Affiliation:
1. Laboratory of Clinical Pharmacy Gifu Pharmaceutical University Gifu‐shi Gifu Japan
2. Department of Clinical Pharmacy Graduate School of Pharmaceutical Sciences Nagoya City University Nagoya‐shi Aichi Japan
3. Laboratory of Pharmaceutical Health Care and Promotion Gifu Pharmaceutical University Gifu‐shi Gifu Japan
4. Department of Pharmacy Gifu Municipal Hospital Gifu‐shi Gifu Japan
5. Department of Psychiatry Gifu Municipal Hospital Gifu‐shi Gifu Japan
Abstract
AbstractObjectiveIn psychiatry, polypharmacy or high psychotropic drug doses increase adverse drug event (ADE) prevalence. However, the full relationship between polypharmacy and ADEs is unclear, and few studies have evaluated dose equivalents for psychotropic drugs for ADEs. Thus, we conducted a retrospective analysis to clarify the effects of polypharmacy and chlorpromazine (CP)‐, diazepam (DAP)‐, and imipramine‐ equivalent doses on all ADEs in inpatients.MethodsPsychiatric inpatients in a Japanese hospital from April 1, 2016 to March 31, 2018, were enrolled. ADE severity and causality were assessed. Multiple logistic regression analyses were performed to evaluate ADE risk factors.ResultsAmong 462 patients analyzed, out of 471 patients enrolled, 145 (31.4%) experienced ADEs. The causality assessment determined that “possible” was 96.5%. The most common ADEs were nervous system disorders (35%). Multiple logistic regression analyses indicated an increase in ADE prevalence with the number of drugs used (≥5; p = 0.026); CP‐equivalent dose (p = 0.048); and endocrine, nutritional, and metabolic disorders (p = 0.045). DAP‐equivalent dose; infectious and parasitic diseases; and injury, poisoning, and consequences of other external causes decreased ADE prevalence (p = 0.047, 0.022, and 0.021, respectively).ConclusionsAvoiding polypharmacy in psychiatric inpatients and adjusting drug regimens to safe equivalent doses could reduce ADEs during hospitalization.