Rutkovska Ieva, Seilis Andis, Neikena Zane, Poplavska Elita
State Agency of Medicines of the Republic of Latvia, Jersikas Street 15, Riga, 1003, Latvia.
Department of Applied Pharmacy, Faculty of Pharmacy, Riga Stradins University, Konsula Street 21, Riga, 1007, Latvia.
Drugs Real World Outcomes. 2023 Dec;10(4):639-649. doi: 10.1007/s40801-023-00394-y. Epub 2023 Oct 12.
A relevant safety concern for the use of valproate (VPA) in women of reproductive age is its teratogenicity. In 2014 European Medicines Agency (EMA) introduced risk minimisation measures (RMMs) to reduce the VPA use by women of reproductive age, where the impact on VPA use was not as large as expected. In 2018, the EMA introduced additional RMMs, and it is essential to assess impact of these interventions.
The objective of this study was to evaluate the impact of the EMA-published RMMs in 2014 and 2018 on the prevalence of VPA use and to describe trends in the prevalence rate and incidence proportion of VPA use in epilepsy, bipolar disorder and off-label indications in Latvia.
This was a nationwide population-based study using a primary care prescription database. The study included women in age groups < 15, 15-49 and > 49 years and men in age group 15-49 years who have received VPA. This study assessed the prevalence rate and the incidence proportion of VPA use. The impact of RMMs on the two study intervention periods [fourth quarter (Q4) 2014 and Q4 2018] in men and women was evaluated using causal impact analysis.
In the study cohort, VPA use in women in the age group 15-49 years decreased after the first and second intervention periods, where after the first intervention period the relative reduction in prevalence of VPA consumption was -7.7 [95% confidence interval (CI) -10%, -5.1%] and after both study periods -6.4% (95% CI -11%, -1.5%). In girls < 15 years of age, valproate use decreased after both intervention periods, while in women > 49 years old VPA use increased. In men aged 15-49 years, an increase after the first period and a non-significant decrease after both intervention periods was observed. The prevalence of valproate use in girls < 15 years and women 15-49 years of age with bipolar disorder, epilepsy and off-label indications decreased per 1000 people during the study period. The incidence proportion of VPA use in women aged 15-49 years decreased each year since the beginning of the study period.
A statistically significant decrease in the prevalence of VPA use was identified among girls < 15 years and women 15-49 years of age. In Latvia, an overall good reaction to the EMA RMMs was observed. The effects go beyond the target population and affect the use of VPA in young girls as well.
育龄女性使用丙戊酸盐(VPA)的一个相关安全问题是其致畸性。2014年,欧洲药品管理局(EMA)引入了风险最小化措施(RMMs),以减少育龄女性使用VPA的情况,但对VPA使用的影响并未达到预期。2018年,EMA又引入了额外的RMMs,评估这些干预措施的影响至关重要。
本研究的目的是评估EMA在2014年和2018年发布的RMMs对VPA使用 prevalence的影响,并描述拉脱维亚癫痫、双相情感障碍及非标签适应症中VPA使用 prevalence率和 incidence proportion的趋势。
这是一项基于全国人口的研究,使用初级保健处方数据库。该研究纳入了年龄小于15岁、15 - 49岁和大于49岁的女性,以及15 - 49岁接受过VPA治疗的男性。本研究评估了VPA使用的 prevalence率和 incidence proportion。使用因果影响分析评估RMMs在两个研究干预期(2014年第四季度和2018年第四季度)对男性和女性的影响。
在研究队列中,15 - 49岁年龄组女性在第一个和第二个干预期后VPA使用减少,在第一个干预期后VPA消费 prevalence的相对降低为-7.7[95%置信区间(CI)-10%,-5.1%],在两个研究期后为-