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The effect of opioid-free anesthesia on the quality of recovery after gynecological laparoscopy: study protocol for a prospective randomized controlled trial

机译:无阿片内麻醉对妇科腹腔镜检查后恢复质量的影响:研究课程促进随机对照试验

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摘要

Because of the indiscriminate use of opioids during the perioperative period, opioid-free anesthesia (OFA) has been increasingly required. Nevertheless, the studies on the detailed techniques and effects of OFA are not sufficient. The Quality of Recovery-40 (QoR-40) questionnaire is a validated assessment tool for measuring recovery from general anesthesia. However, no study has used the QoR-40 to determine if OFA leads to better recovery than standard general anesthesia. Therefore, we aim to perform this study to determine the effects of OFA using dexmedetomidine and lidocaine on the quality of recovery as well as the various postoperative outcomes. The participants (n?=?78) will be allocated to one of the two groups; the study group will receive bolus and infusion of dexmedetomidine and lidocaine, and the control group will receive remifentanil infusion during general anesthesia for gynecological laparoscopy. The other processes including anesthetic and postoperative care will be performed similarly in the two groups. Intraoperative hemodynamic, anesthetic, and nociceptive variables will be recorded. Postoperative outcomes such as QoR-40, pain severity, and opioid-related side effects will be assessed. Additionally, an ancillary cytokine study (inflammatory cytokine, stress hormone, and reactive oxygen species) will be performed during the study period. This will be the first study to determine the effect of OFA, using the combination of dexmedetomidine and lidocaine, on the quality of recovery after gynecological laparoscopy compared with standard general anesthesia using remifentanil. The findings from this study will provide scientific and clinical evidence on the efficacy of OFA.
机译:由于在围手术期期间不分青红皂白种的阿片类药物,因此越来越需要阿片类药物麻醉(OFA)。尽管如此,对OFA的详细技术和效果的研究是不够的。回收 - 40(QOR-40)问卷的质量是一项验证的评估工具,用于从全身麻醉中衡量恢复。然而,没有研究使用QOR-40来确定OFA是否导致更好地恢复,而不是标准的全身麻醉。因此,我们的目的是进行这项研究以确定OFA使用Dexmedetomidine和Lidocaine对恢复质量以及各种术后结果的影响。参与者(n?=?78)将被分配给两组之一;该研究组将接受德克萨梅哌啶和利多卡因的推注和输注,并且对照组将在妇科腹腔镜检查的全身麻醉期间接受雷芬丹尼尼。包括麻醉剂和术后护理的其他方法将在两组中类似地进行。将记录术中血液动力学,麻醉和伤害性变量。将评估术后结果,如QOR-40,疼痛严重程度和与阿片类药物相关的副作用。另外,将在研究期间进行辅助细胞因子研究(炎症细胞因子,胁迫激素和反应性氧)。这将是第一项研究以确定OFA,使用Dexmedetomidine和Lidocaine的组合来确定妇科腹腔镜检查后的恢复质量与使用Remifentanil的标准全身麻醉。本研究的调查结果将提供关于OFA的疗效的科学和临床证据。

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