Novel methodologies using history to document the effects of African American sexual trauma: Perspectives of Gail E. Wyatt, PhD.

This article describes the nearly half a century career of Dr. Gail E. Wyatt, PhD, and her development of novel methodologies and measures of sexual trauma, specifically the Wyatt Sex History Questionnaire and the University of California, Los Angeles, Life Adversities Screener. These approaches broke the silence around experiences of sexual violence, particularly among African Americans, identifying their effects on sexual functioning and mental health. These novel methods are designed without assuming sexual literacy of respondents, knowledge of anatomy, or that discussing sex is easy or common; they include topics that are considered private and may evoke emotions. Trained professionals administering face-to-face interviews can serve to establish rapport and educate the participant or client while minimizing possible discomfort and shame around the disclosure of sexual practices. In this article, four topics are discussed focusing on African Americans, but they may also be relevant to other racial/ethnic groups: (a) breaking the silence about sex, (b) sexual harassment: its disclosure and effects in the workplace, (c) racial discrimination: identifying its effects as a form of trauma, and (d) the cultural relevance of promoting sexual health. Historical patterns of abuse and trauma can no longer be ignored but need to be better understood by psychologists and used to improve policy and treatment standards. Recommendations for advancing the field using novel methods are provided. (PsycInfo Database Record (c) 2023 APA, all rights reserved).

O papel da Santa Casa no sistema público de saúde brasileiro: o levantamento histórico de uma instituição filantrópica / The role of Santa Casa in the Brazilian public health system: a historical survey of a philanthropic institution

Resumo O artigo1 tem por objetivo analisar a evolução da interação entre Santas Casas e o Sistema de Saúde Público brasileiro por meio do levantamento histórico da Santa Casa de Mogi Mirim. Os procedimentos metodológicos foram de abordagem qualitativa e basearam-se em uma coleta de dados por pesquisa documental do levantamento histórico da Santa Casa em questão e do histórico dos principais marcos do sistema de saúde brasileiro. Os dados obtidos foram analisados para identificar o nível de interação entre a Santa Casa e a assistência hospitalar do sistema de saúde em vigor. O resultado desta análise histórico-comparativa demonstrou a intensificação da relação entre a Santa Casa e o sistema público de saúde, partindo de uma interação nula no início do século XIX que se transforma em uma codependência cercada de disputas e com limites muitos tênues no início do século XXI.

Abstract This article1 aims at analyzing the evolution of the interaction between the Santas Casas and the Brazilian Public Health stemmed from the historical research of the Santa Casa de Mogi Mirim. This qualitative research was based on data collected by means of documentary research on the historical survey of the Santa Casa and the Brazilian health system, identifying the level of interaction between the institution and hospital care. The result of this comparative historical analysis demonstrated the intensification of the relationship between Santa Casa and the public health system, starting from a null interaction in the beginning of the 19th century that turns into a codependency with numerous disputes and very subtle limits in the beginning of the 21st century.

The Social Survey, the Metropolitan Life Insurance Company, and the Beginnings of the US Public Health Service's Sickness Surveys.

The earliest sickness survey of the US Public Health Service, which started in 1915, was the Service's first socioeconomic study of an industrial community. It was also the first to define illness as a person's inability to work. The survey incorporated the Metropolitan Life Insurance Company's definition of illness, which, instead of sickness rates, focused on duration of illness as a proxy of time lost from work. This kind of survey took place in the broader context of the reform movements of the Progressive Era and the social surveys conducted in the United States, which led to the creation of the Federal Commission on Industrial Relations, where the Service's sickness survey originated. The Service's focus on the socioeconomic classification of families and definition of illness as the inability to work enabled it to show the strong link between poverty and illness among industrial workers. The leader of the survey, Edgar Sydenstricker, and the Metropolitan Life Insurance Company came up with new ways to measure the health of the population, which also influenced the Service's studies of the effects of the Great Depression on public health and the National Health Survey of 1935-1936. (Am J Public Health. 2021; 111(11):1960-1968. https://doi.org/10.2105/AJPH.2021.306454).

National Health Survey 2019: history, methods and perspectives. / Pesquisa Nacional de Saúde 2019: histórico, métodos e perspectivas.

This article presents the history and construction of the National Health Survey (PNS) 2019, a household survey conducted in partnership with the Brazilian Institute of Geography and Statistics. The objective of PNS 2019 was to provide the country with information on the health determinants, conditionants and needs of the Brazilian population. The expected sample was 108,525 households, considering a 20% non-response rate. The questionnaire had three parts, covering: (i) the household; (ii) all residents of the household, focusing on collection of socioeconomic and health information; and (iii) the selected resident (15 years old or more) for whom lifestyles, chronic diseases, violence, among other topics were investigated, as well as their anthropometric measurements (subsample). The information provided by PNS 2019 will serve as a basis for the (re)formulation of health policies, as well as support for existing actions and programs of the Brazilian National Health System.

Este artigo apresenta o histórico e a construção da Pesquisa Nacional de Saúde (PNS) 2019, inquérito de base domiciliar realizado em parceria com o Instituto Brasileiro de Geografia e Estatística. O objetivo da PNS 2019 foi dotar o país de informações sobre os determinantes, condicionantes e necessidades de saúde da população brasileira. A amostra prevista foi de 108.525 domicílios particulares, considerando-se uma taxa de não resposta de 20%. Seu questionário continha três partes, orientadas para (i) o domicílio, (ii) todos os moradores do domicílio, com enfoque na coleta de informações socioeconômicas e de saúde, e (iii) o morador selecionado (idade ≥15 anos), sendo investigados estilos de vida, doenças crônicas, violências, entre outros temas, e aferidas medidas antropométricas (subamostra). As informações da PNS 2019 servirão de base para a (re)formulação de políticas de saúde e subsídio a ações e programas existentes do Sistema Único de Saúde.

Este artículo presenta la historia y la construcción de la Encuesta Nacional de Salud (PNS) 2019, una encuesta domiciliaria realizada en colaboración con el Instituto Brasileño de Geografía y Estadística. El objetivo de la PNS fue proporcionar al país información sobre los determinantes, las condiciones y las necesidades de salud de la población brasileña. La muestra esperada fue de 108.525 hogares particulares, considerando una tasa de no respuesta del 20%. Su cuestionario contenía tres partes: (i) con respecto al hogar; (ii) dirigido a todos los residentes, centrándose en la recopilación de información socioeconómica y de salud; y (iii) al residente seleccionado (15 años o más) de quien se investigó estilos de vida, enfermedades crónicas, violencia, entre otros temas y se compararon las medidas antropométricas (submuestra). La información de la PNS 2019 servirá como base para la (re)formulación de políticas de salud y para apoyar acciones y programas existentes en el Sistema Único de Salud.

Forty years of national surveys: An overview of children's dental health from 1973-2013.

INTRODUCTION: The first national survey of children's dental health in England and Wales was carried out in 1973. Subsequent surveys, in 1983, 1993 and 2003, included all United Kingdom health departments. The 2013 survey involved England, Wales and Northern Ireland. AIM: To consider all five surveys, from 1973 to 2013, so as to summarise trends in the dental health of children in the UK over the last 40 years. MATERIALS AND METHOD: The 2013 survey was commissioned by the Health &Social Care Information Centre and all surveys used data collected during dental examinations conducted in schools on a random sample of children by NHS dentists, together with a questionnaire to parents of those children. In 2013, a pupil questionnaire for 12- and 15-year-olds was introduced, to complement information received from parents and carers. RESULTS: A total of 69,318 children, aged 5-15 years, were involved, from 1973-2013. Caries prevalence has reduced from 72% to 41% in 5-year-olds, and from 97% to 46% in 15-year-olds in 40 years. Changes in periodontal disease, orthodontic treatment, accidental damage to anterior teeth, tooth surface loss and enamel defects, are also summarised. Behavioural and attitudinal characteristics observed in the 2013 report are listed. CONCLUSIONS: Caries is now concentrated in a minority of children. The prevalence of gingivitis has not changed a great deal in 40 years. About half of those children assessed 'in orthodontic need' receive treatment.

The impact of retirement on health in Canada.

This study estimates the impact of retirement on subsequent health outcomes as measured by self-reported health status. The empirical study is based on seven longitudinal waves of the Canadian National Population Health Survey, spanning 1994 through 2006. To account for biases due to unobserved individual-specific heterogeneity, this study uses a fixed-effects method. The results indicate that retirement has a positive but insignificant impact on self-reported health status. The study further examined this issue using different subgroups based on gender and income and again found that retirement has no significant impact on health status.

