Fred Wilson School of Pharmacy, High Point University, High Point, NC, USA.
Department of Clinical Sciences, Fred Wilson School of Pharmacy, High Point University, High Point, NC, USA.
Ann Pharmacother. 2023 Jan;57(1):71-85. doi: 10.1177/10600280221086639. Epub 2022 May 10.
To review data for bupivacaine/meloxicam extended-release (ER) solution for management of postoperative pain and opioid-sparing effects.
Literature search of PubMed (1946 to August 2021) and ProQuest (1946 to August 2021) was performed using the terms: Zynrelef, HTX-011, and "bupivacaine AND meloxicam." Additional information sources include ClinicalTrials.gov, prescribing information, Heron Therapeutics' Clinical and Economic Evidence Dossier, meeting abstracts, and references of identified articles.
Clinical trials and articles evaluating bupivacaine/meloxicam ER for postoperative pain management.
Bupivacaine is a short-acting local anesthetic. Its efficacy is negatively impacted by the acidic environment of surgical sites. Meloxicam, a nonsteroidal antiinflammatory, reduces inflammation at the surgical site and increases pH propagating bupivacaine movement into the neurons. In Phase 2 and Phase 3 clinical trials, bupivacaine/meloxicam ER was compared with bupivacaine HCl, bupivacaine ER, and meloxicam ER with and without scheduled nonopioid multimodal analgesia (MMA) in bunionectomies, herniorrhaphies, total knee arthroplasty and abdominoplasty. Postoperative pain was well controlled for 72 hours and consistently superior to placebo, with minimal or no opioid use. Wound healing was not impacted and adverse effects were similar to placebo (most commonly nausea, dizziness, constipation, and headaches).
Bupivacaine/meloxicam ER is a viable, safe, nonopioid local anesthetic for sustained 72-hour postoperative pain management mitigating opioid consumption.
Bupivacaine/meloxicam ER is the only dual-acting, extended-release local anesthetic available. It provides effective analgesia in the postoperative setting and successfully reduces or eliminates postoperative opioid consumption.
综述布比卡因/美洛昔康缓释(ER)溶液用于术后疼痛管理和减少阿片类药物的效果的数据。
在 PubMed(1946 年至 2021 年 8 月)和 ProQuest(1946 年至 2021 年 8 月)上使用以下术语进行文献检索:Zynrelef、HTX-011 和“布比卡因和美洛昔康”。其他信息来源包括 ClinicalTrials.gov、处方信息、Heron Therapeutics 的临床和经济证据档案、会议摘要和已确定文章的参考文献。
评估布比卡因/美洛昔康 ER 用于术后疼痛管理的临床试验和文章。
布比卡因是一种短效局部麻醉剂。其疗效受到手术部位酸性环境的负面影响。美洛昔康是非甾体抗炎药,可减少手术部位的炎症并增加 pH 值,促进布比卡因向神经元移动。在 2 期和 3 期临床试验中,布比卡因/美洛昔康 ER 与布比卡因 HCl、布比卡因 ER 以及美洛昔康 ER 进行了比较,同时还与有或没有计划的非阿片类多模式镇痛(MMA)联合使用,用于拇囊炎切除术、疝修补术、全膝关节置换术和腹部整形术。术后疼痛在 72 小时内得到良好控制,明显优于安慰剂,且阿片类药物的使用量最小或没有。伤口愈合没有受到影响,不良反应与安慰剂相似(最常见的是恶心、头晕、便秘和头痛)。
布比卡因/美洛昔康 ER 是一种可行、安全、非阿片类局部麻醉剂,可用于持续 72 小时的术后疼痛管理,减少阿片类药物的消耗。
布比卡因/美洛昔康 ER 是唯一一种双重作用、缓释的局部麻醉剂。它在术后环境中提供有效的镇痛,并成功减少或消除术后阿片类药物的消耗。