Evaluation of long-term oral administration of a sustained release theophylline preparation in children with chronic asthma

Allergol Immunopathol (Madr). 1983 Jan-Feb;11(1):11-4.

Abstract

Over a one-year-period 23 children with chronic asthma were given an oral sustained-release theophylline preparation in twice-daily doses. Constant therapeutic theophylline levels were maintained in 18 children for the whole period, while in 5 subjects the values were in almost all instances below the therapeutic range. In both groups, however, a good clinical effect from the preparation was observed. Only two children reported nausea and mild abdominal pains, whereas other two children had serum theophylline levels above 20 micrograms/ml with no side effects. It is concluded that oral sustained-release theophylline preparation is effective in providing therapeutic drug concentrations on a 12 hr dose schedule, thus avoiding the risk of lower compliance observed in children given normal theophylline tablets.

MeSH terms

  • Administration, Oral
  • Asthma / drug therapy*
  • Child
  • Child, Preschool
  • Delayed-Action Preparations
  • Drug Evaluation
  • Female
  • Humans
  • Male
  • Theophylline / administration & dosage
  • Theophylline / blood
  • Theophylline / therapeutic use*

Substances

  • Delayed-Action Preparations
  • Theophylline