Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 10 de 10
Filtrar
1.
Transgend Health ; 8(4): 307-327, 2023 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-37525832

RESUMO

Purpose: Providing inclusive and comprehensive gender-affirming care is critical to reducing health disparities (gaps in care) experienced by sexual and gender minorities (SGM). Currently, little is known about how medical students and residents are being trained to address the health needs of SGM persons or of the most effective methods. Methods: We conducted a systematic review of the research literature from 2000 to 2020 on the effectiveness of teaching medical students and residents on knowledge, attitudes, and skills in addressing the health of SGM persons and the strength of the research sample, design, and methods used. Results: We identified a total of 36 articles that assessed the impact of medical student and resident education on knowledge, comfort, attitudes, confidence, and skills in working with SGM patients. All studies utilized quasi-experimental designs, and found efficacious results. No study examined the impact of training on patient outcomes. Conclusion: Future studies will need to be powered and designed to assess the impact of training on patient outcomes.

2.
J Low Genit Tract Dis ; 24(2): 232-233, 2020 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-32068616

RESUMO

OBJECTIVE: Transgender men (TGM) are those who identify their sex as male but were assigned female at birth who face marginalization in obstetrics and gynecology (OB/GYN) practices. The following commentary highlights recommendations for creating inclusive OB/GYN spaces and improving outcomes for TGM patients. METHODS: The commentary is written in a call to action style using previously published literature about treatment and guidelines for care of transgender patients to highlight recommendations for creating inclusive OB/GYN spaces for TGM. The GLMA Handbook on LGBT Health and The UCSF Transgender Care Web site were among the resources used to gather information on transgender patient inclusivity in health care settings. RESULTS: Supporting literature was collected that reinstates the need to include framing questions specific to the TGM population during history-taking, creating inclusive clinic settings, and enhancing health care provider training in TGM care. CONCLUSIONS: It is important for TGM who have a vagina, cervix, and/or uterus to have routine gynecological screenings. However, the lack of gender inclusive care in OB/GYN clinics presents a barrier for many TGM and the recommendations emphasized in this commentary will increase sensitivity for the TGM patient population and decrease their marginalization in health care settings.


Assuntos
Pessoas Transgênero , Doenças da Vulva/patologia , Adulto , Feminino , Ginecologia , Humanos , Masculino , Obstetrícia , Resultado do Tratamento , Doenças da Vulva/cirurgia
3.
Ethn Dis ; 29(Suppl 2): 323-328, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31308600

RESUMO

Advancing health equity and reducing disparities through evidence-based policy research requires the expertise, insights, and active participation of various policy stakeholders - particularly those representing vulnerable populations who may be disproportionately affected by such policies. Unfortunately, there are few sustainable settings for these diverse stakeholders to convene, share their knowledge, develop and execute research in a collaborative fashion, and effectively translate evidence-based findings. The development of a health policy-focused center supports the collaborative structure needed to present a unified, multi-disciplinary approach toward informing health policy. The Transdisciplinary Collaborative Center for Health Disparities Research (TCC) at Morehouse School of Medicine (U54MD008173) was funded in 2012 by the National Institute on Minority Health and Health Disparities (NIMHD) as an innovative approach for conducting health policy research and disseminating evidence-based science to diverse stakeholders. This article provides an overview of the research projects, pilot project programs, infrastructure cores, communications, and strategic dissemination activities supported by the TCC.


Assuntos
Equidade em Saúde/organização & administração , Política de Saúde , Grupos Minoritários/legislação & jurisprudência , Humanos , Estados Unidos
4.
Ethn Dis ; 29(Suppl 2): 345-348, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31308603

RESUMO

Health equity is a process, assurance of the conditions for optimal health for all people, which requires valuing all individuals and populations equally, recognizing and rectifying historical injustices, and providing resources according to need. At the heart of health equity is concern about the whole of society, not just a single individual or group. Also, at the heart of health equity is concern about the holes in society, about gaps of opportunity and gaps of being valued that are experienced by many. Strategies to achieve health equity that reflect concern about the w(hole) require the examination of a practical roadmap that combines citizenship (WHOLE) with a gap analysis (HOLE). This shorthand of operationalizing health equity as concern about the (w)hole may prove to be useful in generating further strategies for achieving health equity.


Assuntos
Guias como Assunto/normas , Equidade em Saúde , Política de Saúde/legislação & jurisprudência , Disparidades nos Níveis de Saúde , Disparidades em Assistência à Saúde/organização & administração , Humanos , Estados Unidos
5.
Ethn Dis ; 29(Suppl 2): 359-364, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31308606

RESUMO

Racial/ethnic disparities have long persisted in the United States despite concerted health system efforts to improve access and quality of care among African Americans and Latinos. Cultural competence in the health care setting has been recognized as an important feature of high-quality health care delivery for decades and will continue to be paramount as the society in which we live becomes increasingly culturally diverse. Unfortunately, there is limited empirical evidence of patient health benefits of a culturally competent health care workforce in integrated care, its feasibility of implementation, and sustainability strategies. This article reviews the status of cultural competence education in health care, the merits of continued commitment to training health care providers in integrated care settings, and policy and practice strategies to ensure emerging health care professionals and those already in the field are prepared to meet the health care needs of racially and ethnically diverse populations.


Assuntos
Competência Cultural/organização & administração , Assistência à Saúde Culturalmente Competente/organização & administração , Equidade em Saúde/tendências , Pessoal de Saúde/educação , Qualidade da Assistência à Saúde , Diversidade Cultural , Etnicidade , Humanos , Estados Unidos
6.
Perm J ; 21: 16-018, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28488990

RESUMO

INTRODUCTION: Addressing the multifaceted health and mental health needs of ethnically and culturally diverse individuals is a challenge within the current health care system. Integrated care provides a promising approach to improve mental health treatment-seeking disparities; however, adaptation of care models to impact African Americans is lacking. Although resources to support engagement of diverse populations in depression care exist, little has been developed to tailor patient preferences in accessing and engaging mental health services that are integrated into primary care. OBJECTIVE: Our research seeks to add a cultural focus to the existing literature concerning integrated health care models to help address depression and selected co-occurring chronic health conditions in primary care settings. METHODS: Thirty-two adult patients of an integrated primary care clinic participated in focus groups discussing their individual health experiences. Nine health care practitioners/administrators from five different integrated practice settings in the Atlanta, GA, area participated in key informant interviews. MAIN OUTCOME MEASURES: Transcripts were analyzed for key themes related to depression care, perceived unmet cultural needs, and desired adaptations. RESULTS: Common themes emerged such as the importance of peer-support and community engagement as areas of patient interest. Participants had good knowledge in recognizing depressive symptoms but were less knowledgeable about treatment options and expectations of treatment. The administrative and practitioner perspective suggests that patient preferences are valued and perceived as valid. CONCLUSION: It is critical that strategies and models are developed to improve health care among underserved minorities because current models offer variable efficacy among this population.


Assuntos
Assistência à Saúde Culturalmente Competente/métodos , Prestação Integrada de Cuidados de Saúde/métodos , Disparidades em Assistência à Saúde , Pacientes/estatística & dados numéricos , Médicos/estatística & dados numéricos , Atenção Primária à Saúde , Adulto , Atitude Frente a Saúde , Feminino , Grupos Focais , Georgia , Humanos , Masculino , Fatores Socioeconômicos
7.
Soc Sci (Basel) ; 5(1)2016 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-27713839

RESUMO

Health is a human right. Equity in health implies that ideally everyone should have a fair opportunity to attain their full health potential and, more pragmatically, that no one should be disadvantaged from achieving this potential. Addressing the multi-faceted health needs of ethnically and culturally diverse individuals in the United States is a complex issue that requires inventive strategies to reduce risk factors and buttress protective factors to promote greater well-being among individuals, families, and communities. With growing diversity concerning various ethnicities and nationalities; and with significant changes in the constellation of multiple of risk factors that can influence health outcomes, it is imperative that we delineate strategic efforts that encourage better access to primary care, focused community-based programs, multi-disciplinary clinical and translational research methodologies, and health policy advocacy initiatives that may improve individuals' longevity and quality of life.

