Anesth Analg 2009; 109:1679-1683
© 2009 International Anesthesia Research Society
doi: 10.1213/ANE.0b013e3181b9e904
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.
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