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出境医 / 临床实验 / Assessment of Patients With suspeCted Coronary Artery Disease by Coronary calciUm fiRst strATegy vErsus Usual Care Approach. (ACCURATE)

Assessment of Patients With suspeCted Coronary Artery Disease by Coronary calciUm fiRst strATegy vErsus Usual Care Approach. (ACCURATE)

Study Description
Brief Summary:

The cost of medical care in the United States far exceeds that of all other advanced economies and continues to accelerate at a rate unacceptable to our society, due primarily to the high costs of new imaging technologies and novel drugs (1). Cardiac positron emission tomography (PET) imaging is a powerful new modality for the non-invasive detection of provocable coronary ischemia in patients with low to intermediate-risk chest pain or its equivalent. Intermountain Medical Center (IMC) is performing approximately 6000 clinical cardiac PET scans annually. However, cardiac PET scans are expensive (i.e., billed at >$5,000/scan, average receivable revenue $1500-$2000/scan). Coronary artery calcium (CAC) is a sensitive marker of coronary atherosclerosis. A CAC scan (CACS), performed by multislice computed tomography (CT), is a relatively inexpensive (~$70-$150/scan), low-radiation dose test that marks the presence of coronary atherosclerotic plaque. The absence of CAC has been shown to be associated with very low coronary risk. ACCURATE will test whether a CAC-first strategy (i.e., risk stratification, when CAC ≤ 1, to medical management or to cardiac PET stress testing), performed routinely in symptomatic patients presenting for evaluation of possible coronary artery disease (CAD) prior to the cardiac PET stress test, can be used as a gatekeeper for progression to the expensive rubidium-PET stress (regadenoson) perfusion scan and be a major cost-saver without adversely affecting patient care or outcomes. Routinely, qualifying patients undergo CACS when they present for evaluation of possible but unknown CAD status and are referred for cardiac PET stress testing. In ACCURATE, those with CACS≤1 will then be consented and randomized to either a cardiac PET stress test strategy or a non-PET-driven medical care strategy. Subjects randomized to the cardiac PET stress test strategy will receive appropriate subsequent care depending on the outcome of the cardiac PET scan (i.e., depending on whether ischemia is present or not). Subjects randomized to the CAC-only arm will receive appropriate non-PET driven medical clinical management and follow-up. All participating subjects' electronic medical records will be reviewed indefinitely for clinical outcomes. Initial outcomes will be reported at 1-year, 2-years, and 5-years, with future analyses to be determined by the study investigators.

The objective of this study is to test the hypothesis that PET stress test strategy will results in a decreasing in major adverse cardiac endpoint without exceeding $100,000 per quality-adjusted life year compared to a CAC-first strategy for screening suspected/possible coronary artery disease.


Condition or disease Intervention/treatment Phase
Coronary Artery Disease Diagnostic Test: PET Stress Test Other: Non-PET Medical Management Not Applicable

Study Design
Layout table for study information
Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 2500 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Screening
Official Title: Assessment of Patients With suspeCted Coronary Artery Disease by Coronary calciUm fiRst strATegy vErsus Usual Care Approach
Actual Study Start Date : November 19, 2019
Estimated Primary Completion Date : November 2022
Estimated Study Completion Date : November 2027
Arms and Interventions
Arm Intervention/treatment
Cardiac PET stress testing and test-dependent management
Subjects randomized to the cardiac PET stress test strategy will receive appropriate subsequent care depending on the outcome of the cardiac PET scan (i.e., depending on whether ischemia is present or not).
Diagnostic Test: PET Stress Test
Cardiac positron emission tomography (PET)/computed tomography (CT) and test-result dependent management

Management without stress-imaging
Subjects randomized to the CAC-only arm will receive appropriate non-PET driven medical clinical management and follow-up.
Other: Non-PET Medical Management
Appropriate medical management without cardiac PET stress-imaging

Outcome Measures
Primary Outcome Measures :
  1. Non-inferior major adverse cardiac endpoint (MACE) outcomes [ Time Frame: 1 year ]
    Routine cardiac PET stress test strategy will result in significantly fewer major adverse cardiac endpoint (MACE) outcomes (defined as coronary death, non-fatal myocardial infarction, cardiac arrest, or ischemia driven revascularization) at 1 year compared with a a CAC-first strategy.

  2. Cost-effectiveness [ Time Frame: 5 years ]
    The costs of routine cardiac PET stress test strategy will be less than <$100,000 per quality-adjusted life year (QALY) compared to CAC-first strategy. Cost-effectiveness, categorized by the American Heart Association, will be defined as achieving at least fair cost effectiveness, i.e., as achieving <$100,000/QALY, which is widely accepted as a "willingness-to-pay" threshold, with <$50,000/QALY defined as good cost-effectiveness.


Eligibility Criteria
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Ages Eligible for Study:   50 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Males or females ≥50 years old (i.e., to be of sufficiently high pre-test coronary risk)
  • Cardiac PET regadenoson stress perfusion test has been ordered to assess a possible ischemic etiology of low/intermediate risk chest pain or equivalent symptoms (e.g., exertional dyspnea).
  • Ability to understand and sign a written informed consent form, which must be obtained prior to initiation of any study procedures
  • CAC score of ≥1 per routine CAC first strategy (described above)

Exclusion Criteria:

  1. Disease history: If available for any of the following diseases: prior known CAD, heart transplant, LVAD, untreated severe valve disease (i.e., severe mitral stenosis, severe mitral regurgitation, and/or severe aortic stenosis), or decompensated heart failure (DHF).
  2. Those with a prior CAC score >1.
  3. CAC ≤1 prior to this current episode of cardiac assessment

    • Who ELECT to not receive an updated CAC evaluation OR their referring clinician specifically prefers cardiac PET.
    • CAC evaluation repeated at this current episode of cardiac assessment and is now >1.
  4. Evidence of possible acute coronary syndrome based on an elevated troponin I ≥0.04ng/mL and/or acute ECG changes of ischemia.
  5. Life expectancy <1 year, as assessed by the investigator(s)
  6. Cardiac PET/CT is ordered in the pre-operative risk assessment in higher risk non-thoracic surgery.
  7. Cardiac PET/CT is ordered for assessment of underlying ischemia in those with arrhythmia to guide anti-arrhythmic therapy.
  8. Other conditions that in the opinion of the study investigators and/or referring clinician may increase risk to the subject and/or compromise the quality of the clinical trial.
Contacts and Locations

Contacts
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Contact: Patti Spencer 8015074778 patti.spencer@imail.org

