Coronary Slow Flow Is Not Diagnostic of Microvascular Dysfunction in Patients With Angina and Unobstructed Coronary

Utkarsh Dutta1, Aish Sinha1, Ozan M Demir1

  • 1School of Cardiovascular Medicine and Sciences British Heart Foundation Centre of Excellence and National Institute for Health Research Biomedical Research Centre, King's College London London UK.

Insights

Coronary slow flow phenomenon (CSFP), diagnosed by corrected thrombolysis in myocardial infarction frame count (CTFC), does not reliably diagnose coronary microvascular dysfunction (CMD) or endothelial dysfunction (CED) in patients with angina and unobstructed coronary arteries. Current guidelines recommending CTFC for CMD diagnosis need reevaluation.

Area of Science:

  • Cardiology
  • Vascular Biology
  • Diagnostic Imaging

Background:

  • Current guidelines suggest coronary slow flow phenomenon (CSFP), assessed by corrected thrombolysis in myocardial infarction frame count (CTFC) < 27, can diagnose coronary microvascular dysfunction (CMD) in patients with angina and nonobstructed coronary arteries.
  • CSFP has also been historically considered indicative of coronary endothelial dysfunction (CED).

Purpose of the Study:

  • To validate the utility of CTFC, both as a binary classifier for CSFP and as a continuous variable, in diagnosing CMD and CED.
  • To assess the diagnostic accuracy of CSFP and CTFC in patients presenting with angina and nonobstructed coronary arteries.

Main Methods:

  • Simultaneous coronary pressure and flow velocity measurements were performed in 152 patients with angina and nonobstructed coronary arteries using a dual sensor-tipped guidewire.
  • Measurements were taken at rest, during adenosine-mediated hyperemia (to assess CMD), and during intracoronary acetylcholine infusion (to assess CED).
  • Coronary flow reserve (CFR) < 2.5 defined CMD, and acetylcholine flow reserve (AFR) ≤ 1.5 defined CED.

Main Results:

  • Forty-six patients (30%) exhibited CSFP, characterized by lower flow velocity and higher microvascular resistance compared to controls.
  • CSFP demonstrated poor sensitivity and specificity for diagnosing both CMD (26.7% and 65.2%) and CED (21.1% and 56.0%).
  • Receiver operating characteristic analyses indicated that CTFC could not reliably predict CMD or CED (AUC 0.41 and 0.36, respectively).

Conclusions:

  • In patients with angina and nonobstructed coronary arteries, CSFP and CTFC are not effective diagnostic tools for CMD or CED.
  • The findings suggest that current guidelines supporting the use of CTFC for CMD diagnosis require reconsideration.

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