Thrombophilia is a condition where the blood has an increased tendency to form clots. Blood clots can cause problems such as deep vein thrombosis (DVT) or pulmonary embolus (PE). There are different types of thrombophilia - some are inherited and some are acquired, meaning they usually develop in adult life.

Often thrombophilia is mild, and many people with thrombophilia do not have problems from their condition. Blood tests can diagnose the problem. Thrombophilia does not always require treatment but some people need to take aspirin or warfarin. If you have thrombophilia, be aware of the symptoms of a blood clot and get treatment immediately if you have symptoms.

What do you understand by thrombophilia?

Thrombophilia refers to a groups of conditions where the blood clots more easily than normal. This can lead to unwanted blood clots (called thromboses) forming within blood vessels. These blood clots can cause problems such as deep vein thrombosis (DVT) or pulmonary embolism (PE).

How is thrombophilia caused?

The body has a natural clotting process in the blood, which is altered in thrombophilia.

The normal clotting process is called haemostasis. It helps to stop bleeding if you have an injury such as a cut. When a blood vessel is injured, the clotting process is triggered, and this is called the clotting cascade. The clotting cascade makes the blood solidify into a clot, which sticks to the injured part of the blood vessel. Small particles in the blood called platelets also help to form the clot.

There are also natural chemicals in the blood which act against the clotting system, to stop the blood clotting too much.

Thrombophilia occurs if the normal balance of the clotting system is upset. There may be too much of a clotting factor, or too little of a substance that opposes clotting.

Thrombophilia can cause unwanted blood clots. This does not mean that every person with thrombophilia will get a blood clot. But, it means that you have a higher risk than normal of getting clots. The extra risk will depend on the type of thrombophilia that you have.

What is a thrombosis?

A blood clot that forms within a blood vessel is known medically as a thrombus. Thrombosis is the process that occurs to form a thrombus. A thrombus can block a blood vessel - this blockage is now also known as a thrombosis.

What are the different types of thrombophilia?

Thrombophilias can be classified into inherited or acquired.

The inherited ones are genetic, and may be passed on from parent to child.

Acquired thrombophilias are not inherited, meaning they have nothing to do with your genes. Usually, acquired thrombophilias become apparent in adulthood. They can happen as a result of other medical problems that have developed, or they might be due to problems with the immune system.

It is possible to have a mixed thrombophilia, due partly to genetic and non-genetic factors.

How does thrombophilia develop?

There are no symptoms unless the thrombophilia results in a blood clot.

Many people with thrombophilia do not get a blood clot and have no symptoms at all.

How does blood clot present?

Blood clots can form in arteries and veins. Arteries are blood vessels that take blood away from the heart to the organs and tissues of the body. Veins are blood vessels that bring blood back to the heart, from the rest of the body.

A blood clot in a vein is the most common problem with thrombophilia - this is called venous thrombosis. Possible symptoms are:

  • Pain and swelling in a leg. This occurs if you have a blood clot in a large vein in a leg. This is commonly known as a deep vein thrombosis (DVT).
  • The blood clot may travel to the heart and on into a lung, causing a pulmonary embolus (PE). Possible symptoms are chest pain, pain on deep breathing, shortness of breath or, rarely, collapse.
  • Some types of thrombophilia can cause a blood clot in an unusual site such as the brain, gut or liver. This can cause symptoms in the head or the abdomen (tummy). A blood clot in the liver veins is called Budd-Chiari syndrome.

A blood clot in an artery can occur with some types of thrombophilia. This is called arterial thrombosis. Depending on which artery is affected, a blood clot in an artery can cause a stroke, a heart attack or problems with the placenta during pregnancy. So the possible symptoms of arterial thrombosis due to thrombophilia are:

  • Having a stroke at a relatively young age.
  • Repeated miscarriages.
  • Pregnancy problems: pre-eclampsia, reduced fetal growth or, rarely, fetal death (a stillbirth, or intrauterine death).
  • A heart attack.

