Mathieu-Daudé J C, Deschodt J, Kienlen J, Eledjam J J, Delbord A, du Cailar J
Département d'Anesthésie-Réanimation A, Hôpital Lapeyronie, Montpellier.
Ann Fr Anesth Reanim. 1988;7(5):377-82. doi: 10.1016/s0750-7658(88)80053-4.
The blood concentration of propofol was studied in 14 ASA 1 informed patients, who were to undergo orthopaedic or plastic surgery lasting at least 90 min. Anaesthesia was induced with a 2 mg.kg-1 bolus of propofol together with 0.86 microgram.kg-1 fentanyl. This was followed by a constant rate infusion of propofol and fentanyl, 5 mg.kg-1.h-1 and 3 micrograms.kg-1.h-1 respectively. The mean duration of propofol infusion was 153 +/- 63 min, with extremes of 90 and 315 min. Propofol concentration was measured using gas phase chromatography on total arterial blood; the lower limit of detection was 0.05 mg.l-1. During the infusion, blood concentrations were found between 2 and 4 mg.l-1. It was 2.25 mg.l-1 at the fifth min; this was 80% of the concentration found at the 120th min. There was in fact no statistically significant difference between the values found at the 90th, 120th and 150th min. On stopping the infusion, the concentrations fell rapidly during the first 5 min, and then more slowly. By the 30th min, it had reached a value 4.5 times less than that at the end of the infusion. However, individual variations were found, which could explain delayed recovery. The calculated pharmacokinetic parameters were: elimination half-life = 41.7 +/- 20 min, clearance = 2.14 +/- 0.55 l.min-1 and equilibrium distribution volume = 43.4 +/- 15.2 l. These results are discussed. It is therefore possible to give propofol continuously at a constant rate without having any accumulative effect.
对14例美国麻醉医师协会(ASA)分级为1级的知情患者进行了丙泊酚血药浓度研究,这些患者将接受至少90分钟的骨科或整形手术。用2mg·kg⁻¹的丙泊酚推注联合0.86μg·kg⁻¹的芬太尼诱导麻醉。随后分别以5mg·kg⁻¹·h⁻¹和3μg·kg⁻¹·h⁻¹的速率持续输注丙泊酚和芬太尼。丙泊酚输注的平均持续时间为153±63分钟,范围为90至315分钟。采用气相色谱法测定全动脉血中的丙泊酚浓度;检测下限为0.05mg·l⁻¹。输注期间,血药浓度在2至4mg·l⁻¹之间。第5分钟时为2.25mg·l⁻¹;这是第120分钟时浓度的80%。实际上,在第90、120和150分钟时测得的值之间无统计学显著差异。停止输注后,浓度在最初5分钟内迅速下降,然后下降得更慢。到第30分钟时,其值降至输注结束时的4.5分之一。然而,发现了个体差异,这可能解释恢复延迟的原因。计算得到的药代动力学参数为:消除半衰期=41.7±20分钟,清除率=2.14±0.55l·min⁻¹,平衡分布容积=43.4±15.2l。对这些结果进行了讨论。因此,以恒定速率持续给予丙泊酚不会产生任何蓄积效应。