Departments of Anesthesiology and.
Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, PR China.
Pain. 2024 Sep 1;165(9):e96-e105. doi: 10.1097/j.pain.0000000000003211. Epub 2024 Mar 15.
Moderate-to-severe acute postsurgical pain (APSP) can prolong the recovery and worsen the prognosis of patients who undergo spinal surgery. Esketamine and pregabalin may resolve APSP without causing hyperpathia or respiratory depression after surgery. However, there are other risks, such as dissociative symptoms. We designed a randomized controlled trial to investigate the effect of the combination of these 2 drugs on the incidence of APSP in patients who underwent resection of spinal neoplasms. Patients aged 18 to 65 years were randomized to receive esketamine (a bolus dose of 0.5 mg·kg -1 and an infusion dose of 0.12 mg·kg -1 ·h -1 for 48 hours after surgery) combined with oral pregabalin (75-150 mg/day, starting 2 hours before surgery and ending at 2 weeks after surgery) or an identical volume of normal saline and placebo capsules. The primary outcome was the proportion of patients with moderate-to-severe APSP (visual analog scale score ≥ 40) during the first 48 hours after surgery. Secondary outcomes included the incidence of drug-related adverse events. A total of 90 patients were randomized. The incidence of moderate-to-severe APSP in the combined group (27.3%) was lower than that in the control group (60.5%) during the first 48 hours after surgery (odds ratio = 0.25, 95% CI = 0.10-0.61; P = 0.002). The occurrence of mild dissociative symptoms was higher in the combined group than in the control group (18.2% vs 0%). In conclusion, esketamine combined with pregabalin could effectively alleviate APSP after spinal surgery, but an analgesic strategy might increase the risk of mild dissociative symptoms.
中重度急性术后疼痛(APSP)可延长接受脊柱手术患者的康复时间并使预后恶化。氯胺酮和普瑞巴林可在术后不会引起痛觉过敏或呼吸抑制的情况下缓解 APSP。然而,它们还存在其他风险,例如分离症状。我们设计了一项随机对照试验,以研究这两种药物联合应用于接受脊柱肿瘤切除术的患者中对 APSP 发生率的影响。年龄在 18 至 65 岁之间的患者被随机分为接受氯胺酮(术后 48 小时内给予 0.5mg·kg -1 负荷剂量和 0.12mg·kg -1 ·h -1 输注剂量)联合口服普瑞巴林(75-150mg/天,术前 2 小时开始并在术后 2 周结束)或等量生理盐水和安慰剂胶囊。主要结局是术后 48 小时内中重度 APSP(视觉模拟评分≥40)患者的比例。次要结局包括药物相关不良事件的发生率。共纳入 90 例患者。术后 48 小时内,联合组(27.3%)中中重度 APSP 的发生率低于对照组(60.5%)(比值比=0.25,95%置信区间为 0.10-0.61;P=0.002)。联合组轻度分离症状的发生率高于对照组(18.2%比 0%)。总之,氯胺酮联合普瑞巴林可有效缓解脊柱手术后的 APSP,但镇痛策略可能会增加轻度分离症状的风险。