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1.
J Craniofac Surg ; 23(3): 645-9, 2012 May.
Article in English | MEDLINE | ID: mdl-22565874

ABSTRACT

Velopharyngeal insufficiency (VPI) occurs in more than 20% of patients with a cleft palate after primary palatoplasty. Surgical treatment focuses on pharyngoplasty to narrow the nasopharyngeal space and to decrease the distance needed for palatal closure. Persistent VPI after pharyngoplasty affects more than 20% of patients.From September 2007 to December 2009, 16 children (10 boys and 6 girls) with a mean age of 9.5 years (4-15 years) underwent surgical revision using an AlloDerm sling for persistent VPI after at least 1 previous failed pharyngoplasty. Ten children had previous sphincter pharyngoplasties, and 6 had previous pharyngeal flaps. Surgical technique involves creation of a submucosal tunnel through the limbs of the previous pharyngoplasty or pharyngeal flap. A strip of AlloDerm is threaded circumferentially, and the port is adjusted to the desired aperture.All patients underwent preoperative and postoperative analysis of VPI, including oral pharyngeal and perceptual speech examination by speech pathology with a mean follow-up of 441 days. Acoustic nasometry was used to objectively compare preoperative and postoperative nasalance values. A significant improvement in perceptual resonance was seen in 93.8% of patients, and 87.5% of patients improved to normal or mild resonance (P < 0.001). There was a significant mean reduction of nasalance using the MacKay-Kummer Simplified Nasometric Assessment Procedure test (P < 0.001). Two patients developed postoperative flap dehiscence, with one being revised ultimately to have normal speech resonance.Revision pharyngoplasty using an AlloDerm sling can safely and effectively improve speech in patients with persistent VPI after failed pharyngoplasty. Long-term follow-up studies are ongoing.


Subject(s)
Collagen/therapeutic use , Plastic Surgery Procedures/methods , Velopharyngeal Insufficiency/surgery , Adolescent , Child , Child, Preschool , Female , Humans , Male , Reoperation , Retrospective Studies , Speech Intelligibility , Surgical Flaps , Treatment Failure , Treatment Outcome
2.
J Voice ; 25(6): 709-13, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21439778

ABSTRACT

OBJECTIVES/HYPOTHESIS: Maximum phonation time (MPT), a clinical measurement of the longest time one can phonate a vowel, typically /a/, is a frequently used measure of vocal function, but normative data are lacking for MPT in healthy older adults. The aim of this study was to provide data on MPT in healthy older adults and to determine the effect of advanced age, gender, and repeated measures on MPT. STUDY DESIGN: Prospective. METHODS: Sixty-nine healthy older adult volunteers participated (ie, 15, 26, and 28 in the seventh, eighth, and ninth decades of life, respectively). The effects of age, gender, and repeated measures (three trials in a single session) on MPT were assessed. Mean, standard deviation, compound symmetry covariance, analysis of variance, and analysis of covariance were used for statistical analysis. RESULTS: Neither age group, gender, trial, nor their interactions was statistically significant (P>0.05). Adults in the seventh, eighth, and ninth decades of life had mean MPTs of 22.27 (standard error [SE]=1.56), 22.97 (SE=1.11), and 21.14 (SE=0.97) seconds, respectively. Females and males had mean MPTs of 20.96 (SE=0.92) and 23.23 (SE=0.96) seconds, respectively. Finally, MPTs for trials 1, 2, and 3 were 21.77 (SE=1.09), 21.67 (SE=1.12), and 22.80 (SE=1.27), respectively. CONCLUSIONS: MPTs were longer in this group of older adults than previously reported and did not vary significantly with age or gender. Additionally, across a single short sampling session, measurements were relatively stable across three trials of MPTs.


Subject(s)
Aging/physiology , Phonation , Aged , Aged, 80 and over , Female , Humans , Male , Sex Factors , Time Factors
3.
Laryngoscope ; 121(4): 732-7, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21305558

ABSTRACT

OBJECTIVE: To report our experience with cephalometry in evaluating velopharyngeal dysfunction (VPD) in velocardiofacial syndrome (VCFS) and its utility in assessing the role of cervical spine abnormalities in VPD, prior to surgical correction of VPD. DESIGN: Clinical charts and cephalometric radiographs done prior to surgery for VPD were retrospectively analyzed to ascertain velopharyngeal measurements and cervical spine abnormalities. PATIENTS: Twenty-six patients (age: 6-23 years) with molecularly confirmed VCFS. SETTING: Wake Forest University Health Sciences (1997-2005). MEASUREMENTS: Cranial base angle, nasopharyngeal depth, velum length, and Need ratio at rest, velar dimple location, and velopharyngeal length during phonation; information on presence/absence of submucous cleft palate and cervical spine abnormalities were also obtained. The relationship between C1 anterior arch abnormalities and Need ratio was examined. RESULTS: Seventy-three percent of the VCFS patients had excessive nasopharyngeal depth, 80% had an abnormal Need ratio, 50% had a short velum, 81% had a submucous or occult submucous cleft palate, 90.5% had a cervical spine abnormality (C1 anterior arch abnormalities in 38%) and 11.5% had platybasia. There was a significant difference in the Need ratio between patients with and without C1 anterior arch abnormalities. CONCLUSION: Cephalometry can be used to delineate factors such as C1 vertebral abnormalities, excessive pharyngeal depth, and short velum that contribute to VPD in VCFS. This would help otolaryngologists better understand the anatomy prior to surgical treatment of VPD. This is the first study to highlight the frequent occurrence of C1 anterior arch abnormalities in VCFS.


Subject(s)
Cephalometry/methods , DiGeorge Syndrome/diagnosis , DiGeorge Syndrome/physiopathology , Velopharyngeal Insufficiency/diagnosis , Velopharyngeal Insufficiency/physiopathology , Adolescent , Cervical Vertebrae/abnormalities , Cervical Vertebrae/surgery , Child , Cleft Palate/diagnosis , Cleft Palate/physiopathology , Cleft Palate/surgery , DiGeorge Syndrome/surgery , Female , Humans , Male , Platybasia/diagnosis , Platybasia/physiopathology , Platybasia/surgery , Retrospective Studies , Velopharyngeal Insufficiency/surgery , Young Adult
4.
Ann Otol Rhinol Laryngol ; 115(2): 97-102, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16514790

ABSTRACT

OBJECTIVES: Despite the belief that it represents a central neurologic dysfunctional process, adductor-type spasmodic dysphonia without tremor is usually effectively treated by injection of botulinum toxin A; however, in most cases such injections must be repeated every few months. A promising new surgical procedure is herein reported. METHODS: Under local anesthesia with intravenous sedation, a large laryngoplasty window is created, and under direct vision with intraoperative voice monitoring, fibers from the thyroarytenoid and lateral cricoarytenoid muscles are removed until breathiness occurs. The two sides are staged; that is, one side is done at a time, with surgery on the second side being performed 3 to 6 months after that on the first side, if needed. RESULTS: This was a retrospective, unblinded study of 5 patients who underwent myectomy of the thyroarytenoid and lateral cricoarytenoid muscles. The preliminary results show improved voice fluency in all patients at 5 to 19 months of follow-up. There was no period of prolonged breathiness or dysphagia in any of the patients, and there were no surgical complications. CONCLUSIONS: Myectomy of the thyroarytenoid and lateral cricoarytenoid muscles is a promising new surgical treatment for adductor-type spasmodic dysphonia that may effectively mimic "permanent" botulinum toxin injections.


Subject(s)
Laryngeal Muscles/surgery , Spasm/surgery , Voice Disorders/surgery , Aged , Anesthesia, Intravenous , Anesthesia, Local , Arytenoid Cartilage/surgery , Cricoid Cartilage/surgery , Endoscopy , Female , Follow-Up Studies , Humans , Laryngeal Muscles/physiopathology , Male , Middle Aged , Phonation/physiology , Retrospective Studies , Sound Spectrography , Spasm/physiopathology , Treatment Outcome , Vocal Cords/physiopathology , Voice Disorders/physiopathology
5.
Otolaryngol Head Neck Surg ; 131(5): 606-9, 2004 Nov.
Article in English | MEDLINE | ID: mdl-15523434

ABSTRACT

OBJECTIVE: The efficacy of many of the noninvasive treatments for snoring has not been evaluated in controlled trials. This paper seeks to evaluate the efficacy of an oil-based spray in the treatment of snoring, in a double-blinded, placebo-controlled, crossover trial using objective acoustic analysis and subjective questionnaires. STUDY DESIGN AND SETTING: Participants were randomized to use both oil-based oral spray (treatment) and water-based oral spray (placebo) during a two-night in-home study period. Questionnaires were completed by participant and bed-partner in addition to audio-tape recordings which were analyzed for frequency, duration, and mean energy of snoring. RESULTS: Greatest snoring rate demonstrated 30% = benefit; 40% = no change; 30% = adverse effect (n = 20). Percent time snoring yielded: 30% benefit; 15% no change; 55% adverse effect (n = 20). Study data results for mean energy were (n = 12): benefit = 17%, no change = 33%, adverse effect = 50%. Bed-partner observations (n = 17) demonstrated 37% = benefit; 38% = no change; 25% = adverse effect. CONCLUSION/SIGNIFICANCE: Objective and subjective evaluation of the performance of the oil-based Snoreless spray in comparison to placebo demonstrated a lack of efficacy in snoring reduction.


Subject(s)
Oils/administration & dosage , Snoring/drug therapy , Acoustics/instrumentation , Administration, Topical , Adult , Chronic Disease , Cross-Over Studies , Double-Blind Method , Female , Humans , Lubrication , Male , Middle Aged , Snoring/diagnosis , Tape Recording , Treatment Outcome
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