The addition of adrenaline 5 mug/ml, 1 : 200 000 to 1% etidocaine hydrochloride administered extradurally (L2-3) shortened significantly the onset time for sensory blockade, particularly with respect to the spread of the analgesia from the injection site, and shortened the already rapid onset of motor block. Etidocaine hydrochloride 1% plain caused a slower onset of block, laster longer and produced more profound analgesia over the caudal dermatomes than did 2% lignocaine hydrochloride. The motor block from plain etidocaine was more profound in its extent and lasted longer than that caused by lignocaine. With regard to cardiovascular variables, there were no significant differences between subjects receiving the plain etidocaine and the plain lignocaine. However, subjects receiving etidocaine with adrenaline exhibited increased cardiac stimulation and a decrease in total peripheral resistance over the first 150 min.
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http://dx.doi.org/10.1093/bja/48.9.893 | DOI Listing |
J Pharm Biomed Anal
July 2002
Programa de Pós-Graduação em Ciências Farmacêuticas, Faculdade de Farmácia, Universidade Federal do Rio Grande do Sul (UFRGS), Av. Ipiranga, 2752, Porto Alegre, R/S, CEP 90160-000, Porto Alegre, Brazil.
A spectrophotometric method was developed for the determination of etidocaine hydrochloride (EH) in injectable pharmaceutical preparation. The proposal of this work was to develop a rapid, simple, inexpensive, precise and accurate visible spectrophotometric method. The method is based on the formation of the ion-pair complex by the EH reaction with bromocresol green in the pH 4.
View Article and Find Full Text PDFInt J Pharm
May 2001
Physical Pharmaceutical Chemistry, Uppsala University, Uppsala Biomedical Center, PO Box 574, S-751 23, Uppsala, Sweden.
As part of a general study to improve the iontophoretic delivery of local anaesthetics of the amide type, the diffusion properties of the hydrochloride salts of bupivacaine, etidocaine, lidocaine, mepivacaine, prilocaine and ropivacaine, were studied in a 1% w/w agarose hydrogel. A source drug solution (25 mM) was placed in contact with the gel and, after an appropriate time, the drug concentration profile in the gel was analyzed to give a diffusion coefficient, D. The values of Dx10(10) expressed in m(2) s(-1) were: (bupi) 6.
View Article and Find Full Text PDFOral Surg Oral Med Oral Pathol Oral Radiol Endod
April 2000
The Ohio State University, College of Dentistry, Columbus, OH 43210, USA.
Objective: The purpose of this study was to determine the anesthetic efficacy and heart rate effects of an intraosseous (IO) injection of 1.5% etidocaine with 1:200,000 epinephrine after an inferior alveolar nerve block.
Study Design: In a repeated-measures designed study, 48 subjects randomly received 2 combinations of injections at 2 separate appointments.
J Am Osteopath Assoc
December 1991
Department of Anesthesia, Youngstown Osteopathic Hospital, OH 44505.
Fifteen patients undergoing total hip and total knee replacement were studied prospectively to evaluate postoperative pain relief provided by an epidural infusion of fentanyl citrate, with and without lidocaine hydrochloride, and changes in arterial flow to the lower extremities. The patients were randomly placed in three groups: group 1 received epidural fentanyl, 5 micrograms/mL; group 2 received epidural fentanyl, 5 micrograms/mL with 0.75% solution of lidocaine; and group 3 received epidural fentanyl, 5 micrograms/mL with 1.
View Article and Find Full Text PDFJ Am Dent Assoc
April 1990
Department of Diagnostic Sciences, University of the Pacific School of Dentistry, San Francisco, CA 94115.
Because early research has established the prolonged duration of the effects of etidocaine, this study was performed to determine whether the long-acting local anesthetic can reduce the need for postoperative analgesics after oral surgery.
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