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BackgroundRecent migration trends have shown a notable entry of Latin American asylum seekers to Madrid, Spain.AimTo characterise the profile of asylum-seeking Latin American migrants who are living with HIV in Spain and to outline the barriers they face in accessing HIV treatment.MethodsA prospective cohort study was conducted between 2022 and 2023 with a 6-month follow-up period. Latin American asylum seekers living with HIV were recruited mainly from non-governmental organisations and received care at an HIV clinic in a public hospital in Madrid.ResultsWe included 631 asylum seekers. The primary countries of origin were Colombia (30%), Venezuela (30%) and Peru (18%). The median age was 32â¯years (interquartile range (IQR):â¯28-37), and 553 (88%) were cis men of which 94% were men who have sex with men. Upon their arrival, 49% (nâ¯=â¯309) lacked social support, and 74% (nâ¯=â¯464) faced barriers when attempting to access the healthcare system. Upon entry in Europe, 500 (77%) participants were taking antiretroviral therapy (ART). At their first evaluation at the HIV clinic, only 386 (61%) had continued taking ART and 33% (nâ¯=â¯209) had detectable plasma HIV-1 RNA levels. Six months later, 99% took ART and 98% had achieved an undetectable viral load.ConclusionsLatin American asylum seekers living with HIV in Madrid, Spain encountered barriers to healthcare and to ART. One-third of these individuals presented detectable HIV viral load when assessed in the HIV clinic, highlighting this as an important public health issue.
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Infecciones por VIH , Refugiados , Humanos , Infecciones por VIH/tratamiento farmacológico , Infecciones por VIH/etnología , Infecciones por VIH/diagnóstico , Infecciones por VIH/epidemiología , Refugiados/estadística & datos numéricos , Estudios Prospectivos , Masculino , Adulto , España/epidemiología , Femenino , América Latina/etnología , Accesibilidad a los Servicios de Salud/estadística & datos numéricos , Migrantes/estadística & datos numéricosRESUMEN
Research specific to obsessive-compulsive disorder (OCD) among individuals of Hispanic and Latin American (H/L) ancestry is limited, as are culturally relevant assessment and treatment recommendations. This article discusses the implications of underrepresentation of H/L populations in OCD research and emphasizes the need to consider issues related to assessment, treatment, and structural barriers that hinder delivery of culturally appropriate first-line psychotherapy. Recommendations for assessment and treatment are provided to aid clinicians in distinguishing culturally normative thoughts and behaviors from OCD, as well as to inform the implementation of psychotherapeutic interventions with cultural humility. This manuscript offers recommendations for future research to tackle health equity concerns with respect to assessment and treatment and structural factors limiting access to culturally appropriate psychotherapy. Wide-scale efforts are needed to comprehensively understand how H/L cultures intersect with various OCD presentations and to further disseminate treatments to populations that have historically lacked access to mental health care.
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Hispánicos o Latinos , Trastorno Obsesivo Compulsivo , Psicoterapia , Humanos , Trastorno Obsesivo Compulsivo/terapia , Trastorno Obsesivo Compulsivo/etnología , América Latina/etnología , Psicoterapia/métodos , Asistencia Sanitaria Culturalmente Competente , Competencia CulturalRESUMEN
With increasing violence, political, and economic instability in Latin America, there is a record number of migrants crossing the U.S. southern border. Latin American migrants are often exposed to traumatic events before leaving their home country and during migration. While prior studies document that sex may play a role in types of traumatic exposure, few studies compare differences in traumatic exposure by sex and place of occurrence of recently arrived immigrants. Addressing this gap, we recruited 120 adults who had recently crossed the U.S.-Mexico border. Participants completed questionnaires to characterize trauma exposures in their home country and during their migration journey. Results found that men reported higher levels of exposure to combat situations, while women were more likely to experience sexual assault. Both combat exposure and sexual traumas occurred more often in home countries than during migration. More than half of the full sample reported being threatened with a firearm. These data confirm gender differences in type of trauma and that exposures in the country of origin may provide the impetus to migrate.
