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一项针对接受腰椎融合手术患者的高灾难化认知行为疗法的随机对照试验:TRIBECA 研究。

A randomized controlled TRIal of cognitive BEhavioral therapy for high Catastrophizing in patients undergoing lumbar fusion surgery: the TRIBECA study.

机构信息

Neurosurgical Service, Neurocenter of Southern Switzerland, Lugano, Switzerland.

Department of Neurosurgery, Zuyderland Medical Center, Heerlen/Sittard-Geleen, The Netherlands.

出版信息

BMC Musculoskelet Disord. 2020 Dec 4;21(1):810. doi: 10.1186/s12891-020-03826-w.

Abstract

BACKGROUND

Around 20% of patients undergoing spinal fusion surgery have persistent back or leg pain despite surgery. Pain catastrophizing is the strongest psychological predictor for chronic postsurgical pain. Psychological variables are modifiable and could be target for intervention. However, randomized controlled trials evaluating the effectiveness of psychological interventions to reduce chronic pain and disability after spinal fusion in a population of patients with high preoperative pain catastrophizing scores are missing. The aim of our study is to examine whether an intervention targeting pain catastrophizing mitigates the risk of chronic postsurgical pain and disability. Our primary hypothesis is that targeted perioperative cognitive behavioral therapy decreases the risk of chronic postsurgical pain and disability after spinal fusion surgery in high catastrophizing patients.

METHODS

We will perform a two-center prospective, single-blind, randomized, controlled study comparing lumbar spinal fusion surgery outcome between 2 cohorts. Adult patients selected for lumbar spinal fusion with decompression surgery and a minimum score of 24 on the pain catastrophizing scale will be randomized with 1:1 allocation for either perioperative cognitive behavioral therapy (intervention group) or a perioperative education plus progressive exercise program (control group). Patients randomized to the intervention group will receive six individual sessions of cognitive behavioral therapy, two sessions before the operation and four after. Primary outcome is the Core Outcome Measures Index at 12 months. Secondary outcomes include pain, disability, depression and quality of life.

DISCUSSION

This is the first trial that evaluates the effectiveness of cognitive behavioral therapy as a perioperative tool to improve pain and disability after spinal fusion surgery in comparison with an educational/exercise control intervention, in patients with high levels of pain catastrophizing. If perioperative cognitive behavioral therapy proves to be effective, this might have important clinical implications, reducing the incidence of chronic postsurgical pain and improving outcome after spinal fusion surgery.

TRIAL REGISTRATION

Clinicaltrials ( NCT03969602 ). Registered 31 May 2019.

摘要

背景

尽管接受了手术,仍有约 20%的脊柱融合手术患者持续存在腰背或腿部疼痛。疼痛灾难化是慢性术后疼痛的最强心理预测指标。心理变量是可改变的,可以作为干预的目标。然而,缺乏针对术前疼痛灾难化评分高的患者人群,评估脊柱融合术后心理干预对减少慢性疼痛和残疾的有效性的随机对照试验。我们的研究目的是检验针对疼痛灾难化的干预是否能降低脊柱融合术后慢性疼痛和残疾的风险。我们的主要假设是,针对围手术期认知行为疗法可降低高灾难化患者脊柱融合手术后慢性术后疼痛和残疾的风险。

方法

我们将进行一项为期 12 个月的前瞻性、单盲、随机、对照研究,比较两组腰椎融合手术结果。选择接受减压手术的腰椎融合术且疼痛灾难化量表得分至少为 24 分的成年患者将以 1:1 的比例随机分为围手术期认知行为疗法(干预组)或围手术期教育加渐进性运动方案(对照组)。随机分组至干预组的患者将接受 6 次个体认知行为疗法,术前 2 次,术后 4 次。主要结局为 12 个月时的核心结局测量指标。次要结局包括疼痛、残疾、抑郁和生活质量。

讨论

这是第一项评估认知行为疗法作为围手术期工具,与教育/运动对照干预相比,在疼痛灾难化水平较高的患者中改善脊柱融合手术后疼痛和残疾的有效性的试验。如果围手术期认知行为疗法被证明有效,这可能具有重要的临床意义,可以降低慢性术后疼痛的发生率,改善脊柱融合手术后的结局。

试验注册

Clinicaltrials(NCT03969602)。2019 年 5 月 31 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a7f/7718692/84d10f3a6f02/12891_2020_3826_Fig1_HTML.jpg

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