Department of Palliative, Rehabilitation, and Integrative Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Pharmacy Services, The University of Texas Southwestern Medical Center, Dallas, Texas.
Cancer. 2021 Mar 15;127(6):968-975. doi: 10.1002/cncr.33326. Epub 2020 Nov 24.
There is limited information regarding the true frequency of nonmedical opioid use (NMOU) among patients receiving opioid therapy for cancer pain. Data to guide patient selection for urine drug testing (UDT) as well as the timing and frequency of ordering UDT are insufficient. This study examined the frequency of abnormal UDT among patients with cancer who underwent random UDT and their characteristics.
Demographic and clinical information for patients with cancer who underwent random UDT were retrospectively reviewed and compared with a historical cohort that underwent targeted UDT. Random UDT was ordered regardless of a patient's risk potential for NMOU. Targeted UDT was ordered on the basis of a physician's estimation of a patient's risk for NMOU.
In all, 552 of 573 eligible patients (96%) underwent random UDT. Among these patients, 130 (24%) had 1 or more abnormal results; 38 of the 88 patients (43%) who underwent targeted UDT had 1 or more abnormal results. When marijuana was excluded, 15% of the random group and 37% of the targeted group had abnormal UDT findings (P < .001). It took a shorter time from the initial consultation to detect 1 or more abnormalities with the random test than the targeted test (median, 130 vs 274 days; P = .02). Abnormal random UDT was independently associated with younger age (P < .0001), male sex (P = .03), Cut Down, Annoyed, Guilty, and Eye Opener-Adapted to Include Drugs positivity (P = .001), and higher Edmonton Symptom Assessment System anxiety (P = .01).
Approximately 1 in 4 patients receiving opioids for cancer pain at a supportive care clinic who underwent random UDT had 1 or more abnormalities. Random UDT detected abnormalities earlier than the targeted test. These findings suggest that random UDT is justified among patients with cancer pain.
接受阿片类药物治疗癌痛的患者中,非医疗性阿片类药物使用(NMOU)的真实频率有限。指导患者选择尿液药物检测(UDT)以及进行 UDT 的时间和频率的数据不足。本研究检查了接受随机 UDT 的癌症患者中异常 UDT 的频率及其特征。
回顾性审查了接受随机 UDT 的癌症患者的人口统计学和临床信息,并与接受靶向 UDT 的历史队列进行了比较。随机 UDT 是在不考虑患者 NMOU 风险的情况下进行的。靶向 UDT 是根据医生对患者 NMOU 风险的估计进行的。
共有 573 名符合条件的患者中有 552 名(96%)接受了随机 UDT。在这些患者中,130 名(24%)有 1 项或多项异常结果;88 名接受靶向 UDT 的患者中有 38 名(43%)有 1 项或多项异常结果。排除大麻后,随机组的 15%和靶向组的 37%有异常 UDT 发现(P<.001)。与靶向测试相比,随机测试发现 1 项或多项异常的时间更短(中位数分别为 130 天和 274 天;P=.02)。异常随机 UDT 与年龄较小(P<.0001)、男性(P=.03)、 Cut Down,Annoyed,Guilty,and Eye Opener-Adapted to Include Drugs 阳性(P=.001)和更高的 Edmonton 症状评估系统焦虑(P=.01)独立相关。
在接受姑息治疗诊所阿片类药物治疗癌痛的患者中,约有 1/4 接受随机 UDT 的患者有 1 项或多项异常。随机 UDT 比靶向测试更早发现异常。这些发现表明随机 UDT 是合理的在癌症疼痛患者中。