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硝苯地平与人体术中核心体温

Nifedipine and intraoperative core body temperature in humans.

作者信息

Vassilieff N, Rosencher N, Sessler D I, Conseiller C, Lienhart A

机构信息

Department of Anesthesiology and Intensive Care, Cochin Port-Royal University Hospital, Paris, France.

出版信息

Anesthesiology. 1994 Jan;80(1):123-8. doi: 10.1097/00000542-199401000-00019.

Abstract

BACKGROUND

Initial anesthetic-induced hypothermia results largely from core-to-peripheral redistribution of heat. Nifedipine administration may minimize hypothermia by inducing vasodilation well before induction of anesthesia. Although vasodilation would redistribute heat to peripheral tissues, thermoregulatory responses would maintain core temperature. After equilibration, the patient would be left vasodilated, with a small core-to-peripheral temperature gradient. Minimal redistribution hypothermia may accompany subsequent induction of anesthesia, because heat flow requires a temperature gradient. In contrast, similar vasodilation concurrent with anesthetic-induced vasodilation may augment redistribution hypothermia. Accordingly, the authors tested the hypothesis that nifedipine treatment for 12 h before surgery would minimize intraoperative redistribution hypothermia, whereas nifedipine treatment immediately before induction of anesthesia would aggravate hypothermia.

METHODS

Patients undergoing hip arthroplasty were randomly assigned to: (1) 20 mg long-acting nifedipine orally 12 h before surgery, and 10 mg sublingually 1.5 h before surgery (n = 10); (2) nifedipine 10 mg sublingually just before induction of anesthesia (n = 10); and (3) no nifedipine (control, n = 10). Anesthesia was maintained with isoflurane and 60% nitrous oxide. Administered intravenous fluids were heated, but the patients were not otherwise actively warmed.

RESULTS

Core temperature decreased 0.8 degree C in the first hour of surgery in the patients given nifedipine the night before and the morning of surgery, which was significantly less than in the control group (1.7 degree C in the first hour). In contrast, core temperature decreased 2.0 degrees C in the first hour of surgery in the patients given nifedipine immediately before induction of anesthesia. During the subsequent 70-130 min of anesthesia, core temperature decreased at roughly comparable rates in each group. After 130 min of anesthesia, core temperature in the two nifedipine-treated groups differed by 1.6 degrees C, and the temperatures in all three groups differed significantly.

CONCLUSIONS

Vasodilation induced by nifedipine well before induction of anesthesia minimized redistribution hypothermia, presumably by decreasing the core-to-peripheral tissue temperature gradient. In contrast, redistribution hypothermia was aggravated by administration of the same drug immediately before induction of anesthesia. Drug-induced modulation of vascular tone thus produces clinically important alterations in intraoperative core temperature.

摘要

背景

最初由麻醉引起的体温过低主要是由于热量从核心向周边重新分布所致。硝苯地平给药可能通过在麻醉诱导前很久就引起血管舒张来使体温过低最小化。尽管血管舒张会使热量重新分布到周边组织,但体温调节反应会维持核心体温。平衡后,患者会处于血管舒张状态,核心与周边的温度梯度较小。随后麻醉诱导时可能会伴随最小程度的重新分布性体温过低,因为热流需要温度梯度。相比之下,与麻醉诱导引起的血管舒张同时发生的类似血管舒张可能会加剧重新分布性体温过低。因此,作者检验了这样一个假设,即术前12小时给予硝苯地平治疗会使术中重新分布性体温过低最小化,而在麻醉诱导前即刻给予硝苯地平治疗会加重体温过低。

方法

接受髋关节置换术的患者被随机分为:(1)术前12小时口服20毫克长效硝苯地平,术前1.5小时舌下含服10毫克(n = 10);(2)在麻醉诱导前即刻舌下含服硝苯地平10毫克(n = 10);以及(3)不给予硝苯地平(对照组,n = 10)。使用异氟烷和60%氧化亚氮维持麻醉。静脉输注的液体被加热,但患者未接受其他主动保暖措施。

结果

在前一晚和手术当天早晨给予硝苯地平的患者中,手术第一小时核心体温下降了0.8摄氏度,这明显低于对照组(第一小时下降1.7摄氏度)。相比之下,在麻醉诱导前即刻给予硝苯地平的患者中,手术第一小时核心体温下降了2.0摄氏度。在随后70 - 130分钟的麻醉期间,每组核心体温下降速率大致相当。麻醉130分钟后,两个接受硝苯地平治疗组的核心体温相差1.6摄氏度,且三组的体温有显著差异。

结论

在麻醉诱导前很久由硝苯地平引起的血管舒张使重新分布性体温过低最小化,大概是通过降低核心与周边组织的温度梯度。相比之下,在麻醉诱导前即刻给予同一药物会加重重新分布性体温过低。因此,药物诱导的血管张力调节在术中核心体温方面产生了临床上重要的改变。

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