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The system was now hierarchical with 12 separate trees, six for congenital cardiac anomalies.
However, on the basis of these data, it is very unlikely that cardiac rehabilitation reduces mortality in older patients.
There was no visible tear on the cardiac wall.
Any factor which decreases either cardiac output or peripheral vascular resistance diminishes systemic arterial pressure and hence cerebral perfusion.
Consequently, careful cardiac and peripheral vascular examination should be undertaken in older syncopal patients.
Management options will be discussed again after cardiac catheterisation, and then when the child is admitted for surgery.
Surgical options include fenestration (which benefits patients with high right atrium-left atrium gradient most), partial or complete takedown (associated with high risk), and cardiac transplantation.
Lack of both accuracy and precision becomes more problematic in malformed hearts when cardiac structures are hypoplastic.
The only other cardiac anomaly discovered in these 13 cases was one patient with aortic coarctation.
In our series, 2 of the 4 patients were diagnosed as having right isomerism associated with complex cardiac anomalies.
A 22-month-old boy was referred for corrective cardiac surgery.
In contrast to the previous literature, we have analyzed specifically the presence of congenital cardiac malformations in patients with proven rheumatic heart disease.
Stationary and drifting spiral waves of excitation in isolated cardiac muscle.
Clinical indications for permanent cardiac pacing were: 1) elective, 2) syncope, 3) congestive heart failure.
On cardiac examination, an abnormal four-chamber view was detected, mainly due to dilation of the right atrium.
