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This study aims at reporting the indigenous knowledge of the medicinal flora from the inhabitants of surroundings of the World's largest artificial planted forest "Changa Manga", Pakistan. Data were collected by direct interviews and group meetings from 81 inhabitants including 32 local healers having information regarding the use of indigenous medicinal plants over a period of one year. Different statistical tools were applied to analyze the data including Frequency citation (FC), Relative frequency citation (RFC), Use Value, Factor of informants consensus and fidelity level. This study reported 73 plant species belonging to 37 plant families and 46 genera. The majority of plant species belong to compositae family. The most commonly used medicinal plants were P. hysterophorus L., P. dactylifera L., S. indicum L, P. harmala L., P. emblica L., and A. indica A.Juss. The greatest number of species was used to cure gastrointestinal disorders. The highest fidelity level (68.18%) was of E. helioscopia to cure gastrointestinal disorders. Maximum fresh uses (17) were reported by C. dactylon (L.) Pars. While the highest number of species reporting fresh uses in similar number was 13. In this study, five novel plants are being reported for the first time in Pakistan for their ethnomedicinal worth. Our data reflect unique usage of the medicinal plants in the study area. The statistical tools used in the study proved useful in pointing the most important and disease category specific plants. High use value plant and the new reported medicinal plants might prove an important source of the isolation of pharmacologically active compounds.
Este estudo tem como objetivo relatar o conhecimento indígena sobre a flora medicinal dos habitantes do entorno da maior floresta artificial plantada do mundo, a Changa Manga, no Paquistão. Os dados foram coletados por meio de entrevistas diretas e reuniões em grupo de 81 habitantes, incluindo 32 curandeiros locais, com informações sobre o uso de plantas medicinais indígenas durante o período de um ano. Diferentes ferramentas estatísticas foram aplicadas para analisar os dados, incluindo citação de frequência (FC), citação de frequência relativa (RFC), valor de uso, fator de consenso dos informantes e nível de fidelidade. Este estudo relatou 73 espécies de plantas pertencentes a 37 famílias de plantas e 46 gêneros. A maioria das espécies de plantas pertence à família Compositae. As plantas medicinais mais utilizadas foram P. hysterophorus L., P. dactylifera L., S. indicum L., P. harmala L., P. emblica L. e A. indica A. Juss. O maior número de espécies foi usado para curar distúrbios gastrointestinais. O maior nível de fidelidade (68,18%) foi de E. helioscopia para cura de distúrbios gastrointestinais. Os usos máximos em fresco (17) foram relatados por C. dactylon (L.) Pars. enquanto o maior número de espécies relatando usos frescos em número semelhante foi de 13. Neste estudo, cinco novas plantas estão sendo relatadas pela primeira vez no Paquistão por seu valor etnomedicinal. Nossos dados refletem o uso exclusivo das plantas medicinais na área de estudo. As ferramentas estatísticas utilizadas no estudo mostraram-se úteis para apontar as plantas mais importantes e específicas da categoria de doença. Plantas de alto valor de uso e as novas plantas medicinais relatadas podem ser uma importante fonte de isolamento de compostos farmacologicamente ativos.
Subject(s)
Humans , Plants, Medicinal , Forests , Gastrointestinal Diseases , Indigenous Peoples , Medicine, Traditional , PakistanABSTRACT
Abstract Objective To measure the average time for the diagnosis and for the therapeutic prescription of Continuous Positive Airway Pressure (CPAP) at a hospital in Botucatu Medical School - State University São Paulo, UNESP. Method A retrospective observational study was carried out by collecting data from the electronic medical records of patients over 18-years of age, who had a diagnostic polysomnography testing scheduled between January and December 2017. Result Of the 347 patients eligible for the study, 94 (27.1%) missed follow-up and 103 (29.7%) had a referral for CPAP use. Until February 2021, only 37 (35.9%) of these patients had already acquired and were using the device, the remaining 66 (64.1%) were waiting or gave up the therapy. The mean value of the waiting time interval between the referral of the diagnostic test and its performance was equivalent to 197 days (6.5 months). The mean time between diagnostic polysomnography and CPAP prescription was 440-days (14.5-months), with a total mean time of 624 days (21-months). Conclusion As in other services, the diagnostic-therapeutic flow proved to be highly inefficient, with a long waiting period, difficult access to treatment and a high dropout rate. These findings highlight the need to establish new patient-centered strategies with measures that speed up the flow and facilitate access to CPAP, in order to reduce the morbidity and mortality associated with this condition. Level of evidence Level 3 - Non-randomized controlled cohort/follow-up study Recommendation B.
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Objective: The study aimed to describe the profile and economic burden of patients with depression from the perspective of the Brazilian Private Healthcare System (PHS). Methods: A two-step methodological quantitative-qualitative research design was performed: retrospective descriptive analysis of the Orizon database of patients with at least one claim of depression (F33, F38, or F39) in PHS (2013-2019) and experienced physicians perspective from an expert meeting. Results: 1,802 patients fulfilling the eligibility criteria counted BRL 74,978 million across the 4-year period. Over this period, nearly 60% of patients had a medical appointment (6.6 appointments per patient, on average), 61% had a psychologist, 9.8% had a psychiatrist appointment, and an average of 115.2 exams and 8.7 emergency visits per patient were performed. According to the experts, the economic impact of depression is more significant when considering the indirect costs related to productivity loss and impairment in occupational and interpersonal functioning. Conclusion: Identifying and diagnosing patients with depression and their real burden is challenging; even with significant costs identified in the claim database analyses in the Brazilian PHS, the real impact must be higher if indirect costs are considered. The depressive disorder should be prioritized in the Brazilian PHS to establish more adequate health policies.
