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慢性下腰痛开放性安慰剂对照:5 年随访。

Open-label placebo for chronic low back pain: a 5-year follow-up.

机构信息

ISPA-Instituto Universitário de Ciências Psicológicas, Sociais e da Vida, Rua Jardim do Tabaco, Lisbon, Portugal.

Santa Casa da Misericórdia de Lisboa, Largo Trindade Coelho, Lisbon, Portugal.

出版信息

Pain. 2021 May 1;162(5):1521-1527. doi: 10.1097/j.pain.0000000000002162.

Abstract

Long-term follow-up of patients treated with open-label placebo (OLP) are nonexistent. In this article, we report a 5-year follow-up of a 3-week OLP randomized controlled trial (RCT) in patients with chronic low back pain. We recontacted the participants of original RCT and reassessed their pain, disability, and use of pain medication. We obtained follow-up data from 55 participants (82% of those who took OLP during the parent RCT), with a mean elapsed time between the end of the 3 weeks placebo trial and the follow-up interview of 55 months (SD = 7.85). We found significant reductions in both pain and disability between the baseline assessment immediately before the 3 weeks trial with placebo pills and the original trial endpoint (P < 0.00001 for the 2 primary outcomes of pain and disability). At the 5-year follow-up, we found no significant differences in either outcome between original trial endpoint and follow-up. Improvements persisted after 5 years and were accompanied by substantial reductions compared with baseline in the use of pain medication (from 87% to 38%), comprising analgesics (from 80% to 31%), antidepressants (from 24% to 11%), and benzodiazepines (from 15% to 5%). By contrast, the use of alternative approaches to pain management increased (from 18% to 29%). Although the reduction in pain and medication is comparable with the improvements that occurred in the original study, a major limitation of this long-term follow-up is the absence of controls for spontaneous improvement and new cointerventions. Nonetheless, our data suggest that reductions in pain and disability after OLP may be long lasting.

摘要

长期随访接受开放性安慰剂(OLP)治疗的患者是不存在的。在本文中,我们报告了一项为期 3 周的 OLP 随机对照试验(RCT)的 5 年随访结果,该试验纳入了慢性腰痛患者。我们重新联系了原始 RCT 的参与者,并重新评估了他们的疼痛、残疾和止痛药使用情况。我们从 55 名参与者(在原始 RCT 中接受 OLP 的参与者的 82%)获得了随访数据,在结束 3 周安慰剂试验和随访访谈之间的平均时间间隔为 55 个月(SD=7.85)。我们发现,与安慰剂试验前的基线评估相比,疼痛和残疾在原始试验终点(疼痛和残疾的 2 个主要结局的 P<0.00001)均显著降低。在 5 年随访时,我们发现原始试验终点与随访之间在这两个结局上没有显著差异。在 5 年时,改善仍持续存在,并且与基线相比,止痛药的使用显著减少(从 87%降至 38%),包括镇痛药(从 80%降至 31%)、抗抑郁药(从 24%降至 11%)和苯二氮䓬类(从 15%降至 5%)。相比之下,疼痛管理的替代方法的使用增加(从 18%增至 29%)。尽管疼痛和药物使用的减少与原始研究中的改善相当,但这项长期随访的一个主要局限性是缺乏自发性改善和新的合并干预的对照。尽管如此,我们的数据表明,OLP 后疼痛和残疾的减少可能是持久的。

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