TY - JOUR
T1 - Deprescribing
T2 - Future directions for research
AU - Thompson, Wade
AU - Reeve, Emily
AU - Moriarty, Frank
AU - Maclure, Malcolm
AU - Turner, Justin
AU - Steinman, Michael A.
AU - Conklin, James
AU - Dolovich, Lisa
AU - McCarthy, Lisa
AU - Farrell, Barbara
N1 - Funding Information:
Dr. Thompson reports honoraria for deprescribing presentations from University of Ottawa, University of British Columbia and Ontario Long-Term Care Clinicians Conference. Dr. Reeve reports grants from Australian National Health and Medical Research Council-Australian Research Council , a research award from the Bupa Health Foundation and deprescribing presentation fees from the Pharmacy Association of Nova Scotia and the Swiss Society of Internal Medicine . Dr. McCarthy reports travel support for a presentation from NHS England. Dr. Farrell reports honoraria for deprescribing presentations from College of Psychiatric and Neurologic Pharmacists, European Association of Hospital Pharmacists, Nova Scotia College of Pharmacists. Drs. Farrell and Conklin received a stipend from the Institute for Healthcare Improvement for advice and review of documents related to introducing deprescribing into the US healthcare system.
Funding Information:
Funding for the planning and implementation of the symposium was provided by a Knowledge Mobilization Partnership Program grant through the Centre for Aging and Brain Health Innovation . Additional financial support was provided by the Bruyère Centre for Learning, Research and Innovation , the Canadian Foundation for Healthcare Improvement , CADTH , Medical Pharmacies and the Canadian Deprescribing Network . Funders were not involved in the writing of this report.
Funding Information:
Dr. Thompson reports honoraria for deprescribing presentations from University of Ottawa, University of British Columbia and Ontario Long-Term Care Clinicians Conference. Dr. Reeve reports grants from Australian National Health and Medical Research Council-Australian Research Council, a research award from the Bupa Health Foundation and deprescribing presentation fees from the Pharmacy Association of Nova Scotia and the Swiss Society of Internal Medicine. Dr. McCarthy reports travel support for a presentation from NHS England. Dr. Farrell reports honoraria for deprescribing presentations from College of Psychiatric and Neurologic Pharmacists, European Association of Hospital Pharmacists, Nova Scotia College of Pharmacists. Drs. Farrell and Conklin received a stipend from the Institute for Healthcare Improvement for advice and review of documents related to introducing deprescribing into the US healthcare system.Funding for the planning and implementation of the symposium was provided by a Knowledge Mobilization Partnership Program grant through the Centre for Aging and Brain Health Innovation. Additional financial support was provided by the Bruy?re Centre for Learning, Research and Innovation, the Canadian Foundation for Healthcare Improvement, CADTH, Medical Pharmacies and the Canadian Deprescribing Network. Funders were not involved in the writing of this report. Thank you to the many notetakers and to Salima Suleman for her work in compiling and summarizing the notes from each workshop table. The team also thanks Heera Sen and Stephen Smith for their assistance in preparing these commentaries for publication.
Funding Information:
Funding for the planning and implementation of the symposium was provided by a Knowledge Mobilization Partnership Program grant through the Centre for Aging and Brain Health Innovation. Additional financial support was provided by the Bruyère Centre for Learning, Research and Innovation, the Canadian Foundation for Healthcare Improvement, CADTH, Medical Pharmacies and the Canadian Deprescribing Network. Funders were not involved in the writing of this report.
Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2019/6
Y1 - 2019/6
N2 - A World Café workshop was held at the Bruyère Evidence-Based Deprescribing Guidelines Symposium in March 2018 with 30 participants (researchers, clinicians, policy makers, stakeholders). This workshop explored priorities for future work in the field of deprescribing and deprescribing guidelines through group discussion. The discussions were guided by the following questions: (1) What are deprescribing research priorities (to inform guideline development), (2) What outcome measures are important for developing deprescribing guidelines, and (3) How do we evaluate the implementation and effectiveness of deprescribing guidelines? Discussion from all 3 questions identified 6 main priority areas: (1) conducting high-quality and long-term clinical trials that measure patient-important outcomes, (2) focusing on patient involvement and perspectives, (3) investigating the pharmacoeconomics of deprescribing interventions, (4) understanding deprescribing interventions in different populations, (5) generating evidence on clinical management during deprescribing (e.g. managing adverse drug withdrawal effects, subsequent re-prescribing), and (6) implementing interventions in clinical practice. These topics represent what a group of experienced researchers, clinicians, and stakeholders in the field collectively felt was important to consider for design and implementation of future deprescribing studies. The aim is for these findings to stimulate future discussions and be considered by granting agencies, policy makers, deprescribing research networks, and individual researchers planning future deprescribing studies.
AB - A World Café workshop was held at the Bruyère Evidence-Based Deprescribing Guidelines Symposium in March 2018 with 30 participants (researchers, clinicians, policy makers, stakeholders). This workshop explored priorities for future work in the field of deprescribing and deprescribing guidelines through group discussion. The discussions were guided by the following questions: (1) What are deprescribing research priorities (to inform guideline development), (2) What outcome measures are important for developing deprescribing guidelines, and (3) How do we evaluate the implementation and effectiveness of deprescribing guidelines? Discussion from all 3 questions identified 6 main priority areas: (1) conducting high-quality and long-term clinical trials that measure patient-important outcomes, (2) focusing on patient involvement and perspectives, (3) investigating the pharmacoeconomics of deprescribing interventions, (4) understanding deprescribing interventions in different populations, (5) generating evidence on clinical management during deprescribing (e.g. managing adverse drug withdrawal effects, subsequent re-prescribing), and (6) implementing interventions in clinical practice. These topics represent what a group of experienced researchers, clinicians, and stakeholders in the field collectively felt was important to consider for design and implementation of future deprescribing studies. The aim is for these findings to stimulate future discussions and be considered by granting agencies, policy makers, deprescribing research networks, and individual researchers planning future deprescribing studies.
KW - Deprescribing
KW - Guidelines
KW - Polypharmacy
KW - Research
UR - http://www.scopus.com/inward/record.url?scp=85053131836&partnerID=8YFLogxK
U2 - 10.1016/j.sapharm.2018.08.013
DO - 10.1016/j.sapharm.2018.08.013
M3 - Comment / Debate
C2 - 30241876
AN - SCOPUS:85053131836
SN - 1551-7411
VL - 15
SP - 801
EP - 805
JO - Research in Social and Administrative Pharmacy
JF - Research in Social and Administrative Pharmacy
IS - 6
ER -