Prevalência e fatores associados à realização dos exames de triagem neonatal no Brasil: comparação da PNS 2013 e 2019 / Prevalence of neonatal screening and associated factors in Brazil: a comparison of the 2013 and 2019 National Health Surveys

Resumo Analisou-se a prevalência e fatores associados à realização da Triagem Neonatal Completa (TNC) entre crianças (<2 anos de idade) no Brasil incluídas na Pesquisa Nacional Saúde 2013 (n=4.442) e 2019 (n=5.643). Estudo transversal comparou as estimativas de prevalência e intervalos de confiança de 95% (IC95%) da TNC (testes do olhinho, orelhinha e pezinho). Diferenças foram consideradas estatisticamente significante ao nível de 5%. Regressões de Poisson bruta e ajustada foram realizadas para estimar Razões de Prevalência (RP) e IC95% para a associação das variáveis socioeconômicas, demográficas e de saúde com a TNC. Verificou-se aumento estatisticamente significante da TNC: 67,4% (IC95%: 65,5-69,3) em 2019, ante 49,2% (IC95%: 47,1-51,3) em 2013. Porém, ainda existem desigualdades e defasagens entre os estados da federação e variáveis sociodemográficas. Entre os anos, a TNC foi menor nas crianças de cor/raça parda e preta, dos três piores quintis de renda, sem plano de saúde, cadastradas na Estratégia de Saúde da Família, da região norte, de cidades do interior e da zona rural do Brasil. Apesar de o aumento da prevalência de TNC, desigualdades e defasagens individuais e contextuais permaneceram, indicando os desafios das políticas de saúde.

Abstract This study analyzed the prevalence of complete neonatal screening (CNS) of children aged under 2 years in Brazil and associated factors using data from the 2013 (n=4,442) and 2019 (n=5,643) national health surveys. We conducted a cross-sectional study to compare prevalence of CNS (eye, ear and heel prick tests) adopting 95% confidence intervals (95%CI) and a 5% significance level. Crude and adjusted Poisson regression was performed to estimate prevalence ratios (PR) and 95%CI to assess the association between socioeconomic, demographic and health variables and CNS. There was a statistically significant increase in CNS prevalence, from 49.2% (95%CI: 47.1-51.3) in 2013 to 67.4% (95%CI: 65.5-69.3) in 2019. However, large disparities persist across states and between sociodemographic groups. In both years, CNS prevalence was lowest among brown and black children, those from families in the three lowest income quintiles, children without health insurance, those from families registered in the Family Health Strategy and children living in the North, cities outside the state capital/metropolitan regions and rural areas. Despite the increase in prevalence of CNS, deep individual and contextual inequalities persist, posing challenges for health policies.

The newborn screening tests in Brazil: regional and socioeconomic prevalence and inequalities in 2013 and 2019

Abstract Objective: To analyze the prevalence evolution of Guthrie, hearing, and eye screening testing among newborns in Brazil, between 2013 and 2019, according to demographic and socioeconomic characteristics. Methods: This is a cross-sectional study with data from 5231 infants from the Pesquisa Nacional de Saude (PNS), in 2013, and 6637 infants, in 2019, for the Guthrie test, hearing, and red reflex tests. The authors analyzed the outcomes according to the region of residence, self-reported color/race, having health insurance, and per capita household income. By using bivariate and multivariate Poisson regression models, the prevalence ratios and their respective 95 % Confidence Intervals (CI95%) were calculated for each year. Results: In 2013, Guthrie test, hearing, and red reflex tests were performed in 96.5 % (95%CI 95,8;97,0), 65.8 % (95%CI 63,9;67,7), and 60.4 % (95%CI 58,5;62,3) of infants, respectively. In 2019, the prevalence was 97.8 % (95%CI 97,3;98,2) in the Guthrie test, 81.6 % (95%CI 80,3;82,9) in the hearing test, and 78.6 % (95%CI 77,1;79,9) in the red reflex test. The testing frequency was higher among residents of the Southeast and South regions of Brazil, among infants whose mother or guardian was white, had health insurance, and was in the higher income strata; and the most evident differences were in the eye and hearing testing. Conclusions: The coverage inequalities according to the region of residence, income, and having health insurance highlight the need to use strategies that enable exams to be carried out, with more information about their importance, encompassing actions from primary care, prenatal care to the puerperium, aiming at universal access and equity.

Tendência temporal da incompletude do registro da raça/cor nos sistemas de informação em saúde do Brasil, 2009-2018 / Incomplete recording of race/colour in health information systems in Brazil: time trend, 2009-2018

Resumo Propõe-se avaliar a incompletude e a tendência temporal do preenchimento do campo raça/cor das doenças e agravos mais prevalentes na população negra nos Sistemas de Informação em Saúde do Brasil, 2009-2018. Trata-se de estudo ecológico de tendência temporal e múltiplos grupos. Foi adotada a classificação de Romero e Cunha (2006) para análise da incompletude e utilizados dados secundários do Sistema Nacional de Agravos de Notificação, Sistema de Informações Hospitalares e Sistema de Informações sobre Mortalidade do Brasil e regiões brasileiras, calculada a proporção de subnotificação e a tendência temporal, utilizando o modelo de regressão linear simples, com correção Prais-Winsten (p-valor<0,05). Excetuando-se os registros de mortalidade por causas externas (excelente), tuberculose (bom) e mortalidade infantil (regular), todos os registros apresentaram escore ruim. Observou-se tendência decrescente da proporção de incompletude. A análise por região mostrou que as maiores médias de incompletude foram registradas na região Norte (30,5%), Nordeste (33,3%) e Centro-Oeste (33,0%). As regiões Sudeste e Nordeste foram as que mais apresentaram tendência decrescente. Os resultados visam ampliar a visibilidade acerca das implicações do preenchimento do campo raça/cor para a equidade em saúde.

Abstract This ecological study of time trends and multiple groups evaluated incompleteness in the race/colour field of Brazilian health information system records and the related time trend, 2009-2018, for the diseases and disorders most prevalent in the black population. The Romero and Cunha (2006) classification was applied in order to examine incompleteness using secondary data from Brazil's National Notifiable Diseases System, Hospital Information System and Mortality Information System, by administrative regions of Brazil, while percentage underreporting and time trend were calculated using simple linear regression models with Prais-Winsten correction (p-value<0.05). All records scored poorly except those for mortality from external causes (excellent), tuberculosis (good) and infant mortality (fair). An overall downward trend was observed in percentage incompleteness. Analysis by region found highest mean incompleteness in the North (30.5%), Northeast (33.3%) and Midwest (33.0%) regions. The Southeast and Northeast regions showed the strongest downward trends. The findings intended to increase visibility on the implications of the race/color field for health equity.

Racial and ethnic disparities in premature births among pregnant women in the NISAMI cohort, Brazil / Disparidades étnicas e raciais nos partos prematuros entre gestantes da coorte NISAMI, Brasil

Abstract The incidence of premature birth has increased worldwide, unequally distributed by race/ethnicity. Racism generates economic inequalities, educational disparities, and differential access to health care, which increases the risk of preterm birth. Thus, this study aimed to evaluate the factors associated with preterm birth and racial and ethnic disparities in premature birth among pregnant women attending prenatal care at the Brazilian Unified Health System health units in the urban area of Santo Antônio de Jesus, Bahia, Brazil. This study used data from 938 pregnant women aged between 18 to 45 years within the NISAMI prospective cohort. Premature birth prevalence was 11.8%, with a higher prevalence among black than non-black women (12.9% versus 6.0%, respectively). Maternal age between 18 and 24 years was the only factor associated with premature birth. A higher risk of premature birth was found among black women than non-black women (RR 3.22; 95%CI 1.42-7.32). These results reveal the existence of racial and social inequalities in the occurrence of premature birth.

Resumo A incidência de parto prematuro tem aumentado em todo o mundo, distribuída de forma desigual por raça/etnia. O racismo gera desigualdades econômicas, disparidades educacionais e acesso diferenciado à saúde, o que aumenta o risco de parto prematuro. Assim, este estudo teve como objetivo avaliar os fatores associados à prematuridade e disparidades raciais e étnicas no parto prematuro entre gestantes atendidas durante o pré-natal em unidades de saúde do Sistema Único de Saúde na zona urbana de Santo Antônio de Jesus, Bahia, Brasil. Este estudo utilizou dados de 938 mulheres grávidas com idade entre 18 e 45 anos dentro da coorte prospectiva do NISAMI. A prevalência de prematuridade foi de 11,8%, sendo maior entre as negras do que entre as não negras (12,9% versus 6,0%, respectivamente). A idade materna entre 18 e 24 anos foi o único fator associado ao parto prematuro. Foi encontrado maior risco de prematuridade entre as mulheres negras do que entre as não negras (RR 3,22; IC95% 1,42-7,32). Esses resultados revelam a existência de desigualdades raciais e sociais na ocorrência do parto prematuro.

Characterization of the patterns of care, access, and direct cost of systemic lupus erythematosus in Brazil: findings from the Macunaíma study

Abstract Background A cost of illness (COI) study aims to evaluate the socioeconomic burden that an illness imposes on society as a whole. This study aimed to describe the resources used, patterns of care, direct cost, and loss of productivity due to systemic lupus erythematosus (SLE) in Brazil. Methods This 12-month, cross-sectional, COI study of patients with SLE (ACR 1997 Classification Criteria) collected data using patient interviews (questionnaires) and medical records, covering: SLE profile, resources used, morbidities, quality of life (12-Item Short Form Survey, SF-12), and loss of productivity. Patients were excluded if they were retired or on sick leave for another illness. Direct resources included health-related (consultations, tests, medications, hospitalization) or non-health-related (transportation, home adaptation, expenditure on caregivers) hospital resources. Costs were calculated using the unit value of each resource and the quantity consumed. A gamma regression model explored cost predictors for patients with SLE. Results Overall, 300 patients with SLE were included (92.3% female, mean [standard deviation (SD)] disease duration 11.8 [7.9] years), of which 100 patients (33.3%) were on SLE-related sick leave and 46 patients (15.3%) had stopped schooling. Mean (SD) travel time from home to a care facility was 4.4 (12.6) hours. Antimalarials were the most commonly used drugs (222 [74.0%]). A negative correlation was observed between SF-12 physical component and SLE Disease Activity Index (- 0.117, p = 0.042), Systemic Lupus International CollaboratingClinics/AmericanCollegeofRheumatology Damage Index (- 0.115, p = 0.046), medications/day for multiple co-morbidities (- 0.272, p < 0.001), SLE-specific drugs/day (- 0.113, p = 0.051), and lost productivity (- 0.570, p < 0.001). For the mental component, a negative correlation was observed with medications/day for multiple co-morbidities (- 0.272, p < 0.001), SLE-specific medications/day (- 0.113, p = 0.051), and missed appointments (- 0.232, p < 0.001). Mean total SLE cost was US$3,123.53/patient/year (median [interquartile range (IQR)] US$1,618.51 [$678.66, $4,601.29]). Main expenditure was medication, with a median (IQR) cost of US$910.62 ($460, $4,033.51). Mycophenolate increased costs by 3.664 times (p < 0.001), and inflammatory monitoring (erythrocyte sedimentation rate or C-reactive protein) reduced expenditure by 0.381 times (p < 0.001). Conclusion These results allowed access to care patterns, the median cost for patients with SLE in Brazil, and the differences across regions driven by biological, social, and behavioral factors. The cost of SLE provides an updated setting to support the decision-making process across the country.

