Tong Doris, Wong Jean, Chung Frances, Friedlander Mark, Bremang Joseph, Mezei Gabor, Streiner David
Department of Anesthesia, Toronto Western Hospital, University Health Network, University of Toronto, Ontario, Canada.
Anesthesiology. 2003 Feb;98(2):485-94. doi: 10.1097/00000542-200302000-00030.
The objectives of this study were to compare the incidence, onset, duration and pain scores of transient neurologic symptoms (TNS) with 1% versus 5% hyperbaric lidocaine in spinal anesthesia for short urological procedures in a large prospective study. This study would also evaluate patient satisfaction, and impact of TNS on functional recovery to assess the clinical significance of TNS.
This was a multicenter, double-blind, randomized controlled trial. Four hundred fifty-three patients undergoing short transurethral procedures were randomized to receive 1% or 5% hyperbaric lidocaine. Eighty milligrams of 1% or 5% hyperbaric lidocaine was administered. During the first 3 days after surgery, the presence of TNS, its intensity and duration, and patient functional level were recorded. An intention-to-treat analysis was used.
There was no difference in the incidence of TNS (21% vs. 18%) between 1% versus 5% lidocaine. Patients with TNS had significantly higher pain scores (5.3 +/- 3 vs. 2.3 +/- 3) than patients without TNS during the first 24 h. This difference in pain scores persisted until 72 h postoperatively. There was a significant difference in the daily activities functional scores (2.2 +/- 1 vs. 1.4 +/- 0.8) of TNS non-TNS patients during the first 24 h postoperatively.
There was no difference in the incidence of TNS between the 1% versus 5% spinal lidocaine groups. Pain scores were higher in patients with TNS than those who did not have TNS. During the first 48 h postop, a small proportion of patients who had TNS experienced functional impairment of walking, sitting, and sleeping.
本大型前瞻性研究的目的是比较在短程泌尿外科手术的脊髓麻醉中,1%与5%的高压利多卡因引起的短暂性神经症状(TNS)的发生率、发作情况、持续时间和疼痛评分。本研究还将评估患者满意度以及TNS对功能恢复的影响,以评估TNS的临床意义。
这是一项多中心、双盲、随机对照试验。453例接受短程经尿道手术的患者被随机分配接受1%或5%的高压利多卡因。给予80毫克1%或5%的高压利多卡因。在术后的前3天,记录TNS的存在情况、其强度和持续时间以及患者的功能水平。采用意向性分析。
1%与5%利多卡因组之间TNS的发生率无差异(21%对18%)。在术后的头24小时内,发生TNS的患者的疼痛评分(5.3±3对2.