Department of Health Policy and Management, Richard M. Fairbanks School of Public Health, IUPUI, 1050 Wishard Blvd, RG 5135, Indianapolis, IN 46202-2872, United States of America.
School of Liberal Arts, IUPUI, IN, United States of America.
Drug Alcohol Depend. 2021 Nov 1;228:109108. doi: 10.1016/j.drugalcdep.2021.109108. Epub 2021 Sep 25.
The 2016 Centers for Disease Control and Prevention guideline for prescribing opioids for chronic pain (Guideline hereafter) emphasized tapering patients from long-term opioid therapy (LTOT) when the harms outweigh the benefits.
To examine tapering from LTOT before and after the Guideline release, we conducted a retrospective cohort study of adults with high-dose LTOT (mean of >50 Morphine Milligram Equivalents [MME]/day) from 2014 to 2018 from one Midwest state's Health Information Exchange. We identified tapering (dose reductions in mean MME/day greater than 15%, 30%, 50%) and rapid discontinuation episodes (reduction to zero MME/day) over a 6-month follow-up period relative to a 3-month baseline period. We used segmented regressions to estimate outcomes adjusted for time trends and relevant state laws limiting opioid prescribing.
The Guideline release was associated with statistically significant immediate increase in the patient likelihood of experiencing tapering (15%: 1.8% point [95% confidence interval (CI): 1.2-2.6; 30%: 1.4% point, 95% CI: 0.7-2.2; 50%: 0.8% point, 95% CI: 0.2-1.4) and rapid discontinuation episodes (0.006% point, 95% CI: 0.001-0.01). After the Guideline release, the patient likelihood of tapering increased over time (15%: 0.4% point/month, 95% CI: 0.3-0.5; 30%: 0.3% point/month, 95% CI:0.2-0.4; 50%: 0.3% point/month, 95% CI: 0.2-0.3; rapid discontinuation: 0.01% point/month, 95% CI: 0.007-0.01). Tapering and rapid discontinuation trends was similar among gender and race categories.
The Guideline may be a useful tool in altering opioid prescribing practices, particularly for patients on shorter durations of LTOT.
2016 年疾病控制与预防中心发布的慢性疼痛阿片类药物处方指南(以下简称“指南”)强调,当长期阿片类药物治疗(LTOT)的危害大于益处时,应逐渐减少患者的用药剂量。
为了在指南发布前后检查 LTOT 的减量情况,我们对来自一个中西部州健康信息交换中心的 2014 年至 2018 年期间接受高剂量 LTOT(平均剂量超过 50 毫克吗啡等效剂量[MME]/天)的成年人进行了回顾性队列研究。我们在 6 个月的随访期间,与 3 个月的基线期相比,确定了减量(平均 MME/天减少大于 15%、30%、50%)和快速停药事件(减少到零 MME/天)。我们使用分段回归来估计调整时间趋势和限制阿片类药物处方的相关州法律的结果。
指南的发布与患者接受减量治疗的可能性显著增加有关(15%:1.8%点[95%置信区间(CI):1.2-2.6;30%:1.4%点,95%CI:0.7-2.2;50%:0.8%点,95%CI:0.2-1.4]和快速停药事件(0.006%点,95%CI:0.001-0.01)。指南发布后,患者接受减量治疗的可能性随时间逐渐增加(15%:0.4%点/月,95%CI:0.3-0.5;30%:0.3%点/月,95%CI:0.2-0.4;50%:0.3%点/月,95%CI:0.2-0.3;快速停药:0.01%点/月,95%CI:0.007-0.01)。性别和种族类别之间的减量和快速停药趋势相似。
该指南可能是改变阿片类药物处方实践的有用工具,特别是对于接受 LTOT 治疗时间较短的患者。