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  • Effectiveness and sustainability of deprescribing for hospitalised older patients near end of life: a systematic review

    Author(s)
    Cardona, Magnolia
    Stehlik, Paulina
    Fawzy, Peter
    Byambasuren, Oyungerel
    Anderson, Jarrah
    Clark, Justin
    Sun, Shelley
    Scott, Ian
    Griffith University Author(s)
    Anderson, Jarrah J.
    Fawzy, Peter
    Year published
    2020
    Metadata
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    Abstract
    INTRODUCTION: Polypharmacy is prevalent in hospitals and deprescribing strategies for older people are strongly promoted. However, evidence of their feasibility and sustainability among patients receiving end of life care is lacking. The objective of this review was to ascertain effectiveness and post-discharge sustainability of hospital-initiated deprescribing strategies in older people near the end of life. AREAS COVERED: The authors searched for controlled trials, with low risk of bias and measures of effectiveness post-discharge. Intervention description, duration and healthcare provider engagement were investigated for ...
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    INTRODUCTION: Polypharmacy is prevalent in hospitals and deprescribing strategies for older people are strongly promoted. However, evidence of their feasibility and sustainability among patients receiving end of life care is lacking. The objective of this review was to ascertain effectiveness and post-discharge sustainability of hospital-initiated deprescribing strategies in older people near the end of life. AREAS COVERED: The authors searched for controlled trials, with low risk of bias and measures of effectiveness post-discharge. Intervention description, duration and healthcare provider engagement were investigated for their impact on reduction of number of medications, proportions of patients prescribed inappropriate medications, returns to emergency, hospital admission and adverse events. EXPERT OPINION: Limited evidence suggests hospital-initiated deprescribing interventions may reduce prescribing inappropriateness among older terminal patients in the short term, but evidence beyond 3 months is lacking for significant prevention of adverse events or health service utilisation. Heterogeneity precluded meta-analysis, and short follow-up periods precluded quantitative assessment of sustainability. Trials of older people with terminal conditions with larger sample sizes and longer follow-up periods are needed to confirm the effectiveness and sustainability of deprescribing at the end of life. Objective tools to reliably identify near end-of-life status would be useful in selecting target groups for these interventions.
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    Journal Title
    Expert Opinion on Drug Safety
    DOI
    https://doi.org/10.1080/14740338.2021.1853704
    Note
    This publication has been entered as an advanced online version in Griffith Research Online.
    Subject
    Nanotechnology
    Pharmacology and pharmaceutical sciences
    aged
    controlled trials
    deprescribing
    end-of-life
    polypharmacy
    Publication URI
    http://hdl.handle.net/10072/399636
    Collection
    • Journal articles

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