Schubert A, Licina M G, Glaze G M, Paranandi L
Division of Anesthesiology, Cleveland Clinic Foundation, Ohio 44195-5154.
Can J Anaesth. 1992 Jul;39(6):569-75. doi: 10.1007/BF03008320.
The effect of systemically administered lidocaine on somatosensory evoked potentials (SSEPs) during general anaesthesia has not been widely reported. Knowledge of the influence of anaesthetic agents on evoked potentials assists in interpreting evoked potential waveforms. Accordingly, we studied the behaviour of cortical and subcortical (recorded at the second cervical vertebra) SSEPs after administration of intravenous lidocaine (3 mg.kg-1 bolus followed by infusion at 4 mg.kg-1.hr-1) during a sufentanil-based anaesthetic regimen in 16 patients undergoing abdominal or orthopaedic surgery. When compared to awake baseline recordings, the sufentanil-nitrous oxide, low-dose isoflurane anaesthetic depressed N1 amplitude by approximately 40% and prolonged latency by 10%. Fifteen minutes after establishment of this anaesthetic, the amplitude and latency of N1 were 1.13 +/- 0.56 microV and 19.81 +/- 1.63 msec, respectively. Within five minutes of adding lidocaine, amplitude decreased further to 0.84 +/- 0.39 microV (P = 0.001), while latency was extended to 20.44 +/- 1.48 msec (P = 0.01). Lidocaine did not affect cervical amplitude and prolonged latency only minimally. Despite the observed effects on amplitude and latency, SSEP waveforms were preserved and interpretable. Plasma lidocaine levels obtained at 5, 20, and 40 minutes after lidocaine were 5.17 +/- 1.33, 3.76 +/- 1.14, and 3.66 +/- 0.9 micrograms.dl-1, respectively. Our results indicate that systemically administered lidocaine at therapeutic plasma levels acts synergistically with a sufentanil-based anaesthetic to depress the amplitude and prolong the latency of SSEPs.
全身应用利多卡因对全身麻醉期间体感诱发电位(SSEPs)的影响尚未见广泛报道。了解麻醉药物对诱发电位的影响有助于解读诱发电位波形。因此,我们研究了在以舒芬太尼为基础的麻醉方案中,静脉注射利多卡因(3mg·kg⁻¹推注,随后以4mg·kg⁻¹·小时⁻¹输注)后,16例接受腹部或骨科手术患者的皮质和皮质下(记录于第二颈椎)SSEPs的变化情况。与清醒时的基线记录相比,舒芬太尼 - 氧化亚氮、低剂量异氟烷麻醉使N1波幅降低约40%,潜伏期延长10%。建立该麻醉15分钟后,N1的波幅和潜伏期分别为1.13±0.56微伏和19.81±1.63毫秒。加入利多卡因后5分钟内,波幅进一步降至0.84±0.39微伏(P = 0.001),而潜伏期延长至20.44±1.48毫秒(P = 0.01)。利多卡因对颈椎部位的波幅影响不大,对潜伏期的延长也很轻微。尽管观察到对波幅和潜伏期有影响,但SSEP波形得以保留且可解读。利多卡因注射后5、20和40分钟测得的血浆利多卡因水平分别为5.17±1.33、3.76±1.14和3.66±0.9微克·分升⁻¹。我们的结果表明,治疗血浆水平的全身应用利多卡因与以舒芬太尼为基础的麻醉协同作用,降低SSEPs的波幅并延长其潜伏期。