Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
1.
Pediatr Int ; 54(1): 1-7, 2012 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-22168460

RESUMEN

Chronic pain is a common problem in pediatric practice. The prevalence of chronic pain in children is >30%. Because pain indicates emotional expression as well as the physiological reaction toward infection, injury, and inflammation, both physiological and psychological assessments are essential to determine primary interventions for chronic pain. The Japanese Society of Psychosomatic Pediatrics Task Force of clinical practice guidelines for chronic pain in children and adolescents compiled clinical evidence and opinions of specialists associated with the primary care of pediatric chronic pain in the Japanese 'clinical guidelines for chronic pain in children and adolescents' in 2009, which are presented herein. The guidelines consist of three domains: general introduction to chronic pain; chronic abdominal pain; and chronic headache. Each section contains information on the physiological mechanism, psychological aspects, assessment methods, and primary interventions for pediatric chronic pain. These guidelines are expected to help disseminate knowledge on primary interventions for chronic pain in children and adolescents.


Asunto(s)
Analgésicos/uso terapéutico , Dolor Crónico , Adolescente , Algoritmos , Niño , Dolor Crónico/diagnóstico , Dolor Crónico/psicología , Dolor Crónico/terapia , Humanos , Japón , Pediatría
2.
Brain Dev ; 43(2): 181-185, 2021 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-32878720

RESUMEN

BACKGROUND AND PURPOSE: Bottom shuffling is a locomotion strategy that precedes independent walking in some infants. Shuffling babies are generally considered to have favorable outcomes. The aim of the present study was to reveal clinical features and neurodevelopmental outcomes of shuffling babies who visited a child developmental center. METHODS: We studied 48 shuffling babies who visited Toyota Municipal Child Development Center from April 2007 to March 2015. We excluded patients with cerebral palsy, Down syndrome, or congenital disorders. In 2018, we retrospectively reviewed the clinical charts of the enrolled children. We investigated family history, neurological findings, and the developmental outcome during the follow-up period. RESULTS: During the follow-up period, 20 children (42%) were diagnosed with ASD. Gross motor development in infancy was not different between infants with and without ASD. The rate of poor eye contact at the first visit and a delay in the first word speech were significantly higher in infants with ASD than in infants without ASD. A family history of bottom shuffling was significantly less frequent in infants with ASD (10%) than in those without (39%). CONCLUSION: Some of bottom shufflers may represent ASD during follow-up. Paying attention to social and cognitive functions in shuffling babies is important.


Asunto(s)
Trastorno del Espectro Autista/fisiopatología , Desarrollo Infantil/fisiología , Actividad Motora/fisiología , Trastorno del Espectro Autista/diagnóstico , Trastorno del Espectro Autista/metabolismo , Niño , Preescolar , Femenino , Humanos , Lactante , Japón , Masculino , Estudios Retrospectivos
3.
Int J Dev Neurosci ; 25(6): 367-72, 2007 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-17804189

RESUMEN

Accumulating evidence suggests the possible association between the concentrations of serum brain-derived neurotrophic factor (BDNF) and psychiatric disease with impaired brain development. Yet the reasons remain unclear. We therefore investigated the characteristics of serum BDNF as well as its age-related changes in healthy controls in comparison to autism cases. BDNF was gradually released from platelets at 4 degrees C, reached a maximal concentration after around 24 h, and remained stable until 42 h. At room temperature, BDNF was found to be immediately degraded. Circadian changes, but not seasonal changes, were found in serum levels of BDNF existing as the mature form with a molecular mass of 14 kDa. In healthy controls, the serum BDNF concentration increased over the first several years, then slightly decreased after reaching the adult level. There were no sex differences between males and females. In the autism cases, mean levels were significantly lower in children 0-9 years old compared to teenagers or adults, or to age-matched healthy controls, indicating a delayed BDNF increase with development. In a separate study of adult rats, a circadian change in serum BDNF was found to be similar to that in the cortex, indicating a possible association with cortical functions.


Asunto(s)
Envejecimiento/sangre , Trastorno Autístico/sangre , Factor Neurotrófico Derivado del Encéfalo/sangre , Encéfalo/crecimiento & desarrollo , Encéfalo/metabolismo , Adolescente , Adulto , Distribución por Edad , Animales , Trastorno Autístico/fisiopatología , Plaquetas/metabolismo , Encéfalo/fisiopatología , Factor Neurotrófico Derivado del Encéfalo/química , Corteza Cerebral/crecimiento & desarrollo , Corteza Cerebral/metabolismo , Corteza Cerebral/fisiopatología , Niño , Preescolar , Ritmo Circadiano/fisiología , Femenino , Humanos , Lactante , Recién Nacido , Masculino , Persona de Mediana Edad , Peso Molecular , Ratas , Estaciones del Año , Distribución por Sexo , Manejo de Especímenes , Temperatura , Factores de Tiempo , Regulación hacia Arriba/fisiología
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA