CARDIOVASCULAR
ENGINEERING
Journal for Extracorporeal Circulation, Assist Devices,Transplantation and Artificial Organs

Volume 8, 2003, No 1-2


Zero-Balanced Hemofiltration during and after Cardiopulmonary Bypass in Pigs Results in a Reduction of Plasma Cytokine Levels with no Associated Effects on Cardiorespiratory Function
G. P. Eising, H. Schad, W. Heimisch, A. Bernhard-Abt, U. Ettner, E. Schäffer, P. Tassani, N. Mendler, R. Lange

Background: Investigation of the effects of hemofiltration on cardiorespiratory function, inflammatory responses and tissue fluid accumulation after cardiopulmonary bypass (CPB) in a randomized animal study.
Methods:
26 pigs were subjected to crystalloid primed CPB (90min cardioplegic cardiac arrest, 30min reperfusion). Hemofiltration was performed (n=13) during reperfusion and for 30min postCPB; filtered volume was replaced by equal volumes of ringer’s lactate. PostCPB observation period was 5h.
Results: Following CPB, heart rate was increased, aortic pressure, cardiac output, and dP/dtmax were reduced in both groups. Alveolar-arterial oxygen difference was not affected in control animals, but was transiently increased by 50% after hemofiltration. Pulmonary shunt blood flow was not affected, pulmonary compliance was reduced by 10%-15%, pulmonary vascular resistance was doubled in both groups without intergroup differences. Post mortem left lung water content was 10% higher after hemofiltration compared to controls. PostCPB elevation of plasma levels of TNF-a and IL-10 could be prevented by hemofiltration while myocardial leukocyte infiltration was not different between the two groups.
Conclusions: In an adult porcine model of CPB, hemofiltration with replacement of the hemofiltrate with equal volumes of Ringer’s lactate results in a reduction in TNF and IL-10 plasma levels with no associated effects on heart leukocyte infiltration or immediate post CPB cardiorespiratory function.

(CVE. 2003; 8 (1/2): 87-93)

Key words: cardiopulmonary bypass, hemofiltration, organ dysfunction, systemic inflammatory response, pigs


Gregory P. Eising, M.D.
Klinik für Herz- und Gefäßchirurgie
Deutsches Herzzentrum München
Lazarettstr. 36
D-80636 München
Germany
E-mail: eising@dhm.mhn.de



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