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Buprenorphine Formulations: Clinical Best Practice Strategies Recommendations for Perioperative Management of Patients Undergoing Surgical or Interventional Pain Procedures

机译:丁丙诺啡制剂:对接受手术或介入性疼痛治疗的患者进行围手术期管理的临床最佳实践策略建议

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Background: Starting with approval for clinical use in the treatment of opioid dependence inOctober 2002 by the Food and Drug Administration (FDA), buprenorphine has become an integraltreatment option and in recent years, in chronic pain management. Buprenorphine possesses aunique pharmacodynamic and pharmacokinetic profile that can potentially make perioperativeanalgesia challenging.Objectives: To date no unified guidelines or recommendations are available for buprenorphineproduct management during the perioperative period. The present investigation aims to review theliterature and provide recommendations when encountering a patient on buprenorphine therapywho is scheduled for a surgical or interventional pain procedure.Methods: Clinical studies and reviews were searched using the PubMed National Center forBiotechnology Information database using MeSH terms buprenorphine, buprenorphine andnaloxone, suboxone, perioperative, and postoperative pain.Results: PubMed National Center for Biotechnology Information database search resulted in onerandomized control trial, one prospective case matched cohort, one retrospective cohort, 0 caseseries, 4 case reports, and 6 review articles. Key literature is reviewed and summarized.Limitations: Only 12 articles were included, which permits only limited recommendations drawnfrom this review.Conclusions: The perioperative management of buprenorphine and buprenorphinealoxoneare dependent on several key factors. The nature of the surgery, namely the postoperativeopioid requirement, elective versus emergency surgery, patient characteristics, formulation ofbuprenorphine, and indication for buprenorphine or buprenorphinealoxone therapy must beconsidered when devising a plan. Several options exist when formulating a plan for the perioperativemanagement, including continuing buprenorphine therapy or holding buprenorphine therapy for adefined period of time with or without bridging to alternative opioids. Additionally, social supportpeople and patient motivation should be addressed and optimized, as well as nonopioid adjuvanttherapy should be maximized as applicable to each patient undergoing a surgical or interventionalpain procedure.
机译:背景:丁丙诺啡从2002年10月开始获得美国食品药品监督管理局(FDA)批准用于临床治疗阿片类药物依赖性药物,已成为不可或缺的治疗选择,并且近年来已用于慢性疼痛管理。丁丙诺啡具有独特的药效学和药代动力学特征,可能会给围手术期镇痛带来挑战。目的:迄今为止,围手术期尚无统一的指导原则或建议可用于丁丙诺啡产品的管理。本研究旨在回顾文学并在遇到计划接受手术或介入性疼痛治疗的丁丙诺啡治疗中遇到患者时提供建议。结果:PubMed国家生物技术中心信息数据库搜索结果进行了一项随机对照试验,1例前瞻性病例匹配队列,1例回顾性队列,0例病例系列,4例病例报告和6篇评论文章。局限性:仅纳入12篇文章,仅允许本评论提出有限的建议。结论:丁丙诺啡和丁丙诺啡/纳洛酮的围手术期管理取决于几个关键因素。在制定计划时,必须考虑手术的性质,即术后类鸦片需求,选择性手术与急诊手术,患者特征,丁丙诺啡的配方以及丁丙诺啡或丁丙诺啡/纳洛酮治疗的适应症。在制定围手术期管理计划时,有几种选择,包括继续使用丁丙诺啡治疗或在规定的时间内进行丁丙诺啡治疗,有或没有桥接其他阿片类药物。此外,应解决和优化社会支持者和患者的动机,并且应尽可能将非阿片类药物的辅助疗法应用于接受手术或介入性疼痛治疗的每个患者。

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