Why the study?
Does posterior left thoracic cardiac sympathectomy prevent Horner's syndrome and treat recurrent ventricular arrhythmias in patients with long QT syndrome?
Does posterior left thoracic cardiac sympathectomy prevent Horner's syndrome and treat recurrent ventricular arrhythmias in patients with long QT syndrome?
A posterior approach to left thoracic cardiac sympathectomy appears safe and avoids Horner's syndrome in patients with long QT syndrome.
Supports posterior approach safety without Horner's syndrome in small series; leaves open controlled trials for arrhythmia efficacy in long QT syndrome.
Although high thoracic left sympathectomy via an anterior surgical approach is a highly efficacious treatment for refractory ventricular arrhythmias in patients with the long QT syndrome, the degree of sympathetic denervation has been variable, success of the operation is influenced by anatomical differences between patients, and Horner's syndrome may result. We hypothesized that interruption of sympathetic input to the heart could be accomplished using a posterior thoracic approach to this variable and often complex anatomy by division of the sympathetic chain rather than by direct destruction of the stellate and superior thoracic ganglia with the more conventional anterior, supraclavicular approach. In addition, the posterior approach should decrease the risk of Horner's syndrome by avoiding the ocular sympathetic efferent nerves. This posterior approach is described in five patients with the long QT syndrome and recurrent ventricular arrhythmias. After a mean follow-up of 18 +/- 12 months, all are alive without Horner's syndrome.
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Epstein et al. (1996) studied this question.
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