How do you diagnose thrombophilia?

Thrombophilia may be suspected if a blood relative had a blood clot at a young age (under 40 years), or if you develop a blood clot, which would not be expected, given your age and general health.

One of the most important things is that thrombophilia testing is not done routinely on everyone who has a blood clot. Only certain people need to have these tests - where the result will change how you are treated.

What are the tests for thrombophilia?

Thrombophilia is diagnosed by blood tests.

Tests are done some weeks or months after having a DVT or PE, as the presence of these conditions can affect the results. Usually you have to wait until you have been off anticoagulants, such as warfarin, for 4-6 weeks. If you have recently been pregnant, the tests may have to be delayed by 8 weeks as the results in pregnancy can be much harder to understand.

A sample of blood is taken, and a number of different tests will be done on it, to check different parts of the clotting process. Usually, the tests are done in two stages. The first test is a thrombophilia screen which is some basic clotting tests. If the results of this suggest that thrombophilia is possible, then another blood sample will be taken for more detailed tests.

You may be referred to a haematologist (a doctor specialising in blood conditions). The doctor will usually ask about your history and family history, which will help with interpreting the test results.

Can all thrombophilias be diagnosed on tests?

It is likely that there are some kinds of thrombophilia which we cannot yet identify or test for. This is because there are some people or families who have more blood clots than would normally be expected, yet test negative on the thrombophilia tests. In this situation, you might be advised to have treatment as for thrombophilia, even if you do not have a definite diagnosis.

Therefore, negative tests do not exclude the possibility that you have an inherited increased risk of having blood clots.

Who are the people to be tested for thrombophilia?

Current guidelines suggest that thrombophilia testing should be considered in the following situations:

  • If you have a venous thrombosis or pulmonary embolus under the age of 40.
  • If you have repeated episodes of venous thrombosis or pulmonary embolus or thrombophlebitis (inflamed veins).
  • If you have a venous thrombosis in an unusual site (for example, abdomen or brain) - in some circumstances, as these can be caused by other conditions.
  • Unexplained thromboses in newborn babies.
  • Babies or children with a rare condition called purpurafulminans.
  • If you develop skin necrosis (patches of skin loss due to clots in or under the skin) due to medicines such as warfarin.
  • If you have an arterial thrombosis occurring under the age of 40.
  • If you are a blood relative of someone with certain types of high-risk thrombophilia - such as protein C and S deficiencies, in some circumstances.
  • Some pregnant women who have had a thrombosis in the past due to a mild provoking factor. (However, a pregnant woman with a history of unprovoked thrombosis does not need testing as she needs anticoagulants anyway in pregnancy).
  • If you have a family history of venous thrombosis in at least two relatives.
  • If you have certain blood test results: an unexplained prolonged activated partial thromboplastin time (aPTT) - an abnormal result on a certain type of blood clotting test.
  • Some people with other medical conditions: recurrent miscarriage or fetal death, idiopathic thrombocytopenic purpura (ITP) - a condition affecting blood platelets, or systemic lupus erythematosus (SLE), also referred to as lupus - because these can sometimes be linked to thrombophilia.

Even if there is a known thrombophilia in the family, you may not be tested for it if it is mild and you have not had a blood clot yourself. This is because you are asymptomatic (you have no symptoms) and knowing if you have this inherited defect will not change how you are treated - you probably won't need anticoagulants because it is not known how much your risk of abnormal blood clotting is increased. Use of anticoagulant medication has to be carefully assessed as there are also certain risks, such as bleeding, with its use.

How do you treat thrombophilia?

The first step is for you and your doctor to consider how much risk there is of you getting a blood clot. This risk depends on a combination of things, such as:

  • What type of thrombophilia you have (some are more high-risk for blood clot than others).
  • Your age, weight, lifestyle and other medical conditions.
  • Whether you are pregnant or have recently given birth.
  • Whether you have already had a blood clot.
  • Your family history - whether any close relatives have had a blood clot.

