College of Pharmacy, Ferris State University, Big Rapids, MI.
Department of Pharmacy Practice and Science, University of Kentucky College of Pharmacy, Lexington, KY; Institute for Pharmaceutical Outcomes and Policy, University of Kentucky College of Pharmacy, Lexington, KY.
Pain Physician. 2021 Mar;24(2):E249-E256.
Practice guidelines recommend urine drug monitoring (UDM) at least annually in the setting of chronic opioid therapy as an objective assessment of substance use. However, empirical evidence on who gets tested and how often testing occurs is lacking.
This study investigates 10-year UDM trends in the United States based on 2 factors: (1) the duration of prescription opioid treatment, and (2) having an opioid use disorder (OUD) diagnosis and medications for opioid use disorder (MOUD) prescriptions.
Observational cross-sectional study.
Research was conducted using administrative claims data from Optum's deidentified Clinformatics Data Mart Database for the period 2007 to 2016. The dataset contained information on the plan enrollment and health care claims from 50 states and the District of Columbia.
To examine trends in UDM based on the duration of prescription opioid treatment, persons receiving prescription opioid analgesics were categorized into 4 groups based on the number of days covered: (a) less than 90 days, (b) 90 to 179 days, (c) 180 to 269 days, and (d) at least 270 days. To examine trends based on an OUD diagnosis and MOUD prescriptions, persons diagnosed with OUD were identified and categorized based on the presence of MOUD prescriptions as follows: (a) OUD with buprenorphine (BPN) and naltrexone (NTX) in the same year; (b) OUD with BPN only; (c) OUD with NTX only; (d) OUD with chronic prescription opioid analgesics (>= 90 days); (e) OUD without prescription opioid analgesics, BPN, or NTX; and (f) chronic prescription opioid analgesics (>= 90 days) without an OUD diagnosis. For analysis, the percent receiving UDM was estimated per group per year. Then the data were restricted to those receiving at least one UDM to estimate the average number of UDM per person.
Data included an average of 364,485 persons per year receiving prescription opioid analgesics for chronic use, and 10,277 per year receiving an OUD diagnosis. Among those receiving prescription opioid analgesics, less than 50% received UDM. For those receiving at least one UDM, one additional UDM was performed per person as the duration of opioids increased by 90 days. Among persons with OUD, the percent receiving UDM was the highest for those receiving both BPN and NTX (87%), followed by those receiving BPN only (80%), chronic opioids (79%), NTX only (72%), and those not receiving any MOUD/opioids (54%).
Methadone dispensing for OUD treatments was not captured in administrative claims data.
Although recommended for patients with chronic pain, UDM is provided less than half of the time for these patients. However, once patients received at least one UDM, they would continue to receive it on a fairly regular basis. Compared with those with chronic pain, persons diagnosed with OUD are more likely to receive UDM at a more frequent interval.
实践指南建议在慢性阿片类药物治疗的情况下,至少每年进行一次尿液药物监测(UDM),作为对物质使用的客观评估。然而,缺乏关于谁接受了测试以及测试频率的经验证据。
本研究根据以下 2 个因素调查了美国 10 年来 UDM 的趋势:(1)处方阿片类药物治疗的持续时间,以及(2)患有阿片类药物使用障碍(OUD)诊断和阿片类药物使用障碍治疗药物(MOUD)处方。
观察性横截面研究。
使用 Optum 的匿名 Clinformatics Data Mart 数据库中的管理索赔数据进行研究,时间范围为 2007 年至 2016 年。该数据集包含来自 50 个州和哥伦比亚特区的计划参与和医疗保健索赔信息。
为了根据处方阿片类药物治疗的持续时间检查 UDM 的趋势,将接受处方阿片类药物镇痛剂的患者根据覆盖的天数分为 4 组:(a)少于 90 天,(b)90 至 179 天,(c)180 至 269 天,和(d)至少 270 天。为了根据 OUD 诊断和 MOUD 处方检查趋势,确定患有 OUD 的患者,并根据 MOUD 处方的存在进行如下分类:(a)同年 BPN 和 NTX 治疗的 OUD;(b)仅 BPN 治疗的 OUD;(c)仅 NTX 治疗的 OUD;(d)至少 90 天慢性处方阿片类药物镇痛剂治疗的 OUD;(e)无处方阿片类药物镇痛剂、BPN 或 NTX 的 OUD;和(f)至少 90 天的慢性处方阿片类药物镇痛剂而无 OUD 诊断。在分析中,估计了每年每个组接受 UDM 的百分比。然后,将数据限制为至少接受一次 UDM 的患者,以估计每个人的平均 UDM 次数。
数据包括每年平均有 364485 人接受慢性阿片类药物治疗,每年有 10277 人接受 OUD 诊断。在接受处方阿片类药物治疗的患者中,不到 50%接受了 UDM。对于接受至少一次 UDM 的患者,随着阿片类药物治疗时间延长 90 天,每人接受一次额外的 UDM。在患有 OUD 的患者中,接受 BPN 和 NTX 联合治疗的患者接受 UDM 的比例最高(87%),其次是仅接受 BPN 治疗的患者(80%)、慢性阿片类药物治疗的患者(79%)、仅接受 NTX 治疗的患者(72%)和未接受任何 MOUD/阿片类药物治疗的患者(54%)。
阿片类药物治疗 OUD 的美沙酮配给未包含在行政索赔数据中。
尽管推荐用于慢性疼痛患者,但这些患者接受 UDM 的时间不到一半。然而,一旦患者接受了至少一次 UDM,他们就会继续定期接受 UDM。与患有慢性疼痛的患者相比,被诊断为 OUD 的患者更有可能更频繁地接受 UDM。