Abstract
Objective
Polypharmacy increases the risk of adverse drug events and drug–drug interactions, and contributes to falls, hospital admissions, morbidity and mortality. Veterans with post-traumatic stress disorder often have psychological and physical comorbidities, increasing the likelihood of general and psychotropic polypharmacy. This study investigates the prevalence of general and psychotropic polypharmacy in inpatient veterans with post-traumatic stress disorder, and illustrates potential risks associated with polypharmacy in this population.
Methods
Medical records of 219 veterans admitted to a mental health facility for post-traumatic stress disorder management were retrospectively reviewed. Medication lists on admission were extracted and coded according to Anatomical Therapeutic Chemical Classification classes. The prevalence of general (five or more total medications), psychotropic (two or more N-code medications), and sedative (two or more medications with sedating effects) polypharmacy and Drug Burden Index were calculated. Class combinations were reported, and associations between demographic characteristics and polypharmacy were determined.
Results
Mean age was 62.5 (± 14.6) years. In addition to post-traumatic stress disorder, 90.9% had a diagnosis of at least one other psychiatric condition, and 96.8% had a diagnosis of at least one non-psychiatric medical condition. The prevalence of general polypharmacy was 76.7%, psychotropic polypharmacy was 79.9% and sedative polypharmacy was 75.3%. Drug Burden Index scores ranged from 0 to 8.2, with 66.2% of participants scoring ≥ 1.
Conclusions
This cohort of inpatient veterans with post-traumatic stress disorder had a high prevalence of general, psychotropic and sedative polypharmacy, and were at high risk for drug-related adverse events. This highlights the importance of increasing awareness of polypharmacy and potentially inappropriate drug combinations, and the need for improved medication review by prescribers.
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Details
; Khoo, Andrew 2 ; Saunders-Dow, Elise 1 ; Raguz, Ella 1 ; Taing, Meng-Wong 3 ; Hanjani, Leila Shafiee 4 ; Freeman, Chris 3 ; Crawford, Darrell 1 1 Greenslopes Private Hospital, Gallipoli Medical Research Foundation, Greenslopes, Australia (GRID:grid.413313.7) (ISNI:0000 0004 0406 7034)
2 Toowong Private Hospital, Toowong, Australia (GRID:grid.413313.7)
3 The University of Queensland, Pharmacy Australia Centre of Excellence (PACE), School of Pharmacy, Woolloongabba, Australia (GRID:grid.1003.2) (ISNI:0000 0000 9320 7537)
4 The University of Queensland, Princess Alexandra Hospital, Centre for Health Sciences Research, Faculty of Medicine, Woolloongabba, Australia (GRID:grid.1003.2) (ISNI:0000 0000 9320 7537)





