Naik Bhiken I, Nemergut Edward C, Kazemi Ali, Fernández Lucas, Cederholm Sarah K, McMurry Timothy L, Durieux Marcel E
From the Departments of *Anesthesiology, †Neurosurgery, and ‡Public Health Sciences, University of Virginia, Charlottesville, Virginia.
Anesth Analg. 2016 May;122(5):1646-53. doi: 10.1213/ANE.0000000000001226.
Adult deformity correction spine surgery can be associated with significant perioperative pain because of inflammatory, muscular, neuropathic, and postsurgical pain. α-2 Agonists have intrinsic antinociceptive and antihyperalgesic properties that can potentially reduce both postoperative opioid consumption and pain. We hypothesized that intraoperative dexmedetomidine would reduce postoperative opioid consumption and improve pain scores in deformity correction spine surgery.
Patients undergoing >3 levels of thoracic and/or lumbar spine surgery were enrolled in this prospective randomized double-blind study to receive either dexmedetomidine (1 μg/kg load followed by a continuous infusion of 0.5 μg/kg/h) or saline. Both groups received a single dose of 0.2 mg/kg (ideal body weight) of methadone at the start of surgery. Intraoperative fentanyl was administered based on the clinical and hemodynamic signs suggestive of increased nociception. Postoperative analgesia was provided with a hydromorphone patient-controlled analgesia pump. Opioid consumption and pain scores were recorded at 24, 48, and 72 hours after surgery.
One hundred forty-two participants were enrolled with 131 completing the study. There was no significant difference in demographics (age, sex, weight, and ASA physical status), percentage of participants with preoperative opioid use, and daily median opioid consumption between the groups. The study was terminated early after interim analysis. Intraoperative opioid use was reduced in the dexmedetomidine arm (placebo versus dexmedetomidine, median [25%-75% interquartile range]: 7 [3-15] vs 3.5 [0-11] mg morphine equivalents, P = 0.04) but not at 24 hours: 49 (30-78) vs 61 (34-77) mg morphine equivalents, P = 0.65, or 48 hours: 41 (28-68) vs 40 (23-64) mg morphine equivalents, P = 0.60, or 72 hours: 29 (15-59) vs 30 (14-46) mg morphine equivalents, P = 0.58. The Wilcoxon-Mann-Whitney odds are 1.11 with 97.06% confidence interval (0.71-1.76) for opioid consumption. No difference in pain score, as measured by the 11-point visual analog scale, was seen at 24 hours (placebo versus dexmedetomidine, median [25%-75% interquartile range]: 7 [5-7] vs 6 [4-7], P = 0.12) and 48 hours (5 [3-7] vs 5 [3-6], P = 0.65). There was an increased incidence of bradycardia (placebo: 37% vs dexmedetomidine: 59% P = 0.02) and phenylephrine use in the dexmedetomidine group (placebo: 59% versus dexmedetomidine: 78%, P = 0.03).
Intraoperative dexmedetomidine does not reduce postoperative opioid consumption or improve pain scores after multilevel deformity correction spine surgery.
由于存在炎症性、肌肉性、神经性及术后疼痛,成人脊柱畸形矫正手术可能伴有显著的围手术期疼痛。α-2激动剂具有内在的镇痛和抗痛觉过敏特性,有可能减少术后阿片类药物的使用量并减轻疼痛。我们推测术中使用右美托咪定可减少脊柱畸形矫正手术患者术后阿片类药物的使用量并改善疼痛评分。
本前瞻性随机双盲研究纳入接受3个以上胸椎和/或腰椎节段手术的患者,使其接受右美托咪定(负荷剂量1μg/kg,随后持续输注0.5μg/kg/h)或生理盐水。两组患者均在手术开始时接受单次剂量0.2mg/kg(理想体重)的美沙酮。术中根据提示伤害感受增加的临床和血流动力学体征给予芬太尼。术后通过氢吗啡酮患者自控镇痛泵进行镇痛。记录术后24、48和72小时的阿片类药物使用量及疼痛评分。
142名参与者入组,131名完成研究。两组在人口统计学特征(年龄、性别、体重和美国麻醉医师协会身体状况分级)、术前使用阿片类药物的参与者百分比以及每日阿片类药物使用量中位数方面无显著差异。中期分析后研究提前终止。右美托咪定组术中阿片类药物使用量减少(安慰剂组与右美托咪定组,中位数[25%-75%四分位数间距]:7[3-15]与3.5[0-11]mg吗啡当量,P = 0.04),但术后24小时未减少:49(30-78)与61(34-77)mg吗啡当量,P = 0.65;术后48小时也未减少:41(28-68)与40(23-64)mg吗啡当量,P = 0.60;术后72小时同样未减少:29(15-59)与30(14-46)mg吗啡当量,P = 0.58。阿片类药物使用量的Wilcoxon-Mann-Whitney优势比为1.11,97.06%置信区间为(0.71-1.76)。采用11点视觉模拟量表测量,术后24小时(安慰剂组与右美托咪定组,中位数[25%-75%四分位数间距]:7[5-7]与6[4-7],P = 0.12)和48小时(5[3-7]与5[3-6],P = 0.65)疼痛评分无差异。右美托咪定组心动过缓发生率增加(安慰剂组:37% 对比 右美托咪定组:59%,P = 0.02),使用去氧肾上腺素的情况也增加(安慰剂组:59% 对比 右美托咪定组:78%,P = 0.03)。
在多节段脊柱畸形矫正手术后,术中使用右美托咪定并不能减少术后阿片类药物的使用量或改善疼痛评分。