Why the study?
Is in vitro anticholinergic activity of commonly prescribed medications associated with neuropsychiatric adverse events, and does age affect this relationship?
Is in vitro anticholinergic activity of commonly prescribed medications associated with neuropsychiatric adverse events, and does age affect this relationship?
Older age significantly increases the odds of reporting neuropsychiatric adverse events when exposed to medications with anticholinergic activity, reinforcing the need for cautious prescribing in this population.
May inform cautious prescribing in adults ≥65 years; extends observational data on anticholinergic interactions but remains hypothesis-generating.
This study sought to determine whether the presence of in vitro anticholinergic activity (AA) among different drugs is associated with reporting of neuropsychiatric adverse events (NPAEs) and whether age affects this relationship. Retrospective case/noncase analyses using Australia's spontaneous Adverse Drug Reaction System (ADRS) database containing 150 475 reports determined crude and adjusted reporting odds ratios (RORs) for NPAEs for 23 drugs with various reported in vitro AA. Covariates were age (treated as a dichotomous variable [> or =65 years]), gender, and concomitant use of antipsychotics, benzodiazepines, tricyclic antidepressants, and drugs with recognized inherent anticholinergic properties (anticholinergic drugs). The interaction effect between these covariates and each drug exposure category was examined. Age (> or =65 years) has a significant association with greater odds relative to younger age for reporting NPAEs. Drugs with reported significant AA in vitro were not always associated with RORs greater than 1 for reporting NPAEs, highlighting a dissonance between the in vitro AA index and ADRS observations. Significant interactions were observed between age (> or =65 years) and exposure to cimetidine, anticholinergic drugs, antipsychotics, and tricyclic antidepressants in modifying odds for reporting NPAEs, reinforcing the need for cautious use and monitoring of drugs with AA in older people.
No takes yet. Share an insight, caveat, or question.
Nishtala et al. (2009) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: