Raman Shankar, Lin Mayin, Krishnan Nivedita
Mercy Medical Center, Des Moines, IA, USA.
J Drug Assess. 2018 Jun 29;7(1):43-50. doi: 10.1080/21556660.2018.1487445. eCollection 2018.
The objective of the study was to systematically investigate the outcomes of Liposomal Bupivacaine following major colorectal resections. We conducted a comprehensive literature search of PubMed, Medline, Google scholar, Cochrane Central Registry and clinical trials.gov databases through May 2017 for studies published regarding liposomal bupivacaine. Studies were filtered based on relevance to perioperative analgesia in colorectal resections. Data comparing type of study, techniques of resection, mode of administration of liposomal bupivacaine, details of control group, outcomes were collected. A total of 1008 patients from seven studies were included in this systematic review and meta-analysis. The studies were mostly retrospective or prospective cohort studies with one randomized controlled trial (RCT). Meta-analysis showed that liposomal bupivacaine was associated with decreased length of stay, standard mean difference in days (SMD) - 0.34, (95% confidence intervals [CI] - 0.56, -0.13, = .001) and decreased IV opioid use (expressed as intravenous morphine equivalent in milligrams) in the first 48-72 h, SMD -0.49 (95% CI -0.69, -0.28, < .00001). Pain scores were also significantly low in patients who received liposomal bupivacaine, SMD -0.56 (95% CI -1.07, -0.06, = .03]. There was no significant difference in hospitalization costs between the two groups. Use of liposomal bupivacaine is associated with decreased IV opioid use, length of stay and lower pain scores. However, our data needs to be interpreted cautiously given the relative paucity of randomized controlled trials.
本研究的目的是系统调查脂质体布比卡因用于大肠大手术后的效果。我们对PubMed、Medline、谷歌学术、Cochrane中心注册库和临床试验.gov数据库进行了全面的文献检索,检索截至2017年5月发表的关于脂质体布比卡因的研究。根据与大肠切除围手术期镇痛的相关性对研究进行筛选。收集了比较研究类型、切除技术、脂质体布比卡因给药方式、对照组细节、结果的数据。本系统评价和荟萃分析纳入了来自7项研究的共1008例患者。这些研究大多为回顾性或前瞻性队列研究,其中有1项随机对照试验(RCT)。荟萃分析表明,脂质体布比卡因与住院时间缩短相关,天数的标准平均差(SMD)为-0.34,(95%置信区间[CI]-0.56,-0.13,P = 0.001),且在最初48 - 72小时内静脉注射阿片类药物的使用减少(以毫克静脉注射吗啡当量表示),SMD为-0.49(95% CI -0.69,-0.28,P < 0.00001)。接受脂质体布比卡因的患者疼痛评分也显著较低,SMD为-0.56(95% CI -1.07,-0.06,P = 0.03)。两组之间的住院费用没有显著差异。使用脂质体布比卡因与静脉注射阿片类药物使用减少、住院时间缩短和疼痛评分降低相关。然而,鉴于随机对照试验相对较少,我们的数据需要谨慎解读。