Objetivo: O estudo teve como objetivo descrever o perfil e a carga econômica de pacientes com depressão na perspectiva do Sistema Único de Saúde (SUS). Métodos: Foi realizado um projeto de pesquisa quantitativo-qualitativo metodológico em duas etapas: análise descritiva retrospectiva do banco de dados Orizon de pacientes com pelo menos uma alegação de depressão (F33, F38 ou F39) no PHS (2013- 2019) e perspectiva de médicos experientes de uma reunião de especialistas. Resultados: 1.802 pacientes que preencheram os critérios de elegibilidade totalizaram R$ 74,978 milhões no período de 4 anos. Nesse período, cerca de 60% dos pacientes tiveram consulta médica (6,6 consultas por paciente, em média), 61% tiveram psicólogo, 9,8% consulta com psiquiatra e foram realizados em média 115,2 exames e 8,7 atendimentos de emergência por paciente . Segundo os especialistas, o impacto econômico da depressão é mais significativo quando considerados os custos indiretos relacionados à perda de produtividade e prejuízo no funcionamento ocupacional e interpessoal. Conclusão: Identificar e diagnosticar pacientes com depressão e sua real carga é desafiador; mesmo com custos significativos identificados nas análises da base de sinistros do SUS brasileiro, o impacto real deve ser maior se considerados os custos indiretos. O transtorno depressivo deve ser priorizado na APS brasileira para o estabelecimento de políticas de saúde mais adequadas.
Subject(s)
Costs and Cost Analysis , Depression , Supplemental HealthABSTRACT
Medical mistakes are any unintentional acts which are detrimental to patients' health, most of which have multiple causes or arise from the complexity of modern healthcare systems. Since no medical specialty is free of mistakes, training is needed beginning in undergraduate school to learn how to deal with them. (Acta Med Colomb 2022; 48. DOI:https://doi.org/10.36104/amc.2023.2522).
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Resumo O complexo perfil epidemiológico do país, o envelhecimento populacional e a proporção de pessoas com deficiência apontam para o aumento substancial da demanda por reabilitação. Nesse contexto, foi analisada a distribuição espaço-temporal da oferta de profissionais de fisioterapia, fonoaudiologia e terapia ocupacional no Sistema Único de Saúde (SUS) de 2007 a 2019 nas cinco regiões do Brasil. Foram utilizados dados do Cadastro Nacional de Estabelecimentos em Saúde, as estimativas censitárias do Instituto Brasileiro de Geografia e Estatística e calculados os indicadores da oferta potencial de profissionais e sua evolução relativa. Foi realizada a distribuição espacial da evolução relativa da oferta potencial de profissionais. Para a análise da tendência temporal, adotou-se o modelo de regressão por pontos de inflexão. Houve tendência temporal crescente na oferta potencial das três categorias profissionais no Brasil e em todas as regiões, mas com uma desaceleração do crescimento. Observaram-se diferenciais entre as profissões e as regiões do país, representando um quadro de desigualdade de oferta que precisa ser superado. Resultados que podem subsidiar o controle social e o planejamento nacional para a ampliação do acesso aos serviços de reabilitação
Abstract The complex epidemiological profile of Brazil, the aging population and the proportion of individuals with disabilities have led to a substantial increase in the demand for rehabilitation. The spatiotemporal distribution of the offer of physiotherapy, speech therapy and occupational therapy in the Brazilian public healthcare system from 2007 to 2019 was analyzed for the five macro-regions of the country. Data from the National Register of Health Establishments and census estimates from the Brazilian Institute of Geography and Statistics were used. Indicators of the offer of professionals in these fields services and relative changes in the offer were calculated. The spatial distribution of the relative change in the offer was also determined. A regression model with inflection points was adopted for the analysis of the temporal trend. A growing temporal trend was found in the offer of the three professionals in Brazil as a whole and in all regions of the country, but with a slowdown in growth. Differences were observed in the offer among the regions of the country, revealing healthcare inequality that needs to be overcome. The present findings can assist in planning to expand access to rehabilitation services in the country.
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Resumo O SUS trouxe os princípios de universalidade, integralidade e equidade para nortear as ações e os serviços de saúde, que devem ser livres de preconceito e discriminação. A rede formal de cuidados foi compreendida como a que está institucionalizada e a rede informal é uma rede afetiva. O objetivo da pesquisa foi compreender o acesso à rede de cuidados à saúde na percepção de transexuais em um município da Zona da Mata mineira, por meio da abordagem metodológica qualitativa com estudo descritivo. Foram realizadas entrevistas semiestruturadas com oito pessoas transexuais. As informações foram analisadas por meio da hermenêutica-dialética. Foram identificadas como barreiras à rede formal de cuidados o desrespeito ao uso do nome social nos serviços de saúde e o preconceito dos profissionais. Buscam-se cuidados e informações sobre uso de hormônios nas redes informais. A rede informal acolhe, mas a busca por cuidados somente nessas redes pode trazer riscos à saúde. A pesquisa evidenciou a existência de uma forte rede afetiva no município e a necessidade do estabelecimento de uma sólida rede formal de cuidados para a população transexual com ampla participação da rede informal. A rede formal é instável e não atende as necessidades de saúde dessa população.
