Aporte espiritual/religioso pela enfermagem no tratamento do câncer de mama: revisão integrativa / Spiritual/religious support for nursing in the treatment of breast cancer: integrative review / Apoyo espiritual/religioso de la enfermería en el tratamiento del cáncer de mama: revisión integrativa

Objetivo: analisar na literatura científica a importância da abordagem espiritual/religiosa pela equipe de enfermagem no tratamento do câncer de mama. Método: revisão integrativa, realizada na BDENF, LILACS e SCOPUS. Resultados: foram selecionados seis estudos, evidenciou-se que a abordagem espiritual/religiosa pelos profissionais de enfermagem auxilia para o enfrentamento positivo do câncer de mama. Assim, emergiu a categoria.: Abordagem espiritual/religiosa na assistência de enfermagem e suas repercussões positivas para o enfrentamento do câncer de mama. Conclusão: a categoria da enfermagem integra a rede de apoio social para o alívio do sofrimento, por meio do aporte espiritual/religioso, auxiliando para a minimização de sentimentos negativos associados ao diagnóstico e aos eventos adversos dos tratamentos, sendo importante incluir discussões acerca desta temática na formação de nível técnico e graduação em enfermagem.

Objective: to analyze in the scientific literature the importance of the spiritual/religious approach by the nursing team in the treatment of breast cancer. Method: integrative review, carried out in BDENF, LILACS and SCOPUS. Results: six studies were selected, showing that the spiritual/religious approach by nursing professionals helps to cope positively with breast cancer. Thus, the following category emerged: Spiritual/religious approach in nursing care and its positive repercussions for coping with breast cancer. Conclusion: the nursing category is part of the social support network for relieving suffering, through spiritual/religious support, helping to minimize negative feelings associated with the diagnosis and adverse treatment events, and it is important to include discussions on this topic in technical and undergraduate nursing training.

Objetivos:analizar la importancia del abordaje espiritual/religioso por el equipo de enfermería en el tratamiento del cáncer de mama en la literatura científica. Método: revisión integradora, realizada en BDENF, LILACS y SCOPUS. Resultados: fueron seleccionados seis estudios que demuestran que el abordaje espiritual/religioso por profesionales de enfermería ayuda a enfrentar positivamente el cáncer de mama. Surgió la siguiente categoría: Enfoque espiritual/religioso en los cuidados de enfermería y sus repercusiones positivas para el afrontamiento del cáncer de mama. Conclusión: la categoría de enfermería forma parte de la red de apoyo social para aliviar el sufrimiento, a través del apoyo espiritual/religioso, ayudando a minimizar los sentimientos negativos asociados al diagnóstico y a los eventos adversos de los tratamientos, siendo importante incluir discusiones sobre este tema en la formación técnica y de pregrado de enfermería.

Infertilidade, justiça reprodutiva e pandemia de COVID-19: reflexões sobre acesso e barreiras / Infertility, reproductive justice and the COVID-19 pandemic: reflections on access and barriers / Infertilidad, justicia reproductiva y la pandemia de COVID-19: reflexiones sobre acceso y barreras

Objetivo: refletir sobre o acesso a serviços de saúde para infertilidade e reprodução humana assistida durante o período da pandemia de COVID-19, na perspectiva da justiça reprodutiva. Metodologia: utilizou-se dados do inquérito online da pesquisa Pandemia de COVID-19e práticas reprodutivas de mulheres no Brasil, que obteve 8.313 respostas de mulheres residentes em todas as regiões do país, de 18 anos ou mais. O questionário autoaplicável circulou entre julho e outubro de 2021, contendo questões fechadas e abertas. A análise descritiva das respostas objetivas de 242 mulheres que referiram buscar atendimento para infertilidade contou com o cálculo de frequências simples das variáveis. Já os textos escritos nos espaços abertos do questionário foram submetidos à análise temática. Resultados: o estudo verificou a existência de barreiras institucionais e não institucionais para os cuidados da infertilidade, ambas incrementadas pela pandemia. Conclusão: recomenda-se a efetivação de política pública que garanta acesso pleno a todas as pessoas, haja vista que o tratamento para infertilidade e reprodução assistida tende a se restringir a mulheres cisgênero, de camadas médias e altas, mais escolarizadas e majoritariamente brancas.

Objective: to critically examine access to health services for infertility and assisted human reproduction during the COVID-19 pandemic, emphasizing the perspective of reproductive justice. Methods: data for analysis were derived from the online survey titled COVID-19 Pandemic and Women's Reproductive Practices in Brazil, garnering 8,313 responses from women aged 18 years or older residing in all regions of the country. The self-administered questionnaire circulated from July to October 2021 and comprised both closed and open-ended questions. Descriptive analysis of the objective responses obtained from 242 women actively seeking infertility care involved the calculation of simple frequencies for relevant variables. Responses provided in the open-ended sections of the questionnaire underwent thematic analysis. Results: revealed the presence of both institutional and non-institutional barriers to infertility care, with a notable exacerbation during the pandemic. Conclusion: given that infertility and assisted reproduction treatment predominantly cater to cisgender women from middle and upper socio-economic strata, characterized by higher education levels and mostly white, there is a compelling need for the implementation of public policies that ensure equitable access for all individuals.

Objetivo: reflexionar sobre el acceso a los servicios de salud para la infertilidad y la reproducción humana asistida durante el período de la pandemia de COVID-19, desde la perspectiva de la justicia reproductiva. Metodología: se utilizaron datos de la encuesta en línea de la Pandemia de COVID-19y prácticas reproductivas de las mujeres en Brasil, que obtuvo 8.313 respuestas de mujeres residentes en todas las regiones del país, con edad igual o superior a 18 años. El cuestionario autoaplicado circuló entre julio y octubre de 2021, conteniendo preguntas cerradas y abiertas. El análisis descriptivo de las respuestas objetivas de 242 mujeres que relataron buscar atención por infertilidad implicó el cálculo de frecuencias simples de las variables. Los textos escritos en los espacios abiertos del cuestionario fueron sometidos a análisis temático. Resultados:el estudio verificó la existencia de barreras institucionales y no institucionales para la atención de la infertilidad, ambas aumentadas por la pandemia. Conclusión: se recomiendala implementación de una política pública que garantice el pleno acceso a todas las personas, dado que el tratamiento de la infertilidad y reproducción asistida tiende a estar restringido a mujeres cisgénero de clase media y alta, con mayor educación y en su mayoría blancas.

Saúde, reprodução e sexualidade nos tempos da COVID-19: memórias incorporadas das mulheres no Brasil / Health, reproduction and sexuality in times of COVID-19: embodied memories of women in Brazil / Salud, reproducción y sexualidad en los tiempos de COVID-19: memorias encarnadas de las mujeres en Brasil

Objetivo: compreender como a pandemia de COVID-19 afetou a vida e a saúde das mulheres, com ênfase nos aspectos da saúde sexual e reprodutiva, e refletir sobre os direitos sexuais e reprodutivos e a justiça reprodutiva no contexto da crise sanitária. Metodologia: utilizou-se questionário online com 113 perguntas objetivas e uma questão aberta para comentários. De 8.313 mulheres que responderam ao questionário, 1.838 relataram suas vivências durante a pandemia na questão aberta. Esse material passou por técnicas de análise narrativa e temática e de construção de memória. Resultados: evidenciou-se a ampliação das dificuldades de acesso a serviços de saúde, em especial de saúde sexual e reprodutiva; o aprofundamento das iniquidades na divisão sexual do trabalho, com sobrecarga de trabalho doméstico e profissional; a insegurança econômica; o tensionamentos das relações afetivo-sexuais e maior exposição à violência; e importantes repercussões na saúde psicoemocional. Todos esses aspectos afetaram as experiências de saúde e adoecimento; a vida sexual; e os planos e experiências reprodutivas nos primeiros anos de pandemia. Conclusão: no Brasil, na sobreposição da emergência sanitária com a crise democrática de direitos, fatos sociais e fatos fisiológicos se misturam e se totalizam na experiência histórica e material do corpo sexual e reprodutivo das mulheres, seguindo as linhas de força das precariedades e injustiças de gênero, de raça e de classe. Os relatos das mulheres contribuem para a construção de uma memória coletiva ­não necessariamente unívoca e linear ­da pandemia. Memórias que podem não apenas ilustrar o momento presente, como contribuir para o entendimento e enfrentamento de crises semelhantes futuras.

Objective: this study seeks to comprehend the impact of the COVID-19 pandemic on women's lives and health, with a particular focus on sexual and reproductive health, andto reflect on sexual and reproductive rights and reproductive justice within the context of the health crisis.Methods:employing an online questionnaire featuring 113 objective questions and one open-ended question for free comments, the study gathered responses from 8,313 women. Out of these, 1,838 utilized the open question to articulate their experiences during the pandemic. The collected material underwent analysis using narrative and thematic approaches, along with memory construction techniques.Results:the findings indicate heightened challenges in accessing health services, particularly for sexual and reproductive health. The pandemic deepened inequities in the sexual division of labor, leading to increased domestic and professional workloads, economic insecurity, elevated tensions in affective-sexual relationships, greater exposure to violence, and notable repercussions on psycho-emotional health. These factors collectively influenced women's health/illness experiences, sexual lives, and reproductive plans during the initial years of the pandemic. Conclusion: the intersection of the health crisis with a democratic crisis in rights has intertwined social and physiological factors into the historical and material experiences of women's sexual and reproductive bodies. These experiences follow the trajectories of gender, race, and class-based precariousness and injustices. Women's accounts contribute to the construction of a collective memory of the pandemic that is not necessarily uniform or linear. Beyond illustrating the present moment, these memories aid in understanding and addressing similar crises in the future.

Objetivo: comprender cómo la pandemia de COVID-19 afectó la vida y la salud de las mujeres, con énfasis en aspectos de salud sexual y reproductiva y reflexionar sobre los derechos sexuales y reproductivos y la justicia reproductiva, en el contexto de la crisis sanitaria. Metodología:se utilizó un cuestionario online con 113 preguntas objetivas y una pregunta abierta para comentarios libres al final. De 8.313 mujeres que respondieron el cuestionario, 1.838 relataron sus experiencias durante la pandemia, en este espacio abierto. Este material fue analizado mediante técnicas análisis de narrativa y temática y de construcción de memoria. Resultados: hubo aumento de las dificultades para acceder a los servicios de salud, especialmente de salud sexual y reproductiva, profundización de las inequidades en la división sexual del trabajo, con sobrecarga de trabajo doméstico y profesional, inseguridad económica, tensiones en las relaciones afectivo-sexuales y mayor exposición. a la violencia, e importantes repercusiones en la salud psicoemocional. Todos estos aspectos afectaron las experiencias de salud/enfermedad, la vida sexual, los planes y experiencias reproductivas, en los primeros años de la pandemia. Conclusión: en Brasil, en el solapamiento de la crisis sanitaria con la crisis democrática y de derechos, hechos sociales y hechos fisiológicos se mezclan y totalizan en la experiencia histórica y material de los cuerpos sexuales y reproductivos de las mujeres, siguiendo las líneas de fuerza de la precariedad y las injusticias. de género, raza y clase. Las narrativas de las mujeres contribuyen a la construcción de una memoria colectiva ­no necesariamente unívoca y lineal ­ de la pandemia. Memorias que no sólo pueden ilustrar el momento presente, sino que también contribuyen a comprender y afrontar crisis futuras similares.

