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Myocardial Infarction Prescription Duration Adherence Study

Length of Initial Prescription at Hospital Discharge and Long-term Medication Adherence for Elderly Patients Post-Myocardial Infarction: An Interventional Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03257579
Acronym
MIPAD
Enrollment
20896
Registered
2017-08-22
Start date
2017-09-05
Completion date
2021-07-31
Last updated
2022-03-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Medication Adherence

Keywords

Myocardial Infarction, Adherence, Medication

Brief summary

Quasi-experimental, controlled interrupted time series design, evaluating the impact of the intervention at Hamilton Health Sciences (HHS) where standardized prescriptions and education will be provided and St Joseph's Hospital (SJH) and Niagara Health Services (NHS) where education alone will be provided, with remaining Ontario cardiac sites as a concurrent control group.

Detailed description

The overarching goal of this study is to reduce the morbidity and mortality of post-MI patients through improved long-term cardiac medication adherence. The specific objectives include: 1. Assess the impact on long-term cardiac medication adherence following the implementation of a standardized increase in discharge prescription length to 90-days with 3 repeats in post-MI patients as compared to education alone and usual care; 2. Assess the cost implications of the intervention as compared to usual care; 3. Compare clinical outcomes between longer (\>60 days) versus shorter prescription durations; 4. Collect baseline information to inform a multi-centre interventional study (i.e., simple monthly proportions of 1-year adherence by hospitals in Ontario). Intervention:1. Policy Change implementing a standardized discharge prescription form available on all wards where MI patients are managed at HHS that includes a 90-day supply with 3 repeats for all cardiac medications, and education alone provided at SJH and NHS 2. Educational materials will be disseminated to all involved health care providers (e.g., physicians, residents, nurses) at the start of the intervention period to ensure the new discharge prescriptions are understood and used. Furthermore, extensive outreach to community pharmacies in LHIN IV will be undertaken with help from Ontario Pharmacists' Association (OPA) and Ontario Pharmacy Evidence Network (OPEN). 3\. Education (e.g., emails, mail-outs, site visits) will recur every 3-4 months during the intervention period. Furthermore, monthly monitoring will ensure standardized prescription forms and point of care reminders are implemented at all intervention sites. The intervention group will be exposed to this intervention post-MI and include all eligible patients at HHS/SJH/NHS in the 6-months post-intervention implementation.

Interventions

OTHER90 Day Supply

Policy Change implementing a 90 day standardized discharge prescription form with 3 repeats for all cardiac medications available on all wards where MI patients are managed at Hamilton Health Sciences sites

BEHAVIORALEducation

Education Alone provided at St. Joseph's Hospital and Niagara Health System

Sponsors

Population Health Research Institute
CollaboratorOTHER
Institute for Clinical Evaluative Sciences
CollaboratorOTHER
Hamilton Health Sciences Corporation
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Use of Ontario Drug Benefits (ODB-Age \>65 years, social assistance, and disability); * Cardiac catheterization during an index admission with an MI; * Evidence of obstructive coronary artery disease; * Discharged alive * Ontario Residents (Ontario, Canada)

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Proportion of Patients with High AdherenceOne yearIncreased proportion of patients with high adherence (proportion of days covered (PDC) \>80%) for the combined four cardiac medications classes at one year

Secondary

MeasureTime frameDescription
Difference in adherence of medication classesOne yearDifference in proportion with high adherence (mean PDC \>80%) to the individual cardiac medication classes
Difference in combined and individual medications as measured by Proportion of Days Covered (PDC)One yearDifference in mean of Proportion of Days Covered (PDC \>80%) of the combined cardiac medications as compared to PDC of individual cardiac medications classes as collected by Ontario Drug Benefits usage and reported to the Institute of Clinical Evaluative Sciences (ICES).
Discharge Prescription LengthOne yearDifference in discharge prescription length (\<90 days and ≥90 days)
Clinical outcomes as measured by number of participants who experience death, myocardial infarction, coronary revascularization, and hospital readmissionOne yearDifference in proportion of participants experiencing death, myocardial infarction, coronary revascularization and hospital readmission at one year at each interventional site compared to control sites, as reported by Cardiac Care Network and analyzed by ICES.
Cost implicationsOne yearCost implications of interventions of each arm

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026