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BACKGROUND: Understanding the barriers to and facilitators of participation in research could enhance recruitment rates for biomedical research on Neglected Tropical Diseases (NTDs) and help to avoid the problems associated with poor recruitment. METHODOLOGY/PRINCIPAL FINDINGS: We conducted a systematic review to identify factors related to willingness to participate in biomedical research on Neglected Tropical Diseases (NTDs). Our search included the following databases: Medline/PubMed, Embase (Embase.com), Global Index Medicus (WHO), Web of Science (Core collection), and gray literature. We included studies that analyzed or reported factors associated with willingness to participate in NTD research, using either quantitative methods (such as clinical trials, cohorts, and cross-sectional studies) or qualitative methods (such as focus group discussions, semi-structured interviews, and in-depth interviews). There were no language restrictions, but we excluded review articles, notes, case reports, letters to the editor, editor's notes, extended abstracts, proceedings, patents, editorials, and other editorial materials. Screening of citations, data extraction, and risk of bias assessment was conducted by independent reviewers, according to the study protocol registered on PROSPERO. For analyses, we assessed the frequency of barriers, enablers, and the frequency of recruitment interventions mentioned in the included studies. The protocol for this systematic review was registered under registration number CRD42020212536. (S1 Appendix) We identified 2070 citations, 1470 from the databases, and 600 from other sources. From those, eleven studies were selected for data extraction and analysis. The studies were conducted in Africa, Asia, and North America. Personal health benefits, monetary benefits, and community engagement and sensitization strategies were identified as the main reasons for participating in biomedical research on Neglected Tropical Diseases (NTDs). However, distrust in researchers, lack of knowledge about research methods among potential participants, and previous negative experiences were identified as the main barriers to participating in biomedical research on NTDs. CONCLUSIONS/SIGNIFICANCE: This systematic review provides recommendations for improving adherence to biomedical research on Neglected Tropical Diseases, which can be applied in practice.

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Introduction: Clozapine is an atypical antipsychotic drug eligible for treatment-resistant schizophrenia. It frequently represents the best and the only choice in resistant schizophrenia. However, its use is feared by many professionals due to its possible adverse effects, such as eosinophilia. Case report: We report a case of a young white male suffering from treatment-resistant schizophrenia who rapidly developed eosinophilia after starting clozapine. Discussion: We present a case of a 26-year-old white man diagnosed with schizophrenia with poor clinical response to several antipsychotics owing to which clozapine was started. Psychotic symptoms improved dramatically but a progressively ascendant eosinophilia was reported during serial haematological analyses. The patient remained physically asymptomatic. An exhaustive assessment with ancillary diagnostic tests revealed no cause for eosinophilia. Thus, a diagnosis of clozapine-induced eosinophilia was made. The drug was discontinued and eosinophil count progressively returned to normal but psychotic symptoms worsened. Conclusions: Clozapine treatment is frequently feared due to its possible side effects and complications, delaying its use in refractory schizophrenia. Also, to our knowledge, there are no specific guidelines on how to manage haematological side effects such as eosinophilia. This is problematic as, in some cases, it may lead to an unnecessary withdrawal of clozapine with a worsening of psychotic symptoms. We present a brief discussion of the recent literature on the subject.

Introducción: La clozapina es un fármaco antipsicótico atípico eligible para la esquizofrenia resistente al tratamiento. Con frecuencia representa la mejor y la única opción para la esquizofrenia resistente. Sin embargo, muchos profesionales temen utilizarla por sus posibles efectos adversos, como la eosinofilia. Reporte de caso: Se expone el caso de un joven blanco que sufre esquizofrenia resistente al tratamiento y desarrolló eosinofilia rápidamente tras comenzar el tratamiento con clozapina. Discusión: Varón de 26 años con diagnóstico de esquizofrenia y mala respuesta clínica a varios antipsicóticos, por lo que se inició clozapina. Los síntomas psicóticos mejoraron drásticamente, pero los análisis hematológicos seriados informaron una eosinofilia en ascenso progresivo. El paciente permaneció físicamente asintomático. Una evaluación exhaustiva con pruebas de diagnóstico complementarias no reveló ninguna causa de eosinofilia. Por lo tanto, se diagnosticó eosinofilia inducida por clozapina. Se suspendió el fármaco, el recuento de eosinófilos volvió progresivamente a la normalidad, pero los síntomas psicóticos empeoraron. Conclusiones: A menudo se teme tratar con clozapina por sus posibles efectos secundarios y sus complicaciones, lo cual retrasa su uso en la esquizofrenia refractaria. Además, hasta donde sabemos, no existen pautas específicas sobre cómo tratar los efectos secundarios hematológicos como la eosinofilia. Esto es problemático porque, en algunos casos, puede conducir a suspender innecesariamente la clozapina y que empeoren los síntomas psicóticos. Se presenta una breve discusión de la literatura reciente sobre el tema.

