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au:Fonseca, Marcelo Cunio Machado

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Mirabegron and Anticholinergics in the Treatment of Overactive Bladder Syndrome: A Meta-analysis
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Sartori, Luisa Gracio Ferreira

; Nunes, Bruno Monteiro

; Farah, Daniela

; Oliveira, Leticia Maria de

; Novoa, Claudia Cristina Takano

; Sartori, Marair Gracio Ferreira

; Fonseca, Marcelo Cunio Machado

Revista Brasileira de Ginecologia e Obstetrícia

Journal Metrics
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jun 2023, Volume 45 N. 6 Pages 337 - 346

Abstract: En Pt | Text: En Pt | PDF: En | PDF: Pt

Abstract Objective To compare the use of mirabegron with anticholinergics drugs for the treatment of overactive bladder (OB). Data Source Systematic searches were conducted in EMBASE, PUBMED, Cochrane, and LILACS databases from inception to September 2021. We included RCTs, women with clinically proven OB symptoms, studies that compared mirabegron to antimuscarinic drugs, and that evaluated the efficacy, safety or adherence. Data Collection RevMan 5.4 was used to combine results across studies. We derived risk ratios (RRs) and mean differences with 95% CIs using a random-effects meta-analytic model. Cochrane Collaboration Tool and GRADE was applied for risk of bias and quality of the evidence. Data Synthesis We included 14 studies with a total of 10,774 patients. Fewer total adverse events was reported in mirabegron group than in antimuscarinics group [RR 0.93 (0.89–0.98)]. The risk of gastrointestinal tract disorders and dry mouth were lower with mirabegron [RR 0,58 (0.48–0.68); 9375 patients; RR 0.44 (0.35–0.56), 9375 patients, respectively]. No difference was reported between mirabegron and antimuscarinics drugs for efficacy. The adherence to treatment was 87.7% in both groups [RR 0.99 (0.98–1.00)]. Conclusion Mirabegron and antimuscarinics have comparable efficacy and adherence rates; however, mirabegron showed fewer total and isolated adverse events.

Resumo Objetivo Comparar o uso de mirabegrom com anticolinérgicos para o tratamento da bexiga hiperativa (BH). Fonte de Dados Buscas sistemáticas foram realizadas nas bases de dados EMBASE, PUBMED, Cochrane e LILACS desde o início até setembro de 2021. Incluímos ECR, mulheres com sintomas de BH clinicamente comprovados, estudos que compararam mirabegrom a medicamentos antimuscarínicos e avaliaram a eficácia, segurança ou adesão. Coleta de Dados RevMan 5.4 foi usado para combinar os resultados entre os estudos. Derivamos razões de risco (RRs) e diferenças médias com intervalo de confiança (IC) de 95% usando um modelo meta-analítico de efeitos aleatórios. Cochrane Collaboration Tool e GRADE foi aplicado para risco de viés e qualidade da evidência. Síntese dos Dados Foram incluídos 14 estudos com um total de 10.774 pacientes. Menos eventos adversos totais foram relatados no grupo mirabegrom do que no grupo antimuscarínicos [RR: 0,93 (0,89–0,98)]. O risco de distúrbios do trato gastrointestinal e boca seca foram menores com mirabegrom [RR: 0,58 (0,48–0,68); 9.375 pacientes; RR: 0,44 (0,35–0,56), 9.375 pacientes, respectivamente]. Nenhuma diferença foi relatada entre mirabegrom e drogas antimuscarínicos para eficácia. A adesão ao tratamento foi de 87,7% em ambos os grupos [RR: 0,99 (0,98–1,00)]. Conclusão Mirabegrom e antimuscarínicos têm eficácia e taxas de adesão comparáveis, porém o mirabegrom apresentou menos eventos adversos totais e isolados.

https://doi.org/10.1055/s-0043-1770093

The financial impact of neonatal sepsis on the Brazilian Unified Health System
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Abreu, Mariana Ferreira Carvalho Westerstahl de

; Ogata, Joice Fabíola Meneguel

; Fonseca, Marcelo Cunio Machado

; Sansone, Dayan

; Guinsburg, Ruth

Clinics

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2023, Volume 78 elocation 100277

