Mental and social wellbeing trajectory during the pandemic for vulnerable populations.

Objectives: We investigated changes over time in mental and social wellbeing indicators for vulnerable population subgroups during the pandemic. These groups were younger people, people with disabilities, low-income groups, unemployed, culturally, and linguistically diverse communities (CaLD), and Aboriginal and Torres Strait Islander peoples. Methods: A series of four repeated population representative surveys were conducted in June 2020, September 2020, January 2022, and June 2022. Questions included items on psychological distress, financial hardship, social connection, and life satisfaction. Results: For most groups, social connection and life satisfaction improved in 2022 relative to 2020. Psychological distress and financial hardship showed the opposite pattern, with some groups having worse results in 2022 relative to 2020. People without any vulnerability had better mental health and social wellbeing outcomes at each time point relative to the vulnerable population subgroups. Conclusion: Pandemic-related policies had differential effects over time and for different population groups. Future policies and research need to closely monitor how they impact population subgroups, and the overall results clearly demonstrate the inequity in mental health and social wellbeing outcomes for vulnerable population cohorts.

Social Risk and Dialysis Facility Performance in the First Year of the ESRD Treatment Choices Model.

Importance: The End-Stage Renal Disease Treatment Choices (ETC) model randomly selected 30% of US dialysis facilities to receive financial incentives based on their use of home dialysis, kidney transplant waitlisting, or transplant receipt. Facilities that disproportionately serve populations with high social risk have a lower use of home dialysis and kidney transplant raising concerns that these sites may fare poorly in the payment model. Objective: To examine first-year ETC model performance scores and financial penalties across dialysis facilities, stratified by their incident patients' social risk. Design, Setting, and Participants: A cross-sectional study of 2191 US dialysis facilities that participated in the ETC model from January 1 through December 31, 2021. Exposure: Composition of incident patient population, characterized by the proportion of patients who were non-Hispanic Black, Hispanic, living in a highly disadvantaged neighborhood, uninsured, or covered by Medicaid at dialysis initiation. A facility-level composite social risk score assessed whether each facility was in the highest quintile of having 0, 1, or at least 2 of these characteristics. Main Outcomes and Measures: Use of home dialysis, waitlisting, or transplant; model performance score; and financial penalization. Results: Using data from 125 984 incident patients (median age, 65 years [IQR, 54-74]; 41.8% female; 28.6% Black; 11.7% Hispanic), 1071 dialysis facilities (48.9%) had no social risk features, and 491 (22.4%) had 2 or more. In the first year of the ETC model, compared with those with no social risk features, dialysis facilities with 2 or more had lower mean performance scores (3.4 vs 3.6, P = .002) and lower use of home dialysis (14.1% vs 16.0%, P < .001). These facilities had higher receipt of financial penalties (18.5% vs 11.5%, P < .001), more frequently had the highest payment cut of 5% (2.4% vs 0.7%; P = .003), and were less likely to achieve the highest bonus of 4% (0% vs 2.7%; P < .001). Compared with all other facilities, those in the highest quintile of treating uninsured patients or those covered by Medicaid experienced more financial penalties (17.4% vs 12.9%, P = .01) as did those in the highest quintile in the proportion of patients who were Black (18.5% vs 12.6%, P = .001). Conclusions: In the first year of the Centers for Medicare & Medicaid Services' ETC model, dialysis facilities serving higher proportions of patients with social risk features had lower performance scores and experienced markedly higher receipt of financial penalties.

Examining neighbourhood-level disparities in Black, Latina/o, Asian, and White physical health, mental health, chronic conditions, and social disadvantage in California.

Racial/ethnic minority individuals in the U.S. experience numerous health disparities versus Whites, often due to differences in social determinants. Yet, limited large-scale research has examined these differences at the neighbourhood level. We merged 2021 PLACES Project and 2020 American Community Survey data across 3,211 census tracts (neighbourhoods) defined as majority (>50%) Black, Latina/o, Asian or White. T-tests and hierarchical linear regressions were used to examine differences and associations between neighbourhoods on key health (general health, mental health, obesity, diabetes, cancer, coronary heart disease, chronic obstructive pulmonary disease, stroke), and social outcomes (income, unemployment, age, population density). Results indicated that minority neighbourhoods in California exhibited stark health and social disparities versus White neighbourhoods, displaying worse outcomes on nearly every social and health variable/condition examined; particularly for Black and Latina/o neighbourhoods. Moreover, regression findings revealed that, after considering income, unemployment, and population density, (1) fair/poor mental health and higher percentages of Black, Latina/o and Asian residents in neighbourhoods independently associated with greater neighbourhood fair/poor physical health, and (2) fair/poor mental health significantly associated with greater prevalence of obesity and COPD. This study thus underscores the need to address the profound health and social disparities experienced by minority neighbourhoods for more equitable neighbourhoods.

Inclusion of a Parental Component in a Sports-Based HIV Prevention Program for Dominican Youth.

