CHART-MiCro: Diagnostic and Prognostic Value of Angiography-derived IMR

Sponsor
Shanghai Zhongshan Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04825028
Collaborator
Shanghai 10th People's Hospital (Other)
271
1
6
45.1

Study Details

Study Description

Brief Summary

The importance of the microvasculature in determining clinical outcomes has been highlighted in patients with coronary artery disease (CAD). For patients with stable CAD, despite the success of percutaneous coronary intervention (PCI) in relieving a stenosis in the epicardial coronary artery, microvascular dysfunction may preclude sufficient coronary flow and myocardial perfusion, possibly leading to worse clinical outcome. With the technical development of computational fluid dynamics, angiographic derivation of index of Index of Microcirculatory Resistance (IMR) without pressure wire, hyperemic agents, or theromdilution method is available as a potential alternative for pressure wire-derived IMR. In this regard, the current study will evaluate diagnostic implication of angiography-derived IMR and its prognostic implication after PCI in patients with stable CAD.

Condition or Disease Intervention/Treatment Phase
  • Device: Angiography-drived Index of Microcirculatory Resistance

Detailed Description

The importance of the microvasculature in determining clinical outcomes has been highlighted in patients with coronary artery disease (CAD). For patients with stable CAD, despite the success of percutaneous coronary intervention (PCI) in relieving a stenosis in the epicardial coronary artery, microvascular dysfunction may preclude sufficient coronary flow and myocardial perfusion, possibly leading to worse clinical outcome. With the technical development of computational fluid dynamics, angiographic derivation of IMR without pressure wire, hyperemic agents, or theromdilution method is available as a potential alternative for pressure wire-derived IMR. In this regard, the current study will evaluate diagnostic implication of angiography-derived IMR and its prognostic implication after PCI in patients with stable CAD.

This study cohorts consist with 3 separate cohort: first, internal diagnostic accuracy cohort, which will evaluate correlation between angiography-derived IMR and hyperemic microvascular resistance calculated using Cadmium-Zinc-Telluride Single-Photon Emission Computed Tomography (CZT-SPECT)-derived myocardial blood flow and invasively measured pressure data. For this, 53 consecutive patients with available CZT-SPECT within 3 months of measuring FFR in the left anterior descending coronary artery will be evaluated. Second: external diagnostic cohort, in which diagnostic accuracy of angiography-derived IMR will be assessed in patients with ischemia and no obstructive coronary artery disease (INOCA) and normal controls, whose results were previously published (J Nucl Cardiol. 2020 Sep 30. doi: 10.1007/s12350-020-02252-8.) Among this cohort, 45 patients with no obstructive CAD and normal CZT-SPECT perfusion imaging will be regarded as normal controls, in 35 INOCA patients, vessels with normal corresponding perfusion territory will be regarded as internal control. Third, prognosis cohort, in which 138 consecutive CAD patients received PCI with available angiograms and who were suitable for angiographic fractional flow reserve and IMR measurement will be analyzed. Primary clinical outcome will be cardiac death or congestive heart failure at 2 years from index procedure. Secondary outcome will be any myocardial infarction, ischemia-driven revascularization, definite or probable stent thrombosis, congestive heart failure admission and angina pectoris admission at 2 years from index procedure.

Study Design

Study Type:
Observational
Anticipated Enrollment :
271 participants
Observational Model:
Case-Control
Time Perspective:
Retrospective
Official Title:
Diagnostic Value of Angiography-derived Index of Microvascular Resistance in Coronary Artery Disease Patients and Its Prognostic Implication After Percutaneous Coronary Intervention
Anticipated Study Start Date :
Apr 1, 2021
Anticipated Primary Completion Date :
May 1, 2021
Anticipated Study Completion Date :
Oct 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Internal Diagnostic Accuracy Cohort

Consecutive patients with available CZT-SPECT within 3 months of measuring FFR in the left anterior descending coronary artery. In these patients, correlation between angiography-derived IMR and hyperemic microvascular resistance will be assessed.

