数字肌肉骨骼程序治疗急性和亚急性疼痛后的临床结果:与对照组的观察性纵向研究。

Grace Wang, Manshu Yang, Mindy Hong, Jeffrey Krauss, Jeannie F Bailey
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引用次数: 1

摘要

背景:肌肉骨骼(MSK)疾病的远程康复治疗可能产生与常规治疗相似或更好的结果,但大多数远程康复研究仅针对慢性或术后疼痛。目的:我们的目的是检查参加数字MSK计划的急性和亚急性MSK疼痛个体与非参与者对照组在3,6和12周时的疼痛和功能。方法:我们进行了一项观察性的纵向研究,并与非参与者对照组进行了比较。干预组与物理治疗师进行视频访问,理疗师通过应用程序推荐运动疗法和教育文章。非参与者是那些已注册但由于福利覆盖尚未开始而无法参与的人。我们通过随访3周、6周和12周的调查收集疼痛和功能结果。我们进行了描述性分析、未调整回归和混合效应回归,调整基线特征、时间作为固定效应和时间*组相互作用项。结果:分析包括675名非参与者和262名干预组参与者的数据。与基线相比,在调整基线因素后,干预组在3、6和12周时的疼痛改善程度明显高于非参与者。具体来说,干预组的疼痛评分在3周时与基线相比下降了55.8%,6周时下降了69.1%,12周时下降了73%。干预组的调整疼痛评分从基线时的43.7分(95% CI 41.1-46.2)下降到3周时的19.3分(95% CI 16.8-21.8), 6周时的13.5分(95% CI 10.8-16.2), 12周时的11.8分(95% CI 9-14.6)。相比之下,非参与者的疼痛评分在3周时与基线相比下降了30.8%,在6周时下降了45.8%,在12周时下降了46.7%。非参与者调整后的疼痛评分从基线时的43.8 (95% CI 42-45.5)降至3周时的30.3 (95% CI 27.1-33.5), 6周时的23.7 (95% CI 20-27.5), 12周时的23.3 (95% CI 19.6-27)。经过调整后,在随访中报告疼痛好转或明显好转的参与者比例显著高于干预组参与者,3周时为40.6%,6周时为31.4%,12周时为31.2%。调整后,干预组与非干预组相比,在随访中功能显著改善的参与者比例在3周时显著高于15.2%,在12周时显著高于24.6%。结论:数字MSK程序可能有助于在短期内改善急性和亚急性MSK疼痛患者的疼痛和功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Clinical Outcomes After a Digital Musculoskeletal Program for Acute and Subacute Pain: Observational, Longitudinal Study With Comparison Group.

Background: Telerehabilitation for musculoskeletal (MSK) conditions may produce similar or better outcomes than usual care, but most telerehabilitation studies address only chronic or postsurgical pain.

Objective: We aimed to examine pain and function at 3, 6, and 12 weeks for individuals with acute and subacute MSK pain who took part in a digital MSK program versus a nonparticipant comparison group.

Methods: We conducted an observational, longitudinal study with a nonparticipant comparison group. The intervention group had video visits with physical therapists who recommended exercise therapies and educational articles delivered via an app. Nonparticipants were those who were registered but unable to participate because their benefit coverage had not yet begun. We collected pain and function outcomes through surveys delivered at 3-, 6-, and 12-week follow-ups. We conducted descriptive analyses, unadjusted regression, and mixed effects regression adjusting for baseline characteristics, time as fixed effects, and a time*group interaction term.

Results: The analysis included data from 675 nonparticipants and 262 intervention group participants. Compared to baseline, the intervention group showed significantly more pain improvement at 3, 6, and 12 weeks versus nonparticipants after adjusting for baseline factors. Specifically, the intervention group's pain scores decreased by 55.8% at 3 weeks versus baseline, 69.1% at 6 weeks, and 73% at 12 weeks. The intervention group's adjusted pain scores decreased from 43.7 (95% CI 41.1-46.2) at baseline to 19.3 (95% CI 16.8-21.8) at 3 weeks to 13.5 (95% CI 10.8-16.2) at 6 weeks to 11.8 (95% CI 9-14.6) at 12 weeks. In contrast, nonparticipants' pain scores decreased by 30.8% at 3 weeks versus baseline, 45.8% at 6 weeks, and 46.7% at 12 weeks. Nonparticipants' adjusted pain scores decreased from 43.8 (95% CI 42-45.5) at baseline to 30.3 (95% CI 27.1-33.5) at 3 weeks to 23.7 (95% CI 20-27.5) at 6 weeks to 23.3 (95% CI 19.6-27) at 12 weeks. After adjustments, the percentage of participants reporting that pain was better or much better at follow-up was significantly higher by 40.6% at 3 weeks, 31.4% at 6 weeks, and 31.2% at 12 weeks for intervention group participants versus nonparticipants. After adjustments, the percentage of participants with meaningful functional improvement at follow-up was significantly higher by 15.2% at 3 weeks and 24.6% at 12 weeks for intervention group participants versus nonparticipants.

Conclusions: A digital MSK program may help to improve pain and function in the short term among those with acute and subacute MSK pain.

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4.20
自引率
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发文量
31
审稿时长
12 weeks
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