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Emigrantes e Inmigrantes , Humanos , Masculino , Femenino , Adulto , Emigrantes e Inmigrantes/estadística & datos numéricos , América Latina/etnología , América Latina/epidemiología , Encuestas y Cuestionarios , Factores Sexuales , Adulto Joven , Persona de Mediana Edad , Delitos Sexuales/estadística & datos numéricos , México/epidemiología , México/etnología , Estados Unidos/epidemiología , AdolescenteRESUMEN
PURPOSE: The experience of ethnically diverse parents of children with serious illness in the US health care system has not been well studied. Listening to families from these communities about their experiences could identify modifiable barriers to quality pediatric serious illness care and facilitate the development of potential improvements. Our aim was to explore parents' perspectives of their children's health care for serious illness from Somali, Hmong, and Latin-American communities in Minnesota. METHODS: We conducted a qualitative study with focus groups and individual interviews using immersion-crystallization data analysis with a community-based participatory research approach. RESULTS: Twenty-six parents of children with serious illness participated (8 Somali, 10 Hmong, and 8 Latin-American). Parents desired 2-way trusting and respectful relationships with medical staff. Three themes supported this trust, based on parents' experiences with challenging and supportive health care: (1) Informed understanding allows parents to understand and be prepared for their child's medical care; (2) Compassionate interactions with staff allow parents to feel their children are cared for; (3) Respected parental advocacy allows parents to feel their wisdom is heard. Effective communication is 1 key to improving understanding, expressing compassion, and partnering with parents, including quality medical interpretation for low-English proficient parents. CONCLUSIONS: Parents of children with serious illness from Somali, Hmong, and Latin-American communities shared a desire for improved relationships with staff and improved health care processes. Processes that enhance communication, support, and connection, including individual and system-level interventions driven by community voices, hold the potential for reducing health disparities in pediatric serious illness.
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Grupos Focales , Padres , Investigación Cualitativa , Humanos , Padres/psicología , Femenino , Masculino , Somalia/etnología , Niño , Minnesota , Adulto , Adolescente , Preescolar , Confianza , Investigación Participativa Basada en la Comunidad , Hispánicos o Latinos/psicología , Relaciones Profesional-Familia , Persona de Mediana Edad , Asiático/psicología , América Latina/etnología , Lactante , Enfermedad Crítica/psicología , Enfermedad Crítica/terapiaRESUMEN
Cervical cancer, primarily caused by human papillomavirus (HPV) infection, poses a significant global health challenge. Due to higher levels of poverty and health inequities, Indigenous women worldwide are more vulnerable to cervical cancer than their non-Indigenous counterparts. However, despite constituting nearly 10% of the population in Latin America and the Caribbean (LAC), the true extent of the burden of cervical cancer among Indigenous people in this region remains largely unknown. This article reviews the available information on cervical cancer incidence and mortality, as well as HPV infection prevalence, among Indigenous women in LAC. The limited existing data suggest that Indigenous women in this region face a heightened risk of cervical cancer incidence and mortality compared to non-Indigenous women. Nevertheless, a substantial knowledge gap persists that must be addressed to comprehensively assess the burden of cervical cancer among Indigenous populations, especially through enhancing cancer surveillance across LAC countries. Numerous structural, social and cultural barriers hindering Indigenous women's access to HPV vaccination and cervical cancer screening worldwide have been identified and are reviewed in this article. The discussion highlights the critical role of culturally sensitive education, community engagement, and empowerment strategies in overcoming those barriers. Drawing insights from the success of targeted strategies in certain high-income countries, the present article advocates for research, policies and healthcare interventions tailored to the unique context of LAC countries.
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Infecciones por Papillomavirus , Neoplasias del Cuello Uterino , Humanos , Neoplasias del Cuello Uterino/prevención & control , Femenino , América Latina/etnología , Región del Caribe/etnología , Infecciones por Papillomavirus/prevención & control , Pueblos Indígenas/estadística & datos numéricos , Incidencia , Vacunas contra Papillomavirus/administración & dosificación , Detección Precoz del Cáncer/estadística & datos numéricos , PrevalenciaRESUMEN
Suicide is one of the leading causes of death worldwide (WHO, 2021). Depression is a common precursor to suicide and suicidality; however, individuals' experience of depression and the meaning of suicide differs depending on one's cultural background (Colucci, 2013; Goodmann et al., 2021; Kleinman, 2004). The current study explores the relationship between suicide and depression among six broad cultural groups in a large sample (N = 17,015) of adults representing six broad cultural groups (Latin America, South Asia, former Soviet Bloc, Western English-speakers, Chinese, and Arab World). Participants were recruited to a multilingual depression and suicide screening study via Google Ads (Leykin et al., 2012; Gross et al., 2014). As expected, the presence of depression was associated with suicide attempts. However, cultural group moderated this association, with Chinese participants being most likely to report suicide attempts while screening negative for depression. Although depression remains an important predictor of suicidality, it appears that certain cultural groups may be at higher risk even when depression is not present. Clinicians should consider using culturally adapted assessments for depression and suicidality.