8.
Int J Environ Res Public Health ; 13(1): ijerph13010037, 2015 Dec 22.
Artigo em Inglês | MEDLINE | ID: mdl-26703647

RESUMO

St. Lucia is an island nation in the Eastern Caribbean, with a population of 179,000 people, where chronic health conditions, such as hypertension and diabetes, are significant. The purpose of this pilot study is to create a model for community health education, tracking, and monitoring of these health conditions, research training, and policy interventions in St. Lucia, which may apply to other Caribbean populations, including those in the U.S. This paper reports on phase one of the study, which utilized a mixed method analytic approach. Adult clients at risk for, or diagnosed with, diabetes (n = 157), and health care providers/clinic administrators (n = 42), were recruited from five healthcare facilities in St. Lucia to assess their views on health status, health services, and improving health equity. Preliminary content analyses indicated that patients and providers acknowledge the relatively high prevalence of diabetes and other chronic illnesses, recognize the impact that socioeconomic status has on health outcomes, and desire improved access to healthcare and improvements to healthcare infrastructures. These findings could inform strategies, such as community education and workforce development, which may help improve health outcomes among St. Lucians with chronic health conditions, and inform similar efforts among other selected populations.


Assuntos
Diabetes Mellitus/terapia , Educação em Saúde/métodos , Equidade em Saúde , Política de Saúde , Disparidades nos Níveis de Saúde , Hipertensão/terapia , Vigilância em Saúde Pública , Adulto , Doença Crônica , Diabetes Mellitus/diagnóstico , Diabetes Mellitus/epidemiologia , Feminino , Humanos , Hipertensão/diagnóstico , Hipertensão/epidemiologia , Masculino , Projetos Piloto , Prevalência , Pesquisa Qualitativa , Santa Lúcia/epidemiologia , Estados Unidos
9.
Psychol Serv ; 11(4): 357-68, 2014 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-25383991

RESUMO

Despite decades of research, recognition and treatment of mental illness and its comorbidities still remain a significant public health problem in the United States. Ethnic minorities are identified as a population that is vulnerable to mental health disparities and face unique challenges pertaining to mental health care. Psychiatric illness is associated with great physical, emotional, functional, and societal burden. The primary health care setting may be a promising venue for screening, assessment, and treatment of mental illnesses for ethnic minority populations. We propose a comprehensive, innovative, culturally centered integrated care model to address the complexities within the health care system, from the individual level, which includes provider and patient factors, to the system level, which includes practice culture and system functionality issues. Our multidisciplinary investigative team acknowledges the importance of providing culturally tailored integrative health care to holistically concentrate on physical, mental, emotional, and behavioral problems among ethnic minorities in a primary care setting. It is our intention that the proposed model will be useful for health practitioners, contribute to the reduction of mental health disparities, and promote better mental health and well-being for ethnic minority individuals, families, and communities.


Assuntos
Serviços Comunitários de Saúde Mental , Disparidades nos Níveis de Saúde , Transtornos Mentais/terapia , Saúde Mental , Saúde das Minorias , Competência Clínica , Etnicidade , Humanos , Medicina Integrativa , Transtornos Mentais/etnologia , Grupos Minoritários , Atenção Primária à Saúde , Estados Unidos
10.
J Health Care Poor Underserved ; 24(4 Suppl): 79-93, 2013 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-24241263

RESUMO

The purpose of this cross-sectional pilot study was to determine the prevalence and correlates of depressive symptoms and resiliency among 290 African American women (AAW) in a community-based primary health care center. Descriptive statistics, Pearson product-moment correlation, and logistic regression analyses were conducted. Findings indicate that depressive symptoms are experienced by 49% of the participants, while 10% indicated a history of suicidal ideation. Participants had moderately high resiliency scores that had a statistically significant inverse relationship with depressive symptoms. This suggests that resiliency is potentially a protective factor for depressive symptoms. Depressive symptoms were positively correlated with participants' diagnosis of at least one chronic disease. The strongest predictors of depressive symptoms were previous diagnoses of a mental health condition and unemployment. This study identifies risk and potential protective factors for depression among a clinic sample of AAW.


Assuntos
População Negra , Depressão/epidemiologia , Resiliência Psicológica , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Doença Crônica/epidemiologia , Doença Crônica/psicologia , Centros Comunitários de Saúde , Estudos Transversais , Depressão/psicologia , Feminino , Georgia/epidemiologia , Humanos , Transtornos Mentais/epidemiologia , Pessoa de Meia-Idade , Projetos Piloto , Prevalência , Atenção Primária à Saúde , Fatores de Risco , Desemprego/psicologia , Adulto Jovem
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA