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1.
Anat Cell Biol ; 54(4): 489-500, 2021 Dec 31.
Artigo em Inglês | MEDLINE | ID: mdl-34657839

RESUMO

Dissection and human specimens study remain the gold standard method for teaching anatomy. Due to the increasing health science courses in Brazil, the traditional way of obtaining bodies for scientific purposes, the unclaimed ones, became insufficient. In addition, this source is no longer ethically appropriate according to anatomists. In order to maintain the teaching quality, the Federal University of Juiz de Fora (UFJF) in Brazil, inspired by successful initiatives around the world, created a body donation program; Sempre Vivo. Besides the bureaucratic difficulty faced during its regulation, the implementation of a body donation program requires special attention regarding the religiosity, culture and uniqueness of the city's inhabitants. Informing people can demystify the process, avoid prejudice and increase the number of donors. In this way, an outreach project was designed to publicize Sempre Vivo and raise public awareness. In the first six years, Sempre Vivo reached the mark of 64 registered donors and seven bodies received. The donor's profile corresponds to female (70.3%), 57 years of age, retired (50.8%), spiritist (53.1%) and with 12 years or more of formal education (90.6%). Considering that the UFJF has not received unclaimed bodies for ten years, the program was considered satisfactory up to this level and, in the future, it may be the exclusive source of anatomical specimens. The description of the creation and the publicizing of Sempre Vivo, the overcome challenges, as well as the donors' profile, may encourage and facilitate the foundation of similar programs in Brazil and abroad.

2.
Artigo em Português | LILACS | ID: biblio-1179869

RESUMO

Anatomia e Radiologia são disciplinas amplamente presentes nas grades curriculares de cursos da área da saúde. A interseção entre a Anatomia Radiológica e as tecnologias recentes, como plataformas de ensino interativo, caracteriza-se como uma tendência a ser seguida na esfera educacional, sendo as implicações desse processo ainda não muito debatidas. O Departamento de Anatomia da Universidade Federal de Juiz de Fora iniciou o desenvolvimento de um atlas de anatomia vascular radiológica, o qual apresenta versões impressa e interativa. Possui imagens de angiotomografias computadorizadas feitas em aparelhos multislice de 16 a 128 canais, sendo as imagens de arquivo pessoal dos organizadores. O atlas promove a identificação das estruturas vasculares em questão e propicia a integração do conhecimento adquirido em salas de aula com a visualização de exames de imagem complementares rotineiros. A indiscutível presença de exames de imagem adicionais na rotina dos profissionais da saúde atuais faz com que seja válida a estratégia de integração entre o método tradicional de ensino e as práticas ativas de aprendizagem, as quais vêm ganhando destaque recentemente, devido a sua efetividade na fixação de conhecimentos.


Anatomy and Radiology are subjects widely present in health courses at universities. The intersection between Radiological Anatomy and recent technologies, such as interactive teaching platforms, is characterized as a tendency to be followed in the educational sphere, and the implications of this process are not much debated. The Department of Anatomy of Juiz de Fora Federal University has begun the development of an atlas of radiological vascular anatomy, which features printed and interactived versions. It presents computed tomography images taken on multislice devices from 16 to 128 channels, and the images are from the personal authors' archives. The Radiologic Vascular Atlas provides the identification of vascular structures in study and makes easier the integration of knowledge acquired in classrooms with the visualization of routine complementary imaging exams. The indisputable presence of complementary imaging examinations in the routine of current health professionals makes valid the strategy of integration between the traditional teaching method and active learning practices, which have recently gained prominence, due to its effectiveness in setting knowledge.


Assuntos
Radiologia , Anatomia , Tecnologia Radiológica , Educação Médica
3.
Invest Ophthalmol Vis Sci ; 54(7): 4471-7, 2013 Jul 02.
Artigo em Inglês | MEDLINE | ID: mdl-23737476

RESUMO

PURPOSE: To investigate the pupillary light reflex (PLR) of patients with severe loss of vision due to Leber's Hereditary Optic Neuropathy (LHON) in the context of a proposed preservation of melanopsin-expressing retinal ganglion cells (mRGCs). METHODS: Ten LHON patients (7 males; 51.6 ± 14.1 years), with visual acuities ranging from 20/400 to hand motion perception and severe visual field losses, were tested and compared with 16 healthy subjects (7 males; 42.15 ± 15.4 years) tested as controls. PLR was measured with an eye tracker and the stimuli were controlled with a Ganzfeld system. Pupil responses were measured monocularly, to 1 second of blue (470 nm) and red (640 nm) flashes with 1, 10, 100, and 250 cd/m² luminances. The normalized amplitude of peak of the transient PLR and the amplitude of the sustained PLR at 6 seconds after the flash offset were measured. In addition, optical coherence topography (OCT) scans of the peripapillary retinal nerve fiber layer were obtained. RESULTS: The patient's peak PLR responses were on average 15% smaller than controls (P < 0.05), but 5 out of 10 patients had amplitudes within the range of controls. The patients' sustained PLRs were comparable with controls at lower flash intensities, but on average, 27% smaller to the 250 cd/m² blue light, although there was considerable overlap with the PLR amplitudes of control. All patients had severe visual field losses and the retinal nerve fiber layer thickness was reduced to a minimum around the optic disc in 8 of the 10 patients. CONCLUSIONS: The PLR is maintained overall in LHON patients despite the severity of optic atrophy. These results are consistent with previous evidence of selective preservation of mRGCs.


Assuntos
Atrofia Óptica Hereditária de Leber/fisiopatologia , Reflexo Pupilar/fisiologia , Células Ganglionares da Retina/metabolismo , Opsinas de Bastonetes/metabolismo , Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estimulação Luminosa/métodos , Células Ganglionares da Retina/patologia , Tomografia de Coerência Óptica
4.
Am J Hum Genet ; 80(6): 1064-75, 2007 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-17503325

RESUMO

The present study evaluated the color vision of 44 patients with Duchenne muscular dystrophy (DMD) (mean age 14.8 years; SD 4.9) who were submitted to a battery of four different color tests: Cambridge Colour Test (CCT), Neitz Anomaloscope, Ishihara, and American Optical Hardy-Rand-Rittler (AO H-R-R). Patients were divided into two groups according to the region of deletion in the dystrophin gene: upstream of exon 30 (n=12) and downstream of exon 30 (n=32). The control group was composed of 70 age-matched healthy male subjects with no ophthalmological complaints. Of the patients with DMD, 47% (21/44) had a red-green color vision defect in the CCT, confirmed by the Neitz Anomaloscope with statistical agreement (P<.001). The Ishihara and the AO H-R-R had a lower capacity to detect color defects--5% and 7%, respectively, with no statistical similarity between the results of these two tests nor between CCT and Anomaloscope results (P>.05). Of the patients with deletion downstream of exon 30, 66% had a red-green color defect. No color defect was found in the patients with deletion upstream of exon 30. A negative correlation between the color thresholds and age was found for the controls and patients with DMD, suggesting a nonprogressive color defect. The percentage (66%) of patients with a red-green defect was significantly higher than the expected <10% for the normal male population (P<.001). In contrast, patients with DMD with deletion upstream of exon 30 had normal color vision. This color defect might be partially explained by a retina impairment related to dystrophin isoform Dp260.


Assuntos
Testes de Percepção de Cores/métodos , Percepção de Cores , Defeitos da Visão Cromática/diagnóstico , Deleção de Genes , Distrofia Muscular de Duchenne/genética , Adolescente , Adulto , Estudos de Casos e Controles , Criança , Defeitos da Visão Cromática/classificação , Distrofina/deficiência , Distrofina/genética , Éxons , Humanos , Masculino , Valores de Referência , Sensibilidade e Especificidade
5.
Psicol. USP ; 17(4): 15-33, 2006.
Artigo em Português | Index Psicologia - Periódicos | ID: psi-34309

RESUMO

O sistema visual apresenta muitas funções ao nascimento. O processo de amadurecimento destas funções demanda um tempo variado. Neste trabalho, inicialmente descreveremos como a psicofísica e a eletrofisiologia visual tem colaborado para a medida e o estudo do desenvolvimento de três funções visuais: acuidade visual, sensibilidade ao contraste e visão de cores. Num segundo momento, discutimos sobre como a medida e o desenvolvimento destas funções podem estar prejudicados em patologias que afetam o sistema visual, como a prematuridade e a paralisia cerebral (AU)


Assuntos
Psicofísica , Eletrofisiologia , Acuidade Visual , Sensibilidades de Contraste , Percepção de Cores , Recém-Nascido/psicologia
6.
Psicol. USP ; 17(4): 15-33, 2006.
Artigo em Português | LILACS | ID: lil-457251

RESUMO

O sistema visual apresenta muitas funções ao nascimento. O processo de amadurecimento destas funções demanda um tempo variado. Neste trabalho, inicialmente descreveremos como a psicofísica e a eletrofisiologia visual tem colaborado para a medida e o estudo do desenvolvimento de três funções visuais: acuidade visual, sensibilidade ao contraste e visão de cores. Num segundo momento, discutimos sobre como a medida e o desenvolvimento destas funções podem estar prejudicados em patologias que afetam o sistema visual, como a prematuridade e a paralisia cerebral


Assuntos
Percepção de Cores , Sensibilidades de Contraste , Eletrofisiologia , Psicofísica , Recém-Nascido/psicologia , Acuidade Visual
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