BCS: symptoms & diagnosis
What are the symptoms of Budd-Chiari syndrome?
BCS can appear or ‘present’ as an acute condition which develops rapidly with the following symptoms:
- abdominal pain in the upper right hand side of your abdomen (referred to as the ‘upper right quadrant’)
- ascites
- an enlarged liver due to the build-up of blood (hepatomegaly)
- swelling of legs and ankles
- cramp in legs and feet
- itching
More commonly, BCS can develop in a chronic form, where people are likely to have long-standing ascites and an enlarged liver (hepatomegaly). Very rarely, there is a fulminant form. This is a type of disease with a sudden and severe onset. In fulminant BCS, ascites, hepatomegaly and kidney failure can occur with rapid liver failure. Ascites are present in the majority of people because of portal hypertension.
How is Budd-Chiari syndrome diagnosed?
Like many liver diseases the symptoms of BCS are non-specific, meaning that they can be caused by many conditions other than BCS. Methods of diagnosis include liver function tests (LFTs) and imaging tests with ultrasound and computerised tomography (CT)
Ultrasound, the same technology used in pregnancy, directs sound waves through your skin via a probe device as it is passed over your liver area. Anything solid will bounce back as a reflected sound wave via the probe and will be turned into an image that can be seen on a screen. In BCS, a type of scan known as ‘Doppler’ ultrasound is used to obtain information about blood flow in your arteries and veins and this often gives enough information for BCS to be diagnosed.
A CT scan may also be used. This can obtain pictures, called tomograms, from different angles around your body using computer processing and can also show ‘cross-sections’ of your tissue and organs. This scan can show an enlargement of the liver and changes in the density (thickness) of liver tissue due to abnormal blood flow. A liver biopsy may not be necessary if other tests have helped doctors to identify the reason for liver problems.
Treatment for BCS
The aim of treatment for BCS is to keep your liver function stable by maintaining the flow of blood out of the liver. Doctors will be looking to:
- re-channel the blocked veins if possible
- prevent recurrence or progression of thrombosis
- ease or ‘decompress’ the congestion of blood in your liver
- manage your ascites
- prevent further damage to your liver and allow liver cells to regenerate.
Doctors will try to pinpoint the exact area where blood flow is obstructed to help them understand how your health may be affected (your ‘prognosis’). The severity of BCS can depend on where the clot is located and the number of veins that are affected. Radiologists will use X-ray techniques known as hepatic angiography or venography to examine arteries and veins directly to determine the location and severity of a clot. If the inferior vena cava is being examined, an X-ray called inferior cavography is used. This is usually done under local anaesthetic and you are also likely to be given sedation. It is possible you may be asked to stay in hospital overnight.
These procedures involve inserting a thin, flexible tube (catheter) into a blood vessel through an easily accessible vein in the arm, neck or groin. A dye, referred to as a ‘contrast dye’ or ‘contrast medium’, is then injected through the catheter to light up the blood vessels to make them easier to see in the X-ray. In some cases the scan shows that only the end portion of the vein is blocked and that much of the vein remains clear. In other cases, the vein is more blocked and doctors will need to get to the vein via a tube put into the liver from the tummy.
Once the tube gets to the blockage, doctors can remove the clot and open the vein. This is called venoplasty or angioplasty. The vein is opened with balloons and the interventional radiologist often decides to place a metal spring (stent) within it to keep it open.
If the clot within the hepatic veins was formed recently and is difficult to remove, the catheter tube may be left in the hepatic vein for a day or two to allow clotbusting drugs (thrombolysis) to get rid of the clot. When venoplasty/stent succeeds it usually leads to rapid improvement in the patient’s overall condition.
In some patients, the blockages are too extensive for venoplasty to work. Doctors will look at which treatments are suitable for the symptoms, depending on how severe they are. When ascites or bleeding varices are troublesome, a radiological procedure called TIPS (see Useful words section) may be offered. This lowers pressure in the portal vein. In this procedure a metal or plastic tube (stent) is passed across your liver to make a shunt, or bypass, to make your blood travel straight from the portal vein past the blocked hepatic veins into the inferior vena cava which carries the blood back to the heart. This is done using a needle guided by a catheter inserted through a tiny puncture in your neck. This procedure may be performed either under general anaesthesia or with sedation.
Occasionally another operation may be offered which reverses the flow in the portal vein so that it is taking blood out of the liver rather than into it. The liver still receives enough blood from the hepatic artery to function adequately. This operation uses a vein from the neck to make a new connection which allows the blood to escape from the congested liver. The vein from the neck is grafted on between the mesenteric vein, a vein from which blood normally flows into the portal vein and the inferior vena cava, and is called a meso-caval shunt.
Anticoagulation therapy
Most experts now recommend that patients with BCS should receive life-long anticoagulation therapy, because BCS often means that people’s blood has a tendency to clot too readily. Anticoagulation therapy involves taking medicines and being closely monitored with regular blood tests to check that the levels of clotting are right, to make sure the blood does not clot too readily (which could cause thromboses or blockages) or not well enough (which could cause bleeding).
Liver transplantation
A liver transplant is usually only recommended if other treatments are no longer helpful and your life is threatened by end stage liver disease. In BCS, a liver transplant may be required when:
- an onset of fulminant BCS causes your liver to fail
- your liver stops performing all of its functions adequately, a condition called decompensated cirrhosis
- shunt procedures cannot prevent a further deterioration in your condition.
Liver transplantation is a major operation and if it is not an emergency treatment, you will need to plan it carefully with your medical team, family and friends. Liver transplants offer a good prospect of a full recovery.
Further Information
Looking after yourself when you have BCS?
Being diagnosed with BCS can be worrying and frightening, as it is a serious disease. For many people, the diagnosis can be the end to a long process of feeling something was wrong. Diagnosis also gives patients an opportunity to have effective treatment. Treatments aim to reduce the risk of the disease progressing to a serious outcome, including the risk of death, and to improve quality of life.
To manage your ascites you will be given diuretics and placed on a low-sodium diet. This will mean no added salt on your food and also only eating foods that are very low in salt, avoiding processed and cured foods and snacks such as crisps and biscuits. A dietician can help you adjust your diet.
Like other people with liver disease, you have a higher risk of infections leading to serious complications. You can help protect yourself by maintaining high standards of hygiene and getting vaccinated before travel and for infections such as flu and pneumococcal infection. You may also find that you get tired more easily and need to plan your day to ensure you have enough energy for all your activities.
Living with a long-term serious illness means making adjustments to your way of life and these often take time and patience to achieve. These will affect your family and friends so it may be useful to keep them informed about your condition and feelings (as you judge appropriate), so that they are best able to help and support you. Some people find it useful to join support groups or online forums for people with liver disease or other life-limiting conditions.
Please visit the support section of our website for information on Support groups in your area.