Questionário I-SHARE Brasil: adaptação do português de Portugal para o português do Brasil / I-SHARE Brazil questionnaire: adaptation from Portuguese to Brazilian Portuguese

A pandemia de COVID-19 trouxe desafios acrescidos aos já existentes, em termos de acesso aos serviços, respostas adequadas, garantia de direitos, entre outros, para a área da saúde sexual e reprodutiva no Brasil e no mundo. A pesquisa "International Sexual Health and Reproductive Health Survey" (I-SHARE), um estudo global desenvolvido em mais de 40 países, surge da necessidade de investigar essa situação, sendo necessário criar e adaptar instrumentos capazes de captar esta nova realidade mundial. O objetivo do presente artigo é apresentar o processo de adaptação do questionário I-SHARE de português de Portugal para o português do Brasil. A versão brasileira do questionário I-SHARE incluiu 15 grandes blocos de questões relacionadas a COVID-19, violência e saúde sexual e reprodutiva. A adaptação obrigou a acomodar diferenças linguísticas, culturais e institucionais de diferente natureza. O pré-teste, realizado com 10 pessoas, revelou uma boa aceitação, não se tendo verificado dificuldades de compreensão e análise por parte dos/as participantes. Conclui-se que o questionário I-SHARE Brasil, além de ter servido uma pesquisa particular no contexto da pandemia de COVID-19, poderá ser adaptado a outras realidades e estudos futuros no âmbito da saúde sexual e reprodutiva no Brasil.

The COVID-19 pandemic brought increased challenges regarding access to services, adequate responses, guaranteeing rights, among others, for the area of sexual and reproductive health in Brazil and around the world. The "International Sexual Health and Reproductive Health Survey" (I-SHARE), a global study carried out in more than 40 countries, arises from the need to investigate this situation, making it necessary to create and adapt instruments capable of capturing this new global reality. The objective of this article is to present the process of adapting the I-SHARE questionnaire from Portuguese to Brazilian Portuguese. The Brazilian version of the I-SHARE questionnaire included 15 large blocks of questions related to COVID-19, violence and sexual and reproductive health. Adaptation forced to accommodate linguistic, cultural and institutional differences of different nature. The pre-test, carried out with 10 people, revealed good acceptance, with no difficulties in understanding or analyzing on the part of the participants. It is concluded that the I-SHARE Brazil questionnaire, in addition to having served as a particular research in the context of the COVID-19 pandemic, can be adapted to other realities and future studies in the field of sexual and reproductive health in Brazil.

Do it fast! Early access to specialized care improved long-term outcomes in rheumatoid arthritis: data from the REAL multicenter observational study

Abstract Background Early rheumatoid arthritis (RA) offers an opportunity for better treatment outcomes. In real-life settings, grasping this opportunity might depend on access to specialized care. We evaluated the effects of early versus late assessment by the rheumatologist on the diagnosis, treatment initiation and long-term outcomes of RA under real-life conditions. Methods Adults meeting the ACR/EULAR (2010) or ARA (1987) criteria for RA were included. Structured interviews were conducted. The specialized assessment was deemed "early" when the rheumatologist was the first or second physician consulted after symptoms onset, and "late" when performed afterwards. Delays in RA diagnosis and treatment were inquired. Disease activity (DAS28-CRP) and physical function (HAQ-DI) were evaluated. Student's t, Mann-Whitney U, chi-squared and correlation tests, and multiple linear regression were performed. For sensitivity analysis, a propensity score-matched subsample of early- vs. late-assessed participants was derived based on logistic regression. The study received ethical approval; all participants signed informed consent. Results We included 1057 participants (89.4% female, 56.5% white); mean (SD) age: 56.9 (11.5) years; disease duration: 173.1 (114.5) months. Median (IQR) delays from symptoms onset to both RA diagnosis and initial treatment coincided: 12 (6-36) months, with no significant delay between diagnosis and treatment. Most participants (64.6%) first sought a general practitioner. Notwithstanding, 80.7% had the diagnosis established only by the rheumatologist. Only a minority (28.7%) attained early RA treatment (≤ 6 months of symptoms). Diagnostic and treatment delays were strongly correlated (rho 0.816; p < 0.001). The chances of missing early treatment more than doubled when the assessment by the rheumatologist was belated (OR 2.77; 95% CI: 1.93, 3.97). After long disease duration, late-assessed participants still presented lower chances of remission/low disease activity (OR 0.74; 95% CI: 0.55, 0.99), while the early-assessed ones showed better DAS28-CRP and HAQ-DI scores (difference in means [95% CI]: −0.25 [−0.46, −0.04] and − 0.196 [−0.306, −0.087] respectively). The results in the propensity-score matched subsample confirmed those observed in the original (whole) sample. Conclusions Early diagnosis and treatment initiation in patients with RA was critically dependent on early access to the rheumatologist; late specialized assessment was associated with worse long-term clinical outcomes.

Decreasing delays in the diagnosis and treatment of rheumatoid arthritis in Brazil: a nationwide multicenter observational study

Abstract Background Management delays imply worse outcomes in rheumatoid arthritis (RA) and, therefore, should be minimized. We evaluated changes in diagnostic and treatment delays regarding RA in the last decades in Brazil. Methods Adults fulfilling the ACR/EULAR (2010) criteria for RA were assessed. Delays in diagnosis and treatment, and the frequencies of early management initiation within thresholds (windows of opportunity) of 3, 6, and 12 months from symptoms onset were evaluated. The Mann-Kendall trend test, chi-squared tests with Cramer's V effect sizes and analysis of variance were conducted. Results We included 1116 patients: 89.4% female, 56.8% white, mean (SD) age 57.1 (11.5) years. A downward trend was found in diagnostic (tau = - 0.677, p < 0.001) and treatment (tau = - 0.695, p < 0.001) delays from 1990 to 2015. The frequency of early management increased throughout the period, with ascending effect sizes across the 3-, 6-, and 12-month windows (V = 0.120, 0.200 and 0.261, respectively). Despite all improvements, even in recent years (2011-2015) the diagnostic and treatment delays still remained unacceptably high [median (IQR): 8 (4-12) and 11 (5-17) months, respectively], with only 17.2% of the patients treated within the shortest, 3-month window. Conclusion The delays in diagnosis and treatment of RA decreased during the last decades in Brazil. Improvements (effect sizes) were greater at eliminating extreme delays (≥ 12 months) than in attaining really short management windows (≤ 3 months). Very early treatment was still an unrealistic goal for most patients with RA.

Extra-articular manifestations of rheumatoid arthritis remain a major challenge: data from a large, multi-centric cohort

Abstract Introduction Although Rheumatoid Arthritis (RA) extra-articular manifestations (ExtRA) occurrence has been decreasing over time, they are still a major mortality risk factor for patients. Objective To determine the prevalence of ExtRA in a large cohort, and its association with demographic and clinical variables. Method Cross-sectional and observational study, based on a multi-centric database from a prospective cohort, in which 11 public rheumatology centres enrolled RA patients (1987 ARA or 2010 ACR-EULAR). Data collection began in 08-2015, using a single online electronic medical record. Continuous variables were compared using Mann-Whit-ney U-test, and Fisher's exact test or chi-square test, as appropriate, were used for categorical variables. The level of significance was set at 5% (p < 0.05). Results 1115 patients were included: 89% women, age [mean ± SD] 58.2 ± 11.5 years, disease duration 14.5 ± 12.2 years, positive Rheumatoid Factor (RF, n = 1108) in 77%, positive anti-cyclic citrullinated peptide (ACPA, n = 477) in 78%. Regarding ExtRA, 334 occurrences were registered in 261 patients, resulting in an overall prevalence of 23.4% in the cohort. The comparison among ExtRA and Non-ExtRA groups shows significant higher age (p < 0.001), disease duration (p < 0.001), RF high titers (p = 0.018), Clinical Disease Activity index (CDAI) (p < 0.001), Disease Activity Index 28 (DAS 28) (p < 0.001), and Health Assessment Questionnaire (HAQ) (p < 0.001) in ExtRA group. Treatment with Azathioprine (p = 0.002), Etanercept (p = 0.049) Glucocorticoids (GC) ('p = 0.002), and non-steroidal anti-inflammatory drugs (NSAIDs) (p < 0.001) were more frequent in ExtRA group. Conclusions ExtRA manifestations still show an expressive occurrence that should not be underestimated. Our findings reinforce that long-term seropositive disease, associated with significant disability and persistent inflammatory activity are the key factors related to ExtRA development.

Rhino-orbito-cerebral mucormycosis caused by Rhizopus microsporus var. microsporus in a diabetic patient with COVID-19

Abstract COVID-19 disease caused by the SARS-CoV-2 coronavirus causes a wide range of clinical manifestations, ranging from mild to severe, with the main ones affecting the respiratory tract, such as pneumonia. In patients with greater severity, the high frequency of bacterial and fungal coinfection stands out, a situation related both to the patient's pre-existing comorbidities and due to the hospitalization itself. Cases of mucormycosis associated with COVID-19 were highlighted in the lay and scientific media, with the increase in mycosis cases being directly and indirectly attributed to the viral infection. This report describes a case of rhino-orbito-cerebral mucormycosis in a diabetic patient hospitalized for COVID-19, whose diagnosis was confirmed by identifying the agent Rhizopus microsporus var. microsporus through culture for fungi and PCR examination.

Mulheres das ciências médicas e da saúde e publicações brasileiras sobre Covid-19 / Women of medical and health sciences and Brazilian publications on Covid-19

RESUMO Apesar do aumento histórico da participação feminina na produção científica brasileira, reconfigurações domésticas e laborais para o controle da Covid-19 podem estar reduzindo a produtividade das mulheres cientistas. A pesquisa GenCovid-Br objetivou traçar um panorama da participação feminina nos artigos sobre Covid-19 das ciências médicas e da saúde, disponibilizados no PubMed, com ao menos um autor de filiação brasileira. Das 1.013 publicações até 14 de agosto de 2020, 6,1% foram escritas exclusivamente por mulheres; 17,2%, exclusivamente por homens; grupos mistos respondem por 31,1% com liderança feminina, e 45,6% com liderança masculina. As mulheres participam mais de artigos com primeira autoria feminina (50,1% vs 35,6% nos liderados por homens). Nos artigos de áreas da Medicina Clínica, em que as mulheres são maioria, ocorre menos participação de autoras, o que também acontece em publicações resultantes de colaborações internacionais. Os presentes resultados indicam a possibilidade de ampliação de desigualdades de gênero prévias durante a pandemia de Covid-19. Novos estudos devem aprofundar a investigação sobre a magnitude e os determinantes desse fenômeno, incluindo análises temporais. As políticas institucionais devem considerar as iniquidades de gênero nas avaliações acadêmicas, prevenindo impactos futuros nas carreiras das mulheres, em particular, das jovens pesquisadoras envolvidas na reprodução social.

ABSTRACT Despite the increasing historical participation of women in Brazilian scientific production, domestic and labor reconfiguration for the control of the Covid-19 pandemic is likely to reduce women scientists' productivity. The GenCovid-Br Research aimed to outline a panorama of female production in Covid-19 papers in medical and health sciences, available in PubMed, with at least one author with Brazilian affiliation. From the 1,013 publications by August 14, 2020, 6.1% were written exclusively by women, 17.2% exclusively by men, 31.1% were mixed with female leadership, and 45.6% were mixed with male leadership. Women participated in more papers led by women (50.1% vs. 35.6% in those led by men). Papers in Clinical Medicine, where female researchers are predominant, have fewer female authors, occurring in publications resulting from international collaborations. Our results point to the possible expansion of previous gender inequalities during the Covid-19 pandemic. New studies should deepen the investigation of the magnitude and determinants of such phenomenon, including temporal analyses. Institutional policies must consider gender inequalities in academic assessments, preventing future impacts on women's careers, particularly young researchers involved in social reproduction.

