TY - JOUR
T1 - Speech outcomes in children with 22q11.2 deletion syndrome following surgery for velopharyngeal insufficiency
AU - Jiramongkolchai, Pawina
AU - Kumar, Manvinder S.
AU - Sowder, Derrick
AU - Chinnadurai, Sivakumar
AU - Wootten, Christopher T.
AU - Goudy, Steven L.
N1 - Publisher Copyright:
© 2016 Elsevier Ireland Ltd
PY - 2016/9/1
Y1 - 2016/9/1
N2 - Objective The purpose of this study was to identify prognostic factors associated with improved speech outcomes following surgical correction for velopharyngeal insufficiency (VPI) in pediatric patients with 22q11.2 deletion syndrome (22q11DS). Methods Eighteen patients were identified via retrospective chart review of patients with 22q11DS between 2005 and 2014. Patient characteristics, medical histories, associated comorbidities, surgical procedures, and pre- and postoperative perceptual hypernasality (subjectively rated 1–5 with 5 being the most severe) were gathered for each patient. Results 12 patients (67%) experienced improvement in hypernasality following corrective surgery for VPI. Higher severity of hypernasality preoperatively was found to be indicative of a lower chance of improvement with VPI surgery. Of 8 patients with a preoperative hypernasality score of 5, 3 (38%) showed improvement in hypernasality postoperatively, while 9 out of 10 (90%) of patients with a preoperative hypernasality score less than 5 showed postoperative improvement. Females were also found to have worse speech outcomes compared to males. Conclusion 22q11DS patients presenting with severely hypernasal speech preoperatively are less likely to show improvement in hypernasality following corrective surgery for VPI. Those patients with moderate hypernasality are most likely to benefit from surgery.
AB - Objective The purpose of this study was to identify prognostic factors associated with improved speech outcomes following surgical correction for velopharyngeal insufficiency (VPI) in pediatric patients with 22q11.2 deletion syndrome (22q11DS). Methods Eighteen patients were identified via retrospective chart review of patients with 22q11DS between 2005 and 2014. Patient characteristics, medical histories, associated comorbidities, surgical procedures, and pre- and postoperative perceptual hypernasality (subjectively rated 1–5 with 5 being the most severe) were gathered for each patient. Results 12 patients (67%) experienced improvement in hypernasality following corrective surgery for VPI. Higher severity of hypernasality preoperatively was found to be indicative of a lower chance of improvement with VPI surgery. Of 8 patients with a preoperative hypernasality score of 5, 3 (38%) showed improvement in hypernasality postoperatively, while 9 out of 10 (90%) of patients with a preoperative hypernasality score less than 5 showed postoperative improvement. Females were also found to have worse speech outcomes compared to males. Conclusion 22q11DS patients presenting with severely hypernasal speech preoperatively are less likely to show improvement in hypernasality following corrective surgery for VPI. Those patients with moderate hypernasality are most likely to benefit from surgery.
KW - 22q11.2 microdeletion syndrome
KW - Cleft palate
KW - DiGeorge syndrome
KW - Speech articulation disorder
KW - Velocardiofacial syndrome
KW - Velopharyngeal insufficiency
UR - https://www.scopus.com/pages/publications/84976873318
U2 - 10.1016/j.ijporl.2016.06.044
DO - 10.1016/j.ijporl.2016.06.044
M3 - Article
C2 - 27497383
AN - SCOPUS:84976873318
SN - 0165-5876
VL - 88
SP - 34
EP - 37
JO - International Journal of Pediatric Otorhinolaryngology
JF - International Journal of Pediatric Otorhinolaryngology
ER -