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Cleft Palate Craniofac J ; 41(2): 124-35, 2004 Mar.
Article in English | MEDLINE | ID: mdl-14989693

ABSTRACT

OBJECTIVES: To analyze the results of surgery for velopharyngeal incompetence (VPI) in velocardiofacial syndrome. DESIGN: Prospective data collection, with randomized, blind assessment of speech and velopharyngeal function on lateral videofluoroscopy and nasendoscopy. SETTING: Two-site, tertiary referral cleft unit. PATIENTS: Forty-two consecutive patients with the 22q11 deletion underwent surgery for symptomatic VPI by a single surgeon. INTERVENTIONS: Intraoral examinations, lateral videofluoroscopy (+/- nasendoscopy) and intraoperative evaluation of the position of the velar muscles through the operating microscope. Based on these findings, either a radical dissection and retropositioning of the velar muscles (submucous cleft palate [SMCP repair]) or a Hynes pharyngoplasty (posterior pharyngeal wall augmentation pharyngoplasty) was performed. As anticipated, a proportion of patients undergoing SMCP repair subsequently required a Hynes. The aim of this staged approach was to maximize velar function, thereby enabling a less obstructive pharyngoplasty to be performed. Thus, there were three surgical groups for analysis: SMCP alone, Hynes alone, and SMCP+Hynes. MAIN OUTCOME MEASURES: Blind perceptual rating of resonance and nasal airflow; blind assessment of velopharyngeal function on lateral videofluoroscopy and nasendoscopy; and identification of predictive factors. RESULTS: Significant improvement in hypernasality in all three groups. The SMCP+Hynes group also showed significant improvement in nasal emission. There were significant improvements in the extended and resting velar lengths following SMCP repair and a trend toward increased velocity of closure. CONCLUSIONS: Depending on velopharyngeal anatomy and function, there is a role for SMCP repair, Hynes pharyngoplasty, and a staged combination of SMCP+Hynes, all of which are procedures with a low morbidity.


Subject(s)
Cleft Palate , Heart Defects, Congenital , Oral Surgical Procedures/methods , Velopharyngeal Insufficiency/surgery , Adolescent , Child , Child, Preschool , Chromosome Deletion , Chromosomes, Human, Pair 22 , Cleft Palate/genetics , Female , Heart Defects, Congenital/genetics , Humans , Male , Palatal Muscles/surgery , Pharynx/surgery , Prospective Studies , Random Allocation , Single-Blind Method , Speech Production Measurement , Syndrome , Velopharyngeal Insufficiency/genetics , Video Recording , Voice Disorders/diagnosis
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