Social inequalities in indicators of use of healthcare services by adolescents in Campinas, São Paulo, Brazil / Desigualdades sociais em indicadores de uso de serviços de saúde por adolescentes de Campinas, São Paulo, Brasil / Desigualdades sociales en indicadores de uso de servicios de salud por adolescentes de Campinas, São Paulo, Brasil

Abstract: This study aimed to analyze the prevalence of indicators of use of healthcare services according to sex, income and race/skin color, in adolescents (aged 10-19 years old) based on data from the Health Survey of the Municipality of Campinas (ISACamp), carried out in 2014/2015 in Campinas, São Paulo, Brazil. The chi-square test was used to evaluate the differences between the outcome variables (indicators of use of healthcare service) and sex, income and race/skin color. Adjusted prevalence ratios (PR) were estimated using Poisson multiple regression models. The demand for medical care was high in the last year of the interview (79.2%), mostly attended by the Brazilian Unified National Health System (65.2%), with routine consultations being more prevalent for females (PR = 1.17; 95%CI: 1.01-1.34) and injury for the male population (PR = 0.47; 95%CI: 0.26-0.84). Economic and racial differences were found in the evaluation of the last medical consultation, with a higher prevalence of worse care among those with lower income (PR = 1.46; 95%CI: 1.14-1.87) and black people (PR = 1.27; 95%CI: 1.01-1.61). Inequalities remained for delay or failure to carry out exams (PR = 1.64; 95%CI: 1.02-2.64) and worse quality of dental care (PR = 2.10; 95%CI: 1.38-3.21) in those with lower income. Also, black people had fewer appointments with dentists (PR = 0.90; 95%CI: 0.82-0.99).

Resumo: O estudo objetivou estimar a prevalência dos indicadores de uso de serviços de saúde de acordo com sexo, renda e etnia/cor da pele entre adolescentes (10 a 19 anos) com base nos dados do Inquérito de Saúde no Município de Campinas (ISACamp), realizada em 2014/2015 em Campinas, São Paulo, Brasil. O teste qui-quadrado foi utilizado para avaliar as diferenças entre as variáveis de desfecho (indicadores de utilização de serviços de saúde) e sexo, renda e etnia/cor da pele. As razões de prevalência (RP) ajustadas foram estimadas por meio de modelos de regressão múltipla de Poisson. A demanda por atendimentos médicos foi elevada no último ano da entrevista (79,2%), atendidos majoritariamente pelo Sistema Único de Saúde (65,2%), sendo as consultas de rotina mais prevalentes no sexo feminino (RP = 1,17; IC95%: 1,01-1,34) e lesão na população masculina (RP = 0,47; IC95%: 0,26-0,84). Diferenças econômicas e raciais foram encontradas na avaliação da última consulta médica, com maior prevalência de pior atendimento entre aqueles com menor renda (RP = 1,46; IC95%: 1,14-1,87) e negros (RP = 1,27; IC95%: 1,01-1,61). Desigualdades permaneceram em termos de atraso ou falha na realização de exames (RP = 1,64; IC95%: 1,02-2,64) e pior qualidade do atendimento odontológico (RP = 2,10; IC95%: 1,38-3,21) naqueles com menor renda. E os negros consultaram menos os serviços de dentistas (RP = 0,90; IC95%: 0,82-0,99).

Resumen: El objetivo de este estudio fue estimar la prevalencia de los indicadores de uso de servicios de salud según el sexo, ingresos y etnia/color de la piel entre adolescentes (10 a 19 años) basado en los datos de la Encuesta de Salud de la Ciudad de Campinas (ISACamp), realizada entre 2014 y 2015 en Campinas, São Paulo, Brasil. Se utilizó la prueba de chi-cuadrado para evaluar las diferencias entre las variables de resultado (indicadores de uso de servicios de salud) y sexo, ingresos y etnia/color de la piel. Se estimaron las razones de prevalencia (RP) ajustadas a través de modelos de regresión múltiple de Poisson. La demanda de atención médica fue alta en el último año de la entrevista (el 79,2%), mayoritariamente asistidos por el Sistema Único de Salud (el 65,2%), con las consultas de rutina más frecuentes para el sexo femenino (RP = 1,17; IC95%: 1,01-1,34) y la atención por lesiones más frecuentes para la población masculina (RP = 0,47; IC95%: 0,26-0,84). Se encontraron diferencias económicas y raciales en la evaluación de la última consulta médica, con mayor prevalencia de peor atención entre aquellos con menores ingresos (RP = 1,46; IC95%: 1,14-1,87) y personas negras (RP = 1,27; IC95%: 1,01-1,61). Las desigualdades persistieron en términos de retraso o no realización de exámenes (RP = 1,64; IC95%: 1,02-2,64) y peor calidad de la atención odontológica (RP = 2,10; IC95%: 1,38-3,21) en aquellos con menores ingresos. Y las personas negras fueron las que menos consultaron los servicios de dentistas (RP = 0,90; IC95%: 0,82-0,99).

A carne mais barata do mercado é a carne negra: notas sobre o racismo e a violência obstétrica contra mulheres negras / The cheapest meat on the market is black meat: notes on racism and obstetric violence against Black women

Resumo O presente ensaio tem o intuito de problematizar as iniquidades em saúde, a partir da análise da violência obstétrica direcionada às mulheres negras. Pressupomos que o racismo institucional é chave interpretativa importante para compreender a dinâmica de violências raciais. Adotamos como metodologia, para evidenciar o racismo enfrentado cotidianamente por mulheres negras nos serviços de saúde, a análise descritiva de duas reportagens publicadas no site do G1. Constatamos que o racismo é (re)produtor de negação de direitos, do não acesso aos serviços de saúde, da produção da morte e da não efetivação do Bem Viver para as famílias negras, e isso vem sendo colocado através da produção e reprodução do sofrimento, da violência e do racismo em suas mais diversas expressões. Nessa dinâmica, a efetivação da Política Nacional de Saúde Integral da população negra é mecanismo importante de enfrentamento ao racismo em saúde.

Abstract This essay debates health inequalities by analyzing obstetric violence directed at Black women. We assume that institutional racism is an important interpretive key to understanding the dynamics of racial violence. We adopted the descriptive analysis of two stories published on the G1 website as a methodology to highlight the racism faced daily by Black women in health services. We found that racism (re)produces the denial of rights, non-access to health services, production of death, and non-realization of Good Living for Black families, and this is evidenced by producing and reproducing suffering, violence, and racism in its most diverse expressions. In this dynamic, implementing the National Comprehensive Health Policy for the Black population is an important mechanism for confronting racism in health.

Sobrepeso y obesidad en Chile: Consideraciones para su abordaje en un contexto de inequidad social

Con 3 de cada 4 personas viviendo con sobrepeso u obesidad, la prevalencia de IMC elevado en Chile es de las más altas del continente, mostrando un patrón de distribución inequitativo mediado por determinantes estructurales que modelan el comportamiento en salud (seguridad social, nivel socioeconómico, educación, género, entre otros). Las características socioeconómicas del país, nación de ingresos altos con marcada inequidad, son poco comunes y representan un desafío adicional a la hora de diseñar intervenciones en salud. Una alta concentración de riqueza permite ser clasificado como país de ingresos altos aun cuando la mayor parte de la población pertenecería a una clase social vulnerable, cuyos ingresos se ven acompañados de recursos sociales y simbólicos que dificultan doblemente la adopción de un "estilo de vida" saludable. A pesar de las múltiples estrategias nutricionales implementadas, la prevalencia de sobrepeso y obesidad continúa en aumento. Se postula como gran responsable al insistente uso de modelos basados en elección y responsabilidad individual, que buscan modificar factores de riesgo conductuales (sedentarismo y alta ingesta calórica) sin neutralizar los determinantes estructurales que predisponen esa conducta. Favorablemente, la última Política Nacional de Nutrición reconoce la "determinación social de la alimentación", representando un cambio de paradigma que confiere cierto optimismo y cuya eficacia deberá ser evaluada en los próximos años.

With 3 out of 4 people living with overweight or obesity, the national prevalence of high BMI is among the highest on the continent, thus showing an inequitable distribution pattern mediated by structural determinants that shape health behavior (social security, socioeconomic status, education, gender, among others). The socioeconomic features of the country, a high-income nation with marked inequity, are unusual and represent an additional challenge when designing health interventions. A high concentration of wealth allows it to be classified as a high-income country even though most of the population would belong to a vulnerable social class, whose income is accompanied by social and symbolic resources that make it doubly challenging to adopt a healthy "lifestyle". Despite the multiple nutritional strategies implemented, the prevalence of overweight and obesity continues to increase. The insistent use of models based on individual choice and responsibility, which seek to modify behavioral risk factors (sedentary lifestyle and high caloric intake) without neutralizing the structural determinants predisposing this behavior, is postulated as highly responsible. Favorably, the latest National Nutrition Policy recognizes the "social determination of food", representing a paradigm shift that confers some optimism and whose effectiveness has to be evaluated in the coming years.

A hipótese da equidade inversa na implementação do NASF-AB em municípios do Sul do Brasil / The inverse equity hypothesis in the implementation of NASF-AB in municipalities of Southern Brazil

Resumo O objetivo foi verificar a evolução da implementação do Núcleo Ampliado de Saúde da Família e Atenção Básica (NASF-AB) nos municípios da região Sul do Brasil, de 2008 a 2019, sob à luz da hipótese da equidade inversa. Estudo ecológico considerando 1.188 municípios do Sul do Brasil. As análises foram separadas por estado, com os municípios divididos em quartis de Índice de Desenvolvimento Humano Municipal - Renda. Foi calculado o percentual acumulativo de implementação do NASF-AB no período e a desigualdade entre Q1 (mais rico) e Q4 (mais pobre) verificada por medidas de desigualdade absoluta e relativa. No Paraná o Q1 apresentou maior cobertura do NASF-AB do que o Q4 e, apesar da desigualdade ter reduzido ao final do período, ainda estava bem demarcada, seguindo padrão "top inequality". Em Santa Catarina ocorreu o que prevê a hipótese, com aumento das desigualdades no início e posterior redução quando já existia NASF-AB em cerca de 90% dos municípios do Q1, caracterizando "botton inequality". No Rio Grande do Sul a hipótese foi refutada ao observar, a partir de 2014, maior implementação no Q4 em relação ao Q1.

Abstract The present study aimed to analyze the evolution of the implementation of Family Health and Primary Health Care Expanded Support Centers (NASF-AB, in Portuguese) in the municipalities of Southern Brazil, from 2008 to 2019, in light of the inverse equity hypothesis. This was an ecological study, considering 1,188 municipalities of Southern Brazil. The analyses were separated by state, with municipalities divided into quartiles of Municipal Human Development Index - Income (MHDI-Income). Our study calculated the cumulative percentage of the implementation of NASF-AB within the given period and the inequality between Q1 (richest) and Q4 (poorest), assessed by the absolute and relative inequality measures. In Paraná, Q1 presented a higher coverage of NASF-AB than did Q4, and, although the inequality had decreased at the end of the period, it was still quite distinct, according to the "top inequality" pattern. In Santa Catarina, the predictions of the hypothesis were confirmed, with inequalities found in the beginning of the period and a near 90% decline once NASF-AB had been implemented in the municipalities of Q1, characterizing the "bottom inequality" pattern. In Rio Grande do Sul, the hypothesis was refuted observing that since 2014 there was a greater implementation in Q4 as compared to Q1 was observed.

