Tanaka M
Department of Anesthesia, Akita University, School of Medicine, Japan.
Anesth Analg. 1997 Sep;85(3):639-43. doi: 10.1097/00000539-199709000-00027.
Although a simulated intravenous (I.V.) test dose containing 3 microg isoproterenol results in a reliable heart rate (HR) increase in anesthetized patients, hypotension may limit its clinical utility. The present study was designed to determine the incidence of hypotension and the reliability of smaller doses of isoproterenol. Forty-five healthy adult patients were anesthetized with 1% end-tidal isoflurane and nitrous oxide after endotracheal intubation and were randomized to one of three groups according to the dose of isoproterenol. Isoproterenol 1-, 2-, and 3-microg groups (n = 15 each) received 3 mL of 1.5% lidocaine with 1, 2, and 3 microg isoproterenol I.V., respectively, to simulate an intravascularly administered test dose. HR and systolic blood pressure were measured at 20-s intervals for 4 min after injection. Mean maximal HR increases were 15 +/- 6, 23 +/- 10, and 32 +/- 7 bpm (mean +/- SD) in the isoproterenol 1-, 2-, and 3-microg groups, respectively. However, the incidence and degree of systolic hypotension were similar among groups. Isoproterenol 3 microg produced 100% sensitivity in both the conventional (> or = 20 bpm increase) and the modified (> or = 10 bpm increase) HR criteria, but 2 microg resulted in 100% sensitivity on the modified criterion alone. Isoproterenol 1 microg did not elicit reliable HR changes. Significant correlation was demonstrated between the isoproterenol dose (microg/kg) and the maximal HR increase. Ninety-five percent confidence intervals to increase HR by 10 and 20 bpm were 0.015-0.02 microg/kg and 0.03-0.04 microg/kg, respectively. The application of isoproterenol as a test dose component seems promising, pending detailed studies of neural toxicity. The appropriate dose needs to be tailored according to the patient's weight.
To determine whether an epidural catheter may be in a blood vessel, various vasoactive drugs are often administered. The author found that isoproterenol might be a useful drug in place of epinephrine.
尽管含有3微克异丙肾上腺素的模拟静脉注射试验剂量能使麻醉患者的心率可靠增加,但低血压可能会限制其临床应用。本研究旨在确定低血压的发生率以及较小剂量异丙肾上腺素的可靠性。45例健康成年患者在气管插管后用1%的呼气末异氟醚和氧化亚氮麻醉,并根据异丙肾上腺素的剂量随机分为三组。异丙肾上腺素1微克、2微克和3微克组(每组n = 15)分别静脉注射3毫升含1微克、2微克和3微克异丙肾上腺素的1.5%利多卡因,以模拟血管内给药的试验剂量。注射后每隔20秒测量心率和收缩压,共测量4分钟。异丙肾上腺素1微克、2微克和3微克组的平均最大心率增加分别为15±6、23±10和32±7次/分钟(平均值±标准差)。然而,各组间收缩期低血压的发生率和程度相似。异丙肾上腺素3微克在传统(心率增加≥20次/分钟)和改良(心率增加≥10次/分钟)心率标准下均产生100%的敏感性,但2微克仅在改良标准下产生100%的敏感性。异丙肾上腺素1微克未引起可靠的心率变化。异丙肾上腺素剂量(微克/千克)与最大心率增加之间存在显著相关性。使心率增加10次/分钟和20次/分钟的95%置信区间分别为0.015 - 0.02微克/千克和0.03 - 0.04微克/千克。在对神经毒性进行详细研究之前,将异丙肾上腺素用作试验剂量成分似乎很有前景。合适的剂量需要根据患者体重进行调整。
为确定硬膜外导管是否在血管内,常使用各种血管活性药物。作者发现异丙肾上腺素可能是一种有用的药物,可替代肾上腺素。