经直肠前列腺活检鞍座阻滞:0.25%布比卡因与0.375%罗哌卡因镇痛效果的比较

John Bamigboye, S. Olateju, A. Faponle, A. Salako
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引用次数: 1

摘要

背景:前列腺活检是一种痛苦的过程,疼痛程度与核心活检的数量有关。目的:比较0.25%高压布比卡因和0.375%罗哌卡因用于鞍式阻滞经直肠前列腺活检的镇痛效果。方法:这是一项随机双盲研究。在尼日利亚一家三级医院的Day Case Theatre,80名前列腺活检适应症患者被随机分为两组:B组(布比卡因)和R组(罗哌卡因)。B组接受0.25%布比卡因1ml,R组接受0.375%罗哌卡因1ml用于鞍区阻滞。对两组患者的疼痛评估、家庭准备情况、患者满意度和首次镇痛请求时间进行评估和比较。结果:与罗哌卡因组相比,布比卡因组的感觉阻滞发作较早(11.90±4.10分钟vs 23.70±8.65分钟,p=0.000),感觉阻滞消退较慢(48.73±9.32分钟vs 24.88±4.21分钟,p=0.0000),但回家准备延迟(47.23±15.93分钟vs 29.88±8.58分钟,p=0.00)。布比卡因组在活检期间、活检后即刻和活检后30分钟的疼痛评分较低:分别为p=0.010、p=0.028和p=0.023。布比卡因组首次镇痛时间(48.73±9.33分钟)也长于罗哌卡因组(24.88±4.21分钟),具有统计学意义(p=0.000)。然而,罗哌卡因组的回家准备时间较早。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Saddle Block for Transrectal Prostate Biopsy: A Comparison of the Analgesic Efficacy of 0.25% Bupivacaine and 0.375% Ropivacaine
Background: Prostate biopsy is a painful procedure, and the degree of pain is related to the number of core biopsies taken. Objective: To compare the analgesic properties of hyperbaric bupivacaine 0.25% with 0.375% ropivacaine for saddle block in transrectal prostate biopsy. Methods: This was a randomised double-blinded study. Eighty patients with indications for prostate biopsy presenting at the Day-Case Theatre in a Nigerian tertiary facility were randomised into two equal groups: B (Bupivacaine) and R (Ropivacaine). Group B received 1ml of 0.25% bupivacaine, while Group R received 1ml of 0.375% ropivacaine for saddle block, respectively. Pain assessment, home readiness, patients' satisfaction, and time to first analgesic request were assessed and compared between the two groups. Results: The Bupivacaine group had an earlier onset of sensory block (11.90±4.10 minutes vs 23.70±8.65 minutes, p = 0.000), slower sensory block regression (48.73±9.32 minutes vs 24.88±4.21 minutes, p = 0.000), but delayed home readiness (47.23±15.93 minutes vs 29.88±8.58 minutes, p = 0.000), than patients in the Ropivacaine group. The pain scores during, immediately after and 30 minutes post-biopsy were lower in the Bupivacaine group: p = 0.010, p = 0.028 and p = 0.023 respectively. The time to first analgesic request was also longer in the Bupivacaine group (48.73±9.33 minutes) than for those in the Ropivacaine group (24.88±4.21 minutes) with statistical significance (p = 0.000). Conclusion: Intraoperative analgesic properties were better in the Bupivacaine group than in the Ropivacaine group. However, home readiness was earlier in the Ropivacaine group.
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