首页> 外文期刊>Pain. >Pre-emptive analgesia using intravenous fentanyl plus low-dose ketamine for radical prostatectomy under general anesthesia does not produce short-term or long-term reductions in pain or analgesic use.
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Pre-emptive analgesia using intravenous fentanyl plus low-dose ketamine for radical prostatectomy under general anesthesia does not produce short-term or long-term reductions in pain or analgesic use.

机译:在全身麻醉下使用静脉注射芬太尼加小剂量氯胺酮进行的前列腺癌根治术的先行镇痛不会短期或长期减少疼痛或镇痛效果。

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The aim of the study was to evaluate post-operative pain and analgesic use after pre-operative or post-incisional i.v. fentanyl plus low dose i.v. ketamine vs. a standard treatment receiving i.v. fentanyl but not ketamine. Men undergoing radical prostatectomy under general anesthesia were randomly assigned in a double-blinded manner to one of three groups. Patients received i.v. fentanyl before incision followed by an i.v. bolus dose (0.2 ml kg(-1)) and an i.v. infusion (0.0025 ml kg(-1)min(-1)) of 1 mg ml(-1) ketamine (group 1) or normal saline (groups 2 and 3). Seventy minutes after incision, patients received i.v. fentanyl followed by an i.v. bolus dose (0.2 ml kg(-1)) and an i.v. infusion (0.0025 ml kg(-1)min(-1)) of saline (groups 1 and 3) or ketamine (group 2). Pain, von Frey pain thresholds, and cumulative morphine consumption using patient-controlled analgesia (PCA) were assessed up to 72 h after surgery. 143 patients completed the study (group 1, n = 47, group 2, n = 50, group 3, n = 46). Cumulative PCA morphine (mean+/-SD) did not differ significantly among groups (group 1, 92.3+/-45.9 mg; group 2, 107.2+/-58.4 mg; group 3, 103.6+/-50.4 mg; P = 0.08 for groups 1 vs. 2, and groups 1 vs. 3). On day 3, the hourly rate (mean+/-SEM) of morphine consumption was significantly lower (p < 0.0009) in group 1 (0.61+/-0.013 mg h(-1)) than group 2 (0.86+/-0.011 mg h(-1)) and group 3 (0.89+/-0.008 mg h(-1)). Pain scores and von Frey pain thresholds did not differ significantly among groups. Two-week and 6-month follow-ups did not reveal significant group differences in pain incidence, intensity, disability or mental health. Pre-operative, low-dose administration of i.v. ketamine did not result in a clinically meaningful reduction in pain or morphine consumption when compared with post-incisional administration of ketamine or a saline control condition.
机译:该研究的目的是评估术前或切口后静脉内注射后的术后疼痛和止痛药的使用情况。芬太尼加小剂量静脉注射氯胺酮与接受静脉注射的标准治疗芬太尼,而不是氯胺酮。在全麻下接受根治性前列腺切除术的男性以双盲方式随机分配到三组之一。患者接受静脉注射切开前进行芬太尼推注剂量(0.2 ml kg(-1))和静脉注射输注(0.0025 ml kg(-1)min(-1))1 mg ml(-1)氯胺酮(组1)或生理盐水(组2和3)。切开后70分钟,患者接受静脉输液。芬太尼,然后静脉注射推注剂量(0.2 ml kg(-1))和静脉注射输注(0.0025 ml kg(-1)min(-1))的盐水(第1和3组)或氯胺酮(第2组)。在手术后长达72小时,评估患者使用自控镇痛(PCA)的疼痛,von Frey疼痛阈值和吗啡累积消耗量。 143位患者完成了研究(第1组,n = 47,第2组,n = 50,第3组,n = 46)。各组之间的PCA吗啡累积量(平均值±SD)无显着差异(第1组为92.3 +/- 45.9 mg;第2组为107.2 +/- 58.4 mg;第3组为103.6 +/- 50.4 mg; P = 0.08组1与2,组1与3)。在第3天,第1组(0.61 +/- 0.013 mg h(-1))的吗啡消耗小时率(mean +/- SEM)显着低于第2组(0.86 +/- 0.011 mg(p <0.0009)) h(-1))和第3组(0.89 +/- 0.008 mg h(-1))。各组之间的疼痛评分和冯·弗雷疼痛阈值无显着差异。两周和六个月的随访未显示疼痛发生率,强度,残疾或心理健康方面的显着组差异。术前低剂量静脉注射与切开后施用氯胺酮或生理盐水控制条件相比,氯胺酮并未导致临床上有意义的疼痛或吗啡消耗量减少。

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