Abstract | STUDY OBJECTIVES: DESIGN: Prospective clinical comparison. SETTING: Operating room, Hokkaido University Hospital. PATIENTS: 7 adult ASA physical status II and III patients with impaired renal function undergoing living-related renal transplantation (Group A), 5 adult ASA physical status II and III patients with impaired renal function undergoing elective surgery other than renal transplantation (Group B), and 13 adult ASA physical status I and II patients with normal hepatorenal function undergoing elective surgery (Group C). INTERVENTIONS: MEASUREMENTS: Neuromuscular function was monitored by acceleration of thumb adduction with train-of-four stimulation. Vecuronium 60 microg x kg(-1) was administered as the initial dose via a central catheter, and if the first twitch was more than 3% of the control, another dose of vecuronium 20 microg x kg(-1) was given as necessary. Both onset time and duration of action until 25% recovery were measured. Plasma vecuronium and its metabolite, 3-desacetyl-vecuronium, levels were measured at onset and at 25% recovery in Groups A and C. MAIN RESULTS: The total dose of vecuronium and initial concentration of vecuronium showed no significant difference between Group A and Group C. Duration of action was significantly prolonged in Group A and Group B compared with Group C. CONCLUSIONS:
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Authors | H Sakamoto, K Takita, O Kemmotsu, Y Morimoto, T Mayumi |
Journal | Journal of clinical anesthesia
(J Clin Anesth)
Vol. 13
Issue 3
Pg. 193-7
(May 2001)
ISSN: 0952-8180 [Print] United States |
PMID | 11377157
(Publication Type: Clinical Trial, Comparative Study, Journal Article)
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Chemical References |
- Neuromuscular Nondepolarizing Agents
- Vecuronium Bromide
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Topics |
- Adult
- Anesthesia
- Biotransformation
- Female
- Humans
- Kidney Failure, Chronic
(complications)
- Kidney Function Tests
- Kidney Transplantation
- Male
- Monitoring, Intraoperative
- Neuromuscular Nondepolarizing Agents
(pharmacokinetics)
- Physical Stimulation
- Prospective Studies
- Ulnar Nerve
(physiology)
- Vecuronium Bromide
(pharmacokinetics)
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