L. Monreal et al., COMPARISON OF THE EFFECTS OF LOW-MOLECULAR-WEIGHT AND UNFRACTIONED HEPARIN IN HORSES, American journal of veterinary research, 56(10), 1995, pp. 1281-1285
Thirty healthy male horses were allotted to 3 groups and treated blind
ly during 4 days. Group-1 horses received unfractioned calcium heparin
(100 IU/kg of body weight, SC, q 12 h). Group-2 horses received a sin
gle dose of a low-molecular-weight heparin (50 anti-X(a) IU/kg, SC) ev
ery morning, and a similar volume of saline solution every evening. Gr
oup-3 horses received the vehicle (saline solution), SC, every 12 hour
s. Citrated and EDTA-anticoagulated blood samples were collected befor
e starting the medication (T-0) and once daily 3 hours after each morn
ing injection (T-3, T-27, T-51, and T-75). The PCV, hemoglobin concent
ration, RBC and platelet counts, and clotting times (activated partial
thromboplastin time and thrombin time) were determined, and a microsc
opic examination to detect hemagglutination was performed. Plasma conc
entration of heparin was measured by use of the antifactor X(a) activi
ty assay. Bleeding time was determined on the first and fourth days, u
sing a double-template method. The horses given unfractioned heparin h
ad marked agglutination of erythrocytes after the first injection that
became more pronounced as treatment progressed. Also, significant dec
rease in PCV, hemoglobin concentration, and RBC count was observed dur
ing treatment. Platelet count was significantly decreased after the fi
rst day, and clotting times were significantly prolonged. In contrast
to the horses given unfractioned heparin, those given low-molecular-we
ight heparin did not have any agglutination of erythrocytes during the
4 days of treatment, and there were no significant changes in PCV, he
moglobin concentration, or RBC and platelet counts. Activated partial
thromboplastin time increased slightly in the horses given low-molecul
ar-weight heparin, although the values remained within reference range
. Both groups of horses achieved adequate concentrations of heparin in
plasma for prophylactic purposes, but those given low-molecular-weigh
t heparin achieved those values after the first injection. Bleeding ti
mes were not significantly different between heparin-treated horses an
d horses given saline solution during treatment. We conclude that low-
molecular-weight heparin may be used more safely and conveniently in h
orses, because it does not affect equine erythrocytes, platelets, or c
lotting and bleeding times.