Department of Radiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Cancer Prevention Fellowship Program, Division of Cancer Prevention, Healthcare Delivery Research Program, Division of Cancer Control and Population Sciences, National Cancer Institute, Bethesda, MD, USA.
Cancer Med. 2021 Mar;10(6):2175-2187. doi: 10.1002/cam4.3810. Epub 2021 Feb 26.
Dosing limits in opioid clinical practice guidelines in the United States are likely misapplied to cancer patients, however, opioid use may be difficult to ascertain as they are largely excluded from opioid use studies.
The primary objective was to determine whether cancer patients were more likely to be chronic opioid users after diagnosis. We described prescription opioid use among U.S. older adult cancer patients during two time periods, within 2 years of diagnosis (short-term) and at least 2 years beyond diagnosis (long-term), compared to those without cancer (controls). Among participants in the Prostate, Lung, Colorectal, and Ovarian (PLCO) screening trial with linkages to Medicare Part D data during 2011-2015, we used multivariable logistic regression to estimate the association between cancer diagnosis and opioid use outcomes controlling for demographics. The primary outcome of opioid use was measured with the following metrics: Any opioid use, chronic use (90 consecutive days supply of opioid use while allowing for a 7-day gap between refills), high use (average daily morphine equivalent (MME) ≥120 mg for any 90-day period), and total MME dose above 2,000 mg (MME ).
The short-term cohort included 1,491 cancer patients and 24,930 controls. Any use in the 2-year post-diagnosis period was higher among cancer patients OR 3.3 (95% CI: 3.0-3.7). Chronic use rates were similar by cancer status (4.6% vs. 3.8% for cases and controls, respectively). The long-term cohort included 4,377 cancer patients and 27,545 controls. Rates of any use were similar among cancer patients and controls (63% vs. 59%).
Any opioid use was similar among long-term cancer survivors compared to controls, but differed among short-term survivors for any opioid use and marginally for chronic opioid use.
美国阿片类药物临床实践指南中的剂量限制可能不适用于癌症患者,然而,由于他们在很大程度上被排除在阿片类药物使用研究之外,因此阿片类药物的使用可能难以确定。
主要目的是确定癌症患者在诊断后是否更有可能成为慢性阿片类药物使用者。我们描述了美国老年癌症患者在诊断后 2 年内(短期)和至少 2 年(长期)内与无癌症患者(对照组)相比,处方阿片类药物的使用情况。在 2011-2015 年期间与医疗保险 Part D 数据相关联的前列腺癌、肺癌、结直肠癌和卵巢癌(PLCO)筛查试验的参与者中,我们使用多变量逻辑回归来估计癌症诊断与阿片类药物使用结果之间的关联,同时控制人口统计学因素。阿片类药物使用的主要结果是通过以下指标来衡量的:任何阿片类药物使用、慢性使用(在 90 天的阿片类药物使用期间,允许在每次续药之间有 7 天的间隔)、高使用(任何 90 天期间的平均每日吗啡当量(MME)≥120mg)和总 MME 剂量超过 2000mg(MME)。
短期队列包括 1491 名癌症患者和 24930 名对照。在诊断后 2 年内,癌症患者的任何使用发生率均较高,OR 为 3.3(95%CI:3.0-3.7)。癌症患者和对照组的慢性使用率相似(分别为 4.6%和 3.8%)。长期队列包括 4377 名癌症患者和 27545 名对照。癌症患者和对照组的任何使用发生率相似(分别为 63%和 59%)。
与对照组相比,长期癌症幸存者的任何阿片类药物使用情况相似,但短期幸存者的任何阿片类药物使用情况和慢性阿片类药物使用情况略有不同。