Systemic administration of local anesthetics to relieve neuropathic pain: A systematic review and meta-analysis

被引:162
作者
Tremont-Lukats, IW
Challapalli, V
McNicol, ED
Lau, J
Carr, DB
机构
[1] Tufts Univ New England Med Ctr, Dept Anesthesia, Inst Clin Res & Hlth Policy Studies, Boston, MA 02111 USA
[2] Med Univ S Carolina, Dept Neurol, Charleston, SC 29425 USA
[3] Univ Chicago Hosp, Dept Anesthesia & Crit Care, Chicago, IL 60637 USA
[4] Tufts Univ New England Med Ctr, Dept Anesthesiol, Boston, MA 02111 USA
关键词
D O I
10.1213/01.ANE.0000186348.86792.38
中图分类号
R614 [麻醉学];
学科分类号
100217 [麻醉学];
摘要
We reviewed randomized controlled trials to determine the efficacy and safety of systemically administered local anesthetics compared with placebo or active drugs. Of 41 retrieved studies, 27 trials of diverse quality were included in the systematic review. Ten lidocaine and nine mexiletine trials had data suitable for meta-analysis (n = 706 patients total). Lidocaine (most commonly 5 mg/kg IV over 30-60 min) and mexiletine (median dose, 600 mg daily) were superior to placebo (weighted mean difference on a 0-100 mm pain intensity visual analog scale = -10.60; 95% confidence interval: -14.52 to -6.68; P < 0.00001) and equal to morphine, gabapentin, amitriptyline, and amantadine (weighted mean difference = -0.60; 95% confidence interval: -6.96 to 5.75) for neuropathic pain. The therapeutic benefit was more consistent for peripheral pain (trauma, diabetes) and central pain. The most common adverse effects of lidocaine and mexiletine were drowsiness, fatigue, nausea, and dizziness. The adverse event rate for systemically administered local anesthetics was more than for placebo but equivalent to morphine, amitriptyline, or gabapentin (odds ratio: 1.23; 95% confidence interval: 0.22 to 6.90). Lidocaine and mexiletine produced no major adverse events in controlled clinical trials, were superior to placebo to relieve neuropathic pain, and were as effective as other analgesics used for this condition.
引用
收藏
页码:1738 / 1749
页数:12
相关论文
共 86 条
[1]
The anti-allodynic effects of amitriptyline, gabapentin, and lidocaine in a rat model of neuropathic pain [J].
Abdi, S ;
Lee, DH ;
Chung, JM .
ANESTHESIA AND ANALGESIA, 1998, 87 (06) :1360-1366
[2]
SYSTEMIC LIDOCAINE BLOCKS NERVE INJURY-INDUCED HYPERALGESIA AND NOCICEPTOR-DRIVEN SPINAL SENSITIZATION IN THE RAT [J].
ABRAM, SE ;
YAKSH, TL .
ANESTHESIOLOGY, 1994, 80 (02) :383-391
[3]
Effect of oral mexiletine on capsaicin-induced allodynia and hyperalgesia: A double-blind, placebo-controlled, crossover study [J].
Ando, K ;
Wallace, MS ;
Braun, J ;
Schulteis, G .
REGIONAL ANESTHESIA AND PAIN MEDICINE, 2000, 25 (05) :468-474
[4]
[Anonymous], 1994, J MUSCULOSKELET PAIN, DOI [DOI 10.1300/J094v02n04_05, DOI 10.1300/J094V02N04_05]
[5]
[Anonymous], 2001, Systematic Reviews in Health Care: Meta-Analysis in Context
[6]
The verdict from ALLHAT - Thiazide diuretics are the preferred initial therapy for hypertension [J].
Appel, LJ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 288 (23) :3039-3042
[7]
ATKINSON RL, 1982, INT J OBESITY, V6, P351
[8]
Intravenous lidocaine in central pain -: A double-blind, placebo-controlled, psychophysical study [J].
Attal, N ;
Gaudé, V ;
Brasseur, L ;
Dupuy, M ;
Guirimand, F ;
Parker, F ;
Bouhassira, D .
NEUROLOGY, 2000, 54 (03) :564-574
[9]
THE EFFECT OF INTRAVENOUS LIDOCAINE ON NOCICEPTIVE PROCESSING IN DIABETIC NEUROPATHY [J].
BACH, FW ;
JENSEN, TS ;
KASTRUP, J ;
STIGSBY, B ;
DEJGARD, A .
PAIN, 1990, 40 (01) :29-34
[10]
Backonja MM, 2000, NEUROLOGY, V54, pA81