RESUMO
PURPOSE: 3D visualization is an important part of learning anatomy with cadavers generally used to effectuate this. However, high cost, ethical considerations, and limited accessibility can often limit the suitability of cadavers as teaching tools. Anatomical 3D printed models offer an alternative tool for teaching gross anatomy due to their low cost and accessibility. This study aims to investigate if combing gamification with 3D printed models can enhance the learning experience and be effective for teaching anatomy. METHODS: 3D printed models of the bones of the foot and ankle were generated, and 267 first-year medical students from 2 consecutive cohorts worked in groups to put it together as a puzzle. Participants completed a questionnaire regarding perceptions of 3D models and their knowledge of foot anatomy, before and after the session and were asked to provide comments. RESULTS: Analysis of the responses showed a significant increase in the confidence of the learners in their anatomy knowledge and an increased appreciation of the role that 3D models have in enhancing the learning experience. After the session, there were many comments saying how enjoyable and engaging 3D models were. CONCLUSION: Through the puzzle element of the session, the students were challenged mentally to work out the anatomical features of the foot and ankle. The combined elements of the puzzle and the features of the 3D model assembly made the activity fun and conducive to active learning. The possibility of having fun was not something the students had considered before the session.
Assuntos
Anatomia , Tornozelo , Educação de Graduação em Medicina , Pé , Modelos Anatômicos , Impressão Tridimensional , Estudantes de Medicina , Humanos , Estudantes de Medicina/psicologia , Estudantes de Medicina/estatística & dados numéricos , Educação de Graduação em Medicina/métodos , Pé/anatomia & histologia , Tornozelo/anatomia & histologia , Anatomia/educação , Inquéritos e Questionários , Imageamento Tridimensional , Masculino , Feminino , CadáverAssuntos
Polidactilia/cirurgia , Dedos do Pé/cirurgia , Criança , Dedos/cirurgia , Humanos , Lactente , Recém-NascidoRESUMO
Giant omphalocele is a rare, large abdominal wall defect in which the intra-abdominal organs herniate through the umbilical cord and are covered by a sac. Surgical management of giant omphalocele is challenging, and optimal treatment remains controversial. Two generally accepted treatment options are staged closure and delayed closure. Delayed closure takes place after a period of conservative treatment promoting omphalocele sac epithelialization. We present 3 patients treated by a delayed closure technique for ventral hernia repair. In this technique, the epithelialized omphalocele sac and peritoneum are elevated as flaps, which are used to reconstruct the abdominal wall in multiple layers.
Assuntos
Hérnia Umbilical/cirurgia , Herniorrafia/métodos , Retalhos Cirúrgicos , Pré-Escolar , Terapia Combinada , Tratamento Conservador , Feminino , Hérnia Umbilical/terapia , Humanos , Lactente , Masculino , Fatores de TempoAssuntos
Queimaduras/complicações , Síndrome de Sweet/etiologia , Anti-Inflamatórios/uso terapêutico , Queimaduras/patologia , Feminino , Humanos , Pessoa de Meia-Idade , Prednisolona/uso terapêutico , Síndrome de Sweet/diagnóstico , Síndrome de Sweet/tratamento farmacológico , Resultado do TratamentoRESUMO
A patient with Klippel-Feil syndrome, which was associated with Pierre Robin sequence, bilateral mandibular duplication, and occipital clefts, is described. The management, surgery, and possible etiology are discussed in relation to the relevant literature.
Assuntos
Síndrome de Klippel-Feil/cirurgia , Mandíbula/anormalidades , Mandíbula/cirurgia , Síndrome de Pierre Robin/cirurgia , Vértebras Cervicais/anormalidades , Pré-Escolar , Fissura Palatina/complicações , Fissura Palatina/cirurgia , Humanos , Síndrome de Klippel-Feil/complicações , Masculino , Palato Mole/anormalidades , Síndrome de Pierre Robin/complicações , Distúrbios da Fala/complicaçõesRESUMO
A unilateral upper lateral orbital cleft, fitting the description of the extremely rare Tessier cleft number 9 is reported. The management and surgery of this patient are discussed, and the relevant literature is reviewed. The usefulness of three-dimensional computed tomography reconstructions and plastic models in planning the surgery is discussed.