Natural history and surgical outcomes for isolated discrete subaortic stenosis in children
C V Rohliceka, S Font del Pinoa, M Hoskingb, J Miroc, J-M Côtéd, J Finleye
a Division of
Cardiology, Montréal Children's Hospital, 2300 Tupper Street,
Montréal, Québec H3H 1P3, Canada, b Division of Cardiology,
Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada, c Departement de Cardiologie,
Hôpital Ste Justine, Montréal, Québec, Canada, d Departement
de Cardiologie, Centre Hospitalier de l'Université Laval, Québec,
Québec, Canada, e Division
of Cardiology, Izaak Walton Killam Hospital, Halifax, Nova Scotia,
Canada
Correspondence to: Dr Rohlicek.
Accepted for publication 30 July 1999
OBJECTIVE
To document
the natural history and surgical outcomes for discrete subaortic
stenosis in children.
DESIGN
Retrospective review.
SETTING
Tertiary care
paediatric cardiology centres.
PATIENTS
92 children
diagnosed between 1985 and 1998.
MAIN OUTCOME
MEASURES
Echocardiographic left ventricular
outflow gradient (echograd), and aortic insufficiency (AI).
RESULTS
The mean
(SEM) age at diagnosis was 5.3 (0.4) years; the mean echograd was 30 (2) mm Hg, with AI in 22% (19/87) of patients. The echograd and
incidence of AI increased to 35 (3) mm Hg and 53% (36/68)
(p < 0.05) 3.6 (0.3) years later. The echograd at diagnosis
predicted echograd progression and appearance of AI. 42 patients
underwent surgery 2.2 (0.4) years after diagnosis. Preoperatively
echograd and AI incidence increased to 58 (6) mm Hg and 76% (19/25)
(p < 0.05). The echograd was 26 (4) mm Hg 3.7 (0.4) years
postoperatively, with AI in 82% (31/38) of patients. Surgical
morbidities included complete heart block, need for prosthetic valves,
and iatrogenic ventricular septal defects. Eight patients underwent
reoperation for recurrent subaortic stenosis. The age at diagnosis of
44 patients followed medically and 42 patients operated on did not
differ (5.5 (0.6) v 5.0 (0.6) years,
p < 0.05). However, the echograd at diagnosis in the former was less
(21 (2) v 40 (5) mm Hg, p < 0.05) and
did not increase (23 (2) mm Hg) despite longer follow up (4.1 (0.4)
v 2.2 (0.4) years, p < 0.05). The
incidence of AI at diagnosis and at last medical follow up was also
less (14% (6/44) v 34% (13/38); 40%
(17/43) v 76% (19/25), p < 0.05).
CONCLUSIONS
Many
children with mild subaortic stenosis exhibit little progression of
obstruction or AI and need not undergo immediate surgery. Others with
more severe subaortic stenosis may progress precipitously and will
benefit from early resection despite risks of surgical morbidity and recurrence.
Keywords: subaortic stenosis; congenital heart disease; cardiac surgery
© 1999 by Heart
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