ABSTRACT
For the past decade, resilience research with American Indian/Alaska Native and First Nations/Métis/Inuit adolescents has improved our understanding of how adolescents overcome mental health challenges. A new situation-specific theory is presented to guide nurses in applying the evidence to their practice with Indigenous adolescents in the United States and Canada. The social-ecological resilience of indigenous adolescents (SERIA) theory was derived from integrating ( a ) existing social-ecological frameworks by Bronfenbrenner, Ungar, and Burnette and Figley, ( b ) findings from a systematic review of 78 studies about resilience factors for mental health of Indigenous adolescents, ( c ) clinical experience, and ( d ) Indigenous knowledge.
Subject(s)
Indians, North American , Mental Health , Nursing Theory , Resilience, Psychological , Adolescent , Humans , Canada , Indians, North American/psychology , Inuit , United States , Psychological Theory , Adolescent Health/ethnology , Mental Health/ethnology , Minority Health/ethnologyABSTRACT
Black feminism has so much to offer. Its philosophical, intellectual, and activist practice grounded in the experiences of Black women is a source of healing and liberation. Building on the Black feminist tradition, the current article introduces an intersectional and practical healing framework titled Blafemme Healing. The framework is designed to support individuals in exploring personal healing regardless of their social location while intentionally providing mechanisms for increasing the experience and outcome of wellness, equity, love, liberation, and survival for Black people. The framework includes eight areas, or chambers, that require people's attention if we are to achieve personal and collective wellness. The author, a Black queer cisgender woman pursuing personal and collective wellness and healing through and beyond the field of psychology, uses the biomythography method to introduce and describe Blafemme Healing. (PsycInfo Database Record (c) 2023 APA, all rights reserved).
Subject(s)
Black or African American , Feminism , Minority Health , Women's Health , Female , Humans , Black People , Sexual and Gender Minorities , Women's Health/ethnology , Intersectional Framework , Minority Health/ethnologyABSTRACT
Culturally relevant stressors and protective factors are vital to understanding and effectively supporting Native American/Alaska Native (NA/AN) college students' mental health and well-being. This study examined the theorized pathways among historical loss, well-being, psychological distress, and the proposed cultural buffer of ethnic identity in the indigenist stress-coping model (ISCM). Cross-sectional data were collected via online survey and analyzed using structural equation modeling. Participants were a national sample of 242 NA/AN college students. Participants were predominantly women (n = 185; 76%) and median age was 21 years. Partial support was found for the ISCM. Participants reported frequent thoughts of historical loss, which were associated with lower well-being and higher levels of psychological distress. Ethnic identity moderated the relationship between historical loss and well-being such that those with stronger ethnic identities reported a weaker relationship between historical loss and lower well-being. Results underscore the importance of culturally specific risk and protective factors in NA/AN college students' resiliency and inform needed interventions and systemic change in higher education. (PsycInfo Database Record (c) 2023 APA, all rights reserved).
Subject(s)
American Indian or Alaska Native , Historical Trauma , Mental Health , Social Determinants of Health , Social Identification , Students , Adult , Female , Humans , Male , Young Adult , Adaptation, Psychological , American Indian or Alaska Native/history , American Indian or Alaska Native/psychology , Cross-Sectional Studies , Mental Health/ethnology , Mental Health/history , Students/psychology , Universities , Protective Factors , Historical Trauma/ethnology , Historical Trauma/history , Historical Trauma/psychology , Minority Health/ethnology , Minority Health/history , Social Determinants of Health/ethnology , Social Determinants of Health/history , Resilience, Psychological , Cultural Competency/education , Cultural Competency/psychologyABSTRACT
BACKGROUND: It is important for non-Native persons to understand that the meaning of culture to Native American/Indigenous Peoples is not about esteem, taste or music but rather is described as a cognitive map on how to be. Native American/Indigenous culture can be thought of as all the things and ways in which Native/Indigenous people understand who they are, where they come from and how they are to interact with others. Hundreds of years across many generations have taught that culture-based activities and interventions improve Native/Indigenous health and wellbeing. We explore if increased Native American culture/cultural connectedness is associated with better mental health/well-being and physical health. METHODS: We analyzed data from a two-phased study (N = 259 and N = 102) of 361 urban Native Americans in California (2018-2021). The 29 items validated Cultural Connectedness Scale-California (CCS-CA) measured Native culture/cultural connectedness. Mental health/well-being and physical health were assessed using the: modified Herth Hope Index (mHHI), Satisfaction with Life (SWL), Center for Epidemiologic Studies Depression Scale-Revised (CESD-R-10), Substance Abuse (CAGE-AID), and Health Related Quality of Life (HRQOL). We conducted Pearson correlations and stepwise regression analyses with CCS-CA as the independent (predictor) variable to explore our main research questions: 1) Is increased Native American/Indigenous culture associated with: 1) better mental health/well-being; and 2) better physical health? RESULTS: Increased Native/Indigenous culture (CCS-CA scores) is significantly associated with better mental health/well-being (mHHI, p < .001) and satisfaction with life (SWL, p < .001) predicts good physical health days (HRQOL, p < .001). Increased connection to Native American/Indigenous culture (CCS-CA scores) is significantly associated with decreased risk for depression (CESD-R-10, p < .0) and substance abuse and (CAGE-AID, p < .07). Significant results for culture as protective against risk for substance abuse (CAGE-AID) was most likely affected (p value approaching significance) due to an error in language on the measure (i.e., created double negative). CONCLUSIONS: Native American/Indigenous culture is a predictor of improved outcomes for mental health/well-being and physical healthy days. Native culture is an important social determinant of health. We add to the evidence that Native/Indigenous culture (i.e., cultural connectedness) be considered an important intervention objective and health-related outcome measure.
Subject(s)
American Indian or Alaska Native , Culture , Health , Self Concept , Social Determinants of Health , Social Identification , Humans , American Indian or Alaska Native/ethnology , American Indian or Alaska Native/psychology , Mental Health/ethnology , Quality of Life , Social Determinants of Health/ethnology , Substance-Related Disorders , United States/epidemiology , Psychological Well-Being/psychology , Health/ethnology , Minority Health/ethnology , California , Urban PopulationSubject(s)
COVID-19/ethnology , COVID-19/therapy , Cardiovascular Diseases/ethnology , Cardiovascular Diseases/therapy , Ethnic and Racial Minorities , Health Status Disparities , Healthcare Disparities/ethnology , Minority Health/ethnology , Racism , Attitude of Health Personnel/ethnology , COVID-19/diagnosis , Cardiovascular Diseases/diagnosis , Culturally Competent Care/ethnology , Health Knowledge, Attitudes, Practice/ethnology , Humans , Race Factors , Risk Assessment , Risk Factors , Social Determinants of Health/ethnologySubject(s)
Clinical Trials as Topic , Crohn Disease/therapy , Ethnic and Racial Minorities , Health Status Disparities , Healthcare Disparities/ethnology , Minority Health/ethnology , Patient Selection , Research Subjects , Adult , Crohn Disease/diagnosis , Crohn Disease/ethnology , Female , Humans , Male , Race FactorsABSTRACT
BACKGROUND: Due to the COVID-19 pandemic, there was an uptake of telehealth in cystic fibrosis care. Previous studies show disparities in telehealth use based on socioeconomic status (SES). We aimed to: (1) understand telehealth use and perceptions and (2) identify the facilitators and barriers to telehealth use among people with CF and their families (PwCF) from diverse racial/ethnic and socioeconomic backgrounds. METHODS: We conducted an analysis of the 2020 Cystic Fibrosis State of Care surveys completed by PwCF (PFSoC), CF Care Programs (SoC1) and the CF Foundation Patient Registry (CFFPR). RESULTS: A total of 424 PwCF and 286 programs responded to the PFSoC and SoC1. Among PwCF, 90% self-identified as White, 6% as Hispanic/Latino, and 2% as Black. Racial/ethnic minorities were less likely to have had a telehealth visit (p=.015). This difference was pronounced among the Hispanic/Latino population (p<.01). Telehealth use did not differ by health insurance and was similarly offered independent of financial status. Compared to PwCF who denied financial constraints, those who reported financial difficulties found telehealth more difficult to use (p=.018) and were less likely to think that their concerns (p=.010) or issues that mattered most to them (p=.020) were addressed during telehealth. Programs perceived lack of technology, language barriers, and home conditions as barriers to telehealth in vulnerable populations. CONCLUSION: PFSoC and SoC1 identified differences in telehealth use and care perceptions by ethnicity, race, and socioeconomic characteristics. Further studies are needed to understand how telehealth can change access to CF care in diverse subpopulations.
