L. Kramer et al., Biocompatibility of a cuprophane charcoal-based detoxification device in cirrhotic patients with hepatic encephalopathy, AM J KIDNEY, 36(6), 2000, pp. 1193-1200
Extracorporeal detoxification has been proposed to treat patients with hepa
tic encephalopathy (HE) not responding to standard therapy. To investigate
the biocompatibility of a cuprophane charcoal-based detoxification device,
a prospective, randomized, controlled study was performed. Of 41 consecutiv
e patients with cirrhosis and HE grade II or III who did not improve with c
onventional treatment, 20 patients (median age, 56 years; range, 33 to 71 y
ears; 13 men) were randomly assigned to either ongoing conventional treatme
nt or one additional 6-hour treatment with a sorbent suspension dialysis sy
stem. Main outcome parameters were physiological function and blood paramet
ers of biocompatibility. In the 10 patients undergoing combined conventiona
l and sorbent suspension dialysis treatment, blood pressure remained unchan
ged and body temperature and heart rate increased (P < 0.01). Platelet coun
t decreased (medians, from 75 to 26 g/L; P < 0.001) and international norma
lized ratio increased after combined treatment (2.0 to 2.2; P < 0.001). Thr
ee patients developed bleeding complications during treatment or shortly af
ter. Treated patients showed increases in levels of plasma elastase (104 to
586 <mu>g/L; P = 0.001), tumor necrosis factor-alpha (5.4 to 7.5 pg/mL; P
= 0.04), and interleukin-6 (118 to 139 pg/mL; P = 0.04), but not interferon
-gamma and E-selectin. No changes were observed in the 10 patients treated
conventionally. In conclusion, despite technical refinements compared with
charcoal hemoperfusion, biocompatibility of sorbent suspension dialysis is
still very limited. Clinical complications were apparently caused by blood-
membrane interactions and disseminated intravascular coagulation. We sugges
t further developments in design and appropriate strategies of anticoagulat
ion to improve the biocompatibility of artificial liver support. (C) 2000 b
y the National Kidney Foundation, Inc.