BACKGROUND: Underprivileged youth in the Dominican Republic (DR) are at high risk of acquiring the human immunodeficiency virus (HIV). Protective parenting practices may inhibit sexual risk-taking. OBJECTIVE: We investigated whether parental involvement in a sports-based HIV prevention program increased self-efficacy to prevent HIV and safe sex behavior among Dominican youth. METHOD: The study had a quasi-experimental design with repeated measures. N = 90 participants between 13 and 24 years of age participated in the program through two different trainings, UNICA and A Ganar, both of which had an experimental (i.e., program with parental component) and a control (i.e., program without parental component) condition. RESULTS: Self-efficacy to prevent HIV significantly increased among participants in the experimental condition of UNICA. Self-efficacy for safe sex increased among sexually active participants in the experimental condition of A Ganar. Implications for Impact: These findings are important to meet the United Nations' Sustainable Development Goal of good health and wellbeing, as they suggest that parental involvement in sports-based HIV prevention programs can enhance their positive effects for increasing youth's self-efficacy to practice HIV-preventive behaviors. Randomized control trials and longitudinal studies are needed.

Disparities in refusal of surgery for gynecologic cancer.

OBJECTIVE: To identify sociodemographic and clinical factors associated with refusal of gynecologic cancer surgery and to estimate its effect on overall survival. METHODS: The National Cancer Database was surveyed for patients with uterine, cervical or ovarian/fallopian tube/primary peritoneal cancer treated between 2004 and 2017. Univariate and multivariate logistic regression were used to assess associations between clinico-demographic variables and refusal of surgery. Overall survival was estimated using the Kaplan-Meier method. Trends in refusal over time were evaluated using joinpoint regression. RESULTS: Of 788,164 women included in our analysis, 5875 (0.75%) patients refused surgery recommended by their treating oncologist. Patients who refused surgery were older at diagnosis (72.4 vs 60.3 years, p < 0.001) and more likely Black (OR 1.77 95% CI 1.62-1.92). Refusal of surgery was associated with uninsured status (OR 2.94 95% CI 2.49-3.46), Medicaid coverage (OR 2.79 95% CI 2.46-3.18), low regional high school graduation (OR 1.18 95% CI 1.05-1.33) and treatment at a community hospital (OR 1.59 95% CI 1.42-1.78). Patients who refused surgery had lower median overall survival (1.0 vs 14.0 years, p < 0.01) and this difference persisted across disease sites. Between 2008 and 2017, there was a significant increase in refusal of surgery annually (annual percent change +1.41%, p < 0.05). CONCLUSIONS: Multiple social determinants of health are independently associated with refusal of surgery for gynecologic cancer. Given that patients who refuse surgery are more likely from vulnerable, underserved populations and have inferior survival, refusal of surgery should be considered a surgical healthcare disparity and tackled as such.

Lessons Learned from Health Disparities in Coronavirus Disease-2019 in the United States.

In the United States, the coronavirus disease-2019 (COVID-19) pandemic has disproportionally affected Black, Latinx, and Indigenous populations, immigrants, and economically disadvantaged individuals. Such historically marginalized groups are more often employed in low-wage jobs without health insurance and have higher rates of infection, hospitalization, and death from COVID-19 than non-Latinx White individuals. Mistrust in the health care system, language barriers, and limited health literacy have hindered vaccination rates in minorities, further exacerbating health disparities rooted in structural, institutional, and socioeconomic inequities. In this article, we discuss the lessons learned over the last 2 years and how to mitigate health disparities moving forward.

Experiências de pessoas em situação de rua com o uso de substâncias psicoativas: um estudo no contexto do Distrito Federal / Experiences of homeless people with use of psychoactive substances: a study in the context of federal distric / experiencias de personas en situación de calle con el uso de sustancias psicoactivas: un estudio en el contexto del distrito federal

Investigou-se vivências de pessoas em situação de rua que usam/usaram substâncias psicoativas, a partir de um programa de reinserção social e geração de renda, no Distrito Federal. Trata-se de estudo realizado com quatro adultos a partir de entrevistas semiestruturadas. As informações foram analisadas pela Análise de Conteúdo, gerando as categorias: caracterização do uso de substâncias psicoativas; experiência com programas para usuários de álcool e outras drogas; história de vida e a situação de rua; projeto social e uso de substâncias psicoativas. Como resultados, evidenciou-se como os participantes se relacionam com substâncias psicoativas, como o projeto social investigado se configura como potencializador para transformação de vidas. Conclui-se que a história de vida dos sujeitos está ligada à situação de rua e uso de substâncias psicoativas, destacando-se o potencial transformador de programas sociais, possibilitadores de desenvolvimento econômico e social, e que modelos baseados em abstinência se mostraram ineficazes como forma de tratamento. (AU)

The experiences of homeless people who use/have used psychoactive substances were investigated, based on a program of social reintegrationand income generation, in the Federal District. This is a study carried out with four adults through semi-structured interviews. The information was analyzed by Content Analysis, generating the following categories: characterization of the use of psychoactive substances; experience with programs for users of alcohol and other drugs; life history and the street situation; social project and use of psychoactive substances. As a result, it was evidenced how the participants relate to psychoactive substances, how the investigated social project is configured as a potentiator for the transformation of lives. It is concluded that the life history of the subjects is linked to the homeless situation and the use of psychoactive substances, highlighting the transforming potential of social programs, enabling economic and social development, and that models based on abstinence proved to be ineffective as a way to of treatment. (AU)

Se indagaron las experiencias de personas en situación de calle que consumen/han utilizado sustancias psicoactivas, a partir de un programa de reinserción social y generación de ingresos, en el Distrito Federal. Se trata de un estudio realizado con cuatro adultos a través de entrevistas semiestructuradas. La información fue analizada por Análisis de Contenido, generando las siguientes categorías: caracterización del uso de sustancias psicoactivas; experiencia con programas para usuarios de alcohol y otras drogas; historia de vida y situación de la calle; proyecto social y consumo de sustancias psicoactivas. Como resultado, se evidenció cómo los participantes se relacionan con las sustancias psicoactivas, cómo el proyecto social investigado se configura como un potenciador para la transformación de vidas. Se concluye que la historia de vida de los sujetos está vinculada a la situación de calle y al uso de sustancias psicoactivas, destacando el potencial transformador de los programas sociales, viabilizando el desarrollo económico y social, y que los modelos basados en la abstinencia demostraron ser ineficaces como vía de tratamiento. (AU)

A scoping review on the impact of austerity on healthcare access in the European Union: rethinking austerity for the most vulnerable.

BACKGROUND: There is consensus that the 2008 financial and economic crisis and related austerity measures adversely impacted access to healthcare. In light of the growing debt caused by the COVID-19 crisis, it is uncertain whether a period of austerity will return. OBJECTIVE: This study aims to provide a structured overview of the impact of austerity policies in the EU-28 zone, applied in response to the Great Recession, on access to health care for the adult population, using the five access dimensions by Levesque et al. (2013). METHODS: This study followed the PRISMA extension for Scoping Reviews guideline. Medline (PubMed) and Web of Science were searched between February 2021 and June 2021. Primary studies in the English language published after the 1st of January 2008 reporting on the possible change in access to the healthcare system for the adult population induced by austerity in an EU28 country were included. RESULTS: The final search strategy resulted in 525 articles, of which 75 studies were reviewed for full-text analysis, and a total of 21 studies were included. Results revealed that austerity policy has been primarily associated with a reduction in access to healthcare, described through four main categories: i) Increase in rates of reported unmet needs (86%); ii) Affordability (38%); iii) Appropriateness (38%); iv) and Availability and Accommodation (19%). Vulnerable populations were more affected by austerity measures than the general population when specific safeguards were not in place. The main affected adult vulnerable population groups were: patients with chronic diseases, elderly people, (undocumented) migrants, unemployed, economically inactive people and individuals with lower levels of education or socioeconomic status. CONCLUSION: Austerity measures have led to a deterioration in access to healthcare in the vast majority of the countries studied in the EU-28 zone. Findings should prompt policymakers to rethink the fiscal agenda across all policies in times of economic crisis and focus on the needs of the most vulnerable populations from the health perspective.

An exploration of the inverse care law and market forces in Australian primary health care.

This paper examines the implications of the second sentence in Tudor Harts statement about inverse care - that its operation was strongest when exposed to market forces. In the Australian context, we briefly review some available evidence for inverse care in three groups - Aboriginal and Torres Strait Islander people and those living in remote and socioeconomically disadvantaged areas. We then discuss the extent to which these examples can be attributed to the operation of supply-and-demand within Australia's hybrid fee-for-service system in general practice. Our analysis suggests disparities in workforce supply and the ability of disadvantaged groups to seek preventive and proactive care are critical factors. These, in turn, suggest the need to fund general practice to be responsible for proactive and preventive care of disadvantaged population groups alongside broader structural reforms in workforce, education and taxation.

"We're all one bad day away": Impacts on Food Access in Buffalo, New York during the COVID-19 pandemic.

When COVID-19 arrived in Buffalo, New York in March 2020, there was already significant food insecurity in the region. However, barriers to food access were greatly exacerbated by the pandemic. This study assesses the pandemic's impact on food access in Buffalo through 75 surveys and 30 qualitative interviews conducted with users of food pantries. Results show that, while the pandemic did contribute to food insecurity, many food pantry users were already experiencing chronic food access issues. Specifically, issues related to transportation, stigma, and chronic poverty must be addressed for food insecure households to better endure emergency events like pandemics.

