Correlation between Breakthrough Seizures and Serum Level of Phenytoin and Valproate in Indian Patients

IF 0.4 Q4 PHARMACOLOGY & PHARMACY Journal of Pharmacology & Pharmacotherapeutics Pub Date : 2021-04-01 DOI:10.4103/jpp.jpp_3_21
N. Katoch, A. Bhardwaj, Kapil Suchal, Sangeeta Sharma
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Abstract

Objectives: To determine the optimum range of phenytoin (PHT) and valproate (VAP) levels and find out the critical drug levels below which chances of breakthrough seizures increase in North Indian population. Methodology: A cross-sectional, case-controlled, record-based study was conducted in a quaternary care hospital from September 2018–2019. The case group comprised epilepsy patients on monotherapy with PHT/VAP presenting with breakthrough seizures after at least 6 months of seizure control. Noncompliant, overdose, toxicity, no or partial response, any other psychiatric or neurological disorder, adverse effects, and patients taking two or more antiepileptic drugs were excluded. Results: Data of 100 patients in each group were analyzed. Significantly lower mean levels in cases were observed in PHT (5.74 ± 3.68 mg/L vs. 13.75 ± 4.27 mg/L control) and VAP (24.13 ± 27.39 mg/L vs. 76.37 ± 17.71 mg/L control). A negative correlation of drug levels was observed with age and weight in both the groups. The level/dose ratio in controls (0.05 ± 0.03; 0.09 ± 0.06) was significantly (P < 0.0001) higher than cases (0.02 ± 0.01; 0.02 ± 0.03) in PHT and VAP, respectively. Conclusions: This study identifies the critical levels and level/dose ratio at which the risk of breakthrough seizures increases. A wide level/dose ratio was found in controls, more so in the VAP group. A prospective study with larger group size along with genetic studies should be done to evaluate further.
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印度患者突破性癫痫发作与血清苯妥英钠和丙戊酸钠水平的相关性
目的:确定苯妥英(PHT)和丙戊酸钠(VAP)的最佳剂量范围,并找出印度北部人群突破性癫痫发作机会增加的临界药物水平。方法:于2018年9月至2019年9月在一家四级护理医院进行了一项横断面、病例对照、基于记录的研究。病例组包括接受PHT/VAP单药治疗的癫痫患者,在癫痫发作控制至少6个月后出现突破性发作。排除非依从性、过量、毒性、无反应或部分反应、任何其他精神或神经疾病、不良反应以及服用两种或两种以上抗癫痫药物的患者。结果:对每组100例患者资料进行分析。PHT组(5.74±3.68 mg/L,对照组为13.75±4.27 mg/L)和VAP组(24.13±27.39 mg/L,对照组为76.37±17.71 mg/L)的平均水平显著低于对照组。两组患者的药物水平均与年龄和体重呈负相关。对照组水平剂量比(0.05±0.03;0.09±0.06)显著高于(0.02±0.01);PHT和VAP分别为0.02±0.03)。结论:本研究确定了突破性癫痫发作风险增加的临界水平和水平/剂量比。在对照组中发现了较宽的水平/剂量比,在VAP组中更为明显。应该进行更大群体规模的前瞻性研究以及基因研究来进一步评估。
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CiteScore
0.40
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发文量
37
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