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1.
ABC., imagem cardiovasc ; 34(4): eabc258, 2021. tab, ilus
Article in Portuguese | LILACS | ID: biblio-1361250

ABSTRACT

Introdução: A ecocardiografia é uma ferramenta diagnóstica de crescente utilização na prática clínica, aplicada a diversos cenários médicos. Os cuidados e os processos de manutenção preventiva ou corretiva dos equipamentos são ainda pouco padronizados. O objetivo do presente estudo foi descrever o processo de manutenção atualmente aplicado a equipamentos ecocardiográficos em um laboratório. Descrever o processo inclui a caracterização de danos e aplicações de manutenção preventiva ou corretiva. Métodos: Estudo observacional descritivo e exploratório realizado em centro único. As informações de dados do processo de manutenção de equipamentos ecocardiográficos foram obtidas de arquivos eletrônicos do sistema de gestão de equipamentos de um laboratório de médio porte de um hospital público de nível terciário com características de ensino, no período de 2003 a 2018. Resultados: Foram identificados dez tipos de avarias mais comuns, como dano a programas (23,8%), peças (23,1%) e relacionadas à queda de energia e de acessórios (13,8%). Após a implementação do processo de manutenção preventiva, houve significativa redução dos custos de manutenções (US$ 44.472,10 versus US$ 25.807,59; p= 0,029). Mesmo após a manutenção preventiva, os custos de manutenção corretiva em equipamentos aplicados à ecocardiografia transesofágica (US$ 7.789,17) foram maiores que aqueles a equipamentos aplicados a outras modalidades (US$ 3.184,37 em ecocardiografia transtorácica e US$1.813,00 em estresse). Conclusão: O processo de manutenção de equipamentos ecocardiográficos foi descrito. Danos a equipamentos ecocardiográficos estão relacionados a altos custos, principalmente naqueles aplicados a modalidades especiais, como ecocardiografia transesofágica. As manutenções preventivas reduziram significativamente os custos de manutenção. (AU)


Introduction: Echocardiography is a diagnostic tool that is increasingly used in clinical practice in different medical scenarios; however, the preventive (PM) or corrective maintenance (CM) care and processes for this equipment are still poorly standardized. To describe the maintenance process currently implemented for echocardiographic equipment (ECHO) in a medium-sized laboratory in a tertiary-level public teaching hospital. The description of the process includes damage characterization and MP and MC implementation. Methods: This was a descriptive and exploratory single-center observational study. Data on the maintenance process of echocardiographic equipment were obtained from electronic files from the hospital's equipment management system between 2003 and 2018. Results: Together with the description of the equipment maintenance process, the ten most common types of malfunctions were identified, including software (23.8%), parts (23.1%), and power outage and accessory damage (13.8%). The implementation of the PM process significantly decreased the maintenance costs (USD 44,472.10 vs USD 25,807.59, p = 0.029). Even after the MP, the CM costs related to transesophageal echocardiography equipment (TEE) (USD 7,789.17) were higher than those with other equipment modalities (USD 3,184.37 for transthoracic echocardiography equipment (TTE) and USD 1,813.00 for stress testing). Conclusion: The maintenance process for ECHO equipment was described. ECHO equipment damage has high costs, especially in special modalities such as TEE. PM significantly reduced maintenance costs. (AU)


Subject(s)
Humans , Echocardiography/economics , Equipment Maintenance/methods , Cost-Benefit Analysis/statistics & numerical data , Health Care Economics and Organizations , Equipment and Supplies/economics , Time Factors , Echocardiography, Transesophageal/statistics & numerical data , Ambulatory Care Facilities/organization & administration , Hospitals, Teaching/organization & administration
2.
Rev. Soc. Bras. Med. Trop ; 52: e20180272, 2019. tab, graf
Article in English | LILACS | ID: biblio-1041550

ABSTRACT

Abstract INTRODUCTION: Visceral leishmaniasis (VL) is fatal if not diagnosed and treated. This study aimed to estimate the cost-effectiveness of diagnostic-therapeutic alternatives for VL in Brazil. METHODS: A decision model estimated the life expectancy and costs of six diagnostic-therapeutic strategies. RESULTS: IT LEISH + liposomal amphotericin B emerged the best option, presenting lower costs and higher effectiveness. DAT-LPC + liposomal amphotericin B showed an incremental cost-effectiveness ratio of US$ 326.31 per life year. CONCLUSIONS: These findings indicate the feasibility of incorporating DAT and designating liposomal amphotericin B as the first-line drug for VL in Brazil.


Subject(s)
Humans , Amphotericin B/economics , Cost-Benefit Analysis/statistics & numerical data , Leishmaniasis, Visceral/economics , Meglumine/economics , Antiprotozoal Agents/economics , Brazil , Coombs Test/economics , Amphotericin B/administration & dosage , Sensitivity and Specificity , Fluorescent Antibody Technique, Indirect/economics , Leishmaniasis, Visceral/diagnosis , Leishmaniasis, Visceral/drug therapy , Meglumine/administration & dosage , Antiprotozoal Agents/administration & dosage
3.
Cad. Saúde Pública (Online) ; 35(8): e00108218, 2019. tab, graf
Article in Portuguese | LILACS | ID: biblio-1019622

