1 Xcenda, Palm Harbor, Florida.
3 Analgesic Solutions, Natick, Massachusetts.
J Manag Care Spec Pharm. 2017 Jul;23(7):718-724. doi: 10.18553/jmcp.2017.23.7.718.
Substance abuse disorders among chronic noncancer pain (CNCP) patients add to the clinical challenges and economic burden of caring for such patients. Despite potential risks, some CNCP patients with a history of alcohol abuse or dependence (AAD) and pain that is refractory to nonopioid treatment options may still need opioids for pain management. However, there is a lack of data on adverse outcomes in long-term opioid users with CNCP and a history of substance abuse or AAD disorders.
To compare adverse outcomes and all-cause health care costs among CNCP patients on long-term opioid treatment with and without a previous diagnosis of AAD.
Using MarketScan claims databases (2006-2012), CNCP patients with ≥ 90 days of opioid supply after CNCP diagnosis and continuous enrollment 12 months before CNCP diagnosis (baseline period) and 12 months after opioid start (post-index period) were identified. AAD was defined by diagnosis codes at any time before opioid initiation. Outcomes included opioid overdose, accident, and injury episodes identified by ICD-9-CM diagnoses codes. T-tests and Mann-Whitney tests compared continuous measures, and chi-square and Fisher's exact tests compared categorical measures between those with and without AAD. Multivariable analyses for outcomes were conducted, adjusting for baseline differences between cohorts.
Of 21,203 CNCP patients with long-term opioid treatment, 750 (3.5%) had an AAD diagnosis before opioid initiation. AAD patients were significantly younger (48.4 [SD ± 11.4] years vs. 52.8 [SD ± 14.8] years), less likely to be enrolled in Medicare (17% commercial vs. 4% Medicare), and more likely to be male (67% vs. 48%; all P < 0.001). There were no differences in type or number of CNCP diagnoses or Charlson Comorbidity Index (CCI) scores. Patients with AAD had significantly higher rates of depression and anxiety diagnoses, antidepressant and benzodiazepine use, and drug abuse/dependence diagnoses in the baseline period. Twelvemonth post-index rates of opioid overdose (1.2% vs. 0.2%), accident (7.3% vs. 2.8%), and injury (46.1% vs. 36.8%) were greater in the AAD cohort (all P < 0.001). The differences were nonsignificant for accidents in multivariable analyses. While mean prescription costs were similar ($3,562 vs. $3,312; P = 0.212), AAD patients had significantly higher mean all-cause medical costs ($28,429 vs. $22,082; P < 0.001) and significantly higher all-cause total health care costs ($31,991 vs. $25,395; P < 0.001). The cost differences remained significant in multivariable analyses.
In the first year after long-term opioid initiation, CNCP patients with a previous AAD diagnosis had 5 times the rate of opioid overdose, 2.3 times the rate of accidents, 1.2 times the rate of injury, and higher all-cause health care costs compared with those not diagnosed with AAD.
Funding for this research study and resultant publication was provided by Teva Global Health Economics and Outcomes Research, which fully reviewed the manuscript. Gajria and Yeung are employees of Teva Pharmaceuticals. White was an employee of Teva Pharmaceuticals at the time this research was conducted. Blumberg and Coutinho are employees of Xcenda, which received research funding from Teva Pharmaceuticals for the conduct of this study and for the preparation of this manuscript. Katz has received research funding and consulting fees from Teva Pharmaceuticals unrelated to this study. Study concept and design were contributed by Katz, White, and Blumberg, along with Coutinho and Yeung. Coutinho took the lead in data collection, assisted by the other authors. Data interpretation was performed by Blumberg, Katz, and Gajria, along with the other authors. The manuscript was written by Gajria, Yeung, Coutinho, and Blumberg, along with Katz and White, and revised by Gajria, Blumberg, Katz, and Coutinho, along with Yeung and White.
慢性非癌痛(CNCP)患者的物质滥用障碍增加了此类患者治疗的临床挑战和经济负担。尽管存在潜在风险,但一些有酒精滥用或依赖(AAD)病史且疼痛对非阿片类药物治疗选择无反应的 CNCP 患者仍可能需要阿片类药物进行疼痛管理。然而,长期阿片类药物使用者伴有物质滥用或 AAD 障碍的不良结局数据缺乏。
比较长期使用阿片类药物治疗的 CNCP 患者中,有无 AAD 既往诊断的不良结局和全因医疗保健费用。
使用 MarketScan 索赔数据库(2006-2012 年),确定 CNCP 诊断后至少有 90 天阿片类药物供应且 CNCP 诊断前 12 个月和阿片类药物起始后 12 个月(索引期前)持续入组的患者。任何时间有阿片类药物起始前的诊断代码即可诊断 AAD。结局包括 ICD-9-CM 诊断代码确定的阿片类药物过量、事故和损伤事件。连续变量采用 t 检验和曼-惠特尼检验进行比较,分类变量采用卡方检验和 Fisher 确切概率法进行比较。对结局进行多变量分析,调整队列间的基线差异。
在 21203 名接受长期阿片类药物治疗的 CNCP 患者中,750 名(3.5%)在阿片类药物起始前有 AAD 诊断。AAD 患者明显更年轻(48.4[标准差 ± 11.4]岁 vs. 52.8[标准差 ± 14.8]岁),更不可能参加医疗保险(17%商业保险 vs. 4%医疗保险),更可能为男性(67% vs. 48%;所有 P<0.001)。CNCP 诊断类型或数量或 Charlson 合并症指数(CCI)评分无差异。AAD 患者在基线期有更高的抑郁和焦虑诊断率、抗抑郁药和苯二氮䓬类药物使用率以及药物滥用/依赖诊断率。AAD 队列在索引后 12 个月的阿片类药物过量(1.2% vs. 0.2%)、事故(7.3% vs. 2.8%)和损伤(46.1% vs. 36.8%)发生率更高(所有 P<0.001)。多变量分析中,事故发生率差异无统计学意义。虽然处方费用中位数相似($3562 与 $3312;P=0.212),但 AAD 患者的全因医疗费用中位数更高($28429 与 $22082;P<0.001),全因总医疗保健费用中位数更高($31991 与 $25395;P<0.001)。多变量分析中差异仍然显著。
在长期阿片类药物起始后的第一年,有 AAD 既往诊断的 CNCP 患者阿片类药物过量发生率是未诊断为 AAD 患者的 5 倍,事故发生率是未诊断为 AAD 患者的 2.3 倍,损伤发生率是未诊断为 AAD 患者的 1.2 倍,全因医疗保健费用也高于未诊断为 AAD 患者。
本研究和相关出版物的研究经费由 Teva Global Health Economics and Outcomes Research 提供,该公司对全文进行了审核。Gajria 和 Yeung 是 Teva 制药公司的员工。White 是 Teva 制药公司的员工,在进行这项研究时。Blumberg 和 Coutinho 是 Xcenda 的员工,他们从 Teva 制药公司获得了研究资金,用于进行这项研究和编写本手稿。Katz 与 Teva 制药公司无关的阿片类药物研究获得了研究经费和咨询费。研究概念和设计由 Katz、White 和 Blumberg 以及 Coutinho 和 Yeung 提出。Coutinho 主导了数据收集,其他作者提供了协助。数据解释由 Blumberg、Katz 和 Gajria 以及其他作者进行。手稿由 Gajria、Yeung、Coutinho 和 Blumberg 以及 Katz 和 White 共同撰写,并由 Gajria、Blumberg、Katz 和 Coutinho 以及 Yeung 和 White 共同修订。