Carollo A, Tobar A, Hernandez C
Department of Applied Physics, Faculty of Physics, University of Santiago, Santiago de Compostela, Spain.
Int J Biomed Comput. 1993 Nov;33(3-4):267-76. doi: 10.1016/0020-7101(93)90040-d.
We describe a system for controlling postoperative pain, a phenomenon that is difficult to treat by conventional control methods due to interpatient variability, interferences, non-linearity and the lack of a plausible, well-defined mathematical model. The system consists of two phases. In Phase 1 a closed-loop fuzzy controller implementing a suitable control strategy brings the patient to a zero-pain state. In Phase 2, an open-loop computer-assisted continuous infusion controller maintains a constant concentration of the analgesic (alfentanil) in plasma, subject to an upper safety limit on infusion rate; the set-point of this controller is periodically revised (either maintained or reduced) on the basis of feedback on the duration of zero pain (set-point reduction is necessary because the open-loop system has no means of knowing whether analgesic is accumulating in the patient). Pain is quantified by the patient on a numerical scale of 1 to 10 at 1.5-min intervals during Phase 1 and 9-min intervals during Phase 2. In simulation trials in which a fixed approximate model was used for the effect of sedation on pain while the pharmacokinetics of alfentanil were varied from one simulated patient to another, zero pain was achieved in under 15 min with minimal overshoot in plasma drug concentration and was maintained, with only minor deviation, by means of low drug concentrations.
我们描述了一种用于控制术后疼痛的系统,术后疼痛这种现象由于患者间的变异性、干扰因素、非线性以及缺乏合理的、明确的数学模型,难以通过传统控制方法进行治疗。该系统由两个阶段组成。在阶段1,一个实施合适控制策略的闭环模糊控制器将患者带入零疼痛状态。在阶段2,一个开环计算机辅助持续输注控制器维持血浆中镇痛剂(阿芬太尼)的浓度恒定,但输注速率有一个上限安全限制;该控制器的设定点会根据零疼痛持续时间的反馈定期进行调整(要么维持要么降低)(设定点降低是必要的,因为开环系统无法知道镇痛剂是否在患者体内蓄积)。在阶段1,患者每隔1.5分钟以1至10的数字量表对疼痛进行量化,在阶段2则每隔9分钟进行量化。在模拟试验中,当阿芬太尼的药代动力学在不同模拟患者之间变化时,使用一个固定的近似模型来模拟镇静对疼痛的影响,在15分钟内实现了零疼痛,血浆药物浓度的超调量最小,并且通过低药物浓度得以维持,仅有轻微偏差。