Van Baelen Luk, De Ridder Karin, Antoine Jérôme, Gremeaux Lies
Department of Public Health and Surveillance, Scientific Institute of Public Health, Brussels, Belgium, Rue Juliette Wytsmanstraat, 14, 1050 Brussels, Belgium.
Arch Public Health. 2018 Mar 19;76:17. doi: 10.1186/s13690-018-0254-8. eCollection 2018.
Although gabapentin has been licensed in the European Union only for neuropathic pain and epilepsy for patients who have partial seizures, it has also been prescribed in treatment for substance use disorders. Many studies report the potential risk of abuse of gabapentin by people with substance use disorders. The objective of this paper is to determine if people who have been in treatment for substance use disorders bought gabapentin in a time span that could indicate consumption at a dose that exceeded the maximum approved dose of 3600 mg/day.
This analysis is the result of an observational cross-sectional descriptive study with matching. Two datasets were used and linked at individual level. Subjects were selected based on their first registration in the database of the Treatment Demand Indicator (TDI) between 2011 and 2014, without any exclusion criteria concerning nationality or age. Through linkage with the database of the InterMutualistic Agency (IMA) information on health service use and medication use was determined. In addition, each subject was matched on age, sex and place of residence to four comparators from the general population who were not in specialized treatment. The prevalence of gabapentin purchases in the period between 2008 and 2014 for both populations were compared. Quantification of the amount of gabapentin between two consecutive purchases was used as a proxy for potential abuse.
Out of 30,905 patients in treatment for substance use disorders 2.7% had bought at least once gabapentin in a public pharmacy or received it from a hospital pharmacy, compared to 0.7% in the comparison group ( = 122,142). In both populations, more than half of the patients bought only once or twice gabapentin and about 10.0% bought at least once gabapentin in a time span that could indicate potential abuse. A limitation of the study is that it is only based on reimbursed medication without clinical information.
Through the linkage of the TDI-database and the database of the Belgian health insurance companies, no evidence was found for regular abuse of prescribed gabapentin in Belgium by people in treatment for substance use disorders.
尽管加巴喷丁在欧盟仅被批准用于治疗神经性疼痛以及患有部分性癫痫的患者的癫痫,但它也被用于物质使用障碍的治疗。许多研究报告了物质使用障碍患者滥用加巴喷丁的潜在风险。本文的目的是确定接受物质使用障碍治疗的人是否在一段可能表明其服用剂量超过每日最大批准剂量3600毫克的时间内购买了加巴喷丁。
本分析是一项匹配的观察性横断面描述性研究的结果。使用了两个数据集并在个体层面进行关联。根据2011年至2014年间在治疗需求指标(TDI)数据库中的首次注册情况选择受试者,没有关于国籍或年龄的任何排除标准。通过与互助机构(IMA)的数据库进行关联,确定了健康服务使用和药物使用信息。此外,根据年龄、性别和居住地点,为每个受试者匹配了四名未接受专门治疗的普通人群对照者。比较了这两个人群在2008年至2014年期间购买加巴喷丁的患病率。将连续两次购买之间的加巴喷丁数量量化用作潜在滥用的指标。
在30905名接受物质使用障碍治疗的患者中,2.7%的人至少在公共药房购买过一次加巴喷丁或从医院药房获得过加巴喷丁,而对照组(n = 122142)的这一比例为0.7%。在两个人群中,超过一半的患者仅购买过一两次加巴喷丁,约10.0%的患者在一段可能表明潜在滥用的时间内至少购买过一次加巴喷丁。该研究的一个局限性是它仅基于报销药物,没有临床信息。
通过将TDI数据库与比利时健康保险公司的数据库进行关联,未发现比利时接受物质使用障碍治疗的人经常滥用处方加巴喷丁的证据。