G. Hafner et al., LABORATORY CONTROL OF MINIMAL HEPARINIZATION DURING HEMODIALYSIS IN PATIENTS WITH A RISK OF HEMORRHAGE, Blood coagulation & fibrinolysis, 5(2), 1994, pp. 221-226
For patients undergoing dialysis with a high risk of haemorrhage there
is no standardized procedure for anticoagulation during extracorporea
l circulation. Minimal heparinization with a dose equivalent to half t
hat used for chronic haemodialysis was employed in 49 patients (125 ha
emodialyses) performed after operative interventions (83.3%), after ha
emorrhagic events (5.2%) and after invasive investigations (11.5%). Us
ing a biocompatible membrane and a low molecular weight heparin (bolus
dose 500-1300 U; continuous infusion 100-400 U) it was possible to co
mplete haemodialysis in 74 cases (Group 0) without clots appearing in
the venous bubble trap of the tubing system. In 30 cases (Group 1) onl
y small clots were detected at the end of haemodialysis, and in 13 cas
es (Group 2) larger clots (exceeding a diameter of 1 cm) were found. I
n eight cases (Group 3) partial or complete clot formation occurred in
the tubing. No haemorrhagic complications were observed. Anti-Xa acti
vity, thrombin-antithrombin III complex (TAT) and D-dimer were determi
ned before haemodialysis, 2 h after the start of haemodialysis and on
completion of the procedure. The anti-Xa activities ranged between < 0
.2 and 0.56 U/ml. In contrast, at 2 h there were significant differenc
es (P < 0.05) in the TAT concentrations between Group 0 and the other
groups, as well as between Group 1 and Groups 2 and 3. Significant dif
ferences (P < 0.05) in D-dimer levels occurred only at the end of haem
odialysis. Minimal heparinization in haemodialysis is a practicable al
ternative in patients with a high risk of haemorrhage and extended coa
gulation monitoring is helpful in adjusting heparin dosage.