Mitral Regurgitation
Mitral Regurgitation
Mitral Regurgitation
All advice in this document is derived from the 2017 Expert Consensus Decision Pathway on the Management
of Mitral Regurgitation. The Pathway includes additional advice on these as well as other topics relating to
the management of mitral regurgitation. The information and advice in this tool are meant to support clinical
decision making. They are not meant to represent the only or best course of care, or replace clinical judgment.
This tool was developed as part of ACC’s Emerging Mitral Regurgitation Clinical Care Initiative which was
supported by Founding Sponsor Abbott Vascular.
To provide feedback on this tool, please fill out our feedback survey here.
November 2017
©2017, American College of Cardiology B17205
MITRAL REGURGITATION
ECHO CHECKLISTS TOOL
• Mitral valve morphology, LV and LA volumes, and LV size and systolic function are used together to classify the mechanism and etiology
of MR.
• Mitral valve morphology should be carefully assessed in multiple views using B-mode imaging to evaluate structure and motion and
color flow Doppler (CFD) to localize the origin of MR jet(s).
• Careful measurement of LV and LA volumes and of LV dimensions should be performed according to American Society for
Echocardiography guidelines for chamber quantification.
Assessing MR Severity
• Evaluation of MR severity requires a comprehensive TTE study and assessment whereby multiple parameters are evaluated and
integrated to form a final determination of MR severity. This should include assessment of these parameters listed in the tables
below, and consideration of the strengths and limitations of those parameters (described in further detail in the 2017 ASE Guidelines
for Assessment of Native Valve Regurgitation). It is important to emphasize that no single echocardiographic parameter has the
measurement precision or reproducibility to serve as the sole arbiter of MR severity.
• It is also crucial to record blood pressure, estimated LV systolic pressure in the presence of aortic stenosis or LV outflow obstruction,
heart rate, and rhythm at the time of TTE and to incorporate them when grading MR severity.
• alculation of EROA, a marker of lesion severity, as well as RVol and regurgitant fraction (RF), is strongly recommended for assessing
C
MR severity. They can be measured by several techniques, including the proximal isovelocity surface area (PISA) method, volumetric
methods, and 3D imaging. It is crucial to recognize the technical limitations and imprecision of each method and the overlap of values
obtained.
• In secondary MR, Symptoms, pulmonary congestion on exam or chest x-ray, elevated brain natriuretic peptide (BNP) or N-terminal-
pro-BNP (NT-pro-BNP), and adjunctive findings on TTE or TEE, such as LV or LA dilation and systolic blunting of the pulmonary venous
flow pattern, may be due to the underlying cardiomyopathy and therefore are less helpful in grading MR severity.
• After an initial impression of MR severity is formed, one should next consider whether LA and LV sizes are normal and whether the MR
is holosystolic. For example, if one assesses MR as severe on the basis of a large CFD jet, but LA and LV sizes are normal and the MR is
limited to late systole, the initial impression is most likely an overestimate. One should consider common reasons for overestimation of
MR, such as high MR driving velocity and MR duration limited to very early or very late systole.
• When multiple specific parameters for mild or severe MR align with the initial impression of MR severity, MR can be correctly
graded with high probability of being accurate. Fortunately, this scenario is relatively common in practice, especially with the
finding of mild MR and a structurally normal mitral valve; however, when different parameters are discordant among themselves
or with clinical findings, MR severity should be considered uncertain and further testing pursued. In such cases, TEE may be
sufficient to define leaflet pathology and quantitate MR severity, although it may underestimate MR severity during general anesthesia
due to favorable loading conditions. CMR is generally more accurate and reproducible for quantitating RVol and RF as well as LV
volumes and LVEF.
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Heart Rate:
Rhythm:
Focal calcific or nodular • TEE may identify lesions such as vegetations or flail segments not
thickening detected by TTE, especially in cases of poor image quality.
Diffusely calcified • If the mitral apparatus is structurally normal, significant MR is likely to be
Myxomatous secondary. In such cases, the mechanism of MR still needs to be
Vegetations identified.
Redundant chordae:
Anterior mitral leaflet
Posterior mitral leaflet
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ECHO CHECKLISTS TOOL
Leaflet Mobility
Normal
Redundant, no prolapse
Systolic anterior motion (SAM)
Anterior mitral leaflet
Posterior mitral leaflet
Flail: Anatomic localization: • Flail leaflets or ruptured papillary muscles are usually specific for severe MR.
A1
• Occasionally patients with flail leaflets only have moderate MR by
A2 integrative assessment.
A3
• Rare patients with flail leaflet may experience sudden cardiac death. Early
P1 referral of the patient with flail leaflet might be considered.
P2
P3
Posteromedial commissure
Anterolateral commissure
Prolapse: Anatomic localization: • A common mistake in clinical practice is to misconstrue anterior leaflet
A1 override as prolapse.
A2
A3
P1
P2
P3
Posteromedial commissure
Anterolateral commissure
Mitral Stenosis
Rheumatic
Degenerative
Other
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Carpentier Classification
Normal Leaflet motion (Type I) • May be seen in primary MR due to endocarditis, perforation, or clefts, or in
secondary MR due to pure annular dilation.
Excessive Leaflet motion (Type II) • Most commonly seen with mitral valve prolapse or flail leaflet.
Restricted leaflet motion • Classic for rheumatic mitral valve disease, radiation- or drug-induced injury,
(Type IIIA): during systole and or other inflammatory conditions
diastole
Submitral Morphology
Thickening • Morphology abnormalities should be described and reported in detail by
Calcification size and location.
Retraction
Tumor
Vegetation
MR Mechanism
Primary • Defined by principal involvement of the leaflets and/or chordae tendineae
in the pathologic process (e.g., myxomatous disease, endocarditis).
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Mixed • Due to both primary and secondary causes. Examples of mixed pathology
include:
–Untreated primary MR eventually results in irreversible LV dilation/
dysfunction in which both leaflet prolapse and tethering may coexist
–Patients with long-standing secondary MR due to ischemic heart
disease or atrial fibrillation who subsequently rupture a chord
–Patients with mitral valve prolapse who have a myocardial infarction
or develop a cardiomyopathy
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MITRAL REGURGITATION
ECHO CHECKLISTS TOOL
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MITRAL REGURGITATION
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Regurgitant fraction > 50% • It is recognized that the accepted EROA threshold for severe MR (>0.40
cm2) can be lower in patients with secondary MR and elliptical orifices,
emphasizing the need for an integrative assessment of severity.
• In secondary MR, the shape of the regurgitant orifice is often markedly
crescentic, leading to underestimation of EROA by the PISA method
because the latter assumes a circular orifice. This inaccuracy can be
ameliorated by 3D PISA measurements or direct 3D measurement of
EROA by TTE or TEE.
Mean transmitral Doppler Gradient: • Input concurrently recorded during CW Doppler acquisition
mm Hg @ heart rate
End systolic volume/volume index • LV or LA dilation in chronic primary MR is most often a consequence of
the MR and a strong clue that the MR is severe. Exceptions could occur if
a patient with long-standing mitral valve prolapse and mild MR develops
Left ventricular function
an ischemic or nonischemic cardiomyopathy. On the other hand, when
Ejection fraction (normal > 60%) MR is primary and LV and LA size are normal, severe MR is very unlikely.
Global LV dysfunction
Regional LV Dysfunction
(detail wall motion)
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ECHO CHECKLISTS TOOL
Tricuspid annulus
Normal
Dilated
PA systolic pressure:
mm Hg
Estimated RA pressure:
mm Hg
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©2017, American College of Cardiology B17205