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1.
Am J Kidney Dis ; 29(3): 392-8, 1997 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-9041215

RESUMO

A new method for ascites filtration and reinfusion, which uses a single Cuprophan filter and is performed in the dialysis unit, is reported. Thirty-one procedures were performed in 17 patients with cirrhosis and massive ascites. A mean volume of 8.6 L of ascitic fluid was removed; from this volume, 5 L were ultrafiltered and a concentrated ascitic fluid was reinfused (x = 359.8 mL). The whole procedure was completed in a mean time of 248 minutes. No relevant method-related complications were detected. Moreover, no significant changes in blood urea nitrogen (BUN), creatinine, plasma and urinary electrolytes, or platelet count were found, even in the case of repeated procedures (two to nine times). The reinfused fluid contained a mean value of albumin of 4.7 g/dL and significant amounts of globulins and complement. The overall cost of the materials used in the procedure ($49.46) offered competitive advantages with respect to other types of frequently used methods. In conclusion, we present a safe, effective, and time- and cost-saving technique for ascites reinfusion that represents an advantageous alternative to more complicated and expensive methods or to the currently used medical therapy.


Assuntos
Ascite/terapia , Líquido Ascítico , Cirrose Hepática/terapia , Ascite/economia , Ascite/etiologia , Líquido Ascítico/economia , Custos e Análise de Custo , Diálise/efeitos adversos , Diálise/economia , Diálise/instrumentação , Diálise/métodos , Feminino , Humanos , Infusões Intravenosas/efeitos adversos , Infusões Intravenosas/economia , Infusões Intravenosas/instrumentação , Infusões Intravenosas/métodos , Cirrose Hepática/complicações , Cirrose Hepática/economia , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Recidiva
2.
J Hepatol ; 6(2): 208-13, 1988 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-3411100

RESUMO

In order to document the incidence of hepatitis delta virus (HDV) replication markers and their relationship to HBV replication, 91 HBsAg chronic carriers were studied. Of these, 51 were anti-HD-positive (19 HBeAg-positive and 32 anti-HBe-positive). Liver HDAg was found in 75% of anti-HD-positive patients. Of the 19 patients who had anti-HD and HBeAg, 13 were HBV-DNA-positive. None of the anti-HBe patients were HBV-DNA-positive. No differences with respect to HBV-DNA concentration were observed between anti-HD-positive and -negative patients. Liver HDAg was detected with similar frequency in patients who were HBeAg- and HBV-DNA-positive (63.6%) and in those who were anti-HBe-positive (78.5%), with no statistically significant difference. HBcAg and HDAg were simultaneously detected in 36% of the anti-HD cases. Patients with anti-HD and HBV-DNA had the highest levels of transaminases (SGPT). Our results suggest that in certain patients HDV and HBV replication coexists without mutual inhibition.


Assuntos
Portador Sadio/diagnóstico , DNA Viral/sangue , Vírus da Hepatite B/fisiologia , Hepatite B/diagnóstico , Hepatite D , Adulto , Feminino , Hepatite B/sangue , Antígenos de Superfície da Hepatite B/análise , Vírus da Hepatite B/genética , Vírus Delta da Hepatite/fisiologia , Humanos , Masculino , Replicação Viral
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