Swallowing Disorders in Patients with Chiari Malformation Type I After Decompression Neurosurgery

被引:0
|
作者
Luciana B. de Oliveira
Moisés A. S. de Queiroz
Leonardo J. M. de Macêdo Filho
Nathan A. Shlobin
Andrea Otamendi-Lopez
Priscilla M. E. Barbosa
Andréa C. L. Porto
Euler N. Sauaia Filho
机构
[1] Intensive Care Unit,Division of Speech Pathology
[2] General Hospital of Fortaleza,Health Science Center
[3] University of Fortaleza,Department of Neurological Surgery
[4] Mayo Clinic,Feinberg School of Medicine
[5] Northwestern University,Applied Linguistics Department, Humanities Center
[6] State University of Ceará,Medical Course
[7] CEUMA University,undefined
关键词
“Arnold-Chiari malformation,; “Deglutition disorders,; “Neurosurgery,; “Speech-language pathology,; “Skull base;
D O I
10.1007/s42399-022-01264-4
中图分类号
学科分类号
摘要
The present study aimed to investigate postoperative swallowing disorders in patients diagnosed with CM I after decompression neurosurgery. We selected 54 patients after decompression neurosurgery procedure for CM I from January 2017 to December 2019. We evaluated the speech-language assessment (CSLSA) 24 h after post-surgical extubation. CSLSA observed aspects of posture, sensitivity, tone, and extraoral and intraoral mobility of the FAO and visualizing the functions of breathing, phonation, articulation, chewing, and swallowing. We correlated the severity of the dysphagia and the presence of associated malformations in the CM I patients. In our study, 39 patients were female (mean age 41.3 ± 47.1 years). Thirty-seven patients had associated malformations (p = 0.0243): 21 patients syringomyelia, 11 basilar invagination, and 5 syringomyelia and basilar invagination. Dysphagia was present in 37 of the cases (68.5%; p = 0.0016). Dysphonia in 13 (24.1%; p = 0.4785) and dysarthria in 3 (5.6%; p = 0.0042). We observed in the CSLSA: orofacial hypomobility (29 patients — 53.7%; p = 0.0204), orofacial hyposensitivity (26 patients — 48.1%; p = 0.3023), reduced GAG reflex (24 patients — 44.5%; p = 0.1041), ineffective cough (19 patients — 35.2%; p = 0.0022), ineffective saliva swallowing (18 patients — 33.3%; p = 0.0396), dyspnea (13 patients — 24.1%; p = 0.4785), orofacial hypotonia (11 patients — 20.4%; p = 0.0004), altered cervical auscultation (10 patients — 18.5%; p = 0.0003), and dysarthria (3 patients — 9.3%; p = 0.0042). The presence of associated malformations significantly influenced the appearance of swallowing disorders, the severity of oropharyngeal dysphagia, the post-surgical complications (17 patients — 31.5%; p < 0.001), and the clinical outcomes (p = 0.0029) of patients with CM type I. Decompressive neurosurgery for CM I had low rates of post-surgical complications overall. However, there was a high incidence of dysphagia. The presence of associated malformations is related with poorer prognosis and greater severity of oropharyngeal dysphagia in patients with CM I.
引用
收藏
相关论文
共 50 条
  • [31] Scoliosis in patients with Chiari malformation type I
    Mohammad Hassan A. Noureldine
    Nir Shimony
    George I. Jallo
    Mari L. Groves
    Child's Nervous System, 2019, 35 : 1853 - 1862
  • [32] Assessment of patients with a Chiari malformation type I
    Tam, Sharon Ka Po
    Chia, Jonathan
    Brodbelt, Andrew
    Foroughi, Mansoor
    BRAIN AND SPINE, 2022, 2
  • [33] Posterior fossa decompression with or without duraplasty in patients with Chiari type I malformation: A systematic review
    Xin, Yexin
    Xu, Zhentao
    Dong, Zhaogang
    Xiao, Yilei
    ASIAN JOURNAL OF SURGERY, 2024, 47 (04) : 1961 - 1962
  • [34] Surgical results of posterior fossa decompression for patients with Chiari I malformation
    Ramon Navarro
    Greg Olavarria
    Roopa Seshadri
    Gabriel Gonzales-Portillo
    David G. McLone
    Tadanori Tomita
    Child's Nervous System, 2004, 20 : 349 - 356
  • [35] Surgical results of posterior fossa decompression for patients with Chiari I malformation
    Navarro, R
    Olavarria, G
    Seshadri, R
    Gonzales-Portillo, G
    McLone, DG
    Tomita, T
    CHILDS NERVOUS SYSTEM, 2004, 20 (05) : 349 - 356
  • [36] Timing of syrinx reduction and stabilization after posterior fossa decompression for pediatric Chiari malformation type I
    Chotai, Silky
    Chan, Emily W.
    Ladner, Travis R.
    Hale, Andrew T.
    Gannon, Stephen R.
    Shannon, Chevis N.
    Bonfield, Christopher M.
    Naftel, Robert P.
    Wellons, John C.
    JOURNAL OF NEUROSURGERY-PEDIATRICS, 2020, 26 (02) : 193 - 199
  • [37] Chiari Malformation Type I and sleep disorders: a case report
    Di Munno, G.
    Bartoli, A.
    Corbelli, R.
    SWISS MEDICAL WEEKLY, 2016, 146 : 19S - 19S
  • [38] Incidence and management of postoperative pseudomeningocele and cerebrospinal fluid leak after Chiari malformation type I decompression
    Atchley, Travis J.
    Alam, Yasaman
    Gross, Evan
    Laskay, Nicholas M. B.
    Estevez-Ordonez, Dagoberto
    Schmalz, Philip G. R.
    Fisher, Winfield S., III
    NEUROSURGICAL FOCUS, 2023, 54 (03)
  • [39] Technique for Mini-open Decompression of Chiari Type I Malformation in Adults
    Drapeau, Annie Isabelle
    OPERATIVE NEUROSURGERY, 2017, 13 (04) : 470 - 470
  • [40] Time course of syringomyelia resolution following decompression of Chiari malformation Type I
    Wetjen, Nicholas M.
    Heiss, John D.
    Oldfield, Edward H.
    JOURNAL OF NEUROSURGERY-PEDIATRICS, 2008, 1 (02) : 118 - 123