RESUMO Objetivo: Compreender as perspectivas das mulheres grávidas ou puérperas vivendo com HIV em Sofala, Moçambique, sobre as barreiras e facilidades para seguir as recomendações para a Prevenção da Transmissão Materno-Infantil (PMTCT). Método: estudo qualitativo realizado em três centros de saúde e com um grupo de apoio de pares de mulheres vivendo com HIV, entre outubro de 2020 e março de 2021. Aplicou-se amostra intencional, entrevistas semiestruturadas e análise de conteúdo. Resultados: O estigma social associado a ser HIV positivo e o medo da discriminação, efeitos colaterais dos medicamentos, barreiras econômicas e negação do diagnóstico/tratamento surgiram como barreiras. Como fatores facilitadores: redes de apoio e inspiração dos pares, preocupação inata com a saúde e a família. Finalmente, eles recomendam que a comunidade se eduque mais sobre o HIV. Conclusão: Os resultados deste estudo proporcionam uma compreensão ampla da experiência das mulheres que vivem com o HIV nesta província, possibilitando centrarse em estratégias para melhorar o atendimento às mulheres nos programas de PTMI em Moçambique.

Abstract Objective: To understand the perspectives of pregnant and postpartum women living with HIV in Sofala, Mozambique, regarding barriers and facilitators to following Prevention of Mother-to-Child Transmission (PMTCT) recommendations. Method: Qualitative study conducted in three health centers and with a peer support group of women living with HIV, between October 2020 and March 2021. We applied purposeful sampling, semi-structured interviews, and content analysis. Results: Among the barriers that emerged were the social stigma associated with HIV-positive status and fear of discrimination, side effects of medications, economic barriers, and denial of diagnosis/treatment. As facilitating factors: peer support networks and inspiration, innate concern for health and family. Finally, they recommend that the community should become more educated about HIV. Conclusion: The results of this study give a broad understanding of the experience of women living with HIV in this province, making it possible to focus strategies in improving the care of women in PMTCT programs in Mozambique.

RESUMEN Objetivo: Comprender las perspectivas de las mujeres embarazadas o en posparto viviendo con VIH en Sofala, Mozambique, respecto a las barreras y facilitadores para seguir las recomendaciones para la Prevención de Transmisión Materno Infantil (PTMI). Método: estudio cualitativo realizado en tres centros de salud y con un grupo de apoyo entre pares de mujeres viviendo con VIH, entre octubre de 2020 y marzo de 2021. Aplicamos muestreo intencional, entrevistas semiestructuradas y análisis de contenido. Resultados: Surgieron como barreras el estigma social que conlleva la condición de ser VIH positivo y el miedo a la discriminación, los efectos secundarios de los medicamentos, barreras económicas y la negación al diagnóstico/tratamiento. Como factores facilitadores: redes de apoyo e inspiración de pares, innata preocupación por la salud y la familia. Finalmente, ellas recomiendan que la comunidad se eduque más en materia de VIH. Conclusión: Los resultados de este estudio dan una comprensión amplia acerca de la experiencia de mujeres viviendo con VIH en esta provincia, posibilitando focalizar estrategias para mejorar la atención de las mujeres en los programas de PTMI en Mozambique.

ABSTRACT OBJECTIVE To expose visibility of the health concerns of sexual and gender minority groups in Chile, as well as to provide a platform to advocate for policies that support the health and well-being of sexual and gender minority people in the country. METHODS The health conditions and risk factors of participants identified as sexual and gender minority were compared to those identified as cisgender heterosexual using data from the 2016-2017 National Health Survey. RESULTS Despite reporting higher self-rated health than heterosexual men, gay men had a higher risk of lifetime diagnosis of sexually transmitted infections. Compared to heterosexual women, the prevalence of depression was higher among bisexual women, who were also less likely to have been tested for HIV. Moreover, transgender participants were more likely to report depression and worse self-rated health than cisgender heterosexual participants. CONCLUSION Small sample sizes of sexual and gender minority subgroups might have obscured some differences that would have been observable in larger samples. Despite this, we found statistically significant sexual and/or gender identity differences in several health areas, especially mental, sexual, and overall health.

