Department of Medical and Clinical Pharmacology, CHU Toulouse, Toulouse, Occitanie, France
Department of Psychiatry, Centre Hospitalier Gérard Marchant, Toulouse, France.
BMJ Ment Health. 2024 Apr 12;27(1):e300876. doi: 10.1136/bmjment-2023-300876.
Use of psychostimulants and relative drugs has increased worldwide in treatment of attention-deficit hyperactivity disorder (ADHD) in adolescents and adults. Recent studies suggest a potential association between use of psychostimulants and psychotic symptoms. The risk may not be the same between different psychostimulants.
To assess whether amphetamine or atomoxetine use is associated with a higher risk of reporting symptoms of psychosis than methylphenidate use in adolescents and adults, particularly in patients with ADHD.
Using VigiBase, the WHO's pharmacovigilance database, disproportionality of psychotic symptoms reporting was assessed among adverse drug reactions related to methylphenidate, atomoxetine and amphetamines, from January 2004 to December 2018, in patients aged 13-25 years. The association between psychotic symptoms and psychostimulants was estimated through the calculation of reporting OR (ROR).
Among 13 863 reports with at least one drug of interest, we found 221 cases of psychosis with methylphenidate use, 115 with atomoxetine use and 169 with a prescription of an amphetamine drug. Compared with methylphenidate use, amphetamine use was associated with an increased risk of reporting psychotic symptoms (ROR 1.61 (95% CI 1.26 to 2.06)]. When we restricted the analysis to ADHD indication, we found a close estimate (ROR 1.94 (95% CI 1.43 to 2.64)). No association was found for atomoxetine.
Our study suggests that amphetamine use is associated with a higher reporting of psychotic symptoms, compared with methylphenidate use.
The prescription of psychostimulants should consider this potential adverse effect when assessing the benefit-risk balance.
在青少年和成年人的注意力缺陷多动障碍(ADHD)治疗中,世界范围内使用精神兴奋剂和相关药物的情况有所增加。最近的研究表明,使用精神兴奋剂与精神病症状之间可能存在关联。不同的精神兴奋剂之间的风险可能并不相同。
评估在青少年和成年人中,与使用哌醋甲酯相比,使用安非他命或托莫西汀是否与报告精神病症状的风险更高相关,特别是在 ADHD 患者中。
使用世界卫生组织的药物警戒数据库 VigiBase,评估了 2004 年 1 月至 2018 年 12 月期间,年龄在 13-25 岁之间与哌醋甲酯、托莫西汀和安非他命相关的不良反应报告中,精神病症状报告的比例失调。通过计算报告比值比(ROR)来评估精神病症状与精神兴奋剂之间的关联。
在至少有一种研究药物的 13863 份报告中,我们发现 221 例使用哌醋甲酯的精神病病例,115 例使用托莫西汀的病例和 169 例使用安非他命药物的病例。与使用哌醋甲酯相比,使用安非他命与报告精神病症状的风险增加相关(ROR 1.61(95%CI 1.26-2.06])。当我们将分析限制在 ADHD 适应症时,我们发现了一个接近的估计值(ROR 1.94(95%CI 1.43-2.64))。托莫西汀则没有相关性。
我们的研究表明,与使用哌醋甲酯相比,安非他命的使用与报告精神病症状的风险增加相关。
在评估利益风险平衡时,应考虑到这种潜在的不良反应,来处方精神兴奋剂。