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BACKGROUND: Rheumatic diseases are associated with an increase in overall risks of tuberculosis (TB). The aim of this study was to evaluate the frequency of TB and the frequency of latent TB infection (LTBI), in clinical practice, for juvenile idiopathic arthritis (JIA) patients from high and low risk of TB incidence endemic countries. METHODS: This is an international, multicenter, cross-sectional, observational study of data collection from Brazil and Registry of Portugal at REUMA.PT. The inclusion criteria were patients with Juvenile Idiopathic Arthritis (JIA) with age ≤ 18 years who underwent screening for Mycobacterium tuberculosis infection [tuberculin skin test (TST) and/or interferon gamma release assay (IGRA)]. Chest X-rays and history of exposure to TB were also assessed. RESULTS: 292 JIA patients were included; mean age 14.3 years, mean disease duration 7.5 years, 194 patients (66.4%) performed only TST, 14 (4.8%) only IGRA and 84 (28.8%) both. The frequency of LTBI (10.6%) and TB was similar between the two countries. The reasons for TB screening were different; in Brazil it was performed more often at JIA onset while in Portugal it was performed when starting Disease Modified Anti-Rheumatic Drugs (DMARD) treatment (p < 0.001). Isoniazid therapy was prescribed in 40 (13.7%) patients (31 with LTBI and 9 with epidemiologic risks and/or due to contact with sick people). Only three patients (1%) developed active TB. CONCLUSION: We found nearly 10% of patients with LTBI, a small percentage of patients with treatment due to epidemiologic risks and only 1% with active TB. Distinct reasons and screening methods for LTBI were observed between the two countries.

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Objetivo:Avaliar a evolução da reparação tecidual de úlcera venosa (UV) tratada com plasma rico em plaquetas (PRP). Métodos: Trata-se de relato de caso com aplicação de PRP para tratamento de UV em uma clínica especializada de uma cidade do sul de Minas Gerais. A cada sessão foram coletados 20 mL de sangue distribuídos em quatro tubos com citrato de sódio. O sangue passou por centrifugação para a extração do PRP. O plasma foi aplicado na ferida após a limpeza com água destilada e solução de polihexametileno biguanida. Posteriormente, a lesão foi coberta com gazes impregnada com petrolato e gazes estéreis como cobertura secundária, associado à terapia compressiva elástica. Resultados: Anteriormente à terapia, a úlcera apresentava 1,18 cm² de área. Após quatro semanas de tratamento com PRP, ocorreu a completa cicatrização. Conclusão: O tratamento mostrou-se eficaz e houve 100% de redução de área.

Objective:To evaluate the evolution of tissue repair in venous ulcers treated with platelet-rich plasma. Methods: This is a case report with the application of platelet-rich plasma for the treatment of venous ulcers in a specialized clinic in a city in the south of Minas Gerais. At each session, 20 mL of blood was collected and distributed into four tubes with sodium citrate. The blood was centrifuged to extract platelet-rich plasma. Plasma was applied to the wound after cleaning with distilled water and polyhexamethylene biguanide solution. Subsequently, the lesion was covered with gauze impregnated with petrolatum and sterile gauze as a secondary coverage, associated with elastic compression therapy. Results: Prior to therapy, the ulcer had an area of 1.18 cm². After five weeks of treatment with platelet-rich plasma, complete healing has occurred. Conclusion: Tissue repair occurred after five weeks of treatment without any complications.