ABSTRACT OBJECTIVE To expose visibility of the health concerns of sexual and gender minority groups in Chile, as well as to provide a platform to advocate for policies that support the health and well-being of sexual and gender minority people in the country. METHODS The health conditions and risk factors of participants identified as sexual and gender minority were compared to those identified as cisgender heterosexual using data from the 2016-2017 National Health Survey. RESULTS Despite reporting higher self-rated health than heterosexual men, gay men had a higher risk of lifetime diagnosis of sexually transmitted infections. Compared to heterosexual women, the prevalence of depression was higher among bisexual women, who were also less likely to have been tested for HIV. Moreover, transgender participants were more likely to report depression and worse self-rated health than cisgender heterosexual participants. CONCLUSION Small sample sizes of sexual and gender minority subgroups might have obscured some differences that would have been observable in larger samples. Despite this, we found statistically significant sexual and/or gender identity differences in several health areas, especially mental, sexual, and overall health.

ABSTRACT Introduction: Professionals play a significant role in the perinatal mourning. The relationship they established with parent in this process is critical in facilitating or hindering the quality of health care in this context. Objective: to understand the perspective of health care professionals in relation to perinatal grief. Method: A literature review was carried out in CINAHL, CUIDEN, PsycINFO, PubMed and the Google Scholar databases. A thematic analysis of the selected articles was carried out, allowing to define common thematic categories in these articles. Results: 46 scientific articles, published in the last ten years, were obtained. Three topics were identified: 1) feelings experienced by professionals, including anxiety, guilt, anger, resignation, physical symptoms, frustration, avoidance and emotional pain; 2) needs related to support, such as emotional support, formal training and work experience that allows for a better approach with families and parents; and 3) facilitators of the process, where training, years of professional experience, self-confidence, peer support, multidisciplinary team, religious beliefs and institutional support stand out. Conclusion: Perinatal grief is a complex situation for parents who demand sensitive care. Professionals play a key role in comprehensive support for them, being a demanding process both personally and professionally. Undergraduate and postgraduate training is suggested, encouraging dialogue and support among teams. This would benefit family and professionals, providing effective and quality care in a situation of perinatal grief.

RESUMEN Introducción: Los profesionales tienen un rol significativo en el proceso del duelo perinatal, y la relación que construyan con los padres será decisiva para facilitar u obstaculizar su cuidado. Objetivo: Comprender la perspectiva de los profesionales de la salud con relación al duelo perinatal. Método: Se realizó una búsqueda bibliográfica en las bases de datos CINAHL, CUIDEN, PsycINFO, PubMed y Google Académico. Se realizó un análisis temático de estos, permitiendo delimitar categorías temáticas comunes. Resultados: Se obtuvieron 46 artículos cientificos con menos de 10 años de antiguedad. Se identificaron tres categorias para abordar la experiencia vivida: 1) Sentimientos experimentados por los profesionales, como ansiedad, culpa, resignación, síntomas físicos, frustración y evitación; 2) Necesidades sentidas de apoyo, entre estas, soporte emocional, capacitación formal y experiencia laboral que permitan afrontar de mejor forma el duelo con las familias y el equipo; 3) Facilitadores del proceso, donde se destacan la capacitación, años de trayectoria profesional, confianza en si mismo, apoyo de los pares, equipo multidisciplinario, creencia religiososa y apoyo institucional. Conclusión: El duelo perinatal es una situación dramática para los padres, los cuales demandan un cuidado sensible. Y los profesionales desempeñan un rol clave en el apoyo integral a los padres, siendo un proceso exigente tanto en lo personal como en lo profesional. Se sugiere formación de pregrado y postgrado, fomentando el diálogo y apoyo entre los equipos. De esta forma se beneficiarán los padres, su familia y los profesionales, los cuales podrán otorgar un cuidado efectivo y de calidad en situación de duelo perinatal.

