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体外循环期间瑞芬太尼靶控输注的 Minto 模型性能。

Performance of the Minto model for the target-controlled infusion of remifentanil during cardiopulmonary bypass.

机构信息

Department of Anaesthesiology and Pain Medicine, Seoul National University Hospital, Seoul, South Korea.

CHA Bundang Medical Centre, Department of Anaesthesiology and Pain Medicine, Seongnam-si, South Korea.

出版信息

Anaesthesia. 2017 Oct;72(10):1196-1205. doi: 10.1111/anae.14019.

Abstract

We studied the predictive performance of the Minto pharmacokinetic model during cardiopulmonary bypass in patients undergoing cardiac surgery. Patients received remifentanil target-controlled infusion using the Minto model during total intravenous anaesthesia with propofol. From 56 patients, 275 arterial blood samples were drawn before, during and after bypass to determine the plasma concentration of remifentanil, and the predicted concentrations were recorded at each time. For pooled data, the median prediction error and median absolute prediction error were 21.3% and 21.8%, respectively, and 22.1% and 22.3% during bypass. Both were 148.4% during hypothermic circulatory arrest and measured concentrations were more than three times greater than predicted (26.9 (17.0) vs. 7.1 (1.6) ng.ml ). The Minto model showed considerable bias but overall acceptable precision during bypass. The target concentration of remifentanil should be reduced when using the Minto model during hypothermic circulatory arrest.

摘要

我们研究了米托(Minto)药代动力学模型在心脏手术患者体外循环期间的预测性能。患者在全静脉麻醉下接受丙泊酚和瑞芬太尼靶控输注时使用 Minto 模型。从 56 名患者中抽取了 275 个动脉血样,分别在体外循环前、体外循环中和体外循环后进行检测,以确定瑞芬太尼的血浆浓度,并记录每个时间点的预测浓度。对于合并数据,中位数预测误差和中位数绝对预测误差分别为 21.3%和 21.8%,体外循环期间分别为 22.1%和 22.3%。在低温循环停止期间,两者均为 148.4%,实测浓度是预测浓度的三倍以上(26.9(17.0)vs. 7.1(1.6)ng/ml)。米托模型在体外循环期间显示出相当大的偏差,但总体上具有可接受的精度。在低温循环停止期间使用 Minto 模型时,应降低瑞芬太尼的靶浓度。

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