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Depresión , Intento de Suicidio , Humanos , Masculino , Femenino , Intento de Suicidio/etnología , Intento de Suicidio/estadística & datos numéricos , Intento de Suicidio/psicología , Adulto , Depresión/psicología , Depresión/etnología , Persona de Mediana Edad , Adulto Joven , Comparación Transcultural , Ideación Suicida , Adolescente , América Latina/etnologíaRESUMEN
The pathophysiology of gestational diabetes mellitus (GDM) comprises clinical and genetic factors. In fact, GDM is associated with several single nucleotide polymorphisms (SNPs). This study aimed to build a prediction model of GDM combining clinical and genetic risk factors. A total of 1588 pregnant women from the San Carlos Cohort participated in the present study, including 1069 (67.3%) Caucasian (CAU) and 519 (32.7%) Latin American (LAT) individuals, and 255 (16.1%) had GDM. The incidence of GDM was similar in both groups (16.1% CAU and 16.0% LAT). Genotyping was performed via IPLEX Mass ARRAY PCR, selecting 110 SNPs based on literature references. SNPs showing the strongest likelihood of developing GDM were rs10830963, rs7651090, and rs1371614 in CAU and rs1387153 and rs9368222 in LAT. Clinical variables, including age, pre-pregnancy body mass index, and fasting plasma glucose (FPG) at 12 gestational weeks, predicted the risk of GDM (AUC 0.648, 95% CI 0.601-0.695 in CAU; AUC 0.688, 95% CI 0.628-9.748 in LAT), and adding SNPs modestly improved prediction (AUC 0.722, 95%CI 0.680-0.764 in CAU; AUC 0.769, 95% CI 0.711-0.826 in LAT). In conclusion, adding genetic variants enhanced the prediction model of GDM risk in CAU and LAT pregnant women.
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Diabetes Gestacional , Polimorfismo de Nucleótido Simple , Población Blanca , Adulto , Femenino , Humanos , Embarazo , Glucemia , Índice de Masa Corporal , Diabetes Gestacional/genética , Diabetes Gestacional/epidemiología , Predisposición Genética a la Enfermedad , América Latina/etnología , Factores de Riesgo , Población Blanca/etnología , Población Blanca/genética , EspañaRESUMEN
INTRODUCTION: Detecting imported diseases by migrants and individuals visiting friends and relatives (VFR) is key in the prevention and management of emergent infectious diseases acquired abroad. METHODS: Retrospective descriptive study on migrants and VFR from Central and South America between 2017 and 2022 attended at a National Referral Centre for Tropical Diseases in Madrid, Spain. Demographic characteristics, syndromes and confirmed travel-related diagnoses were obtained from hospital patient medical records. RESULTS: 1654 cases were registered, median age of 42 years, 69.1% were female, and 55.2% were migrants. Most cases came from Bolivia (49.6%), followed by Ecuador (12.9%). Health screening while asymptomatic (31.6%) was the main reason for consultation, followed by Chagas disease follow-up (31%). Of those asymptomatic at screening, 47,2% were finally diagnosed of any disease, mainly Chagas disease (19,7%) and strongyloidiasis (10,2%) CONCLUSION: Our study emphasizes the importance of proactive health screening to detect asymptomatic conditions in migrants and VFR, enabling timely intervention and improved health outcomes. By understanding the unique health profiles of immigrant populations, targeted public health interventions can be devised to safeguard the well-being of these vulnerable groups.
