基于远程医疗的数字认知行为干预治疗全膝关节置换术围手术期焦虑和抑郁。

Journal of pain & relief Pub Date : 2023-01-01 Epub Date: 2023-09-27
Ata Murat Kaynar, Nicole Zharichenko, Ajay D Wasan, Jacques E Chelly
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引用次数: 0

摘要

引言:术前焦虑和抑郁已被证明会使接受单侧全膝关节置换术(TKA)的患者术后疼痛和阿片类药物消耗增加50%。我们假设,在手术前一个月开始使用基于远程医疗的数字认知行为干预计划(RxWell®)可以控制手术前的焦虑和抑郁。材料和方法:这是一项随机对照试验,纳入了接受原发性单侧TKA的患者。至少在手术前一个月,同意参与的患者被要求填写PROMIS®(患者报告结果测量信息系统)情绪焦虑简表8a和PROMIS®情绪抑郁简表8a问卷。T评分≥57的患者在手术前一个月被随机分为无干预组(对照组)或RxWell®方案(治疗组)。这项概念验证研究的主要结果是RxWell®使患者PROMIS焦虑T评分正常化的能力。结果:随机分组到RxWell®组的患者的焦虑和抑郁T评分从随机分组时的64.3±3.0显著降低到手术前的58.5±2.6(n=5,p=0.006),而对照组的T评分没有变化(随机分组时为59.4±4.2,57.7±6.2;n=6,p=0.559)。结论:这些初步数据表明,使用RxWell®程序是在手术前控制焦虑和抑郁的有效方法。相比之下,在没有治疗的情况下,手术前一个多月的焦虑水平似乎保持相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Telemedicine-Based Digital Cognitive Behavioral Intervention for Perioperative Anxiety and Depression for Total Knee Arthroplasty.

Telemedicine-Based Digital Cognitive Behavioral Intervention for Perioperative Anxiety and Depression for Total Knee Arthroplasty.

Telemedicine-Based Digital Cognitive Behavioral Intervention for Perioperative Anxiety and Depression for Total Knee Arthroplasty.

Telemedicine-Based Digital Cognitive Behavioral Intervention for Perioperative Anxiety and Depression for Total Knee Arthroplasty.

Introduction: Preoperative anxiety and depression have been shown to increase postoperative pain and opioid consumption by up to 50% in patients undergoing primary unilateral Total Knee Arthroplasty (TKA). We hypothesized that the use of a telemedicine-based digital Cognitive Behavioral Intervention program (RxWell®) started one month prior to surgery would control anxiety and depression prior to surgery.

Materials and methods: This was a randomized, controlled trial that enrolled patients undergoing primary unilateral TKA. At least a month prior to surgery, patients who gave consent to participate were asked to complete PROMIS® (Patient-Reported Outcomes Measurement Information System) emotional anxiety short form 8a and PROMIS® emotional depression short form-8a questionnaires. Patients with T-scores of ≥ 57 were randomized to either a no intervention (control group) or a RxWell® program (treatment group) for a month prior to surgery. The primary outcome of this proof-of-concept study was the ability of the RxWell® to normalize patients' PROMIS anxiety T scores.

Results: T scores for anxiety and depression among patients randomized to the RxWell® group significantly decreased from 64.3 ± 3.0 at the time of randomization to 58.5 ± 2.6 prior to surgery (n=5, p=0.006), whereas no changes in T scores were recorded in the control group (59.4 ± 4.2 at the time of randomization vs. 57.7 ± 6.2; n=6, p=0.559).

Conclusion: These preliminary data suggest that the use of a RxWell® program represents an effective approach to control anxiety and depression prior to surgery. In contrast, it seems that in the absence of treatment, anxiety level remains similar over a month prior to surgery.

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