Superiorly Based Pharyngeal Flap for Treatment of Velopharyngeal Insufficiency in Patients With 22q11.2 Deletion Syndrome

被引:21
|
作者
Filip, Charles [1 ]
Matzen, Michael [1 ]
Aukner, Ragnhild [2 ]
Moe, Marianne [2 ]
Hogevold, Hans Erik [1 ]
Abyholm, Frank [1 ]
Abrahamsen, Tore Gunnar [3 ]
Tonseth, Kim [1 ]
机构
[1] Oslo Univ Hosp, Rikshosp, Dept Plast & Reconstruct Surg, N-0424 Oslo, Norway
[2] Bredtvet Resource Ctr, Dept Speech & Language Therapy, Cleft Palate Team, Oslo, Norway
[3] Oslo Univ Hosp, Rikshosp, Dept Pediat, N-0424 Oslo, Norway
关键词
Pharyngeal flap; pharyngoplasty; velocardiofacial syndrome; velopharyngeal insufficiency; CARDIO-FACIAL SYNDROME; VELOCARDIOFACIAL SYNDROME; CLEFT-PALATE; INCOMPETENCE; ANOMALIES; SURGERY;
D O I
10.1097/SCS.0b013e31827c84f2
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: There are no previous blinded studies for comparison of preoperative versus postoperative perceptual speech assessments when using a pharyngeal flap for treating velopharyngeal insufficiency (VPI) in patients diagnosed with 22q11.2 deletion syndrome. The aim of the study was to evaluate the effect of superiorly based pharyngeal flap surgery on speech in these patients using blinded judgments of experienced speech therapists. Methods: A retrospective study of 12 consecutive patients who had undergone pharyngeal flap surgery for treatment of VPI between 2002 and 2009 was conducted. Seven girls and 5 boys between 4 and 15 (median, 6) years old at the time of surgery were included in the study. Six patients were born with a submucous cleft palate (including 2 occult), and 1 patient, with an overt cleft palate. The remaining 5 patients had no signs of a palatal pathology. All palatal clefts had been repaired before pharyngeal flap surgery except in 2 patients with occult submucous cleft palate. Preoperative and postoperative audio recordings were blinded for scoring independently by 3 senior speech therapists. Results: There was a significant improvement in hypernasality (P = 0.002), audible nasal emission (P = 0.033), weak pressure consonants (P = 0.008), and speech intelligibility (P = 0.021) after pharyngeal flap surgery. Hyponasality did not develop significantly with surgery. One patient was diagnosed with obstructive sleep apnea. Conclusions: Superiorly based pharyngeal flap resulted in a significant speech improvement in 12 consecutive patients with 22q11.2 deletion syndrome having VPI.
引用
下载
收藏
页码:501 / 504
页数:4
相关论文
共 50 条
  • [21] Health Care Resource Use in Patients With and Without 22q11.2 Deletion Syndrome Undergoing Sphincter Pharyngoplasty for Velopharyngeal Insufficiency
    Wright, Darrell T.
    Nguyen, Shaun A.
    Teufel, Ronald J., II
    White, David R.
    JAMA OTOLARYNGOLOGY-HEAD & NECK SURGERY, 2017, 143 (03) : 286 - 291
  • [22] In Search of the Optimal Surgical Treatment for Velopharyngeal Dysfunction in 22q11.2 Deletion Syndrome: A Systematic Review
    Spruijt, Nicole E.
    ReijmanHinze, Judith
    Hens, Greet
    Vander Poorten, Vincent
    van der Molen, Aebele B. Mink
    PLOS ONE, 2012, 7 (03):
  • [23] Perioperative Risk Factors in Patients With 22q11.2 Deletion Syndrome Requiring Surgery for Velopharyngeal Dysfunction
    Stransky, Carrie
    Basta, Marten
    McDonald-McGinn, Donna M.
    Solot, Cynthia B.
    Drummond, Denis
    Zackai, Elaine
    LaRossa, Don
    Kirschner, Richard
    Jackson, Oksana
    CLEFT PALATE-CRANIOFACIAL JOURNAL, 2015, 52 (02): : 183 - 191
  • [24] Palatal evaluation and treatment in 22q11.2 deletion syndrome
    Jackson, Oksana
    Crowley, T. Blaine
    Sharkus, Robert
    Smith, Robert
    Jeong, Stephanie
    Solot, Cynthia
    McDonald-Mcginn, Donna
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2019, 179 (07) : 1184 - 1195
  • [25] 22q11.2 deletion syndrome and schizophrenia
    Qin, Xianzheng
    Chen, Jiang
    Zhou, Tian
    ACTA BIOCHIMICA ET BIOPHYSICA SINICA, 2020, 52 (11) : 1181 - 1190
  • [26] Camptodactyly and the 22q11.2 deletion syndrome
    Couser, Natario L.
    Pande, Chetna K.
    Walsh, Jonathan M.
    Tepperberg, James
    Aylsworth, Arthur S.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2017, 173 (02) : 515 - 518
  • [27] Adult Height, 22q11.2 Deletion Extent, and Short Stature in 22q11.2 Deletion Syndrome
    Heung, Tracy
    Conroy, Brigid
    Malecki, Sarah
    Ha, Joanne
    Boot, Erik
    Corral, Maria
    Bassett, Anne S.
    GENES, 2022, 13 (11)
  • [28] Schizophrenia and 22q11.2 deletion syndrome
    Bassett A.S.
    Chow E.W.C.
    Current Psychiatry Reports, 2008, 10 (2) : 148 - 157
  • [29] 22q11.2 deletion syndrome: Introduction
    Lajiness-O'Neill, R
    CHILD NEUROPSYCHOLOGY, 2005, 11 (01) : 1 - 3
  • [30] Thrombocytopenia in patients with chromosome 22q11.2 deletion syndrome
    Lawrence, S
    McDonald-McGinn, DM
    Zackai, E
    Sullivan, KE
    JOURNAL OF PEDIATRICS, 2003, 143 (02): : 277 - 278