Portosystemic shunts are a common topic of conversation amongst breeders and owners of small and toy breed dogs. Congenital
portosystemic shunts are being diagnosed with increasing frequency, and many breeders and veterinarians are questioning whether
heredity may play a role in the spread of this disease.
What are Portosystemic Shunts?
A portosystemic shunt is a blood vessel that bypasses liver tissue, carrying blood from the intestines, stomach, spleen, and
pancreas to the heart before it can be filtered and cleansed of proteins, sugars, bacteria, and toxins. Shunts are present
in all fetal mammals and usually close down shortly before or after birth so that the baby's liver takes over the functions
of filtration, storage, and production. In some individuals the shunt doesn't close down or develops in an abnormal place,
and the animal's liver doesn't get enough blood supply to grow or function properly.
Types of Shunts:
Shunts may be congenital (found at birth) or acquired (developing after birth). Dogs with acquired shunts usually have
cirrhosis, or "hardening" of the liver, secondary to severe liver disease. These dogs develop multiple shunting blood
vessels to relieve high blood pressure in the liver. There is no effective surgical treatment for these patients, short
of a liver transplantation.
Congenital shunts are usually single blood vessels that are present at birth. In large breed dogs, they are found inside
of the liver ("intrahepatic") and may be a result of improper or incomplete closure of the fetal shunt. Surgical treatment
of these shunts is possible, but difficult, because of the location of the abnormal blood vessel.
Small and toy breed dogs usually have "extrahepatic" shunts: the blood vessel is located outside of the liver. These shunts
are easier to find and treat and therefore the outcome of surgery is better.
Clinical Signs of Portosystemic Shunts
Clinical signs are often seen at a young age and may include poor growth, behavioral changes (circling, disorientation,
unresponsiveness, staring into space, head pressing, blind staggers), seizures, and quiet demeanor. Many of the clinical
signs may be confused with puppy hypoglycemia (low blood sugar). Other less common signs include diarrhea, vomiting, and
excessive drinking or urinating.
In many animals the signs are seen 1-3 hours after eating meat or puppy chow. Proteins in the food are broken down by intestinal
bacteria to ammonia and other toxins which are absorbed and, instead of being filtered by the liver, are allowed to reach
the brain. The depression and signs are often temporary; once the proteins are emptied from the colon, the signs usually
Some animals may not show clinical signs until they are anesthetized to be castrated or spayed. These animals may take days
to recover from anesthesia, depending on what drugs were used. Other animals show no signs until they are older, when they
develop bladder and kidney problems from excreting toxins and forming urine crystals and stones.
To diagnose a shunt we may need to rule out toxicity, hydrocephalus ("water on the brain"), and low blood sugar in puppies.
We look for abnormalities on bloodwork that indicate poor liver function, such as low protein, albumin, and blood urea
nitrogen, which are chemicals produced by the liver. X-rays of the abdomen may show a small liver, indicating that it is
has not developed properly. Urine sediment may contain ammonium biurate crystals, which look like starfish or spiky balls.
We also run special diagnostic tests. Blood ammonia concentration can be measured; this test will diagnose liver disease
in 90% of affected animals. It is more accurate (95 to 100%) if an ammonia challenge is done, where the puppy is given
ammonia by enema or by mouth and the blood is tested to see if the liver clears the ammonia. Blood for ammonia concentration
measurements must be kept chilled and must be analyzed within 30 minutes after it was drawn.
Even more accurate are bile acid concentrations. A blood sample is taken after a 12 hour fast, and then the puppy is fed a
normal meal. Two hours later another blood sample is taken. Bile acid concentrations are high in most types of liver disease,
including shunts. Bile acid concentrations are altered by hemolysis (breakage of the blood cells) and lipemia (fat in the blood)
but are minimally affected by temperature and storage and can be sent through the mail. These tests tell us that liver disease
is present but do not verify the presence of a shunt. Bile acids levels that are normal after feeding in a 6 or 8 week old
puppy indicate the puppy probably does not have a shunt, as long as there is no hemolysis of the blood sample; therefore this
test can be a good screening tool for breeders.
To be 100% sure that a shunt is present, we either need to use ultrasound (which is more useful in large dogs), a contrast
study with x-rays ("portogram"), nuclear scans ("scintigraphy"), or surgery to find the shunt. Scintigraphy and ultrasound
are not invasive and are therefore the safest tests, with scintigraphy being the most accurate of the two.
Portosystemic shunts must be differentiated from hepatic microvascular dysplasia, a disease that has the same clinical signs,
liver biopsy results, and blood changes. This disease is seen in Yorkies, Cairn terriers, and other small breeds and must be
ruled out by portogram or scintigraphy.
Dogs with shunts that are seizuring or comatose should be given intravenous fluids with dextrose (sugar), intravenous
antibiotics, and warm water enemas. Lactulose syrup can be instilled in the rectum after the enema to decrease toxin
absorption. Some dogs may even need activated charcoal (given by tube through the mouth into the stomach) to absorb
toxins if they are comatose.
Long-term medical treatment for dogs with shunts includes a low protein diet such as Hill's L/D, and drugs such as lactulose
and neomycin or metronidazole to prevent production and absorption of ammonia and other intestinal toxins. Lactulose, a
sugar solution, is extremely safe, although a high dose will cause diarrhea. Some animals do well on medical treatment
alone, but most have shortened life spans because of progressive liver shrinkage and loss of function. Medical treatment
is normally used to stabilize a patient until it is healthy enough to tolerate the surgery.
Most dogs are taken to surgery to have the shunt closed. Because the liver has not developed properly, many dogs cannot
tolerate rapid closure of the shunt. Some veterinarians will partially occlude the vessel, leaving a small amount of shunting
present. Many of these dogs still do well after surgery and about half are able to be taken off of medication and special
diets within 6 months. In some, the clinical signs may recur, and a second surgery may be required to determine whether
further closure can be attempted.
Many veterinarians are now placing ameroid constrictors around the shunts to gradually occlude them. These constrictor rings
will slowly close down over 4-5 weeks, allowing the liver to get used to its new blood supply. Survival rates after ameroid
constrictor placement are about 95%. Most dogs are completely normal within 3 months. While about 1/3 of the dogs may still
have some shunting, less than 15% have any clinical problems.
Most dogs will need to be kept on a low protein diet for at least 6 weeks after surgery. Liver function can be assessed at 2-3
months by rechecking albumin and postprandial bile acids, or by scintigraphy. Dogs can be gradually switched to an adult
maintenance diet after 8 weeks, but should be kept on a low protein diet and lactulose if clinical signs recur.
Portosystemic shunts have been proven to be hereditary in Irish Wolfhounds and Maltese; however, we
also see them frequently in other breeds such as Yorkies, Australian shepherds, and Labrador
retrievers. Currently I am investigating the pedigrees of Yorkshire Terriers, since the odds of
this breed developing shunts are 1,225 times greater than all other breeds combined. At University
of Tennessee Veterinary Teaching Hospital, 35% of our shunt patients are Yorkies; at Washington
State University, one out of seven Yorkshire Terriers presented to Veterinary Hospital for any
reason was found to have a portosystemic shunt. Because of the high prevalence of the disease in
Yorkies, we are determined to search for the cause and to look for a "cure".
Latest Update 2002
As many of you know, I have been completing a study funded by the AKC Canine Health Foundation regarding determination of genetic relationships among Yorkshire Terriers with single congenital portosystemic shunts. Our objectives were to determine whether coefficient of inbreeding was greater in Yorkies with portosystemic shunts (PSS) than Yorkies with normal bile acids (NBA) and to determine whether a common ancestor was present in the pedigrees of dogs with PSS. We excluded pedigrees of full siblings from our analyses so that a wide variety of breedings would be included. Pedigrees were entered into a data collecting system (“The Breeder’s Standard”; Man’s Best Friend Software, Version 5.0.632, 1999). Wright’s coefficient of inbreeding for up to 10 generations was calculated for each dog. Five and eight generation pedigrees were analyzed for common ancestors.
There have never been any reports of shunts closing on their own after
the puppy is over a week of age. Shunts are permanent problems. Over half
of the dogs that have shunts will have progression of their clinical signs
and will die or be euthanized in a year unless they have surgery. About a
third of the dogs that have shunts can be medically managed for 5 or
more years; these are dogs that are older when the diagnosis is made (i.e.
several years old) and don't have any neurologic problems (seizures,
circling, fly biting, star gazing, blanking out) and have relatively
normal blood work (they can make enough protein).