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Published on: June 28, 2019
Comparative Visual Analysis of Coronary Slow Flow and Myocardial Blush Grade in Relation to Invasive Testing for
Andrew P Hill1, Ryan L Wallace1, Abhishek Chaturvedi1
1Section of Interventional Cardiology, MedStar Washington Hospital Center, Washington, District of Columbia, USA.
Angiographic coronary slow flow and myocardial blush grade do not reliably detect coronary microvascular dysfunction (CMD) in patients with angina and non-obstructive coronary arteries. Invasive coronary functional testing is recommended for suspected CMD.
Area of Science:
- Cardiology
- Vascular Biology
- Diagnostic Imaging
Background:
- Coronary slow flow (CSF) and abnormal myocardial blush grade (MBG) are linked to coronary microvascular dysfunction (CMD) and adverse outcomes.
- The diagnostic accuracy of these angiographic markers compared to invasive methods for CMD is not well-established.
Purpose of the Study:
- To evaluate the correlation between angiographic assessments of CSF and MBG and gold-standard invasive coronary functional testing (CFT) for CMD diagnosis.
Main Methods:
- The Coronary Microvascular Disease Registry identified patients with angina and non-obstructive coronary arteries (ANOCA) undergoing invasive CFT.
- CMD was defined by invasive bolus thermodilution (coronary flow reserve < 2.5 and index of microcirculatory resistance > 25).
- CSF and MBG were assessed angiographically and compared between CMD-positive and negative groups.
Main Results:
- Of 304 patients, 26.6% had CMD. No significant differences were observed in the rates of abnormal CSF (8.6% vs. 4.9%) or slow Thrombolysis in Myocardial Infarction frame count (14.8% vs. 15.7%) between CMD-positive and negative groups.
- Similarly, the rates of abnormal MBG were comparable (1.3% vs. 3.1%) across groups.
- Patient demographics showed CMD-positive individuals were slightly older and had lower BMIs.
Conclusions:
- Angiographic CSF and MBG are not reliable indicators of CMD in ANOCA patients.
- Invasive CFT should be considered for definitive CMD diagnosis when clinically suspected.
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