TY - JOUR
T1 - Measurements of Equine Serum Hepatic Indices after Administration of Tetanus Antitoxin
AU - Buechner-Maxwell, Virginia
AU - DiGrassie, Wynne
AU - Dascanio, John
AU - Ward, Daniel
AU - Austin, Scott Matthew
AU - Ley, William
N1 - Funding Information:
Supported by Grand Laboratories, Inc.
PY - 2003/5
Y1 - 2003/5
N2 - Tetanus antitoxin (TAT) was given to 39 horses (1500 IU) intramuscularly; 39 horses (1500 IU) subcutaneously; and 20 horses (25,000 IU) intravenously. Horses were evaluated for clinical evidence of hepatic disease before administration of TAT and on days 1, 2, 14, 60, and 120 after injection. Blood was collected on days 0, 1, 60, and 120 from 9 horses that received TAT by the subcutaneous or intramuscular route, and 5 horses that received TAT intravenously. Serum chemical analysis, which included measurement of total bilirubin concentration, and activity of gamma-glutamyltransferase, aspartate transaminase, and sorbitol dehydrogenase, was performed on the samples. All horses remained clinically normal throughout the 120-day postinjection period. On days 60 and 120 post-IM or SC administration, a statistically significant increase in mean gamma-glutamyltransferase serum concentration was observed compared with pretreatment concentrations, but these values did not exceed the normal reference interval. All other indices did not significantly increase throughout the study. Individually, only one horse had a slight elevation in SDH concentration on day 60 and 120. These findings suggest that administration of TAT rarely causes overt hepatic disease or persistent elevation of hepatic serum indices, regardless of the route of administration.
AB - Tetanus antitoxin (TAT) was given to 39 horses (1500 IU) intramuscularly; 39 horses (1500 IU) subcutaneously; and 20 horses (25,000 IU) intravenously. Horses were evaluated for clinical evidence of hepatic disease before administration of TAT and on days 1, 2, 14, 60, and 120 after injection. Blood was collected on days 0, 1, 60, and 120 from 9 horses that received TAT by the subcutaneous or intramuscular route, and 5 horses that received TAT intravenously. Serum chemical analysis, which included measurement of total bilirubin concentration, and activity of gamma-glutamyltransferase, aspartate transaminase, and sorbitol dehydrogenase, was performed on the samples. All horses remained clinically normal throughout the 120-day postinjection period. On days 60 and 120 post-IM or SC administration, a statistically significant increase in mean gamma-glutamyltransferase serum concentration was observed compared with pretreatment concentrations, but these values did not exceed the normal reference interval. All other indices did not significantly increase throughout the study. Individually, only one horse had a slight elevation in SDH concentration on day 60 and 120. These findings suggest that administration of TAT rarely causes overt hepatic disease or persistent elevation of hepatic serum indices, regardless of the route of administration.
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U2 - 10.1053/jevs.2003.62
DO - 10.1053/jevs.2003.62
M3 - Article
AN - SCOPUS:0346306024
SN - 0737-0806
VL - 23
SP - 220
EP - 224
JO - Journal of Equine Veterinary Science
JF - Journal of Equine Veterinary Science
IS - 5
ER -