Gabapentin and pregabalin for chronic neuropathic and early postsurgical pain: current evidence and future directions

被引:159
作者
Gilron, Ian [1 ,2 ,3 ]
机构
[1] Queens Univ, Dept Anesthesiol & Pharmacol, Kingston, ON K7L 2V7, Canada
[2] Queens Univ, Dept Toxicol, Kingston, ON K7L 2V7, Canada
[3] Queens Univ, Dept Anesthesiol, Kingston Gen Hosp, Kingston, ON K7L 2V7, Canada
关键词
gabapentin; neuropathic pain; postoperative pain; pregabalin;
D O I
10.1097/ACO.0b013e3282effaa7
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Purpose of review Gabapentin and pregabalin bind to the alpha-2-delta calcium channel subunit and represent a novel analgesic drug class. The evidence base supporting their use for chronic neuropathic and early postsurgical pain is reviewed. Recent findings Multiple, large, high-quality trials have demonstrated the safety and efficacy of gabapentin and pregabalin in neuropathic pain. Treatment-related improvement of pain and sleep positively impact upon quality of life. Sedation, dizziness and ataxia are important and relatively common adverse effects, however. Accumulating evidence indicates that gabapentin, and possibly pregabalin, also exert important effects following surgery. Multiple high-quality trials have demonstrated analgesic and opioid-sparing efficacy with gabapentin following various surgical procedures. Gabapentin and pregabalin reduce movement-evoked pain and this can lead to enhanced functional postoperative recovery. Postoperative opioid sparing is of questionable relevance since few trials have shown reduced opioid-related adverse effects. Sedation, dizziness and ataxia have been reported in only a few trials. Future larger-scale perioperative trials focused on safety assessment are needed, however. Summary Gabapentin and pregabalin are efficacious treatments for neuropathic and postsurgical pain. Future research addressing several specific questions would serve to better delineate their optimal roles in treating these and other pain conditions.
引用
收藏
页码:456 / 472
页数:17
相关论文
共 150 条
[1]   A single preoperative dose of gabapentin (800 milligrams) does not augment postoperative analgesia in patients given interscalene brachial plexus blocks for arthroscopic shoulder surgery [J].
Adam, Frederic ;
Menigaux, Christophe ;
Sessler, Daniel I. ;
Chauvin, Marcel .
ANESTHESIA AND ANALGESIA, 2006, 103 (05) :1278-1282
[2]  
Al-Mujadi H, 2006, CAN J ANAESTH, V53, P268, DOI 10.1007/BF03022214
[3]  
Almahrezi A, 2004, J RHEUMATOL, V31, P1228
[4]  
ANDRUSZKIEWICZ R, 1989, SYNTHESIS-STUTTGART, P953
[5]   Gabapentin in the treatment of fibromyalgia - A randomized, double-blind, placebo-controlled, multicenter trial [J].
Arnold, Lesley M. ;
Goldenberg, Don L. ;
Stanford, Sharon B. ;
Lalonde, Justine K. ;
Sandhu, H. S. ;
Keck, Paul E., Jr. ;
Welge, Jeffrey A. ;
Bishop, Fred ;
Stanford, Kevin E. ;
Hess, Evelyn V. ;
Hudson, James I. .
ARTHRITIS AND RHEUMATISM, 2007, 56 (04) :1336-1344
[6]   Myoclonus associated with the use of gabapentin [J].
Asconapé, J ;
Diedrich, A ;
DellaBadia, J .
EPILEPSIA, 2000, 41 (04) :479-481
[7]   EFNS guidelines on pharmacological treatment of neuropathic pain [J].
Attal, N. ;
Cruccu, G. ;
Haanpaa, M. ;
Hansson, P. ;
Jensen, T. S. ;
Nurmikko, T. ;
Sampaio, C. ;
Sindrup, S. ;
Wiffen, P. .
EUROPEAN JOURNAL OF NEUROLOGY, 2006, 13 (11) :1153-1169
[8]   Asterixis related to gabapentin as a cause of falls [J].
Babiy, M ;
Stubblefield, MD ;
Herklotz, M ;
Hand, M .
AMERICAN JOURNAL OF PHYSICAL MEDICINE & REHABILITATION, 2005, 84 (02) :136-140
[9]   Gabapentin for the symptomatic treatment of painful neuropathy in patients with diabetes mellitus - A randomized controlled trial [J].
Backonja, M ;
Beydoun, A ;
Edwards, KR ;
Schwartz, SL ;
Fonseca, V ;
Hes, M ;
LaMoreaux, L ;
Garofalo, E .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 280 (21) :1831-1836
[10]   Gabapentin withdrawal presenting as status epilepticus [J].
Barrueto, F ;
Green, J ;
Howland, MA ;
Hoffman, RS ;
Nelson, LS .
JOURNAL OF TOXICOLOGY-CLINICAL TOXICOLOGY, 2002, 40 (07) :925-928