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极早产儿血糖控制的发展。

Development of blood glucose control for extremely premature infants.

机构信息

Department of Mechanical Engineering, University of Canterbury, New Zealand.

出版信息

Comput Methods Programs Biomed. 2011 May;102(2):181-91. doi: 10.1016/j.cmpb.2010.03.010. Epub 2011 Jan 17.

Abstract

Extremely premature neonates often experience hyperglycaemia, which has been linked to increased mortality and worsened outcomes. Insulin therapy can assist in controlling blood glucose levels and promoting needed growth. This study presents the development of a model-based stochastic targeted controller designed to adapt insulin infusion rates to match the unique and changing metabolic state and control parameters of the neonate. Long-term usage of targeted BG control requires successfully forecasting variations in neonatal metabolic state, accounting for differences in clinical practices between units, and demonstrating robustness to errors that can occur in everyday clinical usage. Simulation studies were used to evaluate controller ability to target several common BG ranges and evaluate controller sensitivity to missed BG measurements and delays in control interventions on a virtual patient cohort of 25 infants developed from retrospective data. Initial clinical pilot trials indicated model performance matched expected performance from simulations. Stochastic targeted glucose control developed using validated patient-specific virtual trials can yield effective protocols for this cohort. Long-term trials show fundamental success, however clinical interface design appears as a critical factor to ensuring good compliance and thus good control.

摘要

极早产儿常经历高血糖,这与死亡率增加和预后恶化有关。胰岛素治疗可以帮助控制血糖水平并促进所需的生长。本研究提出了一种基于模型的随机靶向控制器的开发,旨在根据新生儿独特且不断变化的代谢状态和控制参数,自适应调整胰岛素输注率。靶向 BG 控制的长期使用需要成功预测新生儿代谢状态的变化,考虑到单位之间临床实践的差异,并对日常临床使用中可能出现的误差具有鲁棒性。模拟研究用于评估控制器在靶向几个常见 BG 范围方面的能力,并评估控制器对 BG 测量缺失和控制干预延迟的敏感性,该研究基于从回顾性数据中开发的 25 名虚拟患者队列。初步临床试点试验表明,模型性能与模拟预期性能相匹配。使用经过验证的患者特定虚拟试验开发的随机靶向血糖控制,可以为该队列生成有效的方案。长期试验显示出基本的成功,然而临床接口设计似乎是确保良好依从性从而实现良好控制的关键因素。

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