Risk Stratification in Chest Pain: Impact on the Diagnosis of Acute Coronary Syndrome

Abstract Background The implementation of institutional protocols in the emergency department (ED) for risk stratification in patients with chest pain has been recommended. Objective To assess the sensitivity, specificity and predictive value of an institutional risk stratification protocol for chest pain suggestive of acute coronary syndrome (ACS). Method Cross-sectional study conducted based on the computerized records of patients treated with the use of a chest pain protocol adapted from the Manchester protocol. The level of risk was stratified by applying five colors representing the respective levels. Each color represents a level of severity and a maximum waiting time for receiving medical care. Red and orange were considered to be high priority, while patients with yellow, green or blue indications were considered to represent a low priority. To compare the type of diagnosis and the classification of priority for receiving care, the Pearson's chi-square test was used, considering a significance level of p< 0.05 for all tests. Results The records of 1,074 patients admitted to the cardiology ED were analyzed. Men (54%), with a mean age of 60 ± 15 years, with complaints of chest pain (44%) of moderate intensity (80%) were predominant the study. Of these patients, 19% were classified as high priority, while 81% were considered to represent a low priority. ACS was confirmed in 23% of the patients, with 34% of them being classified as high priority and 66% as low priority. The sensitivity of the risk stratification protocol for chest pain was 33.7% and the specificity was 86.0%, with a positive and negative predictive value of 41.7% and 81.3%, respectively. Conclusion The Institutional risk stratification protocol for chest pain suggestive of ACS presented satisfactory specificity and a low degree of sensitivity. Int J Cardiovasc Sci. 2020; [online].ahead print, PP.0-0

Chronic use of hydroxychloroquine did not protect against COVID-19 in a large cohort of patients with rheumatic diseases in Brazil

Abstract Background: There is a lack of information on the role of chronic use of hydroxychloroquine during the SARS-CoV-2 outbreak. Our aim was to compare the occurrence of COVID-19 between rheumatic disease patients on hydroxychloroquine with individuals from the same household not taking the drug during the first 8 weeks of community viral transmission in Brazil. Methods: This baseline cross-sectional analysis is part of a 24-week observational multi-center study involving 22 Brazilian academic outpatient centers. All information regarding COVID-19 symptoms, epidemiological, clinical, and demographic data were recorded on a specific web-based platform using telephone calls from physicians and medical students. COVID-19 was defined according to the Brazilian Ministry of Health (BMH) criteria. Mann-Whitney, Chi-square and Exact Fisher tests were used for statistical analysis and two binary Final Logistic Regression Model by Wald test were developed using a backward-stepwise method for the presence of COVID-19. Results: From March 29th to May 17st, 2020, a total of 10,443 participants were enrolled, including 5166 (53.9%) rheumatic disease patients, of whom 82.5% had systemic erythematosus lupus, 7.8% rheumatoid arthritis, 3.7% Sjögren's syndrome and 0.8% systemic sclerosis. In total, 1822 (19.1%) participants reported flu symptoms within the 30 days prior to enrollment, of which 3.1% fulfilled the BMH criteria, but with no significant difference between rheumatic disease patients (4.03%) and controls (3.25%). After adjustments for multiple confounders, the main risk factor significantly associated with a COVID-19 diagnosis was lung disease (OR 1.63; 95% CI 1.03-2.58); and for rheumatic disease patients were diagnosis of systemic sclerosis (OR 2.8; 95% CI 1.19-6.63) and glucocorticoids above 10 mg/ day (OR 2.05; 95% CI 1.31-3.19). In addition, a recent influenza vaccination had a protective effect (OR 0.674; 95% CI 0.46-0.98). Conclusion: Patients with rheumatic disease on hydroxychloroquine presented a similar occurrence of COVID-19 to household cohabitants, suggesting a lack of any protective role against SARS-CoV-2 infection. Trial registration Brazilian Registry of Clinical Trials (ReBEC; RBR - 9KTWX6).

Sociodemographic and clinical-pathological study of molecular subtitles of breast carcinoma in a reference unit of Maranhão / Estudo sociodemográfico e clínico-patológico de legendas moleculares de carcinoma de mama em uma unidade de referência do Maranhão

Abstract Objective To evaluate the distribution of the main sociodemographic and clinicalpathological characteristics in women with breast cancer according to the molecular profile by immunohistochemistry. Methods A cross-sectional, retrospective, analytical and quantitative study was performed, with an analysis of 137 medical records from January 2015 to December 2018 of women attending the High Complexity in Oncology Unit of the city of Imperatriz, state of Maranhão, Brazil. The immunohistochemical profile of tumors based on the estrogen and progesterone receptor, Human Epidermal growth factor Receptor-type 2 (HER2) overexpression and Ki67 cell proliferation indexwas defined, fromwhich six molecular subtypes were determined: luminal A, luminal B-HER2 negative, luminal B-HER2 positive, triple negative, overexpression of HER2 and inconclusive. Results A total of 52.6% of the patients were postmenopausal, mean age 52.1 years old, brown (56.2%), had a schooling level < 9 years (40%), staging > IIB (52.6%) and 23.4% hadmetastasis. Invasive ductal carcinoma accounted for 84.7%, tumor size was 2 to 5 cm (48.9%), with lymph node involvement (56.2%), axillary lymphadenectomy in 67.2%, andmastectomy in 73.7% of the patients. Themost frequentmolecular subtype was the luminal B-HER2 negative (36.5%), and the luminal A subtype showed characteristics of better prognosis when compared with the others. Conclusion It was concluded that in the association of molecular subtypes with sociodemographic and clinical-pathological characteristics, there were no statistically significant results obtained, except for complementary therapy, referring to hormone therapy, and there was a high index of metastasis at diagnosis, which was a worrying factor and indicative of failures in the screening and early diagnosis of this population.

Resumo Objetivo Avaliar a distribuição das principais características sociodemográficas e clínico-patológicas em mulheres com câncer de mama segundo o perfil molecular pela imunohistoquímica. Métodos Estudo transversal, retrospectivo, analítico, descritivo e quantitativo, com análise de 137 prontuários do período de janeiro de 2015 a dezembro de 2018 de mulheres atendidas na Unidade de Assistência da Alta Complexidade em Oncologia da cidade de Imperatriz, MA, Brasil. Foi definido o perfil imunohistoquímico dos tumores baseado na avaliação dos receptores de estrogênio e progesterona, superexpressão de HER2 e índice de proliferação celular Ki67, de onde foram determinados seis subtipos moleculares: luminal A, luminal B-HER2 negativo, luminal B-HER2 positivo, triplo negativo, superexpressão de HER2 e inconclusivo. Resultados Foi demonstrado que 52,6% das pacientes eram pós-menopausadas, com idademédia de 52,1 anos, pardas (56,2%), tinhamgrau de escolaridade < 9 anos (40%), estadiamento > IIB (52,6%) e 23,4% tinham metástase. Carcinoma ductal invasivo representou 84,7%, o tamanho tumoral foi de 2 a 5 cm (48,9%), com comprometimento linfonodal (56,2%), com linfadenectomia axilar em 67,2% e mastectomia em 73,7% das pacientes. O subtipo molecularmais frequente foi o luminal B-HER2 negativo (36,5%), e o subtipo luminal A apresentou características de melhor prognóstico em relação aos demais. Conclusão Concluiu-se que na associação dos subtipos moleculares com as características sociodemográficas e clínico-patológicas não se obteve resultados com significância estatística, exceto para terapia complementar, referente à hormonioterapia, e houve elevado índice de metástase ao diagnóstico, o que representou um fator preocupante e indicativo de falhas no rastreio e diagnóstico precoce dessa população.

Revisiting hydroxychloroquine and chloroquine for patients with chronic immunity-mediated inflammatory rheumatic diseases

Abstract Hydroxychloroquine and chloroquine, also known as antimalarial drugs, are widely used in the treatment of rheumatic diseases and have recently become the focus of attention because of the ongoing COVID-19 pandemic. Rheumatologists have been using antimalarials to manage patients with chronic immune-mediated inflammatory rheumatic diseases for decades. It is an appropriate time to review their immunomodulatory and anti-inflammatory mechanisms impact on disease activity and survival of systemic lupus erythematosus patient, including antiplatelet effect, metabolic and lipid benefits. We also discuss possible adverse effects, adding a practical and comprehensive approach to monitoring rheumatic patients during treatment with these drugs.(AU)

Desigualdades de gênero e raça na pandemia de Covid-19: implicações para o controle no Brasil / Gender and race inequalities in the Covid-19 pandemic: implications for control in Brazil

RESUMO Esta revisão narrativa sintetizou evidências científicas sobre desigualdades de gênero e raça na pandemia de Covid-19, enfocando o trabalho produtivo/reprodutivo das mulheres, a violência de gênero e o acesso aos Serviços de Saúde Sexual e Reprodutiva (SSR). Os resultados confirmam que as desigualdades sociais devem ser consideradas para o efetivo controle da pandemia e para a preservação de direitos. Para além dos efeitos diretos do SARS-CoV-2, discute-se que barreiras de acesso a serviços de SSR podem ocasionar o aumento de gravidezes não pretendidas, abortos inseguros e mortalidade materna. O distanciamento social tem obrigado muitas mulheres a permanecer confinadas com seus agressores e dificultado o acesso a serviços de denúncia, incorrendo no aumento da violência de gênero e em desfechos graves à saúde. Como principais responsáveis pelo cuidado, as mulheres estão mais expostas a adoecer nas esferas profissional e doméstica. A conciliação trabalho-família tornou-se mais difícil para elas durante a pandemia. A literatura naturaliza as diferenças de gênero, raça e classe, com ênfase em fatores de risco. Uma agenda de pesquisa com abordagem interseccional é necessária para embasar a formulação de políticas que incorporem os direitos humanos e atendam às necessidades dos grupos mais vulneráveis à Covid-19.

ABSTRACT This narrative review synthesized scientific evidence on gender and race inequalities in the Covid-19 pandemic, focusing on women's productive/reproductive work, gender-based violence, and the access to Sexual and Reproductive Health Services (SRHS). The results demonstrated that social inequalities must be considered for the effective control of the pandemic and for the preservation of rights. Besides the direct effects of SARS-CoV-2, the literature discusses that barriers to access SRHS can lead to an increase in unintended pregnancies, unsafe abortions, and maternal mortality. Also, social distancing has led several women to stay confined with their aggressors, which hinders the access to reporting services, incurring in the increase of gender-based violence and severe outcomes to health. As main responsible for the care, women are more prone to getting the virus in both professional and domestic spheres. The conciliation between work and family has become more difficult for them during the pandemic. Literature naturalizes gender, race, and social class differences, emphasizing risk factors. An intersectional research plan is needed to support the making of public policies that incorporate human rights and meet the needs of the most vulnerable to Covid-19.

Enfrentamento de mulheres que vivenciaram o câncer de mama / Facing women who lived breast cancer / Enfrentamiento de mujeres que viviendo el cáncer de mama

OBJETIVO: conhecer as mulheres que recebem o diagnóstico do câncer de mama. MÉTODO: Estudo qualitativo que utilizou, como referencial teórico, o Interacionismo Simbólico e como metodológico, a Teoria Fundamentada em Dados. Foram entrevistadas treze mulheres em quimioterapia, de um município mineiro, no mês de janeiro de 2014 e, após a análise, surgiu a teoria "Para vivenciar o câncer de mama é necessário que haja um enfrentamento". RESULTADOS: a metodologia permitiu a discussão em três categorias para debate da teoria, sendo elas: recebendo a notícia do diagnóstico e da necessidade dos tratamentos; adaptação ao tratamento; experiências anteriores frente à doença. Verificamos que o enfrentamento surgiu, em todas as etapas da doença, como forma de superar os tratamentos e os aspectos sociais que o câncer trás. CONCLUSÃO: A teoria construída neste estudo demostra que a mulher que vivencia o câncer de mama utiliza-se de aspectos de resiliência para enfrentar a sociedade, da família para oferecer suporte e de aspectos da experiência de vida. Este estudo contribui para impulsionar mudanças, transformações e inovações, tanto em nível pessoal, como profissional e institucional na assistência a essas mulheres

OBJECTIVE: to know how women are diagnosed with breast cancer. METHOD: Qualitative study that used, as theoretical reference, the Symbolic Interactionism and, as methodological, the Theory Based on Data. We interviewed thirteen women in chemotherapy from a town in Minas Gerais in January 2014 and, after the analysis, came up the following the theory: "To experience breast cancer, it's necessary to be a confrontation". RESULTS: the methodology allowed the discussion in three categories to debate the theory. They are: receiving the news about the diagnosis and the necessity for treatments; adaptation to treatment; previous experiences in the face of the disease. We verified that the confrontation arose in all stages of the disease as a way to overcome the treatments and the social aspects that the cancer brings. CONCLUSION: The theory constructed in this study shows that women who experience breast cancer need some resilience to face the society as a whole; family support; and some aspects of life experience. This study contributes to stimulate changes, transformations and innovations, both personally, professionally and institutionally, in these women care

OBJETIVO: conocer cómo las mujeres reciben el diagnóstico del cáncer de mama. MÉTODO: Estudio cualitativo que utilizó como referencial teórico el Interaccionismo Simbólico y, como metodológico, la Teoría Fundamentada en Datos. Se entrevistaron a trece mujeres en quimioterapia de un municipio minero, en el mes de enero de 2014 y, tras el análisis, surgió la teoría "Para vivir el cáncer de mama es necesario que haya un enfrentamiento". RESULTADOS: la metodología permitió la discusión en tres categorias para debate de la teoría. Son ellas: recibiendo la noticia del diagnóstico y de la necesidad de los tratamientos; adaptación al tratamiento; experiencias anteriores frente a la enfermedad. Verificamos que el enfrentamiento surgió en todas las etapas de la enfermedad como forma de superar los tratamientos y los aspectos sociales que el cáncer aporta. CONCLUSIÓN: La teoría construída en este estudio demuestra que la mujer que vive el cáncer de mama utiliza la resiliencia para enfrentar la sociedad; la familia para el soporte; y los aspectos de la experiencia de vida. Este estudio contribuye a impulsar cambios, transformaciones e innovaciones, tanto a nivel personal, como profesional e institucional en la asistencia a esas mujeres

O dilema de uma prática: experiências de aborto em uma maternidade pública de Salvador, Bahia / The dilemma of a practice: experiences of abortion in a public maternity hospital in the city of Salvador, Bahia

Resumo Discute o aborto pelas perspectivas de mulheres internadas em uma maternidade pública de Salvador (BA). Enfatiza a observação participante do cotidiano do hospital e descreve trabalho de campo com técnicas de pesquisa qualitativa e quantitativa. Por perspectiva etnográfica, aborda a experiência hospitalar de mulheres diante da interrupção, voluntária ou não, da gravidez e apresenta o ponto de vista dos profissionais de saúde, argumentando que a forma pela qual a instituição estrutura a atenção ao aborto e os processos de simbolização a ela imbricados afetam profundamente as experiências das mulheres. Aponta que a discriminação contra as mulheres que abortam está integrada a estrutura, organização e cultura institucionais, e não apenas a ações individuais dos profissionais.

Abstract The article discusses abortion and miscarriage from the perspective of women admitted to a public maternity hospital in Salvador (BA), Brazil. Based on qualitative and quantitative research, it draws on participant observation of everyday hospital life. Taking an ethnographic approach, it addresses the hospital experiences of women who had miscarriages or induced abortions, also presenting the views of health professionals. It argues that the way the institution structures care for abortion and miscarriage involves symbolic processes that profoundly affect women’s experiences. The discrimination against women who have had abortions/miscarriages is an integral part of the structure, organization and culture of these institutions, and does not derive solely from the individual actions of healthcare personnel.

Escolas promotoras de saúde / Health promoting schools

O presente trabalho foi desenvolvido no município de Araquari e participaram da pesquisa 22 professores de duas escolas do município, localizadas na área de abrangência de 2 equipes da estratégia saúde da família. Teve como objetivo propor um processo de educação continuada, para que as escolas se tornem promotoras de saúde, por meio da identificação da percepção dos professores em relação aos temas: saúde, promoção e educação em saúde e a necessidade de capacitação nos mesmos temas. Utilizou-se como instrumento de coleta de dados um questionário semi-estruturado com questões abertas e fechadas; análise das respostas foi feita através do método de análise temática proposta por Minayo. Foi possível observar que o conceito de saúde dos professores limita-se ao bem estar físico, assim como o de educação em saúde à transmissão informações sobre cuidados de higiene. Os professores manifestaram interesse pela capacitação de temas relacionados a doenças. Além disso, não há adoção de estratégias para o enfrentamento dos riscos encontrados no ambiente escolar, apesar do espaço físico ser identificado por eles como inadequado e principal condicionante dos acidentes no ambiente escolar. Assim sendo, as autoras consideram que há necessidade imediata de um processo de educação permanente, para que os professores possam ampliar seus conceitos de saúde e trabalhar com os princípios da Escola Promotora de Saúde, em prol da qualidade de vida de todos aqueles que convivem no ambiente escolar.

This work was developed in the municipality of Araquari. Twenty-two teachers from two schools in the municipality participated in the survey. The schools are located in the catchment area of two teams of the family health strategy. The objective was to propose a process of continuing education so that schools become health promoters, through the identification of the teachers' perception regarding the topics: health, health promotion and education, and the need for qualification in the same themes. The tool used for data collection was a semi-structured questionnaire, with open and closed questions; the answers were analyzed through the method of thematic analysis proposed by Minayo. It was possible to see that the teachers' concept of health is limited to physical well-being, and that their concept of health education is restricted to the transmission of information about hygiene care. Teachers are interested in receiving qualification in issues related to diseases. Moreover, there is no strategy for addressing the risks found in the school environment, despite the fact that the physical space is identified by the teachers as inadequate and as the main reason for accidents. Therefore, the authors believe that there is immediate need for a process of continuing education, so that teachers can expand their concepts of health and work with the principles of the Health Promoting School, in support of the quality of life of all who attend the school environment.

