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Controlled infusion of intravenous cardiac drugs using global optimization
OBJECTIVES: The objective of the study is to develop an automatic drug infusion control system during cardiovascular surgery. MATERIALS AND METHODS: Based on the clinical drug dosage analysis, the modeling of cardiovascular system with baroreceptor model is mathematically modeled using compartmental...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444840/ https://www.ncbi.nlm.nih.gov/pubmed/31031469 http://dx.doi.org/10.4103/ijp.IJP_612_18 |
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author | Sowparnika, G. C. Thirumarimurugan, M. Sivakumar, V. M. Vinoth, N. |
author_facet | Sowparnika, G. C. Thirumarimurugan, M. Sivakumar, V. M. Vinoth, N. |
author_sort | Sowparnika, G. C. |
collection | PubMed |
description | OBJECTIVES: The objective of the study is to develop an automatic drug infusion control system during cardiovascular surgery. MATERIALS AND METHODS: Based on the clinical drug dosage analysis, the modeling of cardiovascular system with baroreceptor model is mathematically modeled using compartmental approach, considering the relationship between the volume and flow rate of blood during each heartbeat. This model is then combined with drug modeling of noradrenaline and nitroglycerine by deriving the volume and drug mass concentration equations, based on pharmacokinetics and pharmacodynamics of the drugs. The closed-loop patient models are derived from the open-loop data obtained from the physiology-drug model with covariate as age. The proportional-integral controller is designed based on optimal values obtained from bacterial foraging-oriented particle swarm optimization algorithm. The controllers are implemented individually for each control variable such as aortic pressure and cardiac output (CO), irrespective of varying weights based on the relative gain array analysis which depicts the maximum influence of cardiac drugs on control variables. RESULTS: The physiology-drug model output responses are simulated using MATLAB. The controlled responses of aortic pressure and CO with infusion rate of cardiac drugs are obtained. The robustness of the controller is checked by introducing variations in cardiovascular model parameters. The efficiency of the controller during normal and abnormal conditions is compared using time domain analysis. CONCLUSIONS: The controller design was efficient and can be further improved by designing switching-based controllers. |
format | Online Article Text |
id | pubmed-6444840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-64448402019-04-26 Controlled infusion of intravenous cardiac drugs using global optimization Sowparnika, G. C. Thirumarimurugan, M. Sivakumar, V. M. Vinoth, N. Indian J Pharmacol Research Article OBJECTIVES: The objective of the study is to develop an automatic drug infusion control system during cardiovascular surgery. MATERIALS AND METHODS: Based on the clinical drug dosage analysis, the modeling of cardiovascular system with baroreceptor model is mathematically modeled using compartmental approach, considering the relationship between the volume and flow rate of blood during each heartbeat. This model is then combined with drug modeling of noradrenaline and nitroglycerine by deriving the volume and drug mass concentration equations, based on pharmacokinetics and pharmacodynamics of the drugs. The closed-loop patient models are derived from the open-loop data obtained from the physiology-drug model with covariate as age. The proportional-integral controller is designed based on optimal values obtained from bacterial foraging-oriented particle swarm optimization algorithm. The controllers are implemented individually for each control variable such as aortic pressure and cardiac output (CO), irrespective of varying weights based on the relative gain array analysis which depicts the maximum influence of cardiac drugs on control variables. RESULTS: The physiology-drug model output responses are simulated using MATLAB. The controlled responses of aortic pressure and CO with infusion rate of cardiac drugs are obtained. The robustness of the controller is checked by introducing variations in cardiovascular model parameters. The efficiency of the controller during normal and abnormal conditions is compared using time domain analysis. CONCLUSIONS: The controller design was efficient and can be further improved by designing switching-based controllers. Wolters Kluwer - Medknow 2019 /pmc/articles/PMC6444840/ /pubmed/31031469 http://dx.doi.org/10.4103/ijp.IJP_612_18 Text en Copyright: © 2019 Indian Journal of Pharmacology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Research Article Sowparnika, G. C. Thirumarimurugan, M. Sivakumar, V. M. Vinoth, N. Controlled infusion of intravenous cardiac drugs using global optimization |
title | Controlled infusion of intravenous cardiac drugs using global optimization |
title_full | Controlled infusion of intravenous cardiac drugs using global optimization |
title_fullStr | Controlled infusion of intravenous cardiac drugs using global optimization |
title_full_unstemmed | Controlled infusion of intravenous cardiac drugs using global optimization |
title_short | Controlled infusion of intravenous cardiac drugs using global optimization |
title_sort | controlled infusion of intravenous cardiac drugs using global optimization |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444840/ https://www.ncbi.nlm.nih.gov/pubmed/31031469 http://dx.doi.org/10.4103/ijp.IJP_612_18 |
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