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Enfermedades Transmisibles Importadas , Migrantes , Humanos , Estudios Retrospectivos , Femenino , Masculino , Adulto , Enfermedades Transmisibles Importadas/epidemiología , Enfermedades Transmisibles Importadas/prevención & control , Enfermedades Transmisibles Importadas/diagnóstico , España/epidemiología , Migrantes/estadística & datos numéricos , Persona de Mediana Edad , Viaje/estadística & datos numéricos , Adolescente , América Latina/epidemiología , América Latina/etnología , Adulto Joven , Enfermedad de Chagas/diagnóstico , Enfermedad de Chagas/epidemiología , Enfermedad de Chagas/prevención & control , Niño , Anciano , Medicina Tropical , Derivación y Consulta/estadística & datos numéricos , Emigrantes e Inmigrantes/estadística & datos numéricosRESUMEN
We summarize the clinical trials (CTs) main characteristics, including members of ethnic minorities from Latin America. We carried out a systematic search in six databases. We made a descriptive synthesis of CTs, summarizing the characteristics, interventions, main findings, results, and conclusions reported. 4411 studies were acquired in search strategy, leaving 24 CTs in the final selection. Of these, ten were randomized, four were non-randomized, and the remainder had other designs. Most of the studies were carried out in the population of infants and children (08), ten of the studies included only women, and two studies included men. Nine studies were conducted in Mexico, with the Mayan ethnic minority being mostly evaluated (05). In only 15 it was mentioned that their research was approved by a research ethics committee. Finally, half of the CTs reported funding from international agencies and third reported funding from government agencies. Our results show that that CTs in ethnic minorities are limited and reduced to a few native peoples of the continent.
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Ensayos Clínicos como Asunto , Minorías Étnicas y Raciales , Humanos , América Latina/etnología , Región del Caribe/etnología , Masculino , Femenino , Grupos Minoritarios , Etnicidad/estadística & datos numéricosRESUMEN
The objective of the current research was to investigate the relationship between parenting style, culture, and infant development in a sample of Latin American mother-infant dyads in Toronto, Canada. We examined associations between mothers' self-reported parenting style and infant cognitive and socioemotional development, which we compared to results from mothers belonging to two other Canadian immigrant populations. We further examined whether specific cultural correlates, including affiliation with traditional Latinx cultural beliefs familism and fatalism and acculturation, were associated with positive parenting behaviors in the Latin American sample. Across all three cultural groups, authoritative parenting predicted adaptive socio-emotional development, an effect which differed in magnitude across groups, providing support for the hypothesis that the effect of parenting behaviors on infant development are moderated by culture. Within the Latin American sample, affiliation with the value of familism was associated with higher scores of authoritative parenting, but familism decreased as acculturation to the host culture increased. This research adds to our understanding of factors that contribute to the well-being of Latin American families in Canada. Findings carry implications for provision of infant mental health services to Latin American immigrant families by identifying cultural variables which should be considered when providing parenting interventions to make such interventions more culturally relevant.
La presente investigación examinó la relación entre el estilo de crianza, la cultura y el desarrollo del infante en un grupo muestra de díadas madre-infante latinoamericanas en Toronto, Canadá. Medimos las asociaciones entre el auto reportado estilo de crianza de las madres y el desarrollo cognitivo y socioemocional del infante, lo cual comparamos con resultados de madres que pertenecían a otros dos grupos de población inmigrante canadiense. Examinamos además si componentes culturales específicos, incluyendo creencias cultuales Latinx de familismo y fatalismo, y aculturación, se asociaban con conductas positivas de crianza en el grupo latinoamericano. A lo largo de los tres grupos culturales, la crianza autoritativa predijo puntajes más altos de desarrollo socioemocional del infante, un efecto que difiere en su magnitud entre los grupos, lo cual ofrece apoyo a la hipótesis de que la cultura modera el efecto de las conductas de crianza sobre el desarrollo del infante. Dentro del grupo latinoamericano, la afiliación con el valor del familismo se asoció con puntajes más altos de crianza autoritativa, y una disminución a medida que aumentó la aculturación a la nueva cultura. Esta investigación aumenta nuestra comprensión de los factores que contribuyen al bienestar de las familias latinoamericanas. Los resultados conllevan implicaciones para la provisión de servicios de salud mental infantil a familias inmigrantes latinoamericanas por medio de identificar las variables culturales que deben ser consideradas cuando se ofrezcan intervenciones de crianza para hacer más culturalmente relevantes tales intervenciones.
Nos recherches ont examiné la relation entre le style de parentage, le développement du bébé et la culture chez un échantillon de dyades mère-bébé d'Amérique du Sud à Toronto au Canada. Nous avons mesuré les liens entre le style de parentage auto-rapporté des mères et le développement cognitif et socio-émotionnel, que nous avons comparés aux résultats de mères appartenant à deux autres populations immigrées canadiennes. Nous avons aussi examiné si des corrélats culturels spécifiques comme les croyances culturelles Latinx de familialisme et de fatalisme, et l'acculturation, étaient liées à des comportements de parentage positifs dans l'échantillon latino-américain. Au travers des trois groupes culturels le parentage autoritaire a prédit des scores beaucoup plus élevés de développement socio-émotionnel, un effet qui a varié en magnitude au sein des groupes, soutenant l'hypothèse que l'effet de comportements de parentage sur le développement du bébé est modéré par la culture. Au sein de l'échantillon latino-américain l'affiliation avec la valeur du familialisme était liée à des scores plus élevés de parentage autoritaire, et décroissait au fur et à mesure que l'acculturation à la culture hôte augmentait. Ces recherches s'ajoutent à notre compréhension des facteurs qui contribuent au bien-être des familles latino-américaines. Les résultats ont des implications pour la mise à disposition de services de santé mentale de la petite enfance aux familles immigrées latino-américaines en identifiant des variables culturelles qui devraient être prises en considération lorsqu'on offre des interventions de parentage afin de s'assurer que ces interventions sont pertinentes sur le plan culturel.
