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1.
Asian Pacific Journal of Tropical Medicine ; (12): 407-411, 2014.
Artigo em Inglês | WPRIM | ID: wpr-820695

RESUMO

OBJECTIVE@#To investigate the effects of propofol and ketamine on the cognitive function and immune function in young rats.@*METHOD@#A total of 80 young rats were randomly divided into four groups: Control group, ketamine group (experimental group A), propofol group (experimental group B), ketamine and propofol group (experimental group C). All rats had continuous injection for three times, serum IL-2, IL-4 and IL-10 and whole brain IL-1β level, hippocampal neuronal apoptosis level were measured. The cognitive ability in rats was tested by water maze.@*RESULTS@#Water maze test showed on the 1st d, the maze test latency of the control group, the experimental group B and the experimental group C water were decreased gradually; Compared with the control group after 3 days, the latency of the experimental group A, experimental group B and experimental group C were all decreased, the crossing circle times were also reduced. Hippocampal neuron apoptosis were (2.3 ± 1.7)%, (14.7 ± 6.9)%, (4.2 ± 3.3)%, (10.2 ± 4.8)% in control group, experimental group A, experimental group B and experimental group C, respectively. The neurons apoptosis of experimental group A was significantly increased. The serum IL-4 and IL-10 of the experimental group A, experimental group B and experimental group C after anesthesia were significantly higher than the control group. The whole brain IL-1β of the experimental group A, experimental group B and experimental group C were significantly lower than the control group.@*CONCLUSIONS@#Propofol can reduce anesthesia effect of ketamine on the cognitive function and immune function in the young rats.


Assuntos
Animais , Feminino , Masculino , Ratos , Anestésicos , Toxicidade , Apoptose , Comportamento Animal , Química Encefálica , Hipocampo , Biologia Celular , Injeções Intraperitoneais , Interleucinas , Sangue , Ketamina , Toxicidade , Aprendizagem em Labirinto , Neurônios , Propofol , Toxicidade , Ratos Sprague-Dawley
2.
Chinese Journal of Pediatrics ; (12): 265-269, 2013.
Artigo em Chinês | WPRIM | ID: wpr-359756

RESUMO

<p><b>OBJECTIVE</b>To understand the clinical and epidemiological characteristics of hand-foot-and-mouth disease (HFMD) deceased cases.</p><p><b>METHOD</b>Information of demographics, diagnosis and treatment, clinical symptoms and signs, laboratory test results, and epidemiological contact history of 72 HFMD cases who died between May 2008 and September 2011, in Zhejiang Province, were collected and analyzed.</p><p><b>RESULT</b>The average age of the 72 cases was 1.8 years, 45 were males, accounting for 62.5%, 63 (87.5%) of the cases were scattered children. Eighteen counties reported 2 or more deaths, accounting for 46.1% (18/39) among the counties where the deaths were reported. The deaths occurred mainly in April to August, the peak occurred in May and June. Fever (98.4%, 63/64) and rash (95.1%, 58/61) were the most common symptoms, but the rash was not obvious at the first diagnosis. Fever occurred before the rash (79.0%, 49/62), persisted for 4 days in average. Vomiting (71.9%, 46/64), dyspnea (65.6%, 42/64), cyanosis (53.1%, 34/64) and impaired consciousness (51.6%, 33/64) were often seen among the cases; 53.1% (34/64) cases went to see the doctor on the first day, but 82.5%(52/63)cases were misdiagnosed. Time to diagnosis of HFMD was in average 3 days. About 3 to 4 days after the onset, the disease deteriorated sharply, deaths occurred within 1 day after admission in 78.9%(45/57)of the deceased cases; 85.0% (34/40) cases had high white blood cells level, mainly neutrophils increased, the ratio of neutrophil was more than 70% in 55.6% (15/27) of cases. Enterovirus 71 (EV71) infection was found in 93.3% (56/60) cases, the deceased cases often died of pulmonary hemorrhage (42.9%, 21/49) and encephalitis (34.7%, 17/49). The sanitary conditions of the cases' family were poor (65.5%, 36/55), but 73.3% (33/45) cases had no exposure history.</p><p><b>CONCLUSION</b>The HFMD deceased cases were mostly younger aged boys, scattered children, nonlocal-residents, and had poor sanitation. They were often infected with EV71, had high fever but had no typical rash, no clear exposure history, they had increased leukocyte, and were often misdiagnosed. Three or 4 days after onset, the disease deteriorated abruptly, most cases died within 1 week after onset. To decrease the HFMD mortality, early detection of severe cases should be stressed, and relative measures should be taken. The guardian should be aware of having good sanitary situation and healthy habits.</p>


Assuntos
Animais , Pré-Escolar , Feminino , Humanos , Lactente , Masculino , China , Epidemiologia , Surtos de Doenças , Enterovirus Humano A , Fezes , Virologia , Febre , Patologia , Doença de Mão, Pé e Boca , Epidemiologia , Mortalidade , Patologia , Estudos Retrospectivos , Distribuição por Sexo
3.
Chinese Journal of Stomatology ; (12): 105-108, 2010.
Artigo em Chinês | WPRIM | ID: wpr-245262

RESUMO

<p><b>OBJECTIVE</b>To assess the quality of orthodontic clinical trials published in 4 major dental journals in the past 10 years and establish the reference standard for orthodontic clinical trials and quality control of dental journals.</p><p><b>METHODS</b>All the clinical trials published in Chinese Journal of Stomatology, West China Journal of Stomatology, Journal of Practice Stomatology and Chinese Journal of Orthodontics from 1999 to 2008 were searched. The demographic information of the papers was extracted and the quality of the clinical trials according to the consolidated standards of reporting trials (CONSORT) was assessed.</p><p><b>RESULTS</b>Four hundred and ninety-four clinical trials were retrieved, and 21.3% (105/494) of them were supported by grants. For the study design, only 26.1% (129/494) were prospective studies, and 3.8% (19/494) were randomized clinical trials. It was hard to evaluate precisely due to the lack of information about the details of the study designs. For the randomized clinical trials, the lack of details for randomization, allocation concealment, blinding and intention to treat compromised the quality.</p><p><b>CONCLUSIONS</b>The general quality of clinical trials in orthodontics is poor. It needs to be improved both in the clinical study design and the paper writing.</p>


Assuntos
Humanos , Ensaios Clínicos como Assunto , Padrões de Referência , Odontologia Baseada em Evidências , Ortodontia , Padrões de Referência , Publicações Periódicas como Assunto , Controle de Qualidade , Ensaios Clínicos Controlados Aleatórios como Assunto , Projetos de Pesquisa
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