Desigualdades en la mortalidad por diabetes en México: 2010-2019 / Inequalities in diabetes mortality in Mexico: 2010-2019

Resumen Antecedentes: Se ha demostrado que el impacto de la diabetes mellitus se expresa de manera diferenciada entre los grupos sociales. Objetivo: Estimar las brechas en la desigualdad en la mortalidad por diabetes mellitus a través de medidas absolutas y relativas según distribución geográfica y condiciones sociales. Material y métodos: Se analizaron las muertes registradas en México por diabetes mellitus entre 2010 y 2019 y se calcularon las mediciones de desigualdad a nivel estatal por sexo. Resultados: La tasa de mortalidad nacional por diabetes mellitus ajustada por edad mostró un incremento durante el periodo estudiado. Conclusión: Las desigualdades presentes en la mortalidad por diabetes deben considerarse para el diseño de estrategias de salud.

Abstract Background: The impact of diabetes mellitus has been shown to be differentially expressed between social groups. Objective: To estimate inequality gaps in diabetes mellitus mortality through absolute and relative measures according to geographic distribution and social conditions. Material and methods: Diabetes mellitus-related deaths recorded in Mexico between 2010 and 2019 were analyzed, and inequality measurements at the state level were calculated by gender. Results: National age-adjusted diabetes mellitus mortality rate showed an increase during the study period. Conclusion: The inequalities present in diabetes mortality should be considered for the design of health strategies.

Fatores associados à incidência e à piora do problema de coluna durante a primeira onda da COVID-19 no Brasil / Factors associated with the incidence and worsening of back pain during the first wave of COVID-19 in Brazil

Resumo O artigo tem como objetivo estimar a incidência e o agravamento do problema de coluna (PC) durante a primeira onda da COVID-19 no Brasil, bem como investigar os fatores demográficos, socioeconômicos e as mudanças nas condições de vida associadas. Utilizou-se a ConVid - Pesquisa de Comportamentos, realizada entre abril e maio de 2020, como fonte de dados. Estimou-se o número e a distribuição dos entrevistados que desenvolveram PC e a dos que tiveram agravamento no problema preexistente, seus intervalos de 95% de confiança e o teste qui-quadrado de Pearson. Estimou-se também a razão de chance de desenvolver PC ou ter piora de problema preexistente por meio de modelos de regressão logística múltipla. O PC preexistente foi reportado por 33,9% (IC95% 32,5-35,3) dos entrevistados e mais da metade (54,4%; IC95% 51,9-56,9) teve piora do quadro. A incidência cumulativa de PC na primeira onda da pandemia foi de 40,9% (IC95% 39,2-42,7). Ser mulher, o aumento percebido do trabalho doméstico e o sentimento frequente de tristeza ou depressão foram associados a ambos os desfechos. Os fatores socioeconômicos não foram associados a nenhum dos desfechos. A alta incidência e agravamento do PC durante a primeira onda revelam a necessidade de estudos em períodos mais recentes, dada a longa duração da pandemia.

Abstract The article aims to estimate the incidence and worsening of back pain (BP) during the first wave of COVID-19 in Brazil, as well as to investigate demographic, socioeconomic factors and associated changes in living conditions. ConVid - Behavior Research, applied between April and May 2020, was used as data source. The number and distribution of respondents who developed BP and those who had a worsening of the preexisting problem, their 95% confidence intervals and Pearson's Chi-square test were estimated. The odds ratio of developing BP or worsening a preexisting problem was also estimated using multiple logistic regression models. Pre-existing BP was reported by 33.9% (95%CI 32.5-35.3) of respondents and more than half (54.4%; 95%CI 51.9-56.9) had worsened. The cumulative incidence of BP in the first wave of the pandemic was 40.9% (95%CI 39.2-42.7). Being a woman, the perceived increase in housework and the frequent feeling of sadness or depression were associated with both outcomes. Socioeconomic factors were not associated with any of outcome. The high incidence and worsening of BP during the first wave reveal the need for studies in more recent periods, given the long duration of the pandemic.

Uncovering The Sociological Interpretation of Visual Impairment-Related Inequities and Their Social Determinants in India

Introduction: Determinants of health are divided into four types, such as “Biological-Psychological-Environmental-Social Determinants”. The social determinants of health include gender disparities, economic status, ethnicity, race, geographic isolation, or having a specific health condition. Moreover, the social deter-minants are interdependent and interrelated with one another. There can also be a primary determinant that affects the other determinants. For example, educational level of the patients is associated with knowledge and awareness of eye care and its conditions. However, education might have a different effect than income in should be access of eye care when needed. Methodology: The study is mainly dependent on secondary data analysis. Results: The primary objective of the study is to illustrate the sociological aspects of visual impairment-related inequities and to identify the social determinants of visual impairments and disparities in India. An-other aim of the paper is to present a deeper understanding of how inequities impact the incidence of visual impairment and blindness based on the social determinants of health. The present study adopts the ecological and Commission on Social Determinants of Health (CSDH) framework 2008. We reaffirm the fact that inequi-ties negatively affect the visual impairment and blindness conditions. The national health policies should take into account the social determinants of visual impairment in their policies relating to comprehensive eye care. Social and economic factors are connected with health and welfare; those socio-economic inequalities con-tribute to health inequalities. For reducing the health inequalities around the world, we need effective policy implementation and proper fund pools. Furthermore, committed action on societal determinants of health, sufficient human resources are also necessary to control the health disabilities, include visual impairment

Desigualdades territoriais no financiamento das políticas de educação e de saúde na Espanha e no Brasil / Desigualdades territoriales en la financiación de las políticas de educación y sanidad en España y Brasil / Territorial inequalities in the funding of education and health policies in Spain and Brazil

Resumo O presente artigo compara os modelos e as desigualdades territoriais no financiamento de duas políticas sociais pilares do estado de bem-estar social e com alto grau de descentralização territorial na Espanha e no Brasil: educação e saúde. A análise utiliza bibliografia especializada, legislação nacional e documentos governamentais para descrever as políticas e seus mecanismos de financiamento. Dados fiscais são usados para apresentar os gastos e analisar as desigualdades dos governos subnacionais no financiamento da educação e da saúde nos dois países. A conclusão é que a experiência espanhola apresenta elevado nivelamento de gastos em saúde e educação nas comunidades autônomas do regime comum, com patamares menores de desigualdade que o observado nos estados e municípios brasileiros. O resultado espanhol é decorrente de um processo incremental de aperfeiçoamento do federalismo fiscal, que culminou em um modelo marcado pela priorização e solidariedade territorial no financiamento das políticas sociais. Esse modelo é uma referência para a análise e discussão do caso brasileiro, que configurou seu federalismo fiscal com pouca preocupação em conciliar eficiência e equidade na distribuição dos recursos entre os entes governamentais, mas apresentou avanços importantes em reformas no financiamento da educação e da saúde.

