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1.
BMC Infect Dis ; 19(1): 20, 2019 Jan 07.
Artículo en Inglés | MEDLINE | ID: mdl-30616536

RESUMEN

BACKGROUND: Thus far, studies on Klebsiella pneumoniae carbapenemase (KPC)-producing organisms have only been reported in those with a history of foreign travel, and a specific Japanese KPC-producing isolate has not yet been reported. CASE PRESENTATION: We describe a Japanese patient, with no history of travel to foreign countries, admitted due to aspiration pneumonia, and a KPC-producing isolate detected in his sputum. Fortunately, his pneumonia resolved. His close contacts did not have a history of foreign travel, and the isolate was not detected in other patients. CONCLUSIONS: The potential for KPC-producing organisms to become endemic in Japan is currently of great concern.


Asunto(s)
Proteínas Bacterianas/metabolismo , Infecciones por Klebsiella/microbiología , Klebsiella pneumoniae/metabolismo , Neumonía Bacteriana/microbiología , beta-Lactamasas/metabolismo , Anciano de 80 o más Años , Proteínas Bacterianas/genética , Farmacorresistencia Bacteriana Múltiple/efectos de los fármacos , Humanos , Japón , Infecciones por Klebsiella/tratamiento farmacológico , Infecciones por Klebsiella/etiología , Klebsiella pneumoniae/efectos de los fármacos , Klebsiella pneumoniae/genética , Klebsiella pneumoniae/aislamiento & purificación , Masculino , Neumonía Bacteriana/tratamiento farmacológico , Neumonía Bacteriana/etiología , Salud Pública , Esputo/microbiología , Viaje , beta-Lactamasas/genética
2.
Int Arch Allergy Immunol ; 168(3): 165-72, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26790100

RESUMEN

BACKGROUND: Omalizumab, an anti-immunoglobulin E (IgE) monoclonal antibody, inhibits the binding of circulating IgE to mast cells and basophils, resulting in fewer episodes of airway inflammation, asthma symptoms and exacerbations in patients with severe allergic asthma. Treatment of patients with asthma using omalizumab increases serum total IgE (tIgE) levels. However, little is known about the influence of omalizumab on allergen-specific IgE (sIgE). METHODS: tIgE and sIgE in 47 adult patients with severe asthma were measured with a fluorescent enzyme immunoassay (ImmunoCAP-FEIA) before and after omalizumab treatment. RESULTS: Treatment with omalizumab increased tIgE and sIgE levels. The increases in sIgE by class category after omalizumab treatment were positively correlated with baseline sIgE positivity before treatment. The mean changes in sIgE levels after omalizumab treatment were also correlated with baseline sIgE levels before treatment. The mean changes in tIgE levels were positively correlated with the mean changes in IgE levels against Dermatophagoides pteronyssinus, crude house dust, Japanese cedar and moth. Omalizumab markedly influenced the negative-to-positive seroconversion rate for IgE against Japanese cedar (30.8%), Candida (29.0%) and moth (28.0%). Finally, all patients with negative-to-positive seroconversion for Japanese cedar-specific IgE had cedar pollinosis before beginning omalizumab treatment. CONCLUSIONS: The changes in sIgE levels after omalizumab treatment may be dependent on the baseline sIgE levels. Our data may indicate the presence of undetectable but functional sIgE.


Asunto(s)
Alérgenos/inmunología , Antiasmáticos/uso terapéutico , Asma/tratamiento farmacológico , Inmunoglobulina E/sangre , Omalizumab/uso terapéutico , Adulto , Anciano , Asma/inmunología , Femenino , Humanos , Masculino , Persona de Mediana Edad
3.
Ann Allergy Asthma Immunol ; 115(3): 191-197.e2, 2015 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-26208759

RESUMEN

BACKGROUND: Recent studies have found that serum levels of Staphylococcus aureus enterotoxin (SE)-IgE are higher in patients with severe asthma compared with patients with nonsevere asthma. However, the association between SE-IgE and asthma control is not fully understood. Furthermore, SEA and SEB were the first reported SEs and subdivided into different groups. The influences of SEA-IgE and SEB-IgE on asthma control have not been elucidated. OBJECTIVE: To determine the relevance of SEA- and SEB-IgE in patients with adult asthma and to investigate the association of SEA-IgE, SEB-IgE, and asthma control, respectively. METHODS: The serum concentrations of SEA- and SEB-IgE in 172 adults with asthma were measured with a fluorescent enzyme immunoassay. RESULTS: The prevalence of SEA- and SEB-IgE was 16.2% and 22.1%, respectively. Total IgE levels and the prevalence of atopic dermatitis were higher in SEA-IgE- and SEB-IgE-positive patients than in SEA-IgE- and SEB-IgE-negative patients, respectively; more SEA-IgE- and SEB-IgE-positive patients owned pets. Sensitization to SEA was associated with a younger mean age and a younger mean age at asthma onset. Multiple regression analysis indicated an association between total IgE levels and SEB-IgE. The prevalence of poorly uncontrolled asthma was significantly higher in SEA-IgE-positive patients than in SEA-IgE-negative patients. In addition, fractional exhaled nitric oxide levels were higher in SEA-IgE-positive patients than in SEA-IgE-negative patients. Logistic regression analysis also identified an association between SEA-IgE and poor asthma control. CONCLUSION: Our findings indicate that sensitization to SE, in particular SEA rather than SEB, is associated with poor asthma control in adults with asthma.


Asunto(s)
Asma/inmunología , Asma/terapia , Enterotoxinas/inmunología , Inmunoglobulina E/sangre , Staphylococcus aureus/inmunología , Adulto , Anciano , Anciano de 80 o más Años , Alérgenos/inmunología , Asma/sangre , Estudios Transversales , Femenino , Humanos , Inmunoglobulina E/inmunología , Masculino , Persona de Mediana Edad , Óxido Nítrico/metabolismo , Índice de Severidad de la Enfermedad , Espirometría , Resultado del Tratamiento , Adulto Joven
4.
Psychiatry Clin Neurosci ; 64(2): 207-10, 2010 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-20447015

RESUMEN

The aim of the present study was to investigate the efficacy of Yokukansan in improving behavioral symptoms of frontotemporal dementia. This study was a prospective, open-label trial of daily Yokukansan for 4 weeks in 20 frontotemporal dementia patients. Yokukansan treatment was found to significantly improve scores for the Neuropsychiatric Inventory and the Stereotypy Rating Inventory. No adverse effects or significant changes in physical findings and laboratory data occurred except for hypokalemia in two cases. The results indicate that Yokukansan can alleviate the behavioral symptoms of frontotemporal dementia. (The clinical trial registration number is UMIN000002704).


Asunto(s)
Medicamentos Herbarios Chinos/uso terapéutico , Demencia Frontotemporal/tratamiento farmacológico , Anciano , Anciano de 80 o más Años , Antipsicóticos/uso terapéutico , Femenino , Humanos , Masculino , Pruebas Neuropsicológicas , Selección de Paciente , Proyectos Piloto , Estudios Prospectivos
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