首页> 美国卫生研究院文献>International Journal of Clinical and Experimental Medicine >Flurbiprofen axetil reduces postoperative sufentanil consumption and enhances postoperative analgesic effects in patients with colorectal cancer surgery
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Flurbiprofen axetil reduces postoperative sufentanil consumption and enhances postoperative analgesic effects in patients with colorectal cancer surgery

机译:氟比洛芬酯减少大肠癌手术患者术后舒芬太尼的消耗并增强术后镇痛作用

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摘要

To investigate the effects of different strategies of flurbiprofen axetil (FA) administration on postoperative pain and sufentanil (SF) consumption after open colorectal cancer (CRC) surgery. Forty patients undergoing elective CRC resection were divided into two groups (n = 20 each). Patients in the F50+50 group received 50 mg of intravenous FA 30 min before skin incision and six hours after the first dose; patients in the F100 group received 100 mg of intravenous FA 30 min before skin incision. Perioperative plasma FA (CFA) and SF concentrations (CSF) were determined. Analgesic and sedative efficacy were evaluated using the visual analogue scale (VAS), Bruggman Comfort Scale (BCS), and Ramsay sedation scale. The time to the first PCIA trigger, the number of patients that pressed the PCIA trigger within 24 h after surgery, and the cumulative doses of SF consumption within 6 and 24 h after surgery were recorded. At postoperative 6 and 24 h, CFA was significantly higher, CSF was significantly lower, and the number of patients that pressed the PCIA trigger and the consumption of SF were significantly lower in the F50+50 group compared with the F100 group. At postoperative 4 h, VAS and BCS were significantly lower in the F50+50 group compared with the F100 group (P < 0.05). An administration strategy that maintains a relatively high plasma FA concentration at 6-24 h post-operatively may reduce postoperative inflammatory pain and SF-requirement in patients undergoing CRC resection.
机译:为了研究不同策略的氟比洛芬酯(FA)给药对开放性结直肠癌(CRC)术后术后疼痛和舒芬太尼(SF)的消耗。 40例行选择性CRC切除术的患者分为两组(每组n = 20)。 F50 + 50组的患者在皮肤切开前30分钟和首次给药后6小时接受了50 mg的静脉内FA。 F100组的患者在皮肤切开前30分钟接受100 mg静脉内FA。确定围手术期血浆FA(CFA)和SF浓度(CSF)。使用视觉模拟量表(VAS),布鲁格曼舒适量表(BCS)和Ramsay镇静量表评估镇痛和镇静效果。记录首次PCIA触发的时间,术后24小时内按下PCIA触发的患者人数以及术后6和24 h内的SF累积摄入量。与F100组相比,F50 + 50组在术后6和24 h时,CFA显着升高,CSF显着降低,按下PCIA触发的患者人数和SF的消耗显着降低。术后4 h,F50 + 50组的VAS和BCS明显低于F100组(P <0.05)。术后6-24小时维持相对较高的血浆FA浓度的给药策略可减少接受CRC切除的患者的术后炎症性疼痛和SF需求。

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