Resumen El artículo compara los modelos y las desigualdades territoriales en la financiación de dos políticas sociales que son pilares del estado de bienestar y con un alto grado de descentralización territorial en España y Brasil: la educación y la sanidad. El análisis utiliza literatura especializada, legislación nacional y documentos gubernamentales para describir las políticas y sus mecanismos de financiación. Los datos fiscales se utilizan para analizar las desigualdades de los gobiernos subnacionales en la financiación de la educación y la sanidad en ambos países. La conclusión es que la experiencia española muestra una alta nivelación del gasto en salud y educación en las comunidades autónomas de régimen común, con niveles de desigualdad inferiores a los observados en los estados y municipios brasileños. El resultado español es fruto de un proceso de mejora y perfeccionamiento del federalismo fiscal que culminó en un modelo marcado por la priorización y la solidaridad territorial en la financiación de las políticas sociales. Este modelo es una referencia para el análisis y la discusión del caso brasileño, que ha configurado su federalismo fiscal con poca preocupación por conciliar la eficiencia y la equidad en la distribución de los recursos entre las entidades gubernamentales, pero que ha presentado importantes avances en las reformas de la financiación de la educación y la sanidad.

Abstract The article compares the patterns and territorial inequalities in the funding of two social policies that are pillars of the welfare state and present a high degree of territorial decentralization in Spain and Brazil: education and health. The analysis uses specialist literature, national legislation and government documents to describe the policies and their financing mechanisms. Fiscal data are used to analyze subnational government inequalities in the funding of education and health in both countries. The conclusion is that the Spanish experience has significantly leveled spending on health and education between the autonomous communities of common regime, with lower levels of inequality than those observed in Brazilian states and municipalities. The Spanish result derives from an incremental process of improvement of the country's fiscal federalism, which culminated in a model marked by prioritization and territorial solidarity in the funding of social policies. This model is reference for the analysis and discussion of the Brazilian case, which has configured its fiscal federalism with little concern for reconciling efficiency and equity in the distribution of resources between subnational governments, but which has presented important advances in the reforms of education and health funding.

Desigualdades en salud en mortalidad perinatal durante el Plan Decenal de Salud Pública 2012-2021. Cauca, Colombia

Objetivo: identificar desigualdades en salud asociadas a la mortalidad perinatal durante el Plan Decenal de Salud Pública 2012-2021 en los 42 municipios del Departamento de Cauca Colombia. Métodos: estudio ecológico que abordó el periodo 2012-2021 a partir de datos de fuentes secundarias procedentes del Departamento Administrativo Nacional de Estadística. La población de estudio fueron mujeres entre los 12 y 49 años residentes en Cauca. Se calcularon desigualdades por rangos y modelos de regresión de acuerdo con el Índice de Desigualdad de la Pendiente, el Índice de Desigualdad Relativa y el Índice de Concentración. Resultados: 42 municipios reportaron 3 110 muertes perinatales. La edad media de las mujeres afectadas fue de 25,3 años con predominio del grupo de 20 a 24 años. La región Pacifico reportó la mayor tasa de mortalidad. La pertenencia étnica, el analfabetismo y el Índice de Pobreza Multidimensional, se asociaron estadísticamente con la mortalidad. Se observó una desigualdad más pronunciada en la tasa de mortalidad perinatal en los municipios con condiciones socioeconómicas más desfavorables. Conclusiones: a pesar de la operacionalización del Plan Decenal de Salud Pública, la mortalidad perinatal en el Cauca continúa siendo un reto en el proceso salud/enfermedad. Existe disparidad en la mortalidad perinatal en relación con el nivel socioeconómico; aunque se ha observado disminución en la desigualdad en el transcurso de los años, aún persisten brechas significativas. Los hallazgos subrayan la necesidad de monitorear y dar cuenta de las desigualdades en salud al diseñar, implementar y evaluar las políticas públicas de prevención de la mortalidad perinatal.

Objective: to identify health inequalities associated with perinatal mortality during the Ten-Year Public Health Plan 2012-2021 in the 42 municipalities of the Department of Cauca, Colombia. Methods: ecological study that addressed the period 2012 - 2021 based on data from secondary sources from the National Administrative Department of Statistics. The study population was women between 12 and 49 years of age residing in Cauca. Rank inequalities and regression models were calculated according to the Slope Inequality Index, the Relative Inequality Index and the Concentration Index. Results: 42 municipalities reported 3 110 perinatal deaths. The mean age of the affected women was 25,3 years with a predominance of the 20-24 years age group. The Pacific region reported the highest mortality rate. Ethnicity, illiteracy and the Multidimensional Poverty Index were statistically associated with mortality. There was greater inequality in perinatal mortality in municipalities with worse socioeconomic status. Conclusions: despite the operationalization of the Ten-Year Public Health Plan, perinatal mortality in Cauca continues to be a challenge in the health/disease process. There is disparity in perinatal mortality in relation to socioeconomic level, and although a decrease in inequality has been observed over the years, significant gaps still persist. The findings underscore the need to monitor and account for health inequalities in the design, implementation and evaluation of public policies to prevent perinatal mortality.

Psicologia, Conselho Federal de Psicologia e covid-19: enfrentamento às desigualdades psicossociais no Brasil / Psychology, FCP, and covid-19: facing the psychosocial inequalities in Brazil / Psicología, Consejo Federal de Psicología y covid-19: enfrentando las desigualdades psicosociales en Brasil

A pandemia da covid-19 impôs transformações no cotidiano mundial, em âmbito micro e macroestrutural. Seu impacto psicológico desestabiliza e evidencia desigualdades e vulnerabilidades psicossociais brasileiras. Configura-se como um estudo de perspectiva crítica, com base na Psicologia Sócio-histórica, com o objetivo de mapear os posicionamentos da Psicologia, vindos de diferentes campos, diante das ações de saúde mental. Para tanto, utiliza-se o site do Conselho Federal de Psicologia para a análise de 62 documentos, que resultaram em dois eixos de produção crítica: 1) a relação da Psicologia com o Conselho Federal de Psicologia; e 2) da Psicologia com a sociedade. Revela-se o abismo social entre segmentos da sociedade brasileira; formas de exclusão da população carcerária; violência doméstica contra as mulheres e as crianças; dificuldades de acesso a estratégias sociais, na educação e na saúde, e de superação dos impasses acirrados com a infecção global pelo novo coronavírus. Conclui-se que a diversidade de públicos, temáticas, áreas de atuação e referenciais teóricos materializa um compromisso crítico e científico da Psicologia.(AU)

The COVID-19 pandemic imposed transformations in the world daily life, at the micro and macrostructural levels. Its psychological impact destabilizes and highlights Brazilian inequalities and psychosocial vulnerabilities. This is a critical perspective study, based in socio-historical Psychology, aiming to map the positions of Psychology, from different fields, in the face of mental health actions. To this end, the Federal Council of Psychology website is utilized to analyze 62 documents, which resulted in two axes of critical production: 1) the relation between Psychology and the Federal Council of Psychology; and 2) Psychology with society. They reveal the social gap between segments of Brazilian society; ways of excluding prison po7pulation; domestic violence against women and children; and difficulties in accessing social strategies, in education and health, and in overcoming impasses aggravated by the global infection by the new coronavirus. In conclusion, the diversity of public, themes, areas of professional performance, and theoretical references materialize Psychology's critical and scientific commitment.(AU)

La pandemia del COVID-19 provocó transformaciones globales en lo cotidiano a nivel micro y macroestructural. Su impacto psicológico desestabiliza y destaca las desigualdades y vulnerabilidades psicosociales en Brasil. Esta es una investigación en la perspectiva crítica, basada en la psicología sociohistórica, con el objetivo de mapear las posiciones de la Psicología, procedentes de diferentes campos, frente a las acciones de salud mental. Para este fin, se utiliza el sitio web del Consejo Federal de Psicología para el análisis de 62 documentos, lo que resultó en dos ejes de producción crítica: 1) la relación de la Psicología con el Consejo Federal de Psicología; y 2) de la Psicología con la sociedad. Se revelan la brecha social entre los segmentos de la sociedad brasileña; las formas de exclusión de la población carcelaria; la violencia doméstica contra las mujeres y los niños; y las dificultades para acceder a las estrategias sociales, en la educación y la salud, para superar los impasses agravados por la infección global por el nuevo coronavirus. Se concluye que la diversidad de públicos, temáticas, áreas de actividad y referentes teóricos materializa un compromiso crítico y científico de la Psicología.(AU)

La Epidemiologia en el marco de la Medicina Social / Epidemiology in the framework of social medicine

El Sector Salud necesita un sistema de vigilancia epidemiológica que genere conocimiento, identifique condiciones de vida lo más local posible en unidades territoriopoblación, tiene que proponer intervenciones para superar las iniquidades y desigualdades, equipos de intervención con alta capacidad científica, técnica y resolutiva en cada Red de Salud, que cada red de salud actúe integralmente con plena participación social y comunitaria, revalorizar desde la epidemiologia a la salud intercultural.

The Health Sector needs an epidemiological surveillance system that generates knowledge, identifies living conditions as locally as possible in territory-population units, must propose interventions to overcome iniquities and inequalities, intervention teams with high scientific, technical and resolution capacity in each health network, that each health network acts integrally with full social and community participation, revaluing intercultural health from epidemiology.

Desigualdades de género y las redes de apoyo social en pacientes con tuberculosis

Las desigualdades de género y las redes de apoyo social relacionadas con la tuberculosis conllevan asimetrías de poder, distintas oportunidades para gozar de salud en unos y aumentar la vulnerabilidad a enfermar en otros. El objetivo de este trabajo fue examinar las desigualdades de género según redes de apoyo social en pacientes con tuberculosis. Se realizó una revisión sistematizada en fuentes de datos digitales como Google Académico, SciELO y PudMed. Para la búsqueda se utilizaron las palabras clave: género, desigualdades, redes de apoyo y tuberculosis. Los resultados se limitaron a artículos científicos de revisión y originales, publicados en idioma español e inglés de los últimos 21 años. Se sostiene que las redes de apoyo ante un episodio mórbido resultan condicionadas por las diferencias, pero, sobre todo, por las desigualdades de género dentro de las estructuras sociales. Se concluye que la mayoría de estudios no vinculó la tuberculosis con el género. Las redes de apoyo social cumplieron con una parte fundamental en el proceso salud-enfermedad de las personas con este padecimiento.

Gender inequalities and social support networks related to tuberculosis lead to power asymmetries, health disparities for some, and increased vulnerability to disease for others. The aim of this study was to examine gender inequalities according to social support networks in patients with tuberculosis. A systematic review was conducted in digital data sources such as Google Scholar, SciELO, and PubMed. The search terms used were: gender, inequalities, support networks, and tuberculosis. The results were limited to review and original research articles, published in Spanish and English in the last 21 years. It is argued that support networks in the face of a morbid episode are conditioned by differences, but above all, by gender inequalities within social structures. It is concluded that most studies have failed to associate tuberculosis with gender. Social support networks played a fundamental role in the health-disease process of people with this disease.

