Non-Donors of Organs and Tissues Due to Medical Refusal in a Transplant Referral Service.

BACKGROUND: Obtaining organs for transplants through a deceased donor occurs exclusively through donation. However, some open protocols with potential donors do not become effective donors due to medical refusal. Our aim was to identify the profile of non-donors of organs and tissues due to medical refusal in a state reference service for transplants. METHODS: This is a cross-sectional study with retrospective data collection from medical records of patients who died and had a protocol opened to evaluate brain death and procurement of organs and tissues in 2019. RESULTS: The sample consisted of 27 patients, the majority of whom were female, aged over 71 years, had primary education, and were married. The main causes of medical refusal were age above the recommended age and septicemia. Brain death was mostly confirmed within 12 hours, and the main cause of hospitalization was a vascular event. CONCLUSIONS: Identifying the profile of non-donors due to medical refusal is necessary for services to identify possible misattributed medical contraindications and thus contribute to reducing the disproportion between supply and demand for organs and tissues for transplants.

Global legislation regulating the donation, procurement and distribution processes of organs and tissues from deceased donors for transplants: A scoping review.

Introduction: Organ transplantation is one of the most successful advances in modern medicine. However, a legal system is necessary for its practice to be free from ethical flaws and to respect donors, recipients, and family members. Objective: To map the global legislation regulating the donation, capture and distribution processes of organs and tissues from deceased donors for transplants. Method: A scoping review according to the Joanna Briggs Institute was conducted in the following databases: Medline, CINAHL, Virtual Health Library, SCOPUS, Web of Science, Science Direct, and EMBASE, as well as gray literature, and reported according to the PRISMA extension for scoping reviews. Results: We identified 3302 records, of which 77 were analyzed which enabled mapping the type of consent adopted and the existence of current legislation for harvesting organs and tissues after circulatory and brain death. Conclusion: Opt-out consent predominates in Europe, and there is harvesting after brain and circulatory death. Opt-out predominates in the Americas, while Opt-in and harvesting of organs and tissues after brain death predominate in Asia and Oceania. The procurement of organs and tissues from deceased donors is practically non-existent in Africa.

Chronic kidney disease intervention in primary health care: integrative review

To analyze the knowledge and safety of primary health care professionals in the management of chronic kidney disease in its early stages. Integrative literature review carried out in four steps. The search took place in the following databases: MEDLINE via PubMed, Web of Science, Scopus and BVS. The descriptors used were "Primary Health Care" AND "Kidney Diseases" AND "Health Knowledge, Attitudes, Practice" and the quality of the analysis was checked by means of the Hierarchy of Evidence for Intervention Studies". Fifteen articles were found, with a predominance of qualitative and descriptive method; the results showed insufficient knowledge of health professionals and interest in the best approach in the initial stage of the disease. Thus, it is inferred that the knowledge and security of primary health care professionals depend on individual factors and institutional initiative for the adoption of clinical guidelines and training. Therefore, prepared professionals and organized care, using protocols, would bring benefits both to patients as to the evolution and outcome of the disease and savings to health services.

Fatores de risco para near miss materno: revisão integrativa / Risk factors for maternal near miss: an integrative review / Factores de riesgo para near miss materno: revisión integrativa

Objetivo: sumarizar os principais fatores de risco relacionados ao near miss materno. Método: revisão integrativa da literatura. A busca foi efetuada em 21 de março de 2021, nas bases de dados: NationalLibrary of Medicine - Medline via PubMed; Current Index to Nursing and Allied Health Literature; Science Direct,Elservier's Scopus, Web of Science e no portal da Biblioteca Virtual de Saúde. Os estudos foram avaliados com a Hierarchy of Evidence for Intervention Studies. Resultados: 12 artigos compuseram a revisão, todos de método quantitativo e idioma inglês. As evidências destacaram como risco para near miss materno: distúrbios hipertensivos, complicações hemorrágicas e a sepse puerperal. Demais achados relacionam-se à distância da moradia e dificuldade de acesso aos serviços de saúde além da baixa escolaridade. Conclusões: os fatores de risco para near miss materno se relacionam com pré-natal inadequado, decorrente de questões geográficas e falta de acesso aos serviços, questões econômicas, educacionais e sociais.

Costs related to obtaining organs for transplantation: A systematic review.

INTRODUCTION: The number of transplants in the world is growing, although there is a demand that exceeds supply. It is worth mentioning that the costs for obtaining organs are considered high. However, few studies have been developed on analyzing the costs of obtaining organs and tissues for transplants in order to support the decision-making of managers and health professionals. OBJECTIVE: To summarize the studies related to the cost of obtaining organs for transplants from a deceased donor. METHOD: A systematic literature review was conducted in the following databases: PubMed, Cochrane Library CINAHAL, Virtual Health Library (BVS), SCOPUS, Web of Science and EMBASE, using the following descriptors: Costs and cost analysis; Donor Selection; Tissue and Organ Procurement; Tissue and Organ Harvesting; and Tissue Donors, in studies published until April 2021. The risk of bias assessment was performed using the Joanna Briggs Institute's Checklist for Economic Assessments. It was not possible to perform a meta-analysis due to the heterogeneity of the studies. RESULTS: A total of 1731 studies were identified, of which 11 were analyzed. The cost of kidneys in US dollars (USD) ranged between USD $1672 and USD $25,058. Obtaining a liver ranged from USD $586 to USD $44,478. Heart procurement ranged from USD $633 to USD $24,264. The combined heart-lung transplant ranged from USD $860 to USD $23,203. Obtaining the pancreas ranged from USD $413 to USD $29,708. CONCLUSIONS: Cost of obtaining organs for transplants from a deceased donor is substantial and varies widely across different studies. The overall cost of failures to obtain organs is currently unknown. Understanding organ procurement expenses can help clarify areas in which organ and tissue procurement can improve in cost and efficiency.

Analysis of the temporal trend of mortality from sickle cell anemia in Brazil.

OBJECTIVES: To analyze the temporal trend of mortality from sickle cell anemia in Brazil, by region, in the period 1997-2017. METHODS: epidemiological study, with an ecological design, with a temporal trend, carried out with data from the Mortality Information System. For descriptive analysis, absolute and relative frequencies were used. In the correlation analysis, the ANOVA test was used, followed by Tukey's post-test. The temporal trend was obtained using the cubic polynomial regression test. RESULTS: 6,813 deaths from sickle cell anemia were registered. Brown individuals (50.87%) were more frequent, with a predominance of males (50.4%), aged between 25 and 34 years and a higher incidence of deaths in the Midwest (0.25/100 thousand inhabitants). The time curve showed an increasing trend of deaths in the country between 1997 and 2015 (R2 = 0.98). CONCLUSIONS: sickle cell anemia showed increasing mortality in the 21 years analyzed and alerts health professionals and managers.

Clinical-Epidemiological Characteristics and Mortality in Patients with Sickle Cell Anemia: A Retrospective Cohort Study of 1980 at 2018.

PURPOSE: To analyze the clinical-epidemiological characteristics and mortality in patients with sickle-cell anemia (SCA). PATIENTS AND METHODS: A cohort study with retrospective data, conducted in two reference hospitals for SCA treatment from January 1980 to December 2018, recorded in two reference services. With a 5% significance level, the Chi-Square and Student's t-tests were employed in the inferential statistical analysis. RESULTS: A total of 128 patients with SCA were studied. Diagnosis up to the fifth day of life was made in 10 patients. There were 19 deaths, of which 12 (63.2%) were female, and the average age at death was 27.05 (± 14.78) years. The leading causes of death were septic shock and cardiogenic shock. The use of invasive medical devices was considered a risk factor for death (RR=2.63; 95% CI=1.16-5.96; p=0.018), and monitoring time up to 20 years presented a 31% reduction in the risk of dying (RR=0.31; 95% CI=0.12-0.82; p=0.011) when compared to the monitoring of more than 20 years. CONCLUSION: These findings are to be considered in the treatment of patients with SCA, mainly regarding early diagnosis and access to the treatment immediately afterward, since they are fundamental in improving survival and reducing severe complications.

