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PID controlled fully automated portable duodopa pump for Parkinson's disease patients

机译:PID控制的全自动便携式duodopa泵,用于帕金森氏病患者

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Parkinson's disease (PD) is a neurodegenerative disease that inhibits motor activities due to the impairment of brain cells which produce dopamine. Even though medications as well as Deep Brain Stimulations (DBS) are the two treatment options available to control parkinsonian symptoms, the first one is preferred mostly during the early stages of the disease. Continuous medication through Portable Duodopa Pump (PDP) without feedback is the existing method. This paper focuses on the development of a suitable closed-loop control strategy for traditional PDP; thereby ensuring fully automated drug infusion without wearing off. In fact, the drug infused by the controller is increased proportional to reduction in plasma level of dopamine. This results in the alleviation of side effects caused by incorrect dosages in medication therapy. The main control objective is set-point tracking of the closed-loop system with minimum settling time and good steady state accuracy even in the presence of large time delay, food and exercise disturbances as well as parameter variations present in the system. For achieving this objective, we modified the existing dose-effect model of Levodopa. The proposed model is enriched by (i) Levodopa to dopamine conversion factor, (ii) recirculation time delay and (iii) initial dopamine level present in patient's BP (Blood Plasma). The in-silico analysis of oral medication is used to validate pharmacokinetics (PK), pharmacological activation (PA) and pharmacodynamics of Levodopa. The performance of the proposed fully automatic PDP has been evaluated by traditional Proportional Integral Derivative (PID) controller under two different tuning rules. It is revealed that, both Ziegler-Nichols (ZN) and Particle Swam Optimization (PSO) tuned PID controllers are robust regarding inter-patient variability and the dynamic performance of the later is superior in comparison with the former under intra-patient variability and disturbances. (C) 2019 Elsevier Ltd. All rights reserved.
机译:帕金森氏病(PD)是一种神经退行性疾病,由于产生多巴胺的脑细胞受损而抑制运动活动。尽管药物和深部脑刺激(DBS)是可用于控制帕金森氏症症状的两种治疗方法,但第一种方法主要是在疾病的早期阶段使用。现有的方法是通过便携式Duodopa泵(PDP)连续给药而无反馈。本文着重于为传统的PDP开发合适的闭环控制策略。从而确保全自动输液而不会磨损。实际上,由控制器注入的药物与血浆多巴胺水平的降低成比例地增加。这样可以减轻药物治疗中不正确的剂量引起的副作用。主要控制目标是即使在存在较大的时间延迟,食物和运动干扰以及系统中存在参数变化的情况下,以最少的建立时间和良好的稳态精度对闭环系统进行设定点跟踪。为了实现这一目标,我们修改了左旋多巴的现有剂量效应模型。 (i)左旋多巴至多巴胺转化因子,(ii)再循环时间延迟和(iii)患者的BP(血液血浆)中存在的初始多巴胺水平丰富了所提出的模型。口服药物的计算机模拟分析用于验证左旋多巴的药代动力学(PK),药理激活(PA)和药效学。建议的全自动PDP的性能已通过传统的比例积分微分(PID)控制器在两种不同的调整规则下进行了评估。结果表明,Ziegler-Nichols(ZN)和粒子游优化(PSO)调整的PID控制器在患者间可变性方面均很健壮,而后者在患者内部可变性和干扰下的动态性能优于前者。 (C)2019 Elsevier Ltd.保留所有权利。

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