This information will help your doctor to assess how much risk you have of getting a blood clot, and what type of blood clot could occur. Then you and your doctor can discuss the pros and cons of taking treatment, and if needed, what type of treatment to take.

Possible treatments for thrombophilia are:

Low-dose aspirin
This inhibits the action of platelets, so can help to prevent blood clots. It may also help prevent miscarriage or pregnancy problems, in some types of thrombophilia.

Anticoagulant treatment

Anticoagulation is often called thinning the blood. However, it does not actually thin the blood. It alters certain chemicals in the blood to stop blood clots forming so easily - in effect, it slows down the clotting process. It doesn't dissolve a blood clot either (as some people incorrectly think). The body's own healing mechanisms can then get to work to break up any existing blood clot.

Anticoagulation can greatly reduce the chance of a blood clot from forming. Anticoagulant medication is commonly used to treat a venous thrombosis (such as a DVT) or a PE.
In thrombophilia, anticoagulant medication may be advised if:

  • You have had a blood clot, to prevent another one.
  • You have not had a blood clot, but have a high risk of getting one.
  • You have a temporary situation that puts you at high risk of a blood clot - this may be the case if you are pregnant, within 6 weeks after childbirth, or are immobile for a long period.

There are two main types of anticoagulant: heparin and warfarin. Heparin is taken as an injection once or twice daily. Warfarin is taken as a tablet once daily.

Warfarin is the usual anticoagulant. However, it takes a few days for warfarin tablets to work fully. Therefore, heparin injections (often given just under the skin) are used alongside warfarin in the first few days (usually 5 days) for immediate effect if you currently have a blood clot. If you are starting warfarin and don't have a blood clot (that is, it is just to prevent one), you won't need heparin injections first.

The aim is to get the dose of warfarin just right so the blood will not clot easily, but not too much, which may cause bleeding problems. You will need a regular blood test, called International Normalised Ratio (INR), whilst you take warfarin. The dose is adjusted on an individual basis according to the result of this blood test. The INR is a blood test that measures your blood clotting ability. You need the tests quite often at first, but then less frequently once the correct dose is found.

An INR of 2.5 is usually the aim if you take warfarin to prevent a blood clot in thrombophilia or to treat a DVT or PE, although anywhere in the range 2-3 is usually OK. If you have had recurrent DVTs, or have had a PE whilst on warfarin, you might need a higher INR (even 'thinner' blood). INR blood tests can usually be done in an outpatient clinic, or sometimes by your GP. You may be advised to take warfarin lifelong to prevent blood clots if you have thrombophilia, or you may have short-term treatment for your current DVT or PE (usually 3-6 months).

Heparin is an injectable anticoagulant. Standard heparin is given intravenously (IV), which means directly into a vein - usually in the arm. This type of heparin is given in hospital and monitored with blood tests.

Low molecular weight heparin (LMWH) is injected into the skin on the lower abdomen. It can be given at home, either by a  nurse, or you can be taught to self-inject (or a carer can do it for you). It does not need blood tests to monitor it. Different doses are used for prevention (prophylaxis) and treatment of an existing blood clot. There are different brands of heparin injection; the common ones you might see used are Clexane and Fragmin.

Treatment in pregnancy

If you are pregnant or planning a pregnancy, discuss this with your doctor, and tell your midwife and obstetrician about the thrombophilia. Treatment for thrombophilia may be different in pregnancy because:

Some women with certain types of thrombophilia are advised to take low-dose aspirin while pregnant, to help prevent miscarriage or pregnancy problems.

The pregnancy itself increases the risk of a venous thrombosis - this applies to the whole pregnancy and especially to the 6 weeks after childbirth. So you may be advised to start anticoagulant treatment while pregnant or after childbirth. This will depend on the type of thrombophilia and your medical history.

