4.2 Article

DEFEAT-polypharmacy: deprescribing anticholinergic and sedative medicines feasibility trial in residential aged care facilities

Journal

INTERNATIONAL JOURNAL OF CLINICAL PHARMACY
Volume 41, Issue 1, Pages 167-178

Publisher

SPRINGER
DOI: 10.1007/s11096-019-00784-9

Keywords

Anticholinergic; Deprescribing; Drug burden index; Elderly; Feasibility study; New Zealand; Sedatives

Funding

  1. Lotteries Health Research (LHR)

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Background Prolonged use of anticholinergic and sedative medicines is correlated with worsening cognition and physical function decline. Deprescribing is a proposed intervention that can help to minimise polypharmacy whilst potentially improving several health outcomes in older people. Objective This study aimed to examine the feasibility of implementing a deprescribing intervention that utilises a patient-centred pharmacist-led intervention model; in order to address major deprescribing challenges such as general practitioner time constraints and lack of accessible deprescribing guidelines and processes. Setting Three residential care facilities. Methods The intervention involved a New Zealand registered pharmacist utilising peer-reviewed deprescribing guidelines to recommend targeted deprescribing of anticholinergic and sedative medicines to GPs. Main outcome measure The change in the participants' Drug Burden Index (DBI) total and DBI as required' (PRN) was assessed 3 and 6months after implementing the deprescribing intervention. Results Seventy percent of potential participants were recruited for the study (n=46), and 72% of deprescribing recommendations suggested by the pharmacist were implemented by General Pratitioners(p=0.01; Fisher's exact test). Ninety-six percent of the residents agreed to the deprescribing recommendations, emphasising the importance of patient centred approach. Deprescribing resulted in a significant reduction in participants' DBI scores by 0.34, number of falls and adverse drug reactions, 6months post deprescribing. Moreover, participants reported lower depression scores and scored lower frailty scores 6months after deprescribing. However, cognition did not improve; nor did participants' reported quality of life. Conclusion This patient-centred deprescribing approach, demonstrated a high uptake of deprescribing recommendations and success rate. After 6months, significant benefits were noted across a range of important health measures including mood, frailty, falls and reduced adverse reactions. This further supports deprescribing as a possible imperative to improve health outcomes in older adults.

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