Persistent prescription opioid use and all-cause mortality following the first-year breast cancer survivorship.

IF 4.1 Q2 ONCOLOGY
Rulin C Hechter, Lie Hong Chen, Jiaxiao Shi, Zheng Gu, Moira Brady-Rogers, Rowan T Chlebowski, Reina Haque
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引用次数: 0

Abstract

Background: Harm associated with persistent opioid use beyond the first-year intensive cancer treatment is underinvestigated in cancer survivors. We examined rates and risk factors for persistent opioid use and all-cause mortality after the first-year breast cancer survivorship.

Methods: This retrospective cohort study used electronic health record data from Kaiser Permanente Southern California for women diagnosed with a nonmetastatic breast cancer between 2009 and 2019 who filled 2 or more opioid prescriptions. Rates of persistent opioid use were estimated from first-year survivorship through December 31, 2021. Rate ratios (RRs) and 95% confidence intervals (CIs) for factors associated with persistent use were estimated using a multivariable Poisson regression model. Hazard ratios (HRs) for all-cause mortality associated with persistent opioid use were estimated using multivariable Cox regression models.

Results: Of 14 347 eligible individuals (mean [SD] age = 61.9 [12.5]), 2285 (15.9%) developed persistent opioid use, with an incident rate of 25.5 per 1000 person-years. Risk factors included older age (≥65 vs < 65 years: RR = 1.63, 95% CI = 1.24 to 2.14), smoking (current: 1.89, 1.68 to 2.13; former: 1.30, 1.20 to 1.41), baseline comorbidities (Elixhauser Comorbidity Index 5+ vs 0: 1.70, 1.29 to 2.24), and substance use disorders (1.58, 1.43 to 1.74). All-cause mortality was doubled among individuals with persistent use (51.6, 48.0 to 55.6 per 1000 person-years) than in those without (25.3, 24.2 to 26.4). Persistent use was associated with an increased all-cause mortality (adjusted HR = 1.84, 1.66 to 2.04).

Conclusions: Persistent opioid use was common in breast cancer survivors and associated with increased mortality. Further research is needed to explore factors that may be contributing to increased mortality.

Abstract Image

持续处方阿片类药物使用与乳腺癌第一年生存率后的全因死亡率
背景:在癌症幸存者中,超过第一年强化癌症治疗后持续使用阿片类药物的危害尚不清楚。我们检查了持续使用阿片类药物的比率和风险因素以及乳腺癌存活一年后的全因死亡率。方法:这项回顾性队列研究使用了南加州凯撒医疗机构的电子健康记录数据,用于2009年至2019年期间被诊断为非转移性乳腺癌、服用两种或两种以上阿片类药物处方的女性。从第一年生存率到2021年12月31日,持续阿片类药物使用率进行了估计。使用多变量泊松回归模型估计与持续使用相关因素的比率比(RR)和95%置信区间(CI)。使用多变量Cox回归模型估计与持续使用阿片类药物相关的全因死亡率的风险比(HR)。结果:在14347名符合条件的个体(平均[SD]年龄为61.9[12.5])中,2285名(15.9%)持续使用阿片类药物,发生率为25.5 / 1000人年。危险因素包括年龄较大(≥65岁vs .结论:持续使用阿片类药物在乳腺癌幸存者中很常见,并与死亡率增加相关。需要进一步的研究来探索可能导致死亡率增加的因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JNCI Cancer Spectrum
JNCI Cancer Spectrum Medicine-Oncology
CiteScore
7.70
自引率
0.00%
发文量
80
审稿时长
18 weeks
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