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3.
Dis Colon Rectum ; 64(3): 335-342, 2021 03 01.
Artigo em Inglês | MEDLINE | ID: mdl-32868554

RESUMO

BACKGROUND: There is wide variation in gender distribution in colorectal surgery across different European countries. OBJECTIVE: This study aimed to evaluate female representation, implicit bias, and members' perception on female participation and representation at the European Society of Coloproctology 2017 annual scientific meeting. DESIGN: This was a retrospective mixed-methods cross-sectional observational study. SETTINGS: The study was conducted using data from the 2017 European Society of Coloproctology annual scientific meeting program and attendees. MAIN OUTCOME MEASURES: The primary outcome measure was the percentage of female speakers in the formal program and assessment for implicit bias. Secondary outcomes were the percentage of women attending the conference, the percentage of women serving on committees, and the results of the online survey. METHODS: Female representation was retrospectively quantified by role, session type, and topic. Implicit bias was measured classifying the introductions of speakers by moderators as formal (using a professional title) or informal (using name only), then further stratified by gender. An online survey was disseminated and analyzed to investigate the members' perception as a benchmark analysis. RESULTS: Disparities were found between sexes, with fewer women attending the conference (25%), serving as session chairs (8%), speakers (21%), and on committees (10%) compared with men. There were no differences across sexes regarding the formal or informal introduction. The survey among our members showed that significantly fewer women felt equally endorsed within the society compared with men (33% versus 63%; p < 0.001). LIMITATIONS: The retrospective design with data available to be analyzed was limited by the sessions recorded (27/49) and survey respondents (28%). CONCLUSIONS: Female representation within European Society of Coloproctology as chair, speaker, attendee, and committee member was much lower than male representation, both in absolute numbers and relative to membership. Greater awareness of this disparity and inclusiveness are aims of our society. The impact of these initiatives will be determined by reevaluating these metrics at the 2020 annual meeting. See Video Abstract at http://links.lww.com/DCR/B384. REPRESENTACIN Y POSICIN FEMENINA EN LA SOCIEDAD EUROPEA DE COLOPROCTOLOGA BASADA EN LOS HECHOS Y LAS OPINIONES DE SUS MIEMBROS: ANTECEDENTES:Existe una amplia variabilidad en la distribución de géneros en la cirugía colorrectal en los diferentes países de Europa.OBJETIVO:Evaluar la representación femenina, el sesgo implícito y la percepción de los miembros sobre la participación y representación femenina en el 12° Congreso científico anual de la Sociedad Europea de Coloproctología.DESIGN:Este fué un estudio observacional retrospectivo de métodos mixtos transversales.AJUSTES:Los análisis se realizaron utilizando los datos del programa cintífico de la reunión y los datos de los presentes en el Congreso de la ESCP en 2017.MEDIDAS PRINCIPALES DE RESULTADOS:La principal medida en el resultado fue el porcentaje de disertantes femeninas en el programa definitivo y la evaluación del sesgo implícito. Los resultados secundarios fueron el porcentaje de mujeres que asistieron a la conferencia, trabajaron en los comités y los resultados de la encuesta informática.METODOS:La representación femenina se cuantificó retrospectivamente según el rol, tipo de sesión y temas. Se midió el sesgo implícito clasificando las introducciones de los disertantes por parte de los moderadores de manera formal (usando un título profesional) o informal (usando solamente el nombre), y luego fueron estratificadas por género. Se difundió y analizó una encuesta informática para investigar la percepción de los miembros como análisis de referencia.RESULTADOS:Se encontraron disparidades de género, con menos mujeres presentes en la conferencia (25%), obrando como presidentes de sesión (8%), como disertantes (21%) y como miembros de comités (10%) comparadas con los hombres. No hubo diferencia entre sexos con respecto a la introducción formal o informal. La encuesta informática entre los miembros mostró significativamente que menos mujeres se sentían respaldadas igualitariamente dentro de la sociedad comparadas con los hombres (33% frente a 63%, p<0.001).LIMITACIONES:Diseño retrospectivo de datos limitados a las sesiones grabadas (27/49) y a los encuestados (28%) disponibles para el análisis.CONCLUSIONES:La representación femenina dentro de la Sociedad Europea de Coloproctología como presidente, disertante, asistente ó como miembro del comité fué mucho menor que la representación masculina, tanto en números absolutos como en relación con la membresía. Crear una mayor conciencia de esta disparidad de inclusión son prioridad en nuestra sociedad. El impacto de estas iniciativas se determinará re-evaluando estas variables en reuniones futuras. Consulte Video Resumen en http://links.lww.com/DCR/B384.


Assuntos
Cirurgia Colorretal/ética , Preconceito/ética , Sexismo/estatística & dados numéricos , Sociedades Médicas/ética , Inquéritos e Questionários/estatística & dados numéricos , Adulto , Conscientização , Cirurgia Colorretal/organização & administração , Congressos como Assunto/estatística & dados numéricos , Estudos Transversais , Europa (Continente) , Feminino , Equidade de Gênero , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Distribuição por Sexo , Percepção Social/ética , Sociedades Médicas/organização & administração , Engajamento no Trabalho
7.
Am J Hum Genet ; 104(1): 6-7, 2019 01 03.
Artigo em Inglês | MEDLINE | ID: mdl-30609408

RESUMO

Protections against genetic discrimination advance genetics research and the clinical use of genetics, as well as ensure the ethical use of genetic data. Ten years after the passage of the Genetic Information Nondiscrimination Act (GINA), the American Society of Human Genetics remains a staunch advocate for GINA's strong implementation and for other laws that enhance protections for the public.


Assuntos
Genética Médica/ética , Genética Médica/legislação & jurisprudência , Saúde , Preconceito/legislação & jurisprudência , Preconceito/prevenção & controle , Justiça Social/legislação & jurisprudência , Privacidade Genética/ética , Privacidade Genética/legislação & jurisprudência , Humanos , Preconceito/ética
8.
Cuad Bioet ; 28(92): 99-108, 2017.
Artigo em Espanhol | MEDLINE | ID: mdl-28342437

RESUMO

This article proposes a reflection on the exclusion of particularly vulnerable human beings as a condition for the success of economistic culture and social organization. This fragility can depend on the body side as well as the social aspect: the effects of discrimination are identical. To react to a situation of injustice less and less tolerable, the biolaw touches -as in general the right, if it has a meaning and a specific function, and is not reduced to mere legitimization of the balance of forces or interest of the individuals or the groups better organized and represented- defend the fragility of all violence in the name of equality among human beings which depend on the universal condition of vulnerability, held in its positive aspects by philosophers such as MacIntyre and Nussbaum and many literary geniuses of all times.


Assuntos
Economia , Pessoalidade , Preconceito/ética , Marginalização Social , Populações Vulneráveis , Humanos , Fatores Socioeconômicos
10.
J Med Ethics ; 42(9): 605-10, 2016 09.
Artigo em Inglês | MEDLINE | ID: mdl-27178536

RESUMO

The welfarist account of enhancement and disability holds enhanced and disabled states on a spectrum: the former are biological or psychological states that increase the chances of a person leading a good life in the relevant set of circumstances, while the latter decrease those chances. Here, I focus on a particular issue raised by this account: what should we count as part of an individual's relevant set of circumstances when thinking about enhanced and disabled states? Specifically, is social prejudice relevant to an individual's circumstances in regards to how disabled or enhanced they are? For instance, if an individual is discriminated against on the basis of their skin colour, and this leads to a reduction in their well-being, the welfarist account suggests that their skin colour is a disability. To avoid such a seeming mislabel, Savulescu and Kahane have argued for excluding social prejudice from counting as a relevant circumstance to their welfarist definition of disability. I argue, however, that this exclusion of social prejudice is unsatisfactory and incompatible with the goals of this account.


