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心输出量对猪体内瑞芬太尼和丙泊酚假性稳态浓度的影响。

Influence of cardiac output on the pseudo-steady state remifentanil and propofol concentrations in swine.

机构信息

Department of Anesthesiology and Intensive Care, Hamamatsu University School of Medicine, Hamamatsu, Japan.

出版信息

Acta Anaesthesiol Scand. 2013 Jul;57(6):754-60. doi: 10.1111/aas.12076. Epub 2013 Jan 24.

DOI:10.1111/aas.12076
PMID:23347138
Abstract

BACKGROUND

The propofol concentration during constant infusion is affected by a change in cardiac output, but the effect of this change on remifentanil, which is frequently used in combination with propofol, is unclear.

METHODS

Ten swine were anaesthetised through inhalation of isoflurane and maintained with 1.5% isoflurane. After infusion of remifentanil (0.5 μg/kg/min) and propofol (6 mg/kg/h after 2 mg/kg bolus infusion) for 60 min (baseline 1), cardiac output was increased by continuous infusion of dobutamine and termination of isoflurane (high cardiac output state). Dobutamine infusion was then stopped, 1.5% isoflurane was restarted, and cardiac output was allowed to return to baseline (baseline 2). Finally, cardiac output was decreased by administration of 3% isoflurane (low cardiac output state). Blood samples were collected from the femoral artery at 10, 30, and 60 min after the change to each haemodynamic state.

RESULTS

An inverse relationship was found between cardiac output and the plasma remifentanil and propofol concentrations. The plasma drug concentrations were given by the following equations: [remifentanil] (ng/ml) = 17.5/cardiac output (l/min) + 4.52; and [propofol] (μg/ml) = 3.34/cardiac output + 1.17. The influence of changes in cardiac output on remifentanil were similar to those for coadministered propofol and the influence on the concentration of each drug was greater with decreasing cardiac output.

CONCLUSIONS

The plasma remifentanil concentration is influenced by cardiac output in a similar manner to that of propofol during remifentanil and propofol anaesthesia, although the metabolic sites are different.

摘要

背景

持续输注时丙泊酚的浓度受心输出量变化的影响,但这种变化对瑞芬太尼的影响尚不清楚,瑞芬太尼常与丙泊酚联合使用。

方法

10 头猪通过异氟烷吸入麻醉,并以 1.5%异氟烷维持。输注瑞芬太尼(0.5μg/kg/min)和丙泊酚(2mg/kg 推注后 6mg/kg/h)60min 后(基础状态 1),通过持续输注多巴酚丁胺和停止吸入异氟烷(高心输出量状态)增加心输出量。然后停止多巴酚丁胺输注,重新开始吸入 1.5%异氟烷,使心输出量恢复至基础状态 2。最后,给予 3%异氟烷使心输出量降低(低心输出量状态)。在每个血流动力学状态改变后 10、30 和 60min 从股动脉采集血样。

结果

发现心输出量与瑞芬太尼和丙泊酚的血浆浓度呈反比关系。血浆药物浓度由以下方程给出:[瑞芬太尼](ng/ml)= 17.5/心输出量(l/min)+4.52;[丙泊酚](μg/ml)= 3.34/心输出量+1.17。心输出量变化对瑞芬太尼的影响与联合使用的丙泊酚相似,并且随着心输出量的降低,每种药物浓度的影响更大。

结论

在瑞芬太尼和丙泊酚麻醉期间,瑞芬太尼的血浆浓度受心输出量的影响与丙泊酚相似,尽管代谢部位不同。

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