Levy Anna, Very Etienne, Montastruc François, Birmes Philippe, Jullien Adeline, Richaud Louis
Department of Psychiatry, Psychotherapy, and Art therapy, University Hospital Toulouse (CHU Toulouse), Toulouse, France.
Toulouse NeuroImaging Center, Universit9 de Toulouse, Inserm, UPS, Toulouse, France.
Front Psychiatry. 2022 May 2;13:875636. doi: 10.3389/fpsyt.2022.875636. eCollection 2022.
Hyperammonemic encephalopathy (HAE) is a serious adverse effect of valproate semisodium, which is facilitated by the potential for drug interaction. However, despite frequent co-prescription of valproate semisodium and lithium, the role of this combination in the occurrence of HAE has not been defined in the literature. This case report concerns the occurrence of HAE concomitant with the initiation of lithium in a 29-year-old patient who had been placed on valproate semisodium for a schizoaffective disorder.
Due to a relapse while on a combined antipsychotic and mood-stabilizing therapy (paliperidone palmitate and valproate semisodium), a cross-taper from valproate semisodium to lithium was proposed. The initiation of lithium was accompanied by an acute confusional syndrome, an elevated serum valproate level and hyperammonemia suggestive of drug-induced HAE. The discontinuation of lithium and reduction of valproate semisodium led to neurological improvement, until a recrudescence of psychiatric symptoms justified a rechallenge of the combination within the framework of a new cross-taper. As soon as Lithium was re-initiated, an increase in the serum valproate level and hyperammonemia were again noted.
The mechanisms of valproate-related HAE involve various metabolic pathways. In this case, exploration of the iatrogenic hypothesis focused on the imputability of concomitant cannabis use and co-prescriptions of benzodiazepines, antipsychotics, and in all likelihood, mood stabilizers.
Therefore, this case study suggests that Lithium plays a role in serum valproate level elevation, and supports the hypothesis of an association between an elevated serum valproate level, hyperammonemia and reversible encephalopathy. A more in-depth pharmacokinetic exploration would provide a better understanding of the mechanisms of these interactions and support for the benefit-risk balance associated with this frequent co-prescription.
高氨血症性脑病(HAE)是丙戊酸半钠的一种严重不良反应,药物相互作用可能会促使其发生。然而,尽管丙戊酸半钠和锂盐经常联合使用,但这种联合用药在HAE发生中的作用在文献中尚未明确。本病例报告涉及一名29岁患有分裂情感性障碍且已服用丙戊酸半钠的患者,在开始使用锂盐时并发HAE。
由于在联合使用抗精神病药物和心境稳定剂(棕榈酸帕利哌酮和丙戊酸半钠)治疗期间病情复发,建议从丙戊酸半钠逐步减量换用锂盐。开始使用锂盐时伴有急性意识模糊综合征、血清丙戊酸水平升高和高氨血症,提示药物性HAE。停用锂盐并减少丙戊酸半钠剂量后神经功能有所改善,直到精神症状复发,才在新的逐步减量框架内重新尝试联合用药。锂盐重新开始使用后,血清丙戊酸水平再次升高且出现高氨血症。
丙戊酸相关HAE的机制涉及多种代谢途径。在本病例中,对医源性假说的探究集中在同时使用大麻以及联合使用苯二氮䓬类药物、抗精神病药物,以及很可能联合使用心境稳定剂的责任归属上。
因此,本病例研究表明锂盐在血清丙戊酸水平升高中起作用,并支持血清丙戊酸水平升高、高氨血症与可逆性脑病之间存在关联的假说。更深入的药代动力学探究将有助于更好地理解这些相互作用的机制,并为这种频繁联合用药的获益风险平衡提供支持。