韩雪, 刘玲, 张广华. 右美托咪定对氟比洛芬酯多模式镇痛效果的影响[J]. 中国肿瘤临床, 2017, 44(6): 274-277. DOI: 10.3969/j.issn.1000-8179.2017.06.855
引用本文: 韩雪, 刘玲, 张广华. 右美托咪定对氟比洛芬酯多模式镇痛效果的影响[J]. 中国肿瘤临床, 2017, 44(6): 274-277. DOI: 10.3969/j.issn.1000-8179.2017.06.855
HAN Xue, LIU Ling, ZHANG Guanghua. Influence of dexmedetomidine on the multimodal analgesic effect of flurbiprofen axetil[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2017, 44(6): 274-277. DOI: 10.3969/j.issn.1000-8179.2017.06.855
Citation: HAN Xue, LIU Ling, ZHANG Guanghua. Influence of dexmedetomidine on the multimodal analgesic effect of flurbiprofen axetil[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2017, 44(6): 274-277. DOI: 10.3969/j.issn.1000-8179.2017.06.855

右美托咪定对氟比洛芬酯多模式镇痛效果的影响

Influence of dexmedetomidine on the multimodal analgesic effect of flurbiprofen axetil

  • 摘要:
      目的  观察右美托咪定对氟比洛芬酯多模式镇痛效果的影响。
      方法  选取2016年1月至2016年5月于天津医科大学肿瘤医院择期行直肠癌切除术的肿瘤患者共90例,随机分为A、B、C 3个组,每组30例。A、B两组术前静注氟比洛芬酯行超前镇痛,C组(对照组)静注脂肪乳2 mL。术后镇痛泵配制方法:A组为氟比洛芬酯+右美托咪定+舒芬太尼;B组为氟比洛芬酯+舒芬太尼;C组为舒芬太尼+脂肪乳,三组均加生理盐水至100 mL。分别记录术后4 h(T1)、8 h(T2)、12 h(T3)、24 h(T4)、48 h(T5)咳嗽时疼痛视觉模拟评分(VAS)及Ramsay镇静评分;记录术后24 h止疼泵有效按压次数及舒芬太尼用药量、术前及术后30 min血糖、术前及术后48 h C反应蛋白(C-reaction protein,CRP);观察术后48 h加强镇痛例数及不良反应例数。
      结果  A组T1、T2时Ramsay镇静评分高于B、C组,T1、T2、T3咳嗽时VAS评分、止疼泵有效按压次数、舒芬太尼消耗量、术后血糖和CRP明显小于B、C两组(P<0.05)。A、B两组间不良反应例数差异无统计学意义且均低于C组(均P<0.05)。
      结论  右美托咪定联合氟比洛芬酯多模式镇痛用于直肠癌根治术患者,可增强其镇痛镇静效果,减少应激和炎症反应且不增加不良反应的发生风险。

     

    Abstract:
      Objective  To observe the influence of dexmedetomidine on the multimodal analgesic effect of flurbiprofen axetil on patients subjected to radical resection of rectal carcinoma.
      Methods  Ninety patients who underwent abdominal resection of rectal carcinoma were selected and randomly divided into three groups (30 patients in each group). The patients in groups A and B were intravenously injected with flurbiprofen axetil 30 min before operation to achieve preemptive analgesia, while the patients in group C were pretreated with 2 mL lipid emulsion through intravenous injection. Patient-controlled intravenous analgesia pump was prepared as follows: flurbiprofen axetil + dexmedetomidine + sufentanil for group A; flurbiprofen axetil + sufentanil for group B; and sufentanil + 10 mL lipid emulsion for group C. The three groups were added with saline to obtain the final volume of 100 mL. The flow rate of the analgesic pump was 1 mL/h with single press amount of 1 mL and lock time of 15 min. Visual analog scale (VAS) while coughing and Ramsay sedation scores were recorded at 4 h (T1), 8 h (T2), 12 h (T3), 24 h (T4), and 48 h (T5) after operation. The effective press times and dosage of sufentanil were recorded for 24 h after operation, blood glucose level 30 min before and after operation, and C-reactive protein (CRP) 48 h before and after operation were also monitored. The number of patients with enhanced analgesia and adverse reactions, such as nausea and vomiting, dizziness, headache, itchy skin, urinary retention, respiratory depression, and bradycardia, was recorded for 48 h after operation.
      Results  Ramsay sedation scores of group A at T1 and T2 were higher than those of groups B and C. The VAS scores at T1, T2, and T3 while coughing, effective pumping time of the analgesic pump, post-operational blood glucose level, sufentanil consumption, and CRP of group A were lower than those of groups B and C (P < 0.05). The number of adverse reactions in group A was not significantly different from that in group B. By comparison, this parameter was significantly lower than that in group C (P < 0.05). The enhanced analgesia did not also significantly differ among the three groups.
      Conclusion  Dexmedetomidine combined with flurbiprofen axetil can induce multimodal analgesia, enhance analgesic effects, and reduce stress and inflammatory responses without the risk of increasing the incidence of adverse reactions.

     

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