If you were taking warfarin, you will normally be advised to change to heparin instead. This is because heparin is safer for the unborn baby (there is a significant chance that warfarin could cause fetal abnormalities). Both heparin and warfarin are safe for breast-feeding.

Prevention of venous thrombosis (DVT)

Certain situations can temporarily put you at high risk of having a blood clot, and in these situations you may be advised to take extra treatment for a while. Examples are pregnancy and after childbirth, severe illness, major surgery, or anything which immobilises you, such as travel or an operation. Special stockings such as flight socks or compression stockings may also be advised to help prevent a DVT.

General advice for people with thrombophilia

  • If you are having any medical treatment or surgery, tell your doctor/nurse/pharmacist about the thrombophilia.
  • Be aware of the warning symptoms of a blood clot - get medical help immediately if you suspect one (see above for symptoms).
  • Avoid dehydration by drinking adequate amounts of fluid - dehydration can contribute to blood clots forming.
  • Keep active, and avoid being immobile for long periods - immobility helps cause blood clots in legs (DVT).
  • Caution with medication: some medications increase the risk of a blood clot. For example, the combined oral contraceptive pill (COCP) or patch and hormone replacement therapy (HRT). You may be advised to avoid certain medications, or to change to one which does not affect blood clotting.
  • Keep to a healthy weight - being overweight or obese increases the risk of blood clots in legs.
  • To keep blood vessels healthy (arteries in particular), do not smoke. This is important if you have thrombophilia of a type that can cause blood clots in arteries, as smoking also promotes arterial blood clots.

Are there any complications of thrombophilia - and what is the outlook?

Often there are no complications. Many forms of thrombophilia are mild, so that many people with thrombophilia have no problems from their condition. Also, treatment can successfully prevent complications in many cases.

A pulmonary embolus, stroke, heart attack or a blood clot in the brain or abdomen can all be life-threatening conditions. Early treatment can be life-saving and reduces complications.

As mentioned above, some types (not all) of thrombophilia may increase the chance of problems in pregnancy.

There may also be complications due to anticoagulant treatment. Aspirin, heparin and warfarin can have side-effects, mainly unwanted bleeding, such as internal bleeding from the stomach lining.

Testing relatives

If you or your family has an inherited (genetic) form of thrombophilia, you may be asked to consider tests for yourself or your close relatives. However, the benefits of looking for people with thrombophilia who have not had a blood clot has not yet been proven. This is why there are clear guidelines on who should be tested.

What are the different types of thrombophilia?

Inherited thrombophilias

Factor V Leiden
This is pronounced factor 5 leiden. It is fairly common in people of European origin, and about 1 in 20 Europeans have the factor V Leiden gene. This gene affects the factor V part of the clotting cascade, making the clotting process go on longer. It increases the risk of a blood clot in a vein by about eight times - that is still a relatively low risk, so most people with factor V Leiden do not develop problems. Some people inherit two factor V Leiden genes - one gene from each parent (known as 'homozygous Factor V Leiden'). This is less common, but makes the risk much higher - around eighty times the normal risk.

Prothrombin is a clotting factor, and people with the 20210 gene have a change in their prothrombin which makes the blood clot more easily. About 1 in 50 people of Indian origin have this gene; it is more common in people of South Indian origin. It increases your risk of having a blood clot in a vein to twice the normal risk. This is a relatively low risk, so most people with prothrombin 20210 do not develop a blood clot.

Protein C is a natural anticoagulant chemical in the blood. The deficiency can be genetic, or due to other conditions such as kidney disease. With inherited protein C deficiency, the risk of a blood clot forming varies between families, as each family has a different alteration in the protein C gene. The best guide to your level of risk is whether you or your relatives have had a blood clot. If a child inherits two genes with protein C deficiency (one from each parent - this is very rare), they will have a more severe problem and will get blood clots in the skin soon after birth (a condition called purpurafulminans). This is treated with protein C concentrates and anticoagulant medication.