Device: Angiography-drived Index of Microcirculatory Resistance
From coronary angiographic images, angiography-derived IMR will be calculated based on mathematical calculation. Angiography-derived IMR = (hyperemic Pa x angiography-derived FFR) x (vessel length / {K x V diastole}). Hyperemic Pa will be estimated from resting Pa according to prespecified equation.
Other Names:
  • Angio-IMR
  • CaIMR
  • External Diagnostic Accuracy Cohort

    Patients are subgroup of previously published study (J Nucl Cardiol. 2020 Sep 30. doi: 10.1007/s12350-020-02252-8.), INOCA patients and normal controls confirmed by CZT-SPECT and angiography will be included for the assessment of angiography-derived IMR in diagnosing microvascular dysfunction.

    Device: Angiography-drived Index of Microcirculatory Resistance
    From coronary angiographic images, angiography-derived IMR will be calculated based on mathematical calculation. Angiography-derived IMR = (hyperemic Pa x angiography-derived FFR) x (vessel length / {K x V diastole}). Hyperemic Pa will be estimated from resting Pa according to prespecified equation.
    Other Names:
  • Angio-IMR
  • CaIMR
  • Prognosis Cohort

    Prognosis cohort, in which angiography-derived IMR will be measured in the target vessel after successful revascularization. Those patients have follow-up data after 2 years from index procedure.

    Device: Angiography-drived Index of Microcirculatory Resistance
    From coronary angiographic images, angiography-derived IMR will be calculated based on mathematical calculation. Angiography-derived IMR = (hyperemic Pa x angiography-derived FFR) x (vessel length / {K x V diastole}). Hyperemic Pa will be estimated from resting Pa according to prespecified equation.
    Other Names:
  • Angio-IMR
  • CaIMR
  • Outcome Measures

    Primary Outcome Measures

    1. Diagnostic accuracy [at the index procedure]

      Correlation between angiography-derived IMR and HMR

    2. Major adverse cardiac events [at 28 months from index procedure]

      Major adverse cardiac events (MACE), including cardiac death and readmission due to heart failure.

    Secondary Outcome Measures

    1. A composite of cardiac death, readmission due to heart failure and angina [at 28 months from index procedure]

      A composite of cardiac death, readmission due to heart failure and angina

    2. A composite of cardiac death, readmission due to heart failure, spontaneous MI, target vessel revascularization and angina [at 28 months from index procedure]

      A composite of cardiac death, readmission due to heart failure, spontaneous MI, target vessel revascularization and angina.

    3. Cardiac death [at 28 months from index procedure]

      Cardiac death

    4. Readmission due to heart failure [at 28 months from index procedure]

      Readmission due to heart failure

    5. Spontaneous MI [at 28 months from index procedure]

      Spontaneous MI

    6. Target vessel revascularization [at 28 months from index procedure]

      Target vessel revascularization

    7. Readmission due to angina [at 28 months from index procedure]

      Readmission due to angina

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    19 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • CAD patients with available CZT-SPECT within 3 months of measuring FFR in the left anterior descending coronary artery (Cohort 1)

    • INOCA patients and normal controls confirmed by CZT-SPECT and angiography (Cohort 2)

    • Stable CAD patients received PCI (Cohort 3)

    • analyzable angiograms at the index procedure

    Exclusion Criteria:
    • Previous coronary artery bypass grafting

    • Chronic total occlusion patients

    • limited image quality of coronary angiography

    • Insufficient angiographic project for TIMI frame count

    • Severe tortuosity of target vessel

    • No optimal projection for reconstruction

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Shanghai Tenth People's Hospital Shanghai China 200091

    Sponsors and Collaborators

    • Shanghai Zhongshan Hospital
    • Shanghai 10th People's Hospital

    Investigators

    • Study Chair: Junbo Ge, Professor, Fudan University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Shanghai Zhongshan Hospital
    ClinicalTrials.gov Identifier:
    NCT04825028
    Other Study ID Numbers:
    • ZS-20210328
    First Posted:
    Apr 1, 2021
    Last Update Posted:
    Apr 1, 2021
    Last Verified:
    Mar 1, 2021
    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
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 1, 2021