Yalniz Kudret Yasemin, Baskan Semih
Department of Anesthesiology and Reanimation, Kahramankazan Hamdi Eris Public Hospital, Ankara, Turkey.
Department of Anesthesiology and Reanimation, Ankara Bilkent City Hospital, Ankara Yildirim Beyazit University, Ankara, Turkey.
Medicine (Baltimore). 2025 Mar 21;104(12):e41904. doi: 10.1097/MD.0000000000041904.
This study aimed to compare the efficacy, safety, and discharge times of patients undergoing day-case anorectal surgery using 5 mg hyperbaric bupivacaine versus 5 mg hypobaric bupivacaine. The evaluation was based on Fast-Track Scoring criteria, which assess the suitability of patients for day-case surgery.
A prospective observational study was conducted at Ankara City Hospital, including 80 patients aged 18 to 65 years within American Society of Anesthesiologists I-II risk groups scheduled for day-case anorectal surgery. All patients received spinal anesthesia with either 5 mg of 0.5% hyperbaric bupivacaine or 5 mg of 0.5% hypobaric bupivacaine. Hemodynamic parameters, sensory and motor block durations, time to first analgesic need, urination time, and discharge time were meticulously recorded and analyzed. Statistical analyses were performed using the independent samples t test and Mann-Whitney U test, with significance set at α = 0.05.
The hypobaric group exhibited significantly shorter sensory and motor block durations, enabling faster surgical readiness and earlier discharge. Both groups maintained comparable hemodynamic stability and postoperative complication rates. Shorter discharge times in the hypobaric group may offer potential benefits for patient turnover and cost-effectiveness.
For patients undergoing day-case anorectal surgery, 5 mg hypobaric bupivacaine provides faster recovery and shorter discharge time than hyperbaric bupivacaine, without compromising safety. These findings suggest that hypobaric bupivacaine may be a more suitable choice in day-case settings, contributing to improved resource utilization and patient satisfaction.
本研究旨在比较接受日间肛肠手术的患者使用5毫克高压布比卡因与5毫克低压布比卡因的疗效、安全性和出院时间。评估基于快速通道评分标准,该标准评估患者是否适合日间手术。
在安卡拉市医院进行了一项前瞻性观察性研究,纳入了80例年龄在18至65岁之间、美国麻醉医师协会I-II风险组且计划进行日间肛肠手术的患者。所有患者均接受了5毫克0.5%高压布比卡因或5毫克0.5%低压布比卡因的脊髓麻醉。仔细记录并分析血流动力学参数、感觉和运动阻滞持续时间、首次需要镇痛的时间、排尿时间和出院时间。使用独立样本t检验和曼-惠特尼U检验进行统计分析,显著性设定为α = 0.05。
低压组的感觉和运动阻滞持续时间明显更短,能够更快地准备手术并更早出院。两组的血流动力学稳定性和术后并发症发生率相当。低压组较短的出院时间可能对患者周转和成本效益具有潜在益处。
对于接受日间肛肠手术的患者,5毫克低压布比卡因比高压布比卡因恢复更快、出院时间更短,且不影响安全性。这些发现表明,低压布比卡因在日间手术环境中可能是更合适的选择,有助于提高资源利用和患者满意度。