Vivências de estudantes de enfermagem no início da pandemia da Covid-19: abordagem qualitativa / Experiences of nursing students at the beginning of the Covid-19 pandemic: a qualitative approach

OBJETIVO: Compreender a vivência de estudantes de enfermagem no início da pandemia da Covid-19. MÉTODO: Estudo exploratório, com abordagem qualitativa, realizado com 36 estudantes de enfermagem, matriculados em universidade pública brasileira. Dados coletados por videoconferência e entrevista semiestruturada, submetidos à análise de conteúdo. RESULTADOS: Emergiram duas categorias: "Ser estudante de enfermagem em tempos de pandemia da Covid-19 e ensino remoto de emergência" e "Transformações no cotidiano dos estudantes no início da pandemia". A vivência dos estudantes se revelou exaustiva e estressante, interferindo na saúde e no bem-estar. O cotidiano dos participantes foi marcado por mudanças, sobretudo, na experiência com o ensino remoto de emergência, que exigiu o desenvolvimento de estratégias adaptativas. CONCLUSÃO: O planejamento e o uso de estratégias de promoção da saúde e apoio contínuo aos estudantes que vivenciaram o contexto da pandemia, pelos cursos de enfermagem, tornam-se importantes.

OBJECTIVE: To understand the experience of nursing students at the beginning of the Covid-19 pandemic. METHOD: A exploratory study with a qualitative approach was carried out with 36 nursing students in a Brazilian public university. The data were collected by videoconference, and the semi-structured interviews were submitted for content analysis. RESULTS: Two categories emerged: "Being a nursing student in times of the Covid-19 pandemic and emergency remote teaching" and "Transformations in students' daily lives at the beginning of the pandemic". The students' experiences were exhausting and stressful, interfering with their health and well-being. The participants' daily lives were marked by changes, especially in the experience with emergency remote teaching, which required the development of adaptive strategies. CONCLUSION: The planning and use of health promotion strategies and continuous support for students who experienced the context of the pandemic through nursing programs become important.

Analysis of the temporal trend of mortality from sickle cell anemia in Brazil / Análisis de la tendencia temporal de la mortalidad por anemia de células falciformes en Brasil / Análise da tendência temporal da mortalidade por anemia falciforme no Brasil

ABSTRACT Objectives: To analyze the temporal trend of mortality from sickle cell anemia in Brazil, by region, in the period 1997-2017. Methods: epidemiological study, with an ecological design, with a temporal trend, carried out with data from the Mortality Information System. For descriptive analysis, absolute and relative frequencies were used. In the correlation analysis, the ANOVA test was used, followed by Tukey's post-test. The temporal trend was obtained using the cubic polynomial regression test. Results: 6,813 deaths from sickle cell anemia were registered. Brown individuals (50.87%) were more frequent, with a predominance of males (50.4%), aged between 25 and 34 years and a higher incidence of deaths in the Midwest (0.25/100 thousand inhabitants). The time curve showed an increasing trend of deaths in the country between 1997 and 2015 (R2 = 0.98). Conclusions: sickle cell anemia showed increasing mortality in the 21 years analyzed and alerts health professionals and managers.

RESUMEN Objetivos: analizar tendencia temporal de mortalidad por anemia falciforme en Brasil, por regiones, entre 1997 y 2017. Métodos: estudio epidemiológico, de delineamento ecológico, de tendencia temporal, realizado con datos del Sistema de Informaciones sobre Mortalidad. Utilizado frecuencias absolutas y relativas para análisis descriptivo. Utilizado la prueba ANOVA seguido por la prueba de Tukey en el análisis de correlación. La tendencia temporal fue obtenida mediante la prueba de regresión polinomial cúbico. Resultados: fueron registrados 6.813 óbitos por anemia falciforme. Indivíduos pardos (50,87%) fueron más frecuentes, con predominio del sexo masculino (50,4%), con franja etaria de 25 a 34 años y mayor incidencia de óbitos en Centro-Oeste (0,25/100 mil habitantes). La curva temporal presentó tendencia creciente de óbitos en el país entre 1997 a 2015 (R2 = 0,98). Conclusiones: la anemia falciforme presentó mortalidad creciente en los 21 años analizados y despierta el alerta a profesionales de salud y gestores.

RESUMO Objetivos: analisar a tendência temporal da mortalidade por anemia falciforme no Brasil, por regiões, no período compreendido entre 1997 e 2017. Métodos: estudo epidemiológico, de delineamento ecológico, de tendência temporal, realizado com dados do Sistema de Informações sobre Mortalidade. Para análise descritiva, utilizaram-se frequências absolutas e relativas. Na análise de correlação, utilizou-se o teste ANOVA seguido pelo pós-teste de Tukey. A tendência temporal foi obtida mediante o teste de regressão polinomial cúbico. Resultados: foram registrados 6.813 óbitos por anemia falciforme. Indivíduos pardos (50,87%) foram mais frequentes, com predomínio do sexo masculino (50,4%), com faixa etária de 25 a 34 anos e maior incidência de óbitos no Centro-Oeste (0,25/100 mil habitantes). A curva temporal apresentou tendência crescente de óbitos no país entre 1997 a 2015 (R2 = 0,98). Conclusões: a anemia falciforme apresentou mortalidade crescente nos 21 anos analisados e desperta o alerta aos profissionais de saúde e gestores.

Mask decontamination methods (model N95) for respiratory protection: a rapid review.

BACKGROUND: N95 respiratory protection masks are used by healthcare professionals to prevent contamination from infectious microorganisms transmitted by droplets or aerosols. METHODS: We conducted a rapid review of the literature analyzing the effectiveness of decontamination methods for mask reuse. The database searches were carried out up to September 2020. The systematic review was conducted in a way which simplified the stages of a complete systematic review, due to the worldwide necessity for reliable fast evidences on this matter. RESULTS: A total of 563 articles were retrieved of which 48 laboratory-based studies were selected. Fifteen decontamination methods were included in the studies. A total of 19 laboratory studies used hydrogen peroxide, 21 studies used ultraviolet germicidal irradiation, 4 studies used ethylene oxide, 11 studies used dry heat, 9 studies used moist heat, 5 studies used ethanol, two studies used isopropanol solution, 11 studies used microwave oven, 10 studies used sodium hypochlorite, 7 studies used autoclave, 3 studies used an electric rice cooker, 1 study used cleaning wipes, 1 study used bar soap, 1 study used water, 1 study used multi-purpose high-level disinfection cabinet, and another 1 study used chlorine dioxide. Five methods that are promising are as follows: hydrogen peroxide vapor, ultraviolet irradiation, dry heat, wet heat/pasteurization, and microwave ovens. CONCLUSIONS: We have presented the best available evidence on mask decontamination; nevertheless, its applicability is limited due to few studies on the topic and the lack of studies on real environments.

Estudos econômicos completos sobre tratamentos da anemia falciforme / Estudios económicos completos sobre tratamientos para la anemia falciforme / Comprehensive economic studies on sickle cell anemia treatments

Resumo Objetivo: Analisar os estudos econômicos completos com enfoque nos tratamentos da Anemia Falciforme. Métodos: Estudo de revisão integrativa de literatura desenvolvido mediante coleta de dados nas bases eletrônicas National Library of Medicine - Medline via PubMed; Elservier's Scopus; Current Index to Nursing and Allied Health Literature; Science Direct e Web of Science com descritores indexados no Medical Subject Headings. Os estudos foram selecionados pelo teste de relevância e analisados de acordo com a classificação das análises econômicas em saúde e o sistema de Classificação da qualidade das evidências e a força das recomendações. Resultados: Fizeram parte desta revisão 09 artigos, dos quais sete recuperados na base Elservier's Scopus e dois na Medline via PubMed. Todos estudos completos com enfoque nas perspectivas do uso da Hidroxiureia e da transfusão sanguínea no tratamento da Anemia Falciforme. Conclusão: Não foram identificados estudos realizados no Brasil com este tipo de análise para Anemia Falciforme. Há muito a ser feito mundialmente para avaliação das tecnologias vigentes, reavaliação das utilizadas atualmente e implementação de diagnóstico e tratamento contínuo, com um sistema que garanta uma rede de atenção ativa e eficiente aos pacientes.

Resumen Objetivo: Analizar los estudios económicos completos con enfoque en tratamientos para la anemia falciforme Métodos: Estudio de revisión integradora de la literatura desarrollado mediante la recolección de datos en las bases electrónicas National Library of Medicine - Medline vía PubMed; Elservier's Scopus; Current Index to Nursing and Allied Health Literature; Science Direct y Web of Science con descriptores indexados en Medical Subject Headings. Los estudios fueron seleccionados mediante la prueba de relevancia y analizados de acuerdo con la clasificación de análisis económicos en salud y con el sistema de clasificación de la calidad de las evidencias y la fuerza de las recomendaciones. Resultados: Nueve artículos formaron parte de esta revisión, de los cuales siete fueron encontrados en la base Elservier's Scopus y dos en Medline vía PubMed. Todos son estudios completos con enfoque en las perspectivas del uso de hidroxiurea y transfusión sanguínea para el tratamiento de anemia falciforme. Conclusión: No se identificaron estudios realizados en Brasil con este tipo de análisis de anemia falciforme. Hay mucho por hacer a nivel mundial para evaluar las tecnologías vigentes, revaluar las que se utilizan en la actualidad e implementar el diagnóstico y tratamiento continuo, con un sistema que garantice una red de atención activa y eficiente para los pacientes.

Abstract Objective: To analyze complete economic studies focusing on sickle cell anemia treatments. Methods: Integrative literature review developed by collecting data in the electronic databases National Library of Medicine - Medline via PubMed; Elsevier's Scopus; Current Index to Nursing and Allied Health Literature; Science Direct and Web of Science with descriptors indexed in Medical Subject Headings. The studies were selected by the relevance test and analyzed according to the classification of economic analyses in health and the classification system of evidence quality and strength of recommendations. Results: Nine articles were part of this review, seven of which were retrieved from Elsevier's Scopus and two from Medline via PubMed. All articles reported on studies focusing on the perspectives of using hydroxyurea and blood transfusion in the treatment of sickle cell anemia. Conclusion: No studies were identified that were conducted in Brazil and involved this type of analysis for sickle cell anemia. Much remains to be done worldwide to assess existing technologies, reassess the technologies currently used and implement continuous diagnosis and treatment, by means of a system that guarantees an active and efficient care network for the patients.

Fatores de risco para mortalidade em pacientes com doença falciforme: uma revisão integrativa / Factores de riesgo para la mortalidad en pacientes con enfermedad falciforme: una revisión integradora / Risk factors for mortality in patients with sickle cell disease: an integrative review

RESUMO Objetivo Sumarizar fatores de risco e indicadores de mortalidade em pacientes com doença falciforme. Método Revisão integrativa em periódicos indexados nas bases de dados CINAHL, PubMed/MEDLINE, Science Direct/SCOPUS, SciELO e Web of Science. A questão norteadora foi elaborada por meio da estratégia Population, variable, outcome (PVO). A busca ocorreu no portal de periódicos da Coordenação de Aperfeiçoamento de Pessoal de Nível Superior entre outubro e novembro de 2018. Resultados Dos 19 artigos, 18 eram coorte e um ensaio clínico randomizado. A amostra foi constituída, em sua maioria, pelo sexo feminino e genótipo HbSS. Se repetiram mais a taxa de mortalidade cumulativa e a curva de mortalidade global. Sete estudos identificaram fatores de risco com associação estatisticamente significativa para morte. Os mais frequentes foram o baixo nível de hemoglobina, variáveis hepáticas (enzimas fosfatase alcalina e transaminase glutâmico oxalacética) e cardiovasculares (velocidade de regurgitação da válvula tricúspide ≥ 2,5m/s). Conclusão e implicações para a prática Indicadores de mortalidade constituem ferramentas de manejo de pacientes com doença falciforme e prevenção de riscos e complicações. Há necessidade de estudos sobre os fatores relacionados à mortalidade desses pacientes. A prevenção do óbito, certamente, promoverá uma melhoria na qualidade de vida e na sobrevida dessa população.

RESUMEN Objetivo Resumir los factores de riesgo y los indicadores de mortalidad en pacientes con enfermedad de células falciformes. Método revisión integradora de publicaciones en las bases de datos CINAHL, PubMed/MEDLINE, Science Direct/SCOPUS, SciELO y Web of Science. La pregunta guía basada en Population, variable, outcome (PVO) conduciu la búsqueda en el Portal de revistas de la Coordinación de Mejoramiento de Personal de Nivel Superior, entre octubre-noviembre de 2018, con los descriptores anemia, sickle cell "and" mortality "and" survival y sus sinónimos. Resultados De 18/19 artículos son cohortes y un ensayo controlado aleatorio. La muestra consistió en mujeres y genotipo HbSS. La tasa de mortalidad acumulada y la curva de mortalidad general fueron más repetidas. Siete estudios identificaron factores de riesgo con asociación estadísticamente significativa con la muerte. Los más frecuentes fueron el bajo nivel de hemoglobina, variables hepáticas (fosfatasa alcalina y enzimas glutámicas transaminasas oxalacéticas) y variables cardiovasculares (velocidad de regurgitación de la válvula tricúspide ≥ 2.5m/s). Conclusión e implicaciones para la práctica Los indicadores de mortalidad son herramientas de manejo de los pacientes con esta enfermedad, la prevención de factores de riesgo y complicaciones. Hace necesidad de estudios sobre los factores relacionados con la mortalidad. La prevención de las muertes mejorará la calidad de vida y la supervivencia.

ABSTRACT Objective To summarize the risk factors and mortality indicators in sickle cell disease patients. Method Integrative review searched publications in journals in CINAHL, PubMed/MEDLINE, Science Direct/SCOPUS, SciELO, and Web of Science databases. The guiding question was elaborated through the Population, Variable, Outcome (PVO) strategy and the search was from October-to-November 2018, at the Coordination of Higher Level Personnel Improvement Periodicals' Gate. The keywords anemia, sickle cell "and" mortality "and" survival and their synonyms were used. Results From 18/19 articles were cohort and one randomized controlled trial. The sample consisted mostly of females and HbSS genotype. The cumulative mortality rate and the overall mortality curve were the most repeated. Seven studies identified risk factors with a statistically significant association with death. The most frequent were low hemoglobin level, liver variables (alkaline phosphatase and oxalacetic glutamic transaminase enzymes) and cardiovascular variables (tricuspid valve regurgitation speed ≥ 2.5m/s). Conclusion and implications for practice Mortality indicators are tools for better management of sickle cell disease's patient, prevention of risks and complications. There is a need for further studies on the factors related to mortality of these patients. Preventing the causes that lead to death will certainly improve the quality of life and survival of this population.

Clinical and epidemiological profile of children and adolescents submitted to the hematopoietic cell transplantation / Perfil clínico e epidemiológico de crianças e adolescentes submetidos ao transplante de células-tronco hematopoéticas

The Hematopoietic stem cell transplantation (HSCT) is used in children as a definitive treatment for various oncological, immune deficiencies, hemoglobinopathy, and malignancies diseases that involve the hematological system, congenital metabolism disorders, among others. To characterize the clinical and epidemiological profile of children and adolescents submitted to HSCT at a referral service in the state of Rio Grande do Norte. This is a quantitative, retrospective, observational, descriptive and analytical quantitative approach approaching the medical records of children and adolescents submitted to HSCT in a referral hospital service for this type of transplantation in the state of Rio Grande do Sul North (RN). The final sample consisted of 35 records patients aged between 2 and 18 years old who underwent HSCT from February 2008 to December 2015 and who presented the data necessary for the study. The records analyzed showed a littlemajority of male patients (51.42%) and 60.00% of these men were students and 71.42% lived in the state of the Rio Grande do Norte. According to the clinical characteristics, 34.3% of the patients had Acute Lymphoblastic Leukemia and 25.71% had Acute Myeloid Leukemia as the main diagnosis. Gastrointestinal toxicities were the most frequent (97.1%) and all patients received antineoplastic/chemotherapeutic and antiemetic treatment. The allogeneic HSCT was the most frequently performed (57.14%) and the most used source of Hematopoietic progenitor cells (HPC) was the peripheral blood (54.29%) and 5.71% of these patients developed the Graft versus Host Disease (GVHD), of which one was affected by acute GVHD and another by chronic GVHD. Septsis was the most frequent cause of death (60%). The profile of the clinical variables presented by the children and adolescents of this study shows that the most prevalent diagnosis was ALL, the most frequent toxicities were gastrointestinal, cardiac, respiratory and hematological, the most common HSCT was allogeneic peripheral blood and the greatest cause of mortality was sepsis. These data are similar to studies conducted in North America, Europe and Asia.

O Transplante de Células-Tronco Hematopoéticas (TCTH) é utilizado em crianças como um tratamento definitivo para várias doenças oncológicas, imunodeficiências, hemoglobinopatias, malignidades que envolvem o sistema hematológico, distúrbios de metabolismo congênito, entre outros. Caracterizar o perfil clínico e epidemiológico de crianças e adolescentes submetidos ao TCTH em um serviço de referência do estado do Rio Grande do Norte. Trata de um estudo epidemiológico de abordagem quantitativa, do tipo coorte retrospectiva, observacional, descritivo e analítico onde foram abordados os prontuários de crianças eadolescentes submetidos ao TCTH em um serviço hospitalar de referência para esse tipo de transplante no estado do Rio Grande do Norte (RN). A amostra final foi composta por 35 prontuários de pacientes com idade entre dois e 18 anos que realizaram o TCTH no período de fevereiro de 2008 a dezembro de 2015 e que apresentavam os dados necessários ao estudo. Do total de prontuários analisados houve discreta maioria de pacientes do sexo masculino (51,42%). Destes, 60,00% eram estudantes e 71,42% residiam no estado do RN. De acordo com as características clínicas, 34,3% apresentaram como diagnóstico principal a Leucemia Linfoblástica Aguda e 25,71% a Leucemia Mieloide Aguda. As toxicidades gastrointestinais foram as que mais ocorreram (97,1%) e todos receberam tratamento com antineoplásicos/quimioterápicos e antieméticos. O TCTH alogênico foi o mais frequentemente realizado (57,14%) e a fonte de CPH mais utilizada foi o sangue periférico (54,29%) e 5,71% desenvolveram a Doença do Enxerto Contra Hospedeiro (DECH), dos quais um foi acometido por DECH aguda e outro pela forma crônica. A causa de morte com maior frequência foi a sepse (60%). O perfil das variáveis clínicas apresentadas pelas crianças e adolescents desta pesquisa mostram que o diagnóstico mais prevalente foi o de LLA, as toxicidades que mais ocorreram foram as gastrointestinais, cardíacas, respiratórias e hematológicas, o TCTH mais realizado foi o alogênico de sangue periférico e a maior causa de mortalidade foi a sepse. Tais dados se assemelham aos estudos realizados na América do Norte,Europa e Ásia.

Prevalência da doença falciforme em adultos com diagnóstico tardio / Prevalencia de la anemia falciforme en adultos con diagnóstico tardío / Prevalence of sickle cell disease in adults with delayed diagnosis

Resumo Objetivo: Estimar a prevalência da doença falciforme em adultos com diagnóstico tardio, em tratamento nos ambulatórios de hematologia na rede de saúde do Estado do Mato Grosso do Sul de 2013 a 2017; descrever as características sociodemográficas; verificar associações entre os genótipos em relação a idade atual, os genótipos e a idade ao diagnóstico. Métodos: Estudo transversal, retrospectivo, com dados coletados em dois hospitais de ensino. As variáveis investigadas foram: ano do atendimento, genótipo, sexo, data de nascimento, idade ao diagnóstico, naturalidade e procedência. A prevalência foi estimada por ponto (%) e intervalo de confiança de 95%. Resultados: A prevalência foi 3,9%, com 103 adultos com doença falciforme, sendo 60 do sexo feminino e 43 do masculino. Predominou o genótipo HbSS, seguido pelo HbSC. A mediana de idade foi de 35 para os HbSS e 31 para os HbSC. A mediana de idade ao diagnóstico foi cinco anos para os HbSS e 21 para HbSC. Não houve associação entre idade (anos) dos pacientes e genótipo (teste Qui-quadrado p=0,601) e nem entre genótipo e faixa etária (teste Qui-quadrado p= 0,318). Conclusão: O genótipo mais frequente foi o HbSS, seguido pelo HbSC. O diagnóstico dos pacientes com SC foi mais tardio do que naqueles com genótipo SS. As variáveis sociodemográficas e o diagnóstico tardio alertam para a necessidade de fortalecimento de ações na rede de saúde, que interferem sensivelmente na morbimortalidade de adultos com Doença Falciforme.

Resumen Objetivo: Estimar la prevalencia de la anemia falciforme en adultos con diagnóstico tardío, en tratamiento ambulatorio de hematología de la red de salud del estado de Mato Grosso do Sul de 2013 a 2017; describir las características sociodemográficas; verificar asociaciones entre los genotipos con relación a la edad actual, los genotipos y la edad de diagnóstico. Métodos: Estudio transversal, retrospectivo, con datos recopilados en dos hospitales universitarios. Las variables investigadas fueron: año de atención, genotipo, sexo, fecha de nacimiento, edad de diagnóstico, naturalidad y procedencia. La prevalencia fue estimada por punto (%) e intervalo de confianza de 95%. Resultados: La prevalencia fue 3,9%, con 103 adultos con anemia falciforme, 60 de sexo femenino y 43 masculino. Predominó el genotipo HbSS, seguido de HbSC. La mediana de edad fue 35 años en los HbSS y 31 en los HbSC. La mediana de edad de diagnóstico fue 5 años en los HbSS y 21 en los HbSC. No hubo relación entre edad (años) de los pacientes y genotipo (prueba ⊠2 de Pearson p=0,601) y tampoco entre genotipo y grupo de edad (prueba ⊠2 de Pearson p=0,318). Conclusión: El genotipo más frecuente fue el HbSS, seguido del HbSC. El diagnóstico de los pacientes con SC fue más tardío que el de los de genotipo SS: Las variables sociodemográficas y el diagnóstico tardío advierten sobre la necesidad de fortalecer acciones en la red de salud, que interfieren sensiblemente en la morbimortalidad de adultos con anemia falciforme.

Abstract Objective: To estimate the prevalence of sickle cell disease in adults with delayed diagnosis, receiving treatment at hematology outpatient clinics in the health network of the state of Mato Grosso do Sul, between 2013 and 2017; to describe sociodemographic characteristics; to verify associations between genotypes in relation to current age, the genotypes, and age at diagnosis. Methods: A retrospective, cross-sectional study with data collected at two teaching hospitals. The variables investigated were: year of treatment, genotype, sex, date of birth, age at diagnosis, and city in which they lived. Prevalence was estimated per point, using a 95% confidence interval. Results: The prevalence was 3.9% in 103 adults with sickle cell disease: 60 female and 43 male. The HbSS genotype was predominant, followed by HbSC. The median age was 35 for HbSS, and 31 for HbSC. Median age at diagnosis was five years for HbSS, and 21 for HbSC. No association was found between age (years) of patients and genotype (chi-square test p=0.601), or between genotype and age group (chi-square test p= 0,318). Conclusion: The most frequent genotype was HbSS, followed by HbSC. The diagnosis of patients with hemoglobin SC occurred later in life than those with the hemoglobin SS genotype. Sociodemographic variables and delayed diagnosis warns for the need to strengthen actions in the health network, which interfere significantly in the morbidity and mortality of adults with sickle cell disease.

Condição marcadora para análise da atenção em saúde aos diabéticos pela Estratégia de Saúde da Família / Tracer condition for analysis of attention in health to diabetic patients by family Health Strategy Program

Objetivo: avaliar a assistência prestada por uma equipe da Unidade Básica de Saúde da Família (UBSF) aos pacientes com Diabetes Mellitus (DM). Método: estudo descritivo realizado na ESF Nossa Senhora das Graças, Campo Grande/MS. A população estudada foi composta por usuários da ESF portadores de DM que foram internados. O projeto de pesquisa foi aprovado pelo Comitê de Ética e Pesquisa, CAAE 01679512.9.0000.0021. Os dados foram descritos e analisados e a discussão foi feita à luz da literatura. Resultados: identificou-se 118 pacientes diabéticos cadastrados e um internado por complicações devido ao pé diabético, sendo a taxa de internação esperada para esta população de 0,58/118. Conclusões: o processo de avaliação dos serviços de saúde deve ser permanente, com o aumento do tempo analisado e dos dados coletados, a fim de manter a assistência satisfatória à população assistida.(AU)

Objective: to evaluate the care provided by a team of the Family Health Unit (FHU) to patients with diabetes mellitus (DM). Method: descriptive study performed in the Family Health Strategy Nossa Senhora das Graças, Campo Grande/MS. The study population comprised members of the FHS with DM who were hospitalized. The research project was approved by the Research Ethics Committee, CAAE 01679512.9.0000.0021. Data were described and analyzed and the discussion was made in light of the literature. Results: we identified 118 diabetic patients registered and one hospitalized for complications due to diabetic foot, with an expected hospitalization rate for this population of 0.58/118. Conclusions: the evaluation process of health services should be permanent, with increase of time analyzed and data collected in order to maintain satisfactory assistance to the assisted population.(AU)

Objetivo: evaluar la asistencia prestada por un equipo de la Unidad Básica de Salud de la Familia (UBSF) a los pacientes con Diabetes Mellitus (DM). Método: estudio descriptivo realizado en la ESF Nossa Senhora das Graças, Campo Grande/MS. La población estudiada fue compuesta por usuarios de la ESF portadores de DM que fueron internados. El proyecto de investigación fue aprobado por el Comité de Ética e Investigación, CAAE 01679512.9.0000,0021. Los datos fueron descriptos y analizados y la discusión fue hecha a la luz de la literatura. Resultados: Se identificaron 118 pacientes diabéticos registrados en un internado por complicaciones debido al pie diabético, siendo la tasa esperada para ésta población de 0,58/118. Conclusiones: el proceso de evaluación de los servicios de salud debe ser permanente, con el aumento del tiempo analizado y de los datos recogidos, a fin de mantener la asistencia satisfactoria a la población asistida.(AU)