CarDIA: CCTA to Optimize the Diagnostic Yield of Invasive Angiography

Sponsor
Hamilton Health Sciences Corporation (Other)
Overall Status
Completed
CT.gov ID
NCT03554057
Collaborator
Hamilton Academic Health Sciences Organization (Other)
186
1
43.7
4.3

Study Details

Study Description

Brief Summary

This study aims to reduce patient risk and costs to the healthcare system by improving the diagnostic yield of invasive coronary angiography through existing triage processes to improve risk stratification using Coronary Computed Tomographic Angiography (CCTA) as a first step in low risk patients. All low-risk patients referred for invasive coronary angiography will be potentially eligible for CCTA instead of invasive angiography as a first-line diagnostic test. All CCTAs will be read by both a level 3-trained cardiologist and a radiologist. The results of the CCTA, coupled with evidence-based management recommendations will be sent to the referring physician and an invasive angiogram will be arranged by the HIU triage, only when clearly indicated

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Coronary Computed Tomographic Angiography

Study Design

Study Type:
Observational
Actual Enrollment :
186 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Coronary Computed Tomographic Angiography to Optimize the Diagnostic Yield of Invasive Angiography in Lower Risk Patients
Actual Study Start Date :
Jul 9, 2018
Actual Primary Completion Date :
Feb 28, 2020
Actual Study Completion Date :
Mar 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Intervention Group

All low-risk patients referred for invasive coronary angiography through the Hamilton General Hospital's Heart Investigation Unit Triage will be potentially eligible to receive the intervention over a 12-month period. The intervention will include risk stratification with CCTA at HHS and NHS as an alternative to upfront invasive angiography.

Diagnostic Test: Coronary Computed Tomographic Angiography
All low-risk patients referred for invasive coronary angiography will be potentially eligible to receive the intervention over a 12-month period. The intervention will include risk stratification using Coronary Computed Tomographic Angiography (CCTA) at HHS and NHS as an alternative to upfront invasive angiography. All CCTAs will be read by both a level 3-trained cardiologist and a radiologist. The results of the CCTA, coupled with evidence-based management recommendations will be sent to the referring physician and an invasive angiogram will be arranged only when indicated as per these management recommendations

Control Group

Intervention sites will act as their own controls: outcomes of all eligible patients in the 24-months prior to the implementation of the intervention will be assessed from a routinely collected health administrative database. Eligible patients not undergoing CCTA (patient or physician refusal, or CCTA not available) will be captured and included in the control group as part of a sensitivity analysis during the intervention period

Outcome Measures

Primary Outcome Measures

  1. Diagnostic yield of invasive angiography [Three years]

    Diagnostic yield is defined as the proportion of invasive angiograms that identify significant disease (≥70% stenosis) on a major coronary vessel (>2 mm) or > 50% stenosis in the left main)

Secondary Outcome Measures

  1. Quantitative assessment of angiograms avoided [Three years]

    Number of angiograms avoided due to CCTA bookings

  2. Deviation from management recommendations following CCTA [Three years]

    Number of angiograms performed when not recommended

  3. Protocol deviation as a surrogate for acceptability of the novel triage program [Three years]

    Percentage of patients and physicians refusing to undergo CCTA as a first step

  4. Costing of new strategy [Three years]

    Cost of risk stratification of Coronary Artery Disease in low risk patients

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Non urgent outpatient referral

  2. Canadian Cardiovascular Society class I or II

  3. Indication for invasive angiogram includes: Rule out Coronary Artery Disease (CAD) and Cardiomyopathy

Exclusion Criteria:
  1. Age <18 years old, Men >65 years old or women >75 years old

  2. Patient refusal to provide verbal consent for CCTA at time of triage contact or unable to provide informed consent

  3. Referring physician refusal for their eligible patients to be approached for the CarDIA study

  4. Any prior CCTA

  5. Atrial Fibrillation

  6. Creatinine > 150 mmol/L

  7. Diabetes mellitus

  8. High risk Exercise Stress Test or Functional Imaging

  9. Known severe valvular disease being considered for valve surgery

  10. Any known CAD

  • Prior Acute Coronary Syndrome (ACS)

  • Prior Percutaneous Coronary Intervention (PCI) or Coronary Artery Bypass Graft (CABG)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hamilton General Hospital Hamilton Ontario Canada L8L 2X2

Sponsors and Collaborators

  • Hamilton Health Sciences Corporation
  • Hamilton Academic Health Sciences Organization

Investigators

  • Principal Investigator: Jon-David Schwalm, MD,FRCPC,Msc, Hamilton Health Sciences Corporation
  • Principal Investigator: Tej Sheth, Bsc,FRCPC,MD, Hamilton Health Sciences Corporation

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Hamilton Health Sciences Corporation
ClinicalTrials.gov Identifier:
NCT03554057
Other Study ID Numbers:
  • 4697
First Posted:
Jun 12, 2018
Last Update Posted:
Mar 16, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Hamilton Health Sciences Corporation
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 16, 2022