Academic Urology and Urogynecology, 14044 West Camelback Road, Phoenix, AZ, 85340, USA.
Cleveland Clinic Florida, Department of Gynecology, Section of Female Pelvic Medicine and Reconstructive Surgery, Weston, FL, USA.
Int Urogynecol J. 2023 Aug;34(8):1781-1788. doi: 10.1007/s00192-023-05461-0. Epub 2023 Feb 2.
Dexamethasone is a potent glucocorticoid that may improve quality of recovery (QoR). We hypothesized that standard administration of dexamethasone at induction may improve QoR compared to placebo in subjects undergoing ambulatory vaginal reconstructive surgeries.
This was a randomized prospective clinical trial on subjects scheduled for ambulatory vaginal reconstructive surgery for prolapse and/or urinary incontinence. Intervention arm subjects were administered dexamethasone and the control group, a placebo (normal saline). Timing of administration, anesthesia medications, postoperative pain medications, and antiemetics were standardized. Primary outcome was difference in QoR (QoR-40) scores 24-48 h after surgery. Power analysis estimated that 27 subjects were required in each group to detect a difference in QoR-40 scores with 80% power and an alpha of 0.05.
Fifty-one subjects were enrolled and randomized. 4 withdrew, 1 was excluded, and 46 were analyzed. For the primary outcome, there was no difference in the QoR-40 between the dexamethasone and placebo group (--13.5 vs -19.6, p=0.24). Postoperative nausea vomiting intensity scores were not different (8.33 vs 9.09, p=1). Pain scores were similar in the two groups (6.0 vs 4.7, p=0.12). Although not statistically significant, surgical satisfaction at 6 weeks was better with dexamethasone (23.5 vs 26.9, p=0.09).
Based on this study, a single dose of dexamethasone at the time of induction prior to ambulatory vaginal reconstructive surgery was not associated with improved QoR. Standardized anesthesia protocols may play a role in postoperative nausea, pain control, and thereby QoR in patients undergoing ambulatory vaginal reconstructive surgeries.
地塞米松是一种强效糖皮质激素,可能会改善恢复质量(QoR)。我们假设,在接受门诊阴道重建手术的患者中,与安慰剂相比,在诱导时给予标准剂量的地塞米松可能会改善 QoR。
这是一项针对计划接受脱垂和/或尿失禁门诊阴道重建手术的患者的随机前瞻性临床试验。干预组患者给予地塞米松,对照组给予安慰剂(生理盐水)。管理时间、麻醉药物、术后止痛药物和止吐药均标准化。主要结局是术后 24-48 小时 QoR(QoR-40)评分的差异。功效分析估计每组需要 27 名受试者,以 80%的功效和 0.05 的 alpha 值检测 QoR-40 评分的差异。
共纳入 51 名患者并进行随机分组。4 名患者退出,1 名患者被排除,46 名患者进行了分析。对于主要结局,地塞米松组和安慰剂组的 QoR-40 评分无差异(-13.5 与-19.6,p=0.24)。术后恶心呕吐强度评分无差异(8.33 与 9.09,p=1)。两组疼痛评分相似(6.0 与 4.7,p=0.12)。虽然没有统计学意义,但地塞米松组的手术满意度在 6 周时更好(23.5 与 26.9,p=0.09)。
根据本研究,在接受门诊阴道重建手术前诱导时给予单次剂量地塞米松与改善 QoR 无关。标准化的麻醉方案可能在接受门诊阴道重建手术的患者的术后恶心、疼痛控制,进而 QoR 中发挥作用。