Assuntos
Atenção à Saúde/ética , Pessoas com Deficiência , Preconceito/ética , Qualidade da Assistência à Saúde/ética , Atenção à Saúde/normas , Pessoas com Deficiência/psicologia , Análise Ética , Disparidades nos Níveis de Saúde , Humanos , Qualidade da Assistência à Saúde/normas , Qualidade de Vida/psicologia , Meio Social
11.
Perspect Biol Med ; 58(3): 252-66, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27157343

RESUMO

This article provides an overview of the relevance and import of the U.N. Convention on the Rights of the Child (CRC) to child health practice and pediatric bioethics. We discuss the four general principles of the CRC that apply to the implementation of all rights contained in the document, the right to health articulated in Article 24, and the important position ascribed to parents in fulfilling the rights of their children. We then examine how the CRC is implemented and monitored in law and practice. The CRC and associated principles of child rights provide strategies for rights-based approaches to clinical practice and health systems, as well as to policy design, professional training, and health services research. In light of the relevance of the CRC and principles of child rights to children's health and child health practice, it follows that there is an intersection between child rights and pediatric bioethics. Pediatric bioethicists and child rights advocates should work together to define this intersection in all domains of pediatric practice.


Assuntos
Bioética , Serviços de Saúde da Criança/ética , Direitos Humanos , Nações Unidas , Temas Bioéticos , Criança , Serviços de Saúde da Criança/legislação & jurisprudência , Proteção da Criança/ética , Proteção da Criança/legislação & jurisprudência , Política de Saúde , Pesquisa sobre Serviços de Saúde , Humanos , Pais , Preconceito/ética , Preconceito/legislação & jurisprudência , Determinantes Sociais da Saúde , Valor da Vida
12.
J Health Psychol ; 21(7): 1457-71, 2016 07.
Artigo em Inglês | MEDLINE | ID: mdl-25411197

RESUMO

Psychosocial evaluation is recommended prior to bariatric surgery. Practice guidelines have been published on assessment methods for bariatric surgery candidates, but they have not emphasized ethical issues with this population. This review outlines ethical and professional considerations for behavioral healthcare providers who conduct pre-surgical assessments of bariatric surgery candidates by merging ethical principles for mental health professionals with current practices in pre-surgical assessments. Issues discussed include the following: (a) establishing and maintaining competence, (b) obtaining informed consent, (c) respecting confidentiality, (d) avoiding bias and discrimination, (e) avoiding and addressing dual roles, (f) selecting and using psychological tests, and (g) acknowledging limitations of psychosocial assessments.


Assuntos
Cirurgia Bariátrica/psicologia , Cuidados Pré-Operatórios/ética , Testes Psicológicos , Cirurgia Bariátrica/ética , Viés , Competência Clínica , Confidencialidade/ética , Humanos , Consentimento Livre e Esclarecido/ética , Consentimento Livre e Esclarecido/psicologia , Competência Mental , Preconceito/ética , Preconceito/prevenção & controle , Cuidados Pré-Operatórios/psicologia , Papel Profissional
14.
Monash Bioeth Rev ; 32(1-2): 43-62, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25434064

RESUMO

Disability might be relevant to decisions about life support in intensive care in several ways. It might affect the chance of treatment being successful, or a patient's life expectancy with treatment. It may affect whether treatment is in a patient's best interests. However, even if treatment would be of overall benefit it may be unaffordable and consequently unable to be provided. In this paper we will draw on the example of neonatal intensive care, and ask whether or when it is justified to ration life-saving treatment on the basis of disability. We argue that predicted disability is relevant both indirectly and directly to rationing decisions.


Assuntos
Crianças com Deficiência , Ética Médica , Terapia Intensiva Neonatal/ética , Cuidados para Prolongar a Vida/ética , Atrofias Musculares Espinais da Infância , Suspensão de Tratamento/ética , Austrália , Morte , Tomada de Decisões/ética , Humanos , Lactente , Recém-Nascido , Terapia Intensiva Neonatal/economia , Expectativa de Vida , Cuidados para Prolongar a Vida/economia , Preconceito/ética , Qualidade de Vida , Atrofias Musculares Espinais da Infância/economia , Atrofias Musculares Espinais da Infância/terapia , Reino Unido
16.
Health Soc Work ; 38(3): 135-45, 2013 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-24437019