Terapia ocupacional social e justiça social: diálogos a partir das demandas trans / Social occupational therapy and social justice: dialogues based on the demands of trans populations

Resumo A proposta central deste texto é apresentar reflexões balizadas pelo conceito de justiça social para a terapia ocupacional social a partir das demandas trans levantadas por meio de uma pesquisa que, com base na história oral e técnicas etnográficas, objetivou compreender como pessoas trans constroem e/ou mobilizam, ao longo de suas histórias de vida, estratégias de enfrentamento das condições de marginalização vivenciadas em seus cotidianos, configurando determinados modos de vida. Compreender essas histórias aciona um debate importante no campo da justiça social para a terapia ocupacional social que, para nós, dialoga com a ideia de justiça articulada por Nancy Fraser, baseada em uma concepção que mira à redistribuição econômica e ao reconhecimento simbólico. A aposta que fazemos quando utilizamos essa proposição nos parece potente, sobretudo por oferecer, na sua fundamentação, leituras acerca das desigualdades sociais e dos caminhos possíveis de afirmação de existência. Por isso, se a práxis da terapia ocupacional social propõe articular técnica e politicamente o campo social, é necessário o entendimento dos múltiplos modos de vida, sobretudo das contradições que envolvem essas realidades, dentro daquilo que diz da subjetividade, da história, da cultura, das relações políticas, entre outros elementos que desembocam no cotidiano das pessoas, para se pensar/fazer, junto, possibilidades e caminhos de/para se viver melhor, a partir das negociações sociais.

Abstract The main purpose of this text is to present reflections guided by the concept of social justice for social occupational therapy focusing on the demands of trans individuals brought up through research based on oral history and ethnographic techniques that aimed to understand how these people build and/or mobilize, throughout their life histories, strategies to face the conditions of marginalization experienced in their everyday lives, configuring certain ways of life. The understanding of these histories triggers an important debate in the field of social justice for social occupational therapy that, for us, dialogues with the idea of ​​justice developed by Nancy Fraser, based on a conception that aims at economic redistribution and symbolic recognition. We consider that this is a powerful proposition, mainly because its foundation offers readings about social inequalities and possible ways of affirming existence. Therefore, if the praxis of social occupational therapy proposes to combine the social field technically and politically, it is necessary to understand the multiple ways of life, especially the contradictions that involve these realities, including the subjectivity, history, culture, and political relationships, among other elements in the everyday lives of people, to think/do together possibilities and ways to live better, based on social negotiations.

National Vaccine Coverage Survey 2020: methods and operational aspects / Inquérito Nacional de Cobertura Vacinal 2020: métodos e aspectos operacionais

ABSTRACT Objective: The national vaccination coverage survey on full vaccination at 12 and 24 months of age was carried out to investigate drops in coverage as of 2016. Methods: A sample of 37,836 live births from the 2017 or 2018 cohorts living in capital cities, the Federal District, and 12 inner cities with 100 thousand inhabitants were followed for the first 24 months through vaccine record cards. Census tracts stratified according to socioeconomic levels had the same number of children included in each stratum. Coverage for each vaccine, full vaccination at 12 and 24 months and number of doses administered, valid and timely, were calculated. Family, maternal and child factors associated with coverage were surveyed. The reasons for not vaccinating analyzed were: medical contraindications, access difficulties, problems with the program, and vaccine hesitancy. Results: Preliminary results showed that less than 1% of children were not vaccinated, full coverage was less than 75% at all capitals and the Federal District, vaccines requiring more than one dose progressively lost coverage, and there were inequalities among socioeconomic strata, favorable to the highest level in some cities and to the lowest in others. Conclusion: There was an actual reduction in full vaccination in all capitals and the Federal District for children born in 2017 and 2018, showing a deteriorating implementation of the National Immunization Program from 2017 to 2019. The survey did not measure the impacts of the COVID-19 pandemic, which may have further reduced vaccination coverage.

RESUMO Objetivo: Inquérito nacional de cobertura vacinal aos 12 e 24 meses de idade foi realizado para investigar as quedas nas coberturas a partir de 2016. Métodos: Amostra de 37.836 nascidos vivos das coortes de 2017 e 2018 residentes nas capitais, Distrito Federal (DF) e 12 cidades com mais de 100 mil habitantes, acompanhados nos primeiros 24 meses por registros nas cadernetas de vacinação. Setores censitários foram estratificados segundo condições socioeconômicas, e o mesmo número de crianças foi incluído para cada estrato. Calcularem-se coberturas vacinais de cada vacina e coberturas completas aos 12 e 24 meses, doses aplicadas, válidas e oportunas. Fatores familiares, maternos e da criança associados à cobertura foram pesquisados. Os motivos para não vacinar analisados foram: contraindicações médicas, dificuldades de acesso, problemas no funcionamento do programa e hesitação vacinal. Resultados: Os resultados preliminares mostram que menos de 1% das crianças não foram vacinadas, as coberturas pelo esquema completo são menores que 75% em todas as capitais e no DF, as vacinas com mais de uma dose perdem cobertura progressivamente, há diferenças entre os estratos socioeconômicos, favoráveis aos estratos mais altos em algumas cidades e aos estratos mais baixos em outras. Conclusão: Houve realmente redução da cobertura vacinal em todas as capitais e no DF para as crianças nascidas em 2017 e 2018, denotando piora na execução do Programa Nacional de Imunizações durante os anos de 2017 a 2019. O inquérito realizado não mensurou os impactos da pandemia de COVID-19 que podem ter reduzido ainda mais as coberturas vacinais.