ABSTRACT OBJECTIVE To validate an instrument measuring the cultural competence in health care workers from Chile. METHODS Using Sue & Sue’s theoretical model of cultural competence, we designed a scale, which was assessed by health care workers and experts. Subsequently, the scale was applied to a sample of 483 different health care workers, during 2018 in Santiago de Chile. The analysis included: exploratory and confirmatory factor analysis, estimation of reliability, and analysis of measurement bias. Finally, the level of cultural competence was calculated for every professional who participated in this study. RESULTS The final scale include 14 items that are grouped into three dimensions concordant with the theoretical model: sensitivity to own prejudices, cultural knowledge, and skills to work in culturally diverse environments. This scale showed good fit in factor models, adequate reliability and lack of evidence of measurement bias. Regarding the performance of health care workers, sensitivity showed a lower level compared with the other dimensions evaluated. CONCLUSION The scale for measuring the level of cultural competence in health care workers (EMCC-14) is a reliable instrument, with initial support for its validity, which can be used in the Chilean context. Additionally, the results of this study could guide some possible interventions in the health sector to strengthen the level of cultural competence.

RESUMEN OBJETIVO Validar un instrumento de medición de competencia cultural en trabajadores de salud de Chile. MÉTODOS Utilizando el modelo teórico de Sue y Sue, se diseñó un instrumento de medición el cual fue evaluado por trabajadores de salud y expertos. Este instrumento se aplicó a una muestra diversa de 483 proveedores de salud, durante 2018 en Santiago de Chile. Se realizó análisis factorial exploratorio, confirmatorio, estimación de confiabilidad y análisis de sesgo de medición. Se estimó el nivel de competencia cultural alcanzado por los profesionales. RESULTADOS El instrumento final contó con 14 ítems los cuales se agruparon en tres dimensiones: sensibilidad a los propios prejuicios, conocimiento cultural y habilidades para trabajar en entornos culturalmente diversos. Esta herramienta mostró buen ajuste en los modelos factoriales, adecuada confiabilidad y ausencia de evidencias de sesgo de medición. Los trabajadores de salud evaluados exhibieron un bajo nivel de sensibilidad a los propios prejuicios en comparación con las otras dimensiones evaluadas. CONCLUSIONE La Escala de Medición de Competencia Cultural en trabajadores de salud (EMCC-14) es una herramienta confiable, con soporte inicial para su validez, que puede usarse en el contexto Chileno. Además, los resultados de este estudio podrían guiar algunas posibles intervenciones en el sector de la salud para fortalecer el nivel de competencia cultural.

ABSTRACT OBJECTIVE To validate an instrument measuring the cultural competence in health care workers from Chile. METHODS Using Sue & Sue’s theoretical model of cultural competence, we designed a scale, which was assessed by health care workers and experts. Subsequently, the scale was applied to a sample of 483 different health care workers, during 2018 in Santiago de Chile. The analysis included: exploratory and confirmatory factor analysis, estimation of reliability, and analysis of measurement bias. Finally, the level of cultural competence was calculated for every professional who participated in this study. RESULTS The final scale include 14 items that are grouped into three dimensions concordant with the theoretical model: sensitivity to own prejudices, cultural knowledge, and skills to work in culturally diverse environments. This scale showed good fit in factor models, adequate reliability and lack of evidence of measurement bias. Regarding the performance of health care workers, sensitivity showed a lower level compared with the other dimensions evaluated. CONCLUSION The scale for measuring the level of cultural competence in health care workers (EMCC-14) is a reliable instrument, with initial support for its validity, which can be used in the Chilean context. Additionally, the results of this study could guide some possible interventions in the health sector to strengthen the level of cultural competence.