Subject(s)
COVID-19 , Communication Barriers , Cystic Fibrosis , Minority Health , Telemedicine , COVID-19/epidemiology , COVID-19/prevention & control , Communicable Disease Control/methods , Cystic Fibrosis/economics , Cystic Fibrosis/ethnology , Cystic Fibrosis/psychology , Cystic Fibrosis/therapy , Financial Stress/ethnology , Health Services Accessibility/organization & administration , Health Services Accessibility/trends , Healthcare Disparities/ethnology , Healthcare Disparities/standards , Humans , Minority Health/ethnology , Minority Health/standards , Minority Health/statistics & numerical data , Needs Assessment , Organizational Innovation , SARS-CoV-2 , Socioeconomic Factors , Telemedicine/organization & administration , Telemedicine/standards , United States/epidemiology , Vulnerable Populations/statistics & numerical dataSubject(s)
Atrial Fibrillation/ethnology , Atrial Fibrillation/therapy , Ethnic and Racial Minorities , Healthcare Disparities/ethnology , Patient Selection , Randomized Controlled Trials as Topic , Research Subjects , Atrial Fibrillation/diagnosis , Atrial Fibrillation/physiopathology , Communication Barriers , Cultural Diversity , Female , Health Knowledge, Attitudes, Practice/ethnology , Humans , Language , Male , Minority Health/ethnology , Race Factors , Sex Factors , United States/epidemiologySubject(s)
Clinical Trials as Topic , Minority Health , Patient Selection , Pulmonary Arterial Hypertension , Rare Diseases , Clinical Trials as Topic/methods , Clinical Trials as Topic/organization & administration , Clinical Trials as Topic/standards , Health Services Accessibility , Humans , Minority Health/ethnology , Minority Health/standards , Needs Assessment , Pulmonary Arterial Hypertension/ethnology , Pulmonary Arterial Hypertension/therapy , Rare Diseases/ethnology , Rare Diseases/therapy , Registries/standards , Registries/statistics & numerical data , Social Determinants of Health/ethnology , Social Determinants of Health/standards , Vulnerable Populations/statistics & numerical dataSubject(s)
Health Services Accessibility , Health Status Disparities , Healthcare Disparities/ethnology , Hispanic or Latino , Kidney Transplantation , Minority Health/ethnology , Renal Insufficiency/surgery , Undocumented Immigrants , Health Equity , Humans , Renal Insufficiency/diagnosis , Renal Insufficiency/ethnology , Renal Insufficiency/physiopathologySubject(s)
Clinical Trials as Topic , Ethnic and Racial Minorities , Health Status Disparities , Healthcare Disparities/ethnology , Minority Groups , Minority Health/ethnology , Pancreatic Neoplasms/ethnology , Patient Selection , Research Subjects , Female , Humans , Incidence , Male , Pancreatic Neoplasms/diagnosis , Pancreatic Neoplasms/therapy , Race Factors , Sex FactorsSubject(s)
Ambulatory Care/statistics & numerical data , Ethnicity/statistics & numerical data , Health Services Accessibility , Healthcare Disparities , Medicine/statistics & numerical data , Minority Health , Adult , Ambulatory Care Facilities/statistics & numerical data , Cross-Sectional Studies , Female , Health Services Accessibility/organization & administration , Health Services Accessibility/standards , Health Services Needs and Demand , Health Status Disparities , Healthcare Disparities/ethnology , Healthcare Disparities/statistics & numerical data , Humans , Male , Minority Health/ethnology , Minority Health/standards , Race Factors , Social Determinants of Health , United States/epidemiologySubject(s)
COVID-19 , Emigration and Immigration , Healthcare Disparities , Humanities , Immunization Programs , Minority Health , COVID-19/ethnology , COVID-19/prevention & control , COVID-19 Vaccines/therapeutic use , Healthcare Disparities/ethics , Healthcare Disparities/ethnology , Humanities/ethics , Humanities/trends , Humans , Immunization Programs/ethics , Immunization Programs/legislation & jurisprudence , Minority Health/ethics , Minority Health/ethnology , SARS-CoV-2 , United States/epidemiology , Vaccination Coverage/ethics , Vaccination Coverage/organization & administrationSubject(s)
Culturally Competent Care , Gastroenterology , Liver Diseases , Racism/prevention & control , Systemic Racism/prevention & control , Culturally Competent Care/ethnology , Culturally Competent Care/standards , Culturally Competent Care/trends , Gastroenterology/ethics , Gastroenterology/organization & administration , Gastroenterology/trends , Healthcare Disparities , Humans , Liver Diseases/ethnology , Liver Diseases/therapy , Minority Health/ethnology , Social Determinants of Health , Societies, Medical , United StatesABSTRACT
Harrowing stories reported in the media describe Covid-19 ravaging through families. This essay reports professional experiences of this phenomenon, family clustering, as encountered during the pandemic's spread across Southern California. We identify three ethical challenges following from it: Family clustering impedes shared decision-making by reducing available surrogate decision-makers for incapacitated patients, increases the emotional burdens of surrogate decision-makers, and exacerbates health disparities for and the suffering of people of color at increased likelihood of experiencing family clustering. We propose that, in response to these challenges, efforts in advance care planning be expanded, emotional support offered to surrogates and family members be increased, more robust state guidance be issued on ethical decision-making for unrepresented patients, ethics consultation be increased in the setting of conflict following from family clustering dynamics, and health care professionals pay more attention to systemic and personal racial biases and inequities that affect patient care and the surrogate experience.
Subject(s)
Advance Care Planning , COVID-19/epidemiology , Family Health , Family/psychology , Minority Health , Patient Care , Advance Care Planning/ethics , Advance Care Planning/legislation & jurisprudence , California/epidemiology , Cluster Analysis , Decision Making, Shared , Family Health/ethics , Family Health/ethnology , Health Status Disparities , Humans , Minority Health/ethics , Minority Health/ethnology , Patient Care/ethics , Patient Care/psychology , SARS-CoV-2 , Social Support , Third-Party Consent/ethicsABSTRACT
BACKGROUND: Although cancer screening has led to reductions in the incidence of invasive cervical cancer (ICC) across Canada, benefits of prevention efforts are not equitably distributed. This study investigated the sociodemographic characteristics of women with ICC in British Columbia compared with the general female population in the province. METHODS: In this descriptive study, data of individuals 18 years and older diagnosed with ICC between 2004 and 2013 were obtained from the BC Cancer Registry. Self-reported sociodemographic characteristics were derived from standardized health assessment forms (HAFs) completed upon admission in the BC Cancer Registry. Standardized ratios (SRs) were derived by dividing observed and age-adjusted expected counts by ethnicity or race, language, and marital, smoking and urban-rural status. Differences between observed and expected counts were tested using χ2 goodness-of-fit tests. General population data were derived from the 2006 Census, 2011 National Household Survey and 2011/12 Canadian Community Health Survey. RESULTS: Of 1705 total cases of ICC, 1315 were referred to BC Cancer (77.1%). Of those who were referred, 1215 (92.4%) completed HAFs. Among Indigenous women, more cases were observed (n = 85) than expected (n = 39; SR 2.16, 95% confidence interval [CI] 2.15-2.18). Among visible minorities, observed cases (n = 320) were higher than expected (n = 253; 95% CI 1.26-1.26). Elevated SRs were observed among women who self-identified as Korean (SR 1.78, 95% CI 1.76-1.80), Japanese (SR 1.77, 95% CI 1.74-1.79) and Filipino (SR 1.60, 95% CI 1.58-1.62); lower SRs were observed among South Asian women (SR 0.63, 95% CI 0.62-0.63). Elevated SRs were observed among current smokers (SR 1.34, 95% CI 1.33-1.34) and women living in rural-hub (SR 1.29, 95% CI 1.28-1.31) and rural or remote (SR 2.62, 95% CI 2.61-2.64) areas; the SR was lower among married women (SR 0.90, 95% CI 0.90-0.90). INTERPRETATION: Women who self-identified as visible minorities, Indigenous, current smokers, nonmarried and from rural areas were overrepresented among women with ICC. Efforts are needed to address inequities to ensure all women benefit from cervical cancer prevention.
