Pergolizzi Joseph V, Magnusson Peter, LeQuang Jo Ann, Breve Frank, Mitchell Kailyn, Chopra Maninder, Varrassi Giustino
NEMA Research, Inc., Naples, FL, USA.
Centre for Research and Development, Region Gävleborg/Uppsala University, Gävle, Sweden.
J Pain Res. 2021 Mar 31;14:871-879. doi: 10.2147/JPR.S280572. eCollection 2021.
Transdermal buprenorphine is indicated for chronic pain management, but as its role in the clinical management of acute pain is less clear, this narrative review examines studies of the patch for acute pain, mainly in the postoperative setting. Although perhaps better known for its role in opioid rehabilitation programs, buprenorphine is also an effective analgesic that is a Schedule III controlled substance. Although buprenorphine is a partial agonist at the μ-opioid receptor, it is erroneous to think of the agent as a partial analgesic; it has full analgesic efficacy and unique attributes among opioids, such as a ceiling for respiratory depression and low "drug likeability" among those who take opioids for recreational purposes. Transdermal buprenorphine has been most thoroughly studied for acute pain control in postoperative patients. Postoperative pain follows a distinct and predictable trajectory depending on the type of surgery and patient characteristics. Overall, when the patch is applied prior to surgery and left in place for the prescribed seven days, it was associated with reduced postoperative pain, lower consumption of other analgesics, and patient satisfaction. Transdermal buprenorphine has been evaluated in clinical studies of patients undergoing gynecological surgery, hip fracture surgery, knee or hip arthroscopy/arthroplasty, shoulder surgery, and spinal surgery. Transdermal buprenorphine may also be appropriate pain medication for controlling pain during postsurgical orthopedic rehabilitation programs. Transdermal buprenorphine may result in typical opioid-associated side effects but with less frequency than other opioids. Despite clinical reservations about transdermal buprenorphine and its potential role in acute pain management in the clinical setting, clinical acceptance may be hampered by the fact that it is off-label and buprenorphine is better known as an opioid maintenance agent rather than an analgesic.
透皮丁丙诺啡适用于慢性疼痛管理,但由于其在急性疼痛临床管理中的作用尚不清楚,本文献综述主要研究了该贴片在急性疼痛中的应用,主要是在术后环境中。尽管丁丙诺啡在阿片类药物康复项目中的作用可能更为人所知,但它也是一种有效的镇痛药,属于Ⅲ类受管制物质。虽然丁丙诺啡是μ-阿片受体的部分激动剂,但认为该药物是部分镇痛药是错误的;它具有完全的镇痛效果,且在阿片类药物中具有独特的属性,如呼吸抑制有封顶效应,以及在那些出于娱乐目的服用阿片类药物的人群中“药物成瘾性”较低。透皮丁丙诺啡在术后患者急性疼痛控制方面的研究最为深入。术后疼痛根据手术类型和患者特征遵循独特且可预测的轨迹。总体而言,当在手术前应用该贴片并按规定留置7天时,它与术后疼痛减轻、其他镇痛药消耗量降低以及患者满意度相关。透皮丁丙诺啡已在接受妇科手术、髋部骨折手术、膝关节或髋关节关节镜检查/置换术、肩部手术和脊柱手术的患者的临床研究中进行了评估。透皮丁丙诺啡也可能是控制术后骨科康复项目疼痛的合适止痛药。透皮丁丙诺啡可能会导致典型的阿片类药物相关副作用,但发生频率低于其他阿片类药物。尽管临床上对透皮丁丙诺啡及其在临床环境中急性疼痛管理中的潜在作用存在保留意见,但它未被批准用于该适应症,且丁丙诺啡作为阿片类维持药物而非镇痛药更为人所知,这一事实可能会阻碍其临床应用。