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DOI 10.1046/j.1526-0968.2002.00464.x

Медицинская библиотека · Therapeutic apheresis : official journal of the International Society for Apheresis and the Japanese Society for Apheresis · 2002

Cytokine removal by plasma exchange with continuous hemodiafiltration in critically ill patients.

Nakae Hajime, Asanuma Yoshihiro, Tajimi Kimitaka

Клиническое исследованиеСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

The effectiveness of plasma exchange (PE) with continuous hemodiafiltration (CHDF) in the treatment of critically ill patients was evaluated based on changes in cytokine levels. Twenty-six patients with acute hepatic failure were treated with PE (PE group) or PE and CHDF (PE+CHDF group), and the levels of cytokines such as tumor necrosis factor (TNF)-alpha, interleukin (IL)-6, and IL-8 were determined before and after treatment. Bilirubin levels were significantly lower after treatment in both the PE and PE+CHDF groups. There were no significant differences in TNF-alpha levels before and after treatment in the PE group, but the TNF-alpha level was significantly lower after treatment in the PE+CHDF group. There were no significant differences in the IL-6 levels before and after treatment in both the PE and PE+CHDF groups. There were no significant differences in IL-8 levels before and after treatment in the PE group, but the IL-8 level was significantly lower after treatment in the PE+CHDF group. PE with CHDF therapy was given to 5 patients with acutely aggravated autoimmune diseases, 2 patients with hemorrhagic shock and encephalopathy syndrome, and 3 patients with thrombotic microangiopathy. The results suggested that PE with CHDF therapy are useful in critically ill patients with suspected hypercytokinemia.

Для цитирования: Nakae Hajime, Asanuma Yoshihiro, Tajimi Kimitaka. Cytokine removal by plasma exchange with continuous hemodiafiltration in critically ill patients.. Therapeutic apheresis : official journal of the International Society for Apheresis and the Japanese Society for Apheresis. 2002. DOI: 10.1046/j.1526-0968.2002.00464.x.

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