Streitberger Konrad, Harnik Michael A, Saliba Anna, Bischoff Nina, Blättler Larissa T, Schwegler Kyrill, Baumgartner Christine, Sutter Nora, Wertli Maria M
Department of Anaesthesiology and Pain Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Psychosomatic Medicine, Department of Neurology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Eur J Pain. 2025 May;29(5):e70010. doi: 10.1002/ejp.70010.
High-dose long-term opioid treatment for chronic non-cancer pain (CNCP) has become an increasing burden in industrialised countries. Opioid tapering and withdrawal in patients with CNCP remain challenging. This study evaluated a two-phase inpatient opioid withdrawal (OW) programme aimed at safely discontinuing opioid use in CNCP patients.
This prospective observational study was conducted from 2018 to 2023 at a Swiss tertiary care centre, involving CNCP patients on long-term opioid therapy (≥ 6 months, ≥ 100 mg morphine equivalent daily dose) who had failed outpatient withdrawal attempts. The programme consisted of a withdrawal phase (Phase 1) followed by multimodal pain rehabilitation (Phase 2). Outcomes included the proportion of patients opioid-free after Phase 2 (primary) and at 3 months, pain intensity changes, and adverse events (secondary).
Among the 38 enrolled patients (58% female, median age 54 years [IQR 49, 62]), 34 (89%) completed both phases, and 32 (84%) were opioid-free at the end of Phase 2. At 3 months, 23 patients (61%) remained opioid-free, while 4 (11%) resumed opioids, and 11 (29%) were lost to follow-up. Median pain intensity remained stable after discharge. One patient died by suicide 10 days post-withdrawal.
This two-phase inpatient withdrawal and rehabilitation programme enabled most CNCP patients to discontinue opioids without increased pain intensity, with a majority remaining opioid-free at 3 months. These findings highlight the importance of ongoing psychological support and careful patient selection in OW management.
This study introduces a structured inpatient opioid withdrawal model tailored for chronic non-cancer pain patients on high-dose opioid therapy, demonstrating that high cessation rates can be achieved without worsening pain intensity. By addressing the gap in care for patients who fail outpatient tapering, this research provides clinical insights into optimising withdrawal protocols and highlights the need for targeted resource allocation for intensive, multidisciplinary pain management. These findings support evidence-based decision-making in designing more effective opioid tapering strategies.
在工业化国家,大剂量长期使用阿片类药物治疗慢性非癌性疼痛(CNCP)已成为日益沉重的负担。CNCP患者的阿片类药物减量和戒断仍然具有挑战性。本研究评估了一个两阶段的住院阿片类药物戒断(OW)项目,旨在安全地使CNCP患者停用阿片类药物。
这项前瞻性观察性研究于2018年至2023年在瑞士一家三级护理中心进行,纳入长期接受阿片类药物治疗(≥6个月,每日剂量≥100毫克吗啡当量)且门诊戒断尝试失败的CNCP患者。该项目包括一个戒断阶段(第1阶段),随后是多模式疼痛康复(第2阶段)。结果包括第2阶段结束时(主要指标)和3个月时无阿片类药物使用的患者比例、疼痛强度变化以及不良事件(次要指标)。
在38名入组患者中(58%为女性,中位年龄54岁[四分位间距49, 62]),34名(89%)完成了两个阶段,32名(84%)在第2阶段结束时无阿片类药物使用。在3个月时,23名患者(61%)仍无阿片类药物使用,4名(11%)恢复使用阿片类药物,11名(29%)失访。出院后中位疼痛强度保持稳定。一名患者在戒断后10天自杀身亡。
这个两阶段的住院戒断和康复项目使大多数CNCP患者能够停用阿片类药物且疼痛强度未增加,大多数患者在3个月时仍无阿片类药物使用。这些发现凸显了在OW管理中持续心理支持和仔细选择患者的重要性。
本研究引入了一种为大剂量阿片类药物治疗的慢性非癌性疼痛患者量身定制的结构化住院阿片类药物戒断模型,表明可以在不加重疼痛强度的情况下实现高戒断率。通过解决门诊减量失败患者的护理缺口,本研究为优化戒断方案提供了临床见解,并强调了为强化多学科疼痛管理进行有针对性资源分配的必要性。这些发现支持在设计更有效的阿片类药物减量策略时进行基于证据的决策。