Gannon Emmett, Freeman Matthew, Cornett Chris, Vincent Scott, Powers Sydney, Lyden Elizabeth
Departments of Orthopaedic Surgery.
College of Medicine.
Clin Spine Surg. 2023 Feb 1;36(1):E29-E34. doi: 10.1097/BSD.0000000000001354. Epub 2022 Jun 16.
This is a retrospective observational study.
This study aims to determine the efficacy of liposomal bupivacaine in postoperative analgesia and long-term outcomes in patients undergoing one-level and two-level posterior lumbar fusion.
Multiple studies have investigated the use of liposomal bupivacaine in spine surgery with varying results. The potential benefits of its use include decreasing postoperative opioid use, improved pain control, and a shorter hospital stay. Several studies have supported its use in spine surgery with others showing minimal to no benefit. No studies have investigated its possible impact on long-term outcomes.
A total of 42 patients (22 one-level, 20 two-level) received liposomal bupivacaine injection just before surgical closure and were compared with a historical control group of 42 patients (27 one-level, 15 two-level) that did not receive liposomal bupivacaine. Daily opioid consumption was collected and converted to oral morphine equivalents. Length of stay and daily average pain scores using the visual analog scale were also recorded. In addition, SF-36 bodily pain and physical function outcome measures were collected preoperatively and at 6 months, 1 year and 2 years postoperatively.
The liposomal bupivacaine group was found to have a significantly lower total opioid consumption compared with the control group ( P =0.001). The liposomal bupivacaine group was also found to use significantly fewer opioids on the day of surgery compared with the control group ( P <0.0001). There was no significant difference shown in the average visual analog scale pain scores, length of stay, or long-term outcomes between the 2 groups.
The use of liposomal bupivacaine in one-level and two-level posterior lumbar fusions shows promise as an adjuvant for postoperative analgesia by decreasing postoperative opioid consumption. With the varying results demonstrated with the utilization of liposomal bupivacaine in spine surgery, further investigation is warranted, namely a larger prospective randomized control study.
Level III.
这是一项回顾性观察研究。
本研究旨在确定脂质体布比卡因在接受单节段和双节段后路腰椎融合术患者的术后镇痛效果及长期预后。
多项研究探讨了脂质体布比卡因在脊柱手术中的应用,结果各异。其潜在益处包括减少术后阿片类药物使用、改善疼痛控制及缩短住院时间。一些研究支持其在脊柱手术中的应用,而其他研究显示益处甚微或无益处。尚无研究调查其对长期预后的可能影响。
共有42例患者(22例单节段,20例双节段)在手术关闭前接受脂质体布比卡因注射,并与42例未接受脂质体布比卡因的历史对照组患者(27例单节段,15例双节段)进行比较。收集每日阿片类药物消耗量并换算为口服吗啡当量。记录住院时间及使用视觉模拟量表的每日平均疼痛评分。此外,在术前以及术后6个月、1年和2年收集SF - 36身体疼痛和身体功能结局指标。
发现脂质体布比卡因组的总阿片类药物消耗量显著低于对照组(P = 0.001)。还发现脂质体布比卡因组在手术当天使用的阿片类药物明显少于对照组(P < 0.0001)。两组之间在平均视觉模拟量表疼痛评分、住院时间或长期预后方面无显著差异。
在单节段和双节段后路腰椎融合术中使用脂质体布比卡因,通过减少术后阿片类药物消耗,显示出作为术后镇痛辅助药物的前景。鉴于脂质体布比卡因在脊柱手术中的应用结果各异,有必要进行进一步研究,即更大规模的前瞻性随机对照研究。
三级。