Department of Pharmacy Practice, College of Pharmacy, University of Rhode Island, Kingston, Rhode Island, USA (HAA, ALB, JB, XW, SJK); Department of Biostatistics, Brown University School of Public Health, Providence, Rhode Island, USA (JWH); The Warren Alpert Medical School of Brown University, Providence, Rhode Island, USA (JDR).
J Addict Med. 2021 Apr 1;15(2):99-108. doi: 10.1097/ADM.0000000000000701.
To examine the association between initial patterns of prescription opioid supply (POS) and risk of all-cause mortality among an insured opioid-naïve patient population in the United States (US).
This retrospective observational cohort study used de-identified, administrative health care claims data from a large national insurer (Optum Clinformatics Data Mart) from 2010 to 2015. Participants included insured, cancer-free adults prescribed opioid analgesics. Prescription opioids received during the first 6 months of therapy were used to categorize initial patterns of POS as daily or nondaily. Cox regression was used to estimate the association of initial patterns of POS with all-cause mortality within one year of follow-up, adjusting for baseline covariates to control for confounding.
A total of 4,054,417 patients were included, of which 2.75% had incident daily POS; 54.8% were female; median age was 50 years; mean Charlson comorbidity index (CCI) was 0.21 (standard deviation = 0.77); and mean daily morphine milligram equivalent was 34.61 (95% confidence intervals: 34.59, 34.63). There were 2068 more deaths per 100,000 person-years among patients who were prescribed opioids daily than nondaily. After adjusting for baseline covariates, the hazard of all-cause mortality among patients with incident daily POS was nearly twice that among those prescribed nondaily (hazard ratio [HR] = 1.94; 95% confidence intervals: 1.84, 2.04).
Among insured adult patients with noncancer pain, incident chronic POS was associated with a significantly increased risk of all-cause mortality over at most 1 year of follow-up. Because these results may be susceptible to bias, more research is needed to establish causality.
在美国(US)的一个参保阿片类药物初治患者人群中,研究初始处方阿片类药物供应(POS)模式与全因死亡率之间的关联。
本回顾性观察队列研究使用了来自大型全国保险公司(Optum Clinformatics Data Mart)的匿名行政医疗保健索赔数据,时间范围为 2010 年至 2015 年。参与者包括接受处方阿片类镇痛药治疗的参保、无癌症的成年人。根据治疗的前 6 个月内接受的处方阿片类药物,将初始 POS 模式分类为每日或非每日。Cox 回归用于估计初始 POS 模式与随访 1 年内全因死亡率之间的关联,通过调整基线协变量来控制混杂因素。
共纳入 4054417 名患者,其中 2.75%发生每日 POS;54.8%为女性;中位年龄为 50 岁;平均 Charlson 合并症指数(CCI)为 0.21(标准差=0.77);平均每日吗啡毫克当量为 34.61(95%置信区间:34.59,34.63)。与接受非每日 POS 处方的患者相比,每日 POS 处方患者的每 100000 人年死亡人数多 2068 人。在调整了基线协变量后,每日 POS 患者的全因死亡率的风险几乎是非每日 POS 患者的两倍(风险比[HR] = 1.94;95%置信区间:1.84,2.04)。
在患有非癌性疼痛的参保成年患者中,新发慢性 POS 与最多 1 年的随访期间全因死亡率的显著增加相关。由于这些结果可能容易受到偏差的影响,因此需要进行更多的研究以确定因果关系。