Objetivo:Evaluar la evolución de la reparación tisular en úlceras venosas tratadas con plasma rico en plaquetas. Métodos: Este es un reporte de caso con la aplicación de plasma rico en plaquetas para el tratamiento de úlceras venosas en una clínica especializada en una ciudad del sur de Minas Gerais. En cada sesión se recogieron 20 ml de sangre y se distribuyeron en cuatro tubos con citrato de sodio. La sangre se centrifugó para extraer plasma rico en plaquetas. Se aplicó plasma a la herida después de limpiarla con agua destilada y solución de polihexametileno biguanida. Posteriormente se cubrió la lesión con gasa impregnada de vaselina y gasa estéril como cobertura secundaria, asociada a terapia compresiva elástica. Resultados: Inicialmente la terapia, la úlcera tenía un área de 1,18 cm². Después de cinco semanas de tratamiento con plasma rico en plaquetas, se produjo una curación completa. Conclusión: La reparación del tejido ocurrió después de cinco semanas de tratamiento sin ninguna complicación.

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Introdução:O vitiligo é uma doença caracterizada por máculas hipocrômicas e/ou acrômicas assintomáticas, localizadas ou generalizadas no sistema tegumentar. A despigmentação visível na pele do indivíduo e, usualmente, exposta no cotidiano altera a imagem corporal, impactando na sua qualidade de vida. Objetivo: Avaliar a qualidade de vida das pessoas que convivem com o vitiligo. Método: Trata-se de um estudo transversal realizado com 86 indivíduos com vitiligo. Para a coleta de dados, utilizou-se o questionário Vitiligo-Specific Quality-of-Life Instrument para a qualidade de vida. Resultados: As mulheres (81,4%) em idade adulta (média de 39 anos) com vitiligo apresentaram médio impacto na qualidade de vida, e os fatores que interferiram na qualidade de vida estão relacionados aos cuidados intensificados com a pele, à progressão e à aparência da patologia. Conclusão: A patologia vitiligo interferiu na qualidade de vida dos indivíduos adultos. Os fatores que impactaram na qualidade de vida foram os cuidados intensificados com a pele em atividades de lazer, a preocupação com a progressão da doença e a aparência das manchas hipocrômicas.

Introduction:Vitiligo is a disease characterized by asymptomatic hypochromic and/or achromic macules, localized or generalized in the integumentary system. The visible depigmentation in the skin of the individual and usually exposed in daily life changes the body image, impacting their quality of life. Objective: To evaluate the quality of life of people living with vitiligo. Method: This is a cross-sectional study carried out with 86 individuals with vitiligo. For data collection, the Vitiligo-Specific Quality-of-Life Instrument questionnaire was used for quality of life. Results: Adult women (81.4%) (mean age 39 years old) with vitiligo had a medium impact on quality of life, and the factors that interfered with quality of life are related to intensified skin care, progression, and appearance of the disease. Conclusion: The vitiligo pathology interfered in the quality of life of adults. The factors that impacted quality of life were intensified skin care in leisure activities, the progression of the disease and the appearance of hypochromic spots.

Introducción:El vitíligo es una enfermedad caracterizada por máculas hipocrómicas y/o acrómicas asintomáticas, localizadas o generalizadas en el sistema tegumentario. La despigmentación visible en la piel del individuo y, generalmente expuesta en la vida diaria, cambia la imagen corporal impactando en su calidad de vida. Objetivo:Evaluar la calidad de vida de las personas que viven con vitíligo. Método: Se trata de un estudio transversal realizado con 86 individuos con vitíligo. Para la recolección de datos se utilizó el cuestionario Vitiligo-specific Quality-of-Life Instrument (VitQol) para la calidad de vida. Resultados: Las mujeres adultas (81,4%) (edad media 39 años) con vitíligo tuvieron un impacto medio en la calidad de vida y los factores que interfieren en la calidad de vida están relacionados con el cuidado intensificado de la piel, la progresión y aparición de la patologia. Conclusión:La patología vitíligo interfirió en la calidad de vida de los adultos. Los factores que impactaron en la CV fueron el cuidado intensificado de la piel en las actividades de ocio, la preocupación por la progresión de la enfermedad y la aparición de manchas hipocrómicas.

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Abstract Background: Rheumatic diseases are associated with an increase in overall risks of tuberculosis (TB). The aim of this study was to evaluate the frequency of TB and the frequency of latent TB infection (LTBI), in clinical practice, for juvenile idiopathic arthritis (JIA) patients from high and low risk of TB incidence endemic countries. Methods: This is an international, multicenter, cross-sectional, observational study of data collection from Brazil and Registry of Portugal at REUMA.PT. The inclusion criteria were patients with Juvenile Idiopathic Arthritis (JIA) with age ≤ 18 years who underwent screening for Mycobacterium tuberculosis infection [tuberculin skin test (TST) and/or interferon gamma release assay (IGRA)]. Chest X-rays and history of exposure to TB were also assessed. Results: 292 JIA patients were included; mean age 14.3 years, mean disease duration 7.5 years, 194 patients (66.4%) performed only TST, 14 (4.8%) only IGRA and 84 (28.8%) both. The frequency of LTBI (10.6%) and TB was similar between the two countries. The reasons for TB screening were different; in Brazil it was performed more often at JIA onset while in Portugal it was performed when starting Disease Modified Anti-Rheumatic Drugs (DMARD) treatment (p < 0.001). Isoniazid therapy was prescribed in 40 (13.7%) patients (31 with LTBI and 9 with epidemiologic risks and/or due to contact with sick people). Only three patients (1%) developed active TB. Conclusion: We found nearly 10% of patients with LTBI, a small percentage of patients with treatment due to epide-miologic risks and only 1% with active TB. Distinct reasons and screening methods for LTBI were observed between the two countries.

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Este artigo visa a apresentar uma pesquisa-intervenção voltada para a compreensão da relação entre família e trabalho, em uma unidade mineradora situada no Norte do Brasil. Adotam-se aqui olhares críticos da psicologia sobre o trabalho. Embora não estivessem previstos originalmente, os dados aqui relatados emergiram do campo, derivados do projeto de pesquisa-intervenção contratado pela empresa, que buscava investigar as variáveis psicossociais que diretamente afetam o trabalho de Operadores de retroescavadeira. A necessidade de buscar maior aproximação dos sujeitos de pesquisa motivou a realização de uma intervenção junto às suas famílias. Essa intervenção foi feita a partir de técnicas grupais, como rodas de conversa e visitas domiciliares, seguida pela análise das percepções dos familiares sobre o trabalho dos Operadores e sobre a relação desses com a empresa. Os resultados destacam a importância do conceito de território para compreender os processos de subjetivação das famílias; os vínculos sociais como fator psicossocial protetivo; a imbricada articulação entre o processo de gestão do trabalho e a política de benefícios sociais. Concluímos destacando a importância dos vínculos familiares para a compreensão real da atividade dos Operadores, e reafirmando a noção de centralidade do trabalho, na conformação do território.

This article aims to present an intervention research focused on understanding the relationship between family and work in a mining unit located in Northern Brazil. Psychology's critical views on work are adopted here. Although not originally foreseen, the data reported here emerged from the field, derived from the intervention research project contracted by the company, which sought to investigate the psychosocial variables that directly affect the work of backhoe operators. The need to get closer to the research subjects motivated the realization of an intervention with their families. This intervention was carried out using group techniques, such as conversation circles and home visits, followed by an analysis of family members' perceptions about the operators' work and their relationship with the company. The results highlight the importance of the concept of territory to understand the subjectivation processes of families; social bonds as a protective psychosocial factor; the imbricated articulation between the work management process and the social benefits policy. We conclude by highlighting the importance of family ties for the real understanding of the operators' activity, and reaffirming the notion of the centrality of work in the shaping of the territory.

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OBJECTIVE: To investigate the relationship between body mass index (BMI) and disease activity in patients with Juvenile Idiopathic Arthritis (JIA). METHODS: Patients with JIA, aged ≤18 years, registered at the Rheumatic Diseases Portuguese Register (Reuma.pt) in Portugal and Brazil were included. Age- and sex-specific BMI percentiles were calculated based on WHO growth standard charts and categorized into underweight (P <3), normal weight (3≤P≤85), overweight (85

97). Disease activity was assessed by Juvenile Arthritis Disease Activity Score (JADAS-27). Uni- and multivariate analyses were performed. RESULTS: A total of 275 patients were included. The prevalence of underweight, normal weight, overweight and obesity was 6.9%, 67.3%, 15.3% and 10.5%, respectively. Underweight patients had significantly higher number of active joints (p <0.001), patient's/parent's global assessment of disease activity (PGA) (p=0.020), physician's global assessment of disease activity (PhGA) (p <0.001), erythrocyte sedimentation rate (ESR) (p=0.032) and overall higher JADAS-27 (p <0.001), compared to patients with normal weight, overweight and obesity. In the multivariate regression, underweight persisted significantly associated with higher disease activity, compared to normal weight (B=-9.430, p <0.001), overweight (B=-9.295, p=0.001) and obesity (B=-9.120, p=0.001), when adjusted for age, gender, country, ethnicity, JIA category and therapies used. The diagnosis of RF- (B=3.653, p=0.006) or RF+ polyarticular JIA (B=5.287, p=0.024), the absence of DMARD therapy (B=5.542, p <0.001) and the use of oral GC (B=4.984, p=0.002) were also associated with higher JADAS-27. CONCLUSION: We found an independent association between underweight and higher disease activity in patients with JIA. Further studies are needed to understand the underlying mechanisms of this association.

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Este artigo discute a relação entre o trabalho dos psicólogos e psicólogas e a tecnologia, no contexto marcado pela pandemia da covid-19. Com base na análise da dupla condição da Psicologia, como ciência e profissão, historicamente construída e reproduzida, o texto propõe uma análise crítica da intensificação do uso das Tecnologias de Informação e Comunicação (TIC), com ênfase na atividade de atendimentos clínicos individuais, por se tratar de uma modalidade de serviço em flagrante expansão no atual contexto, em razão das contingências impostas pela pandemia. Como resultados preliminares, evidencia-se o crescimento, sem precedentes, do número de cadastros de psicólogos e psicólogas interessados em realizar atendimento online e observam-se ações dos órgãos reguladores da profissão que objetivam fiscalizar tais práticas e impedir o uso indevido da tecnologia. Ressaltam-se, neste cenário, os riscos da "uberização" do trabalho do psicólogo e psicóloga e de uma retração do campo da Psicologia como profissão.

This article discusses, in the context marked by the Covid-19 pandemic, the relationship between the work of psychologists and technology. Based on the analysis of the double role of Psychology as science and profession, historically constructed and reproduced, the text proposes a critical analysis of the intensified use of Information and Communications Technology (ICT), especially regarding the activity of individual clinical care as a kind of service in clear expansion in the current context, due to the restrictions imposed because of the pandemic. As a preliminary result, it is observed an unprecedented growth of registration numbers of psychologists interested in providing online care, as much as the actions of the professional councils aiming to inspect such practices and prevent the misuse of technology. In this scenario, we stress the risks of the uberization of the psychologist's work, and a shrinking of the professional field.

Este artículo analiza la relación entre el trabajo de los psicólogos y la tecnología, en el contexto marcado por la pandemia Covid-19. A partir del análisis de la doble condición de la Psicología, como ciencia y profesión, históricamente construida y reproducida, el texto propone un análisis crítico de la intensificación del uso de las Tecnologías de Información y Comunicación (TIC), con énfasis en la actividad de atención clínica individual, por ser una modalidad de servicio en flagrante expansión en el contexto actual, debido a las contingencias impuestas por la pandemia. Como resultado preliminar es observado un crecimiento sin precedentes del número de registros de psicólogos interesados en realizar la asistencia en línea, al lado de las acciones de los organismos reguladores de la profesión para inspeccionar tales prácticas. En este contexto, al mismo tiempo, se señalan los riesgos de "uberización" del trabajo del psicólogo y de una retracción del campo de la psicología como profesión.

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