APPLICATION OF A NEW ANTICOAGULANT (NAFAMOSTAT MESILATE) TO CONTROL HEMORRHAGIC COMPLICATIONS DURING EXTRACORPOREAL MEMBRANE-OXYGENATION - A PRELIMINARY-REPORT
M. Nagaya et al., APPLICATION OF A NEW ANTICOAGULANT (NAFAMOSTAT MESILATE) TO CONTROL HEMORRHAGIC COMPLICATIONS DURING EXTRACORPOREAL MEMBRANE-OXYGENATION - A PRELIMINARY-REPORT, Journal of pediatric surgery, 32(4), 1997, pp. 531-535
Bleeding related to systemic heparinization has been considered one of
the major complications associated with extracorporeal membrane oxyge
nation (ECMO). Development of the heparin-bonded system will be essent
ial in reducing hemorrhagic complications, but has not yet been clinic
ally proven, The authors chose an alternative approach of making a dif
ference in the activated clotting time (ACT) values between the patien
t and the ECMO circuit, and decreased only the patient's ACT value, wh
ile keeping the value of the ECMO circuit at an ideal level. For this
purpose, we have used a very short-life anticoagulant, Nafamostat Mesi
late (FUT), while decreasing the dose of heparin, FUT is a synthetic p
rotease inhibitor that has been found to inhibit various kinds of enzy
me activities for coagulation, Twelve newborns who had some hemorrhagi
c complications at various sites before or during ECMO, were selected
to receive FUT The heparin dose was decreased after FUT administration
into the drainage route, FUT and heparin doses were regulated to main
tain the ACT value at the reinfusion route at 190 to 220 seconds. ACT
values at the drainage and the reinfusion routes were simultaneously m
easured. The average time on FUT was 100.3 +/- 86.3 (SD) hours. The av
erage dose of FUT was 0.48 +/- 0.22 mg/kg/h, and that of heparin was 2
1.0 +/- 7.5 U/kg/h. The average ACT value at the reinfusion route was
205.7 +/- 14.0 seconds compared with that at the drainage route of 178
.5 +/- 11.8. The difference was statistically significant (P < .001).
The average difference in ACT values between both routes was 27.1 +/-
7.9 seconds. The bleeding was well controlled by FUT administration in
8 of 12 cases. This report may represent the first clinical use of FU
T in neonatal ECMO, and serve as a preliminary study, Copyright (C) 19
97 by W,B, Saunders Company.