Elevada taxa de insegurança alimentar em unidades de triagem de resíduos no sul do Brasil: insegurança alimentar em recicladores / High food insecurity in recyclers from waste sorting units in southern Brazil: high food insecurity in recyclers

Introdução: No Brasil, existem poucos estudos com recicladores de Unidades de Triagem de Resíduos (UTRs). Vários fenômenos sociais têm sido associados ao aumento da Insegurança Alimentar (IA) em países menos desenvolvidos. O estudo tem como objetivo descrever a prevalência de insegurança alimentar em recicladores.Métodos: Estudo transversal realizado com adultos associados de duas UTRs na cidade de Porto Alegre, sul do Brasil, entre 2017 a 2018. Todas as coletas ocorreram nas UTRs. Os indivíduos tiveram seu estado nutricional avaliado por medidas antropométricas através da aferição de peso, altura e circunferência da cintura. A taxa de Insegurança Alimentar foi avaliada pela Escala Brasileira de Insegurança Alimentar (EBIA) e o risco para uso de substâncias foi avaliado pelo Alcohol, Smoking and Substance Involvement Screening Test (ASSIST).Resultados: Foram avaliados 123 sujeitos, com idade média de 35 ± 13,4 anos, sendo 66% do sexo feminino. Foi identificada uma taxa de IA de 74%, sendo que destes, 16% apresentaram Insegurança Alimentar Grave. Cerca de 57% dos participantes apresentaram sobrepeso ou obesidade e 48% circunferência da cintura aumentada. Em relação ao uso de substâncias, 60,5% relataram abuso de tabaco e 14% de álcool.Conclusão: São necessárias intervenções multidisciplinares para prevenir as situações encontradas e a implementação de políticas públicas voltadas para os atos de promoção da saúde na população de recicladores. É fundamental que tanto a sociedade, quanto o governo reconheçam a existência destes problemas para que medidas efetivas possam ser instituídas.

Introduction: In Brazil, there are few studies with recyclers of Waste Sorting Units (WSUs). Several social phenomena have been associated with increased food insecurity (FI) in less developed countries. The study aims to describe food insecurity prevalence in recyclers.Methods: Cross-sectional study conducted with adults from two WSUs in the city of Porto Alegre, southern Brazil, between 2017 and 2018. All data assessment occurred in WSUs. Anthropometric measurements were assessed by weight, height and waist circumference. Food insecurity was assessed with the Brazilian Food Insecurity Scale (EBIA) and substance use was evaluated by the Alcohol, Smoking and Substance Involvement Screening Test (ASSIST).Results: 123 subjects were evaluated, with a mean age of 35 ± 13.4 years, 66% of which were female. A FI rate of 74% was identified, and of these, 16% had Severe Food Insecurity. About 57% of participants were overweight or obese and 48% presented high waist circumference. Regarding substance use, 60.5% were classified for tobacco abuse and 14% for alcohol abuse.Conclusion: Multidisciplinary interventions are needed to prevent all health issues encountered as well as implementation of public policies for the recyclers' health promotion. It is essential that both society and the government recognize the existence of these problems so that measures can be carried out by health institutions.

Características actuales de la población pediátrica asistida en un centro de salud del primer nivel de atención en 2020-2021: Montevideo, Uruguay / Characteristics of the pediatric population assisted at primary care level in Montevideo, Uruguay / Características da população pediátrica assistida no nível de atenção primária em Montevidéu, Uruguai

Introducción: alrededor del 30% de las enfermedades infantiles responden a factores sociofamiliares y ambientales, asociados a condiciones de vida, dinámica familiar y exposición a sustancias tóxicas. Conocer las características de la población pediátrica que asiste este centro de salud nos ayudará a identificar factores que pueden estar influyendo en su salud. Objetivos: Describir las características clínico-epidemiológicas de la población menor de 15 años que recibió asistencia en el Centro de Salud Badano Repetto en el período 2020-2021. Conocer diferentes variables que pueden influir en la salud de esta población Identificar asociación de variables familiares y socioculturales con el desarrollo en las diferentes edades. Metodología: estudio descriptivo, retrospectivo, corte transversal. Se incluyó una muestra por conveniencia del 15% del total de los niños y adolescentes menores de 15 años asistidos en el centro de salud desde 1/10/2020 hasta 31/3/2021. Variables estudiadas: del niño: sexo, edad, antecedentes perinatales, crecimiento y desarrollo, controles en salud, inmunizaciones, escolarización, actividades extracurriculares. De los padres: edad, nivel educativo, consumo de sustancias psicoactivas, antecedentes patológicos, empleo, privación de libertad. Familia y vivienda: estado civil de los padres, antecedentes de violencia doméstica, convivientes, características de la vivienda, servicios básicos, transferencias directas de ayuda, intervención de equipos de territorio. Fuente de datos: historias clínicas y vía telefónica. Registro en planilla prediseñada. Los resultados se expresan en frecuencias absolutas, relativas y medidas de tendencia central con su rango. Se utilizó test de Chi cuadrado o exacto de Fisher. Nivel de significación: 0,05. Programa Epi Info™ versión 7.2. Consentimiento informado telefónico a padres y asentimiento a adolescentes. Aprobado por el Comité de Ética del CHPR. Resultados: consultaron 2.826 menores de 15 años, se incluyeron 426 (15%), pero solo 263 (62%) fueron analizados, dado que 163 (38%) no pudieron ser contactados telefónicamente. El 52% eran de sexo femenino. Media de edad: 4 años (5 días-14 años), 69% ≤5 años. 83% de los pacientes tenían adecuados controles de salud y 91% estaban al día con sus inmunizaciones. 12% tenían sobrepeso/obesidad. El desarrollo neurológico fue adecuado en 93% en los menores de 5 años y en 56% de los mayores de 5 años de edad. En el caso de aquellos con trastornos del neurodesarrollo mayores de 5 años, 46% tenían trastornos del aprendizaje, 39% trastorno de conducta, 32% trastornos del lenguaje, 10% déficit intelectual. 56% estaba escolarizado, todos en escuelas públicas. En el caso de aquellos que no asistían a la escuela, 4 estaban en edad de asistencia obligatoria (6, 7, 9 y 10 años de edad). 20% de los niños/adolescentes había repetido por lo menos un año en escuela o liceo. Datos perinatales: 14% de las madres consumieron drogas; las más frecuentes fueron tabaco y pasta base de cocaína (PBC). 85% fueron recién nacidos de término, 10% presentaron depresión neonatal. 15% de niños/ adolescentes estuvo expuesto a violencia doméstica y 32% de ellos (12/38) tenía por lo menos un padre con uso de drogas psicoactivas en el domicilio. 21% de los niños/adolescentes expuestos a violencia doméstica tenía una dificultad de aprendizaje. 8% de estos pacientes tenía por lo menos un padre que no había terminado educación primaria y 28% que no había terminado ciclo básico. Se encontró una relación significativa entre uso de drogas psicoactivas, declarada por uno o ambos padres, y violencia doméstica. No se encontró una relación significativa entre alteración del neurodesarrollo y violencia doméstica. Conclusiones: estos hallazgos muestran una población social y económicamente vulnerable, padres con baja escolaridad, uso de pasta base de cocaína durante el embarazo en un porcentaje mayor al reportado nacionalmente, y 15% de niños/adolescentes expuestos a violencia doméstica, pero con un buen número de controles de salud. La mayor fortaleza encontrada por este estudio es la importancia de mantener una buena conexión con estas familias, que mostraron un alto nivel de compromiso con el centro de salud. Esto nos desafía a priorizar la prevención y promoción en salud como herramientas valiosas para adquirir salud de calidad para estos niños/adolescentes. Nuevos estudios, con otras metodologías, serán necesarios para analizar estas variables encontradas.

Introduction: around 30% of childhood diseases are caused by social, environmental and family issues, as well as by life conditions, family dynamics and exposure to toxic substances. Understanding the characteristics of the pediatric population assisted at this Health Center, will help us identify health-threatening factors. Objectives: Describe the clinical and epidemiological characteristics of the population under 15 years of age assisted at Badano Repetto Health Center between 2020 and 2021. Understand the different variables that could influence this population´s health. Identify the link between family, social and cultural variables and neurological development at different ages. Methodology: descriptive, retrospective cross-sectional study. Convenience sampling of 15% of the total number of children and adolescents under 15 years of age, assisted at the Health Center from 10/01/2020 to 3/31/2021. Variables: children: sex, age, perinatal history, growth and neurological development, health checkups, vaccines, school attendance, extracurricular activities. Parents: age, education, psychoactive substance use, pathological background, job, prison. Family and household: parent`s marital status, domestic violence history, cohabitants, housing characteristics, basic household services, government aids, community interventions. Data source: medical records and telephone conversations. Data was recorded on template charts. We used results in absolute and relative frequencies, and their measures of central tendency measures and their range, Chi-square test or Fisher´s exact test. Significance level 0,05. Epi Info Program, version 7.2. Informed parent and adolescent consent. Approved by the CHPR Ethics Committee. Results: out of the 2826 patients under 15 years of age assisted at the clinic, we included 426 (15%), but only 263 (62%) were analyzed, since we were not able to reach 163 (38%) by phone. 52% were female. The average age was 4 years of age (5 days-14 years old). 69% of children were under 5 years old. 83% of patients had adequate number of checkups and 91% had an updated vaccination chart. 12% were overweight/obese. Neurodevelopment was adequate in 93% of those under 5 years of age, and 56% of those over 5 years of age. Regarding those with neurodevelopmental difficulties and over 5 years of age, 46% had learning disabilities, 39% had behavioral disorders, 32% language disorders, 10% intellectual deficit. 56% attended school, all of them public schools. For those who did not attend school, 4 of them were old enough to attend mandatory school (6, 7, 9 and 10 years of age). 20% of the children and adolescents had failed at least one year in school or high school. Perinatal findings: 14% of mothers had substance use during pregnancy, mainly tobacco and cocaine base paste. 85% of them had been born to term, 10% had neonatal depression 15% of children/adolescents had been exposed to domestic violence and 32% of them (12/38) had one parent with psychoactive drug use at home. 21% of children/adolescents exposed to domestic violence had a learning disability. 8% had at least one parent who did not finish primary school and 28% who did not finish middle school. Statistically, a significant link was found between psychoactive substance use, declared by one or both parents, and domestic violence. No statistically significant link was found between neurodevelopmental difficulties and domestic violence. Conclusions: these findings show a socially and economically vulnerable population, parents with little formal education, higher cocaine paste base use during pregnancy than the national statistics and 15% of children/adolescents exposed to domestic violence, even though they a high number of them had received their health checkups. The biggest strength shown by this study is the importance of maintaining a good bond with these families, who showed a high level of commitment with the health center. This leads us to prioritize health prevention and promotion as a valuable tool to achieve health quality standards for these children and adolescents. New studies, using other methodologies, will be necessary to analyze this data.

