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6 岁后患语音障碍儿童的口颜面功能。

Orofacial function in children with Speech Sound Disorders persisting after the age of six years.

机构信息

Division of Speech and Language Pathology, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.

Orofacial Resource Centre for Rare Diseases, Public Dental Service, Mun-H-Center, Gothenburg, Sweden.

出版信息

Int J Speech Lang Pathol. 2020 Oct;22(5):526-536. doi: 10.1080/17549507.2019.1701081. Epub 2020 Mar 1.

DOI:10.1080/17549507.2019.1701081
PMID:32114835
Abstract

: The aim was to investigate, describe and analyse speech characteristics, intelligibility, orofacial function and co-existing neurodevelopmental symptoms in children with SSD of unknown origin, persisting after six years of age.: The study included 61 children with SSD (6-17 years) of unknown origin, referred for a speech and oral motor examination. The severity of SSD was estimated using Percentage Consonants Correct (PCC) and Percentage Vowels Correct (PVC) and assessments of resonance based on Swedish Articulation and Nasality Test (SVANTE). Orofacial function was screened using the Nordic Orofacial Test-Screening (NOT-S). Parents completed the Intelligibility in Context Scale (ICS) and a questionnaire including questions about heredity, medical and neurodevelopmental conditions, and speech development. SSD varied according to PCC (8-95%) and PVC (55-100%) measurements. Percentages of co-occurring disorders included: 51% resonance deviations, 90% intelligibility issues, and 87% orofacial difficulties. The most affected orofacial domains were "Chewing and swallowing" (41%), "Masticatory muscles and jaw function" (38%) and "Sensory function" (38%). The majority (64%) had co-existing dysfunctions relating to general motor and neurodevelopmental disorders. Children with persistent SSD are at risk for orofacial dysfunction, general motor difficulties and other neurodevelopmental disorders and therefore should be screened for co-occurring disorders.

摘要

目的在于调查、描述和分析言语特征、可懂度、口颌功能以及年龄超过 6 岁且病因不明的言语失用症儿童的共存神经发育症状。研究纳入了 61 名病因不明、持续存在言语失用症的儿童(6-17 岁),他们均接受了言语和口腔运动检查。言语失用症的严重程度使用辅音百分比正确(PCC)和元音百分比正确(PVC)以及瑞典言语构音和鼻音测试(SVANTE)的共振评估进行估计。口颌功能使用北欧口颌功能测试筛查(NOT-S)进行筛查。父母完成了语境可懂度量表(ICS)和一份问卷,其中包括遗传、医疗和神经发育状况以及言语发育方面的问题。PCC(8-95%)和 PVC(55-100%)测量结果显示言语失用症存在差异。共存障碍的百分比包括:51%的共振偏差、90%的可懂度问题和 87%的口颌困难。受影响最严重的口颌领域是“咀嚼和吞咽”(41%)、“咀嚼肌和下颌功能”(38%)和“感觉功能”(38%)。大多数(64%)存在与一般运动和神经发育障碍相关的共存功能障碍。持续性言语失用症的儿童存在口颌功能障碍、一般运动困难和其他神经发育障碍的风险,因此应筛查共存障碍。

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