Elevated Serum Concentrations of Lacosamide and Perampanel in a Pediatric Patient Following Coadministration of Clarithromycin for Mycoplasma pneumoniae Pneumonia.

Q2 Medicine
Shotaro Meguro, Toru Imai, Wakako Ishii, Emiko Momoki, Tadayasu Kawaguchi, Kengo Matsuda, Shintaro Watanabe, Susumu Ootsuka
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引用次数: 0

Abstract

Lacosamide (LCM) and perampanel (PER) are antiepileptic drugs eliminated, in part, by cytochrome P450 (CYP) 3A4. However, clinical reports of their interactions are limited. Here, we report the case of a 12-year-old girl with a history of infantile epileptic spasms syndrome, treated with LCM, PER, valproic acid (VPA), and levetiracetam (LEV), who was diagnosed with Mycoplasma pneumoniae pneumonia and prescribed clarithromycin (CAM). Owing to impaired consciousness, serum drug concentrations were measured on multiple occasions during hospitalization. Markedly elevated serum concentrations of LCM (2.3 × baseline) and PER (4.4 × baseline) were observed after initiation of CAM. These concentrations were normalized after CAM was discontinued. Serum concentrations of LEV and VPA remained unchanged. According to the Drug Interaction Probability Scale, interaction was considered probable, with a total score of 5. Clarithromycin likely induced a pharmacokinetic interaction via CYP3A4 inhibition, leading to increased serum concentrations of LCM and PER. Although the concomitant use of CAM with these agents is not contraindicated, the findings of this case suggest caution is warranted. When macrolide therapy is necessary, alternative agents with weaker CYP3A4 inhibition, such as azithromycin, may be preferable.

联合使用克拉霉素治疗肺炎支原体肺炎的儿科患者拉科沙胺和Perampanel的血清浓度升高。
拉科沙胺(LCM)和perampanel (PER)是抗癫痫药物,部分被细胞色素P450 (CYP) 3A4所消除。然而,它们相互作用的临床报告是有限的。在这里,我们报告了一个12岁的女孩,有婴儿癫痫痉挛综合征的病史,治疗LCM, PER,丙戊酸(VPA)和左乙拉西坦(LEV),谁被诊断为肺炎支原体肺炎和处方克拉霉素(CAM)。由于意识受损,住院期间多次测定血清药物浓度。开始CAM后,血清LCM (2.3 ×基线)和PER (4.4 ×基线)浓度明显升高。停用CAM后,这些浓度恢复正常。血清LEV和VPA浓度保持不变。根据药物相互作用概率量表,认为可能发生相互作用,总分为5分。克拉霉素可能通过抑制CYP3A4诱导药代动力学相互作用,导致血清LCM和PER浓度升高。虽然与这些药物同时使用CAM并不是禁忌,但本病例的发现提示谨慎是有必要的。当需要大环内酯类药物治疗时,可选择抑制CYP3A4较弱的替代药物,如阿奇霉素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Pediatric Pharmacology and Therapeutics
Journal of Pediatric Pharmacology and Therapeutics Medicine-Pediatrics, Perinatology and Child Health
CiteScore
2.40
自引率
0.00%
发文量
90
期刊介绍: The Journal of Pediatric Pharmacology and Therapeutics is the official journal of the Pediatric Pharmacy Advocacy Group. JPPT is a peer-reviewed multi disciplinary journal that is devoted to promoting the safe and effective use of medications in infants and children. To this end, the journal publishes practical information for all practitioners who provide care to pediatric patients. Each issue includes review articles, original clinical investigations, case reports, editorials, and other information relevant to pediatric medication therapy. The Journal focuses all work on issues related to the practice of pediatric pharmacology and therapeutics. The scope of content includes pharmacotherapy, extemporaneous compounding, dosing, methods of medication administration, medication error prevention, and legislative issues. The Journal will contain original research, review articles, short subjects, case reports, clinical investigations, editorials, and news from such organizations as the Pediatric Pharmacy Advocacy Group, the FDA, the American Academy of Pediatrics, the American Society of Health-System Pharmacists, and so on.
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