TY - JOUR
T1 - Late antinociception and lower untoward effects of concomitant intrathecal morphine and intravenous buprenorphine in humans
AU - Beltrutti, Diego
AU - Niv, David
AU - Ben-Abraham, Ron
AU - Di Santo, Salvatore
AU - Weinbroum, Avi A.
PY - 2002/9
Y1 - 2002/9
N2 - Study Objective: To evaluate the perioperative antinociceptive effect of intrathecal morphine (a pure μ agonist), intravenous (IV) buprenorphine (a partial μ agonist) or their combination. Design: Randomized, double-blind, placebo-controlled study. Settings: Anesthesiology department of a university-affiliated public hospital. Patients: 45 ASA physical status I, II, and III patients undergoing hysterectomy with general anesthesia. Interventions: Preoperative and postoperative regimens consisted of intrathecal morphine 4.3 μg.kg-1 plus IV 0.9% saline (Group 1), IV buprenorphine 1.3 μg.kg-1 plus intrathecal saline (Group 2), and intrathecal morphine 4.3 μg.kg-1 plus IV buprenorphine 1.3 μg.kg-1 (Group 3; postoperative supplements consisting of IV buprenorphine 1.3 μg.kg-1 plus intrathecal saline). Measurements and Main Results: Group 2 and 3 patients were given three analgesic dosings compared with two dosings in Group 1 (p < 0.001). The duration of action in Group 2 was significantly shorter (p = 0.001) than in the other two groups. The 12-hour postoperative pain intensity and sedation in Group 3 was significantly lower (p < 0.05) than in the other groups. Side effects (mainly pruritus and nausea and vomiting) were significantly fewer (p < 0.05) in Groups 2 and 3 (26% and 28%, respectively) than in Group 1 (46%). Conclusions: The concomitant administration of intrathecal morphine and IV buprenorphine alleviates pain sensation and minimizes sedation more effectively than when given after the administration of either drug separately. In addition, IV buprenorphine affords a reduction in side effects.
AB - Study Objective: To evaluate the perioperative antinociceptive effect of intrathecal morphine (a pure μ agonist), intravenous (IV) buprenorphine (a partial μ agonist) or their combination. Design: Randomized, double-blind, placebo-controlled study. Settings: Anesthesiology department of a university-affiliated public hospital. Patients: 45 ASA physical status I, II, and III patients undergoing hysterectomy with general anesthesia. Interventions: Preoperative and postoperative regimens consisted of intrathecal morphine 4.3 μg.kg-1 plus IV 0.9% saline (Group 1), IV buprenorphine 1.3 μg.kg-1 plus intrathecal saline (Group 2), and intrathecal morphine 4.3 μg.kg-1 plus IV buprenorphine 1.3 μg.kg-1 (Group 3; postoperative supplements consisting of IV buprenorphine 1.3 μg.kg-1 plus intrathecal saline). Measurements and Main Results: Group 2 and 3 patients were given three analgesic dosings compared with two dosings in Group 1 (p < 0.001). The duration of action in Group 2 was significantly shorter (p = 0.001) than in the other two groups. The 12-hour postoperative pain intensity and sedation in Group 3 was significantly lower (p < 0.05) than in the other groups. Side effects (mainly pruritus and nausea and vomiting) were significantly fewer (p < 0.05) in Groups 2 and 3 (26% and 28%, respectively) than in Group 1 (46%). Conclusions: The concomitant administration of intrathecal morphine and IV buprenorphine alleviates pain sensation and minimizes sedation more effectively than when given after the administration of either drug separately. In addition, IV buprenorphine affords a reduction in side effects.
KW - Buprenorphine
KW - Drug administration: concomitant
KW - Morphine: intrathecal
KW - Pain, postoperative
UR - http://www.scopus.com/inward/record.url?scp=0036710559&partnerID=8YFLogxK
U2 - 10.1016/S0952-8180(02)00397-5
DO - 10.1016/S0952-8180(02)00397-5
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C2 - 12393113
AN - SCOPUS:0036710559
SN - 0952-8180
VL - 14
SP - 441
EP - 446
JO - Journal of Clinical Anesthesia
JF - Journal of Clinical Anesthesia
IS - 6
ER -