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1.
Res. Biomed. Eng. (Online) ; 31(4): 343-351, Oct.-Dec. 2015. tab, graf
Article in English | LILACS | ID: biblio-829447

ABSTRACT

Abstract Introduction: This work concerns the assessment of a novel system for mechanical ventilation and a parameter estimation method in a bench test. The tested system was based on a commercial mechanical ventilator and a personal computer. A computational routine was developed do drive the mechanical ventilator and a parameter estimation method was utilized to estimate positive end-expiratory pressure, resistance and compliance of the artificial respiratory system. Methods The computational routine was responsible for establishing connections between devices and controlling them. Parameters such as tidal volume, respiratory rate and others can be set for standard and noisy ventilation regimes. Ventilation tests were performed directly varying parameters in the system. Readings from a calibrated measuring device were the basis for analysis. Adopting a first-order linear model, the parameters could be estimated and the outcomes statistically analysed. Results Data acquisition was effective in terms of sample frequency and low noise content. After filtering, cycle detection and estimation took place. Statistics of median, mean and standard deviation were calculated, showing consistent matching with adjusted values. Changes in positive end-expiratory pressure statistically imply changes in compliance, but not the opposite. Conclusion The developed system was satisfactory in terms of clinical parameters. Statistics exhibited consistent relations between adjusted and estimated values, besides precision of the measurements. The system is expected to be used in animals, with a view to better understand the benefits of noisy ventilation, by evaluating the estimated parameters and performing cross relations among blood gas, ultrasonography and electrical impedance tomography.

2.
An. acad. bras. ciênc ; 81(1): 3-12, Mar. 2009. graf, tab
Article in English | LILACS | ID: lil-506847

ABSTRACT

Optimal control theory provides a very interesting quantitative method that can be used to assist the decision making process in several areas of application, such as engineering, biology, economics and sociology. The main idea is to determine the values of the manipulated variables, such as drug doses, so that some cost function is minimized, subject to physical constraints. In this work, the cost function reflects the number of CD4+T cells, viral particles and the drug doses. It is worth noticing that high drug doses are related to more intense side-effects, apart from the impact on the actual cost of the treatment. In a previous paper by the authors, the LQR - Linear Quadratic Regulator approach was proposed for the computation of long period maintenance doses for the drugs, which turns out to be of state feedback form. However, it is not practical to determine all the components of the state vector, due to the fact that infected and uninfected CD4+T cells are not microscopically distinguishable. In order to overcome this difficulty, this work proposes the use of Extended Kalman Filter to estimate the state, even though, because of the nonlinear nature of the involved state equations, the separation principle may not be valid. Extensive simulations were then carried out to investigate numerically if the control strategy consisting of the feedback of estimated states yielded satisfactory clinical results.


A teoria de controle ótimo apresenta um método quantitativo muito interessante que pode ajudar no processo de tomada de decisão em algumas áreas de aplicação, tais como engenharia, biologia, economia e sociologia. A principal idéia é determinar os valores das variáveis controladas, tais como doses de medicamentos, onde alguma função-custo é minimizada, sujeito às restrições físicas. Neste trabalho, a função-custo reflete o número de células CD4+T, partículas virais e doses de medicamentos. É fato que altas dosagens de medicamentos estão relacionadas à maior intensidade de efeitos colaterais, além do impacto no custo real do tratamento. Num prévio trabalho nosso, foi proposta a abordagem LQR - Regulador Linear Quadrático para o cálculo das doses de manutenção para os medicamentos, as quais dependiam de ser realimentadas pelo estado. Entretanto, a determinação de todos os componentes do vetor de estado não seria prática, devido ao fato de que células infectadas e não infectadas são indistingüíveis no microscópio. Para contornar essa dificuldade, este trabalho propõe o uso do Filtro de Kalman Estendido para estimar o estado, ainda que, devido à natureza não linear das equações de estado envolvidas, o princípio da separação não seja válido. Simulações extensivas foram realizadas para investigar numericamente se a estratégia de controle consistindo da realimentação de estados estimados produz resultados clínicos satisfatórios.


Subject(s)
Humans , Anti-HIV Agents/administration & dosage , HIV Infections/drug therapy , Models, Biological , Linear Models , Time Factors
3.
An. acad. bras. ciênc ; 74(3): 379-392, Sept. 2002. ilus, tab, graf
Article in English | LILACS | ID: lil-320132

ABSTRACT

Numerical optimization techniques are useful in solving problems of computing the best inputs for systems described by mathematical models and when the objectives can be stated in a quantitative form. This work concerns the problem of optimizing the drug doses in the treatment of AIDS in terms of achieving a balance between the therapeutic response and the side effects. A mathematical model describing the dynamics of HIV viruses and CD4 cells is used to compute the short term optimal drug doses in the treatments of patients with AIDS by a direct method of optimization using a cost function of Bolza type. The model parameters were fitted to actual published clinical data. In order to simplify the numerical procedures, the control law is expressed as a series and the sub-optimal control is obtained by truncating the higher terms. When the patient reaches a clinically satisfactory state, the LQR - Linear Quadratic Regulator technique is used to determine the long period maintenance doses for the drugs. The doses computed using the LQR technique tend to be smaller than equivalent constant-dose therapy in terms of increase in the counts of CD4+T cells and reduction of the density of free viruses


Subject(s)
Humans , Acquired Immunodeficiency Syndrome/drug therapy , Anti-HIV Agents , HIV Protease Inhibitors , Models, Theoretical , Reverse Transcriptase Inhibitors , Acquired Immunodeficiency Syndrome/immunology , Anti-HIV Agents , CD4 Lymphocyte Count , CD4-Positive T-Lymphocytes , Computer Simulation , HIV , HIV Protease Inhibitors , Linear Models , Reverse Transcriptase Inhibitors , Time Factors , Treatment Outcome
4.
An. acad. bras. ciênc ; 71(4,pt.1): 589-97, dez. 1999. tab, graf
Article in English | LILACS | ID: lil-247922

ABSTRACT

In recent years, many researchers in the field of biomedical sciences have made successful use of mathematical models to study, in a quatitative way, a multitude of phenomena such as those found in disease dynamics, control of physiological systems, optimization of drug therapy, economics of the preventive medicine and many other applications. The availability of good dynamic models have been providing means for simulation and design of novel control strategies in the context of biological events. This work concerns a particular model related to HIV infection dynamics which is used to allow a comparative evaluation of schemes for treatment of AIDS patients. The mathematical model adopted in this work was proposed by Nowak & Bangham, 1996 and describes the dynamics of viral concentration in terms of interaction with CD4 cells and the cytotoxic T lymphocytes, which are responsible for the defense of the organism. Two conceptually distinct techniques for drug therapy are analyzed: Open Loop Treatment, where a priori fixed dosage is prescribed and Closed Loop Treatment, where the doses are adjusted according to results obtained by laboratory analysis. Simulation results show that the Closed Loop Scheme can achieve improved quality of the treatment in terms of reduction in the viral load and quatity of administered drugs, but with the inconvenience related to the necessity of frequent and periodic laboratory analysis.


Subject(s)
Humans , Acquired Immunodeficiency Syndrome/drug therapy , Computer Simulation , Drug Administration Schedule , Mathematics
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