Abstract SUS brought the principles of universality, integrality, and equity to guide health actions and services, which must be free from any form of prejudice and discrimination. The formal care network was understood as the one that is institutionalized, and the informal network is an affective network. This research aimed to understand the access to the health care network in the perception of transsexuals in a municipality in Zona da Mata, Minas Gerais, through the qualitative methodological approach with descriptive study. Semi-structured interviews were conducted with eight transsexual people. The information was analyzed using hermeneutics-dialectics. Barriers to the formal care network were disrespect to the use of the social name in health services, prejudice, and unpreparedness of professionals. Therefore, care and information on hormone use are sought in informal networks. The informal network welcomes, but the search for care only in these networks can bring health risks. The research showed the existence of a strong affective network in the municipality and the need to establish a solid formal care network for the transsexual population with wide participation in the informal network, since the formal network is unstable and does not meet health needs of that population.
Subject(s)
Humans , Male , Female , Adult , User Embracement , Transsexualism , Qualitative Research , Gender Diversity , Health Services Accessibility/trendsABSTRACT
The objective of this study is to determine how the Indian health care system is performing relative to health care system of the Kingdom of Saudi Arabia (KSA), given that it is facing sustained financial pressure, increasing population and demand for quality care. This is an observational study using secondary data from major international organizations, ministries of health, other government and non- government agencies in India and KSA. In order to measure the performance of health care systems, four domains such as population and healthcare coverage, healthcare spending, health system capacity and health status were considered. In comparison with KSA, India spends a very low expenditure on healthcare and markedly lower health workforce density. Due to lower healthcare expenditure, India's health services outcomes and health status are low compared to KSA. Although Indian healthcare system has undergone notable progress in the last two decades, it is lagging behind in many healthcare system parameters. If India wants to reach a high performing and a nation with good health outcomes comparable with other G20 member countries, it needs to invest more on primary healthcare, health workforce, strengthening public healthcare system, and prevention and treatment for non-communicable diseases.
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Introducción: la fibromialgia (FM) es una enfermedad crónica caracterizada por dolor musculoesquelético y un espectro de síntomas somáticos. Se asocia a un alto costo y compromiso en la calidad de vida de los pacientes, razón por la que es necesaria una política pública en atención primaria de salud (APS) en Chile, que contribuya con el diagnóstico temprano, tratamiento y seguimiento. Métodos: revisión bibliográfica narrativa centrada en las características de la FM, tratamiento y políticas públicas vigentes (Chile, España y Uru-guay), utilizando PubMed, Cochrane, Epistemonikos, Google Scholar y GreyLit. La búsqueda se realizó desde el 3 de septiembre al 11 de diciembre de 2020. Resultados: la prevalencia global de la FM alcanza el 2,7%, con una proporción mujeres y hombres de 3:1. Se estima una prevalencia entre 1 a 2% y un alto impacto en la calidad de vida y un alto costo asociado a discapacidad. Uruguay y España han implementado políticas públicas para FM, con enfoque principal en atención de salud integral y plan de reinserción laboral. En Chile, no existe la incorporación de la FM en ningún programa de salud que garantice el acceso y tratamiento. Conclusión: la FM es una enfermedad polisintomática, que impacta en la calidad de vida de los pacientes. Dada su prevalencia a nivel nacional, retraso en el diagnóstico e inicio de un tratamiento, se ve justificada una política pública. En el presente artículo se propone la creación de Unidades de Fibromialgia en APS, cuyas características consideren aspectos de interdisciplinaridad y territorialidad que permitan un acceso rápido a diagnóstico, tratamiento, seguimiento, derivación oportuna a especialistas y educación a los pacientes y profesionales.
Introduction: Fibromyalgia (FM) is a chronic musculoskeletal disease related to a somatic symptoms spectrum. It is associated with high economic costs and the deterioration of patients' quality of life. That explains why a public policy in the primary healthcare system (PHS) is necessary for Chile to contribute to early diagnosis, treatment, and follow-up. Methods: Narrative bibliographic review, focused on the FM clinical characteristics, their treatment, and current public policies about FM in Chile, Spain, and Uruguay. We utilized PubMed, Cochrane, Epistemonikos, Google Scholar, and Greylist as search engines from September 3rd to December 11th, 2020. Results: The FM global prevalence is 2.7%, with a proportion female: male 3:1, and in Chile is between 1.1% to 3.9%, with a high impact on the quality of life and high cost related to disability. Uruguay and Spain have implemented public policies about FM, especially in diagnosis and treat-ment. In Chile, there are not any health programs that guarantee access and early treatment to FM. Conclusion: FM is a polysymptomatic disease, which impacts to quality of life of patients. Given its prevalence in Chile, and the delay in diagnosis and treatment, a public policy is justified. This article proposes the creation of Fibromyalgia Units in PHC whose characteristics consider aspects of interdisciplinary and territorial that allow access and opportune treatment to FM, follow-up, timely referral to specialists, and pain education to patients.
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ABSTRACT BACKGROUND: Cardiac rehabilitation (CR) barriers are well-understood in high-resource settings. However, they are under-studied in low-resource settings, where access is even poorer and the context is significantly different, including two-tiered healthcare systems and greater socioeconomic challenges. OBJECTIVE: To investigate differences in characteristics of patients attending publicly versus privately funded CR and their barriers to adherence. DESIGN AND SETTING: Observational, cross-sectional study in public and private CR programs offered in Brazil. METHODS: Patients who had been attending CR for ≥ 3 months were recruited from one publicly and one privately funded CR program. They completed assessments regarding sociodemographic and clinical characteristics and the CR Barriers Scale. RESULTS: From the public program, 74 patients were recruited, and from the private, 100. Participants in the public program had significantly lower educational attainment (P < 0.001) and lower socioeconomic status (P < 0.001). Participants in the private program had more cognitive impairment (P = 0.015), and in the public program more anxiety (P = 0.001) and depressive symptoms (P = 0.008) than their counterparts. Total barriers among public CR participants were significantly higher than those among private CR participants (1.34 ± 0.26 versus 1.23 ± 0.15/5]; P = 0.003), as were scores on 3 out of 5 subscales, namely: comorbidities/functional status (P = 0.027), perceived need (P < 0.001) and access (P = 0.012). CONCLUSION: Publicly funded programs need to be tailored to meet their patients' requirements, through consideration of educational and psychosocial matters, and be amenable to mitigation of patient barriers relating to presence of comorbidities and poorer health status.
Subject(s)
Humans , Cardiac Rehabilitation , Brazil , Cross-Sectional Studies , Delivery of Health CareABSTRACT
Abstract We analyze how the interactions between the trans population and the Chilean healthcare system shape specific processes of malaise associated with gender transition ("tránsito de género"). Adopting psychoanalytic and transfeminist conceptual approaches, as well as a biographical methodology, we examine autobiographical narratives of three trans subjects. We discuss three topics: childhood as a critical period for gender transition and malaise; the role of institutions; and the ways through which subjects manage malaise. We argue that trans subjects face specific sociocultural conditions that lead to unique processes of malaise associated with gender transition. We show how politicization and the construction of an institutional framework, bodily aesthetical modifications, and the self-administration of medical knowledge emerge as some of the paths to navigate the gender transition process. Besides, we foreground the notion of "transitioning" ("transicionar") by considering the criticism voiced by the participants. By using this notion, they interrogate the rigidity and psychopathologization of identity that is implicitly present in the notion of gender transition, as well as they enrich the transfeminist discourse in favor of their agency/autonomy.
Resumo Analisamos como as interações entre a população trans e o sistema de saúde chileno conformam processos específicos de mal-estar associados à transição de gênero ("tránsito de género"). Adotando abordagens conceituais psicanalíticas e transfeministas, bem como uma metodologia biográfica, examinamos narrativas autobiográficas de três sujeitos trans. Discutimos três tópicos: a infância como um período crítico para a transição e mal-estar de gênero; o papel das instituições; e as maneiras pelas quais os sujeitos lidam com o mal-estar. Argumentamos que sujeitos trans enfrentam condições socioculturais específicas que levam a processos únicos de mal-estar associados à transição de gênero. Mostramos como a politização e a construção de um arcabouço institucional, as modificações estéticas corporais e a autogestão do saber médico surgem como alguns dos caminhos para navegar o processo de transição de gênero. Além disso, colocamos em primeiro plano a noção de "transição" ("transicionar") considerando as críticas expressas pelos participantes. Ao utilizar essa noção, interrogam a rigidez e a psicopatologização da identidade que está implicitamente presente na noção de transição de gênero, bem como enriquecem o discurso transfeminista em favor de sua agência/autonomia.
Subject(s)
Humans , Child , Gender Identity , Health Services , Chile , Delivery of Health Care , NarrationABSTRACT
La pandemia de COVID-19 generó en la comunidad odon- tológica argentina un profundo desconcierto e incertidumbre frente a su práctica profesional, su economía y su cuidado. Mediante un cuestionario difundido a través de redes so- ciales en octubre de 2020, se formularon preguntas vinculadas al ejercicio profesional en ese contexto y otras en las que se incluyeron variables referidas a signos de ansiedad, depresión y resiliencia. Los odontólogos presentaron signos de estrés, ansiedad, tensión emocional, dificultad para conciliar el sueño, senti- mientos de culpa y sensación de soledad. Manifestaron casi en su totalidad que su esfuerzo y el cuidado de su persona frente a este nuevo paradigma no son valorados por el sistema de salud y que se evidencia en la escasa retribución que perciben por sus prestaciones. Las conclusiones tienen el mandato del cambio pues los datos arrojados por la encuesta y el sentir manifestado con vehemencia y desolación ponen sobre la mesa la necesidad de iniciar una nueva etapa (AU)
The COVID-19 pandemic created a profound state of be- wilderment and uncertainty among dentists regarding their professional practice, economy and personal care. An online survey posted on social media in October 2020 asked ques- tions about professional practice in this context and other variables such as signs of anxiety, depression and resilience. Dentists reported signs of stress, anxiety, emotional tension, difficulty to get to sleep, and feelings of guilt and loneliness. Most of them felt that the efforts they made to do their job and ensure their personal care in this new paradigm were not valued by the healthcare system, as reflected by the low compensation for their services. From the data obtained through the survey and the feelings of vehemence and grief expressed by respondents, it is concluded there is a need for action and change (AU)
Subject(s)
Humans , Professional Practice , Dental Care/standards , Dentists/psychology , COVID-19/prevention & control , Argentina , Self Care , Dentists/economics , COVID-19/economics , COVID-19/psychology , Occupational Diseases/prevention & controlABSTRACT
Qinghai province is located in the northeastern part of the Tibetan Plateau, and is an underdeveloped province of inland China. Chinese government gives high priority to the improvement of the wellbeing of Qinghai people, and have provided great supports in aspects of policy, funding, and professional resource to the development of health care and medical system in Qinghai. Great progress has been made, and wellness of residents in Qinghai has been significantly improved. This article reviews the strategies and measures from central and provincial government in improving health care of Qinghai province under the leadership of the Communist Party of China.
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Humans , China , Delivery of Health Care , GovernmentABSTRACT
Resumen Introducción: este artículo tiene por objetivo estimar las propiedades psicométricas de la Escala de Reacciones ante Experiencias de Trato Desigual en Salud de Baeza-Rivera (2015) y establecer si existen diferencias estadísticamente significativas entre quienes se atienden en el sistema privado y público y la pertenencia o no a la etnia mapuche. Materiales y métodos: participaron 337 personas cuyo promedio de edad fue de 31 años, en su mayoría mujeres. El 57 % reportó ser usuario del sistema público de salud y el 32 % declaró su pertenencia a la etnia mapuche. Se realizó un análisis factorial exploratorio, análisis de confiabilidad y Anova factorial. Resultados: los hallazgos dan cuenta de un instrumento con adecuadas propiedades psicométricas, que puede usarse en población con características similares a la muestra empleada. Además, se observa que existen diferencias estadísticamente significativas en función del sistema de salud en que se atiende la persona y la pertenencia a la etnia mapuche. Conclusiones: el instrumento tiene adecuadas propiedades psicométricas que presenta dos factores relacionados, que sirve para ser utilizado en contextos de salud, lo que permite comprender los procesos de salud-enfermedad.
Abstract Introduction: This study aimed to estimate the psychometric properties of the Scale of Reactions to Experiences of Unequal Treatment in Health, from Baeza-Rivera (2015), and to determine any statistically significant differences between those using the private and public healthcare systems and those belonging to the Mapuche ethnic group. Materials and Methods: The Scale of Reactions to Experiences of Unequal Treatment in Health was used in 337 participants (mostly women) with a mean age of 31 years. Of these, 57% reportedly used the public healthcare system and 32% belonged to the Mapuche ethnic group. Subsequently, exploratory factor analysis and reliability analysis using Cronbach's alpha and factorial analysis of variance were conducted. Results: The findings demonstrated that this scale has ideal psychometric properties, such as reliability and factorial validity, and it can be used in a population with characteristics similar to those of the sample population used in this study. Additionally, statistically significant differences were observed between those using the healthcare systems and those belonging to the Mapuche ethnic group. Conclusions: This scale shows adequate psychometric properties, such as the two related factors reliability and factorial validity, and can be used in health-related contexts, thus allowing for an understanding of health-disease processes.
Resumo Introdução: este artigo tem por objetivo estimar as propriedades psicométricas da Escala de Reações ante Experiências de Trato Desigual em Saúde, de Baeza-Rivera (2015), e estabelecer se existem diferenças estatisticamente significativas entre quem se atendem no sistema privado e público e a pertença ou não à etnia mapuche. Materiais e métodos: participaram 337 pessoas cuja média de idade foi de 31 anos, em sua maioria mulheres, 57% reportou ser usuário do sistema público de saúde e 32% declarou pertencer à etnia mapuche. Se realizou análise fatorial exploratório, análise de confiabilidade e a Anova fatorial. Resultados: se conta com um instrumento com adequadas propriedades psicométricas, que pode ser utilizado em população com características similares à amostra utilizada. Adicionalmente, se observa que existem diferenças estatisticamente significativas em função do sistema de saúde em que se atende a pessoa e a pertença ou não a etnia mapuche. Conclusões: o instrumento tem adequadas propriedades psicométricas, apresenta dois fatores relacionados, e serve para ser utilizado em contextos de saúde, permitindo compreender os processos de saúde-doença.
Subject(s)
Humans , Adult , Health Services Accessibility , Psychometrics , RacismABSTRACT
Abstract Considering the growing number of cases requiring emergency care as a result of SARS-CoV-2 in the Brazilian State of Rio de Janeiro, this study focuses on mapping the health infrastructure of the municipalities of the state, comparing the Structure Efficiency Index (IEE) before (2016) and after the COVID-19 pandemic. The article fills a gap in the academic literature, informing public health policies specialists and technicians, as well as policy and decision-makers, about the capacity of municipalities to face the problem. We calculated the Structure Efficiency Index (IEE) of the states' 92 municipalities and positioned them on the pandemic curve. It was possible to verify that the government of the State of Rio de Janeiro needs to start acting to suppress COVID-19, maintaining the policy of providing more hospital beds, and purchasing equipment. However, it is also necessary to consider the particularities and deficiencies of each region, as the policy to transfer patients to places with available beds can contribute to the spread of the disease.
Resumen Considerando el número creciente de casos de atención de emergencia procedentes del SARS-CoV-2, en el estado de Río de Janeiro, este estudio se centra en el mapeo de la infraestructura de salud en los municipios de dicho estado, con el fin de informar a los especialistas, técnicos, formuladores y tomadores de decisiones de políticas de salud pública sobre la capacidad de cada localidad para enfrentar el problema. Para esto, calculamos el índice de eficiencia de estructura (IEE) colocando los 92 municipios del estado en la curva de la pandemia. Se pudo verificar que el Gobierno del Estado de Río de Janeiro debe comenzar a actuar para suprimir la COVID-19 manteniendo la política de apertura o reapertura de camas y adquisición de equipos. Sin embargo, también se deben considerar las particularidades y deficiencias de cada región, ya que la política de traslado de pacientes postrados a otras regiones con camas disponibles puede propagar la enfermedad.
Resumo Considerando um número crescente de casos de atendimento de emergência, provenientes do SARS-CoV-2, no Estado do Rio de Janeiro, o presente estudo se concentra no mapeamento da infraestrutura de saúde nos municípios do Estado, comparando o Índice de Eficiência em Estrutura antes (2016) e após a pandemia da COVID-19. O artigo preenche uma lacuna acadêmica ao informar aos especialistas, técnicos, formuladores e tomadores de decisão de políticas públicas de saúde, sobre a capacidade de cada localidade para enfrentar o problema. Para isso, calculamos o Índice de Eficiência da Estrutura (IEE), alocando os 92 municípios do Estado na curva de pandemia. Foi possível verificar que o Governo do Estado do Rio de Janeiro precisa começar a atuar na supressão da COVID-19, mantendo a política de abertura, ou reabertura, de leitos e aquisição de equipamentos. No entanto, também é necessário considerar as particularidades e deficiências de cada região, pois a política de transferência dos acamados para outras regiões com leitos disponíveis pode espalhar a doença.
Subject(s)
Humans , Male , Female , Public Policy , Health Infrastructure , Health Systems , Coronavirus Infections , Municipal Management , Health Management , EfficiencyABSTRACT
Abstract COVID-19 arrived to Latin America early in March 2020. Currently, strategies are being developed in Colombia focusing on the quarantine and social and economic capital reactivation, whereby the expected results are not being obtained. In this article, we propose to review scientific evidence-based literature where information on the operation and adaptation of health systems, and social, economic and solidarity sectors of Colombia is presented. The purpose is to identify COVID-19 implications in the network that provides health services, quality of life and health-disease prognosis in the country, which is not prepared to face crises of social nature and of health systems, as well as the economic and solidarity impacts that are brought about by pandemics and crude episodes of disease.
Resumen COVID-19 llegó a Latinoamérica a principios de marzo de 2020. Actualmente, en Colombia se desarrollan estrategias enfocadas en la cuarentena y la reactivación del capital social y económico, con las cuales no se están obteniendo los resultados esperados. En este artículo se propone revisar literatura basada en evidencia científica en la que se exponga información del funcionamiento y adaptación de los sistemas de salud, sectores sociales, económicos y solidarios de Colombia. El objetivo es identificar las implicaciones de COVID-19 en la red prestadora de servicios de salud, calidad de vida, pronóstico de salud-enfermedad en el país, el cual no está preparado para afrontar crisis de orden social, de sistemas de salud e impactos económicos y solidarios que conllevan las pandemias y episodios graves de enfermedad.
Subject(s)
Humans , Pneumonia, Viral/epidemiology , Public Health , Coronavirus Infections/epidemiology , Delivery of Health Care/organization & administration , Quality of Life , Colombia/epidemiology , Pandemics , Betacoronavirus/isolation & purification , SARS-CoV-2 , COVID-19ABSTRACT
Since the outbreak of the new coronavirus epidemic, novel coronavirus has infected nearly 100,000 people in more than 110 countries. How to face this new coronavirus epidemic outbreak is an important issue. Basic reproduction number (R0) is an important parameter in epidemiology; The basic reproduction number of an infection can be thought of as the expected number of cases directly generated by one case in a population where all individuals are susceptible to infection. Epidemiology dynamics is a mathematical model based on a susceptibility-infection-recovery epidemic model. Researchers analyzed the epidemiological benefits of different transmission rates for the establishment of effective strategy in prevention and control strategies for epidemic infectious diseases. In this review, the early use of TCM for light and ordinary patients, can rapidly improve symptoms, shorten hospitalization days and reduce severe cases transformed from light and normal. Many TCM formulas and products have wide application in treating infectious and non-infectious diseases. The TCM theoretical system of treating epidemic diseases with TCM and the treatment scheme of integrated Chinese and Western medicine have proved their effectiveness in clinical practice. TCM can cure COVID-19 pneumonia, and also shows that the role of TCM in blocking the progress of COVID-19 pneumonia.
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Objetivo: Estimar o impacto orçamentário em cinco anos da incorporação da técnica de SET (single embryo transfer) sequencial no Sistema de Saúde Suplementar brasileiro (SSSB). Métodos: Foram consideradas taxas de nascidos vivos de 41% e de gemelaridade de 2% e 30% para SET e DET (double transfer embryo), respectivamente. Os custos dos procedimentos foram, em sua maioria, obtidos das tabelas SIMPRO, CBHPM e CMED. Para a estimativa da população elegível, foram consideradas mulheres de 20 a 35 anos registradas no Datasus e taxas de infertilidade e de uso de fertilização in vitro (FIV) da literatura. Estimou-se em 20% e 80% o uso de SET sequencial e DET, respectivamente, com incorporação da primeira em 45%, 50%, 55%, 65% e 75% dos casos nos cinco anos subsequentes. Resultados: Considerando cenários com reembolso de um a dois ciclos de SET sequencial e inclusão ou não do valor dos medicamentos, o impacto orçamentário em cinco anos seria entre R$ 10.231.387 e R$ 16.123.874 em operadoras de grande porte, R$ 1.054.174 e R$ 1.661.297 em operadoras de médio porte e R$ 173.700 e R$ 273.738 em operadoras de pequeno porte. Em cenário com aumento progressivo do uso de SET sequencial sem alteração no modelo de reembolso atual, foi estimada economia de R$ 59.319.276 para o SSSB em cinco anos. Conclusões: O uso de SET sequencial (vs. DET) em procedimentos de FIV é potencialmente menos oneroso para o SSSB referente a custos de pré-natal, parto e complicações. Em cenário de incorporação progressiva, o custo incremental foi estimado em R$ 8-13 mil/paciente.
Objective: To estimate the five-year budget impact of incorporating the sequential single embryo transfer (SET) technique into the Brazilian Supplementary Healthcare System (BSHS). Methods: Live birth rates of 41% and multiple pregnancy rates of 2% and 30% were considered for SET and DET (double transfer embryo), respectively. The costs of the procedures were mostly obtained from e SIMPRO, CBHPM and CMED tables. To estimate the eligible population, we considered women aged 20-35 years registered in DATASUS, and infertility and in vitro fertilization (IVF) rates from the literature. The use of sequential SET and DET was estimated as 20% and 80%, respectively, with incorporation of the first in 45%, 50%, 55%, 65% and 75% of cases in the subsequent five years. Results: Considering scenarios with reimbursement of 1 to 2 cycles of sequential SET and inclusion or not of the drugs in the reimbursement, the budget impact in five years would be between BRL 10,231,387-16,123,874 in large operators, BRL 1,054,174-1,661,297 in midsize operators and BRL 173,700-273,738 in small operators. In a scenario of progressive increase of the use of sequential SET with no change in the current reimbursement model, we estimated a saving of BRL 59,319,276 for the BSHS in five years. Conclusions: The use of sequential SET (vs. DET) in IVF procedures is potentially less costly for BSHS for prenatal, child-birth and complication costs. In the scenario of progressive incorporation and full reimbursement of the procedure, the incremental cost was estimated at BRL 8-13 thousands/patient.
Subject(s)
Costs and Cost Analysis , Supplemental Health , Single Embryo Transfer , InfertilityABSTRACT
Surgical Engineering Society realizó una investigación, la primera revisión como pioneros en LATAM, desde el año 2015, que desarrolla el tema de las últimas tecnologías de robótica médica creadas en América del Norte, Europa y Asia, que se importan para aplicarlas en el sistema de salud de Perú y América Latina Los sistemas robóticos para cirugía, rehabilitación y asistencia se presentan cubriendo la descripción del diseño del control y las especificaciones técnicas. Además, el manejo del paciente mediante robots se analiza con herramientas de diagnóstico, pronóstico y tratamiento. El proceso para evaluar los nuevos inventos de los dispositivos robóticos y llevarlo al mercado se introduce donde en las tres etapas que se muestran a continuación: innovación, asuntos regulatorios y aplicación biomédica. Además, hay un alto porcentaje de población con discapacidad en América Latina, por lo tanto, es necesario que más científicos biomédicos se especialicen en robótica para comenzar a desarrollar nuevas ideas y mejorar el manejo del paciente. Finalmente, las nuevas tecnologías creadas en América Latina deben ser asequibles, simples y eficientes para apoyar la situación económica de la atención médica en el continente y brindar los mejores estándares de calidad para mejorar los resultados del tratamiento en los pacientes.
Surgical Engineering Society conducted a research, the First Review as the pioneers in LATAM, since year 2015, which develops the topic of the latest Medical Robotics technologies created in North América, Europe and Asia, which are imported to apply in the Healthcare System of Peru and Latin America. The robotic systems for surgery, rehabilitation and assistance are presented covering the description of control design and technical specifications. Besides, the patient management using robots is analyzed with diagnosis, prognosis and treatment tools. The process to evaluate the new inventions of robotic devices and bring to the market is introduced where three stages are shown as the following: innovation, regulatory affairs and biomedical application. Moreover, there is a high percentage of population with disability in Latin America, therefore, it is necessary that more biomedical scientists be specialized in robotics to start developing new ideas to improve the patient management. Finally, the new technologies created in Latin America must be affordable, simply and effcient in order to support the healthcare economic situation in the continent and give the best quality standards to improve treatment outcomes on patients.
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Objetivos: Os objetivos deste estudo são calcular o custo de um surto de esclerose múltipla sob a perspectiva de uma operadora de saúde privada e o impacto orçamentário da adoção de natalizumabe em primeira linha para esclerose múltipla remitente-recorrente altamente ativa (EMRRAA). Métodos: Para o cálculo do custo do surto, duas abordagens foram adotadas: para surtos que não levam a hospitalizações, foi aplicada uma pesquisa a 33 médicos neurologistas para identificação do consumo de recursos. Microcusteio foi realizado com base em bases de dados públicas. Para o cálculo do custo de surtos que levam a hospitalizações, foi utilizada uma base de contas médicas. Para o cálculo do impacto orçamentário, foi construído um modelo baseado em prevalência. Foram assumidos os seguintes custos: custo de aquisição de natalizumabe, custo de infusão de natalizumabe e custo de surtos. Taxa de ocorrência de surtos para natalizumabe e para seus comparadores, disponível apenas no sistema público, foi obtida em estudos clínicos e metanálises. O caso-base foi realizado considerando-se uma operadora que atende 100 mil vidas na região Sudeste. Análise de sensibilidade foi realizada. Resultados: O custo calculado de um surto foi de R$ 14.157,21. O impacto orçamentário calculado para adoção de natalizumabe para EMRRAA foi de R$ 0,64 por beneficiário por ano, ou 0,02% das despesas assistenciais de uma operadora de saúde suplementar, ou 0,02% de suas receitas de contraprestações. A análise de sensibilidade confirma que o impacto não chega a 1 real por beneficiário por ano e atinge, no máximo, 0,03% das despesas assistenciais. Conclusão: Dados os altos benefícios clínicos de natalizumabe, o impacto orçamentário de sua adoção para primeira linha de EMRRAA é considerado baixo. O impacto pode estar superestimado, visto que não foram considerados custos de progressão da doença.
Objetivos: The goals of this study are to evaluate the cost of a multiple sclerosis relapse and the budget impact of adopting natalizumab as first-line therapy for HARRMS, both from a private payer perspective. Methods: For calculating the cost of a relapse, two approaches were adopted: for relapses not resulting in hospitalizations, a research with 33 physicians was made to obtain resource utilization data. Microcosting was performed using public data sources. For calculating costs of relapses leading to hospitalizations, we analyzed a claims database. To calculate the budget impact of adopting natalizumab as per its label indication, we built a prevalence-based model. The following costs were included: drug acquisition, drug infusion and relapses costs. The relapses rates for natalizumab and its comparators present in the public system were calculated based on clinical trials and meta-analysis. The base case was calculated assuming a hypothetical payer covering one hundred lives in the southeastern region of Brazil. Sensitivity analysis was performed. Results: The calculated relapse cost was R$ 14,157.21. The calculated budget impact for adopting natalizumab for HARRMS was R$ 0.64 per person per year, or 0.02% of the payer's healthcare expenditures, or 0.02% of its revenue. The sensibility analysis confirmed that the budget impact does not reach one real per person per year and does not exceed 0.03% of healthcare expenses. Conclusion: Given the high clinical benefits of adopting Tysabri, its budget impact can be considered low. The results might be overestimated, since disability progression costs were not accounted in the calculations
Subject(s)
Humans , Health Systems , Supplemental Health , Natalizumab , Multiple SclerosisABSTRACT
Further healthcare system reform calls for desirable pathway design. This paper introduced the logical framework of the new healthcare system reform pathway design and typical practical experience in Hangzhou.Known for " Internet+Smart healthcare" forerunner, Hangzhou has pioneered the reform of public hospitals and the construction of smart handy service for the public.With the aim of fully protecting the health rights and interests of urban and rural residents, comprehensive policy has been taken to deepen the reform of public hospitals; with the comprehensive promotion of contracted services and the primary level sharing of resources as a carrier, we will build a hierarchical medical service system of vertical linkage.We will also innovate and practice the governing philosophy of " Medicine has its limitations but we have the courage to overcome, service is boundaryless and we must pursue excellence".Promotion of party building in the industry also ranks high.Deepening the reform of " one visit for all" in the field of medical and health services as a measure to enhance people′s sense of gain; The " public-private partnership" to encourage the development of the social governance system and legalization in healthcare proves successful at this stage. However, there are still many challenges in the information security maintenance of smart healthcare, the balance of stakeholder interests in public hospitals, the all-round advancement of hierarchical medical service, standardizing and streamlining the reform of " one visit for all".