TY - JOUR
T1 - Hemoperfusion with a polymyxin B fiber column decreases clotting activity
AU - Kushi, Hidehiko
AU - Miki, Takahiro
AU - Sakagami, Yuichiro
AU - Sato, Jun
AU - Saito, Takeshi
AU - Tanjoh, Katsuhisa
PY - 2009/12
Y1 - 2009/12
N2 - We investigated whether hemoperfusion with a polymyxin B column (DHP-PMX) was able to improve coagulation abnormalities in patients with sepsis. Sixteen patients with sepsis were enrolled in the study. They all had signs of systemic inflammatory response syndrome due to infection and a mean arterial blood pressure ≥65mm Hg (irrespective of the use of catecholamines). A thermodilution catheter was inserted prior to DHP-PMX for intravenous infusion, and DHP-PMX was performed twice within 24 h for 3 h each time. Circulating levels of thrombin-antithrombin complex (TAT), plasmin-α2 plasmin inhibitor complex (PIC), the TAT/PIC ratio, and plasminogen activator inhibitor-1 (PAI-1) were measured six times. Before DHP-PMX, the TAT level was 24.5 ± 8.3 ng/mL, the PIC level was 2.5 ± 1.1 μg/mL, the TAT/PIC ratio was 13.9 ± 3.5, and the PAI-1 level was 143.0 ± 24.4 ng/L. The TAT level, TAT/PIC ratio, and PAI-1 were all significantly lower (P < 0.05) after 48 hr compared with before DHP-PMX, but no significant change of PIC was observed. In these patients with sepsis, fibrinolysis was inhibited by PAI-1, whereas clotting activity was significantly increased. This coagulation/fibrinolysis imbalance was improved by DHP-PMX. The present results suggest that indirect inhibition of clotting activity can be achieved in patients with sepsis through adsorption of lipopolysaccharide by DHP-PMX.
AB - We investigated whether hemoperfusion with a polymyxin B column (DHP-PMX) was able to improve coagulation abnormalities in patients with sepsis. Sixteen patients with sepsis were enrolled in the study. They all had signs of systemic inflammatory response syndrome due to infection and a mean arterial blood pressure ≥65mm Hg (irrespective of the use of catecholamines). A thermodilution catheter was inserted prior to DHP-PMX for intravenous infusion, and DHP-PMX was performed twice within 24 h for 3 h each time. Circulating levels of thrombin-antithrombin complex (TAT), plasmin-α2 plasmin inhibitor complex (PIC), the TAT/PIC ratio, and plasminogen activator inhibitor-1 (PAI-1) were measured six times. Before DHP-PMX, the TAT level was 24.5 ± 8.3 ng/mL, the PIC level was 2.5 ± 1.1 μg/mL, the TAT/PIC ratio was 13.9 ± 3.5, and the PAI-1 level was 143.0 ± 24.4 ng/L. The TAT level, TAT/PIC ratio, and PAI-1 were all significantly lower (P < 0.05) after 48 hr compared with before DHP-PMX, but no significant change of PIC was observed. In these patients with sepsis, fibrinolysis was inhibited by PAI-1, whereas clotting activity was significantly increased. This coagulation/fibrinolysis imbalance was improved by DHP-PMX. The present results suggest that indirect inhibition of clotting activity can be achieved in patients with sepsis through adsorption of lipopolysaccharide by DHP-PMX.
KW - Direct hemoperfusion
KW - Plasmin-α2 plasmin inhibitor complex
KW - Polymyxin B column
KW - Sepsis
KW - Thrombin antithrombin complex
UR - https://www.scopus.com/pages/publications/71949113218
U2 - 10.1111/j.1744-9987.2009.00776.x
DO - 10.1111/j.1744-9987.2009.00776.x
M3 - Article
C2 - 19954477
AN - SCOPUS:71949113218
SN - 1744-9979
VL - 13
SP - 528
EP - 533
JO - Therapeutic Apheresis and Dialysis
JF - Therapeutic Apheresis and Dialysis
IS - 6
ER -