Locations
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United States, Utah
Intermountain Healthcare Hospitals and Clinics Recruiting
Salt Lake City, Utah, United States, 84107
Contact: Kirk U Knowlton, MD    801-507-4701    kirk.knowlton@imail.org   
Contact: Jeffrey L Anderson, MD    801-507-4757    jeffreyl.anderson@imail.org   
Sponsors and Collaborators
Intermountain Health Care, Inc.
Investigators
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Principal Investigator: Kirk U Knowlton, MD Intermountain Medical Center
Principal Investigator: Jeffrey L Anderson, MD Intermountain Medical Center
Tracking Information
First Submitted Date  ICMJE May 31, 2019
First Posted Date  ICMJE June 4, 2019
Last Update Posted Date April 5, 2021
Actual Study Start Date  ICMJE November 19, 2019
Estimated Primary Completion Date November 2022   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: February 7, 2020)
  • Non-inferior major adverse cardiac endpoint (MACE) outcomes [ Time Frame: 1 year ]
    Routine cardiac PET stress test strategy will result in significantly fewer major adverse cardiac endpoint (MACE) outcomes (defined as coronary death, non-fatal myocardial infarction, cardiac arrest, or ischemia driven revascularization) at 1 year compared with a a CAC-first strategy.
  • Cost-effectiveness [ Time Frame: 5 years ]
    The costs of routine cardiac PET stress test strategy will be less than <$100,000 per quality-adjusted life year (QALY) compared to CAC-first strategy. Cost-effectiveness, categorized by the American Heart Association, will be defined as achieving at least fair cost effectiveness, i.e., as achieving <$100,000/QALY, which is widely accepted as a "willingness-to-pay" threshold, with <$50,000/QALY defined as good cost-effectiveness.
Original Primary Outcome Measures  ICMJE
 (submitted: May 31, 2019)
  • Non-inferior major adverse cardiac endpoint (MACE) outcomes [ Time Frame: 1 year ]
    Using a CAC-first strategy will result in non-inferior major adverse cardiac endpoint (MACE) outcomes (defined as within 1 absolute percentage point MACE, defined as coronary or heart failure death, non-fatal myocardial infarction, heart failure hospitalization, cardiac arrest, or unstable angina requiring revascularization) at 1 year compared with a routine cardiac PET stress test strategy.
  • Cost-effectiveness [ Time Frame: 5 years ]
    A CAC-first strategy will be more cost-effective than a routine cardiac PET stress test strategy. Cost-effectiveness, categorized by the American Heart Association, will be defined as achieving at least fair cost effectiveness, i.e., as achieving an additional quality-adjusted life year (QALY) for <$100,000, which is widely accepted as a "willingness-to-pay" threshold, with <$50,000/QALY defined as good cost-effectiveness.
Change History
Current Secondary Outcome Measures  ICMJE Not Provided
Original Secondary Outcome Measures  ICMJE Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE Assessment of Patients With suspeCted Coronary Artery Disease by Coronary calciUm fiRst strATegy vErsus Usual Care Approach.
Official Title  ICMJE Assessment of Patients With suspeCted Coronary Artery Disease by Coronary calciUm fiRst strATegy vErsus Usual Care Approach
Brief Summary

The cost of medical care in the United States far exceeds that of all other advanced economies and continues to accelerate at a rate unacceptable to our society, due primarily to the high costs of new imaging technologies and novel drugs (1). Cardiac positron emission tomography (PET) imaging is a powerful new modality for the non-invasive detection of provocable coronary ischemia in patients with low to intermediate-risk chest pain or its equivalent. Intermountain Medical Center (IMC) is performing approximately 6000 clinical cardiac PET scans annually. However, cardiac PET scans are expensive (i.e., billed at >$5,000/scan, average receivable revenue $1500-$2000/scan). Coronary artery calcium (CAC) is a sensitive marker of coronary atherosclerosis. A CAC scan (CACS), performed by multislice computed tomography (CT), is a relatively inexpensive (~$70-$150/scan), low-radiation dose test that marks the presence of coronary atherosclerotic plaque. The absence of CAC has been shown to be associated with very low coronary risk. ACCURATE will test whether a CAC-first strategy (i.e., risk stratification, when CAC ≤ 1, to medical management or to cardiac PET stress testing), performed routinely in symptomatic patients presenting for evaluation of possible coronary artery disease (CAD) prior to the cardiac PET stress test, can be used as a gatekeeper for progression to the expensive rubidium-PET stress (regadenoson) perfusion scan and be a major cost-saver without adversely affecting patient care or outcomes. Routinely, qualifying patients undergo CACS when they present for evaluation of possible but unknown CAD status and are referred for cardiac PET stress testing. In ACCURATE, those with CACS≤1 will then be consented and randomized to either a cardiac PET stress test strategy or a non-PET-driven medical care strategy. Subjects randomized to the cardiac PET stress test strategy will receive appropriate subsequent care depending on the outcome of the cardiac PET scan (i.e., depending on whether ischemia is present or not). Subjects randomized to the CAC-only arm will receive appropriate non-PET driven medical clinical management and follow-up. All participating subjects' electronic medical records will be reviewed indefinitely for clinical outcomes. Initial outcomes will be reported at 1-year, 2-years, and 5-years, with future analyses to be determined by the study investigators.

