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心脏输出量对麻醉猪苏芬太尼药代动力学的影响。

Influence of Cardiac Output on the Pharmacokinetics of Sufentanil in Anesthetized Pigs.

机构信息

From the Department of Anesthesiology, University of Erlangen-Nuremberg, Erlangen, Germany.

出版信息

Anesthesiology. 2018 May;128(5):912-920. doi: 10.1097/ALN.0000000000002160.

Abstract

BACKGROUND

Sufentanil is used for general anesthesia and analgesia. The study aim was to determine the effect of pharmacologically induced changes in cardiac output on the pharmacokinetics of sufentanil in anesthetized pigs.

METHODS

Twenty-four pigs were randomly assigned to low, high, and control cardiac output groups. Cardiac output was decreased or increased from baseline by at least 40%, or maintained within ± 10% of baseline, respectively. Sufentanil was administered as a bolus followed by a continuous infusion for 120 min. Timed arterial samples were drawn for sufentanil concentration measurements.

RESULTS

Data from 20 animals were analyzed. The cardiac outputs (means ± SD) were 2.9 ± 0.7, 5.4 ± 0.7, and 9.6 ± 1.6 l/min in the low, control, and high cardiac output groups, respectively. The parameters of the two-compartment pharmacokinetic model for these cardiac outputs were: CL1: 0.9, 1.2, and 1.7 l/min; CL2: 0.9, 3.1, and 6.9 l/min; V1: 1.6, 2.9, and 5.2 l; and V2: 27.5, 47.0, and 79.8 l, respectively. Simulated sufentanil doses to maintain a target plasma concentration of 0.5 ng/ml for 3 h were 99.5, 128.6, and 157.6 μg for cardiac outputs of 3, 5, and 7 l/min, respectively. The context-sensitive half-times for these cardiac outputs increased from 3.1 to 19.9 and 25.9 min, respectively.

CONCLUSIONS

Cardiac output influences the pharmacokinetics of sufentanil. Simulations suggest that in the case of increased cardiac output, the dose should be increased to avoid inadequate drug effect at the expense of prolonged recovery, whereas for low cardiac output the dose should be reduced, and a faster recovery may be expected.

摘要

背景

舒芬太尼用于全身麻醉和镇痛。本研究旨在确定心脏输出量的药理学变化对麻醉猪舒芬太尼药代动力学的影响。

方法

24 头猪随机分为低、高和对照心输出量组。心输出量分别比基线减少或增加至少 40%,或维持在基线的±10%以内。舒芬太尼以推注方式给药,随后持续输注 120 分钟。定时抽取动脉样本以测量舒芬太尼浓度。

结果

20 只动物的数据进行了分析。低、对照和高心输出量组的心脏输出量(平均值±标准差)分别为 2.9±0.7、5.4±0.7 和 9.6±1.6 l/min。对于这些心输出量,双室药代动力学模型的参数为:CL1:0.9、1.2 和 1.7 l/min;CL2:0.9、3.1 和 6.9 l/min;V1:1.6、2.9 和 5.2 l;和 V2:27.5、47.0 和 79.8 l。模拟舒芬太尼剂量以维持 3 小时 0.5 ng/ml 的目标血浆浓度分别为 99.5、128.6 和 157.6 μg,用于 3、5 和 7 l/min 的心输出量。这些心输出量的上下文敏感半衰期分别从 3.1 增加到 19.9 和 25.9 分钟。

结论

心输出量影响舒芬太尼的药代动力学。模拟表明,在心脏输出量增加的情况下,应增加剂量以避免药物作用不足,代价是恢复时间延长,而对于低心输出量,应减少剂量,并有望更快恢复。

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