The clinical use of tramadol hydrochloride

被引:76
作者
Bamigbade, TA [1 ]
Langford, RM [1 ]
机构
[1] Univ London St Bartholomews Hosp Med Coll, Anaesthe Lab, London EC1A 7BE, England
来源
PAIN REVIEWS | 1998年 / 5卷 / 03期
关键词
D O I
10.1191/096813098668122984
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The attributes of tramadol hydrochloride provide the clinician with a useful analgesic for short- and long-term use in the hospital and community settings. The two enantiomers of tramadol, and its principle metabolite O-desmethyltramadol, produce relief of moderate to severe pain across the range of acute and chronic pain states by combining synergistically weak opioid and monoaminergically-mediated antinociceptive mechanisms. Tramadol is demonstrably inferior to morphine in severe pain; however, it is free of some of the clinically significant adverse effects seen with other opioid analgesics of similar efficacy, particularly respiratory depression. Tramadol causes minimal dependence and tolerance and has very low abuse potential; consequently it is not scheduled as a controlled drug. Tramadol also lacks the prostaglandin inhibition-mediated adverse effects of the nonsteroidal anti-inflammatory drugs. Although data reflect 20 years of clinical experience with tramadol, intraoperative experience remains limited due to historical concerns of accidential awareness with an outdated anaesthetic technique that has been superseded.
引用
收藏
页码:155 / 182
页数:28
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共 132 条
  • [1] ALON E, 1981, ANAESTHESIST, V30, P623
  • [2] [Anonymous], 1995, REV CONTEMP PHARMACO
  • [3] Actions of tramadol, its enantiomers and principal metabolite, O-desmethyltramadol, on serotonin (5-HT) efflux and uptake in the rat dorsal raphe nucleus
    Bamigbade, TA
    Davidson, C
    Langford, RM
    Stamford, JA
    [J]. BRITISH JOURNAL OF ANAESTHESIA, 1997, 79 (03) : 352 - 356
  • [4] BAMIGBADE TA, 1997, BRIT J ANAESTH, V80, pP558
  • [5] BAMIGBADE TA, 1997, 8 WORLD C PAIN VANC, P261
  • [6] A COMPARISON OF EPIDURAL TRAMADOL AND EPIDURAL MORPHINE FOR POSTOPERATIVE ANALGESIA
    BARAKA, A
    JABBOUR, S
    GHABASH, M
    NADER, A
    KHOURY, G
    SIBAI, A
    [J]. CANADIAN JOURNAL OF ANAESTHESIA-JOURNAL CANADIEN D ANESTHESIE, 1993, 40 (04): : 308 - 313
  • [7] COMPARISON OF THE EFFICACY AND TOLERABILITY OF TRAMADOL, PETHIDINE AND NALBUPHINE IN CHILDREN WITH POSTOPERATIVE PAIN - AN OPEN RANDOMIZED STUDY
    BARSOUM, MW
    [J]. CLINICAL DRUG INVESTIGATION, 1995, 9 (04) : 183 - 190
  • [8] ANAPHYLACTOID REACTIONS AND HISTAMINE-RELEASE DO NOT OCCUR AFTER APPLICATION OF THE OPIOID TRAMADOL
    BARTH, H
    GIERTZ, H
    SCHMAL, A
    LORENZ, W
    [J]. AGENTS AND ACTIONS, 1987, 20 (3-4): : 310 - 313
  • [9] Barth H, 1987, PAIN S, V30, pS231, DOI 10.1016/0304-3959(87)91523-5
  • [10] BECKER R, 1990, ASSESS EFFECT ORALLY