Institute for Clinical and Evaluative Sciences, Toronto, Ontario, Canada (JKE, ASW, PK); Centre for Addiction and Mental Health, Toronto, Ontario, Canada (PK); Northern Ontario School of Medicine, Sudbury, Ontario, Canada (JKE, AMF, DCM).
J Addict Med. 2019 May/Jun;13(3):182-187. doi: 10.1097/ADM.0000000000000476.
Benzodiazepine (BZD) use is common in patients who are engaged in methadone as a treatment for opioid use disorder. BZD prescribing is generally discouraged for this patient population due to the increased risk of BZD dependence and BZD use disorder, medication-assisted treatment (MAT) discontinuation, and opioid-overdose death. However, some patients have concurrent mental health disorders, where BZD use may be clinically indicated. This study evaluates the impact of prescribed BZD on MAT outcomes.
Linking urine drug screening data (UDS) and prescribing information from single-payer health records, we conducted a retrospective Kaplan-Meier analysis between patients using prescribed and nonprescribed BZD with methadone treatment retention as the primary outcome. Data are from a network of 52 outpatient clinics in Ontario, Canada, between January 1, 2006 and June 30, 2013.
We identified 3692 patients initiating methadone-assisted treatment for the first time; 76% were BZD-/UDS- (no BZD prescription and <30% screens positive for BZD); 13% were BZD+/UDS-; 6% BZD-/UDS+; and 6% BZD+/UDS+. Using 1-year treatment retention as a primary outcome, patients using nonprescribed BZD (BZD-/UDS+) were twice as likely (adjusted odds ratio 0.38, 95% confidence interval 0.27-0.53) to discontinue treatment as those not using BZD (BZD-/UDS-), or those using BZD in a prescribed manner (BZD+/UDS+).
Our findings suggest that prescribed BZD can be used during methadone MAT without impacting a patient's retention in MAT, but nonprescribed BZD use is predictive of treatment discontinuation. Importantly, we urge both the physician and patient to seek alternative clinical options to BZD prescribing, due to the potential for developing physical dependence (and BZD use disorder) to BZD and the risks of negative interactions with opioids.
苯二氮䓬类药物(BZD)在接受美沙酮治疗阿片类药物使用障碍的患者中很常见。由于 BZD 依赖和 BZD 使用障碍、药物辅助治疗(MAT)停药以及阿片类药物过量死亡的风险增加,一般不建议为这一患者群体开具 BZD 处方。然而,一些患者同时患有精神健康障碍,BZD 的使用可能在临床上是有指征的。本研究评估了处方 BZD 对 MAT 结局的影响。
通过将尿液药物检测(UDS)数据与单一支付者健康记录中的处方信息相联系,我们对接受美沙酮治疗的患者进行了一项回顾性 Kaplan-Meier 分析,以 MAT 保留作为主要结局。数据来自加拿大安大略省 52 家门诊诊所的网络,时间为 2006 年 1 月 1 日至 2013 年 6 月 30 日。
我们确定了 3692 名首次接受美沙酮辅助治疗的患者;76%为 BZD-/UDS-(无 BZD 处方,且 UDS 中 BZD 阳性率<30%);13%为 BZD+/UDS-;6%为 BZD-/UDS+;6%为 BZD+/UDS+。以 1 年治疗保留率作为主要结局,与未使用 BZD(BZD-/UDS-)或使用 BZD 处方方式(BZD+/UDS+)的患者相比,使用非处方 BZD(BZD-/UDS+)的患者停止治疗的可能性增加了一倍(调整后的优势比 0.38,95%置信区间 0.27-0.53)。
我们的研究结果表明,在接受美沙酮 MAT 期间,可以开具处方 BZD,而不会影响患者对 MAT 的保留率,但非处方 BZD 的使用与治疗停药相关。重要的是,由于可能对 BZD 产生身体依赖(和 BZD 使用障碍)以及与阿片类药物发生负性相互作用的风险,我们敦促医生和患者寻求替代的临床选择,而不是开 BZD 处方。