Oikkonen M, Rosenberg P H, Neuvonen P J
Anaesthesia. 1984 Jul;39(7):660-5. doi: 10.1111/j.1365-2044.1984.tb06474.x.
The antipyrine (phenazone) half-life was determined in 20 surgical patients to discover whether there are changes in hepatic metabolic rate during or immediately after anaesthesia compared with the pre-anaesthetic rate. Nine patients received enflurane (mean duration 8.6, SD 2.0 hours) and six patients had a balanced anaesthetic without enflurane (duration 4.4, SD 3.3 hours). A further five patients received a spinal anaesthetic with bupivacaine. The changes in antipyrine half-life were inconsistent, and there was no evidence of competitive metabolic inhibition by general anaesthesia. Antipyrine half-lives did not correlate with serum fluoride levels or urinary fluoride excretion in the case of enflurane. The mean serum inorganic fluoride concentration rose to 29 mumol/litre, and two patients had potentially nephrotoxic concentrations (64 and 50 mumol/litre) after 8 hours of exposure to enflurane though without any evident harmful effects.
测定了20例外科手术患者的安替比林(非那宗)半衰期,以探究与麻醉前相比,麻醉期间或麻醉刚结束后肝脏代谢率是否有变化。9例患者接受恩氟烷麻醉(平均时长8.6小时,标准差2.0小时),6例患者接受不含恩氟烷的平衡麻醉(时长4.4小时,标准差3.3小时)。另有5例患者接受布比卡因脊髓麻醉。安替比林半衰期的变化并不一致,且没有证据表明全身麻醉存在竞争性代谢抑制。在恩氟烷麻醉的情况下,安替比林半衰期与血清氟化物水平或尿氟排泄无关。平均血清无机氟浓度升至29微摩尔/升,2例患者在暴露于恩氟烷8小时后出现了潜在肾毒性浓度(64和50微摩尔/升),但未出现任何明显有害影响。