ABSTRACT

Resumo: O câncer renal é a 13ª neoplasia mais frequente no mundo. Entre 2012 e 2016, representou 1,48% das mortes por câncer no Brasil. A terapia de escolha para o tratamento de câncer renal metastático são os inibidores de tirosina quinase (ITK), sunitinibe e pazopanibe. Este artigo avalia o custo-efetividade do pazopanibe comparado ao sunitinibe no tratamento de câncer renal metastático. Foi realizada uma análise de custo-efetividade sob a perspectiva de um hospital federal do Sistema Único de Saúde. No modelo de árvore de decisão foram aplicados os desfechos de efetividade e segurança dos ITK. Os dados clínicos foram extraídos de prontuários e os custos diretos consultados em fontes oficiais do Ministério da Saúde. O custo de 10 meses de tratamento, englobando o valor dos ITK, procedimentos e manejo de eventos adversos, foi de R$ 98.677,19 para o pazopanibe e R$ 155.227,11 para o sunitinibe. Os medicamentos apresentaram efetividade estatisticamente equivalente e diferença estatisticamente significativa para o desfecho de segurança, no qual o pazopanibe obteve o melhor resultado. O pazopanibe, nesse contexto, é a tecnologia dominante quando os custos de tratamento são associados aos de manejo de eventos adversos.


Abstract: Renal cancer is the 13th most frequent neoplasm in the world. From 2010 to 2014, renal cancer accounted for 1.43% of cancer deaths in Brazil. The treatment of choice for metastatic renal cancer is tyrosine kinase inhibitors (TKI) sunitinib and pazopanib. This article assesses cost-effectiveness between pazopanib and sunitinib in the treatment of metastatic renal cancer. A cost-effectiveness study was performed from the perspective of a federal hospital under the Brazilian Unified National Health System (SUS). TKI effectiveness and safety outcomes were applied to the decision tree model. Clinical data were extracted from patient charts, and direct costs were consulted from official Ministry of Health sources. The cost of 10 months of treatment, including the costs of the TKI, procedures and management of adverse events, was BRL 98,677.19 for pazopanib and BRL 155,227.11 for sunitinib. The drugs displayed statistically equivalent effectiveness and statistically different safety outcomes, with pazopanib displaying better results. In this setting, pazopanib is the dominant technology when the treatment costs are analyzed together with the costs of managing adverse events.


Resumen: El cáncer renal es la 13ª neoplasia más frecuente en el mundo. Entre 2010 y 2014, representó un 1,43% de las muertes por cáncer en Brasil. La terapia de elección para el tratamiento de cáncer renal metastásico son los inhibidores de tirosina quinasa (ITK), sunitinib y pazopanib. Este artículo evalúa el costo-efectividad entre pazopanib y sunitinib en el tratamiento de cáncer renal metastásico. Se realizó un análisis de costo-efectividad desde la perspectiva de un hospital federal del Sistema Único de Salud. En el modelo de árbol de decisión se aplicaron los desenlaces de efectividad y seguridad de los ITK. Los datos clínicos se extrajeron de registros médicos, y los costos directos consultados en fuentes oficiales del Ministerio de Salud. El costo de 10 meses de tratamiento, englobando el valor de los ITK, procedimientos y gestión de eventos adversos, fue de BRL 98.677,19 con el pazopanib y BRL 155.227,11 con el sunitinib. Los medicamentos presentaron efectividad estadísticamente equivalente y diferencia estadísticamente significativa para el desenlace de seguridad, en el que el pazopanib obtuvo el mejor resultado. El pazopanib, en este contexto, es la tecnología dominante cuando los costes de tratamiento están asociados a los de la gestión de eventos adversos.


Subject(s)
Humans , Male , Female , Adult , Aged , Pyrimidines/economics , Sulfonamides/economics , Cost-Benefit Analysis/statistics & numerical data , Protein Kinase Inhibitors/economics , Sunitinib/economics , Kidney Neoplasms/drug therapy , Antineoplastic Agents/economics , Pyrimidines/administration & dosage , Sulfonamides/administration & dosage , Treatment Outcome , Protein Kinase Inhibitors/administration & dosage , Kaplan-Meier Estimate , Sunitinib/administration & dosage , Indazoles , Middle Aged , National Health Programs , Neoplasm Metastasis , Antineoplastic Agents/administration & dosage
4.
Salud colect ; 15: e1962, 2019. tab, graf
Article in Spanish | LILACS | ID: biblio-1004640

ABSTRACT

RESUMEN En Argentina, los nuevos medicamentos pueden ser autorizados presentando el certificado de aprobación en al menos uno de los 15 países considerados de alta vigilancia sanitaria, sin necesidad de realizar una evaluación propia de eficacia, seguridad o valor terapéutico agregado por el nuevo producto. En este artículo, evaluamos los nuevos medicamentos comercializados en Argentina en el año 2016, utilizando diferentes enfoques: su aprobación por otras agencias reguladoras, demostración de eficacia en ensayos clínicos aleatorizados, tipo de desenlaces estudiados, calificación del valor terapéutico agregado por medio de dos escalas reconocidas y el precio de venta al público. Se concluye que, como reflejo de lo que ocurre en los países desarrollados, los nuevos medicamentos ingresan con precios exorbitantes, pero la mayoría no representa un avance terapéutico significativo. El resultado es un aumento de riesgos para los pacientes y una sobrecarga para los sistemas de financiación públicos y privados.


