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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 27, No 3, May/June 2016

AFRICA

149

Echocardiographic and catheterisation assessment of patients

before the procedure showed no significant differences between

the basic features of the two groups. The degree of mitral valve

stenosis, mitral valve scores and MR (2

+

) were similar between

the two groups (

p

=

0.73,

p

=

0.58 and

p

=

0.74, respectively).

BMVs were performed successfully on both groups. Adequate

mitral valve area and a decrease in MVG were obtained.

BMV was assessed as successful in 60 (92.3%) patients in the

HBRS group and in 61 (96.8%) in the EBRS group (

p

=

0.03). The

mean of the calculated balloon reference sizes was significantly

higher in the HBRS than in the EBRS group [26.3

±

1.2 mm, 95%

confidence interval (CI): 26.1–26.6 vs 25.2

±

1.1, 95% CI: 25.0–

25.4, respectively;

p

=

0.007]. The final inflated balloon sizes were

similar between the groups (25.6

±

0.9 mm, 95% CI: 25.3–25.9

vs 25.9 mm

±

1.0 mm, 95% CI: 25.1–25.8, respectively;

p

=

0.34).

The post-procedural results of the patients are presented in

Table 4. A greater decrease in the trans-mitral mean gradient

was observed in the EBRS group but it was not statistically

significant (

p

=

0.06). In the EBRS group, larger MVAs were

achieved than in the HBRS group (1.6

±

0.3 cm

2

, 95% CI:

1.56–1.69 vs 1.7

±

0.3 cm

2

, 95% CI: 1.57–1.74, respectively;

p

=

0.02). The incidence of significant MR (3–4

+

) was lower than

in the HBRS group (

p

=

0.05 by echocardiography and

p

=

0.03

by ventriculography). Also, 2

+

degree MR was significantly less

developed in the EBRS patients (

p

=

0.01).

Discussion

In recent years, Inoue balloon mitral commissurotomy has

become the treatment of choice in many patients with rheumatic

mitral stenosis. The main target of this procedure is to resolve

the stenotic mitral orifice without causing extensive damage

to the commissures, leaflets and subvalvular apparatus, thus

leading to excessive mitral regurgitation. The most common

serious complication is haemopericardium, with an incidence

of 0 to 2.0%.

17

Severe MR is another important and common

serious complication after BMV.

18

Many studies have shown that acute procedural results,

including final MVA and post-procedural MR, independently

predict the long-term outcome after BMV.

8

When severe mitral

regurgitation occurs after BMV, surgical treatment is required at

some point. Most mild but significant cases of MR are caused by

commissural split, chordal rupture or leaflet laceration.

Table 1. Background characteristics of study patients

HBRS

(

n

=

65)

EBRS

(

n

=

63)

p-

value

Age (years)

35.4

±

6.2

31.4

±

5.1

0.12

Gender,

n

(%)

Male

18 (27.7)

17 (27)

0.67

Female

47 (72.3)

46 (73)

0.58

Weight (kg)

66.2

±

10.9

70.1

±

11.1

0.14

Height (cm)

162

±

9

163

±

9

0.62

CVD

3

1

0.09

Atrial fibrillation

14

12

0.53

NYHA

1

16

12

0.62

2

41

42

3

8

9

EBRS, echocardiographic balloon reference sizing; HBRS, height-based balloon

reference sizing; F, female; M, male; CVD, cerebrovascular disease; NYHA,

New York Heart Association functional classification.

Table 2. Pre-procedural echocardiographic

data of study participants

HBRS

(

n

=

65)

EBRS

(

n

=

63)

p-

value

LVDD (mm)

46

±

2.4

47

±

2.5

0.81

LVSD (mm)

29

±

1.5

29

±

1.4

0.78

LA (mm)

49

±

6

47

±

6

0.51

LVEF (%)

64

±

5

65

±

5

0.54

MVA (cm

2

)

1.1

±

0.2

1.0

±

0.3

0.13

MV Wilkins score

8.7

±

1.1

9.1

±

1.4

0.38

MV max gradient (mmHg)

22.4

±

5.5

21

±

5.3

0.34

MV mean gradient (mmHg)

9.5

±

4.2

9.7

±

4.5

0.69

MR

0

20

19

0.52

1

+

42

39

2

+

3

5

EBRS, echocardiographic balloon reference sizing; HBRS, height-based balloon

reference sizing; LVDD, left ventricular end-diastolic diameter; LVSD, left

ventricular end-systolic diameter; LA, left atrium; LV EF, left ventricular ejec-

tion fraction; MVA, mitral valve area; MV, mitral valve; MR, mitral regurgita-

tion.

Table 3. Pre-procedural catheterisation

data of study participants

HBRS

(

n

=

65)

EBRS

(

n

=

63)

p-

value

PA pressure (mmHg)

49

±

15

51

±

16

0.91

RV pressure (mmHg)

48

±

14

49

±

15

0.82

RA pressure (mmHg)

7.5

±

2

9.1

±

2.4

0.14

MV mean pressure (mmHg)

9.9

±

4.1

10.4

±

4.4

0.32

MR

0

21

20

0.69

1

+

41

39

2

+

3

4

EBRS, echocardiographic balloon reference sizing; HBRS, height-based balloon

reference sizing; PA, pulmonary artery; RV, right ventricle; RA, right atrium;

MV, mitral valve; MR, mitral regurgitation.

Table 4. Post-procedural catheterisation

data of study participants

HBRS

(

n

=

65)

EBRS

(

n

=

63)

p-

value

Estimated reference MBS (mm)

26.3

±

1.2 25.2

±

1.1

0.02

Final balloon size

25.6

±

0.9 25.9

±

1.0

0.34

MVA (cm

2

)

1.6

±

0.2 1.7

±

0.3 0.02

Transmitral mean gradient (mm Hg)

3.2

±

0.3 3.0

±

0.3 0.04

PAP (mmHg)

28

±

8

29

±

7

0.81

MR severity,

n

(%)

Echocardiography

0

10

14

0.03

1

+

41

43

2

+

11

5

3–4

+

3

1

Catheterisation

0

9

13

0.04

1

+

39

42

2

+

13

6

3–4

+

4

2

EBRS, echocardiographic balloon reference sizing; HBRS, height-based balloon

reference sizing; MBS, mitral balloon size; MVA, mitral valve area; PAP, pulmo-

nary artery pressure; MR, mitral regurgitation.