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Safer medicines To reduce falls and refractures for OsteoPorosis (#STOP): a study protocol for a randomised controlled trial of medical specialist-initiated pharmacist-led medication management reviews in primary care

  • Rebekah Jane Moles
  • , Lin Perry
  • , Justine M Naylor
  • , Jacqueline Center
  • , Peter Ebeling
  • , Gustavo Duque
  • , Gabor Major
  • , Christopher White
  • , Christopher Yates
  • , Matthew Jennings
  • , Mark Kotowicz
  • , Thach Tran
  • , Dana Bliuc
  • , Lei Si
  • , Kathryn Gibson
  • , Benjamin Joseph Basger
  • , Patrick Bolton
  • , Stephen Barnett
  • , Geraldine Hassett
  • , Ayano Kelly
  • Barbara Bazarnik, Wafaa Ezz, Kate Luckie, Stephen Ross Carter
  • The University of Sydney
  • University of Technology Sydney Faculty of Health
  • Ingham Institute for Applied Medical Research
  • Garvan Institute of Medical Research
  • Monash University
  • The University of Melbourne
  • John Hunter Hospital
  • University of New South Wales, Australia
  • The Royal Melbourne Hospital
  • Liverpool Women’s Hospital
  • Deakin University - Geelong Campus at Waurn Ponds
  • The George Institute for Global Health
  • University of Wollongong, Wollongong, NSW, Australia
  • Ingham Institute

Allbwn ymchwil: Cyfraniad at gyfnodolyn › Erthygl › adolygiad gan gymheiriaid

2 Wedi eu Llwytho i Lawr (Pure)

Crynodeb

INTRODUCTION: Minimal trauma fractures (MTFs) often occur in older patients with osteoporosis and may be precipitated by falls risk-increasing drugs. One category of falls risk-increasing drugs of concern are those with sedative/anticholinergic properties. Collaborative medication management services such as Australia's Home Medicine Review (HMR) can reduce patients' intake of sedative/anticholinergics and improve continuity of care. This paper describes a protocol for an randomised controlled trial to determine the efficacy of an HMR service for patients who have sustained MTF.

METHOD AND ANALYSIS: Eligible participants are as follows: ≥65 years of age, using ≥5 medicines including at least one falls risk-increasing drug, who have sustained an MTF and under treatment in one of eight Osteoporosis Refracture Prevention clinics in Australia. Consenting participants will be randomised to control (standard care) or intervention groups. For the intervention group, medical specialists will refer to a pharmacist for HMR focused on reducing falls risk predominately through making recommendations to reduce falls risk medicines, and adherence to antiosteoporosis medicines. Twelve months from treatment allocation, comparisons between groups will be made. The main outcome measure is participants' cumulative exposure to sedative and anticholinergics, using the Drug Burden Index. Secondary outcomes include medication adherence, emergency department visits, hospitalisations, falls and mortality. Economic evaluation will compare the intervention strategy with standard care.

ETHICS AND DISSEMINATION: Approval was obtained via the New South Wales Research Ethics and Governance Information System (approval number: 2021/ETH12003) with site-specific approvals granted through Human Research Ethics Committees for each research site. Study outcomes will be published in peer-reviewed journals. It will provide robust insight into effectiveness of a pharmacist-based intervention on medicine-related falls risk for patients with osteoporosis. We anticipate that this study will take 2 years to fully accrue including follow-up.

TRIAL REGISTRATION NUMBER: ACTRN12622000261718.

Iaith wreiddiolSaesneg
Rhif yr erthygle072050
CyfnodolynBMJ Open
Cyfrol13
Rhif cyhoeddi8
Dynodwyr Gwrthrych Digidol (DOIs)
StatwsCyhoeddwyd - 24 Awst 2023
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