ABSTRACT In Argentina, new drugs can be authorized by presenting the drug's certificate of approval in at least one of 15 countries considered to have rigorous health surveillance, without needing to carry out a local evaluation of the efficacy, safety or added therapeutic value of the new product. In this article, we evaluate the new drugs commercialized in Argentina in 2016 using different approaches: their approval by other regulatory agencies, the demonstration of their efficacy in randomized clinical trials, types of outcomes studied, rating of their added therapeutic value using two widely recognized scales, and their sale price to the public. It is concluded that, as a reflection of what occurs in developed countries, new drugs enter the market at exorbitant prices, but the majority do not represent a significant therapeutic advancements. The result is increased risks to patients and an overburdening of the public and private funding systems.


Subject(s)
Humans , Drug Costs/statistics & numerical data , Cost-Benefit Analysis/statistics & numerical data , Drug Approval , Drug Evaluation , Argentina , Randomized Controlled Trials as Topic
5.
Braz. j. infect. dis ; 22(1): 1-10, Jan.-feb. 2018. tab
Article in English | LILACS | ID: biblio-951627

ABSTRACT

ABSTRACT Background: Influenza burden in Brazil is considerable with 4.2-6.4 million cases in 2008 and influenza-like-illness responsible for 16.9% of hospitalizations. Cost-effectiveness of influenza vaccination may be assessed by different types of models, with limitations due to data availability, assumptions, and modelling approach. Objective: To understand the impact of model complexity, the cost-utility of quadrivalent versus trivalent influenza vaccines in Brazil was estimated using three distinct models: a 1-year decision tree population model with three age groups (FLOU); a more detailed 1-year population model with five age groups (FLORA); and a more complex lifetime multi-cohort Markov model with nine age groups (FLORENCE). Methods: Analysis 1 (impact of model structure) compared each model using the same data inputs (i.e., best available data for FLOU). Analysis 2 (impact of increasing granularity) compared each model populated with the best available data for that model. Results: Using the best data for each model, the discounted cost-utility ratio of quadrivalent versus trivalent influenza vaccine was R$20,428 with FLOU, R$22,768 with FLORA (versus R$20,428 in Analysis 1), and, R$19,257 with FLORENCE (versus R$22,490 in Analysis 1) using a lifetime horizon. Conceptual differences between FLORA and FLORENCE meant the same assumption regarding increased all-cause mortality in at-risk individuals had an opposite effect on the incremental cost-effectiveness ratio in Analysis 2 versus 1, and a proportionally higher number of vaccinated elderly in FLORENCE reduced this ratio in Analysis 2. Discussion: FLOU provided adequate cost-effectiveness estimates with data in broad age groups. FLORA increased insights (e.g., in healthy versus at-risk, paediatric, respiratory/non-respiratory complications). FLORENCE provided greater insights and precision (e.g., in elderly, costs and complications, lifetime cost-effectiveness). Conclusion: All three models predicted a cost per quality-adjusted life year gained for quadrivalent versus trivalent influenza vaccine in the range of R$19,257 (FLORENCE) to R$22,768 (FLORA) with the best available data in Brazil (Appendix A).


Subject(s)
Humans , Male , Female , Infant , Child, Preschool , Child , Adolescent , Adult , Middle Aged , Aged , Young Adult , Influenza Vaccines/economics , Vaccination/economics , Models, Economic , Influenza, Human/economics , Influenza, Human/prevention & control , Brazil , Reproducibility of Results , Decision Support Techniques , Age Factors , Vaccination/statistics & numerical data , Cost-Benefit Analysis/methods , Cost-Benefit Analysis/statistics & numerical data , Risk Assessment , Quality-Adjusted Life Years , Hospitalization/economics
6.
Braz. J. Pharm. Sci. (Online) ; 53(3): e00178, 2017. tab, graf
Article in English | LILACS | ID: biblio-889385

ABSTRACT

ABSTRACT Human insulin is provided by the Brazilian Public Health System (BPHS) for the treatment of diabetes, however, legal proceedings to acquire insulin analogs have burdened the BPHS health system. The aim of this study was to perform a cost-effectiveness analysis to compare insulin analogs and human insulins. This is a pharmacoeconomic study of cost-effectiveness. The direct medical cost related to insulin extracted from the Ministry of Health drug price list was considered. The clinical results, i.e. reduction in glycated hemoglobin (HbA1c), were extracted by meta-analysis. Different scenarios were structured to measure the uncertainties regarding the costs and reduction in HbA1c. Decision tree was developed for sensitivity of Incremental Cost Effectiveness Ratio (ICER). A total of fifteen scenarios were structured. Given the best-case scenario for the insulin analogs, the insulins aspart, lispro, glargine and detemir showed an ICER of R$ 1,768.59; R$ 3,308.54; R$ 11,718.75 and R$ 2,685.22, respectively. In all scenarios in which the minimum effectiveness was proposed, lispro, glargine and detemir were dominant strategies. Sensitivity analysis showed that the aspart had R$ 3,066.98 [95 % CI: 2339.22; 4418.53] and detemir had R$ 6,163.97 [95% CI: 3919.29; 11401.57] for incremental costs. We concluded there was evidence that the insulin aspart is the most cost-effective.


