Attenuation of Pain in a Randomized Trial by Suppression of Peripheral Nociceptive Activity in the Immediate Postoperative Period

• Published in: Anesthesia and analgesia Vol. 95; no. 5; pp. 1351 - 1357
• Main Authors: Gordon, Sharon M., Brahim, Jaime S., Dubner, Ronald, McCullagh, Linda M., Sang, Christine, Dionne, Raymond A.
• Format: Journal Article
• Language: English
• Published: United States International Anesthesia Research Society 01.11.2002
• Subjects: Acetaminophen - administration & dosage; Acetaminophen - therapeutic use; Adult; Analgesics, Non-Narcotic - administration & dosage; Analgesics, Non-Narcotic - therapeutic use; Analgesics, Opioid - administration & dosage; Analgesics, Opioid - therapeutic use; Anesthesia, General; Anesthesia, Local; beta-Endorphin - blood; Codeine - administration & dosage; Codeine - therapeutic use; Double-Blind Method; Female; Humans; Male; Nociceptors - drug effects; Pain Measurement; Pain, Postoperative - drug therapy; Peripheral Nervous System - drug effects; Surveys and Questionnaires
• ISSN: 0003-2999
• DOI: 10.1097/00000539-200211000-00047

Peripheral neuronal barrage from tissue injury produces central nervous system changes that contribute to the maintenance of postoperative pain. The therapeutic approaches to blocking these central changes remain controversial, because previous studies have not differentiated presurgical interventions from those administered after tissue injury, yet before pain onset. In this study, we evaluated the relative contributions of blockade of nociceptive input during surgery or during the immediate postoperative period on pain suppression. Subjects were randomly allocated to one of four groupspreoperative 2% lidocaine, postoperative 0.5% bupivacaine, both, or placebo injections. General anesthesia was induced and third molars extracted. Pain was assessed over 4 h and at 24 and 48 h. The β-endorphin in blood samples increased twofold during surgery, which is indicative of activation of the peripheral nociceptive barrage in response to painful stimuli. Pain was decreased in the immediate postoperative period in the bupivacaine groups, whereas it increased in the lidocaine group over time. Pain intensity was less 48 h after surgery in the groups whose postoperative pain was blocked by the administration of bupivacaine, but no effect was demonstrated for the preoperative administration of lidocaine alone. These results in the oral surgery pain model suggest that minimizing the peripheral nociceptive barrage during the immediate postoperative period decreases pain at later time periods. In contrast, blocking the intraoperative nociceptive barrage does not appear to contribute significantly to the subsequent reduction in pain.