RESUMEN OBJETIVO Validar un instrumento de medición de competencia cultural en trabajadores de salud de Chile. MÉTODOS Utilizando el modelo teórico de Sue y Sue, se diseñó un instrumento de medición el cual fue evaluado por trabajadores de salud y expertos. Este instrumento se aplicó a una muestra diversa de 483 proveedores de salud, durante 2018 en Santiago de Chile. Se realizó análisis factorial exploratorio, confirmatorio, estimación de confiabilidad y análisis de sesgo de medición. Se estimó el nivel de competencia cultural alcanzado por los profesionales. RESULTADOS El instrumento final contó con 14 ítems los cuales se agruparon en tres dimensiones: sensibilidad a los propios prejuicios, conocimiento cultural y habilidades para trabajar en entornos culturalmente diversos. Esta herramienta mostró buen ajuste en los modelos factoriales, adecuada confiabilidad y ausencia de evidencias de sesgo de medición. Los trabajadores de salud evaluados exhibieron un bajo nivel de sensibilidad a los propios prejuicios en comparación con las otras dimensiones evaluadas. CONCLUSIONE La Escala de Medición de Competencia Cultural en trabajadores de salud (EMCC-14) es una herramienta confiable, con soporte inicial para su validez, que puede usarse en el contexto Chileno. Además, los resultados de este estudio podrían guiar algunas posibles intervenciones en el sector de la salud para fortalecer el nivel de competencia cultural.

Resumen Las voluntades anticipadas en salud tienen como finalidad que la persona manifieste de manera anticipada su voluntad sobre los cuidados y el tratamiento de su salud, lo cual le permite expresar personalmente y de forma previa sus preferencias. Esta revisión de la literatura tiene por objetivo describir el concepto y la estructura de las voluntades anticipadas, así como los aspectos éticos involucrados durante el cuidado del paciente. Con las palabras clave “Advanced Health Care Directive” AND “Ethical Implication” y sus símiles en español (voluntades anticipadas, implicaciones éticas), se revisaron cinco bases de datos: ProQuest, Philosophy (JSTOR), PubMed, Web of Science y SciELO; las publicaciones se agruparon entre los años 2010 y 2018. Se obtuvieron 31 artículos de los cuales se realizó una lectura crítica. Los resultados de esta revisión fueron agrupados en las siguientes categorías: concepto, estructura, situaciones clínicas donde se aplican las voluntades anticipadas, fortalezas y limitaciones; así como los aspectos éticos involucrados. Actualmente, son más comunes las vivencias relacionadas con las situaciones al final de la vida, donde la persona pierde su capacidad de decidir y no puede manifestar sus deseos, por lo que es imposible conocer su voluntad. Gran parte de los profesionales de la salud no tienen capacitación adecuada sobre el desarrollo y la aplicación de las voluntades anticipadas, escenario que se convierte en una oportunidad para la investigación y profundización sobre el tema. Las voluntades anticipadas son una herramienta que proporciona al equipo de salud información fidedigna de los valores y deseos del paciente, por lo que es importante capacitar a estos profesionales para brindar una atención respetuosa y de calidad.

Abstract Advance healthcare directives are intended for the individual to personally express their will and preferences about healthcare and treatment ahead of time. This literature review aims to describe the concept and structure of advance directives and the ethical aspects involved in patient care. Using the keywords “Advance Healthcare Directive” AND “Ethical Implication” and its Spanish equivalents (voluntades anticipadas, implicaciones éticas), five databases were accessed: ProQuest, Philosophy (JSTOR), PubMed, Web of Science and Scielo. Publications were narrowed down to the 2010-2018 period. Thirty-one articles were obtained and read critically. Results of this review were grouped into the following categories: concept, structure, clinical situations in which advance directives apply, strengths and limitations, as well as the ethical aspects involved. End of life-related experiences in which a person loses their ability to make decisions and cannot express their wishes, so it is impossible to know their will, are more common nowadays. Most health workers are not appropriately trained in the preparation and application of advance directives, which becomes an opportunity to research and delve deeper into the subject. Advance directives are a tool that gives health workers reliable information on a patient’s values and wishes, so it is vital to train them to provide respectful quality care.

Resumo As diretivas antecipadas de vontade na saúde têm como finalidade que o paciente manifeste, de maneira antecipada, sua vontade e preferências sobre os cuidados e o tratamento de sua saúde. Esta revisão da literatura tem como objetivo descrever o conceito e a estrutura das diretivas antecipadas de vontade, bem como os aspectos éticos envolvidos durante o cuidado do paciente. Com as palavras-chave “advanced health care directive” AND “ethical implication” e seus equivalentes em espanhol (“voluntades anticipadas”, “implicaciones éticas”), foram revisadas cinco bases de dados: ProQuest, Philosophy (JSTOR), PubMed, Web of Science e SciELO; as publicações são de 2010 a 2018. Foram obtidos 31 artigos, dos quais foi realizada uma leitura crítica. Os resultados desta revisão foram agrupados nas seguintes categorias: conceito, estrutura, situações clínicas em que são aplicadas as diretivas antecipadas de vontade, fortalezas, limitações, bem como aspectos éticos envolvidos. Atualmente, são mais comuns as vivências relacionadas com as situações no final da vida, em que a pessoa perde sua capacidade de decidir e não pode manifestar seus desejos, portanto é impossível conhecer sua vontade. Grande parte dos profissionais da saúde não tem capacitação adequada sobre o desenvolvimento e a aplicação das diretivas antecipadas de vontade, o que se torna uma oportunidade para pesquisar e aprofundar sobre o tema. As diretivas antecipadas de vontade são uma ferramenta que proporciona, à equipe de saúde, informação fidedigna dos valores e desejos do paciente, por isso é importante capacitar os profissionais para oferecer uma atenção respeitosa e de qualidade.

Abstract It was proposed to know the health vulnerability and health care needs of immigrants in Chile, through a qualitative exploratory study. The findings suggest that their vulnerability would be due to their irregular status, precarious work and low incomes, when they do. Health conditions are common morbidity, mental and reproductive health. Acculturation and a positive attitude towards self-care would be protective factors. An important barrier to access is the illegal status of some immigrants; as the ignorance of the Chilean health system. It is suggested to socialize health policies for migrants and to expand targeted strategies for their health care.

Resumen Se propuso conocer la vulnerabilidad sanitaria y necesidades de salud de personas inmigrantes en Chile, a través de un estudio cualitativo exploratorio. Los hallazgos indican que su vulnerabilidad estaría dada por su condición irregular, trabajo precario y bajos ingresos, cuando lo tienen. Las afecciones de salud son morbilidad común, de salud mental y reproductiva. La aculturación y actitud positiva hacia el autocuidado serían factores protectores. Importante barrera de acceso es la situación ilegal de algunos inmigrantes; y el desconocimiento del sistema sanitario chileno. Se sugiere socializar políticas sanitarias para migrantes y expandir estrategias dirigidas para su atención de salud.

Abstract: Objective: To explore the social determinants of health (SDH) of international migrant children, from the perceptions of caregivers, health workers and local authorities in eight municipalities in Chile. Materials and methods: A secondary analysis of data was conducted from a qualitative study that took place between 2014 and 2017. The original study involved semi-structured interviews and focus groups. The secondary thematic analysis of data included all emerging issues related to international migrant children and their living conditions, including use of health services. Results: Findings were grouped according to the model of social determinants of health, which allow a reflection on living conditions of international migrant children and their health situation. Conclusion: This research shows the impact of SDH on international migrant children in Chile, highlighting relevant issues around this group.

Resumen: Objetivo: Explorar los determinantes sociales de la salud (DSS) de niños migrantes, a partir de las percepciones de cuidadores y trabajadores/autoridades de salud en las zonas más densas de población migrante en Chile. Material y métodos: Se realizó un análisis de datos secundario de un estudio realizado entre los años 2014 y 2017 desde un paradigma cualitativo de investigación. El estudio original incluyó entrevistas semiestructuradas y grupos focales. El análisis temático secundario de datos contempló todos los temas emergentes referidos a niños migrantes y condiciones de vida, incluyendo utilización de servicios de salud. Resultados: Los DDS fueron agrupados de acuerdo con el Modelo de Determinantes Sociales de la Salud, el cual permite reflexionar en torno a las condiciones de vida de niños migrantes y su situación de salud. Conclusión: Esta investigación muestra el impacto de los DSS en salud de niños migrantes en Chile, resaltando temáticas relevantes en torno a este grupo.

Abstract: Objective: To explore the social determinants of health (SDH) of international migrant children, from the perceptions of caregivers, health workers and local authorities in eight municipalities in Chile. Materials and methods: A secondary analysis of data was conducted from a qualitative study that took place between 2014 and 2017. The original study involved semi-structured interviews and focus groups. The secondary thematic analysis of data included all emerging issues related to international migrant children and their living conditions, including use of health services. Results: Findings were grouped according to the model of social determinants of health, which allow a reflection on living conditions of international migrant children and their health situation. Conclusion: This research shows the impact of SDH on international migrant children in Chile, highlighting relevant issues around this group.

Resumen: Objetivo: Explorar los determinantes sociales de la salud (DSS) de niños migrantes, a partir de las percepciones de cuidadores y trabajadores/autoridades de salud en las zonas más densas de población migrante en Chile. Material y métodos: Se realizó un análisis de datos secundario de un estudio realizado entre los años 2014 y 2017 desde un paradigma cualitativo de investigación. El estudio original incluyó entrevistas semiestructuradas y grupos focales. El análisis temático secundario de datos contempló todos los temas emergentes referidos a niños migrantes y condiciones de vida, incluyendo utilización de servicios de salud. Resultados: Los DDS fueron agrupados de acuerdo con el Modelo de Determinantes Sociales de la Salud, el cual permite reflexionar en torno a las condiciones de vida de niños migrantes y su situación de salud. Conclusión: Esta investigación muestra el impacto de los DSS en salud de niños migrantes en Chile, resaltando temáticas relevantes en torno a este grupo.

Abstract: Objective: To describe the main barriers and facilitators perceived by the health care workers for the implementation of Pre- and Post-Ductal Oxygen Saturation (SPPD) as a detection method of Con genital Heart Disease in newborns, prior to hospital discharge. Material and Method: From a cons tructivist research paradigm, a case study was carried out in three public hospitals in the Metropoli tan Region, Chile, two of them are high-complexity hospitals. The first one, the NEW Hospital, has recently started its activity, and the second one, the OLD Hospital, has been operating for many years. The third one, the RURAL Hospital, is a low-complexity institution, located near Santiago. Data were collected through individual semi-structured interviews and focus groups to Nursing Technicians (TENS), Midwives and Physicians. The interviews were recorded and transcribed. Thematic content analysis is performed using the NVivo11 qualitative software. The investigation was approved by the Ethics Committee recognized by the hospitals involved. Results: In the NEW Hospital, where the SPPD was implemented more than a year ago, barriers are detected at execution level, especially in oximeter inputs and on weekends. In the OLD Hospital and the RURAL Hospital, in which the SPPD was not implemented, the main perceived barriers are concentrated in insufficient knowledge about their usefulness, economic aspects, work overload, and organizational aspects. In the NEW Hospital, the main facilitators for the application of SPPD were its simplicity, economy, and the fact that it is an important contribution to the safety of newborns discharged. Conclusion: The disposition regar ding the practice of PPDS as a screening, varies in the 3 hospitals explored. To achieve this goal it is recommended to overcome organizational, management and economic barriers. Although there is a need to train the personnel in charge of screening, there is good disposition given the importance for the health of the RN. The flow of referral after screening for positive SPPD is quite clear.

Resumen: Objetivo: Describir principales barreras y facilitadores percibidos por equipo de salud para la implementación de Saturometría Pre y Post Ductal (SPPD) como método de detección de Cardiopatías Congénitas (CC), en recién nacidos (RN) previo al alta hospitalaria. Material y Método: Desde un paradigma constructivista de investigación, se realizó un estudio de caso en tres hospitales públicos de la región metropolitana: Dos de ellos son hospitales de alta complejidad. Uno; el Hospital NUE VO, inició su actividad recientemente y el otro; el Hospital ANTIGUO, lleva muchos años funcionando. El tercero; el Hospital RURAL, es un establecimiento de baja complejidad, ubicado cerca de Santiago. Los datos se recolectaron mediante entrevistas semiestructuradas individuales y grupos focales a Técnicos de Enfermería (TENS), Matrones y Médicos. Las entrevistas fueron grabadas y transcritas. Se efectúa análisis de contenido temático, utilizando el software cualitativo NVivo11. La investigación contó con aprobación de Comité de Ética, reconocido por los Hospitales involucrados. Resultados: En el Hospital NUEVO, donde la SPPD se implementó hace más de un año, las barreras se detectan a nivel de ejecución, especialmente en insumos del saturador y en los fines de semana. En el Hospital ANTIGUO y el Hospital RURAL, en los cuáles la SPPD no encontraba implementada, las principales barreras percibidas se sintetizan en insuficiente conocimiento acerca de su utilidad, aspec tos económicos, sobrecarga laboral y aspectos organizacionales. En el Hospital NUEVO los princi pales facilitadores para la aplicación de la SPPD fueron su sencillez, economía y el ser un importante aporte para la seguridad de los recién nacidos dados de alta. Conclusión: La disposición frente a la práctica de SPPD a modo de screening varía en los 3 hospitales explorados. Para lograr dicha meta se recomienda subsanar barreras organizacionales, de gestión y económicas. Aunque falta capacitar al personal a cargo de screening, existe buena disposición dada la importancia para la salud del RN. El flujo de derivación posterior a screening de SPPD positivo está bastante claro.

ABSTRACT Objective To describe, based on the perceptions of adolescents and health service staff, the ways in which adolescent boys interact with sexual and reproductive health services, the changes perceived in this area over time, and the Espacios Amigables strategy (‘Friendly Spaces’ for adolescent health) to reach out to boys. Methods An ethnographic, qualitative study was conducted in Friendly Spaces for adolescent and young adult health in five municipalities belonging to Chile's Metropolitan Region. The research methods used were semi-structured interviews (N = 38), discussion groups (N = 5), and participant observation. Results A masculinities perspective was [TN: “un enfoque de masculinidades”. Or simply: “Masculine perspectives were…”] felt to be missing in adolescent sexual and reproductive health care, which is perceived to be an area geared primarily toward females. Most adolescent boys perceive health services as distant and visit them only in case of emergency. Male attendance is low at sexual and reproductive health services in Friendly Spaces within primary health care centers. However, services outside these centers attract boys in larger numbers, for example, one that is exclusively devoted to providing adolescent health care and integrated services in schools. Conclusions Greater provision of adolescent sexual and reproductive health services does not necessarily translate into increased male access. For such an increase to occur, it is important to engage boys in addressing issues that capture their interest, bring health services closer to them, strengthen intersectoral work, and incorporate a masculinities perspectives in their care.

RESUMEN Objetivo Describir, a partir de las percepciones de adolescentes y personal de atención de salud, las formas en que los adolescentes varones se relacionan con la atención de salud sexual y reproductiva, las transformaciones percibidas en este ámbito y las estrategias desplegadas por Espacios Amigables para la atención de salud adolescente para acercarse a ellos. Métodos Estudio cualitativo etnográfico en Espacios Amigables para la atención de adolescentes y jóvenes de cinco municipios de la Región Metropolitana de Chile. Se utilizaron las técnicas de entrevistas semiestructuradas (N = 38), grupos de discusión (N = 5) y observación participante. Resultados Se identifica una falta de perspectiva de masculinidades en la atención de salud sexual y reproductiva en adolescentes, que se percibe como un ámbito enfocado principalmente para el género femenino. La mayoría de los adolescentes varones percibe a los servicios de salud como distantes y acuden principalmente en casos de emergencia. Se identifica una baja asistencia de hombres a servicios de salud sexual y reproductiva en Espacios Amigables ubicados en centros de atención primaria de salud. Sin embargo, aquellos ubicados fuera de estos como, por ejemplo, un centro exclusivo de atención de salud adolescente y servicios integrados en las escuelas, convocan a mayor número de varones. Conclusiones Una mayor oferta de servicios de salud sexual y reproductiva para adolescentes no necesariamente implica un aumento en el acceso de hombres. Para que esto suceda, es importante invitarlos desde temáticas que les resulten de interés, acercar los servicios de salud hacia donde ellos están, potenciar el trabajo intersectorial, e incorporar un enfoque de masculinidades para su atención.

