Departments of Anesthesiology, Perioperative, and Pain Medicine and.
Orthopedic Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.
Pain. 2021 Jun 1;162(6):1828-1839. doi: 10.1097/j.pain.0000000000002185.
Placebo effects have traditionally involved concealment or deception. However, recent evidence suggests that placebo effects can also be elicited when prescribed transparently as "open-label placebos" (OLPs), and that the pairing of an unconditioned stimulus (eg, opioid analgesic) with a conditioned stimulus (eg, placebo pill) can lead to the conditioned stimulus alone reducing pain. In this randomized control trial, we investigated whether combining conditioning with an OLP (COLP) in the immediate postoperative period could reduce daily opioid use and postsurgical pain among patients recovering from spine surgery. Patients were randomized to COLP or treatment as usual, with both groups receiving unrestricted access to a typical opioid-based postoperative analgesic regimen. The generalized estimating equations method was used to assess the treatment effect of COLP on daily opioid consumption and pain during postoperative period from postoperative day (POD) 1 to POD 17. Patients in the COLP group consumed approximately 30% less daily morphine milligram equivalents compared with patients in the treatment as usual group during POD 1 to 17 (-14.5 daily morphine milligram equivalents; 95% CI: [-26.8, -2.2]). Daily worst pain scores were also lower in the COLP group (-1.0 point on the 10-point scale; 95% CI: [-2.0, -0.1]), although a significant difference was not detected in average daily pain between the groups (-0.8 point; 95% CI: [-1.7, 0.2]). These findings suggest that COLP may serve as a potential adjuvant analgesic therapy to decrease opioid consumption in the early postoperative period, without increasing pain.
安慰剂效应传统上涉及隐瞒或欺骗。然而,最近的证据表明,当以“开放性安慰剂”(OLP)透明地开处方时,也可以引发安慰剂效应,并且将无条件刺激(例如阿片类镇痛药)与条件刺激(例如安慰剂丸)配对可以导致单独的条件刺激减轻疼痛。在这项随机对照试验中,我们研究了在脊柱手术后康复期间,在术后即刻将条件作用与 OLP 相结合(COLP)是否可以减少每日阿片类药物的使用和术后疼痛。患者被随机分配到 COLP 或常规治疗组,两组都可以不受限制地使用典型的基于阿片类的术后镇痛方案。广义估计方程方法用于评估 COLP 对术后第 1 天至第 17 天(POD1 至 POD17)期间每日阿片类药物消耗量和疼痛的治疗作用。与常规治疗组相比,COLP 组患者在 POD1 至 17 期间每天消耗的吗啡毫克当量减少了约 30%(-14.5 毫克吗啡当量;95%CI:[-26.8,-2.2])。COLP 组患者的每日最差疼痛评分也较低(10 分制下降 1.0 分;95%CI:[-2.0,-0.1]),尽管两组之间的平均每日疼痛差异无统计学意义(-0.8 分;95%CI:[-1.7,0.2])。这些发现表明,COLP 可能作为一种潜在的辅助镇痛疗法,在不增加疼痛的情况下,减少术后早期阿片类药物的消耗。
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