Department of Anesthesiology and Critical Care, Peking University First Hospital, Beijing, China.
Department of Anesthesiology, Handan Central Hospital, Handan, Hebei, China.
PLoS One. 2018 Aug 14;13(8):e0202008. doi: 10.1371/journal.pone.0202008. eCollection 2018.
Dexmedetomidine in combination with opioids has been used for postoperative analgesia. The purpose of this study was to investigate the impacts of dexmedetomidine supplemented intravenous analgesia on morphine consumption and subjective sleep quality in elderly patients after open abdominal surgery.
This was a pilot randomized controlled trial. 58 elderly patients (age ≥ 60 years) who underwent open abdominal surgery were randomized to receive either dexmedetomidine supplemented morphine analgesia (0.5 mg/ml morphine plus 2 μg/ml dexmedetomidine in 100 ml normal saline, DEX group) or morphine analgesia (0.5 mg/ml morphine in 100 ml normal saline, CTRL group) for 72 hours after surgery. Patient-controlled analgesia pump was programmed to deliver a 2ml bolus with a lockout interval of 8 minutes and a background infusion at a rate of 1 ml/h. The primary endpoint was 72-hour morphine consumption. Secondary endpoints included pain intensity, subjective sleep quality, and 30-day complications and mortality after surgery.
The 72-hour morphine consumption was lower in the DEX group than in the CTRL group (median 39.0 mg [interquartile range 37.3, 41.0] in the DEX group vs. 49.0 mg [45.5, 50.0] in the CTRL group; median difference -9.0 mg [95% CI -10.0, -6.0], P < 0.001). The intensity of pain within 48 hours was lower (P<0.001 at 4, 12 and 48 hours, P = 0.007 at 24 hours) whereas the subjective quality of sleep was higher (P = 0.031 during the night of surgery and P<0.001 during the 1st night after surgery, respectively) in the DEX group than in the CTRL group. The incidence of 30-day complications did not differ significantly between groups, but it was slightly lower in the DEX group (P = 0.060). There were no significant differences between groups regarding 30-day mortality and the incidences of adverse events.
For elderly patients after open abdominal surgery, dexmedetomidine supplemented analgesia decreases morphine consumption, improves analgesic effects and subjective sleep quality without increasing adverse events.
Chinese Clinical Trial Registry ChiCTR-IPR-14005620.
右美托咪定联合阿片类药物已被用于术后镇痛。本研究旨在探讨右美托咪定静脉辅助镇痛对老年开腹手术后患者吗啡消耗和主观睡眠质量的影响。
这是一项前瞻性随机对照试验。58 例(年龄≥60 岁)接受开腹手术的老年患者随机分为接受右美托咪定联合吗啡镇痛(0.5mg/ml 吗啡加 2μg/ml 右美托咪定于 100ml 生理盐水,DEX 组)或吗啡镇痛(0.5mg/ml 吗啡于 100ml 生理盐水,CTRL 组)治疗 72 小时。患者自控镇痛泵设定为 2ml 推注,锁定间隔 8 分钟,背景输注速度为 1ml/h。主要终点是 72 小时吗啡消耗量。次要终点包括疼痛强度、主观睡眠质量以及术后 30 天并发症和死亡率。
DEX 组 72 小时吗啡消耗量低于 CTRL 组(中位数 39.0mg[四分位距 37.3,41.0]与 49.0mg[45.5,50.0];中位数差值-9.0mg[95%CI-10.0,-6.0],P<0.001)。48 小时内疼痛强度较低(P<0.001,4、12 和 48 小时,P=0.007,24 小时),DEX 组主观睡眠质量较高(P=0.031,手术当晚,P<0.001,术后第一晚)。两组 30 天并发症发生率无显著差异,但 DEX 组略低(P=0.060)。两组 30 天死亡率和不良事件发生率无显著差异。
对于老年开腹手术后患者,右美托咪定辅助镇痛可减少吗啡消耗,改善镇痛效果和主观睡眠质量,而不增加不良事件。
中国临床试验注册中心 ChiCTR-IPR-14005620。