RESUMO Objetivo Descrever, a partir das percepções dos jovens e do pessoal de saúde, as formas como os adolescentes do sexo masculino se relacionam com a atenção de saúde sexual e reprodutiva, as transformações percebidas neste âmbito e as estratégias para atenção de saúde do adolescente por espaços amigáveis para o alcance deste grupo. Métodos Foi realizado um estudo qualitativo etnográfico em espaços amigáveis para atenção de saúde de adolescentes e jovens em cinco municípios da região metropolitana do Chile. Foram empregados os métodos de entrevistas semiestruturadas (N = 38) e grupos de discussão (N = 5) e a técnica de observação participante. Resultados Foi verificada a falta de uma perspectiva de masculinidades na atenção de saúde sexual e reprodutiva para adolescentes, que se percebe como sendo voltada principalmente ao sexo feminino. A maioria dos adolescentes e jovens percebe os serviços de saúde como distantes e recorrem a eles sobretudo em situações de emergência. Foi observada pouca assistência ao sexo masculino nos serviços de saúde sexual e reprodutiva em espaços amigáveis situados em unidades de atenção primária à saúde. No entanto, a frequência dos jovens é maior nos espaços localizados fora destas unidades, como em um centro exclusivo de atenção de saúde do adolescente e serviços integrados em escolas. Conclusões Uma maior oferta de serviços de saúde sexual e reprodutiva para adolescentes não implica necessariamente maior acesso do sexo masculino. Para isso, é importante atrair os jovens com assuntos do interesse deles, acercar os serviços de saúde de onde eles estão, reforçar o trabalho intersetorial e incorporar um enfoque de masculinidades à atenção.

ABSTRACT Objectives To investigate the perceptions of primary health workers (PHW) about the challenges of health care for migrants. Materials and methods A qualitative multicase study was conducted in eight communes of Chile, using the snowball technique, where 101 PHW and local authorities were recruited. Semi-structured interviews and focal groups were conducted, achieving information saturation. Results The findings were grouped into two major thematic axes: 1. Technical and administrative difficulties, and 2. Perception of cultural barriers. According to the PHW, although regulations have been established and health care strategies have been generated for the migrant population, these are mostly not stable or known to all PHW. They are also not easy to implement in the various realities investigated. The absence of records on the number of migrants accessing the health system makes it difficult to design specific interventions. Additionally, health care has complications, and the PHW do not necessarily have tools that allow them to provide a care that is culturally sensitive to the needs of the migrant community. Conclusions The findings put into question the new challenges in health that Chile is facing in the face of the growing migrant population. The needs perceived by PHW are: stability and clarity in the regulations in force in relation to access and provision of services, training in regulations and the concrete way in which they should operate, and sensitization in cultural competence.

RESUMEN Objetivos Indagar en las percepciones de los trabajadores de salud primaria (TSP) sobre los desafíos de atención de salud para población migrante. Materiales y métodos Se realizó un estudio cualitativo de caso múltiple en ocho comunas de Chile, mediante la técnica de bola de nieve se reclutó a 101 TSP y autoridades locales. Se realizaron entrevistas semiestructuradas y grupos focales, logrando saturación de información. Resultados Los hallazgos fueron agrupados en dos grandes ejes temáticos: 1. Dificultades técnicas y administrativas, y 2. Percepción de barreras culturales. De acuerdo a los TSP, pese a que se han establecido normativas y se han generado estrategias de atención en salud para población migrante, estas, en su mayoría, no son estables ni conocidas por todos los TSP. Tampoco son fáciles de implementar en las diversas realidades investigadas. La ausencia de registros sobre el número de migrantes que accederán al sistema sanitario, dificulta el diseño de intervenciones específicas. Adicionalmente, la atención en salud presenta complicaciones, y los TSP no necesariamente poseen herramientas que les permitan brindar una atención que sea culturalmente sensible a las necesidades de la comunidad migrante. Conclusiones Los hallazgos ponen en discusión los nuevos desafíos en salud que enfrenta Chile frente a la creciente población migrante. Las necesidades percibidas por TSP son: estabilidad y claridad en las normativas vigentes en relación a acceso y prestación de servicios, capacitación en normativas y la manera concreta en la que estas deben operar, y sensibilización en competencia cultural.