Abstract: En | Text: En | PDF: En

Abstract Objective To evaluate the hospital cost of newborn infants diagnosed with sepsis from the perspective of the Brazilian Public Health System over 11 years. Method Cross-sectional study that analyzed secondary data from the databases of the Hospital Information System of the Brazilian Public Health System. Infants hospitalized between 0‒29 days after birth with a diagnosis of sepsis from 2008 to 2018 were included. The diagnosis used in the study was the one that the hospital considered the main diagnosis at admission. Costs were analyzed in US dollars and reflected the amount paid by the Brazilian Public Health System to the hospitals for the informed diagnosis upon admission. The costs were evaluated as the total per admission, and they were compared among Brazilian geographic regions, among etiologic agents, and between neonates with the diagnosis of sepsis that survived or died. Results From 2008 to 2018, 47,554 newborns were hospitalized with sepsis (148.04 cases per 100,000 live births), with an average cost of US$ 3345.59 per hospitalization, ranging from US$ 2970.60 in the North region to US$ 4305.03 in the Midwest. Among sepsis with identified agents, the highest mean cost was related to Gram-negative agents, and the lowest to Streptococcus agalactiae sepsis. Patients with sepsis who died had a higher cost than the survivors (t-test; p= 0.046). Conclusions The evaluation of costs related to neonatal sepsis in the country during an 11-year period shows the economic impact of morbidity that may be avoided by improving the quality of neonatal care.

https://doi.org/10.1016/j.clinsp.2023.100277

Uma análise de custo-efetividade de propofol versus midazolam para sedação de pacientes adultos admitidos à unidade de terapia intensiva
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Andrade, Teresa Raquel

; Salluh, Jorge Ibrain Figueira

; Garcia, Raphaela

; Farah, Daniela

; Silva, Paulo Sérgio Lucas da

; Bastos, Danielle F.

; Fonseca, Marcelo Cunio Machado

Revista Brasileira de Terapia Intensiva

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sep 2021, Volume 33 N. 3 Pages 428 - 433

Abstract: Pt En | Text: Pt En | PDF: Pt | PDF: En

RESUMO Objetivo: Construir um modelo de custo-efetividade para comparar o uso de propofol com o de midazolam em pacientes críticos adultos sob uso de ventilação mecânica. Métodos: Foi construído um modelo de árvore decisória para pacientes críticos submetidos à ventilação mecânica, o qual foi analisado sob a perspectiva do sistema privado de saúde no Brasil. O horizonte temporal foi o da internação na unidade de terapia intensiva. Os desfechos foram custo-efetividade por hora de permanência na unidade de terapia intensiva evitada e custo-efetividade por hora de ventilação mecânica evitada. Foram obtidos os dados do modelo a partir de metanálise prévia. Assumiu-se que o custo da medicação estava incluído nos custos da unidade de terapia intensiva. Conduziram-se análises univariada e de sensibilidade probabilística. Resultados: Pacientes mecanicamente ventilados em uso de propofol tiveram diminuição de sua permanência na unidade de terapia intensiva e na duração da ventilação mecânica, respectivamente, em 47,97 horas e 21,65 horas. Com o uso de propofol, ocorreu redução média do custo de U$2.998,971 em comparação ao uso do midazolam. A custo-efetividade por hora de permanência na unidade de terapia intensiva evitada e por hora de ventilação mecânica evitada foi dominante, respectivamente, em 94,40% e 80,8% do tempo. Conclusão: Ocorreu diminuição significante do custo associado ao uso de propofol, no que se refere à permanência na unidade de terapia intensiva e à duração da ventilação mecânica para pacientes críticos adultos.

ABSTRACT Objective: To build a cost-effectiveness model to compare the use of propofol versus midazolam in critically ill adult patients under mechanical ventilation. Methods: We built a decision tree model for critically ill patients submitted to mechanical ventilation and analyzed it from the Brazilian private health care system perspective. The time horizon was that of intensive care unit hospitalization. The outcomes were cost-effectiveness per hour of intensive care unit stay avoided and cost-effectiveness per hour of mechanical ventilation avoided. We retrieved data for the model from a previous meta-analysis. We assumed that the cost of medication was embedded in the intensive care unit cost. We conducted univariate and probabilistic sensitivity analyses. Results: Mechanically ventilated patients using propofol had their intensive care unit stay and the duration of mechanical ventilation decreased by 47.97 hours and 21.65 hours, respectively. There was an average cost reduction of US$ 2,998.971 for propofol when compared to midazolam. The cost-effectiveness per hour of intensive care unit stay and mechanical ventilation avoided were dominant 94.40% and 80.8% of the time, respectively. Conclusion: There was a significant reduction in costs associated with propofol use related to intensive care unit stay and duration of mechanical ventilation for critically ill adult patients.

https://doi.org/10.5935/0103-507x.20210068 48 downloads

Who is going to turn on the ventilators?
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Fonseca, Marcelo Cunio Machado

; Araújo, Gabriela Tannus Branco de

; Scorza, Fulvio Alexandre

; Silva, Paulo Sérgio Lucas da

; Andrade, Teresa Raquel de Moraes

; Farah, Daniela

; Sansone, Dayan

einstein (São Paulo)