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Emigrantes e Inmigrantes , Responsabilidad Parental , Niño , Femenino , Humanos , Lactante , Canadá , Desarrollo Infantil , Hispánicos o Latinos/psicología , América Latina/etnología , Madres/psicología , Responsabilidad Parental/psicología , Cultura , Valores Sociales/etnologíaRESUMEN
OBJECTIVES: To reduce disparities in HIV care outcomes among Latin American and Caribbean (LAC) immigrants living with HIV in the U.S., it is necessary to identify factors influencing HIV care in this population. A systematic review that provides a comprehensive understanding of factors influencing retention in HIV care and viral suppression among LAC immigrants living with HIV in the U.S. is lacking. This systematic review used the Immigrant Health Services Utilization theoretical framework to provide an understanding of these factors. DESIGN: We searched for peer-reviewed publications in MEDLINE, EMBASE, CINAHL, PsycINFO, and ASSIA, from January 1996 to June 2020. RESULTS: A total of 17 qualitative (n = 10) and quantitative (n = 7) studies were included in the review. The most commonly reported general and immigrant-specific factors appearing in studies were undocumented immigration status, HIV stigma, homophobia, cultural norms, values and beliefs, family and social support, language barriers, structure, complexity and quality of the U.S. healthcare delivery system, and patient-provider relationship. CONCLUSION: These findings highlight the importance of considering immigrant-specific factors along with general factors to improve the provision of HIV care services and HIV care outcomes among LAC immigrant populations.
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Emigrantes e Inmigrantes , Infecciones por VIH , Hispánicos o Latinos , Humanos , Emigrantes e Inmigrantes/estadística & datos numéricos , Hispánicos o Latinos/estadística & datos numéricos , Infecciones por VIH/etnología , Infecciones por VIH/terapia , América Latina/etnología , Estados Unidos , Región del Caribe/etnología , Respuesta Virológica Sostenida , Retención en el Cuidado/estadística & datos numéricos , Disparidades en el Estado de Salud , Factores de RiesgoRESUMEN
BACKGROUND: Chagas disease is a parasitic disease endemic to Latin America, but it has become a disease of global concern due to migration flows. Asymptomatic carriers may host the parasite for years, without knowing they are infected. The aim of this study is to assess prevalence of Chagas disease and evaluate the participants' level of knowledge between Latin American migrants attending a community-based screening campaign. METHODS: Three community-based campaigns were performed in Alicante (Spain) in 2016, 2017 and 2018, including educational chats and blood tests for Trypanosoma cruzi serology. Participants completed a questionnaire assessing knowledge about the mechanisms of transmission, disease presentation, diagnosis, and treatment. People seropositive for T. cruzi underwent diagnostic confirmation by two different tests. Results were analyzed by multivariable logistic regression and expressed as adjusted odds ratios (aORs), adjusting for age, sex, and time in Spain. RESULTS: A total of 596 participants were included in the study; 17% were aged under 18 years. Prevalence in adults was 11% [54/496; 95% confidence interval (CI): 8.3-14.5%] versus 0% among children. All but one case were in Bolivians. Diagnosis was independently associated with having been born in Bolivia (aOR: 102, 95% CI: 13-781) and a primary school-level education (aOR: 2.40, 95% CI: 1.14-5.06). Of 54 people diagnosed with Chagas disease (most of whom were asymptomatic), 42 (77.7%) returned to the clinic at least once, and 24 (44.4%) received treatment. Multivariable analysis showed that coming from Argentina (aOR: 13, 95% CI: 1.61-1188) or Bolivia (aOR: 1.90, 95% CI: 1.19-3.39) and having received information about Chagas disease in Spain (aOR: 4.63, 95% CI: 2.54-8.97) were associated with a good level of knowledge on the disease. Having primary level studies (aOR: 0.59, 95% CI: 0.34-0.98) and coming from Ecuador (aOR: 4.63, 95% CI: 2.52-847) were independently associated with a lower level of knowledge. CONCLUSIONS: Community-based interventions are a good strategy for diagnosing neglected diseases such as Chagas disease in non-endemic countries and for identifying and treating infected, asymptomatic individuals.
