Literature DB >> 8657431

Analgesic efficacy and safety of tramadol enantiomers in comparison with the racemate: a randomised, double-blind study with gynaecological patients using intravenous patient-controlled analgesia.

Stefan Grond1, Thomas Meuser, Detlev Zech, Ulrike Hennig, Klaus A Lehmann.   

Abstract

The opioid analgesic tramadol is a racemate and consists of 50% (+)- and 50% (-)-enantiomer. This study investigated analgesic efficacy and safety of both enantiomers after intravenous (i.v.) injection in comparison with the racemate. Ninety-eight patients recovering from major gynaecological surgery under opioid-free halothane anaesthesia were treated in a randomised, double-blind study with (+)-tramadol, (-)-tramadol or the racemate. Following an individualised i.v. loading dose up to a maximum of 200 mg, patient-controlled analgesia with demand doses of 20 mg was made available for 24 h. The primary criterion was of efficacy was the decrease of pain intensity on a 5-point verbal rating scale from severe or maximum pain to mild or no pain intensity on a 5-point verbal rating scale from severe or maximum pain to mild or no pain within the first hour after the loading dose. The secondary criterion was patient satisfaction with pain relief during the 24-h observation period stated in the final interview. Patients who terminated the study prematurely were evaluated as non-responders. Of patients treated with (+)-tramadol, tramadol racemate, and (-)-tramadol, 12%, 15%, and 53% of treated patients, respectively, terminated the study prematurely because of inefficacy. Of patients treated with (+)-tramadol, racemate or (-)-tramadol 67%, 48% and 38%, respectively, were considered responders regarding the primary criterion of efficacy (P = 0.061), and 82%, 76%, or 41% with respect to the secondary criterion (P = 0.001). Assessment of laboratory screening, adverse events, vital signs and blood gas monitoring showed no serious drug-related events. Nausea and vomiting were the most frequently reported non-serious side effects and were most often seen with (+)-tramadol. Taking into account both efficacy and safety aspects, the racemate seems to be superior to either enantiomer alone.

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Year:  1995        PMID: 8657431     DOI: 10.1016/0304-3959(94)00274-I

Source DB:  PubMed          Journal:  Pain        ISSN: 0304-3959            Impact factor:   6.961


  12 in total

Review 1.  [Tramadol in acute pain].

Authors:  K A Lehmann
Journal:  Drugs       Date:  1997       Impact factor: 9.546

Review 2.  Clinical pharmacology of tramadol.

Authors:  Stefan Grond; Armin Sablotzki
Journal:  Clin Pharmacokinet       Date:  2004       Impact factor: 6.447

Review 3.  A risk-benefit assessment of tramadol in the management of pain.

Authors:  L Radbruch; S Grond; K A Lehmann
Journal:  Drug Saf       Date:  1996-07       Impact factor: 5.606

4.  Population pharmacokinetic/pharmacodynamic modelling of the analgesic effects of tramadol in pediatrics.

Authors:  María J Garrido; Walid Habre; Ferdinand Rombout; Iñaki F Trocóniz
Journal:  Pharm Res       Date:  2006-08-09       Impact factor: 4.200

Review 5.  Tramadol: a review of its use in perioperative pain.

Authors:  L J Scott; C M Perry
Journal:  Drugs       Date:  2000-07       Impact factor: 9.546

6.  Serum concentrations of tramadol enantiomers during patient-controlled analgesia.

Authors:  S Grond; T Meuser; H Uragg; H J Stahlberg; K A Lehmann
Journal:  Br J Clin Pharmacol       Date:  1999-08       Impact factor: 4.335

Review 7.  Pharmacology and clinical experience with tramadol in osteoarthritis.

Authors:  W A Katz
Journal:  Drugs       Date:  1996       Impact factor: 9.546

8.  Pharmacokinetics of tramadol following intravenous and oral administration in male rhesus macaques (Macaca mulatta).

Authors:  K R Kelly; B H Pypendop; K L Christe
Journal:  J Vet Pharmacol Ther       Date:  2014-12-09       Impact factor: 1.786

Review 9.  The mu-opioid receptor agonist/noradrenaline reuptake inhibition (MOR-NRI) concept in analgesia: the case of tapentadol.

Authors:  Thomas M Tzschentke; Thomas Christoph; Babette Y Kögel
Journal:  CNS Drugs       Date:  2014-04       Impact factor: 5.749

10.  Estimation of the minimum effective dose of tramadol for postoperative analgesia in infants using the continual reassessment method.

Authors:  Yue'e Dai; Dongxu Lei; Zhenghua Huang; Yan Yin; G Allen Finley; Yunxia Zuo
Journal:  Front Med       Date:  2012-08-10       Impact factor: 4.592

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