Owen R T
Freelance Medical Writer, Crewe, Cheshire, United Kingdom.
Drugs Today (Barc). 2013 Aug;49(8):475-82. doi: 10.1358/dot.2013.49.8.2006992.
A multivesicular liposomal formulation of bupivacaine which can provide prolonged postsurgical pain relief has been developed. Two pivotal placebo-controlled phase III trials, one in hemorrhoidectomy and one in bunionectomy procedures, showed that wound infiltration of the suspension at the end of surgery could provide analgesia for up to 72 hours, reduce the amount of opiate rescue medications, the time to their first use and increase patient satisfaction. Liposomal bupivacaine was generally well tolerated, with no signal of QTc prolongation or evidence of impaired wound healing. A small open U.S. health economic study showed benefits (versus patient-controlled analgesia) for the preparation in decreasing total opioid use, length of hospital stay and total hospital costs. Further larger studies are warranted, in particular using bupivacaine hydrochloride as the comparator.
一种可提供延长术后疼痛缓解效果的布比卡因多泡脂质体制剂已被研发出来。两项关键的安慰剂对照III期试验,一项针对痔切除术,另一项针对拇囊炎切除术,结果表明在手术结束时将该混悬液进行伤口浸润可提供长达72小时的镇痛效果,减少阿片类急救药物的用量、首次使用时间,并提高患者满意度。脂质体布比卡因总体耐受性良好,没有QTc延长的迹象,也没有伤口愈合受损的证据。一项小型的美国卫生经济学开放性研究表明,该制剂(与患者自控镇痛相比)在减少总阿片类药物使用量、住院时间和总住院费用方面具有益处。有必要开展进一步更大规模的研究,尤其是以盐酸布比卡因作为对照。