Subject(s)
Cost-Benefit Analysis/statistics & numerical data , Insulin, Long-Acting/analysis , Insulins/analysis , Insulin, Short-Acting/analysis , Unified Health System/statistics & numerical data , Glycated Hemoglobin , Costs and Cost Analysis , Diabetes Mellitus/drug therapy , Insulin Aspart/analysis , Insulin Detemir , Insulin/supply & distribution
7.
s.l; s.n; 2016.
Non-conventional in Spanish | BRISA, LILACS | ID: biblio-833289

ABSTRACT

Galsulfasa es un tratamiento de alto costo y con evidencia de baja calidad de un beneficio que no se traduce en desenlaces clínicos importantes relevantes como calidad de vida y la mortalidad de los pacientes con MPS, resultando en un balance bastante incierto entre el costo y su beneficio. 3.2. En condiciones habituales de práctica médica, la galsulfasa no alcanzó a lograr los objetivos primarios en un paciente con diagnóstico de Mucopolisacaridosis tipo VI. Se recomienda no brindar cobertura al medicamento galsulfasa en mucopolisacaridosis tipo VI.(AU)


Subject(s)
Cost-Benefit Analysis/statistics & numerical data , Mucopolysaccharidosis VI/drug therapy , N-Acetylgalactosamine-4-Sulfatase/adverse effects , Technology Assessment, Biomedical
8.
Einstein (Säo Paulo) ; 13(4): 600-603, Oct.-Dec. 2015. tab
Article in Portuguese | LILACS | ID: lil-770503

ABSTRACT

ABSTRACT Objective To identify the financial resources and investments provided for preventive medicine programs by health insurance companies of all kinds. Methods Data were collected from 30 large health insurance companies, with over 100 thousand individuals recorded, and registered at the Agência Nacional de Saúde Suplementar. Results It was possible to identify the percentage of participants of the programs in relation to the total number of beneficiaries of the health insurance companies, the prevention and promotion actions held in preventive medicine programs, the inclusion criteria for the programs, as well as the evaluation of human resources and organizational structure of the preventive medicine programs. Conclusion Most of the respondents (46.7%) invested more than US$ 50,000.00 in preventive medicine program, while 26.7% invested more than US$ 500,000.00. The remaining, about 20%, invested less than US$ 50,000.00, and 3.3% did not report the value applied.


RESUMO Objetivo Identificar os recursos financeiros e os investimentos disponibilizados para os programas de medicina preventiva em operadoras de saúde suplementar de todos os tipos. Métodos Foram levantados dados referentes a 30 operadoras de saúde registradas na Agência Nacional de Saúde Suplementar, de grande porte, com registro acima de 100 mil vidas. Resultados Foi possível identificar o porcentual de participantes dos programas em relação ao número total de beneficiários da operadora, as ações de prevenção e promoção realizadas nos programas de medicina preventiva, os critérios de inclusão nos programas, bem como a avaliação dos recursos humanos e da estrutura organizacional dos programas de medicina preventiva pesquisadas. Conclusão A maior parte dos pesquisados (46,7%) investiu mais de US$ 50,000.00 no programa de medicina preventiva, enquanto 26,7% investiram mais de US$ 500,000.00. Os restantes, cerca de 20%, investiram menos de US$ 50,000.00 e 3,3% não informaram o valor aplicado.


Subject(s)
Adolescent , Adult , Aged , Aged, 80 and over , Child , Child, Preschool , Humans , Infant , Infant, Newborn , Middle Aged , Young Adult , Health Care Costs/statistics & numerical data , Health Promotion/organization & administration , Insurance Benefits/statistics & numerical data , Insurance, Health/organization & administration , Preventive Medicine/organization & administration , Private Sector/organization & administration , Brazil , Cost-Benefit Analysis/statistics & numerical data , Health Resources/economics , Insurance, Health/classification , Program Evaluation/economics , Surveys and Questionnaires
9.
Braz. j. pharm. sci ; 50(2): 345-352, Apr-Jun/2014. tab, graf
Article in English | LILACS | ID: lil-722193

ABSTRACT

Brazilian Guidelines to HCV treatment (2007) recommended that the first choice treatment for patients with chronic hepatitis C (CHC) and genotype 2 or 3 is interferon alpha (IFN) plus ribavirin (RBV) for 24 weeks. The aim of this study is compare the cost and effectiveness to Hepatitis C treatment in patients with genotype 2 or 3 of peginterferon alpha (PEG) as the first choice of treatment within PEG for those that do not respond to IFN. The target population is CHC patients with genotype 2 or 3 in Brazil. The interventions are: PEG-SEC (first IFN plus RBV for 24 weeks, after, for non-responders and relapsers subsequently PEG plus RBV for 48 weeks); PEG-FIRST24 (PEG+RBV for 24 weeks). The type of the study is cost-effectiveness analysis. The data sources are: Effectiveness data from meta-analysis conducted on the Brazilian population. Treatment cost from Brazilian micro costing study is converted into USD (2010). The perspective is the Public Health System. The outcome measurements are Sustained Viral Response (SVR) and costs. PEG-FIRST24 (SVR: 87.8%, costs: USD 8,338.27) was more effective and more costly than PEG-SEC (SVR: 79.2%, costs: USD 5,852.99). The sensitivity analyses are: When SVR rates with IFN was less than 30% PEG-FIRST is dominant. On the other hand, when SVR with IFN was more then 75% PEG-SEC is dominant (SVR=88.2% and costs USD $ 3,753.00). PEG-SEC is also dominant when SVR to PEG24 weeks was less than 54%. In the Brazilian context, PEG-FIRST is more effective and more expensive than PEG-SEC. PEG-SEC could be dominant when rates of IFN therapy are higher than 75% or rates of PEG24 therapy are lower than 54%.