Users' and providers' perspectives on technological procedures for 'normal' childbirth in a public maternity hospital in Salvador, Brazil / Perspectivas de usuarios y proveedores sobre procedimientos tecnológicos para el parto 'normal' en una maternidad pública de Salvador, Brasil

OBJECTIVE: To reveal the effect of cultural practices on the way in which normal birth is conducted in a public hospital in Brazil. MATERIAL AND METHODS: This article about a public maternity hospital in Salvador, Brazil, compares the points of view of providers and users on four technological normal childbirth procedures: trichotomy, episiotomy, oxytocin infusion, and epidural analgesia. Fieldwork carried out from 2002 to 2003 combined qualitative and quantitative methods. RESULTS: Institutional practices make childbirth unnecessarily difficult for women. Nonetheless, most women accept the conditions because the medical procedures make sense according to their cultural understandings. Service providers support the use of such procedures, although doctors are aware that they contradict recommendations found in scientific medical literature. This article argues that from the perspective of both providers and users, the technological procedures are infused with a culturally specific set of meanings and values. CONCLUSIONS: Policymakers must address the cultural understandings of both users and health care professionals in order to improve maternal healthcare in public hospitals in Brazil.

OBJETIVO: Revelar el efecto de las prácticas culturales en el parto normal en un hospital público en Brasil. MATERIAL Y MÉTODOS: Este artículo sobre el parto en una maternidad pública de Salvador, Brasil, compara el punto de vista de los proveedores de servicios de salud y los usuarios de dichos servicios con respecto a cuatro procedimientos para el parto normal: tricotomía, episiotomía, infusión de oxitocina y analgésico epidural. La investigación, realizada entre 2002 y 2003, utilizó métodos cualitativos y cuantitativos. RESULTADOS: La práctica institucional hace que el parto sea innecesariamente dificultoso para las mujeres, sin embargo, la mayoría de ellas aceptan las condiciones, porque los procedimientos médicos tienen sentido dentro de su comprensión cultural. Los proveedores de servicios apoyan el uso de los procedimientos, aunque los doctores están concientes de que están en contra de las recomendaciones estipuladas en la literatura médica científica. El artículo sostiene que desde el punto de vista de ambos, los proveedores de servicios y los usuarios, los procedimientos tecnológicos están cargados de significados y valores culturalmente específicos. CONCLUSIONES: Para lograr mejorar los cuidados en las maternidades de los hospitales públicos del Brasil, los diseñadores de políticas deben tomar en consideración los entendimientos culturales tanto de los usuarios como de los profesionales de salud.

Re-significando a dor e superando a solidão: experiências do parto entre adolescentes de classes populares atendidas em uma maternidade pública de Salvador, Bahia, Brasil / Re-signifying pain, overcoming loneliness: childbirth experiences among working-class adolescents in a public maternity hospital in Salvador, Bahia, Brazil

Este artigo examina o parto em uma maternidade pública de Salvador, Bahia, Brasil, com base na perspectiva de mulheres jovens e adolescentes, a maioria das quais negras e de classes populares. O estudo, de caráter antropológico, baseia-se na análise de entrevistas e na etnografia do hospital, particularmente do centro obstétrico. As mulheres descrevem o trabalho de parto como dominado pelo medo, solidão e dor, sensações que se transformam em amor com o nascimento da criança. Enfocando o parto como um processo biossocial, o trabalho mostra como as jovens produzem significados durante o processo de parturição, enquanto se encontram envolvidas nas interações sociais próprias ao parto hospitalar, particularmente com os profissionais de saúde. Do ponto de vista simbólico, as parturientes experienciam o parto como um rito de passagem que legitima a maternidade, em um contexto social e institucional que, ao contrário, deslegitima a reprodução sexual de mulheres negras, jovens e de baixa renda e estigmatiza a maternidade na adolescência.

Do corpo sedutor ao corpo invisivel: a menopausa em uma perspectiva antropologica / From the seductive body to the invisible body: the menopause from a anthropology perspective

Esta dissertação enfoca a menopausa, a partir de uma abordagem sócio-antropológica. Uma pesquisa qualitativa com mulheres de 45-55 anos, pertencentes às camadas médias da cidade de Salvador é a base empírica deste estudo. Procedeu-se a um levantamento bibliográfico no campo da biomedicina, cuja interpretação informa, de modo fundamental, a apreensão da menopausa nas sociedades ocidentais. Estudos críticos à medicina, especialmente aqueles que enfocam o olhar médico sobre a menopausa, e algumas investigações etnográficas sobre o tema são brevemente resenhados. A menopausa é considerada como um evento síntese do processo de transformações corporais, associada ao curso do envelhecimento feminino, sobre o qual pesa um forte demarcador de gênero. A partir do cotejamento com a literatura antropológica consultada, assim como com dados de outros estudos sobre o tema é possível afirmar que, a despeito do intenso processo de mudanças relativas ao status feminino, permanece uma representação negativa acerca da menopausa. Sua ocorrência continua sendo interpretada como um sinal contundente do envelhecimento feminino, com diferentes implicações para os sujeitos nele envolvidos, sobretudo aquelas circunscritas às restrições de possibilidades de novos encontros afetivo-sexuais. Contudo, uma nova caracterização relativa às mulheres da faixa etária e camada social enfocada parece estar ocorrendo, propiciada pelo intenso processo de mudanças sociais, que impactaram mais positivamente, segundo as entrevistadas, sobretudo mulheres de sua geração