首页> 外文期刊>Obstetrics and Gynecology: Journal of the American College of Obstetricians and Gynecologists >Improving continuous wound infusion effectiveness for postoperative analgesia after cesarean delivery: a randomized controlled trial.
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Improving continuous wound infusion effectiveness for postoperative analgesia after cesarean delivery: a randomized controlled trial.

机译:剖宫产术后提高镇痛效果的连续伤口输注效果:一项随机对照试验。

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OBJECTIVE: To evaluate in which anatomical layer (above the fascia or below the fascia) continuous wound infusion of local anesthetic, combined with nonsteroidal antiinflammatory drugs, through a multiorifice catheter has the best effectiveness during the first 48 hours on postoperative pain intensity after elective cesarean delivery. METHODS: Fifty-six women undergoing elective cesarean delivery under spinal anesthesia were randomly allocated to receive 48-hour continuous wound infusion either above the fascia or below the fascia using ropivacaine and ketoprofene through a multiholed wound catheter. No other systemic analgesics were used, except for rescue patient-controlled intravenous morphine. Evaluation by a blinded investigator included visual analog scale scores at rest and at movement, morphine consumption, patient satisfaction, residual pain at 1 and 6 months, and undesirable side effects. RESULTS: Continuous wound infusion below the fascia resulted in significantly reduced pain at rest and total postoperative morphine consumption (15.7 mg, 95% confidence interval 9.7-20.7 mg) compared with wound administration above the fascia (26.4 mg, 95% confidence interval 18.1-34.7). No undesirable side effects or residual pain requiring treatment were recorded in both groups, whereas analgesia and satisfaction were excellent. CONCLUSION: After cesarean delivery, continuous wound infusion over 48 hours with ropivacaine and ketoprofene through a multiholed wound catheter inserted below the fascia results in better analgesia when compared with administration above the fascia. CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov, www.clinicaltrials.gov, NCT01160913. LEVEL OF EVIDENCE: I.
机译:目的:评估在选择性剖宫产术后头48小时内,通过多孔导管在局部解剖层(筋膜上方或筋膜下方)连续伤口局部麻醉药与非甾体类抗炎药的组合输注对效果最佳的效果交货。方法:将56名在脊髓麻醉下接受选择性剖宫产的妇女随机分配,以罗哌卡因和酮丙烯通过多孔伤口导管在筋膜上方或筋膜下方接受48小时连续伤口输注。除抢救患者控制的静脉内吗啡外,未使用其他全身镇痛药。盲人研究者的评估包括静止和运动时的视觉模拟量表评分,吗啡消耗量,患者满意度,1和6个月时的残留疼痛以及不良副作用。结果:与在筋膜上方伤口给药(26.4 mg,95%置信区间18.1)相比,在筋膜下方连续输注伤口可显着减少静息痛和术后总吗啡消耗量(15.7 mg,95%置信区间为9.7-20.7 mg)。 34.7)。两组均未记录到不良副作用或需要治疗的残留疼痛,而止痛和满意度均极佳。结论:剖宫产后,通过筋膜下插入的多孔伤口导管连续48小时使用罗哌卡因和酮基芬输注伤口,与在筋膜上给药相比,镇痛效果更好。临床试验注册:ClinicalTrials.gov,www.clinicaltrials.gov,NCT01160913。证据级别:I.

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