Department of Pharmacy, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Guangdong Provincial Key Laboratory of New Drug Design and Evaluation, Guangzhou, China.
J Clin Lab Anal. 2024 Apr;38(8):e25025. doi: 10.1002/jcla.25025. Epub 2024 Apr 2.
This study aimed to indicate whether a declined plasma concentration of valproic acid (VPA) induced by co-administration of meropenem (MEPM) could affect the antiepileptic efficacy of VPA.
We retrospectively reviewed data of hospitalized patients who were diagnosed with status epilepticus or epilepsy between 2010 and 2019. Patients co-administered VPA and MEPM during hospitalization were screened and assigned to the exposure group, while those co-administerd VPA and other broad-spectrum antibiotics were allocated to the control group.
The exposure group and control group included 50 and 11 patients, respectively. With a similar dosage of VPA, the plasma concentration of VPA significantly decreased during co-administration (24.6 ± 4.3 μg/mL) compared with that before co-administration (88.8 ± 13.6 μg/mL, p < 0.0001), and it was partly recovered with the termination of co-administration (39.8 ± 13.2 μg/mL, p = 0.163) in the exposure group. The inverse probability of treatment weighting estimated the treatment efficacy via changes in seizure frequency, seizure duration, and concomitant use of antiepileptic drugs, which were not significantly different between the exposure and control groups. In the exposure group, there was no significant differences in seizure frequency between the periods of before-during and before-after (p = 0.074 and 0.153, respectively). Seizure duration during VPA-MEPM co-administration was not significantly different from that before co-administration (p = 0.291).
In this study, the reduced plasma concentration of VPA induced by the co-administration of MEPM did not affect the antiepileptic efficacy of VPA. This conclusion should be interpreted with caution, and more research is warranted.
Chinese Clinical Trial Registry: ChiCTR2000034567. Registered on 10 July 2020.
本研究旨在探讨美罗培南(MEPM)合用是否会降低丙戊酸(VPA)的血药浓度从而影响 VPA 的抗癫痫疗效。
我们回顾性分析了 2010 年至 2019 年期间因癫痫持续状态或癫痫住院的患者数据。筛选出住院期间合用 VPA 和 MEPM 的患者并分为暴露组,将合用 VPA 和其他广谱抗生素的患者分为对照组。
暴露组和对照组分别纳入 50 例和 11 例患者。与合用前相比,合用期间 VPA 的血药浓度(24.6±4.3μg/mL)明显降低(88.8±13.6μg/mL,p<0.0001),且在停止合用后部分恢复(39.8±13.2μg/mL,p=0.163)。逆概率治疗加权法(inverse probability of treatment weighting,IPTW)通过发作频率、发作持续时间和抗癫痫药物的使用变化来估计治疗效果,暴露组和对照组之间无显著差异。在暴露组中,VPA-MEPM 合用期间和合用前后的发作频率无显著差异(p=0.074 和 0.153)。VPA-MEPM 合用期间的发作持续时间与合用前无显著差异(p=0.291)。
本研究中,MEPM 合用降低了 VPA 的血药浓度,但并未影响 VPA 的抗癫痫疗效。这一结论应谨慎解读,需要进一步研究。
中国临床试验注册中心:ChiCTR2000034567。注册于 2020 年 7 月 10 日。