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1.
Ned Tijdschr Tandheelkd ; 127(9): 473-480, 2020 Sep.
Artigo em Holandês | MEDLINE | ID: mdl-33011752

RESUMO

The practical training in dental schools in the Netherlands is largely organised within the walls of the educational institution, while many other medical educational programmes provide practical training to a large extent in the professional environment. The external practical internship is a form of practical learning with which positive experience has been gained in foreign dental schools, both by students and dentist-supervisors. The Dutch dental schools have a joint plan to set up practical internships in dental practices for master's students in the final year of their education. The aim of such an internship is that students in the last phase of their programme learn to apply the acquired knowledge and skills in an actual professional environment. This includes both clinical and dental treatment and the ability to organise oral health care for patients and everything that comes with it. This article describes the outline of this programme.


Assuntos
Internato e Residência , Currículo , Educação em Odontologia , Educação Continuada em Odontologia , Humanos , Países Baixos , Paladar
2.
Neuromuscul Disord ; 26(6): 354-60, 2016 06.
Artigo em Inglês | MEDLINE | ID: mdl-27132120

RESUMO

Dysphagia in Duchenne muscular dystrophy (DMD) worsens with age, with increasingly effortful mastication. The aims of this study were to describe mastication problems in consecutive stages in a group of patients with DMD and to determine related pathophysiological aspects of masticatory muscle structure, tongue thickness, bite force and dental characteristics. Data from 72 patients with DMD (4.3 to 28.0 years), divided into four clinical stages, were collected in a cross sectional study. Problems with mastication and the need for food adaptations, in combination with increased echogenicity of the masseter muscle, were already found in the early stages of the disease. A high percentage of open bites and cross bites were found, especially in the later stages. Tongue hypertrophy also increased over time. Increased dysfunction, reflected by increasingly abnormal echogenicity, of the masseter muscle and reduced occlusal contacts (anterior and posterior open bites) were mainly responsible for the hampered chewing. In all, this study shows the increasing involvement of various elements of the masticatory system in progressive Duchenne muscular dystrophy. To prevent choking and also nutritional deficiency, early detection of chewing problems by asking about feeding and mastication problems, as well as asking about food adaptations made, is essential and can lead to timely intervention.


Assuntos
Má Oclusão/patologia , Mastigação/fisiologia , Músculos da Mastigação/fisiopatologia , Distrofia Muscular de Duchenne/fisiopatologia , Adolescente , Força de Mordida , Criança , Pré-Escolar , Humanos , Masculino , Má Oclusão/diagnóstico por imagem , Má Oclusão/fisiopatologia , Músculos da Mastigação/diagnóstico por imagem , Distrofia Muscular de Duchenne/diagnóstico por imagem , Distrofia Muscular de Duchenne/patologia , Inquéritos e Questionários , Ultrassonografia , Adulto Jovem
3.
J Oral Rehabil ; 42(6): 430-8, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-25600935

RESUMO

Patients with Duchenne muscular dystrophy (DMD) experience negative effects upon feeding and oral health. We aimed to determine whether the mandibular range of motion in DMD is impaired and to explore predictive factors for the active maximum mouth opening (aMMO). 23 patients with DMD (mean age 16.7 ± 7.7 years) and 23 controls were assessed using a questionnaire about mandibular function and impairments. All participants underwent a clinical examination of the masticatory system, including measurement of mandibular range of motion and variables related to mandibular movements. In all patients, quantitative ultrasound of the digastric muscle and the geniohyoid muscle and the motor function measure (MFM) scale were performed. The patients were divided into early and late ambulatory stage (AS), early non-ambulatory stage (ENAS) and late non-ambulatory stage (LNAS). All mandibular movements were reduced in the patient group (P < 0.001) compared to the controls. Reduction in the aMMO (<40 mm) was found in 26% of the total patient group. LNAS patients had significantly smaller mandibular movements compared to AS and ENAS (P < 0.05). Multiple linear regression analysis for aMMO revealed a positive correlation with the body height and disease progression, with MFM total score as the strongest independent risk factor (R(2) = 0.71). Mandibular movements in DMD are significantly reduced and become more hampered with loss of motor function, including the sitting position, arm function, and neck and head control. We suggest that measurement of the aMMO becomes a part of routine care of patients with DMD.


Assuntos
Mandíbula/fisiopatologia , Músculos da Mastigação/fisiopatologia , Distrofia Muscular de Duchenne/fisiopatologia , Amplitude de Movimento Articular/fisiologia , Adolescente , Adulto , Estudos de Casos e Controles , Criança , Humanos , Modelos Lineares , Masculino , Fatores de Risco , Inquéritos e Questionários , Adulto Jovem
4.
Neuromuscul Disord ; 24(8): 684-92, 2014 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-24969130

RESUMO

Patients with Duchenne muscular dystrophy (DMD) report masticatory and swallowing problems. Such problems may cause complications such as choking, and feeling of food sticking in the throat. We investigated whether masticatory performance in DMD is objectively impaired, and explored predictive factors for compromised mastication. Twenty-three patients and 23 controls filled out two questionnaires about mandibular function, and underwent a clinical examination of the masticatory system and measurements of anterior bite force and masticatory performance. In the patients, moreover, quantitative ultrasound of the tongue and motor function measurement was performed. The patients were categorized into ambulatory stage (early or late), early non-ambulatory stage, or late non-ambulatory stage. Masticatory performance, anterior bite force and occlusal contacts were all reduced in the patient group compared to the controls (all p < 0.001). Mastication abnormalities were present early in the disease process prior to a reduction of motor function measurement. The early non-ambulatory and late non-ambulatory stage groups showed less masticatory performance compared to the ambulatory stage group (p < 0.028 and p < 0.010, respectively). Multiple linear regression analysis revealed that stage of the disease was the strongest independent risk factor for the masticatory performance (R(2) = 0.52). Anterior bite force, occlusal contacts and masticatory performance in DMD are severely reduced.


Assuntos
Força de Mordida , Mastigação , Distrofia Muscular de Duchenne/fisiopatologia , Adolescente , Adulto , Estudos de Casos e Controles , Criança , Estudos de Coortes , Progressão da Doença , Humanos , Modelos Lineares , Masculino , Boca/diagnóstico por imagem , Boca/fisiopatologia , Distrofia Muscular de Duchenne/diagnóstico por imagem , Exame Físico , Fatores de Risco , Inquéritos e Questionários , Ultrassonografia , Adulto Jovem
5.
Neurology ; 73(21): 1787-91, 2009 Nov 24.
Artigo em Inglês | MEDLINE | ID: mdl-19933981

RESUMO

OBJECTIVE: In patients with spinal muscular atrophy (SMA) type II, feeding problems and dysphagia are common, but the underlying mechanisms of these problems are not well defined. This case control study was designed to determine the underlying mechanisms of dysphagia in SMA type II. METHODS: Six children with SMA type II and 6 healthy matched controls between 6.4 and 13.4 years of age were investigated during swallowing liquid and solid food in 2 different postures using surface EMG (sEMG) of the submental muscle group (SMG) and a video fluoroscopic swallow study (VFSS). RESULTS: The VFSS showed postswallow residue of solid food in the vallecula and above the upper esophageal sphincter (UES), which can be responsible for indirect aspiration. Better results in swallowing were achieved in a more forward head position. These findings were supported by the sEMG measurements of the SMG during swallowing. CONCLUSIONS: Dysphagia in spinal muscular atrophy type II is due to a neurologic dysfunction (lower motor neuron problems from the cranial nerves in the brainstem) influencing the muscle force and efficiency of movement of the tongue and the submental muscle group in combination with a biomechanical component (compensatory head posture). The results suggest an integrated treatment with an adapted posture during meals and the advice of drinking water after meals to prevent aspiration pneumonias.


Assuntos
Paralisia Bulbar Progressiva/etiologia , Transtornos de Deglutição/etiologia , Atrofias Musculares Espinais da Infância/complicações , Adolescente , Estudos de Casos e Controles , Criança , Deglutição/fisiologia , Eletromiografia/métodos , Comportamento Alimentar , Feminino , Humanos , Masculino , Avaliação de Resultados em Cuidados de Saúde , Postura/fisiologia , Gravação em Vídeo/métodos
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