O protocolo brasileiro de tratamento da Hepatite C (2007) recomendava como primeira escolha para pacientes com hepatite C crônica e portadores de genótipo 2 ou 3 o tratamento com interferona alfa (IFN) associada à ribavirina (RBV), por 24 semanas. O objetivo deste estudo é comparar o custo e a efetividade para pacientes com hepatite C crônica e portadores do genótipo 2 ou 3 o uso de peguinterferon (PEG) como primeiro escolha com o PEG como secunda escolha para aqueles que não responderam ao tratamento com IFN. A população alvo compreende pacientes com hepatite C crônica portadores de genótipo 2 ou 3 no Brasil. As intervenções são: PEG-SEC (IFN + RBV por 24 semanas, para os não respondedores e recidivantes tratamento subsequente com PEG + RBV por 48 semanas; PEG-FIRST24 (PEG + RBV por 24 semanas). O tipo de estudo envolvido é Análise de Custo Efetividade. Os dados de efetividade são provenientes de um metanálise de estudos brasileiros e os dados de custo do tratamento de um estudo de custo do contexto brasileiro. A perspectiva é o Sistema Público de Saúde. Os desfechos avaliados foram Resposta Viral Sustentada (RVS) e Custos. PEG-FIRST24 (RVS: 87,8%, costs: USD 8.338,27) foi mais efetivo e apresentou maior custo que PEG-SEC (RVS: 79,2%, custo USD 5.852,99). A análise de sensibilidade demonstrou que PEG-SEC é dominado por PEG-FIRST24 quando RVS com IFN for menor que 30%. Por outro lado, quando RVS com IFN for maior que 75% PEG-SEC é dominante (RVS=88.2% e custo USD $ 3.753,00). PEG-SEC é também dominante quando RVS para PEG24 for menor que 54%. Conclusão: No contexto brasileiro, PEG-FIRST é mais efetivo e mais custoso que PEG-SEC. PEG-SEC poderia ser dominante quando as taxas de RVS do tratamento com IFN forem superiores a 75% ou as taxas de PEG24 forem inferiores a 54%.


Subject(s)
Therapeutics/economics , Cost-Benefit Analysis/statistics & numerical data , Hepatitis C, Chronic/classification , Genotype , Costs and Cost Analysis/classification , Interferon Regulatory Factor-2/classification , Interferon Regulatory Factor-3
10.
Salud pública Méx ; 53(supl.3): s375-s385, 2011. graf
Article in Spanish | LILACS | ID: lil-625717

ABSTRACT

OBJETIVO: Presentar y analizar información de costo-efectividad de intervenciones propuestas por la Iniciativa Mesoamericana de Salud (IMS) en las áreas de nutrición infantil, inmunizaciones, paludismo, dengue y salud materno-infantil y reproductiva. MATERIAL Y MÉTODOS: Se llevó a cabo una revisión sistemática de la literatura de evaluaciones económicas publicadas entre el año 2000 y agosto 2009 sobre intervenciones en las áreas de la salud mencionadas, en los idiomas inglés y español. RESULTADOS: Las intervenciones en nutrición y de salud materno-infantil mostraron ser altamente costo-efectivas (con rangos menores a US$200 por año de vida ajustado por discapacidad [AVAD] evitado para nutrición y US$100 para materno-infantil). En dengue sólo se encontró información sobre la aplicación de larvicidas, cuya razón de costo efectividad estimada fue de US$40.79 a US$345.06 por AVAD evitado. Respecto al paludismo, las intervenciones estudiadas resultaron costo-efectivas (

OBJECTIVE: Present and analyze cost-effectiveness information of public health interventions proposed by the Mesoamerican Health Initiative in child nutrition, vaccination, malaria, dengue, and maternal, neonatal, and reproductive health. MATERIAL AND METHODS: A systematic literature review was conducted on cost-effectiveness studies published between January 2000 and August 2009 on interventions related to the health areas previously mentioned. Studies were included if they measured effectiveness in terms of Disability-Adjusted Life Year (DALY) or death averted. RESULTS: Child nutrition and maternal and neonatal health interventions were found to be highly cost-effective (most of them below US$200 per DALY averted for nutritional interventions and US$100 for maternal and neonatal health). For dengue, information on cost-effectiveness was found just for application of larvicides, which resulted in a cost per DALY averted ranking from US$40.79 to US$345.06. Malarial interventions were found to be cost-effective (below US$150 per DALY averted or US$4,000 per death averted within Africa). In the case of pneumococcus and rotavirus vaccination, cost-effectiveness estimates were always above one GDP per capita per DALY averted. CONCLUSIONS: In Mesoamerica there are still important challenges in child nutrition, vaccination, malaria, dengue and maternal, neonatal, and reproductive health, challenges that could be addressed by scaling-up technically feasible and cost-effective interventions.


Subject(s)
Animals , Child , Female , Humans , Pregnancy , Bibliometrics , Cost-Benefit Analysis/statistics & numerical data , Health Promotion/statistics & numerical data , Public Health/statistics & numerical data , Central America , Child Health Services/economics , Child Health Services/organization & administration , Child Health Services/statistics & numerical data , Costs and Cost Analysis , Dengue/prevention & control , Developing Countries , Health Promotion/economics , Health Promotion/organization & administration , Immunization Programs/economics , Immunization Programs/organization & administration , Immunization Programs/statistics & numerical data , International Cooperation , Malaria/prevention & control , Malnutrition/prevention & control , Maternal Health Services/economics , Maternal Health Services/organization & administration , Maternal Health Services/statistics & numerical data , Mexico , Mosquito Control/economics , Mosquito Control/organization & administration , Mosquito Control/statistics & numerical data , Preventive Health Services/economics , Preventive Health Services/organization & administration , Preventive Health Services/statistics & numerical data , Reproductive Health Services/economics , Reproductive Health Services/organization & administration , Reproductive Health Services/statistics & numerical data
11.
Colomb. med ; 41(4): 315-322, oct.-dic. 2010. tab, ilus
Article in English | LILACS | ID: lil-573024