Protein S is also a natural anticoagulant chemical in the blood. Protein S deficiency is rare. The risk of a blood clot forming varies between families, and the best guide to your risk is to look at whether other relatives have had a blood clot.

Antithrombin deficiency Antithrombin is another of the natural anticoagulant chemicals in the blood. There are different types of antithrombin deficiency, both genetic and due to other diseases. The inherited form is rare, affecting about 1 in 2,000 people.

Antithrombin deficiency is a fairly severe type of thrombophilia. The risk of having a blood clot varies between families, but can be increased by 25-50 times the normal risk. With this condition, a blood clot can occur not only in the legs or lung, but also in the veins of the arms, gut, brain or liver. About 1 in 2 people with antithrombin deficiency gets a blood clot before the age of 30, but others may reach old age without problems.

With this condition, if you do develop a blood clot, you may be advised to take long-term warfarin medication. However, this must be decided on an individual basis. Also, treatment with antithrombin concentrates can be given when there is a higher risk of having blood clot - for example, if you are having major surgery.

With pregnancy, anticoagulant treatment with heparin is usually needed. Treatment with antithrombin concentrates can also be used.

Note: children can have antithrombin deficiency; parents need to be aware so that they can detect signs of a blood clot. Although most children don't get a blood clot, they are at risk of them in situations such as surgery. Some newborn babies develop blood clots too. Anticoagulant treatment or antithrombin concentrate may be needed. Parents who have antithrombin deficiency themselves and are expecting a child, should discuss this with their doctor.

Dysfibrinogenaemia This is a rare genetic defect where fibrinogen (a clot-dissolving chemical) does not work normally. There may be increased clotting, increased bleeding or both.
Combined inherited thrombophilias Some people inherit more than one thrombophilia gene - for example, factor V Leiden plus prothrombin 20210. With combined thrombophilias, the risk of developing a blood clot is multiplied and there is a much greater risk than with either condition alone.

Acquired thrombophilias

Acquired thrombophilias are not inherited, and usually start in adulthood.

Antiphospholipid syndrome
This is called APS for short. It is also known as Hughes' syndrome. It is caused by certain antibodies (immune system chemicals) in the blood, which are called antiphospholipid antibodies. APS can cause a blood clot to form in arteries and small blood vessels, as well as in veins.

APS can affect pregnancy in some cases. Many women with APS do not have problems in pregnancy. However, APS may cause miscarriage, or other problems - growth restriction of the fetus, pre-eclampsia or, rarely, fetal death. These problems can be reduced by treatment.

APS can be treated with low-dose aspirin, which is helpful in pregnancy. If you have had a blood clot, then warfarin is usually advised instead (or heparin if you are pregnant.
Other acquired conditions Other conditions can increase the risk of a blood clot. Some doctors classify these as thrombophilias. Examples are: certain disorders affecting platelets, some bone marrow disorders, some kidney problems, inflammatory bowel disease and advanced cancer.

Mixed inherited/acquired thrombophilias

These are due to both genetic and non-genetic causes.


This is a raised level of a chemical called homocysteine in the blood, which is thought to increase the risk of arterial and venous blood clots because it damages blood vessels. This is a relatively mild condition, but it can add to the risk factors for having a blood clot. Vitamin B12 and folic acid may help.

Paroxysmal nocturnal haemoglobinuriaThis is a rare condition affecting the bone marrow. It can lead to venous blood clots, often in unusual sites such as the veins of the gut, liver or brain. Anticoagulation may be needed, and there are other treatments too for this condition.

Elevated factor VIII This is pronounced 'factor 8'. It is due to abnormally high levels of factor VIII, which is one of the blood chemicals that promotes clotting. Depending on the actual level of factor VIII, it can increase the clotting risk by about six times - this is a relatively low risk for getting a blood clot

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