RESUMO

This article examines and unpacks the "black box" of cultural competence in health interventions with racial and ethnic minority populations. The analysis builds on several recent reviews of evidence-based efforts to reduce health disparities, with a focus on how cultural competence is defined and operationalized. It finds that the use of multiple similar and indistinct terms related to cultural competence, as well as the lack of a mutually agreeable definition for cultural competence itself, has resulted in an imprecise concept that is often invoked but rarely defined and only marginally empirically validated as an effective health intervention. This article affirms the centrality of cultural competence as an essential values-based component of optimal social work practice, while also suggesting future directions for operationalizing, measuring, and testing cultural competence to build an evidence base on whether and how it works to reduce health disparities.


Assuntos
Competência Cultural/ética , Atenção à Saúde/normas , Acessibilidade aos Serviços de Saúde/normas , Disparidades em Assistência à Saúde/etnologia , Saúde das Minorias , Serviço Social/normas , Atenção à Saúde/ética , Acessibilidade aos Serviços de Saúde/ética , Disparidades em Assistência à Saúde/ética , Humanos , Preconceito/ética , Preconceito/etnologia , Discriminação Social/ética , Discriminação Social/etnologia , Serviço Social/ética
17.
Nurs Ethics ; 20(4): 382-91, 2013 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-23166143

RESUMO

Significant minority populations confer richness and diversity to British society. Responsive end-of-life care is a universal need that has ascended the public agenda following myriad reports of inadequate provision. Nevertheless, the potential exists for unwitting discrimination when caring for terminally ill patients on the basis of their religion or faith. Recent implementation of the Equality Act 2010, together with the government and professional initiatives, promises to positively impact upon this area of contemporary relevance and concern, although the extent to which facilitative policies can truly enhance patient care will depend upon how these are translated into care at the bedside. The contributions of health professionals will be central in meeting the challenges and seizing the opportunities for meeting the religion and faith interests of patients of South Asian descent.


Assuntos
Disparidades em Assistência à Saúde/ética , Religião e Medicina , Assistência Terminal/ética , Povo Asiático , Disparidades em Assistência à Saúde/legislação & jurisprudência , Humanos , Cuidados de Enfermagem/ética , Direitos do Paciente , Preconceito/ética , Preconceito/legislação & jurisprudência , Assistência Terminal/legislação & jurisprudência
18.
Rev. cuba. enferm ; 21(1)ene.-abr. 2005.
Artigo em Espanhol | LILACS, CUMED | ID: lil-412722

RESUMO

El trabajo hace un análisis de las iniquidades en salud vistas con un enfoque de género, desde el prisma de la Bioética, disciplina que establece un puente entre el hombre y su medio social y natural, a la luz de los valores morales. A partir de la definición de las iniquidades en salud y cómo ellas se reflejan en el caso de la mujer, se hace una exposición del tratamiento a la mujer a lo largo de la historia con énfasis en los aspectos relacionados con la salud sexual y reproductiva, desde la adolescencia y haciendo también alusión al abuso, el maltrato y la violencia, para concluir con el debate teórico acerca de los fundamentales principios éticos o de prima fascie, cuya violación afecta doblemente a la mujer(AU)


The work makes an analysis of the iniquities in health done with a gender focus, from the prism of the Bioética, it disciplines that it establishes a bridge between the man and its half social and natural one, by the light of the moral values. Starting from the definition of the iniquities in health and how they are reflected in the case of the woman, an exhibition is made from the treatment to the woman along the history with emphasis in the aspects related with the sexual and reproductive health, from the adolescence and also making allusion to the abuse, the abuse and the violence, to conclude with the theoretical debate about the fundamental ethical principles or of cousin fascie whose violation affects the woman doubly(AU)


Assuntos
Humanos , Feminino , Preconceito/ética , Direitos da Mulher/métodos , Bioética , Disparidades nos Níveis de Saúde , Identidade de Gênero , Fatores Socioeconômicos , Saúde Reprodutiva
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