ABSTRACT

Objective: To estimate the economic impact of the introduction of heptavalent pneumococcal conjugate vaccine (PCV-7) in high risk populations of Colombia. Methods: A full economic evaluation was done regarding potential introduction of PCV-7. A cost-effectiveness study from the perspective of the third payer was done using a Decision Model. The model considered two alternatives: with and without vaccination. As measurement of results the avoided events were taken [cases, hospitalizations, deaths and Life-Years Saved (LYS)]. In addition the net costs and the incremental cost-effectiveness ratio (ICER) were evaluated. Results: In a cohort of 70 thousand children of under 2 years old in situation of high risk, can generate 532 deaths that would produce a little more than 21 thousand Years of Life Lost (YLL) with costs between 7.7 and 13.3 million dollars. If we vaccinate this same cohort the deaths can be reduced to 355, and the costs of burden of disease would be between 5.7 and 10 million dollars. It is estimated a reduction of 25% of the costs of burden of disease and of 33% of the deaths. In addition the ICER by YLS would be between 590 and 762 dollars. Conclusion: The introduction of the Heptavalent Pneumococcal Conjugate Vaccine in populations of high risk is highly cost effective in Colombia.


Objetivo: Evaluar económicamente la introducción de la vacuna heptavalente de neumococo en poblaciones de alto riesgo en Colombia. Métodos: Se realizó un análisis de costo-efectividad desde la perspectiva del tercer pagador utilizando un modelo de decisiones que consideró dos alternativas: con y sin programa de vacunación. Como medida de resultados se tomaron los eventos evitados [casos, hospitalizaciones, muertes y años de vida salvados (AVS)]. Además, se valoraron los costos netos y la razón de costo-efectividad incremental (RCEI). Resultados: En una cohorte de 70 mil niños menores de dos años en situación de alto riesgo (bajo peso al nacer), se puede generar 532 muertes que producirían un poco más de 21 mil años de vida perdidos. Los costos de atención estarían entre 7,7 y 13,3 millones de dólares. Si vacunásemos esta misma cohorte con la vacuna conjugada heptavalente las muertes se reducirían a 355 y los costos de la carga estarían entre 5,7 y 10 millones de dólares. Es decir, una reducción cerca de 25% de los costos de la carga y 33% de las muertes. Además el CEI por AVS estaría entre 590 y 762 dólares del año 2006. Conclusiones: La introducción de la vacuna contra neumococo en poblaciones de alto riesgo (bajo peso al nacer) en Colombia es altamente costo-efectiva.


Subject(s)
Humans , Infant, Newborn , Cost-Benefit Analysis/statistics & numerical data , Cost-Benefit Analysis/methods , Pneumonia/diagnosis , Pneumonia/immunology , Pneumonia/prevention & control , Vaccination
12.
Rio de Janeiro; s.n; 2010. 37 p. ilus, tab.
Thesis in Portuguese | LILACS | ID: lil-601247

ABSTRACT

O estudo teve como objetivo avaliar a razão de custo-efetividade, sob a perspectiva do Sistema Único de Saúde - SUS, do tratamento da anemia de pacientes em Terapia Renal Substitutiva. Duas alternativas foram comparadas: um novo medicamento recentemente registrado no Brasil, o Ativador Contínuo de Receptor de Eritropoetina (Continuous Erythropoitin Receptor Activador), CERA, e outro, atualmente disponível no sistema de saúde brasileiro, a Eritropoetina Recombinante Humana - EPO-rHu. Métodos: Um modelo de Markov simulou o curso de uma coorte de pacientes em Terapia Renal Substitutiva tratados com CERA e Epo-Hu por quatro anos. A qualidade de vida associada ao uso dos medicamentos foi estimada de forma indireta, por meio de entrevista qualificada com os profissionais cuidadores, previamente submetida e aprovada pelo Comitê de Ética em Pesquisa local. Foi realizada análise de sensibilidade no modelo proposto através da variação dos parâmetros: doses dos medicamentos, custo das estratégias, taxas de desconto e efetividade utilizados para sua construção. Resultados: A média da qualidade de vida atribuída aos pacientes tratados foi 6,3 para Epo-rHu, 7,8 para o CERA e 9,3 para os pacientes transplantados. O modelo demonstrou que a estratégia mais custo-efetiva é a terapêutica com a Epo-rHu, com um custo por QALY de R$21.052,00. O custo incremental por QALY ganho associado ao CERA foi de 72.974,00. Conclusão: A utilização mensal do medicamento CERA está associada à maior qualidade de vida quando comparada a EPO-rHu. No entanto, a terapia com o novo medicamento não se mostrou mais custo-efetiva frente ao tratamento com EPO-rHu.


Subject(s)
Humans , Male , Female , Cost-Benefit Analysis/economics , Cost-Benefit Analysis/statistics & numerical data , Cost-Benefit Analysis/trends , Cost-Benefit Analysis , Anemia/economics , Renal Replacement Therapy , Unified Health System , Drug Evaluation/economics , Erythropoietin , Clinical Trials as Topic/economics , Erythropoietin/therapeutic use , Receptors, Erythropoietin
13.
J Health Popul Nutr ; 2008 Dec; 26(4): 388-96
Article in English | IMSEAR | ID: sea-713

ABSTRACT

The study was done to evaluate the cost-effectiveness of a national rotavirus vaccination programme in Brazilian children from the healthcare system perspective. A hypothetical annual birth-cohort was followed for a five-year period. Published and national administrative data were incorporated into a model to quantify the consequences of vaccination versus no vaccination. Main outcome measures included the reduction in disease burden, lives saved, and disability-adjusted life-years (DALYs) averted. A rotavirus vaccination programme in Brazil would prevent an estimated 1,804 deaths associated with gastroenteritis due to rotavirus, 91,127 hospitalizations, and 550,198 outpatient visits. Vaccination is likely to reduce 76% of the overall healthcare burden of rotavirus-associated gastroenteritis in Brazil. At a vaccine price of US$ 7-8 per dose, the cost-effectiveness ratio would be US$ 643 per DALY averted. Rotavirus vaccination can reduce the burden of gastroenteritis due to rotavirus at a reasonable cost-effectiveness ratio.


Subject(s)
Brazil , Child, Preschool , Cohort Studies , Cost-Benefit Analysis/statistics & numerical data , Female , Gastroenteritis/economics , Humans , Infant , Male , Rotavirus/drug effects , Rotavirus Infections/economics , Rotavirus Vaccines/economics
14.
JPMI-Journal of Postgraduate Medical Institute. 2008; 22 (2): 136-139
in English | IMEMR | ID: emr-88494

ABSTRACT

To evaluate the role of metoclopramide and dimenhydrinate in controlling postoperative nausea and vomiting [PONV] and its cost effectiveness in gynaecological laparoscopy. This study was conducted in the department of anaesthesiology and intensive care unit, Pakistan Institute of Medical Sciences, Islamabad from June 2004 to March 2006. Ninety nine female patients belonging to American society of Anaesthesiologist [ASA] grading ASA-1 to ASA-111, scheduled for laparoscopic surgery, who did not fall in exclusion criteria were finally included. Anaesthetic technique was standardized for all patients. Injection Metocloparamide 10 mg and injection Dimenhydrinate 50 mg were administered 20 min before the procedure was over. At the end of procedure patients were transferred to the recovery room for observation for 10 hours. Four point verbal descriptive scale [VDS] was used to identify the presence and severity of PONV. Four out of 99 [4.04%] patients developed nausea soon after regaining consciousness and did not demand any medication for relief. Three [3.03%] patients developed vomiting. It was single episode and no rescue medication was needed. Most of the symptoms developed with in 10 -30 minutes of reversal. Metocloparamide and dimenhydrinate is a good combination to combat PONV and is costeffective in laparoscopic gynaecological surgery


Subject(s)
Humans , Female , Postoperative Nausea and Vomiting/classification , Laparoscopy/adverse effects , Dimenhydrinate/administration & dosage , Dimenhydrinate , Metoclopramide/administration & dosage , Metoclopramide , Cost-Benefit Analysis/statistics & numerical data , Gynecologic Surgical Procedures/adverse effects
15.
Rev. cienc. adm. financ. segur. soc ; 14(1): 91-93, ene. - jun. 2006. ilus
Article in Spanish | LILACS | ID: lil-581886

ABSTRACT

En este artículo se presentan las principales características de la morbilidad por enfermedades cardiovasculares y el costo en que incurre la Caja Costarricense de Seguro Social en la atención de las mismas.


Subject(s)
Humans , Cost-Benefit Analysis/statistics & numerical data , Cardiovascular Diseases , Health Care Costs/statistics & numerical data , Costs and Cost Analysis/statistics & numerical data , Costa Rica
16.
Rev. argent. cir ; 85(1/2): 61-68, jul.ago. 2003. ilus
Article in Spanish | LILACS | ID: lil-383874

ABSTRACT

Antecedentes: La cirugía craneofacial tiene por objeto la exéresis completa de todos los tumores que en forma presunta o confirmada invaden la base del cráneo, ya sea por una lesión facial que progrese en sentido craneal o de un tumor encefálico que lo haga caudalmente. Objetivo: Comunicar resultados, costo-beneficio y calidad de vida alcanzada. Lugar de aplicación: Hospital público terciario especializado en el tratamiento de tumores. Diseño: Prospectivo. Población: 42 operaciones en 39 enfermos, 61 por ciento masculinos. La localización fue mayor en seno maxilar y etmoides. La patología fue maligna en el 94,8 por ciento. El 35,9 por ciento era virgen de tratamiento. Método: Cirugía sólo del primario en 90,4 por ciento, extendida a órbita en el 30,9 por ciento y al cuello en el 9,5 por ciento. En el 69 por ciento fueron anteriores y en el resto laterales. En 17 operaciones fue necesario algún procedimiento reconstructivo de partes blandas. Resultados: Se produjeron complicaciones en el 59,5 por ciento. La más frecuente fue la supuración local, seguida de la pérdida de LCR. El 50 por ciento de la muestra tuvo la posibilidad de estar vivo a los 27,5 meses. Los costos alcanzaron una media de $4698. La calidad de vida mejoró en el 55 por ciento. Conclusiones: La cirugía craneofacial es un procedimiento sencillo, económico, seguro y efectivo para tratar estos enfermos


Subject(s)
Humans , Male , Adult , Female , Middle Aged , Facial Neoplasms , Head and Neck Neoplasms , Cost-Benefit Analysis/statistics & numerical data , Carcinoma, Squamous Cell/surgery , Carcinoma, Squamous Cell/mortality , Skull/surgery , Face , Facial Neoplasms , Salivary Glands, Minor/surgery , Head and Neck Neoplasms , Prospective Studies , Quality of Life , Plastic Surgery Procedures , Salivary Gland Neoplasms , Survival Analysis , Survival Rate , Treatment Outcome
17.
Rev. mex. ortop. traumatol ; 15(2): 78-93, mar.-abr. 2001. tab
Article in Spanish | LILACS | ID: lil-310754

ABSTRACT

En el presente artículo se hace una exhaustiva revisión bibliográfica de las investigaciones y resultados clínicos de las drogas más utilizadas para el tratamiento de la osteoporosis, así como de la efectividad de cada una de ellas para prevenir una fractura. También se discuten los problemas más importantes para prevenir, diagnosticar y tratar esta enfermedad con un costo beneficio razonable. Al final se discuten algunas estrategias y sugerencias para definir si es necesaria o no una intervención farmacológica, y si ésta se considera necesaria, de qué tipo debe ser.


Subject(s)
Ribulose-Bisphosphate Carboxylase , Calcitonin , Alendronate , Diphosphonates , Fluorides , Fractures, Bone/prevention & control , Osteoporosis, Postmenopausal/drug therapy , Treatment Outcome , Cost-Benefit Analysis/statistics & numerical data
18.
Rev. nutr ; 14(supl): 21-26, 2001. tab, graf
Article in Portuguese | LILACS | ID: lil-341272

ABSTRACT

Neste estudo, analisou-se a influência do tamanho das plantas de produção de refeições, as Unidades de Alimentação e Nutrição da Divisão de Alimentação COSEAS/USP, nos custos das refeições produzidas em 1997, a preços de abril de 1998. O número de refeições produzidas em cada Unidade de Alimentação e Nutrição foi utilizado como proxy do tamanho de cada planta de produção. Foram calculados os custos unitários de refeições, abrangendo a totalidade do universo em 1997. A comparação com os preços, por categoria de usuários, permitiu o cálculo da margem de contribuição. Os principais resultados foram: não há relação entre os custos unitários de gêneros alimentícios e a planta de produção, mas quanto maior a planta menores são os custos diretos unitários. O cálculo da margem de contribuição permitiu confirmar a existência da política da Universidade de subsídio às refeições oferecidas a sua comunidade


Subject(s)
Collective Feeding/economics , Cost-Benefit Analysis/statistics & numerical data , Food Services/statistics & numerical data
19.
Rev. bioméd. (México) ; 9(2): 103-7, abr.-jun. 1998. tab
Article in Spanish | LILACS | ID: lil-248113

ABSTRACT

Introducción. La mediación de progesterona de origen ovárico, es un prodecidimiento que permite determinar la funcionalidad reproductiva de las hembras de todos los mamíferos domésticos, inclusive en la mujer. En México, la tecnología del radioinmunoanálisis (RIA) es la más utilizada para medir progesterona sanguínea. Sin embargo, no existe alguna industria mexicana que se dedique a producir estuches comerciales. En el presente trabajo se estimó el costo de producción de dos técnicas de RIA en fase líquida para medir progesterona sanguínea. Material y métodos. A partir de los insumos primarios (anticuerpo, calibrador o analito y trazador) se establecieron y validaron dos técncias de RIA para medir progesterona sanguínea. La técnica A utilizó anticuerpos antipropgesterona inducidos en conejo y extraídos del suero sanguíneo. La técnica B utilizó anticuerpos antiprogesterona inducidos en gallina de postura y extraídos de la yema del huevo. Resultados. La sensibilidad de ambas técnicas de RIA permitió detectar valores relativamente bajos de la hormona, lo suficiente para poder detectar actividad luteal. El costo de producción por tubo (de USD 0.14 a 0.20) disminuyó conforme aumentó el rendimiento del anticuerpo. Discusión. En nuestro medio la producción de anticuerpos contra progesterona para establecer un RIA es una alternativa viable y disminuiría el costo de utilización de esta técnica


Subject(s)
Animals , Rabbits , Cost-Benefit Analysis/statistics & numerical data , Egg Yolk/immunology , Antibody Formation/immunology , Biomarkers/analysis , Biomarkers/blood , Poultry/immunology , Progesterone/analysis , Progesterone/blood , Rabbits/blood , Rabbits/immunology , Immunologic Techniques/economics , Immunologic Techniques
20.
Säo Paulo; s.n; 1997. 164 p. ilus, tab, graf.
Thesis in Portuguese | LILACS, SES-SP | ID: lil-198287

ABSTRACT

Este trabalho refere-se ao estudo dos programas governamentais de saúde pública, especialmente ao controle e combate ao mosquito Aedes aegypti, vetor transmissor do dengue, doença endêmica na América Latina e que caminha a curto prazo para um nível epidêmico de dengue hemorrágico, em várias regioes da América Latina e Caribe. É abordado aqui a situaçäo epidemiológica de três Regiöes-Estados latinos-americanos: Costa Rica, Venezuela e o Estado de Säo Paulo (Brasil). Na parte econômica, foco principal deste estudo, é feita uma análise sobre seus recursos orçamentários destinados com esse programa de controle do dengue, sobre seus custos totais e unitários de produçäo e custos-efetividade também, no período de 1990-1994.


Subject(s)
Humans , Dengue/prevention & control , Cost-Benefit Analysis/statistics & numerical data , Budgets/statistics & numerical data , National Health Programs/economics , Venezuela/epidemiology , Brazil/epidemiology , Costa Rica/epidemiology , Dengue/epidemiology
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