首页> 外文期刊>Journal of Thoracic Disease >The effectiveness of preemptive analgesia for relieving postoperative pain after video-assisted thoracoscopic surgery (VATS): a prospective, non-randomized controlled trial
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The effectiveness of preemptive analgesia for relieving postoperative pain after video-assisted thoracoscopic surgery (VATS): a prospective, non-randomized controlled trial

机译:先发型镇痛对术后胸腔诊断(VATS)缓解术后疼痛的有效性:前瞻性,非随机对照试验

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Background: The effectiveness of preemptive analgesia (PA) for relieving postoperative pain and reducing the side effects of analgesics following video-assisted thoracoscopic surgery (VATS) has not yet been determined. This study intends to test the clinical application value of PA in the perioperative period of VATS. Methods: From January 2018 to August 2018, we divided patients who underwent VATS in our hospital into a trial group (PA group) and a control group (traditional analgesia group, TA group). The PA group received a PA program, and the TA group was administered a conventional postoperative analgesia scheme. We compared the two groups according to the intensity of postoperative pain using the numeric rating scale (NRS), the incidence rate of analgesic drug-related adverse reactions, and the severity of stress-induced inflammation. Results: One hundred five cases from the PA group, and 80 cases from the TA group were included in the analysis. There were no significant differences between the two groups in baseline characteristics (P0.05). The PA group had a lower incidence rate of side effects from the analgesics compared to the TA group, and there was a statistical difference at 48 and 72 hours after surgery (P0.05). The PA group had a slightly lower score than the TA group for postoperative resting pain. However, this difference was not statistically significant (P0.05). The motion pain NRS score of the PA group was lower than the TA group, and although there were no significant differences at 4, 24, and 48 hours (P0.05), there was a statistically significant difference at 72 hours (P0.05). In the subset of patients with motion pain NRS ≥3 points, the PA group was marginally higher than the TA group at 4 hours (P0.05) but was lower than the TA group at 24, 48, and 72 hours, with a statistically significant difference at 24 and 72 hours (P0.05). There were no statistically significant differences in perioperative stress indexes between the two groups (P0.05). Conclusions: PA can relieve postoperative pain following VATS and reduce the incidence rate of analgesic drug-related adverse effects.
机译:背景:尚未确定尚未确定止血术后疼痛和降低镇痛药副作用术后止痛药(VATS)后止痛药的副作用的有效性。本研究旨在在大桶围手术期的临床应用价值。方法:2018年1月至2018年8月,我们将患者分为医院,进入试验组(PA组)和对照组(传统镇痛组,TA组)。 PA组接受了PA程序,TA组进行了常规的术后镇痛计划。我们根据术后疼痛的强度比较了两组使用数值评定量表(NRS),镇痛药物相关的不良反应的发生率和应激诱导的炎症的严重程度。结果:涉及PA组的一百五种案例,分析中包括80例TA组患者。基线特征中的两组之间没有显着差异(P> 0.05)。与TA组相比,PA组与镇痛药的副作用发生率较低,手术后48和72小时有统计学差异(P <0.05)。 PA组的得分略低于TA组,用于术后休息疼痛。然而,这种差异在统计学上没有统计学意义(P> 0.05)。 PA组的运动疼痛NRS得分低于TA组,虽然4,24和48小时没有显着差异(p> 0.05),但在72小时的统计学上有显着差异(P <0.05 )。在运动疼痛NRS≥3分的患者的子集中,PA组在4小时内比TA组略微高(P> 0.05),但低于24,48和72小时的TA组,具有统计学24和72小时的显着差异(P <0.05)。两组之间的围手术期应激指数没有统计学显着差异(P> 0.05)。结论:PA可缓解VATS后术后疼痛,降低镇痛药有关的不良反应的发生率。

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