Alfonsi P, Brusset A, Levy R, Gauneau P, Chauvin M
Département d'Anesthésie-Réanimation, Hôpital Ambroise-Paré, Boulogne.
Ann Fr Anesth Reanim. 1991;10(6):543-7. doi: 10.1016/s0750-7658(05)80292-8.
This study aimed to compare the haemodynamic effects of two different glucose-free bupivacaine solutions is thirty patients aged more than 70 years (mean age 82 years) undergoing hip surgery under spinal anaesthesia. They were randomly assigned to two groups, group A to receive 2.5 ml of a 0.5% bupivacaine solution, and group B 10 ml of a 0.125% solution in normal saline. All the patients were therefore given the same dose of bupivacaine, 12.5 mg. Lorazepam (1 mg orally) was administered to all for premedication two hours beforehand. Those patients taking antihypertensive agents were given their last dose on the eve of surgery. Lactated Ringer's solution (500 ml) was infused to all before the spinal puncture. Systolic (Pasys), mean and diastolic arterial pressures, and heart rate, were recorded every minute before volume loading, and for 30 minutes after the start of the spinal anaesthesia. Ephedrine (3 mg every two minutes if required) was given whenever Pasys decreased by more than 30% of the pre-induction value. The upper level of sensory blockade was assessed by the pin-prick test, and the quality of motor blockade with the Bromage scale. The cephalad spread of the solutions was similar, as well as the haemodynamic profile in each group. The total dose of ephedrine required in each group was not significantly different. It may therefore be concluded that, in the elderly, the upper level of, and the haemodynamic changes due to, spinal anaesthesia do not depend on the concentration or the volume of glucose-free bupivacaine solution.
本研究旨在比较两种不同的无糖布比卡因溶液对30例70岁以上(平均年龄82岁)行脊髓麻醉下髋关节手术患者的血流动力学影响。他们被随机分为两组,A组接受2.5毫升0.5%布比卡因溶液,B组接受10毫升0.125%布比卡因生理盐水溶液。所有患者接受的布比卡因剂量均为12.5毫克。术前两小时给所有患者口服1毫克劳拉西泮进行术前用药。服用抗高血压药物的患者在手术前夕给予最后一剂。在脊髓穿刺前给所有患者输注500毫升乳酸林格氏液。在扩容前每分钟记录收缩压(Pasys)、平均动脉压和舒张压以及心率,并在脊髓麻醉开始后30分钟内记录。每当Pasys下降超过诱导前值的30%时,按需每两分钟给予麻黄碱(3毫克)。通过针刺试验评估感觉阻滞的上限,并用Bromage量表评估运动阻滞的质量。两组溶液向头端的扩散以及血流动力学情况相似。每组所需麻黄碱的总剂量无显著差异。因此可以得出结论,在老年人中,脊髓麻醉的上限以及由此引起的血流动力学变化并不取决于无糖布比卡因溶液的浓度或体积。