Department of Anesthesiology, Advocate Illinois Masonic Medical Center, Chicago, IL, United States.
College of Liberal Arts & Sciences, University of Illinois at Urbana Champaign, IL, United States.
Expert Opin Drug Saf. 2021 Sep;20(9):1005-1033. doi: 10.1080/14740338.2021.1921142. Epub 2021 May 11.
: The healthcare expenditures in the United States are substantial for the management of refractory, chronic low back pain (CLBP). The objective of this review is to summarize and evaluate the safety profiles of different pharmacological treatment options used in the management of CLBP.: The authors conducted a search of randomized controlled trials (RCTs) assessing the safety profiles of different pharmacological agents used in the management of CLBP. This narrative review covered corticosteroids, opioids, antidepressants, gabapentinoids, nonsteroidal anti-inflammatory drugs, muscle relaxants, anti-nerve growth factor antibodies and topical agents, as monotherapy or in combination.: The risk-benefit ratio of a particular treatment is a subject driving the ongoing development of pharmaceuticals. The most commonly reported AEs across all drug classes are of gastrointestinal nature, followed by neurological and skin-related. These AEs include nausea, dizziness, constipation, arthralgia, headache, dry mouth, pruritus, etc. The majority of the AEs reported are not life-threatening, although they may lower patients' quality of life, thus, affecting their compliance. One of the biggest limitations of our review stems from the paucity of safety assessments in published RCTs. Advances in our understanding of the neurobiology of pain will promote development of new therapeutic strategies.
美国在治疗难治性、慢性下腰痛(CLBP)方面的医疗支出巨大。本综述的目的是总结和评估用于 CLBP 管理的不同药物治疗选择的安全性概况。
作者对评估用于 CLBP 管理的不同药物治疗安全性概况的随机对照试验(RCT)进行了检索。本叙述性综述涵盖了皮质类固醇、阿片类药物、抗抑郁药、加巴喷丁类药物、非甾体抗炎药、肌肉松弛剂、抗神经生长因子抗体和局部制剂,作为单一疗法或联合疗法。
特定治疗的风险效益比是推动药物不断发展的一个主题。所有药物类别中最常见的不良反应都是胃肠道性质的,其次是神经和皮肤相关的。这些不良反应包括恶心、头晕、便秘、关节痛、头痛、口干、瘙痒等。大多数报告的不良反应并不危及生命,但可能会降低患者的生活质量,从而影响其依从性。我们综述的最大限制之一源于已发表 RCT 中安全性评估的缺乏。我们对疼痛神经生物学理解的进步将促进新治疗策略的发展。