脑外伤后的慢性疼痛:合作护理方法。

IF 1.3 Q3 REHABILITATION
Frontiers in rehabilitation sciences Pub Date : 2024-08-26 eCollection Date: 2024-01-01 DOI:10.3389/fresc.2024.1398856
Mary C Curran, Sylvia Lucas, Jesse R Fann, Jennifer M Zumsteg, Jeanne M Hoffman
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引用次数: 0

摘要

导言:慢性疼痛是创伤性脑损伤(TBI)后的常见症状,经常会限制日常活动,并与社区参与减少等负面结果相关。尽管慢性疼痛有负面影响,但很少有创伤性脑损伤患者得到有效治疗。本文介绍了一种协作护理(CC)干预--"TBI 护理",该疗法专门用于治疗 TBI 患者的慢性疼痛,强调专家临床医生的意见、认知行为疗法(CBT)技术以及其他非药物方法来减少疼痛干扰。方法:79 名参与者参与了来自两家学术医疗康复诊所的 CC 干预,每周对疼痛强度、干扰和药物使用情况进行评估。通过在最后一次治疗和/或加强治疗中与护理经理(CM)面谈,收集参与者对干预的反馈意见。医疗服务提供者的反馈则通过干预后的保密调查收集:90%的参与者至少接受了护理经理(CM)12次目标疗程中的11次,其中大部分是通过电话进行的。参与者平均认可了 7 个疼痛位置。所有参与者都接受了疼痛教育、自我监控技能、目标设定/行为激活和放松训练。由心理医生每周跟踪的疼痛干扰评分(对活动和享受的影响)在各疗程中显著下降。89% 的参与者获得了 CBT 技能建议,65% 的参与者获得了针对疼痛干扰的其他治疗转介,43% 的参与者获得了护理协调。75% 的参与者在第一次和最后一次疗程中都报告了 6 种或更多的药物/补充剂,建议主要针对头痛治疗进行更改。参与者和医疗服务提供者的反馈都很积极:讨论:"创伤性脑损伤护理 "是一种新颖的以患者为中心的CC方法,其实施灵活,符合创伤性脑损伤和慢性疼痛患者的需求,参与者参与度高,参与者和医疗服务提供者满意度高。这种方法优先考虑疼痛自我管理策略和其他非药物治疗方法,同时优化药物治疗,在干预期间显著降低了自我报告的疼痛干扰和疼痛强度。在创伤性脑损伤中使用CC模式是可行的,它成功地改善了慢性疼痛循证治疗的可及性,并提高了疼痛干扰和疼痛强度的治疗效果:临床试验注册:ClinicalTrials.gov,标识符 NCT03523923。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chronic pain after traumatic brain injury: a collaborative care approach.

Introduction: Chronic pain is common after traumatic brain injury (TBI), frequently limits daily activities, and is associated with negative outcomes such as decreased community participation. Despite the negative impact of chronic pain, few people with TBI receive effective treatment. This paper describes a collaborative care (CC) intervention, TBI Care, adapted specifically to treat chronic pain in people living with TBI, emphasizing expert clinician input, cognitive behavioral therapy (CBT) techniques, and other non-pharmacological approaches for decreasing pain interference.

Methods: 79 participants engaged in the CC intervention from two academic medical rehabilitation clinics with weekly assessments of pain intensity, interference, and medication use. Participant feedback on the intervention was gathered by interview with the care manager (CM) at the last treatment session and/or booster session. Provider feedback was gathered by a confidential survey post intervention.

Results: Ninety percent of participants received at least 11 of the target 12 sessions with a care manager (CM), the majority occurring over the phone. Participants endorsed an average of 7 pain locations. All participants received pain education, skills in self-monitoring, goal setting/behavioral activation and relaxation training. Pain interference scores (impact on activity and enjoyment), tracked weekly by the CM, significantly decreased across sessions. 89% of participants received recommendations for CBT skills, 65% received referrals for additional treatments targeting pain interference, and 43% received care coordination. 75% of participants reported 6 or more medications/supplements at both the first and last session, with changes recommended primarily for headache treatment. Feedback from participants and providers was positive.

Discussion: TBI Care, a novel patient-centered CC approach, was flexibly delivered, tailored to the needs of those living with TBI and chronic pain, with a high level of participant engagement, and satisfaction among participants and providers. This approach, prioritizing pain self-management strategies and other non-pharmacological approaches, along with optimizing pharmacological treatment, led to significant reductions in self-reported pain interference and intensity during the intervention. Using a CC model in TBI is feasible and successfully improved access to evidence-based treatments for chronic pain as well as outcomes for pain interference and intensity.

Clinical trial registration: ClinicalTrials.gov, identifier NCT03523923.

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