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The Journal of Thoracic and Cardiovascular Surgery, Vol 101, 526-535, Copyright © 1991 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
MP Leung, R McKay, A Smith, RH Anderson and R Arnold
To establish noninvasive criteria by which to manage infants with critical
aortic stenosis, we examined 20 heart specimens from infants under 3 months
of age and reviewed the clinical course and real time echocardiograms of 20
patients in the same age group. All 20 infants underwent open valvotomy,
and in five cases both echocardiographic and postmortem measurements were
available for the same heart. The anatomic specimens showed a spectrum of
valvular, ventricular, and vascular abnormalities that could be accurately
identified by echocardiography. A small left ventricular cavity was usually
associated with a narrow ventriculoarterial junction, small ascending
aorta, and narrow subaortic region. In these hearts, the mitral valve had a
single or grossly hypoplastic papillary muscle with short or "arcuate"
tendinous cords. A dilated left ventricular cavity had wider inflow and
outflow orifices, and the tension apparatus of the mitral valve was either
normal or supported by hypertrophic papillary muscles, at the other end of
the spectrum. The survivors (n = 15) and nonsurvivors (n = 5) of open
valvotomy showed significant differences in the echocardiographic
dimensions of the left ventricle (p less than 0.005), the subaortic region
(p less than 0.05), the ventriculoaortic junction (p less than 0.05), the
ascending aorta (p less than 0.005), and the mitral valve orifice (p less
than 0.001). Moreover, the papillary muscle of the mitral valve was
invariably single or hypoplastic with short tendinous cords in the early
nonsurvivors. Infants with unfavorable cardiac anatomy tended to present
earlier (p less than 0.05) and to have a lower systemic blood pressure (p
less than 0.05), and they required prostaglandin E2 to maintain right
ventricular support of the circulation through a persistent arterial duct.
This study suggests that patients with a small left ventricle
(echocardiographic inflow dimension less than 25 mm), a narrow
ventriculoaortic junction (less than 5 mm), and a small mitral valve
orifice (less than 9 mm) will not achieve a satisfactory surgical result
from aortic valvotomy. Such patients should be considered for cardiac
transplantation or the Norwood-type of palliation for hypoplastic left
heart syndrome.
ARTICLES
Critical aortic stenosis in early infancy. Anatomic and echocardiographic substrates of successful open valvotomy
Royal Liverpool Children's Hospital, England.
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