Improving medication prescribing-related outcomes for vulnerable elderly in transitions on high-risk medications (IMPROVE-IT HRM): a pilot randomized trial protocol.

Clinical pharmacology High-cost user High-risk medications Hospital discharge Major polypharmacy Medication management Medication safety Pilot RCT Seniors

Journal

Pilot and feasibility studies
ISSN: 2055-5784
Titre abrégé: Pilot Feasibility Stud
Pays: England
ID NLM: 101676536

Informations de publication

Date de publication:
10 Apr 2024
Historique:
received: 25 08 2023
accepted: 25 03 2024
medline: 11 4 2024
pubmed: 11 4 2024
entrez: 10 4 2024
Statut: epublish

Résumé

Seniors with recurrent hospitalizations who are taking multiple medications including high-risk medications are at particular risk for serious adverse medication events. We will assess whether an expert Clinical Pharmacology and Toxicology (CPT) medication management intervention during hospitalization with follow-up post-discharge and communication with circle of care is feasible and can decrease drug therapy problems amongst this group. The design is a pragmatic pilot randomized trial with 1:1 patient-level concealed randomization with blinded outcome assessment and data analysis. Participants will be adults 65 years and older admitted to internal medicine services for more than 2 days, who have had at least one other hospitalization in the prior year, taking five or more chronic medications including at least one high-risk medication. The CPT intervention identifies medication targets; completes consult, including priorities for improving prescribing negotiated with the patient; starts the care plan; ensures a detailed discharge medication reconciliation and circle-of-care communication; and sees the patient at least twice after hospital discharge via virtual visits to consolidate the care plan in the community. Control group receives usual care. Primary outcomes are feasibility - recruitment, retention, costs, and clinical - number of drug therapy problems improved, with secondary outcomes examining coordination of transitions in care, quality of life, and healthcare utilization and costs. Follow-up is to 3-month posthospital discharge. If results support feasibility of ramp-up and promising clinical outcomes, a follow-up definitive trial will be organized using a developing national platform and medication appropriateness network. Since the intervention allows a very scarce medical specialty expertise to be offered via virtual care, there is potential to improve the safety, outcomes, and cost of care widely. ClinicalTrials.gov identifier: NCT04077281.

Sections du résumé

BACKGROUND BACKGROUND
Seniors with recurrent hospitalizations who are taking multiple medications including high-risk medications are at particular risk for serious adverse medication events. We will assess whether an expert Clinical Pharmacology and Toxicology (CPT) medication management intervention during hospitalization with follow-up post-discharge and communication with circle of care is feasible and can decrease drug therapy problems amongst this group.
METHODS METHODS
The design is a pragmatic pilot randomized trial with 1:1 patient-level concealed randomization with blinded outcome assessment and data analysis. Participants will be adults 65 years and older admitted to internal medicine services for more than 2 days, who have had at least one other hospitalization in the prior year, taking five or more chronic medications including at least one high-risk medication. The CPT intervention identifies medication targets; completes consult, including priorities for improving prescribing negotiated with the patient; starts the care plan; ensures a detailed discharge medication reconciliation and circle-of-care communication; and sees the patient at least twice after hospital discharge via virtual visits to consolidate the care plan in the community. Control group receives usual care. Primary outcomes are feasibility - recruitment, retention, costs, and clinical - number of drug therapy problems improved, with secondary outcomes examining coordination of transitions in care, quality of life, and healthcare utilization and costs. Follow-up is to 3-month posthospital discharge.
DISCUSSION CONCLUSIONS
If results support feasibility of ramp-up and promising clinical outcomes, a follow-up definitive trial will be organized using a developing national platform and medication appropriateness network. Since the intervention allows a very scarce medical specialty expertise to be offered via virtual care, there is potential to improve the safety, outcomes, and cost of care widely.
TRIAL REGISTRATION NUMBER BACKGROUND
ClinicalTrials.gov identifier: NCT04077281.

Identifiants

pubmed: 38600599
doi: 10.1186/s40814-024-01484-6
pii: 10.1186/s40814-024-01484-6
doi:

Banques de données

ClinicalTrials.gov
['NCT04077281']

Types de publication

Journal Article

Langues

eng

Pagination

60

Subventions

Organisme : CIHR
ID : TEG-165595)
Pays : Canada

Informations de copyright

© 2024. The Author(s).

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Auteurs

Anne Holbrook (A)

Division of Clinical Pharmacology and Toxicology, Department of Medicine, McMaster University, Hamilton, ON, Canada. holbrook@mcmaster.ca.
Clinical Pharmacology Research, Research Institute of St. Joes Hamilton, Hamilton, ON, Canada. holbrook@mcmaster.ca.
Department of Health Research Methods, Evidence and Impact (HEI), McMaster University, Hamilton, ON, Canada. holbrook@mcmaster.ca.

Dan Perri (D)

Division of Clinical Pharmacology and Toxicology, Department of Medicine, McMaster University, Hamilton, ON, Canada.
Digital Solutions, St. Joseph's Healthcare Hamilton, Hamilton, Canada.

Mitch Levine (M)

Division of Clinical Pharmacology and Toxicology, Department of Medicine, McMaster University, Hamilton, ON, Canada.
Department of Health Research Methods, Evidence and Impact (HEI), McMaster University, Hamilton, ON, Canada.

Lawrence Mbuagbaw (L)

Department of Health Research Methods, Evidence and Impact (HEI), McMaster University, Hamilton, ON, Canada.
Department of Anesthesia, McMaster University, Hamilton, ON, Canada.
Department of Pediatrics, McMaster University, Hamilton, ON, Canada.
Biotatistics Unit, Research Institute of St. Joes Hamilton, Hamilton, ON, Canada.
Centre for Development of Best Practices in Health (CDBPH), Yaoundé Central Hospital, Yaoundé, Cameroon.
Division of Epidemiology and Biostatistics, Department of Global Health, Stellenbosch University, Cape Town, South Africa.

Sarah Jarmain (S)

Medical and Academic Affairs, St. Joseph's Healthcare Hamilton, Hamilton, ON, Canada.

Lehana Thabane (L)

Department of Health Research Methods, Evidence and Impact (HEI), McMaster University, Hamilton, ON, Canada.
Biotatistics Unit, Research Institute of St. Joes Hamilton, Hamilton, ON, Canada.
Faculty of Health Sciences, University of Johannesburg, Johannesburg, South Africa.

Jean-Eric Tarride (JE)

Department of Health Research Methods, Evidence and Impact (HEI), McMaster University, Hamilton, ON, Canada.
Center for Health Economic and Policy Analysis, McMaster University, Hamilton, ON, Canada.
Programs for Assessment of Technology in Health (PATH), The Research Institute of St. Joes Hamilton, Hamilton, ON, Canada.

Lisa Dolovich (L)

Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, ON, Canada.
Department of Family Medicine, McMaster University, Hamilton, ON, Canada.

Sylvia Hyland (S)

Institute for Safe Medication Practices Canada, North York, ON, Canada.

Victoria Telford (V)

Clinical Pharmacology Research, Research Institute of St. Joes Hamilton, Hamilton, ON, Canada.

Jessyca Silva (J)

Clinical Pharmacology Research, Research Institute of St. Joes Hamilton, Hamilton, ON, Canada.

Carmine Nieuwstraten (C)

Pharmacy Services, St. Joseph's Healthcare Hamilton, Hamilton, ON, Canada.

Classifications MeSH