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1.
Brain Dev ; 42(10): 747-755, 2020 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-32622762

RESUMO

OBJECTIVES: To investigate the prevalence and background of children with medical complexity (CMC) and its secular trend in Japan. METHODS: CMC were defined as patients under the age of 20 years requiring medical care and devices. The patients were enrolled using the national health insurance claims data of three hospitals and two rehabilitation centers in Tottori Prefecture. The study period was divided into three periods: Period 1, 2007-2010; Period 2, 2011-2014; and Period 3, 2015-2018. RESULTS: A total of 378 CMC were enrolled. The prevalence of CMC was 1.88 per 1000 population among subjects aged <20 years in 2018, and it increased by approximately 1.9 times during the study period. The number of CMC who presented with severe motor and intellectual disabilities did not change from Period 1 to Period 3. Meanwhile, the number of CMC who had relatively preserved motor and intellectual abilities increased from 58 to 98. The proportion of CMC who required respiratory management and oxygen therapy increased by 1.3 and 1.8 times, respectively. By contrast, the proportion of CMC who need tube feeding decreased significantly between periods 1 and 3 (P < 0.05). CONCLUSIONS: The prevalence of CMC increased almost twice during the 12-year study period; however, the increase in the number of patients with relatively preserved motor and intellectual abilities was pronounced. This study showed that the need for medical care and devices differed based on the underlying disorders and severity of CMC; therefore, individualized medical, welfare, and administrative services and education about the various types of CMC must be provided.


Assuntos
Atenção à Saúde/tendências , Crianças com Deficiência/estatística & dados numéricos , Pessoas com Deficiência Mental/estatística & dados numéricos , Adolescente , Criança , Pré-Escolar , Atenção à Saúde/economia , Atenção à Saúde/métodos , Equipamentos e Provisões/provisão & distribuição , Feminino , Humanos , Japão/epidemiologia , Estudos Longitudinais , Masculino , Prevalência , Adulto Jovem
2.
Brain Dev ; 40(4): 361-365, 2018 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-29277332

RESUMO

A 3-year-old girl suffered from anti-N-methyl-d-aspartate (anti-NMDA) receptor encephalitis after resolution of herpes simplex virus encephalitis (HSE). Methylprednisolone pulse and immunoglobulin therapies showed little effect, but the patient completely recovered after six courses of monthly cyclophosphamide pulse therapy and successive maintenance on mycophenolate mofetil for one year. Anti-NMDA receptor antibody in the cerebrospinal fluid (CSF) was minimally detected during the prodromal febrile period and then was seen to be markedly elevated at the onset of second encephalopathy phase. CSF interleukin (IL)-6, and 10, tumor necrosis factor-α, interferon gamma, C-X-C motif ligands (CXCL)10 and 13, chemokine ligand 2, and migration inhibitory factor showed a second peak during the prodromal period and were reduced at the onset of anti-NMDA receptor encephalitis. These suggest the presence of cytokine/chemokine phase between the initial HSE and the secondary autoimmune encephalitis phases. Treatment strategy during the early stage of this entity should be further explored.


Assuntos
Encefalite Antirreceptor de N-Metil-D-Aspartato/líquido cefalorraquidiano , Encefalite Antirreceptor de N-Metil-D-Aspartato/imunologia , Citocinas/líquido cefalorraquidiano , Encefalite por Herpes Simples/líquido cefalorraquidiano , Encefalite por Herpes Simples/imunologia , Encefalite Antirreceptor de N-Metil-D-Aspartato/terapia , Autoanticorpos/líquido cefalorraquidiano , Biomarcadores/líquido cefalorraquidiano , Pré-Escolar , Progressão da Doença , Encefalite por Herpes Simples/terapia , Feminino , Humanos , Receptores de N-Metil-D-Aspartato/imunologia
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