Table 2.
Diagnosis, prognostic value, and treatment of coronary microvascular dysfunction in different clinical settings
Type of CMD | Specific diseases | Diagnosis | Impact on outcome | Treatment |
---|---|---|---|---|
Type 1 | RF MVA |
TTDE TTDE, CMR |
Unknown* Documented |
RF control RF control, see Figure 4 |
Type 2 | HCM COCM PVB9 Myocarditis AFD Amyloidosis AS |
CMR, PET CMR, PET A-Ch CMR, PET CMR, PET CMR, PET |
Documented Unknown Unknown Unknown Unknown Unknown |
Alcohol septal ablation? Allopurinol Unknown Beta-galactosidase? Unknown Beta-blockers, Ivabradine? |
Type 3 | Stable angina MVO after pPCI |
Angina after PCI BG, STR, CMR |
Unknown Documented |
Angiogenesis See Figure 5 |
Type 4 | PCI CABG |
Tn raise Tn raise |
Documented Documented |
Statins, alpha-blockers? Statins |
A-ch, acetylcholine test; AFD, Anderson-Fabry's disease; AS, aortic stenosis; BG, blush grade; CABG, coronary aortic bypass graft; CMD, coronary microvascular dysfunction; CMR, cardiac magnetic resonance; COCM, congestive cardiomyopathy; HCM, hypertrophic cardiomyopathy; MVA, microvascular angina; MVO, microvascular obstruction; PET: positron emission tomography; pPCI, primary percutaneous coronary intervention; PVB, Parvovirus B9; RF, risk factors; STR, ST segment resolution; Tn, troponin; TTDE, transthoracic Doppler echocardiography.
It is unknown the incremental prognostic value of coronary microvascular dysfunction in addition to that conveyed by risk factors