COMPARISON OF DROPERIDOL, HALOPERIDOL AND PROCHLORPERAZINE AS POST-OPERATIVE ANTI-EMETICS

被引:62
作者
LOESER, EA
BENNETT, G
STANLEY, TH
MACHIN, R
机构
[1] Department of Anesthesiology, University of Utah College of Medicine, Salt Lake City, 84132, Utah
关键词
D O I
10.1007/BF03013781
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
The results of this study demonstrate that prochlorperazine, haloperidol and droperidol are all effective post-operative anti-emetic compounds when compared to saline but vary in onset of activity and duration of action. Haloperidol has the shortest onset of action, being effective within 30-minutes of intravenous administration. Prochlorperazine has an intermediate onset of action and droperidol is the slowest of the three compounds but the only one to provide significant anti-emesis 4-24 hours following administration. Our data suggest that a combination of haloperidol and droperidol may be more effective as an anti-emetic than any one of the compounds used alone. © 1979 Canadian Anesthesiologists.
引用
收藏
页码:125 / 127
页数:3
相关论文
共 11 条
  • [1] USE OF HALOPERIDOL FOR TREATMENT OF POSTOPERATIVE NAUSEA AND VOMITING - DOUBLE-BLIND PLACEBO-CONTROLLED TRIAL
    BARTON, MD
    LIBONATI, M
    COHEN, PJ
    [J]. ANESTHESIOLOGY, 1975, 42 (04) : 508 - 512
  • [2] BORISON HL, 1953, PHARMACOL REV, V5, P193
  • [3] ABSORPTION, METABOLISM AND EXCRETION OF DROPERIDOL BY HUMAN SUBJECTS FOLLOWING INTRAMUSCULAR AND INTRAVENOUS ADMINISTRATION
    CRESSMAN, WA
    PLOSTNIEKS, J
    JOHNSON, PC
    [J]. ANESTHESIOLOGY, 1973, 38 (04) : 363 - 369
  • [4] FORSMAN A, 1976, CURR THER RES CLIN E, V20, P319
  • [5] GOODMAN, 1975, PHARMALOGICAL BASIS, P166
  • [6] PATTON CM, 1974, ANESTH ANALG, V53, P361
  • [7] SHIELDS KG, 1971, ANESTH ANAL CURR RES, V50, P1017
  • [8] SOUDIJN W, 1974, International Anesthesiology Clinics, V12, P145, DOI 10.1097/00004311-197412020-00017
  • [9] SOUDIJN W., 1967, EUR J PHARMACOL, V1, P47, DOI 10.1016/0014-2999(67)90065-9
  • [10] TORNETTA FJ, 1972, ANESTH ANAL CURR RES, V51, P964