JOURNAL HOME CME HOME THIS MONTH PAST ISSUES ETOC COLLECTIONS
AUTHORS REVIEWERS EDITORIAL BOARD FEEDBACK RSS HELP
A&A International Anesthesia Research Society
 QUICK SEARCH:   [advanced]


     


Anesth Analg 2009; 109:1679-1683
© 2009 International Anesthesia Research Society
doi: 10.1213/ANE.0b013e3181b9e904
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a colleague
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Movafegh, A.
Right arrow Articles by Nabavian, O.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Movafegh, A.
Right arrow Articles by Nabavian, O.
Related Collections
Right arrow Clinical Pharmacology
Right arrow Regional Anesthesia
Right arrow Pharmacology


ANALGESIA

An Ultra-Low Dose of Naloxone Added to Lidocaine or Lidocaine-Fentanyl Mixture Prolongs Axillary Brachial Plexus Blockade

Ali Movafegh, MD, Behrang Nouralishahi, MD, Mustafa Sadeghi, MD, and Omid Nabavian, MD

From the Department of Anesthesiology and Critical Care, Dr. Ali Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.

Address correspondence and reprint requests to Mustafa Sadeghi, MD, Department of Anesthesiology and Critical Care, Dr Ali Shariati Hospital, North Karegar St., Tehran 1411713135, Iran. Address e-mail to sadeghi{at}movafegh.com.

Abstract

INTRODUCTION: In this prospective, randomized, double-blind study, we evaluated the effect of an ultra-low dose of naloxone added to lidocaine and fentanyl mixture on the onset and duration of axillary brachial plexus block.

METHODS: One hundred twelve patients scheduled for elective forearm surgery under axillary brachial plexus block were randomly allocated to receive 34 mL lidocaine 1.5% with 3 mL of isotonic saline chloride (control group, n = 28), 34 mL lidocaine 1.5% with 2 mL (100 µg) of fentanyl and 1 mL of isotonic saline chloride (fentanyl group, n = 28), 34 mL lidocaine 1.5% with 2 mL saline chloride and 100 ng (1 mL) naloxone (naloxone group, n = 28), or 34 mL lidocaine 1.5% with 2 mL (100 µg) of fentanyl and 100 ng (1 mL) naloxone (naloxone + fentanyl group, n = 28). A multiple stimulation technique was used in all patients. After performing the block, sensory and motor blockades of radial, median, musculocutaneous, and ulnar nerves were recorded at 5, 15, and 30 min. The onset time of the sensory and motor blockades was defined as the time between the last injection and the total abolition of the pinprick response and complete paralysis, respectively. The duration of sensory and motor blocks was considered as the time interval between the complete block and the first postoperative pain and complete recovery of motor functions.

RESULTS: Sensory and motor onset times were longer in the naloxone (sensory onset time: 15 ± 3, and motor onset time: 21 ± 4) and naloxone + fentanyl group than control or fentanyl groups (sensory onset time: 10 ± 3 min in control group, 10 ± 4 min in fentanyl group, and 17 ± 3 min in naloxone + fentanyl group, motor onset time: 15 ± 5 min in control group, 14 ± 7 min in fentanyl group, and 17.3 ± 3.4 min in naloxone + fentanyl group) (P < 0.001). The duration of time to first postoperative pain and motor blockade was significantly longer in the naloxone (92 ± 10 and 115 ± 10 min) and naloxone + fentanyl groups (98 ± 12 and 122 ± 16 min) than control (68 ± 7 and 89 ± 11 min) and fentanyl groups (68 ± 11 and 90 ± 12 min) (P < 0.001). The time to first postoperative pain was significantly longer in the naloxone and naloxone + fentanyl groups than in the control or fentanyl groups (P < 0.001).

CONCLUSIONS: The addition of an ultra-low dose of naloxone to lidocaine 1.5% solution with or without fentanyl solution in axillary brachial plexus block prolongs the time to first postoperative pain and motor blockade but also lengthens the onset time.







Lippincott, Williams & Wilkins Anesthesia & Analgesia® is published for the International Anesthesia Research Society® by Lippincott Williams & Wilkins and Stanford University Libraries' HighWire Press®. Copyright 2009 by the International Anesthesia Research Society. Online ISSN: 1526-7598   Print ISSN: 0003-2999 HighWire Press
Copyright © 2009 by the International Anesthesia Research Society.