Harvard Pilgrim Health Care Institute, Department of Population Medicine, Harvard Medical School, Boston, Massachusetts2Section of General Internal Medicine, Department of Medicine, Boston Medical Center, Boston University School of Medicine, Boston, Mass.
Harvard Pilgrim Health Care Institute, Department of Population Medicine, Harvard Medical School, Boston, Massachusetts.
JAMA Intern Med. 2015 Jun;175(6):978-87. doi: 10.1001/jamainternmed.2015.0914.
In the second half of 2010, abuse-deterrent extended-release oxycodone hydrochloride (OxyContin; Purdue Pharma) was introduced and propoxyphene was withdrawn from the US market. The effect of these pharmaceutical market changes on opioid dispensing and overdose rates is unknown.
To evaluate the association between 2 temporally proximate changes in the opioid market and opioid dispensing and overdose rates.
DESIGN, SETTING, AND PARTICIPANTS: Claims from a large national US health insurer were analyzed, using an interrupted time series study design. Participants included an open cohort of 31.3 million commercially insured members aged 18 to 64 years between January 1, 2003, and December 31, 2012, with median follow-up of 20 months (last follow-up, December 31, 2012).
Introduction of abuse-deterrent OxyContin (resistant to crushing or dissolving) on August 9, 2010, and market withdrawal of propoxyphene on November 19, 2010.
Standardized opioid dispensing rates and prescription opioid and heroin overdose rates were the primary outcomes. We used segmented regression to analyze changes in outcomes from 30 quarters before to 8 quarters after the 2 interventions.
Two years after the opioid market changes, total opioid dispensing decreased by 19% from the expected rate (absolute change, -32.2 mg morphine-equivalent dose per member per quarter [95% CI, -38.1 to -26.3]). By opioid subtype, the absolute change in dispensing by milligrams of morphine-equivalent dose per member per quarter at 2 years was -11.3 (95% CI, -12.4 to -10.1) for extended-release oxycodone, 3.26 (95% CI, 1.40 to 5.12) for other long-acting opioids, -8.19 (95% CI, -9.30 to -7.08) for propoxyphene, and -16.2 (95% CI, -18.8 to -13.5) for other immediate-release opioids. Two years after the market changes, the estimated overdose rate attributed to prescription opioids decreased by 20% (absolute change, -1.10 per 100,000 members per quarter [95% CI, -1.47 to -0.74]), but heroin overdose increased by 23% (absolute change, 0.26 per 100,000 members per quarter [95% CI, -0.01 to 0.53]).
Opioid dispensing and prescription opioid overdoses decreased substantially after 2 major changes in the pharmaceutical market in late 2010. Pharmaceutical market interventions may have value in combatting the prescription opioid overdose epidemic, but heroin overdose rates continue to increase. Complementary strategies to identify and treat opioid abuse and addiction are urgently needed.
2010 年下半年,引入了具有防滥用缓释羟考酮盐酸盐(OxyContin;普渡制药),并将丙氧芬从美国市场撤出。这些药物市场变化对阿片类药物配药和过量率的影响尚不清楚。
评估阿片类药物市场的 2 个时间相近的变化与阿片类药物配药和过量率之间的关联。
设计、地点和参与者:利用大型美国全国性健康保险公司的索赔数据,采用中断时间序列研究设计进行分析。参与者包括 2003 年 1 月 1 日至 2012 年 12 月 31 日期间年龄在 18 至 64 岁之间的 3130 万商业保险成员的开放队列,中位随访时间为 20 个月(最后一次随访为 2012 年 12 月 31 日)。
2010 年 8 月 9 日推出防滥用羟考酮(耐粉碎或溶解)和 2010 年 11 月 19 日丙氧芬撤出市场。
标准化阿片类药物配药率以及处方阿片类药物和海洛因过量率是主要结局。我们使用分段回归分析了 2 次干预前 30 个季度和后 8 个季度的结果变化。
在阿片类药物市场变化后的两年内,总阿片类药物配药量比预期减少了 19%(绝对变化,每成员每季度减少 32.2 毫克吗啡等效剂量[95%置信区间,-38.1 至-26.3])。按阿片类药物亚型,每成员每季度吗啡等效剂量的配药量的绝对变化在 2 年内为:延长释放羟考酮减少 11.3(95%置信区间,-12.4 至-10.1);其他长效阿片类药物增加 3.26(95%置信区间,1.40 至 5.12);丙氧芬减少 8.19(95%置信区间,-9.30 至-7.08);其他即时释放阿片类药物减少 16.2(95%置信区间,-18.8 至-13.5)。市场变化两年后,归因于处方阿片类药物的估计过量率下降了 20%(绝对变化,每 10 万成员每季度减少 1.10[95%置信区间,-1.47 至-0.74]),但海洛因过量增加了 23%(绝对变化,每 10 万成员每季度增加 0.26[95%置信区间,-0.01 至 0.53])。
2010 年末药物市场的 2 项重大变化后,阿片类药物配药和处方阿片类药物过量明显减少。药物市场干预措施可能在对抗处方阿片类药物过量流行方面具有价值,但海洛因过量率仍在继续上升。迫切需要寻找和治疗阿片类药物滥用和成瘾的补充策略。