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首页> 外文期刊>European Journal of Obstetrics, Gynecology and Reproductive Biology: An International Journal >Combination of pre-emptive port-site and intraoperative intraperitoneal ropivacaine for reduction of postoperative pain: a prospective cohort study
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Combination of pre-emptive port-site and intraoperative intraperitoneal ropivacaine for reduction of postoperative pain: a prospective cohort study

机译:先发制人的入位与术中腹膜内罗哌卡因联合用于减轻术后疼痛的前瞻性队列研究

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Objective: To evaluate the effectiveness of intraoperatively applied local ropivacaine added to standard analgesic therapy in reducing postoperative pain intensity and opioid requirement under routine hospital conditions.Study design: In this prospective controlled cohort study, 303 consecutive patients receiving a gynaecological laparoscopic intervention at the Jena University Hospital were included. The study cohort (n = 168) received, in addition to standard pain management, a port-site (PS) infiltration with ropivacaine prior to incision and intraperitoneal (IP) instillation at the end of surgery. On the first postoperative day patients answered a validated questionnaire, and requirement of rescue analgesics was assessed. Results: Pain intensity was assessed on an 11-point numeric rating scale (NRS) from 0 = no pain to 10 = most severe pain. Reported pain intensity for movement-related pain was significantly lower (p = .001)in the study group compared with the control group (4.4 (SD 2.4) vs. 5.3 (SD 2.2) respectively). Minimal pain intensity after operation was also significantly lower in the study cohort (2.6 (SD 1.7) vs. 2.1 (SD 1.8), (p = .007)). Significantly fewer patients required rescue opioids for analgesia in the ropivacaine cohort (p = .001). The requested dose of rescue opioid (piritramide) in this cohort was also lower (p = .035) with 6.5 mg (SD 4.9) vs. 8.7 mg (SD 6.6), and demanded later (p = .001) with 4.3 h after surgery vs. 3.1 h. Patients in the study cohort experienced less nausea (p = .046). Higher satisfaction scores with pain management were reported in the ropivacaine group 12.7 (SD 2.5) vs. 11.6 (SD 2.8) (p <.001) (16-point NRS with 0 = not at all, 15 = completely satisfied).Conclusion: Addition of pre-emptive port-site plus intraperitoneal ropivacaine to standard postoperative analgesic therapy reduced postoperative pain intensity and opioid consumption in gynaecological laparoscopy.
机译:目的:评价在常规医院条件下术中局部应用罗哌卡因联合标准镇痛治疗可降低术后疼痛强度和阿片类药物需求的有效性。研究设计:在这项前瞻性对照队列研究中,连续303例在耶拿接受妇科腹腔镜手术的患者包括大学医院。该研究队列(n = 168)除接受标准的疼痛处理外,还接受了罗哌卡因的切口入位(PS)浸润,并在手术结束时进行了腹膜内滴注(IP)。术后第一天,患者回答了经过验证的问卷,并评估了急救镇痛药的需求。结果:疼痛强度以11点数字评分量表(NRS)进行评估,从0 =无疼痛到10 =最严重的疼痛。与对照组相比,研究组报告的与运动有关的疼痛的疼痛强度显着降低(p = .001)(分别为4.4(标准差2.4)和5.3(标准差2.2))。在研究队列中,手术后的最小疼痛强度也显着降低(2.6(SD 1.7)vs. 2.1(SD 1.8),(p = .007))。罗哌卡因组中需要镇痛用阿片类药物的患者明显减少(p = .001)。在该队列中,抢救性阿片类药物(吡咯酰胺)的要求剂量也较低(p = .035)(6.5 mg(SD 4.9)与8.7 mg(SD 6.6)),并在以后的4.3 h(p = .001)手术vs. 3.1小时研究队列中的患者较少出现恶心(p = .046)。罗哌卡因组的疼痛控制满意度较高,分别为12.7(SD 2.5)和11.6(SD 2.8)(p <.001)(16分NRS,0表示完全不满意,15表示完全满意)。在标准的术后镇痛治疗中,先发制人的前置位加上腹膜内罗哌卡因可降低妇科腹腔镜手术后的疼痛强度和阿片类药物的消耗。

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