Division of Health Outcomes, College of Pharmacy, University of Texas at Austin, Austin, Texas, USA.
Pharmacotherapy Division, College of Pharmacy, University of Texas at Austin, San Antonio, Texas, USA.
Clin Drug Investig. 2021 Mar;41(3):245-253. doi: 10.1007/s40261-021-01009-6. Epub 2021 Feb 12.
Gabapentin and pregabalin have been considered relatively safe opioid-sparing adjuncts for pain management. However, rising prescribing trends, presence of gabapentinoids in opioid-related overdoses, and the growing body of evidence regarding gabapentinoid misuse and abuse, have caused gabapentinoids to emerge as a drug class of public health concern. This study aimed to assess the prevalence of, and factors associated with gabapentinoid use and misuse.
This retrospective study of Texas Medicaid data from 1/1/2012 to 30/8/2016 included patients aged 18-63 years at index date, with ≥ 1 gabapentinoid prescription, and continuously enrolled 6 months pre-index and 12 months post-index. Gabapentinoid misuse was defined as ≥ 3 claims exceeding daily doses of 3600 mg for gabapentin and 600 mg for pregabalin. Age, gender, concurrent opioid use, neuropathic pain diagnoses and gabapentinoid type were independent variables. Descriptive and inferential statistics were used.
Of included subjects (N = 39,000), 0.2% (N = 81) met study criteria for gabapentinoid misuse. Overall, the majority (76.4%) of gabapentinoid users were aged 41-63 years with a mean ± SD age of 48.2 ± 10.7 years. Those patients meeting the study criteria for gabapentinoid misuse were significantly younger (45.1 ± 11.0 vs 48.2 ± 10.7, p = 0.0084). Majority of the study sample was female (68.1%). However, a significantly higher proportion of males met the study criteria for gabapentinoid misuse compared to females (0.3% vs 0.2%, p = 0.0079). Approximately one-half (51.9%) of the study sample had neuropathic pain, and gabapentinoid misuse was significantly higher in neuropathic pain patients compared to those without neuropathic pain (0.3% vs 0.1%, p = 0.0078). Over three-quarters (77.4%) of patients were using gabapentin; however, gabapentinoid misuse was significantly higher among pregabalin users (0.4% vs 0.2%, p = 0.0003). Approximately 20% (17.3%) of gabapentinoid users had ≥ 90 days of concurrent opioid use. However, there was no significant difference in gabapentinoid misuse among patients with concurrent opioid use compared to patients without (0.3% vs 0.2%, p = 0.1440). Factors significantly associated with misuse included: male sex (odds ratio [OR] 0.486; 95% confidence interval [CI] 0.313-0.756; p = 0.0013); neuropathic pain (OR 2.065; 95% CI 1.289-3.308; p = 0.0026); and pregabalin versus gabapentin use (OR 2.337, 95% CI 1.492-3.661; p = 0.0002). Concurrent opioid use was not significantly associated with gabapentinoid misuse (OR 1.542, 95% CI 0.920-2.586; p = 0.1006).
Prevalence of gabapentinoid misuse was low (0.2%) among Texas Medicaid recipients. Younger age, male gender, neuropathic pain diagnosis and pregabalin use were significantly associated with higher levels of gabapentinoid misuse.
加巴喷丁和普瑞巴林被认为是相对安全的阿片类药物辅助药物,可用于疼痛管理。然而,开处方的趋势不断上升,加巴喷丁类药物出现在阿片类药物相关过量的药物中,以及关于加巴喷丁类药物滥用和误用的证据不断增加,导致加巴喷丁类药物成为公共卫生关注的药物类别。本研究旨在评估德克萨斯州医疗补助数据中加巴喷丁类药物的使用和滥用的流行率以及相关因素。
本研究回顾性分析了 2012 年 1 月 1 日至 2016 年 8 月 30 日期间德克萨斯州医疗补助数据,纳入了索引日期时年龄在 18-63 岁之间、至少有 1 份加巴喷丁类药物处方、并且在索引前 6 个月和索引后 12 个月持续入组的患者。将加巴喷丁类药物滥用定义为≥3 次用药,每日剂量超过 3600 毫克的加巴喷丁和 600 毫克的普瑞巴林。年龄、性别、同时使用阿片类药物、神经病理性疼痛诊断和加巴喷丁类药物类型是自变量。使用描述性和推断性统计方法。
在纳入的研究对象(N=39000)中,有 0.2%(N=81)的患者符合加巴喷丁类药物滥用的研究标准。总体而言,大多数(76.4%)加巴喷丁类药物使用者的年龄为 41-63 岁,平均年龄为 48.2±10.7 岁。符合加巴喷丁类药物滥用研究标准的患者明显更年轻(45.1±11.0 岁比 48.2±10.7 岁,p=0.0084)。研究样本中大多数是女性(68.1%)。然而,与女性相比,男性中符合加巴喷丁类药物滥用研究标准的比例显著更高(0.3%比 0.2%,p=0.0079)。研究样本中有大约一半(51.9%)的患者患有神经病理性疼痛,与没有神经病理性疼痛的患者相比,神经病理性疼痛患者中加巴喷丁类药物滥用的比例显著更高(0.3%比 0.1%,p=0.0078)。超过四分之三(77.4%)的患者使用加巴喷丁;然而,普瑞巴林使用者的加巴喷丁类药物滥用率显著更高(0.4%比 0.2%,p=0.0003)。大约 20%(17.3%)的加巴喷丁类药物使用者有≥90 天的同时使用阿片类药物。然而,与没有同时使用阿片类药物的患者相比,同时使用阿片类药物的患者中加巴喷丁类药物滥用的比例没有显著差异(0.3%比 0.2%,p=0.1440)。与滥用显著相关的因素包括:男性(比值比[OR]0.486;95%置信区间[CI]0.313-0.756;p=0.0013);神经病理性疼痛(OR 2.065;95% CI 1.289-3.308;p=0.0026);以及普瑞巴林与加巴喷丁的使用(OR 2.337;95% CI 1.492-3.661;p=0.0002)。同时使用阿片类药物与加巴喷丁类药物滥用没有显著相关性(OR 1.542;95% CI 0.920-2.586;p=0.1006)。
在德克萨斯州医疗补助受助人中,加巴喷丁类药物滥用的流行率较低(0.2%)。年龄较小、男性、神经病理性疼痛诊断和普瑞巴林的使用与更高水平的加巴喷丁类药物滥用显著相关。