Association between trajectories of prescription opioid use and risk of opioid use disorder and overdose among US nonmetastatic breast cancer survivors

被引:0
|
作者
Chang, Ching-Yuan [1 ]
Jones, Bobby L. [1 ]
Hincapie-Castillo, Juan M. [2 ]
Park, Haesuk [1 ,3 ]
Heldermon, Coy D. [4 ]
Diaby, Vakaramoko [1 ,3 ]
Wilson, Debbie L. [1 ]
Lo-Ciganic, Wei-Hsuan [5 ,6 ,7 ]
机构
[1] Univ Florida, Coll Pharm, Dept Pharmaceut Outcomes & Policy, Gainesville, FL 32611 USA
[2] Univ N Carolina, Dept Epidemiol, Chapel Hill, NC 27599 USA
[3] Univ Florida, Coll Pharm, Ctr Drug Evaluat & Safety, Gainesville, FL 32611 USA
[4] Univ Florida, Coll Med, Dept Med, Gainesville, FL 32611 USA
[5] Univ Pittsburgh, Sch Med, Div Gen Internal Med, Pittsburgh, PA 15260 USA
[6] Univ Pittsburgh, Ctr Pharmaceut Policy & Prescribing, Pittsburgh, PA 15260 USA
[7] North Florida South Georgia Vet Hlth Syst, Geriatr Res Educ & Clin Ctr, Gainesville, FL 32608 USA
关键词
Prescription opioid; Opioid use disorder; Opioid overdose; Breast cancer; Medicare; PROPENSITY SCORE METHODS; CHRONIC PAIN; PRESCRIBING PATTERNS; THERAPY; REGRESSION; GUIDELINE; OUTCOMES; SURGERY; EVENTS; STATES;
D O I
10.1007/s10549-023-07205-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To examine the association between prescription opioid use trajectories and risk of opioid use disorder (OUD) or overdose among nonmetastatic breast cancer survivors by treatment type.Methods This retrospective cohort study included female nonmetastatic breast cancer survivors with at least 1 opioid prescription fill in 2010-2019 Surveillance, Epidemiology and End Results linked Medicare data. Opioid mean daily morphine milligram equivalents (MME) calculated within 1.5 years after initiating active breast cancer therapy. Group-based trajectory models identified distinct opioid use trajectory patterns. Risk of time to first OUD/overdose event within 1 year after the trajectory period was calculated for distinct trajectory groups using Cox proportional hazards models. Analyses were stratified by treatment type.Results Four opioid use trajectories were identified for each treatment group. For 38,030 survivors with systemic endocrine therapy, 3 trajectories were associated with increased OUD/overdose risk compared with early discontinuation: minimal dose (< 5 MME; adjusted hazard ratio [aHR] = 1.73 [95% CI 1.43-2.09]), very low dose (5-25 MME; 2.67 [2.05-3.48]), and moderate dose (51-90 MME; 6.20 [4.69-8.19]). For 9477 survivors with adjuvant chemotherapy, low-dose opioid use was associated with higher OUD/overdose risk (aHR = 7.33 [95% CI 2.52-21.31]) compared with early discontinuation. For 3513 survivors with neoadjuvant chemotherapy, the differences in OUD/OD risks across the 4 trajectories were not significant.Conclusions Among Medicare nonmetastatic breast cancer survivors receiving systemic endocrine therapy or adjuvant chemotherapy, compared with early discontinuation, low-dose or moderate-dose opioid use were associated with six- to sevenfold higher OUD/overdose risk. Breast cancer survivors at high-risk of OUD/overdose may benefit from targeted interventions (e.g., pain clinic referral).
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收藏
页码:561 / 577
页数:17
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