Subject(s)
Early Detection of Cancer , Healthcare Disparities , Minority Health , Preventive Health Services , Rural Health/statistics & numerical data , Uterine Cervical Neoplasms , British Columbia/epidemiology , Demography , Early Detection of Cancer/methods , Early Detection of Cancer/statistics & numerical data , Female , Healthcare Disparities/standards , Healthcare Disparities/statistics & numerical data , Humans , Incidence , Middle Aged , Minority Health/ethnology , Minority Health/statistics & numerical data , Neoplasm Invasiveness , Neoplasm Staging , Preventive Health Services/organization & administration , Registries/statistics & numerical data , Risk Factors , Smoking/epidemiology , Socioeconomic Factors , Uterine Cervical Neoplasms/epidemiology , Uterine Cervical Neoplasms/pathologySubject(s)
Anxiety , COVID-19 , Cigarette Smoking , Depression , Minority Health , Preventive Health Services , Smoking , Anxiety/epidemiology , Anxiety/etiology , Anxiety/psychology , COVID-19/epidemiology , COVID-19/prevention & control , COVID-19/psychology , Cigarette Smoking/epidemiology , Cigarette Smoking/psychology , Cigarette Smoking/therapy , Depression/epidemiology , Depression/etiology , Depression/psychology , Global Health/trends , Health Services Needs and Demand , Healthcare Disparities , Humans , Minority Health/ethnology , Minority Health/trends , Physical Distancing , Preventive Health Services/methods , Preventive Health Services/standards , SARS-CoV-2 , Smoke-Free Policy , Smoking/epidemiology , Smoking/psychology , Smoking/trends , Smoking Cessation/ethnology , Smoking Cessation/methods , Smoking Prevention , Socioeconomic FactorsABSTRACT
Importance: Criminalizing immigrant policies, a form of structural racism, are associated with preterm birth; however, to date, few population studies have examined this association by race and nativity status or examined the association of inclusive immigrant policies with preterm birth. Objective: To assess the extent to which variation in preterm birth by race/ethnicity and nativity status is associated with state-level criminalizing vs inclusive immigrant policies. Design, Setting, and Participants: This retrospective, cross-sectional study analyzed birth record data from all 50 states and the District of Columbia in 2018, as well as state-level indicators of inclusive and criminalizing immigrant policies. White, Black, Asian, and Latina women who had singleton births were included in the study. Statistical analysis was performed from June 1, 2020, to February 5, 2021. Two continuous variables were created to capture the number of criminalizing vs inclusive immigrant policies in effect as of 2017 in each state. Main Outcomes and Measures: The main outcome measure was preterm birth (<37 weeks' gestation). Results: Among the 3â¯455â¯514 live births that occurred in 2018, 10.0% were preterm, and 23.2% were to mothers born outside the US. Overall, for women born outside the US, each additional state-level inclusive policy was associated with a 2% decrease in preterm birth (adjusted odds ratio [aOR], 0.98 [95% CI, 0.96-1.00]); there were no significant associations between inclusive policies and preterm birth among women born in the US. In models examining the combined associations of criminalizing and inclusive immigrant policies with preterm birth, each additional criminalizing policy was associated with a 5% increase in preterm birth among Black women born outside the US (aOR, 1.05 [95% CI, 1.00-1.10]). Each additional inclusive immigrant policy was associated with a lower likelihood of preterm birth for Asian women born in the US (aOR, 0.95 [95% CI, 0.93-0.98]) and White women born outside the US (aOR, 0.97 [95% CI, 0.95-0.99]). No significant associations were found among other groups. Conclusions and Relevance: This study suggests that criminalizing immigrant policies are associated with an increase in preterm birth specifically for Black women born outside the US. Inclusive immigrant policies are associated with a decrease in preterm birth for immigrants overall, Asian women born in the US, and White women born outside the US. No associations were found between criminalizing or inclusive immigrant policies and preterm birth among Latina women.
Subject(s)
Emigrants and Immigrants/statistics & numerical data , Minority Health/ethnology , Pregnancy Outcome/ethnology , Premature Birth/ethnology , Cross-Sectional Studies , Female , Humans , Infant, Newborn , Minority Health/statistics & numerical data , Pregnancy , Pregnancy Outcome/epidemiology , Premature Birth/epidemiology , Retrospective Studies , Socioeconomic FactorsABSTRACT
COVID-19 reveals longstanding health inequities among minority patients.