[The "shoeleather epidemiology" or the reinvention of medical survey. Alice Hamilton and industrial medicine in early 20th century America]. / L' "épidémiologie de la bottine" ou l'enquête médicale réinventée. Alice Hamilton et la médecine industrielle dans l'Amérique du premier XXe siècle.

Dr. Alice Hamilton (1869-1970) was a pioneer in industrial medicine, a new discipline that emerged with a new interest in working conditions and occupational hazards within an era of unprecedented industrial growth. From various sources, including her reports after she visited Arizona copper belt in 1919, my paper emphasizes the innovation of Hamilton's approach,"shoeleather epidemiology". She went to the source of information in workshops, plants and construction sites, observed the very concrete part of industrial work, interviewed many stakeholders in and around the workplace, making a methodological toolbox for industrial surveys. Her method combined an old medical practice (the medical inquiry) and a new clinical field (the plant) and placed the worker as a patient in the core of the issue of occupational health and safety.

Birth defects surveillance in China.

BACKGROUND: Birth defects are a global public health problem because of their large contribution to infant mortalities and disabilities. It is estimated that 4%-6% of Chinese newborns are affected by birth defects every year. Surveillance is a basic approach to understanding the occurrence and associated factors of birth defects. The Ministry of Health of China initiated a national hospital-based birth defects monitoring system 20 years ago. Nearly every province in this country has established its own surveillance system in the past. The authors reviewed the result of the monitoring system at different administrative levels in China. DATA SOURCES: Available publications on the surveillance of birth defects and data from national and provincial birth defects surveillance systems were reviewed to evaluate the effectiveness of the surveillance systems. RESULTS: According to the 2009 data, the national hospital-based birth defects surveillance system monitored over 1.3 million births, which accounted for more than 8% of births in China. In addition, 30 provincial hospital-based surveillance programs covered a birth population of more than 3.6 million (22% of births in China). Great achievements have been made in terms of case ascertainment, data quality control, and online reporting. But the surveillance systems in China still have some limitations. A short ascertainment period may miss some internal anomalies, inherited metabolic diseases, and malformed fetus aborted before the 28th gestational week. Discrepancies in antenatal or postnatal diagnosis of birth defects between surveillance institutes may affect the detection rate and introduce biases. Absence of baseline data and lack of integrated database systems limit the application of surveillance data to etiological studies and affect the process of decision-making. CONCLUSIONS: The surveillance system for birth defects is prerequisite to propose, conduct and assess any interventions for the disease. To meet the need of study and prevention of birth defects, measures should be taken to improve the national and provincial birth defects surveillance systems in China.

How the 1932 and 1947 mental surveys of Aberdeen schoolchildren provide a framework to explore the childhood origins of late onset disease and disability.

OBJECTIVES: To describe the discovery and development of the Aberdeen 1921 and 1936 birth cohort studies. STUDY DESIGN: The Aberdeen birth cohort studies were started in 1998 when the Scottish Mental Survey archives of the Scottish Council for Research in Education were re-discovered and permissions granted to follow-up survivors born in 1921 or 1936 and then aged about 77 or 64 years and who had entered (or were about to enter) the age of greatest risk for Alzheimer's disease (AD). MAIN OUTCOME MEASURES: Sources of attrition from the study, exposures to childhood adversity, nutritional, genetic and life style factors of possible relevance to extent of age-related cognitive decline and the timing of onset of dementia. RESULTS: By 2010, the feasibility of following up more than 75% of Scottish Mental Survey survivors living in the Aberdeen area without dementia was well-established, dementia ascertainment to age about 88 years was completed in the 1921 birth cohort and was underway in the 1936 born cohort. CONCLUSION: These databases are available to other bone fide research groups wishing to test specific hypotheses that may either replicate their own findings or make best use of the data collected in the Aberdeen studies.

[The electrocardiographic survey]. / O inquérito eletrocardiográfico.

