THEOPHYLLINE Flashcards
THEOPHYLLINE INDICATIONS
For Uniphyllin Continus® -
- Chronic asthma
- Reversible airways obstruction,
- Severe acute asthma
SAME BRAND OF THEOPHYLLINE SHOULD BE MAINTAINED
Therapeutic drug monitoring
Target plasma-theophylline concentration of 10–20 mg/litre (55–110 micromol/litre) is required for satisfactory bronchodilation, although a lower plasma-theophylline concentration of 5–15 mg/litre may be effective.
Adverse effects can occur within the range 10–20 mg/litre and both the frequency and severity increase at concentrations above 20 mg/litre.
Plasma-theophylline concentration is measured 5 days after starting oral treatment and at least 3 days after any dose adjustment. A blood sample should usually be taken 4–6 hours after an oral dose of a modified-release preparation (sampling times may vary—consult local guidelines).
When to measure plasma levels
Plasma-theophylline concentration is measured 5 days after INITIATION
At least 3 days after any dose adjustment
A blood sample should usually be taken 4–6 hours after an oral dose of a modified-release preparation (sampling times may vary—consult local guidelines).
Dose adjustments due to interactions for theophylline
Dose adjustment may be necessary if smoking started or stopped during treatment.
Theophylline is metabolised in the liver. The plasma-theophylline concentration is increased in heart failure, hepatic impairment, and in viral infections.
The plasma-theophylline concentration is decreased in smokers, and by alcohol consumption.
If a patient wants to reduce or quit smoking?
Dosage of theophylline should be decreased
TOXICITY EFFECTS - SICK + FAST
VOMITING
AGITATION
DILATED PUPILS
TACHYCARDIA + ARRHYTHMIAS
HYPERGLYCEAMIA
CONVULSIONS
TREAT TOXICITY WITH ACTIVATED CHARCOAL