Pulmonary embolism 

Introduction 

A pulmonary embolism is a blood clot in the pulmonary artery, which transports blood from the heart to the lungs 

How common are pulmonary embolisms?

In the UK, around 3-4 people per 10,000 are diagnosed with a pulmonary embolism each year. However, this is thought to be an underestimate and the actual number of cases is likely to be higher.

Studies conducted in America and Europe have found the annual incidence of pulmonary embolism to be 4-21 people per 10,000 of the population.

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A pulmonary embolism is a blood clot in the pulmonary artery, which is the blood vessel that transports blood from the heart to the lungs.

It is a serious and potentially life-threatening condition as it can prevent the blood from reaching your lungs.

When the blood leaves the heart it is low in oxygen and needs to reach the lungs to pick up oxygen.

Pulmonary embolism symptoms

The signs and symptoms of a pulmonary embolism can sometimes be difficult to recognise because they can vary between individuals. However, the main symptoms include:

  • chest pain – a sharp, stabbing pain that may be worse when you breathe in
  • shortness of breath – which can come on suddenly or develop gradually
  • coughing – which is usually dry, but may include coughing up blood or mucus that contains blood
  • feeling faint, dizzy or passing out

You should visit your GP immediately if you have a combination of these symptoms.

Read more about the symptoms of a pulmonary embolism.

Causes of a pulmonary embolism

Pulmonary embolisms often occur when part or all of a blood clot travels from one of the deep veins in your legs up into your lungs.

A blood clot in one of the deep veins of the legs is known as deep vein thrombosis (DVT). DVT can occur for no apparent reason, but it often develops after long periods of inactivity, such as during a long-haul flight or if you are ill in hospital.

DVT can also occur during pregnancy, as a result of some medical conditions, such as cancer or heart failure, or if the wall of a blood vessel becomes damaged.

Read more about the causes of a pulmonary embolism.

Treating a pulmonary embolism

Pulmonary embolisms are treated with anticoagulant medicines, which reduce the blood's clotting ability and prevent blood clots from getting bigger.

You will be prescribed an anticoagulant called warfarin, which will help break down any blood clots and ensure that the blood flow to your lungs is uninterrupted.

As it can take a while for warfarin to start working, you will also be prescribed another anticoagulant called heparin. This will have an immediate blood-thinning effect and you will need to take it for the first few days.

As part of your treatment, you will also need to have regular blood tests to check that the dose of warfarin you are receiving is correct. If it is too high, you may experience bleeding, and if it is too low you may have further blood clots.

Keeping mobile will also help you to maintain good blood circulation and prevent further blood clots from forming.

Read more about treating a pulmonary embolism.

Preventing a pulmonary embolism

A pulmonary embolism can sometimes occur after surgery, particularly if surgery is on the lower half of your body.

Blood vessel damage and being inactive while in hospital increases your risk of developing blood clots. Your risk is also increased if you:

  • are 40 years of age or over
  • have had a blood clot in the past
  • have a family history of blood clots
  • are overweight or obese

As well as taking warfarin while in hospital to help thin your blood, wearing compression stockings may also be recommended. They fit tightly around your lower legs and encourage the blood to flow more quickly around your body.

You can also reduce your risk of developing a pulmonary embolism if you:

Read more about preventing a pulmonary embolism.




Last reviewed: 22/12/2011

Next review due: 22/12/2013

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Comments are personal views. Any information they give has not been checked and may not be accurate.

Gillflower said on 30 January 2013

I had a fall and broke a bone in my foot. I was put in a temporary cast up to my knee and the following day this was replaced with a knee high walking boot. After a day or so I began to feel short of breath but thought it was due to walking with crutches and the after effects of falling downstairs in the first place. As it was Christmas I carried on but became more and more short of breath. Climbing the stairs was like climbing Everest. Eventually after 6 days I went back to the Minor Injuries Unit where I gone with my foot injury. They took a heart reading, blood pressure etc. the next thing I knew was they had called an ambulance and I was taken to A & E at another hospital where I was diagnosed with a very large saddle embolism and some smaller ones. I spent 6 days there before being discharged on warfarin for the next 6 months. I was very lucky as by the time I got to A & E my condition had deteriorated. It is taking longer than I expected to feel anything like normal. I still get tired quickly and my chest hurts especially when out in the recent cold weather. I'm hoping to dispense with the walking boot this week after seeing the orthopaedic chap. It is good to read other people's experiences and to know that the things I feel are a normal part of healing.

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justingirl69 said on 16 October 2012

Hi i'd been complaining about pains in my legs for a while , i went to hospital and the doctors and they said it was down to my weight and stress and i was given anti depressant tablets. months later i started getting pains in my chest and getting shortness of breath. it turned out to be blood clots in both my lungs{ pulmanary embolism}. i think this could have been avoided i told my doctor and the hospital that it runs in the family, { my sister, uncle,auntieand cousins } all have had blood clots, yet they chose not to look into this.

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wendy42 said on 15 October 2012

I was diagnosed with a PE after having taken HRT for approx. 18 months. At the time I was unaware of any problem with my blood. After treatment (as described above) I found out that there is a history of DVTs in the family. A sister & 2 cousins in Australia. My doctors then tested my blood & I have Factor V Leiden which is Protein C resistant. Surely a simple blood test by my doctor (before prescribing HRT) could possibly have prevented the PE. I also think that again, a simple blood test on all young women before being presribed 'the pill' (the cause of my sister's DVT). It seems the culture is to prescribe 'medication' before checking a person's suitability for it. Surely this would save the NHS money as well as the distress, or possible dire consequences for families affected.
Having lived in France for 6 years we were sent for routine blood tests regularly, where they have specialised centres. Have also travelled to Australia where they also have specialised clinics for Haemotology .

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