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The Journal of Thoracic and Cardiovascular Surgery, Vol 95, 868-875, Copyright © 1988 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
R Taillefer and AC Duranceau
Fifteen patients with oculopharyngeal muscular dystrophy underwent
cricopharyngeal myotomy for palliation of dysphagia. The aim of this work
was to assess the effectiveness of this operation by using a radionuclide
pharyngeal emptying study as a new quantitative method in addition to
clinical and manometric evaluation. Radionuclide study was performed with
the patient in both the upright and the supine positions after ingestion of
15 ml of water labeled with sulfur colloid 99mTc. Computerized data were
acquired at 0.5 second intervals for 15 minutes and a pharyngeal
time-activity curve was generated. Four quantitative parameters were
evaluated: the time for pharyngeal clearance of 25%, 50%, and 75% of the
ingested radioactive water and the pharyngeal stasis at 15 minutes.
Manometric studies were also performed before and after cricopharyngeal
myotomy. The pharyngeal clearance of 25%, 50%, and 75% of the water and
pharyngeal stasis at 15 minutes were all improved by cricopharyngeal
myotomy, decreasing from 1.2 to 0.9 second (p less than 0.04), 4.2 to 2
seconds (p less than 0.005), 15 to 7 seconds (p less than 0.02), and 10.3%
to 6% (p less than 0.01), respectively. Both pharyngoesophageal and
tracheobronchial symptoms were also significantly improved by
cricopharyngeal myotomy. Manometric evaluation showed a decrease of the
upper esophageal sphincter closing pressure from 60.1 mm Hg before to 28.2
mm Hg after the operation (p less than 0.001), and the resting pressure
decreased from 34.4 to 15.7 mm Hg (p less than 0.0005). Cricopharyngeal
myotomy significantly improves both symptoms and pharyngeal emptying in
patients with oculopharyngeal muscular dystrophy.
ARTICLES
Manometric and radionuclide assessment of pharyngeal emptying before and after cricopharyngeal myotomy in patients with oculopharyngeal muscular dystrophy
Division of Nuclear Medicine, Hotel-Dieu de Montreal Hospital, Universite de Montreal, Quebec, Canada.
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