Do QT-Prolonging Drugs Cause Major Adverse Cardiac Events in Hospitalized Adults?

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorSt. Joseph's Healthcare Hamilton

About this trial

There are 28 non-cardiology medications from multiple families costing more than $13 billion annually in Canada, categorized as 'Known' QT-prolonging medications (QTPmeds) based on very low levels of evidence. The association between many commonly used medications listed as known QTPmeds and actual major adverse cardiac events (MACE) is weak. Meanwhile, QTPmeds-related warnings are ubiquitous in every healthcare setting, triggering 'hard stop' disruption millions of times per day to front line clinicians. Poor quality medication safety alerts are increasingly recognized as a source of inferior patient care and provider burnout which detracts from healthcare sustainability.

In this study, anonymized hospital electronic medical record data from more than 990,000 adult patients across Ontario will be used to compare patients who experience MACE with those who do not, measuring their real-time exposure to QT-prolonging drugs. Additionally, machine-learning techniques will also be used to find which patient or treatment factors best predict risk.

The objectives of this study are to 1) Investigate whether exposure to one or more 'Known' QTPmed is associated with an increased risk of MACE after adjusting for confounders; and 2) Identify predictors and their relative importance for QTPmeds-associated MACE.

In summary, QT-prolonging medications have the potential to cause very serious adverse events, including death. However, it is not sufficiently clear which patients under which circumstances suffer events, or when is QT prolongation a useful surrogate marker for harm. Meanwhile, ubiquitous medication alerts related to QT-prolonging medications are at best imprecise and at worst, misleading, costly and potentially dangerous. Now that data resources are available with the data elements, structure and sample size required to rigorously assess this association, this study will address this question to improve patient safety, provider satisfaction and the cost-effectiveness of care.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult patients 18 years of age or older

Admitted to St. Joseph's Healthcare Hamilton or GEMINI hospitals between December 2017 and March 2025

Disqualifiers

Patients <18 years old

Outpatient encounters

Trial population

This is a retrospective observational study using de-identified electronic-medical-record data from St. Joseph's Healthcare Hamilton and GEMINI hospitals; no direct participant enrollment or consent is required.

Trial design

Design model

Case-control

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

990,000 Participants
are grouped into 2 trial groups
Group A: Exposed (Known QTPmeds)
Group B: Unexposed (no known QTP meds)

Trial outcomes

Primary outcomes

1

Composite of major adverse cardiac events (MACE)

Time to first MACE during hospitalization, defined as incidence of any of the following: Mortality, non-fatal cardiac arrest, ventricular arrythmia including torsades de pointes, and syncope

Time frame
From first exposure to the end of hospitalization, which would typically be up to 4 weeks follow-up.

Secondary outcomes

1

Overall Mortality

In-hospital death

Time frame
From first exposure to the end of hospitalization, which would typically be up to 4 weeks follow-up.
2

Non-fatal cardiac arrest

Cardiac arrest based on diagnosis or Code Blue or resuscitation with CPR where the patient survives

Time frame
From first exposure to the end of hospitalization, which would typically be up to 4 weeks follow-up.
3

Ventricular arrhythmias

Includes Ventricular fibrillation or tachycardia or torsades de pointes

Time frame
From first exposure to the end of hospitalization, which would typically be up to 4 weeks follow-up.
4

Syncope

Syncopal event based on diagnosis - brief loss of consciousness

Time frame
From first exposure to the end of hospitalization, which would typically be up to 4 weeks follow-up.

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

St. Joseph's Healthcare Hamilton

Lead sponsor

McMaster University

Collaborator

Canadian Institutes of Health Research (CIHR)

Collaborator