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Neurology. 2010 Nov 23;75(21):1912-9. doi: 10.1212/WNL.0b013e3181fef115.

Aspiration and swallowing in Parkinson disease and rehabilitation with EMST: a randomized trial.

Author information

1
PO Box 117420, University of Florida, Gainesville, FL 32611, USA. michi81@ufl.edu

Abstract

OBJECTIVE:

Dysphagia is the main cause of aspiration pneumonia and death in Parkinson disease (PD) with no established restorative behavioral treatment to date. Reduced swallow safety may be related to decreased elevation and excursion of the hyolaryngeal complex. Increased submental muscle force generation has been associated with expiratory muscle strength training (EMST) and subsequent increases in hyolaryngeal complex movement provide a strong rationale for its use as a dysphagia treatment. The current study's objective was to test the treatment outcome of a 4-week device-driven EMST program on swallow safety and define the physiologic mechanisms through measures of swallow timing and hyoid displacement.

METHODS:

This was a randomized, blinded, sham-controlled EMST trial performed at an academic center. Sixty participants with PD completed EMST, 4 weeks, 5 days per week, for 20 minutes per day, using a calibrated or sham, handheld device. Measures of swallow function including judgments of swallow safety (penetration-aspiration [PA] scale scores), swallow timing, and hyoid movement were made from videofluoroscopic images.

RESULTS:

No pretreatment group differences existed. The active treatment (EMST) group demonstrated improved swallow safety compared to the sham group as evidenced by improved PA scores. The EMST group demonstrated improvement of hyolaryngeal function during swallowing, findings not evident for the sham group.

CONCLUSIONS:

EMST may be a restorative treatment for dysphagia in those with PD. The mechanism may be explained by improved hyolaryngeal complex movement.

CLASSIFICATION OF EVIDENCE:

This intervention study provides Class I evidence that swallow safety as defined by PA score improved post EMST.

PMID:
21098406
PMCID:
PMC2995389
DOI:
10.1212/WNL.0b013e3181fef115
[Indexed for MEDLINE]
Free PMC Article

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