The clinical application of S-(+)-ketamine.

被引:43
作者
Himmelseher, S
Pfenninger, E
机构
[1] Univ Ulm Klinikum, Anasthesiol Klin, D-89075 Ulm, Germany
[2] Tech Univ, Klinikum Rechts Isar, Inst Anasthesiol, Munich, Germany
来源
ANASTHESIOLOGIE INTENSIVMEDIZIN NOTFALLMEDIZIN SCHMERZTHERAPIE | 1998年 / 33卷 / 12期
关键词
intravenous anaesthetics; S-(+)-ketamine; pharmacology; anaesthetic and analgesic potency; clinical applications;
D O I
10.1055/s-2007-994851
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
The intravenous anaesthetic ketamine is a racemic mixture of two equimolar doses of enantiomers. After stereoselective separation, the right-handed S(+)-isomer is now clinically available. Since anaesthetic and analgesic pharmacological studies have shown that S(+)-ketamine is approximately two times as potent as racemic ketamine, the clinical effects of S(+)-ketamine were evaluated in comparison to ketamine-racemate at dose relation of 1:2 in several therapeutic investigations. The studies disclosed that both drugs caused a similar activation of the endocrine stress response and a comparable stimulation of the sympathoadrenergic system. However, application of S(+)-ketamine was associated with a remarkably smoother emergence period, a profound postoperative analgesia, a more rapid recovery of cerebral functions, and a greater preference by the study persons. The incidence of psychotomimetic phenomena appeared to be negligibly less after S(+)-ketamine in comparison to racemic ketamine, but their quality was described as far less unpleasant. Clinical use of S(+)-ketamine administered at one-half of the usual dose is thus not only associated with a reduction of undesirable adverse effects without altering ketamine's anaesthetic and analgesic potency, but also offers distinctive improvements due to the reduced drug load. Moreover, increasing experimental evidence supports a remarkable neuroprotective effect of S(+)-ketamine, which may become a promising drug for new therapeutic approaches to neuroprotection.
引用
收藏
页码:764 / 770
页数:7
相关论文
共 43 条
[1]  
ADAMS HA, 1992, ANAESTHESIST, V41, P588
[2]  
Adams HA, 1995, ANAESTHESIST, V44, pS540
[3]   S-(+)-ketamine. Cardiovascular interactions during total intravenous anaesthesia and analgosedation [J].
Adams, HA .
ANAESTHESIST, 1997, 46 (12) :1081-1087
[4]   TOTAL IV ANESTHESIA WITH S-(+)-KETAMINE IN GERIATRIC ORTHOPEDIC-SURGERY - ENDOCRINE STRESS-RESPONSE, CARDIOVASCULAR REACTIONS, AND RECOVERY [J].
ADAMS, HA ;
BAUER, R ;
GEBHARDT, B ;
MENKE, W ;
BALTESGOTZ, B .
ANAESTHESIST, 1994, 43 (02) :92-100
[5]  
Adams HA, 1997, ANAESTHESIST, V46, P1026, DOI 10.1007/s001010050503
[6]   Endocrine responses to S-(+)-ketamine [J].
Adams, HA .
ANAESTHESIST, 1997, 46 (Suppl 1) :S30-S37
[7]   Ketamine decreases intracranial pressure and electroencephalographic activity in traumatic brain injury patients during propofol sedation [J].
Albanese, J ;
Arnaud, S ;
Rey, M ;
Thomachot, L ;
Alliez, B ;
Martin, C .
ANESTHESIOLOGY, 1997, 87 (06) :1328-1334
[8]   Effect of racemic mixture and the (S+)-isomer of ketamine on temporal and spatial summation of pain [J].
ArendtNielsen, L ;
Nielsen, J ;
PetersenFelix, S ;
Schnider, TW ;
Zbinden, AM .
BRITISH JOURNAL OF ANAESTHESIA, 1996, 77 (05) :625-631
[9]  
Bornscheuer A, 1997, ANAESTHESIST, V46, P1043, DOI 10.1007/s001010050504
[10]   ISOMERISM AND ANESTHETIC DRUGS [J].
CALVEY, TN .
ACTA ANAESTHESIOLOGICA SCANDINAVICA, 1995, 39 :83-90