971 resultados para Artificial life simulation


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In the present work the life cycle of Psammolestes tertius was studied. The mean length, in days, fromeach stage was: 26.3 (± 1.7) (1st), 28.6 (± 1.8) (2nd), 28.4 (± 1.8) (3rd), 32.2 (± 1.9) (4th) and 33.5 (± 5.8) (5th). The mean egg incubation period was 15.7 days (± 1.7). Overall mortality was 48.9% and egg viability was 65.7%.

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ABSTRACT - It is the purpose of the present thesis to emphasize, through a series of examples, the need and value of appropriate pre-analysis of the impact of health care regulation. Specifically, the thesis presents three papers on the theme of regulation in different aspects of health care provision and financing. The first two consist of economic analyses of the impact of health care regulation and the third comprises the creation of an instrument for supporting economic analysis of health care regulation, namely in the field of evaluation of health care programs. The first paper develops a model of health plan competition and pricing in order to understand the dynamics of health plan entry and exit in the presence of switching costs and alternative health premium payment systems. We build an explicit model of death spirals, in which profitmaximizing competing health plans find it optimal to adopt a pattern of increasing relative prices culminating in health plan exit. We find the steady-state numerical solution for the price sequence and the plan’s optimal length of life through simulation and do some comparative statics. This allows us to show that using risk adjusted premiums and imposing price floors are effective at reducing death spirals and switching costs, while having employees pay a fixed share of the premium enhances death spirals and increases switching costs. Price regulation of pharmaceuticals is one of the cost control measures adopted by the Portuguese government, as in many European countries. When such regulation decreases the products’ real price over time, it may create an incentive for product turnover. Using panel data for the period of 1997 through 2003 on drug packages sold in Portuguese pharmacies, the second paper addresses the question of whether price control policies create an incentive for product withdrawal. Our work builds the product survival literature by accounting for unobservable product characteristics and heterogeneity among consumers when constructing quality, price control and competition indexes. These indexes are then used as covariates in a Cox proportional hazard model. We find that, indeed, price control measures increase the probability of exit, and that such effect is not verified in OTC market where no such price regulation measures exist. We also find quality to have a significant positive impact on product survival. In the third paper, we develop a microsimulation discrete events model (MSDEM) for costeffectiveness analysis of Human Immunodeficiency Virus treatment, simulating individual paths from antiretroviral therapy (ART) initiation to death. Four driving forces determine the course of events: CD4+ cell count, viral load resistance and adherence. A novel feature of the model with respect to the previous MSDEMs is that distributions of time to event depend on individuals’ characteristics and past history. Time to event was modeled using parametric survival analysis. Events modeled include: viral suppression, regimen switch due virological failure, regimen switch due to other reasons, resistance development, hospitalization, AIDS events, and death. Disease progression is structured according to therapy lines and the model is parameterized with cohort Portuguese observational data. An application of the model is presented comparing the cost-effectiveness ART initiation with two nucleoside analogue reverse transcriptase inhibitors (NRTI) plus one non-nucleoside reverse transcriptase inhibitor(NNRTI) to two NRTI plus boosted protease inhibitor (PI/r) in HIV- 1 infected individuals. We find 2NRTI+NNRTI to be a dominant strategy. Results predicted by the model reproduce those of the data used for parameterization and are in line with those published in the literature.

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A Work Project, presented as part of the requirements for the Award of a Masters Degree in Management from the NOVA – School of Business and Economics

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A fim de obter metodologias que permitam estabelecer, com segurança, o diagnóstico "post-mortem " da infecção chagásica, adaptou-se o xenodiagnóstico artificial a necropsiados com diferentes tempos de óbito. O testefoi positivo em três (30%) de dez chagásicos autopsiados. O tempo decorrido entre o êxito letal e o início do repasto pelos triatomineos destes chagásicos foi de duas horas, duas horas e quinze minutos e sete horas, respectivamente. Discutem-se os fatores que podem explicara sobrevivência do Trypanosoma cruzi no hospedeiro morto bem como as aplicações práticas do achado.

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Dissertação para obtenção do Grau de Mestre em Engenharia e Gestão da Água

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Foram realizados, simultaneamente, os xenodiagnósticos natural e artificial em 57 pacientes chagásicos, na fase crônica, com idades entre 26 e 83 anos, sendo 26 do sexo masculino e 31 do feminino, todos com sorologia reativa. Este estudo teve a finalidade de verificar a sensibilidade do método artificial, visando à sua utilização, em rotina de laboratório. Aplicaram-se 40 Dipetalogaster maximus de 1° estádiopara cada paciente tanto no xmodiagnóstico natural quanto no artificial. O xenodiagnóstico artificial foi significativamente mais sensível do que o natural para detectar o Trypanosoma cruzi, uma aplicaçao do artificial foi igual à do método natural aplicado três vezes. A "xenopositividade'' foi de 35,1%, sendo significativamente maior no sexo masculino, nas faixas etárias de 56 a 65 anos e 66 a 83 anos. Estes resultados mostram a viabilidade e a possibilidade do uso do xenodiagnóstico artificial em rotina de laboratório.

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Based on the presentation and discussion at the 3rd Winter School on Technology Assessment, December 2012, Universidade Nova de Lisboa (Portugal), Caparica Campus, PhD programme on Technology Assessment

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Materials Science Forum Vols. 730-732 (2013) pp 433-438

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Dissertação para obtenção do Grau de Doutor em Engenharia Química

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No combate à doença de Chagas no Brasil, foi utilizado como primeira medida o controle químico, erradicando o Triatoma infestans, o mais importante vetor, tal combate vem favorecendo o aparecimento de vetores secundários, como Triatoma sordida and Panstrongylus megistus, espécies que podem eventualmente ser encontradas no domicílio, como os triatomíneos provenientes de Bernardino de Campos e Sete Barras por nós examinados que foram encontrados no domicílio e positivos para o T. cruzi, sugerindo que, apesar da doença de Chagas estar controlada no Estado de São Paulo, existe a necessidade de aprimorar os conhecimentos sobre o comportamento destes vetores para que mudanças nas medidas de controle sejam introduzidas.