Introdução: cerca de 30% das doenças infantis são causadas por questões sociais, ambientais e familiares, bem como por condições de vida, dinâmica familiar e exposição a substâncias tóxicas. Compreender as características da população pediátrica atendida neste Centro de Saúde, nos ajudará a identificar fatores de risco à saúde. Objetivos: Descrever as características clínico-epidemiológicas da população menor de 15 anos de idade atendida no Centro de Saúde Badano Repetto no período 2020-2021. Compreender diferentes variáveis que podem influenciar a saúde dessa população. Identificar uma relação entre as variáveis familiares e socioculturais e o desenvolvimento em diferentes idades. Metodologia: estudo descritivo, retrospectivo, transversal. Foi incluída uma amostra por conveniência de 15% de todas as crianças e adolescentes menores de 15 anos atendidos no Centro de Saúde entre 01/10/2020 e 31/03/2021. Variáveis estudadas: da criança: sexo, idade, história perinatal, crescimento e desenvolvimento, controles de saúde, imunizações, escolaridade, atividades extracurriculares. Dos pais: idade, escolaridade, consumo de substâncias psicoativas, histórico médico, emprego, privação de liberdade. Família e habitação: estado civil dos pais, história de violência doméstica, coabitantes, características da moradia, serviços básicos, transferências de ajuda de custo, intervenção das equipes no território. Fonte de dados: prontuários e enquetes telefônicas. Cadastro em planilha padrão. Os resultados são expressos em frequências absolutas e relativas e medidas de tendência central com sua amplidão. Utilizou-se o teste do qui-quadrado ou exato de Fisher. Nível de significância 0,05. Programa Epi Info™ versão 7.2. Consentimento informado por telefone pais e consentimento dos adolescentes. Aprovado pelo Comitê de Ética do CHPR. Resultados: 2.826 crianças menores de 15 anos consultadas, 426 (15%) foram incluídas, mas 263 (62%) foram analisadas, pois 163 (38%) não puderam ser contatadas por telefone. 52% eram do sexo feminino. Idade média 4 anos (5 dias -14 anos), 69% ≤ 5 anos. 83% dos pacientes possuíam controles de saúde adequados e 91% estavam com suas imunizações em dia. 12% com sobrepeso/obesidade. O desenvolvimento neurológico foi adequado em 93% dos menores de 5 anos e em 56% dos maiores de 5 anos. No caso dos portadores de transtornos de neurodesenvolvimento com mais de 5 anos, 46% apresentavam transtorno de aprendizagem, 39% transtorno de conduta, 32% transtorno de linguagem, 10% déficit intelectual. 56% estavam na escola, todos em escolas públicas. No caso dos que não frequentaram a escola, 4 deles estavam em idade em idade escolar obrigatória (6, 7, 9 e 10 anos). 20% das crianças/adolescentes repetiram pelo menos um ano na escola ou no ensino médio. Dados perinatais: 14% das mães usavam drogas; pasta base de tabaco e maiormente pasta base de cocaína (PBC). 85% eram recém-nascidos a termo, 10% tinham depressão neonatal. 15% das crianças/adolescentes foram expostos à violência doméstica e 32% deles (12/38) tinham pelo menos um dos pais que usava drogas psicoativas em casa. 21% das crianças/adolescentes expostas à violência doméstica tinham dificuldade de aprendizagem. 8% desses pacientes possuíam pelo menos um dos pais com escola primária incompleta e 28% com ensino médio incompleto. Encontrou-se relação significativa entre o uso de drogas psicoativas, declarado por um ou ambos os pais, e a violência doméstica. Não foi encontrada relação significativa entre transtornos do neurodesenvolvimento e violência doméstica. Conclusões: esses achados mostram uma população social e economicamente vulnerável, pais com baixa escolaridade, uso de pasta base de cocaína durante a gravidez em porcentagem superior ao reportado a nível nacional, e 15% de crianças/adolescentes expostos à violência doméstica, mas com um alto número de controles de saúde. A maior fortaleza encontrada por este estudo é a importância de manter um bom vínculo com essas famílias, que demonstraram alto nível de comprometimento com o centro de saúde. Isso nos leva a priorizar a prevenção e promoção da saúde como ferramentas valiosas para a aquisição de saúde de qualidade para essas crianças/adolescentes. Novos estudos, com outras metodologias, serão necessários para poder analisar essas variáveis encontradas.

Huddling with families after disaster: Human resilience and social disparity.

Disasters, from hurricanes to pandemics, tremendously impact human lives and behaviors. Physical closeness to family post-disaster plays a critical role in mental healing and societal sustainability. Nonetheless, little is known about whether and how family colocation alters after a disaster, a topic of immense importance to a post-disaster society. We analyze 1 billion records of population-scale, granular, individual-level mobile location data to quantify family colocation, and examine the magnitude, dynamics, and socioeconomic heterogeneity of the shift in family colocation from the pre- to post-disaster period. Leveraging Hurricane Florence as a natural experiment, and Geographic Information System (GIS), machine learning, and statistical methods to investigate the shift across the landfall (treated) city of Wilmington, three partially treated cites on the hurricane's path, and two control cities off the path, we uncover dramatic (18.9%), widespread (even among the partially treated cities), and enduring (over at least 3 months) escalations in family colocation. These findings reveal the powerful psychological and behavioral impacts of the disaster upon the broader populations, and simultaneously remarkable human resilience via behavioral adaptations during disastrous times. Importantly, the disaster created a gap across socioeconomic groups non-existent beforehand, with the disadvantaged displaying weaker lifts in family colocation. This sheds important lights on policy making and policy communication to promote sustainable family colocation, healthy coping strategies against traumatic experiences, social parity, and societal recovery.

Interprofessional Collaborative Practice Improves Access to Care and Healthcare Quality to Advance Health Equity.

ABSTRACT: Healthcare disparites exist in cardiovascular care, including heart failure. Care that is not equitable can lead to higher incidence of heart failure, increased readmissions, and poorer outcomes. The Heart Failure Transitional Care Services for Adults Clinic is an interprofessional collaborative practice that provides guideline-directed medical therapy and education to underserved patients with heart failure. Little is known regarding healthcare equity and quality metrics in relation to interprofessional teams. Thus, the purpose of this study was to examine if an interprofessional collaborative practice care delivery model can affect access to care and healthcare quality outcomes in underserved patients with heart failure. As evidenced by control charts over a two and a half year period, the Heart Failure Transitional Care Services for Adults Clinic was able to show improvements in access to care and quality metrics results without variation. An interprofessional collaborative practice can be an effective delivery model to address health equity and quality of care outcomes.

Medical avoidance among marginalized groups: the impact of the COVID-19 pandemic.

Medical avoidance is common among U.S. adults, and may be emphasized among members of marginalized communities due to discrimination concerns. In the current study, we investigated whether this disparity in avoidance was maintained or exacerbated during the onset of the COVID-19 pandemic. We assessed the likelihood of avoiding medical care due to general-, discrimination-, and COVID-19-related concerns in an online sample (N = 471). As hypothesized, marginalized groups (i.e., non-White race, Latinx/e ethnicity, non-heterosexual sexual orientation, high BMI) endorsed more general- and discrimination-related medical avoidance than majoritized groups. However, marginalized groups were equally likely to seek COVID-19 treatment as majoritized groups. Implications for reducing medical avoidance among marginalized groups are discussed.

Assessment of a Crisis Standards of Care Scoring System for Resource Prioritization and Estimated Excess Mortality by Race, Ethnicity, and Socially Vulnerable Area During a Regional Surge in COVID-19.

Importance: Crisis standards of care (CSOC) scores designed to allocate scarce resources during the COVID-19 pandemic could exacerbate racial disparities in health care. Objective: To analyze the association of a CSOC scoring system with resource prioritization and estimated excess mortality by race, ethnicity, and residence in a socially vulnerable area. Design, Setting, and Participants: This retrospective cohort analysis included adult patients in the intensive care unit during a regional COVID-19 surge from April 13 to May 22, 2020, at 6 hospitals in a health care network in greater Boston, Massachusetts. Participants were scored by acute severity of illness using the Sequential Organ Failure Assessment score and chronic severity of illness using comorbidity and life expectancy scores, and only participants with complete scores were included. The score was ordinal, with cutoff points suggested by the Massachusetts guidelines. Exposures: Race, ethnicity, Social Vulnerability Index. Main Outcomes and Measures: The primary outcome was proportion of patients in the lowest priority score category stratified by self-reported race. Secondary outcomes were discrimination and calibration of the score overall and by race, ethnicity, and neighborhood Social Vulnerability Index. Projected excess deaths were modeled by race, using the priority scoring system and a random lottery. Results: Of 608 patients in the intensive care unit during the study period, 498 had complete data and were included in the analysis; this population had a median (IQR) age of 67 (56-75) years, 191 (38.4%) female participants, 79 (15.9%) Black participants, and 225 patients (45.7%) with COVID-19. The area under the receiver operating characteristic curve for the priority score was 0.79 and was similar across racial groups. Black patients were more likely than others to be in the lowest priority group (12 [15.2%] vs 34 [8.1%]; P = .046). In an exploratory simulation model using the score for ventilator allocation, with only those in the highest priority group receiving ventilators, there were 43.9% excess deaths among Black patients (18 of 41 patients) and 28.6% (58 of 203 patients among all others (P = .05); when the highest and intermediate priority groups received ventilators, there were 4.9% (2 of 41 patients) excess deaths among Black patients and 3.0% (6 of 203) among all others (P = .53). A random lottery resulted in more excess deaths than the score. Conclusions and Relevance: In this study, a CSOC priority score resulted in lower prioritization of Black patients to receive scarce resources. A model using a random lottery resulted in more estimated excess deaths overall without improving equity by race. CSOC policies must be evaluated for their potential association with racial disparities in health care.

Sexual Victimization, Self-Efficacy to Refuse Sex While Drinking, and Regretting Alcohol-Involved Sex among Underserved Youth in Kampala, Uganda.

The purposes of this study were to determine whether youth who have experienced sexual victimization (SV) have lower self-efficacy to refuse sex and to identify intervention strategies for rape survivors to mitigate further health-risks and harm. Cross-sectional data from the 2014 Kampala Youth Survey (n = 1134) of youth aged 12 to 18 years recruited from Uganda Youth Development Link drop-in centers were used to conduct the analyses. Multivariable statistics were computed to determine the correlates (i.e., sex, education, homelessness, problem drinking, and SV) for (1) self-efficacy to refuse sex, (2) self-efficacy to refuse sex while drinking, and (3) regretting sex due to alcohol use. Among participants, 16.9% reported SV (79% were female and 21% were male). In the final adjusted model, self-efficacy to refuse sex while drinking was only associated with homelessness (OR: 0.52; 95% CI: 0.36, 0.74). Previous SV was not associated with lower self-reports of self-efficacy to refuse sex compared to those who had not experienced SV. Additionally, SV was not associated with increased reports of regrets for sex attributed to alcohol use. Alcohol prevention strategies for the most at-risk youth, including homeless youth, are warranted to improve self-efficacy to refuse sex among youth living in the slums of Kampala.

Challenges in providing special care dentistry during COVID-19 pandemic: a survey of public dental care services in Italy.

BACKGROUND: The aim of this paper was to assess COVID-19 pandemic impact over the public health care services (HCS) involved in special care dentistry (SCD). METHODS: Customized questionnaire was sent to 45 HCS involved in SCD. Healthcare personnel (HP) on duty, safety of HCS, time of suspension and reduction of routine dental practice in special needs patients (SNP), kind of SNP mostly penalized during pre-COVID period/T1, lockdown (phase 1/T2) and post pandemic reopening (phase 2/T3) were analyzed by statistical means (P<0.05). RESULTS: 21 questionnaires were returned. A significant decrease of median number of HP during T2 was observed. Prevalence of COVID-19 infection among HP was not significantly different between T2 vs. T3. Medical surveillance of HP during T2 was significantly lower than during T3. Patients with lack of cooperation were the most disadvantaged during both phases dental procedures were significantly lower between T1 and T2 and between T1 and T3 as well. Patients with lack of cooperation and/or living in residential care homes were the most disadvantaged in relation to access to dental care during both phases. CONCLUSIONS: COVID-19 pandemic determined significant restrictions in daily access to routine oral care resulting in reduction of preventive evaluations and decline of oral health in a population which is already at a higher risk of oral pathologies. Our data reveal that reduction of dental procedures, healthcare professionals and days of suspension of clinical activity were still considerable also in T3 with respect to T1 and in some cases not significantly different from T2.

Physician Specialties Involved in Thyroid Cancer Diagnosis and Treatment: Implications for Improving Health Care Disparities.

CONTEXT: Little is known about provider specialties involved in thyroid cancer diagnosis and management. OBJECTIVE: Characterize providers involved in diagnosing and treating thyroid cancer. DESIGN/SETTING/PARTICIPANTS: We surveyed patients with differentiated thyroid cancer from the Georgia and Los Angeles County Surveillance, Epidemiology and End Results registries (N = 2632, 63% response rate). Patients identified their primary care physicians (PCPs), who were also surveyed (N = 162, 56% response rate). MAIN OUTCOME MEASURES: (1) Patient-reported provider involvement (endocrinologist, surgeon, PCP) at diagnosis and treatment; (2) PCP-reported involvement (more vs less) and comfort (more vs less) with discussing diagnosis and treatment. RESULTS: Among thyroid cancer patients, 40.6% reported being informed of their diagnosis by their surgeon, 37.9% by their endocrinologist, and 13.5% by their PCP. Patients reported discussing their treatment with their surgeon (71.7%), endocrinologist (69.6%), and PCP (33.3%). Physician specialty involvement in diagnosis and treatment varied by patient race/ethnicity and age. For example, Hispanic patients (vs non-Hispanic White) were more likely to report their PCP informed them of their diagnosis (odds ratio [OR]: 1.68; 95% CI, 1.24-2.27). Patients ≥65 years (vs <45 years) were more likely to discuss treatment with their PCP (OR: 1.59; 95% CI, 1.22-2.08). Although 74% of PCPs reported discussing their patients' diagnosis and 62% their treatment, only 66% and 48%, respectively, were comfortable doing so. CONCLUSIONS: PCPs were involved in thyroid cancer diagnosis and treatment, and their involvement was greater among older patients and patients of minority race/ethnicity. This suggests an opportunity to leverage PCP involvement in thyroid cancer management to improve health and quality of care outcomes for vulnerable patients.