医学
麻醉
随机对照试验
氯胺酮
安慰剂
食管切除术
萧条(经济学)
可视模拟标度
医院焦虑抑郁量表
评定量表
不利影响
焦虑
简短疼痛清单
疼痛量表
疾病严重程度
病人自控镇痛
多中心试验
临床试验
生活质量(医疗保健)
外科
腹部外科
作者
Hongwei Zhang,Feng Yin,Lantao Li,Xuefei Li,Weiwei Xu,Yi Zhou,Liang Jin,Hongyan Lin,Xihua Lu,Jianjun Yang,Hai Yu
标识
DOI:10.1080/07853890.2026.2704297
摘要
Background Patients undergoing minimally invasive esophagectomy (MIE) frequently experience moderate-to-severe postoperative pain and anxiety-depressive symptoms, compromising postoperative quality of recovery (QoR). Esketamine is a promising adjunct for analgesia and anxiolysis; however, the effect of low-dose esketamine on patient-centered recovery outcomes in MIE remains unclear.Methods In this double-blinded, multicenter randomized controlled trial, patients scheduled for elective McKeown esophagectomy were allocated to esketamine (0.25 mg/kg loading dose and 0.125 mg/kg/h continuous infusion during surgery) or placebo (equivalent volume and rate of saline). The primary outcome was the QoR-15 score on postoperative day (POD) 2. Secondary outcomes included QoR-15 scores on POD 1, 3, 7 and 30. Hospital Anxiety and Depression Scale - Anxiety Subscale (HADS-A) and Depression Subscale (HADS-D) scores, numeric rating scale (NRS) pain scores, and the Brief Pain Inventory (BPI) scores on POD 1 to 3, and safety evaluations.Results A total of 198 patients were analyzed (esketamine, n = 98; placebo, n = 100). Intraoperative esketamine significantly improved QoR-15 scores on POD 2 (116.9 ± 9.4 vs. 110.2 ± 9.8, p < 0.001) and POD 3 (123.6 ± 7.2 vs. 116.8 ± 8.4, p < 0.001) compared with placebo. HADS-A and HADS-D scores were lower in the esketamine group on POD 1 to 3 (all p < 0.001). Additionally, esketamine recipients reported significantly lower NRS scores at rest and during movement and BPI scores for pain severity and pain interference items (all p < 0.001). There were no significant between-group differences in safety outcomes.Conclusions Intraoperative low-dose esketamine improved early, patient-reported recovery after MIE by enhancing analgesia and reducing postoperative anxiety and depression without increasing adverse events.Trial registration Chinese Clinical Trial Register (identifier: ChiCTR2400088916).
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