Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
1.
Invest Radiol ; 49(8): 505-8, 2014 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-24619209

RESUMO

OBJECTIVE: This study was designed to evaluate the dialysability of gadoteric acid in patients with end-stage renal disease (ESRD) requiring hemodialysis. Gadoteric acid is used for magnetic resonance imaging. It is cleared from the blood exclusively by glomerular filtration. In an attempt to decrease the occurrence of nephrogenic systemic fibrosis, hemodialysis has been advocated immediately after injection of gadolinium-based contrast agents in patients with ESRD. METHODS: Ten patients with ESRD underwent 3 consecutive 4-hour hemodialysis sessions after a single intravenous injection (0.1 mmol/kg) of gadoteric acid. Blood samples were drawn from the vascular access just before and immediately after the end of each 4-hour session. Additional sampling was performed during session 1. RESULTS: Gadoteric acid was efficiently eliminated, with mean (95% confidence interval) clearance values (mL/min) of 224.6 (216.0-233.9) at 0.5 hours and 225.9 (215.6-237.2) at 1.5 hours during session 1. The gadolinium concentration decrease after a 4-hour hemodialysis (vs the corresponding predialysis values) was 97% after session 1. The decrease in gadolinium concentration after session 3 was 99.7% compared with the predialysis concentration of session 1. These percentages are similar to those reported after hemodialysis for other gadolinium-based contrast agents. No adverse effects related to gadoteric acid were reported. CONCLUSION: Although no unconfounded case of nephrogenic systemic fibrosis has been reported so far after injection of gadoteric acid, hemodialysis can be efficiently used to remove this molecule in patients with ESRD already undergoing long-term hemodialysis.


Assuntos
Extravasamento de Materiais Terapêuticos e Diagnósticos/sangue , Compostos Heterocíclicos/sangue , Compostos Heterocíclicos/farmacocinética , Falência Renal Crônica/sangue , Falência Renal Crônica/terapia , Rim/metabolismo , Compostos Organometálicos/sangue , Compostos Organometálicos/farmacocinética , Diálise Renal , Adulto , Idoso , Disponibilidade Biológica , Meios de Contraste/efeitos adversos , Meios de Contraste/farmacocinética , Extravasamento de Materiais Terapêuticos e Diagnósticos/etiologia , Extravasamento de Materiais Terapêuticos e Diagnósticos/prevenção & controle , Feminino , Compostos Heterocíclicos/efeitos adversos , Humanos , Masculino , Taxa de Depuração Metabólica , Pessoa de Meia-Idade , Compostos Organometálicos/efeitos adversos , Segurança do Paciente , Reprodutibilidade dos Testes , Sensibilidade e Especificidade
2.
Clin Infect Dis ; 38(10): 1350-6, 2004 May 15.
Artigo em Inglês | MEDLINE | ID: mdl-15156469

RESUMO

A 37-year-old Belgian patient presented with acute nephropathia epidemica (NE) shortly after a camping holiday in southern France. Unusual symptoms were initial noncardiogenic lung involvement, followed by severe acute renal failure, acute acalculous cholecystitis, presence of immunoblasts in the bone marrow, and hemolytic anemia, presenting as hemolytic uremic syndrome. Positive immunoglobulin (Ig) A and rising IgG titers against Puumala hantavirus (PUUV) were detected, but IgM remained negative on days 8 and 20. The results of reverse-transcriptase-polymerase chain reaction performed on day 8 were positive for PUUV. This is the first report of an iatrogenically IgM-negative hantavirus case due to the selective removal of heavy-weight molecules during plasma exchange via the centrifugation technique. This is also the first report of proven NE from the Mediterranean part of France.


Assuntos
Infecções por Hantavirus/imunologia , Febre Hemorrágica com Síndrome Renal/imunologia , Imunoglobulina M/imunologia , Orthohantavírus , Adulto , Ensaio de Imunoadsorção Enzimática , França , Febre Hemorrágica com Síndrome Renal/virologia , Humanos , Doença Iatrogênica , Masculino
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA