右美托咪定复合芬太尼静脉自控镇痛对老年患者术后睡眠及认知功能的影响

吴晓丽, 李向南, 盛如意, 钱静, 袁从虎

吴晓丽, 李向南, 盛如意, 钱静, 袁从虎. 右美托咪定复合芬太尼静脉自控镇痛对老年患者术后睡眠及认知功能的影响[J]. 实用临床医药杂志, 2019, 23(8): 32-34, 38. DOI: 10.7619/jcmp.201908008
引用本文: 吴晓丽, 李向南, 盛如意, 钱静, 袁从虎. 右美托咪定复合芬太尼静脉自控镇痛对老年患者术后睡眠及认知功能的影响[J]. 实用临床医药杂志, 2019, 23(8): 32-34, 38. DOI: 10.7619/jcmp.201908008
WU Xiaoli, LI Xiangnan, SHENG Ruyi, QIAN Jing, YUAN Conghu. Effect of dexmedetomidine combined with fentanil on postoperative sleep quality and cognitive function in elderly patients with patient-controlled intravenous analgesia[J]. Journal of Clinical Medicine in Practice, 2019, 23(8): 32-34, 38. DOI: 10.7619/jcmp.201908008
Citation: WU Xiaoli, LI Xiangnan, SHENG Ruyi, QIAN Jing, YUAN Conghu. Effect of dexmedetomidine combined with fentanil on postoperative sleep quality and cognitive function in elderly patients with patient-controlled intravenous analgesia[J]. Journal of Clinical Medicine in Practice, 2019, 23(8): 32-34, 38. DOI: 10.7619/jcmp.201908008

右美托咪定复合芬太尼静脉自控镇痛对老年患者术后睡眠及认知功能的影响

详细信息
  • 中图分类号: R614

Effect of dexmedetomidine combined with fentanil on postoperative sleep quality and cognitive function in elderly patients with patient-controlled intravenous analgesia

  • 摘要:
      目的  探讨右美托咪定复合芬太尼静脉自控镇痛(PCIA)对老年患者术后睡眠和认知功能的影响。
      方法  选择拟行胸科手术需使用静脉镇痛泵的老年患者40例,随机分为对照组(芬太尼组)和实验组(右美托咪定+芬太尼组)各20例。术后对照组镇痛泵配方为芬太尼15 μg/kg+托烷司琼5 mg混合生理盐水到100 mL, 实验组镇痛泵配方为芬太尼15 μg/kg+右美托咪定1.0 μg/kg+托烷司琼5 mg混合生理盐水到100 mL, 2组均48 h后撤泵。观察2组患者术前1 d、手术当天及术后3 d的睡眠时间并评价睡眠质量,记录术前1 d及术后1、3、7 d的简易精神状态量表(MMSE)评分以及术后认知功能障碍(POCD)发生率。
      结果  与对照组相比,实验组手术当天和术后2 d的睡眠时间显著更长,睡眠质量评分显著升高(P < 0.05); 实验组术后1、3 d的MMSE评分显著高于对照组(P < 0.05); 实验组术后1、3 d的POCD发生率显著低于对照组(P < 0.05)。
      结论  老年手术患者术后应用右美托咪定复合芬太尼静脉自控镇痛,有助于改善患者术后睡眠剥夺状态,且认知功能降低少。
    Abstract:
      Objective  To investigate the effect of dexmedetomidine combined with fentanil on postoperative sleep quality and cognitive function in elderly patients with patient-controlled intravenous analgesia(PCIA).
      Methods  Forty elderly patients underwent thoracic surgery were randomly divided into control group(fentanil group, n=20) and experimental group C (fentanil plus dexmedetomidine group, n=20), The control group was mixed 15 μg/kg fentanil and 5 mg tropisetron into 100 mL of normal saline in patient-controlled intravenous analgesia pump, and experimental group contained 15 μg/kg fentanil, 1.0 μg/kg dexmedetomidine and 5 mg tropisetron in 100 mL of normal saline. The pump was withdrawn after 48 h. The total steep time, sleep quality were recorded at 1 d before surgery and on the day of surgery, and at 3 d after surgery. The Mini-Mental Status Examination (MMSE) were recorded at 1 d before surgery and 1, 3, 7 d after surgery, and the incidence of postoperative cognitive dysfunction was observed.
      Results  Compared with control group, the sleep time of experimental group on the surgery day and at 2 d after surgery was longer (P < 0.05); the sleep quality were significantly higher(P < 0.05); the MMSE scores of experimental group on the first and third postoperative day were higher(P < 0.05), and the incidence of POPD was lower than that in the control group(P < 0.05).
      Conclusion  Dexmedetomidine combined with fentanil administered for postoperative analgesia in elderly patients shows better efficacy in improvement of sleep status, and improve the postoperative cognitive function.
  • 表  1   2组患者一般情况、麻醉时间、手术时间比较(x±s)

    组别 n 年龄/岁 身高/cm 体质量/kg ASAⅠ级/例 ASAⅡ级/例 麻醉时间/min 手术时间/min
    对照组 20 14 6 67.0±3.0 165.0±16.0 66.0±8.0 7 13 260.0±19.0 236.0±14.0
    实验组 20 13 7 68.0±4.0 166.0±18.0 67.0±8.0 8 12 263.0±17.0 232.0±13.0
    下载: 导出CSV

    表  2   2组患者患者不同时点睡眠时间比较(x±s)  h

    组别 n 术前1 d 手术当天 术后1 d 术后2 d 术后3 d
    对照组 20 8.2±0.8 5.6±0.7 6.3±0.6 6.5±0.5 7.2±0.7
    实验组 20 8.1±0.7 6.9±0.6* 7.2±0.4* 7.3±5.6* 7.5±0.6
    与对照组比较, *P < 0.05。
    下载: 导出CSV

    表  3   2组患者不同时点睡眠质量比较(x±s)  cm

    组别 n 术前1 d 手术当天 术后1 d 术后2 d 术后3 d
    对照组 20 8.9±0.8 5.5±0.7 6.3±0.8 7.1±0.5 7.7±0.6
    实验组 20 9.0±0.7 7.7±0.6* 8.3±0.4* 7.9±0.7* 8.3±0.5
    与对照组比较, *P < 0.05。
    下载: 导出CSV

    表  4   2组患者不同时点MMSE评分比较(x±s)  

    组别 n 术前1 d 术后1 d 术后3 d 术后7 d
    对照组 20 28.4±0.9 23.6±0.8 25.3±0.8 27.2±0.6
    实验组 20 28.5±0.9 26.5±0.9* 27.6±0.7* 28.3±0.7
    与对照组比较, *P < 0.05。
    下载: 导出CSV

    表  5   2组患者术后POCD发生情况比较[n(%)]

    组别 n 术后1 d 术后3 d 术后7 d
    对照组 20 6(30.0) 4(20.0) 1(5.0)
    实验组 20 2(10.0)* 1(5.0)* 0
    与对照组比较, *P < 0.05。
    下载: 导出CSV
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出版历程
  • 收稿日期:  2019-01-09
  • 录用日期:  2019-03-04
  • 网络出版日期:  2020-12-03
  • 发布日期:  2019-04-27

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