Why the study?
Does high-dose dipyridamole infusion provoke abnormal left ventricular filling patterns in patients with syndrome X compared to normal subjects and CAD patients?
Does high-dose dipyridamole infusion provoke abnormal left ventricular filling patterns in patients with syndrome X compared to normal subjects and CAD patients?
Patients with syndrome X exhibit abnormal left ventricular filling patterns during dipyridamole-induced ST depression similar to CAD patients, suggesting diffuse myocardial ischemia without regional wall motion abnormalities.
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May indicate microvascular ischemia in syndrome X; leaves open diagnostic role of dipyridamole-induced filling changes.
The left ventricular filling and regional wall motion patterns were compared in 6 normal subjects, 20 patients with coronary artery disease, and 10 patients with syndrome X by means of Doppler and two-dimensional echocardiography during high-dose (0.9 mg/kg body weight in 10 min) dipyridamole infusion. During the procedure none of the normal subjects had chest pain or significant ST depression (greater than 0.1 mV) whereas 10 of 20 patients with coronary artery disease had ST depression, 3 with chest pain. Six patients with syndrome X had ST depression, 5 with chest pain. Regional wall motion abnormalities were identified in 6 patients with coronary artery disease who had ST depression but none were detected in normals or in patients with syndrome X. Compared with normals (-2.1 +/- 3.5%) there was a significant difference in percentage decrease in the peak early filling velocity in patients with coronary artery disease and ST depression (-10.3 +/- 6.2%; p less than 0.01) and in patients with syndrome X and ST depression (-9.4 +/- 6.9%; p less than 0.05). These findings indicate that, in the presence of dipyridamole-induced ST depression, patients with syndrome X have an abnormal left ventricular filling pattern similar to that observed in patients with coronary artery disease. This suggests that myocardial ischemia occurs in patients with syndrome X but the absence of regional wall motion abnormality suggests that it is diffuse.
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Nadazdin et al. (1991) studied this question.
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