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Enfermedad de Chagas/diagnóstico , Migrantes/estadística & datos numéricos , Trypanosoma cruzi/aislamiento & purificación , Adulto , Enfermedad de Chagas/epidemiología , Servicios de Salud Comunitaria , Investigación Participativa Basada en la Comunidad , Estudios Transversales , Diagnóstico Precoz , Humanos , América Latina/etnología , Tamizaje Masivo , Persona de Mediana Edad , Enfermedades Desatendidas/epidemiología , Prevalencia , España/epidemiologíaRESUMEN
In this work, we propose a quantitative model for the 2019 Chilean protests. We utilize public data for the consumer price index, the gross domestic product, and the employee and per capita income distributions as inputs for a nonlinear diffusion-reaction equation, the solutions to which provide an in-depth analysis of the population dynamics. Specifically, the per capita income distribution stands out as a solution to the extended Fisher-Kolmogorov equation. According to our results, the concavity of employee income distribution is a decisive input parameter and, in contrast to the distributions typically observed for Chile and other countries in Latin America, should ideally be non-negative. Based on the results of our model, we advocate for the implementation of social policies designed to stimulate social mobility by broadening the distribution of higher salaries.
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Demografía/estadística & datos numéricos , Producto Interno Bruto/estadística & datos numéricos , Renta/estadística & datos numéricos , Política Pública/tendencias , Chile/etnología , Humanos , América Latina/etnología , Modelos Teóricos , Dinámica Poblacional , Factores SocioeconómicosRESUMEN
Self-perception of ethnicity is a complex social trait shaped by both, biological and non-biological factors. We developed a comprehensive analysis of ethnic self-perception (ESP) on a large sample of Latin American mestizos from five countries, differing in age, socio-economic and education context, external phenotypic attributes and genetic background. We measured the correlation of ESP against genomic ancestry, and the influence of physical appearance, socio-economic context, and education on the distortion observed between both. Here we show that genomic ancestry is correlated to aspects of physical appearance, which in turn affect the individual ethnic self-perceived ancestry. Also, we observe that, besides the significant correlation among genomic ancestry and ESP, specific physical or socio-economic attributes have a strong impact on self-perception. In addition, the distortion among ESP and genomic ancestry differs across age ranks/countries, probably suggesting the underlying effect of past public policies regarding identity. Our results indicate that individuals' own ideas about its origins should be taken with caution, especially in aspects of modern life, including access to work, social policies, and public health key decisions such as drug administration, therapy design, and clinical trials, among others.
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Etnicidad/genética , Etnicidad/psicología , Autoimagen , Adulto , Anciano , Escolaridad , Femenino , Antecedentes Genéticos , Humanos , América Latina/etnología , Masculino , Persona de Mediana Edad , Fenotipo , Factores SocioeconómicosAsunto(s)
Enfermedad de Chagas/epidemiología , Emigrantes e Inmigrantes , Conocimientos, Actitudes y Práctica en Salud , Hispánicos o Latinos , Animales , California/epidemiología , Humanos , América Latina/etnología , Factores Socioeconómicos , Triatoma/parasitología , Trypanosoma cruzi/aislamiento & purificaciónRESUMEN
OBJECTIVE: A previous survey investigated postmenopausal vaginal atrophy in a sample of women across Latin America. To help implement a tailored approach to improve postmenopausal care and outcomes in Brazil, we consider results from the survey for this country. METHODS: A total of 2509 postmenopausal women resident in Argentina, Brazil, Chile, Colombia, or Mexico completed an online questionnaire. The Brazilian cohort comprised 504 women. RESULTS: Over half of the Brazilian cohort (56%) reported experiencing symptoms of vaginal atrophy; most described them as moderate or severe (76%), and almost half (48%) experienced symptoms for at least 1 year. Three-quarters of the Brazilian cohort (75%) were unaware of the chronic nature of the condition. Upon experiencing symptoms of vaginal atrophy, 92% had visited a health-care provider to discuss treatment options. Overall, 56% were aware of some form of local hormone therapy and 40% of those affected by vaginal atrophy had used such treatment. CONCLUSION: Postmenopausal women in Brazil are likely to benefit from increased awareness of the symptoms of vaginal atrophy. Health-care providers can potentially improve outcomes by helping women to understand the chronic nature of the condition and available treatment options. Women may be open to education pre menopause, before symptoms occur.
