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British Journal of Anaesthesia, Vol 78, Issue 5 507-514, Copyright © 1997 by The Board of Management and Trustees of the British Journal of Anaesthesia


CLINICAL INVESTIGATIONS

Central nervous and cardiovascular effects of i.v. infusions of ropivacaine, bupivacaine and placebo in volunteers

K. Knudsen, M. B. Suurkula, S. Blomberg, J. Sjovall and N. Edvardsson
Department of Anaesthesia and Intensive Care, Sahlgrenska University Hospital, S-413 45 Goteborg; Department of Clinical Physiology, Sahlgrenska University Hospital, S-413 45 Goteborg; Division of Cardiology, Sahlgrenska University Hospital, S-413 45 Goteborg; Clinical Research and Development, Astra Pain Control AB, S-151 85 Sodertalje, Sweden

We have compared the incidence of CNS symptoms and changes in echocardiography and electrophysiology during i.v. infusions of ropivacaine, bupivacaine and placebo. Acute tolerance of i.v. infusion of 10 mg min-1 was studied in a crossover, randomized, double-blind study in 12 volunteers previously acquainted with the CNS effects of lignocaine. The maximum tolerated dose for CNS symptoms was higher after ropivacaine in nine of 12 subjects and higher after bupivacaine in three subjects. The 95% confidence limits for the difference in mean dose between ropivacaine and bupivacaine were -30 and 7 mg. The maximum tolerated unbound arterial plasma concentration was twice as high after ropivacaine (P < 0.001). Muscular twitching occurred more frequently after bupivacaine (P < 0.05). The time to disappearance of all symptoms was shorter after ropivacaine (P < 0.05). A threshold for CNS toxicity was apparent at a mean free plasma concentration of approximately 0.6 mg litre-1 for ropivacaine and 0.3 mg litre-1 for bupivacaine. Bupivacaine increased QRS width during sinus rhythm compared with placebo (P < 0.001) and ropivacaine (P < 0.01). Bupivacaine reduced both left ventricular systolic and diastolic function compared with placebo (P < 0.05 and P < 0.01, respectively), while ropivacaine reduced only systolic function (P < 0.01).
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M. W. B. Hartmannsgruber, D. G. Silverman, T. M. Halaszynski, V. Bobart, S. J. Brull, C. Wilkerson, A. W. Loepke, and P. G. Atanassoff
Comparison of Ropivacaine 0.2% and Lidocaine 0.5% for Intravenous Regional Anesthesia in Volunteers
Anesth. Analg., September 1, 1999; 89(3): 727 - 727.
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A. J Fox and D. J Rowbotham
Recent advances: Anaesthesia
BMJ, August 28, 1999; 319(7209): 557 - 560.
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H. Wulf, J. Biscoping, B. Beland, B. Bachmann-Mennenga, and J. Motsch
Ropivacaine Epidural Anesthesia and Analgesia Versus General Anesthesia and Intravenous Patient-Controlled Analgesia with Morphine in the Perioperative Management of Hip Replacement
Anesth. Analg., July 1, 1999; 89(1): 111 - 111.
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E. U. M. Nystrom, J. E. Heavner, and C. W. Buffington
Blood Pressure Is Maintained Despite Profound Myocardial Depression During Acute Bupivacaine Overdose in Pigs
Anesth. Analg., May 1, 1999; 88(5): 1143 - 1148.
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