The objective of this study is to test the hypothesis that PET stress test strategy will results in a decreasing in major adverse cardiac endpoint without exceeding $100,000 per quality-adjusted life year compared to a CAC-first strategy for screening suspected/possible coronary artery disease.

Detailed Description Not Provided
Study Type  ICMJE Interventional
Study Phase  ICMJE Not Applicable
Study Design  ICMJE Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Screening
Condition  ICMJE Coronary Artery Disease
Intervention  ICMJE
  • Diagnostic Test: PET Stress Test
    Cardiac positron emission tomography (PET)/computed tomography (CT) and test-result dependent management
  • Other: Non-PET Medical Management
    Appropriate medical management without cardiac PET stress-imaging
Study Arms  ICMJE
  • Cardiac PET stress testing and test-dependent management
    Subjects randomized to the cardiac PET stress test strategy will receive appropriate subsequent care depending on the outcome of the cardiac PET scan (i.e., depending on whether ischemia is present or not).
    Intervention: Diagnostic Test: PET Stress Test
  • Management without stress-imaging
    Subjects randomized to the CAC-only arm will receive appropriate non-PET driven medical clinical management and follow-up.
    Intervention: Other: Non-PET Medical Management
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Recruiting
Estimated Enrollment  ICMJE
 (submitted: May 31, 2019)
2500
Original Estimated Enrollment  ICMJE Same as current
Estimated Study Completion Date  ICMJE November 2027
Estimated Primary Completion Date November 2022   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion Criteria:

  • Males or females ≥50 years old (i.e., to be of sufficiently high pre-test coronary risk)
  • Cardiac PET regadenoson stress perfusion test has been ordered to assess a possible ischemic etiology of low/intermediate risk chest pain or equivalent symptoms (e.g., exertional dyspnea).
  • Ability to understand and sign a written informed consent form, which must be obtained prior to initiation of any study procedures
  • CAC score of ≥1 per routine CAC first strategy (described above)

Exclusion Criteria:

  1. Disease history: If available for any of the following diseases: prior known CAD, heart transplant, LVAD, untreated severe valve disease (i.e., severe mitral stenosis, severe mitral regurgitation, and/or severe aortic stenosis), or decompensated heart failure (DHF).
  2. Those with a prior CAC score >1.
  3. CAC ≤1 prior to this current episode of cardiac assessment

    • Who ELECT to not receive an updated CAC evaluation OR their referring clinician specifically prefers cardiac PET.
    • CAC evaluation repeated at this current episode of cardiac assessment and is now >1.
  4. Evidence of possible acute coronary syndrome based on an elevated troponin I ≥0.04ng/mL and/or acute ECG changes of ischemia.
  5. Life expectancy <1 year, as assessed by the investigator(s)
  6. Cardiac PET/CT is ordered in the pre-operative risk assessment in higher risk non-thoracic surgery.
  7. Cardiac PET/CT is ordered for assessment of underlying ischemia in those with arrhythmia to guide anti-arrhythmic therapy.
  8. Other conditions that in the opinion of the study investigators and/or referring clinician may increase risk to the subject and/or compromise the quality of the clinical trial.
Sex/Gender  ICMJE
Sexes Eligible for Study: All
Ages  ICMJE 50 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers  ICMJE No
Contacts  ICMJE
Contact: Patti Spencer 8015074778 patti.spencer@imail.org
Listed Location Countries  ICMJE United States
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT03972774
Other Study ID Numbers  ICMJE 1051080
Has Data Monitoring Committee Yes
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
IPD Sharing Statement  ICMJE
Plan to Share IPD: Undecided
Responsible Party Intermountain Health Care, Inc.
Study Sponsor  ICMJE Intermountain Health Care, Inc.
Collaborators  ICMJE Not Provided
Investigators  ICMJE
Principal Investigator: Kirk U Knowlton, MD Intermountain Medical Center
Principal Investigator: Jeffrey L Anderson, MD Intermountain Medical Center
PRS Account Intermountain Health Care, Inc.
Verification Date April 2021

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP