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J Thorac Cardiovasc Surg 1994;107:629-0630
© 1994 Mosby, Inc.


Letters to the Editor

Invited letter concerning: Balloon dilation of stenotic aortic valve in children—An intraoperative study (J THORAC CARDIOVASC SURG 1992;104:1709-13)

John F. Keane, MD

Department of Cardiology
Boston Childrens Hospital
Boston, MA 02115

To the Editor:

The article of Solymar and coworkers, "Balloon Dilation of Stenotic Aortic Valve in Children: An Intraoperative Study," is of interest to interventional cardiologists and surgeons in this field.

In this report, 10 patients with significant valvular obstruction, aged 3 through 17 years, underwent balloon dilation during cardiopulmonary bypass, with a balloon that was at least the size of the anulus in six. Immediately after the dilation, it was determined by visual inspection that a surgical valvuloplasty was necessary in all cases, without valve replacement. The authors reported that the angioplasty result was too extensive in one case, caused rupture into a valve leaflet in three cases, produced too short a separation in three cases, and was close to optimum only in the other three patients. At follow-up, on the basis of echocardiographic data, the average instantaneous gradient was 33 mm Hg, representing a reduction of about 55% to 60%. Aortic regurgitation was present at follow-up in eight patients but was mild in most. In the authors' view, the site and extent of the ruptures created by balloon dilation seemed inferior to results of surgical commissurotomy, and valve morphologic characteristics appeared to be an important determinant of outcome. The investigators emphasized their commendable degree of medical-surgical cooperation, which surely is not unique to their institution.

Surgical valvotomy in children with aortic stenosis is generally regarded as a palliative procedure, with valve replacement likely at some point in their lifetime. In the recently completed Natural History Study,Go 1 within 25 years after valvotomy in childhood, some 35% of patients have required reoperation; 51% had aortic regurgitation, deemed moderate or severe in 12%.

Balloon angioplasty in recent years has been introduced as an alternative first procedure. As performed in the catheterization laboratory, it is of course extremely different from the procedure undertaken by the authors. A balloon 90% of the anulus size is used first, after which cardiac output and residual gradient measurements and aortography for regurgitation are carried out before proceeding further. Because survivorship at 25 years in those with a peak-to-peak gradient of less than 50 mm Hg is 92% (Natural History Study), stenosis as great as this has been accepted by most investigators as an end point.

Because of the wide variation in valve morphologic characteristics, it is little short of miraculous that balloon angioplasty is as effective as it is in reducing the degree of stenosis. In our own and others' experience,Go Go 2-5 gradient reduction seems to be comparable with that in surgical series, although follow-up duration is obviously less. The major complication with balloon angioplasty to date is aortic regurgitation, new or increased in 31% to 43%.Go Go 3, 4 In most patients, this regurgitation is mild at most.

It is nevertheless clear that some patients have severe regurgitation after angioplasty. In our own 7-year experience of more than 130 patients aged 1 year or older at dilation, eight are known to date to have undergone valve replacement and one has undergone a valvuloplasty. Among these, three had had a prior surgical valvotomy. Operation, primarily for regurgitation, was performed in six patients; in one of these the valve was platelike, without any recognizable cusp or commissure formation, and would have required valve replacement even if the operation had been the initial procedure (Fig. 1).



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Fig. 1. . Aortic valve excised from 17-year-old patient. The patient had severe regurgitation after balloon dilation 7 months earlier. The valve is platelike, without sinuses or commissures evident. (Courtesy of Dr. E. Nowicki, Portland, Maine.)

 
The major contribution of this article, in my opinion, is that a surgical procedure was accomplished in all of this small group without valve replacement. On the basis of data to date, economic and patient considerations, for the immediate future it is likely that balloon valvuloplasty will become the initial procedure, with operation for those in whom excessive regurgitation is induced. As experience accumulates it is hoped that (1) those valves suitable for balloon dilation can be identified, and (2) should excessive regurgitation result from angioplasty, those valves that can be repaired surgically without replacement can be recognized.

References

  1. Keane JF, Driscoll DJ, Gersony WM, et al. Long-term follow up of congenital aortic stenosis, pulmonary stenosis, and ventricular septal defect. Circulation 1993;87(Suppl):I16-27.
  2. Helgason H, Keane JF, Fellows KE, Kulik TJ, Lock JE. Balloon dilation of the aortic valve: studies in normal lambs and in children with aortic stenosis. J Am Coll Cardiol 1987;9:816-22.[Abstract]
  3. Sholler GF, Keane JF, Perry SB, Sanders SP, Lock JE. Balloon dilation of congenital aortic valve stenosis: results and influence of technical and morphological features on outcome. Circulation 1988;78:351-60.[Abstract/Free Full Text]
  4. Shaddy RE, Boucek MM, Sturtevant JE, Ruttenberg HD, Orsmond GS. Gradient reduction, aortic valve regurgitation and prolapse after balloon aortic valvuloplasty in 32 consecutive patients with congenital aortic stenosis. J Am Coll Cardiol 1990;16:451-6.[Abstract]
  5. Witsenburg M, Cromme-Dijkhuis AH, Frohn-Mulder IME, Hess J. Short- and midterm results of balloon valvuloplasty for valvular aortic stenosis in children. Am J Cardiol 1992;69:945-50.[Medline]




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