Coves-Orts Francisco Javier, Borrás-Blasco Joaquín, Navarro-Ruiz Andrés, Murcia-López Ana, Palacios-Ortega Francisco
Intensive Care Unit, Hospital General Universitario de Elche, Cami de l'Almazara 11, Elche 03203, Alicante, Spain.
Ann Pharmacother. 2005 Mar;39(3):533-7. doi: 10.1345/aph.1E358. Epub 2005 Feb 8.
To report a probable interaction between meropenem and valproic acid that resulted in the development of epileptic seizures.
A 21-year-old woman presented to our emergency department because of a new-onset, generalized tonic-clonic seizure and was admitted to the intensive care unit. Treatment with valproic acid 1000 mg as a continuous intravenous infusion over 24 hours was initiated. On day 6, the serum concentration of valproic acid was 52.5 microg/mL. On day 13, treatment with intravenous meropenem 1 g 3 times daily was started. On day 15, when the patient was afebrile, numerous myoclonic episodes occurred involving her arms and face; the serum concentration of valproic acid at that time was 42 mug/mL. The valproic acid dose was increased to 2880 mg. Two days later, a generalized tonic-clonic seizure occurred despite the increased dosage, and the plasma concentration of valproic acid fell to 7 microg/mL. The valproic acid dose was increased the following day to 3600 mg; however, the serum concentrations remained <10 microg/mL. On day 19, based on the results of a blood culture and the suspicion of an interaction between meropenem and valproic acid, meropenem therapy was suspended. The serum concentration of valproic acid was 52.4 microg/mL on day 27. Three days later, the patient was asymptomatic and was discharged.
Coadministration of valproic acid and other drugs that are metabolized by the hepatic cytochrome P450 isoenzyme system can lead to clinically relevant interactions by induction or inhibition of enzymes in shared metabolic pathways. In view of studies in experimental models, the interaction between carbapenem antibiotics and valproic acid is at least possible. Use of the Naranjo probability scale indicated a probable relationship between acute seizures and a meropenem-valproic acid interaction in this patient.
This case report provides strong evidence for an interaction between valproic acid and meropenem. Clinicians should be aware of this potential interaction that may be associated with a serious adverse effect as the result of the decrease of the valproic acid serum concentrations.
报告美罗培南与丙戊酸之间可能存在的相互作用,该相互作用导致癫痫发作。
一名21岁女性因新发全身性强直阵挛发作就诊于我院急诊科,并被收入重症监护病房。开始以1000mg丙戊酸持续静脉输注24小时进行治疗。第6天,丙戊酸血清浓度为52.5μg/mL。第13天,开始每日3次静脉注射1g美罗培南治疗。第15天,患者无发热时,出现累及手臂和面部的多次肌阵挛发作;此时丙戊酸血清浓度为42μg/mL。丙戊酸剂量增至2880mg。两天后,尽管剂量增加,仍发生全身性强直阵挛发作,丙戊酸血浆浓度降至7μg/mL。次日丙戊酸剂量增至3600mg;然而,血清浓度仍<10μg/mL。第19天,根据血培养结果及怀疑美罗培南与丙戊酸之间存在相互作用,暂停美罗培南治疗。第27天丙戊酸血清浓度为52.4μg/mL。三天后,患者无症状并出院。
丙戊酸与其他经肝细胞色素P450同工酶系统代谢的药物合用时,可通过诱导或抑制共同代谢途径中的酶而导致具有临床意义的相互作用。鉴于在实验模型中的研究,碳青霉烯类抗生素与丙戊酸之间的相互作用至少是有可能的。使用纳伦霍概率量表表明该患者急性发作与美罗培南 - 丙戊酸相互作用之间可能存在关联。
本病例报告为丙戊酸与美罗培南之间的相互作用提供了有力证据。临床医生应意识到这种潜在的相互作用,其可能因丙戊酸血清浓度降低而导致严重不良反应。