In order to investigate the prevalence of chagasic heart disease in Brazil, a national electrocardiographic survey was carried out from 1977 to 1981. A total of 5,347 electrocardiograms (ECG) were performed and paired by age and gender. The results obtained in relation with the autochthonous cases, were distributed by Brazilian states, as follows: Rio Grande do Sul (1,078), Minas Gerais (760), Bahia (612), Paraná (400), Paraiba (340), Piauí (218), Sergipe (216), Goiás (176), Pernambuco (170), Ceará (136) and Alagoas 134. The higher proportions of altered ECGs among seropositive individuals were found in the States of Goiás (63.6%), Minas Gerais (57.6%), Ceará (57.3%), Paraná (54.5%), Piauí (53.2%) and Paraiba (52.3%). Among the control individuals, these proportions were respectively 25%, 25.7%, 25%, 12.5%, 22.9% and 26.5%. A significant statistical difference of altered ECGs between positive and negative individuals was verified in all the States, with a single exception (Alagoas). The estimation of the gradient showed to be higher in Paraná State (42%), followed by Goiás (38.6%), Ceará (32.3%), Minas Gerais (31.9%), Piauí (30.3%), Paraíba (25.8%), Pernambuco (22.3%), Bahia (18.9%), Sergipe (16.7%), Rio Grande do Sul (9.9%) and Alagoas (7.5%). Concerning the distribution of the electrocardiographical alterations found in the eleven states, the main alterations find among the seropositive group were: ventricular extrasystoles, complete right bundle branch block, left anterior fascicular block, the association of complete right bundle branch block with left anterior fascicular block and primary alterations of the ST segment and of the T wave. Furthermore, these ECG alterations were more prevalent in the group of infected individuals.

[Summary of results from the national surveys]. / Síntese dos resultados dos inquéritos nacionais.

This article aims to correlate the main results of three large national surveys on Chagas disease (entomologic, seroprevalence and electrocardiographic) carried out in Brazil from late 1970's to early 1980's, which served as baseline for definition of the control measures adopted in the country. The proportion of infected people was much higher in areas where Triatoma infestans, the most efficient vector of Chagas disease among the five principal species involved in transmission at that time, was predominant. Similar result was observed in places where Triatoma sordida was dispersed, mainly in the country's central region, which corresponds to its native area. This finding is due to the coincidence observed in the geographic distribution of both vectors, since T. sordida is not considered to play an important role in transmission. In the Northeastern semi-arid, endemic area for Triatoma brasiliensis and Triatoma pseudomaculata, rates of human infection were much lower, although both vectors may have some relevance in the maintenance of the disease. As for areas with Panstrongylus megistus, human infection varied according to the levels of domiciliation. Whenever domiciled, like in the humid northeastern coastal area, its involvement in transmission can be clearly demonstrated. In some parts of Bahia State it represented the exclusive vector of the disease. Based upon the results of the seroprevalence survey an electrocardiographic study was carried out in 11 Brazilian states, which showed marked differences in the presence of cardiac alterations when comparing different areas of the country.

Epidemiology and health care reform: the National Health Survey of 1935-1936.

The National Health Survey undertaken in 1935 and 1936 was the largest morbidity survey until that time. It was also the first national survey to focus on chronic disease and disability. The decision to conduct a survey of this magnitude was part of the larger strategy to reform health care in the United States. The focus on morbidity allowed reformers to argue that the health status of Americans was poor, despite falling mortality rates that suggested the opposite. The focus on chronic disease morbidity proved to be an especially effective way of demonstrating the poor health of the population and the strong links between poverty and illness. The survey, undertaken by a small group of reform-minded epidemiologists led by Edgar Sydenstricker, was made possible by the close interaction during the Depression of agencies and actors in the public health and social welfare sectors, a collaboration which produced new ways of thinking about disease burdens.

The impact of the HIV/AIDS epidemic on kinship resources for orphans in Zimbabwe.

The extended family has been recognized as a major safety net for orphans in sub-Saharan Africa. However, the mortality crisis associated with HIV/AIDS may drastically reduce the availability of relatives and thus undermine traditional forms of mutual support. In this article, the microsimulator SOCSIM is used to estimate and project quantities such as the number of living uncles, aunts, siblings, and grandparents available to orphans. The model is calibrated to the setting of Zimbabwe, using data from demographic and Health Surveys and estimates and projections of demographic rates from the United Nations. The article shows that there is a lag of more than ten years between the peak in orphanhood prevalence and the peak in scarcity of grandparents for orphans. The results indicate that a generalized HIV/AIDS epidemic has a prolonged impact on children and orphans that extends well beyond the peak in mortality. A rapid increase in the number of orphans is followed by a steady reduction in the number of living grandparents for orphans. Consequently, the burden of double orphans (both of whose parents have died) is likely to shift to uncles and aunts. In Zimbabwe, the number of living uncles and aunts per double orphan decreased between 1980 and 2010, but it is expected to increase progressively during the next few decades. Changes in kinship structure have important social consequences that should be taken into account when seeking to address the lack of care for orphans.