病毒抑制(HIV-1 RNA)的可能性。
{"title":"Gender and Racial/Ethnic Disparities in HIV Care and Viral Suppression at Jail Entry.","authors":"Jocelyn T Vaughn, Caryn E Peterson, Jana L Hirschtick, Lawrence J Ouellet, Ronald C Hershow, Sage J Kim","doi":"10.1007/s40615-024-02230-7","DOIUrl":"10.1007/s40615-024-02230-7","url":null,"abstract":"<p><p>Women and racial/ethnic minorities living with HIV are less likely than White men to be engaged in HIV treatment when entering US jails. Few studies have examined the intersection of gender and race/ethnicity among incarcerated populations. The \"Enhancing Linkages to HIV Primary Care and Services in Jail Settings Initiative\" (EnhanceLink) was a 10-site prospective cohort study of 1,270 people living with HIV in correctional facilities between 2008 and 2011. Using data from this study (N = 1,096), we assessed the likelihood of having a usual source of HIV care, utilizing ART, and viral suppression (HIV-1 RNA < 200 copies/ml) within 30 days of incarceration among the following groups, stratified by current gender and race/ethnicity, relative to non-Hispanic White men: Non-Hispanic Black women, non-Hispanic Black men, Hispanic/Latina (Hispanic) women, Hispanic men, and non-Hispanic White women. Compared to non-Hispanic White men, non-Hispanic Black women were 20% less likely to report that they had access to HIV care before incarceration after adjusting for age, sexual orientation, incarceration history, and medical comorbidities (prevalence ratio (PR) = 0.8, 95% CI: 0.7-0.9, p = 0.0002). Non-Hispanic Black, Hispanic, and Non-Hispanic White women were 30% less likely to utilize ART (respectively) than White men after adjusting for the same potential confounders (PR = 0.7, 95% CI: 0.6-0.9, p = 0.002; PR = 0.7, 95% CI: 0.5-0.9, p = 0.02; PR = 0.7, 95% CI: 0.5-1.0, p = 0.03). Our findings underscore the importance of culturally informed, community-based HIV interventions that promote equitable access to HIV care.</p>","PeriodicalId":16921,"journal":{"name":"Journal of Racial and Ethnic Health Disparities","volume":" ","pages":"104-116"},"PeriodicalIF":2.4,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12795891/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142729595","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2024-11-29DOI: 10.1007/s40615-024-02234-3
Hayden M Ventresca, Parker A Kell, Tyler A Toledo, Erin N Street, Felicitas A Huber, Natalie M Hellman, Taylor V Brown, Claudia N Vore, Kayla Trevino, Joanna O Shadlow, Jamie L Rhudy
The COVID-19 pandemic disproportionately impacted minoritized individuals. This study examined the relationships between pandemic-related stressors/distress and bodily pain in 79 Native American (NA) and 101 non-Hispanic White (NHW) participants from the Oklahoma Study of Native American Pain Risk. Online surveys were administered in May/June 2020 (wave 1), March/April 2021 (wave 2), and Sept/Oct 2021 (wave 3). Pandemic-related stressors (e.g., resource loss and added responsibilities) and distress were assessed from a custom-built questionnaire. Bodily pain was assessed from pain items on the Patient Health Questionnaire-15 (PHQ-15). The results indicate NAs and NHWs reported similar pandemic-related stressors and distress at wave 1, which remained at similar levels across all waves in NHWs. By contrast, stressors and distress increased in NAs at waves 2 and 3. Moreover, bodily pain was higher in NAs than NHWs across all waves. Regression-based multilevel analyses predicting bodily pain found that NHWs with more pandemic-related stressors/distress experienced more bodily pain, but stress/distress did not predict bodily pain in NAs. Findings demonstrated that NAs experienced more bodily pain and pandemic-related stressors/distress than NHWs. However, pandemic-related stressors/distress did not further exacerbate NA pain as observed in NHWs. This implies NAs may have demonstrated resiliency that buffered the pronociceptive effects of pandemic-related stress.
{"title":"COVID-19 Pandemic-Related Stressors, Distress, and Bodily Pain in Native Americans: Results from the Oklahoma Study of Native American Pain Risk.","authors":"Hayden M Ventresca, Parker A Kell, Tyler A Toledo, Erin N Street, Felicitas A Huber, Natalie M Hellman, Taylor V Brown, Claudia N Vore, Kayla Trevino, Joanna O Shadlow, Jamie L Rhudy","doi":"10.1007/s40615-024-02234-3","DOIUrl":"10.1007/s40615-024-02234-3","url":null,"abstract":"<p><p>The COVID-19 pandemic disproportionately impacted minoritized individuals. This study examined the relationships between pandemic-related stressors/distress and bodily pain in 79 Native American (NA) and 101 non-Hispanic White (NHW) participants from the Oklahoma Study of Native American Pain Risk. Online surveys were administered in May/June 2020 (wave 1), March/April 2021 (wave 2), and Sept/Oct 2021 (wave 3). Pandemic-related stressors (e.g., resource loss and added responsibilities) and distress were assessed from a custom-built questionnaire. Bodily pain was assessed from pain items on the Patient Health Questionnaire-15 (PHQ-15). The results indicate NAs and NHWs reported similar pandemic-related stressors and distress at wave 1, which remained at similar levels across all waves in NHWs. By contrast, stressors and distress increased in NAs at waves 2 and 3. Moreover, bodily pain was higher in NAs than NHWs across all waves. Regression-based multilevel analyses predicting bodily pain found that NHWs with more pandemic-related stressors/distress experienced more bodily pain, but stress/distress did not predict bodily pain in NAs. Findings demonstrated that NAs experienced more bodily pain and pandemic-related stressors/distress than NHWs. However, pandemic-related stressors/distress did not further exacerbate NA pain as observed in NHWs. This implies NAs may have demonstrated resiliency that buffered the pronociceptive effects of pandemic-related stress.</p>","PeriodicalId":16921,"journal":{"name":"Journal of Racial and Ethnic Health Disparities","volume":" ","pages":"149-162"},"PeriodicalIF":2.4,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142750903","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2024-11-14DOI: 10.1007/s40615-024-02232-5
Abigail E Lantz, Ryan Gebert, Jiannong Li, Jose A Oliveras, Edna R Gordián, Jaileene Perez-Morales, Steven Eschrich, Dung-Tsa Chen, Marilin Rosa, Julie Dutil, Harold I Saavedra, Teresita Muñoz-Antonia, Idhaliz Flores, William D Cress
Background: Herein, we report the characterization of four cohorts of breast cancer patients including (1) non-Hispanic Whites in Florida, (2) non-Hispanic Blacks in Florida, (3) Hispanics in Florida, and (4) Hispanics in Puerto Rico.
Methods: Data from female breast cancer patients were collected from cancer registry (n = 9361) and self-reported patient questionnaires (n = 4324). Several statistical tests were applied to identify significant group differences.
Results: Breast cancer patients from Puerto Rico were least frequently employed and had the lowest rates of college education among the groups. They also reported more live births and less breastfeeding. Both Hispanic groups reported a higher fraction experiencing menstruation at age 11 or younger (Floridian Hispanics [38%] and Puerto Ricans [36%]) compared to non-Hispanic Whites (20%) and non-Hispanic Blacks (22%). Non-Hispanic Black and Puerto Rican women were significantly older at breast cancer diagnosis than their non-Hispanic White and Floridian Hispanic counterparts. The Puerto Rican and non-Hispanic Black groups more frequently had pathology stage T2 or higher primary breast tumors at diagnosis (non-Hispanic Whites [29%], non-Hispanic Blacks [39%], Floridian Hispanics [33%], Puerto Ricans [46%]). The Puerto Rican (73%, 95% CI [66, 82]) and non-Hispanic Black (79%, 95% CI [75, 84]) groups demonstrate reduced 5-year survival compared to non-Hispanic Whites (89%, 95% CI [86, 92]) and Floridian Hispanics (89%, 95% CI [86, 90]).
Conclusions: These findings demonstrate that Puerto Rican breast cancer patients suffer significant breast cancer health disparities relative to non-Hispanic Whites and Hispanics from Florida similar to the disparities observed for non-Hispanic Blacks. Future work must seek to better understand and address these disparities.
背景:在此,我们报告了四组乳腺癌患者的特征,包括:(1) 佛罗里达州的非西班牙裔白人;(2) 佛罗里达州的非西班牙裔黑人;(3) 佛罗里达州的西班牙裔人以及 (4) 波多黎各的西班牙裔人:从癌症登记(9361 人)和患者自我报告问卷(4324 人)中收集了女性乳腺癌患者的数据。结果:来自波多黎各的乳腺癌患者与来自美国的乳腺癌患者之间存在明显的群体差异:结果:波多黎各乳腺癌患者的就业率最低,大学教育率也最低。他们还报告了更多的活产和更少的母乳喂养。与非西班牙裔白人(20%)和非西班牙裔黑人(22%)相比,两个西班牙裔群体在 11 岁或 11 岁以下月经初潮的比例较高(佛罗里达西班牙裔[38%]和波多黎各人[36%])。非西班牙裔黑人和波多黎各妇女确诊乳腺癌时的年龄明显大于非西班牙裔白人和弗洛里达西班牙裔妇女。波多黎各人和非西班牙裔黑人群体在确诊时更常患有病理 T2 期或更高的原发性乳腺肿瘤(非西班牙裔白人[29%]、非西班牙裔黑人[39%]、弗洛里达西班牙裔[33%]、波多黎各人[46%])。波多黎各人(73%,95% CI [66,82])和非西班牙裔黑人(79%,95% CI [75,84])群体的 5 年存活率低于非西班牙裔白人(89%,95% CI [86,92])和弗洛里达西班牙裔(89%,95% CI [86,90]):这些研究结果表明,波多黎各乳腺癌患者与非西班牙裔白人和佛罗里达州西班牙裔人相比,在乳腺癌健康方面存在显著差异,这与非西班牙裔黑人的差异类似。今后的工作必须设法更好地了解和解决这些差异。
{"title":"Worse Clinical and Survival Outcomes in Breast Cancer Patients Living in Puerto Rico Compared to Hispanics, Non-Hispanic Blacks, and Non-Hispanic Whites from Florida.","authors":"Abigail E Lantz, Ryan Gebert, Jiannong Li, Jose A Oliveras, Edna R Gordián, Jaileene Perez-Morales, Steven Eschrich, Dung-Tsa Chen, Marilin Rosa, Julie Dutil, Harold I Saavedra, Teresita Muñoz-Antonia, Idhaliz Flores, William D Cress","doi":"10.1007/s40615-024-02232-5","DOIUrl":"10.1007/s40615-024-02232-5","url":null,"abstract":"<p><strong>Background: </strong>Herein, we report the characterization of four cohorts of breast cancer patients including (1) non-Hispanic Whites in Florida, (2) non-Hispanic Blacks in Florida, (3) Hispanics in Florida, and (4) Hispanics in Puerto Rico.</p><p><strong>Methods: </strong>Data from female breast cancer patients were collected from cancer registry (n = 9361) and self-reported patient questionnaires (n = 4324). Several statistical tests were applied to identify significant group differences.</p><p><strong>Results: </strong>Breast cancer patients from Puerto Rico were least frequently employed and had the lowest rates of college education among the groups. They also reported more live births and less breastfeeding. Both Hispanic groups reported a higher fraction experiencing menstruation at age 11 or younger (Floridian Hispanics [38%] and Puerto Ricans [36%]) compared to non-Hispanic Whites (20%) and non-Hispanic Blacks (22%). Non-Hispanic Black and Puerto Rican women were significantly older at breast cancer diagnosis than their non-Hispanic White and Floridian Hispanic counterparts. The Puerto Rican and non-Hispanic Black groups more frequently had pathology stage T2 or higher primary breast tumors at diagnosis (non-Hispanic Whites [29%], non-Hispanic Blacks [39%], Floridian Hispanics [33%], Puerto Ricans [46%]). The Puerto Rican (73%, 95% CI [66, 82]) and non-Hispanic Black (79%, 95% CI [75, 84]) groups demonstrate reduced 5-year survival compared to non-Hispanic Whites (89%, 95% CI [86, 92]) and Floridian Hispanics (89%, 95% CI [86, 90]).</p><p><strong>Conclusions: </strong>These findings demonstrate that Puerto Rican breast cancer patients suffer significant breast cancer health disparities relative to non-Hispanic Whites and Hispanics from Florida similar to the disparities observed for non-Hispanic Blacks. Future work must seek to better understand and address these disparities.</p>","PeriodicalId":16921,"journal":{"name":"Journal of Racial and Ethnic Health Disparities","volume":" ","pages":"130-140"},"PeriodicalIF":2.4,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12281488/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142622040","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-01-30DOI: 10.1007/s40615-024-02281-w
Iris María Muñoz-Del-Pino, Francisco Javier Saavedra-Macías, Elvira Pérez-Vallejos
Previous studies have suggested that COVID-19 led to an increase in stigma towards the Asian population with a negative impact on their health. This study aims to explore this phenomenon and its impact on health through the qualitative analysis of semi-structured interviews conducted with 26 people of Asian origin living in Spain from September 2020 to September 2021. Among the results, it was found that, prior to the pandemic, discrimination was mostly verbal. After the outbreak of the pandemic, some participants, who were blamed and referred to as "COVID", experienced fear and physical aggression. Among the health effects, mental and social disturbances such as feeling like "permanent foreigners", worrying about being stigmatized or fear of interacting with others were prominent. The main protective factor was the support network, including education and community cohesion as main determinants. Future research is needed to analyse the evolution of this stigma after the pandemic and to explore in detail its impact on health.
{"title":"\"Am I the only one who will Spread the Virus?\": Impact of Public Stigma Towards the East Asian Population Living in Spain Related to COVID-19.","authors":"Iris María Muñoz-Del-Pino, Francisco Javier Saavedra-Macías, Elvira Pérez-Vallejos","doi":"10.1007/s40615-024-02281-w","DOIUrl":"10.1007/s40615-024-02281-w","url":null,"abstract":"<p><p>Previous studies have suggested that COVID-19 led to an increase in stigma towards the Asian population with a negative impact on their health. This study aims to explore this phenomenon and its impact on health through the qualitative analysis of semi-structured interviews conducted with 26 people of Asian origin living in Spain from September 2020 to September 2021. Among the results, it was found that, prior to the pandemic, discrimination was mostly verbal. After the outbreak of the pandemic, some participants, who were blamed and referred to as \"COVID\", experienced fear and physical aggression. Among the health effects, mental and social disturbances such as feeling like \"permanent foreigners\", worrying about being stigmatized or fear of interacting with others were prominent. The main protective factor was the support network, including education and community cohesion as main determinants. Future research is needed to analyse the evolution of this stigma after the pandemic and to explore in detail its impact on health.</p>","PeriodicalId":16921,"journal":{"name":"Journal of Racial and Ethnic Health Disparities","volume":" ","pages":"689-702"},"PeriodicalIF":2.4,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12795974/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143066374","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}