Curr Med Res Opin. 2012 Sep;28(9):1485-96. doi: 10.1185/03007995.2012.713338. Epub 2012 Aug 2.
To examine opioid prescription claims before and after initiation of pregabalin in patients with a diagnosis of diabetic peripheral neuropathy (DPN).
This retrospective analysis used a national commercial database of integrated inpatient, outpatient, and prescription claims to identify adults with a DPN diagnosis code within 360 days prior to the first claim for pregabalin between January 1, 2006 and March 31, 2008. Prescription claims for pregabalin or opioids were analyzed in nine consecutive 60-day periods from 180 days before through 360 days after the first pregabalin claim. It was not possible to establish drug administration dates, compliance rates, indications for opioid use, or reasons for treatment discontinuation.
Of the 8004 adults who met eligibility criteria, 6080 (76%) received an opioid within the 180 days before and/or 360 days after their first prescription for pregabalin, including 3956 (49%) both before and after, 1580 (20%) after only, and 544 (7%) before only. The percentage of patients with pregabalin claims covering ≥20 of 60 days (within 60-day periods) was 99% (day 1-60), 63% (day 61-120), 50% (day 121-180), 45% (day 181-240), 42% (day 241-300), and 39% (day 301-360). The percentage of patients with opioid claims covering ≥20 of 60 days within the 60-day periods remained stable (range, 25-30%). Among patients with opioid claims, 73-76% received only short-acting opioids, 6-7% received only long-acting opioids, and 18-20% received both short- and long-acting opioids. In the first year, 982 (12%) patients had opioid claims covering ≥20 of 60 days in every 60-day period (i.e., persistent use of opioids). Coexisting musculoskeletal (95%) or neuropathic (61%) pain conditions were frequent.
A majority of patients with DPN receive an opioid before and/or after their first pregabalin claim. Pregabalin neither interferes with nor replaces opioid use for pain management in patients with DPN. Although nearly 1 in 8 patients received opioids throughout the study period, most claims were for short-acting opioids. The majority of this DPN sample had other pain conditions, including musculoskeletal and neuropathic pain conditions. These results highlight the frequency of opioid use with pregabalin, particularly short-acting opioids.
在开始使用普瑞巴林治疗糖尿病周围神经病变 (DPN) 的患者中,检查阿片类药物处方的情况。
本回顾性分析使用了一个全国性的综合住院、门诊和处方数据库,以确定在 2006 年 1 月 1 日至 2008 年 3 月 31 日期间首次使用普瑞巴林前 360 天内有 DPN 诊断代码的成年人。从第一次使用普瑞巴林前 180 天到后 360 天,对普瑞巴林或阿片类药物的处方进行了九个连续的 60 天分析。无法确定药物管理日期、遵医嘱率、阿片类药物使用的适应证以及治疗停止的原因。
在符合入选标准的 8004 名成年人中,有 6080 名(76%)在首次使用普瑞巴林前 180 天内和/或后 360 天内接受了阿片类药物治疗,其中 3956 名(49%)在前后均接受了治疗,1580 名(20%)仅在后期接受了治疗,544 名(7%)仅在前期接受了治疗。在 60 天内(60 天期间)至少有 20 天的普瑞巴林治疗的患者比例为 99%(第 1-60 天)、63%(第 61-120 天)、50%(第 121-180 天)、45%(第 181-240 天)、42%(第 241-300 天)和 39%(第 301-360 天)。在 60 天期间内,有阿片类药物治疗的患者中至少有 20 天接受阿片类药物治疗的比例保持稳定(范围为 25-30%)。在有阿片类药物治疗的患者中,73-76%接受的仅是短效阿片类药物,6-7%接受的仅是长效阿片类药物,18-20%接受的是短效和长效阿片类药物的联合治疗。在第一年,982 名(12%)患者在每个 60 天期间(即持续使用阿片类药物)的阿片类药物治疗覆盖≥20 天。共存的肌肉骨骼(95%)或神经病变(61%)疼痛状况很常见。
大多数 DPN 患者在首次使用普瑞巴林前和/或后接受阿片类药物治疗。普瑞巴林既不会干扰也不会替代 DPN 患者的疼痛管理中阿片类药物的使用。尽管近 1/8 的患者在整个研究期间都接受了阿片类药物治疗,但大多数是短期阿片类药物。该 DPN 样本的大多数患者还有其他疼痛状况,包括肌肉骨骼和神经病变疼痛状况。这些结果突出了普瑞巴林治疗中阿片类药物的使用频率,特别是短期阿片类药物的使用频率。