RecruitingNCT03733262

Targeted Deprescribing in Patients on Hemodialysis

Implementation of Deprescribing and Patient Education Tools in Hemodialysis Units to Decrease Polypharmacy


Sponsor

University Health Network, Toronto

Enrollment

480 participants

Start Date

Oct 1, 2022

Study Type

OBSERVATIONAL

Conditions

Summary

Hemodialysis (HD) patients take more pills per day on average than any other chronically ill patient population. On average, an HD patient takes 19 medications per day, of which 70% may not be appropriate. The reason the medications may not be appropriate is that HD patients are rarely included in clinical trials for new medications and therefore the efficacy and safety data that exists for the general population may not actually apply to them. Tools to guide the re-assessment and discontinuation (deprescribing) of these specific medications that lack evidence for efficacy and safety in HD patients are needed. These tools will help reduce the amount of medications being taken and the potential negative consequences of taking so many medications (e.g. adverse drug reactions, drug interactions, non-adherence, increased risk of cognitive impairment, impaired balance and falls, and increased risk of morbidity, hospitalization, and mortality). Nine medications that are often inappropriately prescribed to HD patients have been identified by the investigators. These medications are: Alpha-1 Blockers, Anticonvulsants, Benzodiazepines \& Z-Drugs, Loop Diuretics, Prokinetic Agents, Proton Pump Inhibitors, Quinine, Urate Lowering Agents, and Statins. The investigators developed and validated tools to help medical teams in outpatient HD units with identifying and stopping these medications in their patients. The next step will be to perform a study where test these tools are tested in practice at multiple HD centers across Canada. This initiative should decrease the average number of medications per patient and inappropriate medication use in the HD units where these tools are used. The overall objective of this study is to improve current clinical practice by optimizing medication use and prescribing patterns in the HD units across Canada.


Eligibility

Min Age: 18 Years

Inclusion Criteria3

  • + years
  • Have been receiving outpatient HD treatment at one of the four study sites for at least the past three months
  • Able to read and understand English and provide consent

Exclusion Criteria1

  • \- Acute starts to HD

Interventions

OTHERDe-prescribing Trial

Validated de-prescribing algorithms will be applied for any patients identified as taking one of the 9 study drugs in order to determine whether or not physician should consider a deprescribing trial. If they are are identified as candidates for deprescribing and consent to participate in the trial, they will enter the Deprescribing Trial group and begin the deprescribing trial.


Locations(4)

Providence Health Care

Vancouver, British Colombia, Canada

Manitoba Renal Program

Winnipeg, Manitoba, Canada

Nova Scotia Health Authority

Halifax, Nova Scotia, Canada

University Health Network

Toronto, Ontario, Canada

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT03733262