癌症患者和非癌症患者的长期阿片类药物治疗轨迹和过量

BMJ oncology Pub Date : 2023-01-01 Epub Date: 2023-07-03 DOI:10.1136/bmjonc-2022-000023
Jessica S Merlin, Anne C Black, Amanda M Midboe, Lara Troszak, Steven M Asch, Amy Bohnert, Brenda T Fenton, Karleen F Giannitrapani, Peter Glassman, Robert D Kerns, Maria Silveira, Karl A Lorenz, Erica A Abel, William C Becker
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引用次数: 0

摘要

大多数癌症患者都会经历疼痛,阿片类药物是治疗的基石。我们的目标是(1)确定长期阿片类药物治疗(LTOT)的模式或轨迹及其在癌症和非癌症患者中的相关性;(2)考虑到癌症的潜在调节作用,评估轨迹与阿片类药过量风险之间的关联。我们对美国退伍军人健康管理局数据库中有癌症和无癌症LTOT事件的个体进行了回顾性队列研究(N=44 351;N=285 772)。我们研究了LTOT轨迹与所有国际疾病分类(ICD)-9定义和ICD-10定义的意外和故意阿片类药物相关过量之间的关系。在没有癌症的患者中观察到并在癌症患者中复制的阿片类药物接收轨迹为:低剂量/稳定趋势、低剂量/降级趋势、中等剂量/稳定倾向、中等剂量-二次下降趋势升级和高剂量-二次下降趋势升级。较高的剂量和不断上升的轨迹显著预测了首次服药过量的时间;这两种低剂量轨迹具有相似、较低的风险。中等剂量、中等剂量/二次下降上升和高剂量/二次下降上升趋势的条件HR(99%CI)分别为1.84(1.18至2.85)、2.56(1.54至4.25)和2.41(1.37至4.26)。轨迹对用药过量时间的影响没有因癌症的存在而不同;当限制在癌症3/4期患者时,重复了推论。癌症患者面临阿片类药物过量风险,如无癌症患者。未来的研究应寻求扩大和解决我们对癌症患者阿片类药物风险的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-term opioid therapy trajectories and overdose in patients with and without cancer.

Objective: Pain is experienced by most patients with cancer and opioids are a cornerstone of management. Our objectives were (1) to identify patterns or trajectories of long-term opioid therapy (LTOT) and their correlates among patients with and without cancer and (2) to assess the association between trajectories and risk for opioid overdose, considering the potential moderating role of cancer.

Methods and analysis: We conducted a retrospective cohort study among individuals in the US Veterans Health Administration (VHA) database with incident LTOT with and without cancer (N=44,351; N=285,772, respectively) between 2010-2017. We investigated the relationship between LTOT trajectory and all International Classification of Diseases-9 and 10-defined accidental and intentional opioid-related overdoses.

Results: Trajectories of opioid receipt observed in patients without cancer and replicated in patients with cancer were: low-dose/stable trend, low-dose/de-escalating trend, moderate-dose/stable trend, moderate-dose/escalating with quadratic downturn trend, and high-dose/escalating with quadratic downturn trend. Time to first overdose was significantly predicted by higher-dose and escalating trajectories; the two low-dose trajectories conferred similar, lower risk. Conditional hazard ratios (99% CI) for the moderate-dose, moderate-dose/escalating with quadratic downturn and high-dose/escalating with quadratic downturn trends were 1·84 (1·18, 2·85), 2·56 (1·54, 4·25), and 2·41 (1·37, 4·26), respectively. Effects of trajectories on time to overdose did not differ by presence of cancer; inferences were replicated when restricting to patients with stage 3/4 cancer.

Conclusion: Patients with cancer face opioid overdose risks like patients without cancer. Future studies should seek to expand and address our knowledge about opioid risk in cancer patients.

Trial registration: None.

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