Key result
Phenobarbitone outperforms isoniazid and metoprolol in detecting partial compliance over prior weeks.
Why the study?
Long half-life compounds are considered more appropriate pharmacological indicators of treatment compliance, but short half-life markers and measurements of short half-life therapeutic drugs are frequently used without clear comparison.
Answers are grounded in this paper and cite their sources.
Phenobarbitone measurement may better detect partial compliance over weeks than short-acting markers in volunteers; leaves open real-world patient utility.
Although, long half-life compounds appear to be more appropriate pharmacological indicators of compliance with treatment, short half-life markers or measurements of short half-life therapeutic drugs are frequently used. 2. We have compared the usefulness of low-dose phenobarbitone (a long half-life indicator), low dose isoniazid (a short half-life marker) and controlled release metoprolol (Metros) (a controlled release formulation of a short half-life 'therapeutic' drug) in seven volunteers with simulated partial (two thirds) compliance. 3. Detection of isoniazid metabolites in urine had an 83% sensitivity and 94% specificity for detecting ingestion within the previous 24 h and 100% sensitivity and 82% specificity for detecting ingestion within the past 6 h but gave no indication of the longer term pattern of compliance. 4. At 28 days (a time when steady-state would be obtained for all three drugs) phenobarbitone plasma levels were 70% (66-76%)--median and interquartile range--of the expected steady-state level if compliance had been complete. Corresponding figures for metoprolol were 82% (37-100%). 5. Measurement of phenobarbitone was much superior to isoniazid or metoprolol measurements in reflecting partial compliance over the previous 1 to 4 weeks.
No takes yet. Share an insight, caveat, or question.
Hardy et al. (1990) studied Simulated partial compliance (n=7). Low-dose phenobarbitone vs. Low-dose isoniazid and controlled release metoprolol was evaluated on Plasma levels as a percentage of expected steady-state level at 28 days. Measurement of phenobarbitone was superior to isoniazid or metoprolol in reflecting partial compliance over the previous 1 to 4 weeks.
Synapse has enriched 10 related papers. Consider them for comparative context: