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1.
Ned Tijdschr Tandheelkd ; 127(9): 473-480, 2020 Sep.
Article in Dutch | MEDLINE | ID: mdl-33011752

ABSTRACT

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.


Subject(s)
Internship and Residency , Curriculum , Education, Dental , Education, Dental, Continuing , Humans , Netherlands , Taste
2.
Neuromuscul Disord ; 26(6): 354-60, 2016 06.
Article in English | MEDLINE | ID: mdl-27132120

ABSTRACT

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.


Subject(s)
Malocclusion/pathology , Mastication/physiology , Masticatory Muscles/physiopathology , Muscular Dystrophy, Duchenne/physiopathology , Adolescent , Bite Force , Child , Child, Preschool , Humans , Male , Malocclusion/diagnostic imaging , Malocclusion/physiopathology , Masticatory Muscles/diagnostic imaging , Muscular Dystrophy, Duchenne/diagnostic imaging , Muscular Dystrophy, Duchenne/pathology , Surveys and Questionnaires , Ultrasonography , Young Adult
3.
J Oral Rehabil ; 42(6): 430-8, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25600935

ABSTRACT

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.


Subject(s)
Mandible/physiopathology , Masticatory Muscles/physiopathology , Muscular Dystrophy, Duchenne/physiopathology , Range of Motion, Articular/physiology , Adolescent , Adult , Case-Control Studies , Child , Humans , Linear Models , Male , Risk Factors , Surveys and Questionnaires , Young Adult
4.
Neuromuscul Disord ; 24(8): 684-92, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24969130

ABSTRACT

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.


Subject(s)
Bite Force , Mastication , Muscular Dystrophy, Duchenne/physiopathology , Adolescent , Adult , Case-Control Studies , Child , Cohort Studies , Disease Progression , Humans , Linear Models , Male , Mouth/diagnostic imaging , Mouth/physiopathology , Muscular Dystrophy, Duchenne/diagnostic imaging , Physical Examination , Risk Factors , Surveys and Questionnaires , Ultrasonography , Young Adult
5.
Neurology ; 73(21): 1787-91, 2009 Nov 24.
Article in English | MEDLINE | ID: mdl-19933981

ABSTRACT

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.


Subject(s)
Bulbar Palsy, Progressive/etiology , Deglutition Disorders/etiology , Spinal Muscular Atrophies of Childhood/complications , Adolescent , Case-Control Studies , Child , Deglutition/physiology , Electromyography/methods , Feeding Behavior , Female , Humans , Male , Outcome Assessment, Health Care , Posture/physiology , Video Recording/methods
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