...
首页> 外文期刊>Pain medicine : >'My Surgical Success': Effect of a Digital Behavioral Pain Medicine Intervention on Time to Opioid Cessation After Breast Cancer Surgery-A Pilot Randomized Controlled Clinical Trial
【24h】

'My Surgical Success': Effect of a Digital Behavioral Pain Medicine Intervention on Time to Opioid Cessation After Breast Cancer Surgery-A Pilot Randomized Controlled Clinical Trial

机译:“我的手术成功”:乳腺癌手术后的数字行为疼痛医学干预对阿片类药物的影响 - 试点随机对照临床试验

获取原文
获取原文并翻译 | 示例

摘要

Objective. This study aims to assess the feasibility of digital perioperative behavioral pain medicine intervention in breast cancer surgery and evaluate its impact on pain catastrophizing, pain, and opioid cessation after surgery. Design and Setting. A randomized controlled clinical trial was conducted at Stanford University (Palo Alto, CA, USA) comparing a digital behavioral pain medicine intervention ("My Surgical Success" [MSS]) with digital general health education (HE). Participants. A convenience sample of 127 participants were randomized to treatment group. The analytic sample was 68 patients (N = 36 MSS, N = 32 HE). Main Outcomes. The primary outcome was feasibility and acceptability of a digital behavioral pain medicine intervention (80% threshold for acceptability items). Secondary outcomes were pain catastrophizing, past seven-day average pain intensity, and time to opioid cessation after surgery for patients who initiated opioid use. Results. The attrition rate for MSS intervention (44%) was notably higher than for HE controls (18%), but it was lower than typical attrition rates for e-health interventions (60-80%). Despite greater attrition for MSS, feasibility was demonstrated for the 56% of MSS engagers, and the 80% threshold for acceptability was met. We observed a floor effect for baseline pain catastrophizing, and no significant group differences were found for post-surgical pain catastrophizing or pain intensity. MSS was associated with 86% increased odds of opioid cessation within the 12-week study period relative to HE controls (hazard ratio = 1.86, 95% confidence interval = 1.12-3.10, P = 0.016). Conclusions. Fifty-six percent of patients assigned to MSS engaged with the online platform and reported high satisfaction. MSS was associated with significantly accelerated opioid cessation after surgery (five-day difference) with no difference in pain report relative to controls. Perioperative digital behavioral pain medicine may be a low-cost, accessible adjunct that could promote opioid cessation after breast cancer surgery.
机译:客观的。本研究旨在评估乳腺癌手术中数字围手术期行为止痛药干预的可行性,并评估手术后对疼痛灾难,疼痛和阿片类药物的影响。设计和设置。随机对照临床试验在斯坦福大学(Palo Alto,CA,USA)进行了比较了数字行为止痛药干预(“我的手术成功”[MSS]),具有数字普通健康教育(他)。参与者。 127名参与者的便利样本被随机分为治疗组。分析样本为68名患者(n = 36毫秒,n = 32 HE)。主要结果。主要结果是数字行为止痛药干预的可行性和可接受性(可接受性项目的80%阈值)。二次结果是疼痛灾难性,过去七天的平均疼痛强度,并且手术后的阿片类药物戒烟时间,用于开始阿片类药物的患者。结果。 MSS干预的磨损率(44%)显着高于他的控制(18%),但它低于电子健康干预措施的典型磨损率(60-80%)。尽管MSS更大的消磨,但是对于56%的MSS引擎证明了可行性,并且满足了80%的可接受性阈值。我们观察到基线疼痛灾害灾害的楼层效果,并且没有发现外科疼痛灾害或疼痛强度的显着群体差异。 MSS与相对于他控制的12周的研究期内的阿片类药物戒烟的可能性增加了86%(危险比= 1.86,95%置信区间= 1.12-3.10,P = 0.016)。结论。 56%的患者分配给与在线平台进行的MSS并报告高满意度。在手术后(五天差异)后,MSS与显着加速的阿片样物质停止有关,疼痛报告无差异相对于控制。围手术期数字行为疼痛药物可能是一种低成本,可访问的辅助药物,可促进乳腺癌手术后的阿片类药物。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号