Journal Metrics
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2021, Volume 19 elocation eAO6211

Abstract: Pt En | Text: Pt En | PDF: Pt | PDF: En

RESUMO Objetivo Analisar a pandemia da COVID-19 no Brasil, um país de dimensões continentais, considerado uma economia emergente, mas com inúmeras diferenças regionais, abordando a disponibilidade de recursos humanos, especialmente para unidades de terapia intensiva. Métodos Foi acessado o banco de dados do Cadastro Nacional de Estabelecimentos de Saúde. Os profissionais de saúde que atuavam nos cuidados para COVID-19 foram georreferenciados. O número de profissionais foi correlacionado com os parâmetros utilizados pela Organização Mundial da Saúde. De acordo com a Associação de Medicina Intensiva Brasileira, correlacionaram-se os dados de leitos de terapia intensiva adulta em cada unidade federativa com o número de profissionais para cada dez leitos de terapia intensiva. Os números de profissionais, leitos e casos foram, então, organizados por unidade federativa. Resultados O número de médicos por 100 mil habitantes seguiu as recomendações da Organização Mundial da Saúde; mas não o número de enfermeiras. O número de intensivistas, enfermeiros, técnicos de enfermagem especializados em terapia intensiva e fisioterapeutas respiratórios, necessário a cada dez leitos de terapia intensiva, não foi suficiente para nenhuma dessas categorias profissionais. Uma equipe completa desses especialistas esteve disponível para 10% dos leitos de terapia intensiva do Brasil. Conclusão Há carência de profissionais para unidade de terapia intensiva, como demonstrado no Brasil. Os recursos físicos da terapia intensiva, para serem usados de forma eficiente, precisam de recursos humanos extremamente especializados; portanto, o planejamento de recursos humanos é tão crucial quanto o planejamento de recursos físicos e estruturais.

ABSTRACT Objective To analyze the COVID-19 pandemic in Brazil, a continental-sized country, considered as an emerging economy but with several regional nuances, focusing on the availability of human resources, especially for intensive care units. Methods The database of the National Registry of Health Facilities was accessed. Healthcare professionals in the care of COVID-19 were georeferenced. We correlated the number of professionals with the parameters used by the World Health Organization. According to the Brazilian Intensive Care Medicine Association, we correlated the data for adult intensive care unit beds in each state with the number of professionals for each ten intensive care unit beds. The number of professionals, beds, and cases were then organized by state. Results The number of physicians per 100 thousand inhabitants followed the World Health Organization recommendations; however, the number of nurses did not. The number of intensivists, registered nurses, nurse technicians specialized in intensive care, and respiratory therapists, necessary for every ten intensive care beds, was not enough for any of these professional categories. A complete team of critical care specialists was available for 10% of intensive care unit beds in Brazil. Conclusion There is a shortage of professionals for intensive care unit, as we demonstrated for Brazil. Intensive care physical resources to be efficiently used require extremely specialized human resources; therefore, planning human resources is just as crucial as planning physical and structural resources.

https://doi.org/10.31744/einstein_journal/2021ao6211 28 downloads

Willingness to pay for short- and long-acting contraceptives among female adolescents and their parents in Brazil:a pilot study
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Farah, Daniela

; Girão, Manoel João Batista Castello

; Fonseca, Marcelo Cunio Machado

einstein (São Paulo)

Journal Metrics
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2021, Volume 19 elocation eAO6376

Abstract: Pt En | Text: Pt En | PDF: Pt | PDF: En

RESUMO Objetivo Avaliar a disposição de mulheres adolescentes e seus pais a pagar por métodos contraceptivos reversíveis de longa e curta duração, além de suas perspectivas ao usá-los. Métodos Este é um estudo transversal com adolescentes de 13 a 19 anos e seus pais. Foi feita uma pesquisa para estimar a disposição a pagar por métodos anticoncepcionais. Os valores estão expressos em média±desvio-padrão em Reais (R$). Foi feita a correlação de Spearman para nível socioeconômico dos pais, idade das adolescentes e seus pontos de vista. Os tipos de métodos e as perspectivas de adolescentes e pais foram analisados pelo teste χ2. Para determinar a concordância entre os pares e sua disposição a pagar, foi usado o gráfico de Bland-Altman. Resultados Foram coletadas 165 pesquisas. O método de curta duração foi significativamente mais aceitável para pagar que o de longa duração, por ambos pais e filhas. Os pais e suas filhas estavam dispostos a pagar, do próprio bolso, R$ 52,25±22,48 e R$ 51,63±21,24, pelo método contraceptivo reversível de curta duração, e R$ 176,83±130,34 e R$ 174,83±143,64, pelo de longa duração, respectivamente. A análise de Bland-Altman indicou concordância sobre ambas as perspectivas e o preço a que estavam dispostos a pagar por cada método anticoncepcional. Conclusão Pais e adolescentes estão mais dispostos a pagar pelos métodos reversíveis de curta duração. Houve concordância entre o pai e a filha para os valores pagos por cada método.

