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CLINICAL COMPARISON OF ATRACURIUM AND VECURONIUM (ORG NC 45)
ROBERTSON, E.N ; BOOIJ, L.H.D.J ; FRAGEN, R.J ; CRUL, J.F
British journal of anaesthesia : BJA, 1983-02, Vol.55 (2), p.125-129
[Peer Reviewed Journal]
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Title:
CLINICAL COMPARISON OF ATRACURIUM AND VECURONIUM (ORG NC 45)
Author:
ROBERTSON, E.N
;
BOOIJ, L.H.D.J
;
FRAGEN, R.J
;
CRUL, J.F
Subjects:
Pancuronium - analogs & derivatives
;
Atracurium
;
Pancuronium - pharmacology
;
Pancuronium - administration & dosage
;
Humans
;
Middle Aged
;
Neuromuscular Blocking Agents - pharmacology
;
Neuromuscular Blocking Agents - administration & dosage
;
Dose-Response Relationship, Drug
;
Neuromuscular Nondepolarizing Agents - administration & dosage
;
Neuromuscular Nondepolarizing Agents - pharmacology
;
Heart Rate - drug effects
;
Isoquinolines - pharmacology
;
Time Factors
;
Vecuronium Bromide
;
Muscle Contraction - drug effects
;
Adolescent
;
Adult
;
Aged
;
Blood Pressure - drug effects
;
Isoquinolines - administration & dosage
;
Index Medicus
Is Part Of:
British journal of anaesthesia : BJA, 1983-02, Vol.55 (2), p.125-129
Description:
The potency, histamine releasing ability, cardiovascular effects, and pharmacodynamics of vecuronium and atracurium were investigated in 64 healthy patients following administration i.v. Cumulative dose-response curves showed vecuronium to be 4.4 times as potent as atracurium. Using the calculated EQ90 of each drug (43 g kg−1 for vecuronium and 188 fig kg−1 for atracurium), vecuronium had a significantly more rapid onset time and shorter duration of action than atracurium. When three times the ED90 doses were used (129 gkg−1 for vecuronium and 564 g kg−1 for atracurium), no statistically significant differences in the pharmacodynamics were seen between the two drugs, although vecuronium tended to be shorter-acting. There was no clinical evidence of histaminr release during the study. No clinically significant changes in arterial pressure or heart rate were seen after the injection of either drug, although vecuronium caused a statistically significant decrease in heart rate (≏5%) at 5 and 10 min after administration. Both drugs would appear to have certain advantages over existing non-depolarizing neuromuscular blocking drugs.
Publisher:
England: Elsevier Ltd
Language:
English
Identifier:
ISSN:
0007-0912
EISSN:
1471-6771
DOI:
10.1093/bja/55.2.125
PMID:
6131682
Source:
© ProQuest LLC All rights reserved
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