FRANK J. MILNE STATE-OF-THE-ART LECTURE
the liver trying to regenerate/repair itself. Both unconjugated (mean, 12.5; range, 9.3–17.2 mg/dL) and conjugated bilirubins (mean; 2.7; range, 0.9–4.7 mg/dL) are increased, with conjugated often com- prising less than 20% of the total. Prolongation of PT and PTT are almost always present, and a small number of the horses have thrombocytopenia, likely indicating disseminated intravascular coagulation. Bile acids, anion gap, and lactate are almost always noticeably increased. Blood glucose is frequently in the 140–170-mg/dL range and no horse in our last 14 cases was hypoglycemic. Ammonia concentra- tion in our last 14 cases has ranged from 91 to 495 mmol/L (normal, 90 mmol/L). Signalment and history are important in the di- agnosis of Theiler’s disease: Any adult horse with clinical signs of acute fulminant hepatic failure that has received serum (especially TAT) or plasma ap- proximately 4–10 weeks earlier would likely have Theiler’s disease as the top differential. If the horse has appropriate signs and laboratory findings of Theiler’s disease but no history of recent blood product administration and there is no suspicious toxic cause for the hepatic failure then nonbiologic origin acute hepatitis should be considered. Ultra- sound examination of the liver in horses with Thei- ler’s disease may seem unremarkable other than the liver is sometimes hard to image due to its small size; if the liver is seen it may seem hypoechoic. I generally do not perform a liver biopsy on a horse with “classic” Theiler’s disease as the utility of a liver biopsy is marginal because histologic data will not change therapy. Unfortunately, in many cases a diagnosis is often made at necropsy where the liver is almost always smaller than normal (Fig. 6). Measurement of liver weight in comparison with body weight (BW) in our last 13 cases of Theiler’s disease found that the liver in Theiler’s disease horses was 1.0% of BW and normal controls were 1.6% of BW, suggesting a 40% decrease in hepatic size following disease. Affected livers show severe centrilobular or massive liver necrosis/apopto- sis,77,84–86 with portal areas often less severely af- fected but with a mononuclear cell infiltration and slight-to-moderate bile duct proliferation, some- times with fibrosis. Vasculitis has been occasion- ally reported in horses with Theiler’s disease77,86 and was found in three of 12 of our most recent necropsy cases at Cornell (Sean McDonough, per- sonal communication). Alzheimer type II astro- cytes are present in the brain in virtually all the cases.
Treatment focuses on treating HE when present
or preventing it from occurring (HE treatment, page 92), along with supportive care including fluids, nu- tritional support (page 95), antioxidant treatments, anti-inflammatory and antibiotic treatments. Pen- toxifylline, 7.5 mg/kg by mouth (PO) or IV (com- pounded), two or three times daily, may be helpful in decreasing systemic inflammation, which undoubt- edly occurs with Theiler’s disease. A bactericidal
Fig. 6. Livers from two horses of similar body weight, normal liver on left and shrunken Theiler’s disease liver on the right.
antibiotic (e.g., ceftiofur) should be administered in all cases of acute liver failure to inhibit bacterial translocation (gut to blood). Bacterial transloca- tion is of increased risk in acute fulminant liver disease because of loss of Kupffer cell numbers and function, in addition to the potential for increased intestinal permeability resulting from ischemia and congestion of the intestine. Acetylcysteine has been proposed as an antioxidant treatment for acute fulmi- nant liver failure in humans.98 Acetylcysteine is best known as the specific treatment for acetaminophen toxicity but as a potential glutathione donor and anti- oxidant, it could have value in treating other acute fulminant liver diseases. I have administered the sterile acetylcysteine solution marketed for nebuli- zation by slow intravenous administration (up to 100 mg/kg) by mixing in 5% dextrose. A prepara- tion labeled for intravenous use in humans is not available in the United States and the sterile nebu- lization product is used in human hospitals. Horses with Theiler’s disease have a guarded to
poor prognosis if there is fulminant HE. Horses that continue to eat for 3 days and have supportive treatments may then make a quick recovery. My experience is that horses with Theiler’s disease are usually either dead or “on their road to recovery” within 3–5 days. There are no proven long-term consequences in horses that recover.
Newly Discovered Equine Hepatitis Viruses
Recently, three distinct equine hepatitis viruses have been discovered in horses: nonprimate hepa-
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