ABSTRACT Objective To evaluate willingness to pay for short- and long-acting reversible contraceptive methods among female Brazilian adolescents and their parents, as well as their perspective on using such methods. Methods This is a cross-sectional study of female adolescents aged 13 to 19 years and their parents. We surveyed to estimate their willingness to pay for contraceptive methods. The values are expressed as mean±standard deviation in Brazilian reals (R$). Spearman correlation was employed for socioeconomic status of parents, age of adolescents and their standpoints. The methods types and adolescent and parent perspectives were analyzed by the test χ2. To determine an agreement between pairs and their willingness to pay, we used the Bland-Altman plot. Results A total of 165 surveys were collected. Short-acting method was significantly more acceptable to pay than the long-action method, by both parents and their daughters. Parents and their daughters are willing to pay out-of-pocket R$ 52,25±22,48 and R$ 51,63±21,24 for short-acting reversible contraception method, and R$ 176,83±130,34 and R$ 174,83±143,64, for long-acting method, respectively. Bland-Altman analysis indicated an agreement on both perspectives and the price they are willing to pay for each contraceptive method. Conclusion Parents and adolescent daughters are more willing to pay for short-acting methods. We showed an agreement between the parent and the daughter for the values paid for each method.

https://doi.org/10.31744/einstein_journal/2021ao6376 32 downloads

Antibody indexes in COVID-19 convalescent plasma donors: Unanswered questions
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Bonetti, Tatiana Carvalho de Souza

; Latini, Flavia Roche Moreira

; Invitti, Adriana Lukow

; Fonseca, Marcelo Cunio Machado

; Scorza, Fulvio Alexandre

; Saldanha, Maira Garcia

; Bellucco, Fernanda T.

; Bacarov, Natalia B.S.

; Soane, Michel M.

; Girão, Manoel João Batista Castelo

Clinics

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2021, Volume 76 elocation e2818

Abstract: En | Text: En | PDF: En

OBJECTIVE: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is characterized by high contagiousness, as well as variable clinical manifestations and immune responses. The antibody response to SARS-CoV-2 is directly related to viral clearance and the antibodies' ability to neutralize the virus and confer long-term immunity. Nevertheless, the response can also be associated with disease severity and evolution. This study correlated the clinical characteristics of convalescent COVID-19 patients with immunoglobulin A (IgA) and IgG anti-SARS-CoV-2 antibodies. METHODS: This study included 51 COVID-19 health care professionals who were candidates for convalescent plasma donation from April to June 2020. The subjects had symptomatic COVID-19 with a polymerase chain reaction-confirmed diagnosis. We measured anti-SARS-CoV-2 IgA and IgG antibodies after symptom recovery, and the subjects were classified as having mild, moderate, or severe symptoms. RESULTS: Anti-SARS-CoV-2 antibodies were positive in most patients (90.2%). The antibody indexes for IgA and IgG did not differ significantly between patients presenting with mild or moderate symptoms. However, they were significantly higher in patients with severe symptoms. CONCLUSIONS: Our study showed an association between higher antibody indexes and severe COVID-19 cases, and several hypotheses regarding the association of the antibody dynamics and severity of the disease in SARS-CoV-2 infection have been raised, although many questions remain unanswered.

https://doi.org/10.6061/clinics/2021/e2818 174 downloads

Which children account for repeated admissions within 1 year in a Brazilian pediatric intensive care unit?,
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Silva, Paulo Sérgio Lucas da

; Fonseca, Marcelo Cunio Machado

Jornal de Pediatria

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sep 2019, Volume 95 N. 5 Pages 559 - 566

Abstract: Pt En | Text: Pt En | PDF: Pt | PDF: En

Resumo: Objetivo: Apesar dos estudos terem focado em reinternações precoces ou reinternações durante a mesma internação na unidade de terapia intensiva pediátrica, pouco se sabe sobre essas crianças com internações recorrentes. Buscamos avaliar as características dos pacientes reinternados em 1 ano em uma unidade de terapia intensiva pediátrica brasileira. Métodos: Este foi um estudo retrospectivo realizado em uma unidade de terapia intensiva pediátrica terciária. O resultado foi o número máximo de reinternações por cada criança em qualquer período de 365 dias durante um período de acompanhamento de 5 anos. Resultados: Do total de 758 internações elegíveis, 75 pacientes (9,8%) foram de reinternações. Esses pacientes representaram 33% de todos os dias de cuidados com os internados na unidade de terapia intensiva pediátrica. O tempo mediano para a reinternação foi 73 dias para todas as reinternações. A regressão logística mostrou que as doenças crônicas complexas (razão de chance de 1,07), deficiência cognitiva grave a moderada (razão de chance de 1,08) e uso de suporte de aparelhos tecnológicos (razão de chance de 1,17) foram associados às reinternações. As múltiplas internações apresentaram duração significativamente prolongada na ventilação mecânica (8 em comparação a 6 dias), maior tempo de internação na unidade de terapia intensiva pediátrica (7 em comparação a 4 dias) e tempos de internação (20 em comparação a 9 dias) e maior taxa de mortalidade (21,3% em comparação a 5,1%), em comparação às internações iniciais. Conclusão: A taxa de reinternações na unidade de terapia intensiva pediátrica em 1 ano foi baixa, porém foi associada a um número relevante de cuidados durante internação e piores resultados. Um índice de reinternação de 30 dias pode ser inadequado para refletir a grande número de reinternações na unidade de terapia intensiva pediátrica. Os pacientes com doenças crônicas complexas, estado funcional ruim ou suporte de aparelhos tecnológicos correm maior risco de reinternações. Estudos futuros devem abordar o impacto das intervenções qualitativas sobre os serviços de saúde e as internações recorrentes.

Abstract Objective: While studies have focused on early readmissions or readmissions during the same hospitalization in a pediatric intensive care unit, little is known about the children with recurrent admissions. We sought to assess the characteristics of patients readmitted within 1 year in a Brazilian pediatric intensive care unit. Methods: This was a retrospective study carried out in a tertiary pediatric intensive care unit. The outcome was the maximum number of readmissions experienced by each child within any 365-day interval during a 5-year follow-up period. Results: Of the 758 total eligible admissions, 75 patients (9.8%) were readmissions. Those patients accounted for 33% of all pediatric intensive care unit bed care days. Median time to readmission was 73 days for all readmissions. Logistic regression showed that complex chronic conditions (odds ratio 1.07), severe to moderate cognitive disability (odds ratio 1.08), and use of technology assistance (odds ratio 1.17) were associated with readmissions. Multiple admissions had a significantly prolonged duration of mechanical ventilation (8 vs. 6 days), longer length of pediatric intensive care unit (7 vs 4 days) and hospital stays (20 vs 9 days), and higher mortality rate (21.3% vs 5.1%) compared with index admissions. Conclusion: The rate of pediatric intensive care unit readmissions within 1 year was low; however, it was associated with a relevant number of bed care days and worse outcomes. A 30-day index of readmission may be inadequate to mirror the burden of pediatric intensive care unit readmissions. Patients with complex chronic conditions, poor functional status or technology assistance are at higher risk for readmissions. Future studies should address the impact of qualitative interventions on healthcare and recurrent admissions.

https://doi.org/10.1016/j.jped.2018.04.009 597 downloads

It is impossible to know the way if we do not know where to start: tidal volume, driving pressure, and positive end-expiratory pressure
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Fonseca, Marcelo Cunio Machado

; Carvalho, Werther Brunow de

Revista da Associação Médica Brasileira

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jan 2017, Volume 63 N. 1 Pages 1 - 3

Abstract: En | Text: En | PDF: En

https://doi.org/10.1590/1806-9282.63.01.1 1666 downloads

Sponsored multicentric clinical research conducted in Brazil in the respiratory area - losses and gains
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Carvalho, Andréa Kelly da Silveira

; Nascimento, Oliver Augusto

; Fonseca, Marcelo Cunio Machado

; Pereira, Eanes Delgado Barros

; Jardim, José Roberto

Revista da Associação Médica Brasileira

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apr 2016, Volume 62 N. 2 Pages 131 - 137

Abstract: Pt En | Text: Pt En | PDF: Pt | PDF: En

Resumo Objetivo: avaliar nos centros de pesquisas clínicas patrocinadas na área respiratória no Brasil o perfil, a logística e a estrutura. Método: questionários foram respondidos por pesquisadores principais (29) e subinvestigadores (30) de 39 centros de pesquisa relativos a identificação e formação dos pesquisadores, instalações dos centros e vantagens e desvantagens quanto à participação nas pesquisas patrocinadas. Resultados: setenta e cinco por cento (75,6%) dos centros se localizavam nas regiões Sul e Sudeste do Brasil. A maioria dos investigadores principais eram homens com média de idade de 53,4 anos. As pesquisas na área respiratória se concentravam no estudo da asma e da doença pulmonar obstrutiva crônica (DPOC). Oitenta por cento dos pesquisadores citaram a demora na Comissão Nacional de Ética em Pesquisa (Conep) e na Agência Nacional de Vigilância Sanitária (Anvisa) como fator de entrave para a realização das pesquisas. As vantagens em participar das pesquisas clínicas foram a atualização própria ou da equipe envolvida, com rendimento adicional para a equipe. A principal desvantagem apontada pelos pesquisadores foi a baixa compensação financeira em relação ao volume de trabalho e disponibilidade de tempo. A mediana de profissionais por centro de pesquisa foi de seis pessoas, com predominância de médicos. Conclusão: o número de centros na área respiratória no Brasil ainda é relativamente pequeno. As equipes apresentam boa formação para a realização das pesquisas. Asma e DPOC são as doenças mais estudadas pelas pesquisas clínicas patrocinadas. O principal entrave é a demora da Conep e da Anvisa. Os fatores que levam os investigadores a participarem variam desde atualização própria/equipe até questões financeiras para a equipe e o centro; a principal desvantagem relatada é a baixa remuneração diante da demanda de trabalho exigida.

Summary Objective: To evaluate the sponsored centers for clinical trial in the respiratory care setting in Brazil: profile; logistics and structure. Methods: Principal investigators (29) and subinvestigators (30) of 39 research centers completed the questionnaires that addressed personal identification and training of researchers, the centers' facilities and advantages and/or disadvantages of performing sponsored trials. Results: 75.6% of the centers were located in southern and southeastern Brazil. Most principal investigators were men with a mean age of 53.4 years. The clinical trials in the respiratory care setting focus on asthma and chronic obstructive pulmonar disease (COPD). 80% of the researchers cited delay of the Conep and Anvisa as a barrier to performing research. The advantages of participating in clinical trials were updating knowledge of the researcher and the team, and additional income for the team. The main disadvantages mentioned by the researchers included low financial compensation for the performed workload, and time availability. The median number of professionals per research center was six people, predominantly physicians. Conclusion: The number of research centers in the respiratory care setting in Brazil is still relatively small. The teams have good training for performing the clinical trials. Asthma and COPD are the most studied diseases in sponsored clinical trials. The main barrier is delay by the Conep and Anvisa. The factors that lead investigators to participate range from being updated along with the team, to site and staff financial issues; the main disadvantage is the low compensation for the required workload demand.

https://doi.org/10.1590/1806-9282.62.02.131 1261 downloads

10.

Costs of hospitalization in preterm infants: impact of antenatal steroid therapy
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Ogata, Joice Fabiola Meneguel

; Fonseca, Marcelo Cunio Machado

; Miyoshi, Milton Harumi

; Almeida, Maria Fernanda Branco de

; Guinsburg, Ruth

Jornal de Pediatria

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feb 2016, Volume 92 N. 1 Pages 24 - 31

Abstract: Pt En | Text: Pt En | PDF: Pt | PDF: En

RESUMO OBJETIVO: Estimar os custos da internação hospitalar de prematuros cujas mães receberam ou não corticoide antenatal (CEA). MÉTODO: Coorte retrospectiva de prematuros sem malformações congênitas com idade gestacional de 26 a 32 semanas, nascidos entre janeiro/2006 e dezembro/2009, em hospital público, terciário e universitário brasileiro. Coletaram-se dados demográficos maternos e dos recém-nascidos (RN), a morbidade neonatal e o uso de recursos de saúde durante a internação hospitalar. Os custos foram analisados pela técnica de microcosting. RESULTADOS: Dos 220 nascidos que obedeciam a critérios de inclusão, 211 (96%) prontuários foram revisados: 170 receberam CEA e 41 não receberam a medicação. Analisando-se toda a população, houve redução de 14-37% entre os diferentes componentes do custo nos pacientes expostos ao CEA, sem significância estatística. Na análise de prematuros que receberam alta hospitalar vivos, o grupo com CEA teve redução de 24-47% nos vários componentes dos custos hospitalares, com diminuição significativa dos dias de internação em terapia intensiva. Os nascidos com peso < 1.500 g, considerando-se somente os sobreviventes, são aqueles que mais se beneficiaram da administração do CEA, com redução significativa de todos os componentes dos custos em 30-50%, diminuição de 36% no custo total (p = 0,008). Para o grupo com idade gestacional < 30 semanas, também sobreviventes, houve diminuição do custo total de 38% (p = 0,008) e redução de 49% dos dias de internação em UTI neonatal (p = 0,011). CONCLUSÕES: O CEA reduz o custo hospitalar de prematuros que sobrevivem à internação após o parto, principalmente naqueles abaixo de 1.500 g e 30 semanas de idade gestacional.

