Lee Y Y S, Wong S M, Hung C T
Department of Anaesthesia, Queen Elizabeth Hospital, Hong Kong, China.
Br J Anaesth. 2007 Apr;98(4):477-83. doi: 10.1093/bja/aem040. Epub 2007 Mar 1.
We explored the sympatholytic property of dexmedetomidine, especially its role in intraocular pressure (IOP) reduction, haemodynamic stability, and attenuation of extubation response.
In this double-blind, randomized, controlled trial approved by the Hospital Ethics Committee, 60 patients undergoing elective vitreoretinal surgery were allocated to two groups, receiving either placebo or dexmedetomidine. A loading dose of dexmedetomidine 2.5 microg kg(-1) h(-1) (or placebo in same volume) was infused for 10 min immediately before induction of anaesthesia with propofol, followed by a maintenance dexmedetomidine or placebo infusion at 0.4 microg kg(-1) h(-1) till 30 min before the end of the operation. Anaesthesia was maintained with isoflurane, oxygen, and air mixture. IOP was measured before the loading dose and 1 min after tracheal intubation. The mean arterial pressure (MAP) and heart rate (HR) during loading, induction, maintenance, extubation, and recovery period were measured. The degree of strain on extubation was graded from 0 to 5.
The use of vasopressor/labetalol/atropine and the reduction in IOP were comparable between the two groups. There was a significant variation in MAP and HR over time within group, but not between groups. The median degree of strain was significantly lower (P = 0.049), and the time to reach Aldrete score of 10 shorter (P = 0.031) in the dexmedetomidine group.
Dexmedetomidine can be used without undue haemodynamic fluctuation and can decrease the excitatory response during extubation. The reduction in IOP with dexmedetomidine was comparable with placebo.
我们探讨了右美托咪定的交感神经阻滞特性,尤其是其在降低眼压(IOP)、血流动力学稳定性及减轻拔管反应方面的作用。
在本医院伦理委员会批准的双盲、随机、对照试验中,60例行择期玻璃体视网膜手术的患者被分为两组,分别接受安慰剂或右美托咪定。在使用丙泊酚诱导麻醉前10分钟,立即静脉输注负荷剂量的右美托咪定2.5微克/千克/小时(或等体积的安慰剂),随后以0.4微克/千克/小时的速度持续输注右美托咪定或安慰剂直至手术结束前30分钟。采用异氟烷、氧气和空气混合维持麻醉。在输注负荷剂量前及气管插管后1分钟测量眼压。测量负荷期、诱导期、维持期、拔管期及恢复期的平均动脉压(MAP)和心率(HR)。将拔管时的应激程度从0至5级进行评分。
两组间血管升压药/拉贝洛尔/阿托品的使用情况及眼压降低程度相当。组内MAP和HR随时间有显著变化,但组间无差异。右美托咪定组的应激程度中位数显著更低(P = 0.049),达到Aldrete评分为10分的时间更短(P = 0.031)。
右美托咪定可在不引起过度血流动力学波动的情况下使用,并可降低拔管时的兴奋反应。右美托咪定降低眼压的效果与安慰剂相当。