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Subtherapeutic Acetazolamide Doses as a Noninvasive Method for Assessing Medication Adherence
Author(s) -
Hampson Aidan J.,
Schroeder Jennifer R.,
Ellefsen Kayla N.,
Yammine Luba,
Epstein David H.,
Preston Kenzie L.,
Huestis Marilyn A.,
Verrico Christopher D.
Publication year - 2020
Publication title -
clinical pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.941
H-Index - 188
eISSN - 1532-6535
pISSN - 0009-9236
DOI - 10.1002/cpt.1929
Subject(s) - acetazolamide , medicine , clinical trial , excretion , pharmacokinetics , creatinine , urinary system , adverse effect , pharmacology , intensive care medicine
Adherence monitoring is a vital component of clinical efficacy trials, as the regularity of medication consumption affects both efficacy and adverse effect profiles. Pill‐counts do not confirm consumption, and invasive plasma assessments can only assist post hoc assessments. We previously reported on the pharmacokinetics of a potential adherence marker to noninvasively monitor dosage consumption during a trial without breaking a blind. We reported that consumption cessation of subtherapeutic 15 mg acetazolamide (ACZ) doses showed a predictable urinary excretion decay that was quantifiable for an extended period. The current study describes the clinical implementation of 15 mg ACZ doses as an adherence marker excipient in distinct cohorts taking ACZ for different “adherence” durations. We confirm that ACZ output did not change (accumulate) during 18–20 days of adherence, and developed and assessed urinary cutoffs as nonadherence indicators. We demonstrate that whereas an absolute concentration cutoff (989 ng/mL) lacked sensitivity, a creatinine normalized equivalent (1,376 ng/mg ACZ) was highly accurate at detecting nonadherence. We also demonstrate that during nonadherent phases of three trials, creatinine‐normalized urinary ACZ elimination was reproducible within and across trials with low variability. Excretion was first order, with a decay half‐life averaging ~ 2.0 days. Further, excretion remained quantifiable for 14 days, providing a long period during which the date of last consumption might be determined. We conclude that inclusion of 15 mg ACZ as a dosage form adherence marker excipient, provides a reliable and sensitive mechanism to confirm medication consumption and detect nonadherence during clinical efficacy trials.