Individualization of Theophylline Dosage Using a Single Serum Sample Following a Test Dose
- 1 January 1982
- journal article
- research article
- Published by American Academy of Pediatrics (AAP) in Pediatrics
- Vol. 69 (1) , 70-73
- https://doi.org/10.1542/peds.69.1.70
Abstract
Because formulas for theophylline requirement based on weight alone carry the risk of overdosing and toxicity, this study was designed to test a clearance nomogram for determining daily theophylline requirement after a known initial dose of theophylline. Twenty asthmatic children who had not taken theophylline for at least 36 hours fasted and were given one dose of anhydrous theophylline (5 mg/kg). Six hours later the serum level was measured and the appropriate dosage of sustained-release theophylline to achieve a serum level of 10 µg/ml was selected from the clearance nomogram. Three to seven days later a six-hour theophylline level was obtained. Of 20 patients, therapeutic levels of 10 to 20 µg/ml were achieved in 15, and the remaining five patients had levels close to this (range 6.2 to 16.0 µg/ml). The dosage requirement per 24 hours ranged from 10 to 32 mg/kg/24 hr. This method of determining theophylline requirements for children required measurement of the serum theophylline level only once for the determination of a safe and effective daily dose. It is especially valuable when follow-up is difficult and is a safe way to avoid serious overdosing while being certain of effective dosing.This publication has 3 references indexed in Scilit:
- Oral theophylline dosage for the management of chronic asthmaThe Journal of Pediatrics, 1978
- Oral aminophylline therapy. Increased dosage requirements in childrenJAMA, 1977
- Theophylline-Induced Seizures in AdultsAnnals of Internal Medicine, 1975