Sternlicht Andrew, Shapiro Max, Robelen Gary, Vellayappan Usha, Tuerk Ingolf A
Department of Anesthesiology and Pain Medicine, Tufts University School of Medicine, Boston, MA, USA.
Department of Urology, Steward St Elizabeth's Medical Center, Tufts University School of Medicine, Boston, MA, USA.
Local Reg Anesth. 2014 Dec 12;7:69-74. doi: 10.2147/LRA.S64515. eCollection 2014.
Transversus abdominis plane (TAP) infiltration has been increasingly used for postsurgical analgesia in abdominal/pelvic procedures; however, duration/extent of analgesia with standard local anesthetics is limited. This pilot study assessed the preliminary efficacy and safety of two volumes of liposome bupivacaine administered via TAP infiltration in patients undergoing robotic laparoscopic prostatectomy.
In this single-center, open-label, prospective study, patients older than 18 years received TAP infiltration with liposome bupivacaine immediately after surgery. The first 12 patients received a total volume of 20 mL liposome bupivacaine (266 mg); the next 12 received 40 mL liposome bupivacaine (266 mg). The liposome bupivacaine was diluted with 0.9% normal saline. The primary efficacy measure was duration of analgesia, measured by time to first opioid administration. Secondary outcome measures included patient-assessed pain scores, opioid use, and opioid-related adverse events (AEs).
Twenty-four patients received liposome bupivacaine (20 mL, n=12; 40 mL, n=12) and were included in the primary analysis. Three refused participation in a 10-day follow-up visit and did not complete the study. Median time to first opioid administration after surgery was 23 and 26 minutes for the 20 and 40 mL groups, respectively. Mean total amount of postsurgical opioids ranged from 25.4 to 27.3 mg; after hospital discharge to day 10, both groups required a mean of 0.7 oxycodone/acetaminophen tablets/day. Mean pain scores of 4.4 and 5.3 were reported at 1 hour and 3.1 and 3.9 at 2 hours postsurgery, with 20 and 40 mL doses, respectively. Neither group had mean scores higher than 3.0 at any further assessments. No opioid-related or treatment-related serious AEs were reported.
Median time to first opioid administration did not differ between the two groups. No differences in secondary outcomes were observed on the basis of volume administered. These initial findings suggest further study of liposome bupivacaine administered via TAP infiltration as part of a multimodal analgesic regimen in laparoscopic robotic prostatectomy may be warranted.
腹横肌平面(TAP)阻滞已越来越多地用于腹部/盆腔手术后镇痛;然而,使用标准局麻药时镇痛的持续时间/范围有限。这项前瞻性试验评估了在接受机器人腹腔镜前列腺切除术的患者中,经TAP阻滞注射两种剂量脂质体布比卡因的初步疗效和安全性。
在这项单中心、开放标签的前瞻性研究中,18岁以上患者在手术后立即接受脂质体布比卡因TAP阻滞。前12例患者接受总量20 mL脂质体布比卡因(266 mg);接下来的12例接受40 mL脂质体布比卡因(266 mg)。脂质体布比卡因用0.9%生理盐水稀释。主要疗效指标是镇痛持续时间,通过首次使用阿片类药物的时间来衡量。次要结局指标包括患者评估的疼痛评分、阿片类药物使用情况及阿片类药物相关不良事件(AE)。
24例患者接受了脂质体布比卡因(20 mL组12例;40 mL组12例)并纳入主要分析。3例拒绝参加10天的随访,未完成研究。20 mL组和40 mL组术后首次使用阿片类药物的中位时间分别为23分钟和26分钟。术后阿片类药物的平均总量为25.4至27.3 mg;出院至第10天,两组每天平均需要0.7片羟考酮/对乙酰氨基酚片。术后1小时,20 mL和40 mL剂量组的平均疼痛评分分别为4.4和5.3,术后2小时分别为3.1和3.9。在任何进一步评估中,两组的平均评分均未高于3.0。未报告阿片类药物相关或治疗相关的严重AE。
两组首次使用阿片类药物的中位时间无差异。根据给药剂量,次要结局指标未观察到差异。这些初步研究结果表明,对于腹腔镜机器人前列腺切除术,作为多模式镇痛方案的一部分进一步研究经TAP阻滞注射脂质体布比卡因可能是必要的。