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Aceptación de la Atención de Salud/psicología , Posmenopausia/psicología , Vagina/patología , Enfermedades Vaginales/psicología , Salud de la Mujer/estadística & datos numéricos , Atrofia , Brasil/epidemiología , Brasil/etnología , Femenino , Conocimientos, Actitudes y Práctica en Salud , Humanos , América Latina/epidemiología , América Latina/etnología , Persona de Mediana Edad , Aceptación de la Atención de Salud/etnología , Posmenopausia/etnología , Encuestas y Cuestionarios , Enfermedades Vaginales/epidemiología , Enfermedades Vaginales/etnología , Salud de la Mujer/etnologíaRESUMEN
AIMS/HYPOTHESIS: Non-Western immigrants to Europe are at high risk for type 2 diabetes. In this nationwide study including incident cases of type 2 diabetes, the aim was to compare all-cause mortality (ACM) and cause-specific mortality (CSM) rates in first- and second-generation immigrants with native Swedes. METHODS: People living in Sweden diagnosed with new-onset pharmacologically treated type 2 diabetes between 2006 and 2012 were identified through the Swedish Prescribed Drug Register. They were followed until 31 December 2016 for ACM and until 31 December 2012 for CSM. Analyses were adjusted for age at diagnosis, sex, socioeconomic status, education, treatment and region. Associations were assessed using Cox regression analysis. RESULTS: In total, 138,085 individuals were diagnosed with type 2 diabetes between 2006 and 2012 and fulfilled inclusion criteria. Of these, 102,163 (74.0%) were native Swedes, 28,819 (20.9%) were first-generation immigrants and 7103 (5.1%) were second-generation immigrants with either one or both parents born outside Sweden. First-generation immigrants had lower ACM rate (HR 0.80 [95% CI 0.76, 0.84]) compared with native Swedes. The mortality rates were particularly low in people born in non-Western regions (0.46 [0.42, 0.50]; the Middle East, 0.41 [0.36, 0.47]; Asia, 0.53 [0.43, 0.66]; Africa, 0.47 [0.38, 0.59]; and Latin America, 0.53 [0.42, 0.68]). ACM rates decreased with older age at migration and shorter stay in Sweden. Compared with native Swedes, first-generation immigrants with ≤ 24 years in Sweden (0.55 [0.51, 0.60]) displayed lower ACM rates than those spending >24 years in Sweden (0.92 [0.87, 0.97]). Second-generation immigrants did not have better survival rates than native Swedes but rather displayed higher ACM rates for people with both parents born abroad (1.28 [1.05, 1.56]). CONCLUSIONS/INTERPRETATION: In people with type 2 diabetes, the lower mortality rate in first-generation non-Western immigrants compared with native Swedes was reduced over time and was equalised in second-generation immigrants. These findings suggest that acculturation to Western culture may impact ACM and CSM in immigrants with type 2 diabetes but further investigation is needed. Graphical abstract.
Asunto(s)
Diabetes Mellitus Tipo 2/mortalidad , Emigrantes e Inmigrantes/estadística & datos numéricos , Mortalidad/etnología , Adulto , África/etnología , Anciano , Asia/etnología , Estudios de Cohortes , Diabetes Mellitus Tipo 2/tratamiento farmacológico , Escolaridad , Europa (Continente)/etnología , Femenino , Humanos , América Latina/etnología , Masculino , Persona de Mediana Edad , Medio Oriente/etnología , Clase Social , Suecia/epidemiologíaRESUMEN
We wanted to explore possible differences in disease presentation, frequency, and age of onset of dementia with Lewy bodies (DLB) between first-generation immigrants (FGI) and patients born in Belgium (PBIB). We conducted a retrospective study on all patients of our Memory Clinic between June 1, 2010 and January 31, 2020. A synucleinopathy was diagnosed in 150 of 2702 patients (5.5%): 91 received a diagnosis of DLB (3.4%). FGI were two times more likely to receive a diagnosis of DLB, due to a higher prevalence in North-Africans and Latin-Americans. Visual hallucinations were less frequent in North-Africans than in other immigrants. FGI were younger than PBIB and reported more often parasomnia. Our data suggest a higher risk for DLB in certain immigrant groups. Especially for North-African patients, a genetic factor can be suspected, namely mutations in Leucine-rich repeat kinase 2 (LRRK2). Memory clinics with a high rate of FGI may provide interesting data and insights into the prevalence of DLB, genetic and environmental differences.
