Patients who are critically ill with acute renal failure and sepsis have ex
tremely high mortality rates. While it seems reasonable that eliminating th
e inflammatory mediators (such as cytokines, chemokines, tumor necrosis fac
tor-alpha, etc.) by continuous renal replacement therapy (CRRT) would be ef
fective, studies show that only insubstantial numbers of these mediators ar
e removed in comparison with endogenous clearance. Mass removal seems only
to be effective when highly permeable membranes (sieving coefficient of app
roximately 1.0) are used, there is a filtrate volume greater than 2 liters/
hour, and when the half-life of the substance to be eliminated is greater t
han 60 minutes. Removal of cytokines by membrane adsorption is another poss
ibility. However, because the membrane surfaces are saturated after a few h
ours, frequent filter changes are necessary for them to generate effective
adsorption of these mediators. Despite filter changes, only a brief and tra
nsient drop in the TNF plasma level has been observed. Controlled clinical
trials are needed to determine whether or not CRRT actually has a beneficia
l effect on the systemic inflammatory response syndrome (SIRS).