ABSTRACT OBJECTIVE: To estimate the costs of hospitalization in premature infants exposed or not to antenatal corticosteroids (ACS). METHOD: Retrospective cohort analysis of premature infants with gestational age of 26-32 weeks without congenital malformations, born between January of 2006 and December of 2009 in a tertiary, public university hospital. Maternal and neonatal demographic data, neonatal morbidities, and hospital inpatient services during the hospitalization were collected. The costs were analyzed using the microcosting technique. RESULTS: Of 220 patients that met the inclusion criteria, 211 (96%) charts were reviewed: 170 newborns received at least one dose of antenatal corticosteroid and 41 did not receive the antenatal medication. There was a 14-37% reduction of the different cost components in infants exposed to ACS when the entire population was analyzed, without statistical significance. Regarding premature infants who were discharged alive, there was a 24-47% reduction of the components of the hospital services costs for the ACS group, with a significant decrease in the length of stay in the neonatal intensive care unit (NICU). In very-low birth weight infants, considering only the survivors, ACS promoted a 30-50% reduction of all elements of the costs, with a 36% decrease in the total cost (p = 0.008). The survivors with gestational age <30 weeks showed a decrease in the total cost of 38% (p = 0.008) and a 49% reduction of NICU length of stay (p = 0.011). CONCLUSION: ACS reduces the costs of hospitalization of premature infants who are discharged alive, especially those with very low birth weight and <30 weeks of gestational age.

https://doi.org/10.1016/j.jped.2015.03.004 2775 downloads

11.

Ilusão ou realidade, arte abstrata ou concreta? Modelos em saúde: eles respondem as perguntas?
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Fonseca, Marcelo cunio Machado

Revista da Associação Médica Brasileira

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jun 2012, Volume 58 N. 3 Pages 269 - 271

Abstract: Pt | Text: Pt | PDF: Pt

2694 downloads

12.

Sedação da criança submetida à ventilação pulmonar mecânica: estamos avançando
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Fonseca, Marcelo Cunio Machado

; Carvalho, Werther Brunow de

Revista Brasileira de Terapia Intensiva

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mar 2011, Volume 23 N. 1 Pages 4 - 5

Abstract: Pt | Text: Pt | PDF: Pt

3176 downloads

13.

Consenso brasileiro do tratamento da fibromialgia
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Heymann, Roberto Ezequiel

; Paiva, Eduardo dos Santos

; Helfenstein Junior, Milton

; Pollak, Daniel Feldman

; Martinez, José Eduardo

; Provenza, José Roberto

; Paula, Ana Patrícia

; Althoff, Antonio Carlos

; Souza, Eduardo José do R. e

; Neubarth, Fernando

; Lage, Lais Verderame

; Rezende, Marcelo Cruz

; Assis, Marcos Renato de

; Lopes, Maria Lucia Lemos

; Jennings, Fabio

; Araújo, Rejane Leal C. da Costa

; Cristo, Valéria Valim

; Costa, Evelin Diana Goldenberg

; Kaziyama, Helena Hideko S.

; Yeng, Lin Tchia

; Iamamura, Marta

; Saron, Thais Rodrigues Pato

; Nascimento, Osvaldo J. M.

; Kimura, Luiz Koiti

; Leite, Vilnei Mattioli

; Oliveira, Juliano

; Araújo, Gabriela Tannus Branco de

; Fonseca, Marcelo Cunio Machado

Revista Brasileira de Reumatologia

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feb 2010, Volume 50 N. 1 Pages 56 - 66

Abstract: Pt | Text: Pt | PDF: Pt

92318 downloads Cited 22 times in SciELO

14.

Cost effectiveness of peginterferon alfa-2B combined with ribavirin for the treatment of chronic hepatitis C in Brazil
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Fonseca, Marcelo Cunio Machado

; Araújo, Gabriela Tannus Branco de

; Araújo, Denizar Vianna

Brazilian Journal of Infectious Diseases

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jun 2009, Volume 13 N. 3 Pages 191 - 199

Abstract: En | Text: En | PDF: En

The treatment of chronic hepatitis C (CHC) with peginterferon alpha-2b/ribavirin (PegIFN + Rib) produced larger sustained viral response (SVR) compared to the conventional (non-pegylated) interferon/ribavirin (IFN + Rib), but its cost-effectiveness was not assessed in Brazil. We developed a Markov model to mirror the natural disease history and cohorts of patients with hepatitis C virus (HCV), that received PegIFN + Rib or IFN + Rib treatment for 48 or 24 weeks, according to viral genotype and liver histology. The SVRs for the treatments PegIFN + Rib and IFN + Rib were respectively 48% and 34% (genotype 1), and 88% and 80% (genotype non-1). Three Delphi panels were conducted with hepatologists and intensivists, and another one with oncologists. The costs are expressed in 2006 Brazilian Reais (R$) and the benefits were discounted at 3%. In genotype 1 HCV patients, PegIFN + Rib increases the life expectancy (LE) in 0.51 year, and the quality-adjusted life years (QALY) in 0.78, as compared to IFN + Rib. In genotype non-1 HCV patients, PegIFN + Rib increases the LE in 0.29 years and the QALY in 0.44 years, as compared to IFN + Rib. The incremental cost-effectiveness rate, considering all the genotypes, was of R$19,848.34 per QALY. Peginterferon alpha-2b with ribavirin is a cost-effective therapy for the treatment of naïve CHC adult patients compared to the interferon alpha-2b and ribavirin regime, irrespective of the viral genotype.

2937 downloads

15.

Validação do questionário de qualidade de vida (King's Health Questionnaire) em mulheres brasileiras com incontinência urinária
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Fonseca, Eliana Suelotto Machado

; Camargo, Adriana Luciana Moreno

; Castro, Rodrigo de Aquino

; Sartori, Marair Gracio Ferreira

; Fonseca, Marcelo Cunio Machado

; Lima, Geraldo Rodrigues de

; Girão, Manoel João Batista de Castello

Revista Brasileira de Ginecologia e Obstetrícia

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may 2005, Volume 27 N. 5 Pages 235 - 242

Abstract: Pt En | Text: Pt En | PDF: Pt | PDF: En

OBJETIVO: a proposta deste estudo foi traduzir e validar o King's Health Questionnaire (KHQ) para mulheres brasileiras com incontinência urinária. MÉTODOS: 134 pacientes com incontinência urinária, confirmada pelo estudo urodinâmico, foram recrutadas em ambulatório de Uroginecologia. Inicialmente, traduzimos o questionário KHQ para a língua portuguesa (do Brasil) de acordo com critérios internacionais. Devido às diferenças da língua, fizemos a adaptação cultural, estrutural, conceitual e semântica do KHQ, para que as pacientes compreendessem as questões. Todas as pacientes responderam duas vezes o KHQ, no mesmo dia, com dois entrevistadores distintos, com intervalo de 30 minutos de uma entrevista para a outra. Depois de 7 a 14 dias, a aplicação do questionário foi repetida numa segunda visita. Foram testadas a confiabilidade (consistência interna intra e inter-observador) e validade do constructo e discriminativa. RESULTADOS: foram necessárias várias adaptações culturais até obtermos a versão final. A consistência interna intra-observador (alfa de Cronbach) das diversas dimensões oscilou de moderada a alta (0,77-0,90) e a consistência interna inter-observador oscilou de 0,66 a 0,94. Na validação do constructo, obtivemos correlação de moderada a forte entre os domínios específicos para incontinência urinária e manifestações clínicas que, sabidamente, afetam a qualidade de vida dessas pacientes. CONCLUSÃO: o KHQ foi adaptado ao idioma português e para a cultura brasileira, mostrando grande confiabilidade e validade, devendo ser incluído e utilizado em qualquer estudo brasileiro de incontinência urinária.

PURPOSE: the proposal of the present study was to translate and to validate King's Health Questionnaire (KHQ) for Brazilian women with urinary incontinence. METHODS: a hundred and thirty-four patients with urinary incontinence, confirmed by urodynamic study, were enrolled from the outpatient clinic of Uroginecology. Initially, we translated the KHQ into the Brazilian Portuguese language in agreement with international criteria. Due to language and cultural differences we performed a cultural, structural, conceptual, and semantic adaptation of the KHQ, in order to make sure that patients were able to fully understand the questions. All patients answered the KHQ twice on the same day, within an interval of 30 min, applied by two different interviewers. After 7 to 14 days, on a second visit, the questionnaire was applied again. Reliability (intra- and interobserver internal consistency), construct and discriminative validity were tested. RESULTS: several cultural adaptations were necessary until we reached the final version. The intra-observer internal consistency (alpha of Cronbach) of the several dimensions varied from moderate to high (0.77-0.90), and the interobserver internal consistency varied from 0.66 to 0.94. Moderate to strong correlation was detected among the specific KHQ urinary incontinence dominions and clinical urinary incontinence manifestations known to affect the quality of life of these patients. CONCLUSION: KHQ was adapted to the Portuguese language and to the Brazilian culture, showing great reliability and validity. It should be included and used in any Brazilian urinary incontinence clinical trial.

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