Asunto(s)
Emigrantes e Inmigrantes/psicología , Enfermedad por Cuerpos de Lewy/etnología , Enfermedad por Cuerpos de Lewy/psicología , Trastornos de la Memoria/etnología , Trastornos de la Memoria/psicología , Servicio Ambulatorio en Hospital , África del Norte/etnología , Anciano , Anciano de 80 o más Años , Bélgica/etnología , Europa (Continente)/etnología , Femenino , Humanos , América Latina/etnología , Enfermedad por Cuerpos de Lewy/diagnóstico , Masculino , Trastornos de la Memoria/diagnóstico , Persona de Mediana Edad , Estudios RetrospectivosRESUMEN
The US Hispanic population is large and rapidly growing, with serious healthcare disparities. Alarmingly, 67% of Hispanic adults with a mental illness go untreated. Attempts to increase treatment rates have had limited success, likely partly due to stigma beliefs. There is an urgent need to develop and utilize a Spanish language stigma assessment tool. The current study is the first to do so, translating the Beliefs Toward Mental Illness (BTMI; Hirai et al., 2018) scale into Spanish (S-BTMI). Our psychometric findings with English-Spanish bilingual Latinx undergraduate students suggest that the S-BTMI can be a reliable measure of mental illness stigma. The BTMI's 4-factor solution was confirmed by the S-BTMI. Language invariance tests for the S-BTMI and BTMI demonstrated metric invariance and partial scalar invariance. The S-BTMI's factors produced strong internal consistency and two-week test-retest reliability. A previous Latinx sample's BTMI scores were similar to the current S-BTMI scores, except for greater endorsement of incurability beliefs for the Spanish version. Average stigma levels were fairly low in the current sample. Use of the BTMI-S can improve our understanding of stigma, and its relationships to language, culture, acculturation, and treatment-seeking in Latinx communities.
Asunto(s)
Hispánicos o Latinos/psicología , Lenguaje , Trastornos Mentales/etnología , Trastornos Mentales/psicología , Encuestas y Cuestionarios/normas , Traducción , Aculturación , Adolescente , Adulto , Femenino , Humanos , América Latina/etnología , Estudios Longitudinales , Masculino , Trastornos Mentales/diagnóstico , Persona de Mediana Edad , Psicometría/métodos , Reproducibilidad de los Resultados , Estigma Social , Adulto JovenRESUMEN
OBJECTIVES: To describe and compare the main clinical characteristics and outcome measures in hospitalized patients with confirmed coronavirus disease 2019 (COVID-19) according to geographical area of origin. METHODS: A retrospective analysis of patients hospitalized with confirmed COVID-19 at a referral centre in Madrid, Spain, during March-May 2020 was performed. Recorded variables (age, gender, intensive care unit (ICU) admission, outcome), and geographical area of origin were compared for Europeans and non-Europeans (Latin Americans, Asians and Africans). RESULTS: In total, 2345 patients with confirmed COVID-19 hospitalized during the study period were included in the study. Of these, 1956 (83.4%) were European and 389 (16.6%) were non-European (of whom over 90%, 354/389, were Latin American). Non-Europeans were significantly younger than Europeans (mean 54 (SD 13.5) versus 70.4 (SD 15.1) years, p < 0.001); the majority were male (1420/2345, 60.6%), with no significant differences in gender between Europeans and non-Europeans (1197/1956 (61.2%) male in the European group versus 223/389 (57.3%) male in the non-European group, p 0.15). In-hospital mortality overall was higher in Europeans (443/1956, 22.7%) than in non-Europeans (40/389, 10.3%) (p < 0.001), but there were no significant differences when adjusted for age/gender (OR 1.27, 95% CI 0.86-1.88). Non-Europeans were more frequently admitted to ICU (71/389, 18.3%) compared with Europeans (187/1956, 9.6%) (p < 0.001) and a difference in ICU admission rate was also found when adjusted for age/gender (OR 1.43, 95% CI 1.03-1.98). CONCLUSIONS: No significant differences in mortality were observed between Europeans and non-Europeans (mainly Latin Americans), but an increase in ICU admission rate was found in non-Europeans.