M. Kikura et al., HEPARIN NEUTRALIZATION WITH METHYLENE-BLUE, HEXADIMETHRINE, OR VANCOMYCIN AFTER CARDIOPULMONARY BYPASS, Anesthesia and analgesia, 83(2), 1996, pp. 223-227
There are no clinically available alternatives for reversing heparin i
n protamine-allergic patients. This study examined the ability of meth
ylene blue, hexadimethrine, and vancomycin to reverse circulating hepa
rin so that these compounds can be carefully examined in future placeb
o-controlled studies in humans. Heparin activity in blood obtained fro
m extracorporeal circuits was reversed by adding protamine (13.5, 27.0
, 81.1, 135.1, and 270.3 mu g/mL), methylene blue (13.5, 27.0, 135.1,
202.7, 270.3, 337.8, 405.4, 473.0, 540.5, and 810.8 mu g/mL), hexadime
thrine (6.8, 13.5, 20.3, 27.0, 81.1, and 135.1 mu g/mL), or vancomycin
(13.5, 27.0, 135.1, 270.3, 540.5, and 810.8 mu g/mL), and activated c
lotting times (ACTs) were measured with kaolin (n = 18). Heparinase-AC
T was obtained to determine complete reversal. Heparin concentrations
were 3.3 +/- 0.3 U/mL with ACT values of 485 +/- 97 s. The ACT at a pr
otamine concentration of 81.1 mu g/mL and at hexadimethrine concentrat
ions of 81.1 and 135.1 mu g/mL was not statistically different from he
parinase-ACT; however, methylene blue or vancomycin did not reverse th
e anticoagulation at any concentrations. Hexadimethrine can reverse he
parin-induced anticoagulation after cardiopulmonary bypass as well as
protamine, although methylene blue or vancomycin did not neutralize he
parin in vitro.