Objectives: (1) To determine how swallow function in patients with myotonic
muscular dystrophy (MD) differs from that of healthy controls, (2) to iden
tify the contributors to and predictors of improvement, and (3) to evaluate
strategies that facilitate swallowing.
Design: Observational.
Setting: University medical center.
Participants: Eighteen adults with myotonic MD (age range, 24-58yr) and 60
healthy adult control subjects (age range, 18-73yr).
Interventions: Swallow facilitation strategies.
Main Outcome Measures: Between-group comparisons of mean bolus transit time
s, onsets of swallow gestures, and displacement measures obtained by dynami
c lateral view videofluoroscopy,
Results: The MD patients' bolus transit times were significantly longer, an
d onsets of some swallow gestures were significantly delayed. Upper esophag
eal sphincter opening was prolonged (myotonic MD,.61 +/-.13s; control,.5 +/
-.11s). Hyoid displacement was significantly less in men with myotonic MD (
1.9 +/-.05cm) than in male controls (2.4 +/- .68cm); this difference was no
t observed between control and myotonic women. Of particular importance was
the markedly reduced pharyngeal constriction found in the MD group.
Conclusions: Weakness associated with the disease, as opposed to myotonia,
was the most significant contributor to impairment. Persons at risk for asp
iration may be identified by a measure of pharyngeal area. Selected strateg
ies to facilitate pharyngeal clearing are worthwhile.