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Correlation between serum and salivary phenytoin concentrations in Thai epileptic children
Sahas Liamsuwan1, Ulailuk Jaiweerawattana
1Division of Child Neurology, Queen Sirikit National Institute of Child Health, Department of Medical Services, Ministry of Public Health, College of Medicine, Rangsit University, Bangkok, Thailand. liamsuwan@hotmail.com
Insights
Saliva can effectively monitor phenytoin levels in Thai children with epilepsy, showing a strong correlation with serum levels. This offers a less invasive alternative to blood tests for managing medication dosages.
Area of Science:
- Pediatric Neurology
- Clinical Pharmacology
- Biomarker Analysis
Background:
- Epilepsy management in children requires precise drug level monitoring.
- Phenytoin is a common antiepileptic drug, but blood collection can be challenging in pediatric patients.
- Exploring alternative, less invasive methods for phenytoin monitoring is crucial.
Purpose of the Study:
- To investigate the correlation between serum and salivary phenytoin concentrations in Thai epileptic children.
- To establish predictive equations for phenytoin levels based on saliva samples.
Main Methods:
- Studied Thai children (5-12 years) with epilepsy on phenytoin monotherapy.
- Collected blood and saliva samples for phenytoin level measurement using fluorescence-polarization immunoassay.
- Excluded patients with specific health conditions or poor compliance.
Main Results:
- A close linear correlation (R=0.880, R²=0.967) was found between serum and salivary phenytoin levels.
- Equations were derived to predict serum and salivary phenytoin levels from drug dosage.
- Adverse drug reactions were observed in 6.6% of patients.
Conclusions:
- Salivary phenytoin monitoring is a viable and highly correlated alternative to serum monitoring in Thai children.
- This approach can simplify drug management, reduce patient distress, and improve adherence.
- The derived equations can aid in adjusting phenytoin dosage regimens in clinical practice.
Objective:
To study the correlation between serum and salivary phenytoin concentration in Thai epileptic children.
Material And Method:
Children aged 5 to 12 years with diagnosed epilepsy who received phenytoin monotherapy seen in the neurological clinic at Queen Sirikit National Institute of Child Health were studied. The recruited patients were required to have good compliance, normal albumin level, and no evidence of cancer, HIV infection, hepatic, renal and salivary glands disease. Blood and saliva samples were collected and measured phenytoin level by fluorescence-polarization immunoassay technique.
Results:
Thirty patients, 19 males and 11 females, were studied. The average (mean +/- SD) age and weight were 8.24 +/- 2.09 years and 27.76 +/- 9.86 Kilograms. Both serum and salivary phenytoin levels correlated with phenytoin doses as exponential type (R2 = 0.4188, 0.3682, respectively). Equations for describing serum and salivary phenytoin levels by phenytoin dose were y = 0.7403e(0.3952x) and y = 0.1431e(0.3072x) respectively. Serum and salivary phenytoin levels were closely correlated as linear type (R = 0.880, R2 = 0.967). The obtained equation of this relationship was y = 10.165x, where y = serum phenytoin level and x = salivary phenytoin level. Adverse drug reactions were found in 5 patients (6.6%), horizontal nystagmus 2 cases, hirsutism 2 cases and gingival hyperplasia 1 case.
Conclusion:
High correlation between serum and salivary phenytoin levels supported the use of saliva instead of blood for phenytoin monitoring in Thai children which were difficult in blood collection and had psychological trauma. The obtained equations in the present study could be applied for adjusting the dosage regimen and monitoring by using salivary phenytoin level in clinical practice.
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