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Mitral stenosis (MS) is the most common sequelae of rheumatic heart disease and is characterized by diffuse fibrous thickening of the margins of the mitral valve (MV) leaflets and fusion of the commissures. Untreated, severe MS can lead to significant derangement of the functional status of patients and reduced long-term survival. Since its introduction in the 1980s, percutaneous balloon mitral valvuloplasty (PBMV) has proven to be an effective and durable treatment option for selected patients with rheumatic MS. Although it is more challenging, PBMV has also been utilized in patients with nonrheumatic MS (e.g., calcific MS). This chapter focuses on the contemporary indications, patient selection, and techniques of PBMV.
PBMV is recommended for symptomatic patients with severe MS (mitral valve area [MVA] <1.5 cm 2 , stage D) and favorable valve morphology in the absence of contraindications ( Fig. 14.1 ). The goal of PBMV for patients with rheumatic MS is to directly affect the main valvular pathology by inducing an effective commissural split without a significant increase in mitral regurgitation (MR). Hence, in symptomatic patients, the main determinants of patient selection for PBMV are the anatomic features of the mitral apparatus. Other considerations include the patient’s age, functional status, and the presence or absence of atrial fibrillation or pulmonary hypertension.
Patients who are being considered for PBMV should undergo a comprehensive assessment with transthoracic ± transesophageal echocardiography (TEE). The MV and subvalvular apparatus need to be systematically evaluated for favorable and unfavorable features for PBMV. Attempts have been made to incorporate certain individual characteristics into a holistic scoring system to predict optimal PBMV results. The Wilkins echocardiography score is the most commonly used scoring system for PBMV. This score incorporates four echocardiographic characteristics of the mitral apparatus, including leaflet mobility, leaflet thickness, leaflet calcification, and subvalvular thickening ( Table 14.1 ). Each component is given a 1- to 4-point score. Patients with Wilkins scores ≤8 are, in general, suitable for PBMV. When the Wilkins score is >10, the risk of complications, including severe MR requiring urgent or emergent MV replacement, is significantly higher. Patients with a Wilkins score between 8 and 10 may be considered for PBMV on an individual basis. A simpler scoring system is the Lung and Cormier score, which divides the valvular anatomy into three groups, with patients in group 1, 2, and 3 considered optimal, intermediate, and borderline candidates for PBMV, respectively ( Table 14.2 ). Newer scoring systems to predict PBMV outcomes have been proposed. , These scores incorporate novel predictors of PBMV outcomes, such as commissural morphology, leaflet displacement, commissural calcium, and commissural fusion. These scoring systems have weaknesses and strengths. One fundamental criticism applying to all scoring systems is that they are mainly derived from single-center experience and with a limited number of operators. Furthermore, assessment of the subvalvular apparatus is difficult in most patients, despite TEE. Most of the echocardiographic assessments are qualitative, which makes the reproducibility of a specific scoring system more challenging. Nevertheless, using any of these scoring systems might help the operator in predicting the outcome and potential complications that should be discussed with the patient as part of the informed consent and shared decision-making.
Grade | Leaflet Mobility |
---|---|
1 | Highly mobile with only leaflet tips restricted |
2 | Leaflet midportions and base portions have normal mobility |
3 | Valve continues to move forward in diastole, mainly from the base |
4 | No or minimal forward movement of the leaflets in diastole |
Leaflet Thickening | |
1 | Leaflets near normal in thickness (4-5 mm) |
2 | Middle of the leaflets normal, considerable thickening of margins (5-8 mm) |
3 | Thickening extending through the entire leaflets (5-8 mm) |
4 | Considerable thickening of all leaflet tissue (>8-10 mm) |
Leaflet Calcifications | |
1 | A single area of increased brightness on echocardiogram |
2 | Scattered areas of brightness confined to leaflet margins |
3 | Brightness extending into the midportions of the leaflets |
4 | Extensive brightness throughout much of the leaflet tissue |
Subvalvular Thickening | |
1 | Minimal thickening just below the mitral leaflets |
2 | Thickening of chordal structures extending to one of the chordal lengths |
3 | Thickening extended to distal third of the chords |
4 | Extensive thickening and shortening of all chordal structures extending to the papillary muscles |
Echocardiographic Group | Mitral Valve Anatomy | Suitability for PBMV |
---|---|---|
Group 1 | Pliable, noncalcified anterior mitral leaflet and mild subvalvular disease (thin chordae ≥10 mm long) | + |
Group 2 | Pliable, noncalcified anterior mitral leaflet and severe subvalvular disease (thickened chordae <10 mm long) | ± |
Group 3 | Calcification of mitral valve of any extent, as assessed by fluoroscopy, whatever the state of the subvalvular apparatus | − |
The presence of greater-than-moderate MR is considered an absolute contraindication to PBMV. Relative contraindications include a Wilkins score >10, left atrial or left atrial appendage thrombus, severe or bicommissural calcification, absence of bicommissural fusion, severe mitral annular calcification, international normalized ratio (INR) >1.5 or bleeding diathesis, and other significant coronary or valvular pathology requiring surgery.
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