Sinnott C J, Garfield J M, Thalhammer J G, Strichartz G R
Pain Research Center, Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Anesthesiology. 2000 Oct;93(4):1045-52. doi: 10.1097/00000542-200010000-00028.
Adding sodium bicarbonate to lidocaine to enhance its efficacy during peripheral nerve block is controversial. The authors studied the effect of adding sodium bicarbonate to lidocaine with and without epinephrine versus equivalent alkalinization by sodium hydroxide (NaOH) on onset, degree, and duration of peripheral nerve block.
Part I examined alkalinization by sodium bicarbonate versus NaOH to pH 7.8 on 0.5% lidocaine, with and without epinephrine (1:100,000), prepared from crystalline salt. Part II examined 0.5% and 1.0% commercial lidocaine solutions, with and without epinephrine, either unalkalinized or alkalinized with sodium bicarbonate or NaOH. With NaOH, pH was adjusted to 7.8, but with sodium bicarbonate, no pH adjustments were made to simulate clinical conditions.
In part I, addition of either NaOH or sodium bicarbonate to 0.5% lidocaine without epinephrine produced a faster onset than did unalkalinized lidocaine, without effecting degree or duration of block. In solutions with epinephrine there were no differences in onset, degree, or duration between lidocaine alkalinized with sodium bicarbonate versus NaOH. In part II, addition of sodium bicarbonate or NaOH to 1.0% commercial lidocaine without epinephrine did not accelerate onset compared with the unalkalinized solution. However, adding sodium bicarbonate decreased the degree and duration of block by 25% and more than 50%, respectively, compared with lidocaine unalkalinized and alkalinized with NaOH. With epinephrine, sodium bicarbonate hastened onset without effecting degree and duration compared with the unalkalinized solution.
With 1% commercial lidocaine without epinephrine, sodium bicarbonate decreases the degree and duration of block. However, in solutions with epinephrine, sodium bicarbonate hastens onset, without effecting degree or duration.
在周围神经阻滞期间添加碳酸氢钠以增强利多卡因的疗效存在争议。作者研究了在利多卡因中添加碳酸氢钠(有无肾上腺素)与用氢氧化钠(NaOH)进行等效碱化对周围神经阻滞的起效时间、程度和持续时间的影响。
第一部分研究了将碳酸氢钠与NaOH碱化至pH 7.8对由结晶盐制备的0.5%利多卡因(有无肾上腺素[1:100,000])的影响。第二部分研究了0.5%和1.0%市售利多卡因溶液,有无肾上腺素,未碱化或用碳酸氢钠或NaOH碱化。使用NaOH时,将pH调节至7.8,但使用碳酸氢钠时,不进行pH调节以模拟临床情况。
在第一部分中,向不含肾上腺素的0.5%利多卡因中添加NaOH或碳酸氢钠比未碱化的利多卡因起效更快,且不影响阻滞程度或持续时间。在含肾上腺素的溶液中,用碳酸氢钠碱化的利多卡因与用NaOH碱化的利多卡因在起效时间、程度或持续时间上没有差异。在第二部分中,与未碱化溶液相比,向不含肾上腺素的1.0%市售利多卡因中添加碳酸氢钠或NaOH并未加速起效。然而,与未碱化和用NaOH碱化的利多卡因相比,添加碳酸氢钠分别使阻滞程度和持续时间降低了25%和超过50%。对于含肾上腺素的溶液,与未碱化溶液相比,碳酸氢钠加快了起效速度,且不影响阻滞程度和持续时间。
对于不含肾上腺素的1%市售利多卡因,碳酸氢钠会降低阻滞程度和持续时间。然而,在含肾上腺素的溶液中,碳酸氢钠可加快起效速度,且不影响阻滞程度和持续时间。