N. Ammash et Ca. Warnes, CEREBROVASCULAR EVENTS IN ADULT PATIENTS WITH CYANOTIC CONGENITAL HEART-DISEASE, Journal of the American College of Cardiology, 28(3), 1996, pp. 768-772
Objectives. We sought to determine the frequency of spontaneous cerebr
ovascular events in adult patients,vith cyanotic congenital heart dise
ase and to evaluate any contributing factors. Background. Cerebrovascu
lar events are a serious complication of cyanotic congenital heart dis
ease in infants and children but are said to be uncommon in adults. Me
thods. Between 1988 and 1995, 162 patients with cyanotic congenital he
art disease (mean age 37 Sears, range 19 to 70) were retrospectively e
valuated for any well documented cerebrovascular events that occurred
at greater than or equal to 18 gears of age, Events related to procedu
res, endocarditis or brain abscess were excluded. Results. Twenty-two
patients (13.6%) had 29 cerebrovascular events (1/100 patient-years),
There mas no significant difference between those with and without a c
erebrovascular event in terms of age, smoking history, degree of eryth
rocytosis, ejection fraction or use of aspirin or warfarin (Coumadin).
Patients who had cerebrovascular event had a significantly increased
tendency to develop hypertension, atrial fibrillation, microcytosis (m
ean corpuscular volume <82) and history of phlebotomy (p < 0.05). Even
when patients with hypertension or atrial fibrillation were excluded,
there was an increased risk of cerebrovascular events associated with
microcytosis (p < 0.01). Conclusions. Adults with cyanotic congenital
heart disease are at risk of having cerebrovascular events. This risk
is increased in the presence of hypertension, atrial fibrillation, hi
story of phlebotomy and microcytosis, the latter condition having the
strongest significance (p < 0.005). This finding leads us to endorse a
more conservative approach toward phlebotomy and a more aggressive ap
proach toward treating microcytosis in adults with cyanotic congenital
heart disease.