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1.
Orv Hetil ; 157(7): 268-74, 2016 Feb 14.
Artículo en Húngaro | MEDLINE | ID: mdl-26853728

RESUMEN

INTRODUCTION: Self-expandable metal and plastic stents can be applied in the palliative endoscopic treatment of patients with unresectable malignant biliary obstruction. The use of metal stentsis recommended if the patient's life expectancy is more than four months. AIM: To compare the therapeutic efficacy and cost-effectiveness of metal and plastic stents in the treatment of malignant biliary obstruction. METHOD: The authors retrospectively enrolled patients who received metal (37 patients) or plastic stent (37 patients). The complication rate, stent patency and cumulative cost of treatment were assessed in the two groups. RESULTS: The complication rate of metal stents was lower (37.84% vs. 56.76%), but the stent patency was higher compared with plastic stents (19.11 vs. 8.29 weeks; p = 0.0041). In the plastic stent group the frequency of hospitalization of patients in context with stent complications (1.18 vs. 2.32; p = 0.05) and the necessity of reintervention for stent dysfunction (17 vs. 27; p = 0.033) were substantially higher. In this group multiple stent implantation raised the stent patency from 7.68 to 10.75 weeks. There was no difference in the total cost of treatment of malignant biliary obstruction between the two groups (p = 0.848). CONCLUSIONS: Considering the cost of treatment and the burden of patients the authors recommend self-expandable metal sten timplantation if the life expectancy of patients is more than two months. In short survival cases multiple plastic stent implantation is recommended.


Asunto(s)
Neoplasias del Sistema Biliar/complicaciones , Procedimientos Quirúrgicos del Sistema Biliar/economía , Procedimientos Quirúrgicos del Sistema Biliar/métodos , Colestasis/etiología , Stents Metálicos Autoexpandibles/economía , Stents/economía , Adulto , Anciano , Anciano de 80 o más Años , Colangiopancreatografia Retrógrada Endoscópica , Colestasis/diagnóstico por imagen , Análisis Costo-Beneficio , Femenino , Humanos , Hungría , Masculino , Persona de Mediana Edad , Cuidados Paliativos/economía , Cuidados Paliativos/métodos , Plásticos , Estudios Retrospectivos
2.
Scand J Gastroenterol ; 50(2): 174-81, 2015 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-25384624

RESUMEN

OBJECTIVE: Influenza vaccination is recommended for inflammatory bowel disease (IBD) patients on immunosuppressive therapy. The objective was to evaluate the antibody and cell-mediated immune response to the split and whole virion influenza vaccine in patients with IBD treated with anti-TNF-α and immunosuppressive therapy. PATIENTS AND METHODS: One hundred and fifty-six immunocompromised IBD patients were vaccinated. Fifty-three patients (control group) refused vaccination. Split virion vaccine and whole virion vaccine were used. Serum samples were obtained for pre- and postimmunization antibody titers to influenza vaccine (A/California/7/2009 [H1N1], A/Victoria/361/2011 [H3N2], B/Wisconsin/1/2010-like B/Hubei-Wujiagang/158/2009). Cell-mediated response was evaluated using an interferon (INF)-γ, interleukine (IL)-2 and tumor necrosis factor (TNF)-α ELISA. RESULTS: Postimmunization titers of both influenza subtypes increased significantly after the administration of split virion vaccines compared to the controls and to those who received whole virion vaccine. The antibody titers of Influenza B also increased significantly in patients immunized with split vaccine and treated with anti-TNF-α therapy. After influenza vaccination, the level of serum IL-2 significantly decreased. No serious side effects developed occurred after influenza vaccination, and the influenza-like symptoms did not differ significantly between vaccinated versus control patients. The relapse of the disease was observed in only 10% of the patients and was more common in vaccinated than in control subjects. CONCLUSION: Split virion vaccines seem to be more effective than whole virion vaccines. Measuring the antibody responses is worthwhile in patients treated with immunosuppressants to determine the efficacy of influenza vaccination.


Asunto(s)
Anticuerpos Antivirales/sangre , Terapia Biológica/métodos , Inmunosupresores/uso terapéutico , Enfermedades Inflamatorias del Intestino/terapia , Vacunas contra la Influenza/uso terapéutico , Adulto , Femenino , Humanos , Inmunidad Celular , Inmunidad Humoral , Gripe Humana/prevención & control , Alphainfluenzavirus/inmunología , Betainfluenzavirus/inmunología , Interferón gamma/sangre , Interleucina-2/sangre , Masculino , Estudios Prospectivos , Factor de Necrosis Tumoral alfa/sangre , Vacunación , Virión/inmunología
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