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Pulmonary hypertension is high pressure inside the pulmonary arteries, which are the vessels carrying blood from the right-hand side of the heart to the lungs.
It is a serious medical condition as it results in damage to the right-hand side of the heart (see below for a full explanation of what happens), making the heart less efficient at pumping blood around the body and getting oxygen to the muscles. This leads to symptoms such as:
See Pulmonary hypertension – Symptoms for more.
If it is not treated, pulmonary hypertension can cause heart failure, which is when the heart struggles to pump enough blood around the body. This can be fatal.
How common is pulmonary hypertension?
There are many different types of pulmonary hypertension and some are associated with underlying health conditions, particularly conditions affecting the heart or lungs. Pulmonary hypertension may be more common in people with:
Generally, pulmonary hypertension can affect people of almost any age, although some types are more common in young women and some in people aged over 40.
One type of pulmonary hypertension, called pulmonary arterial hypertension (PAH), is more common in women and affects two to four people in every million each year. It is estimated that there are nearly 2,200 adults in England and Wales with PAH.
For more information on the different types of pulmonary hypertension and why they occur, see Pulmonary hypertension – Causes.
Pulmonary hypertension is a serious condition that usually gets progressively worse. There may be a delay in getting a diagnosis, as the symptoms can be quite general (see Pulmonary hypertension – Diagnosis).
The symptoms, such as breathlessness, can significantly affect your quality of life as you may be unable to continue with your regular activities. It is important that you start treatment as soon as possible to improve your symptoms.
If you already have an underlying condition which is causing your pulmonary hypertension, this should be treated first. In some cases this can prevent permanent damage to your pulmonary arteries.
In the 1980s people lived for an average of less than three years after being diagnosed with PAH. Now, new medicines mean that people may be able to survive longer. One study found that around two-thirds of people lived longer than five years after their diagnosis.
The course of the disease will depend on how quickly your condition is diagnosed, how advanced your symptoms are and whether you have an underlying health condition.
What happens in pulmonary hypertension
In a healthy person, the blood travelling through the pulmonary arteries from the right-hand side of the heart picks up oxygen when it reaches the lungs. Oxygen-rich blood from the lungs then returns to the left-hand side of the heart, where it is pumped around the body to the muscles, which is where the oxygen is needed.
During exercise, when the demand for oxygen increases, the heart beats more quickly and the pulmonary arteries normally widen to let more blood flow through to the lungs.
However, if you have pulmonary hypertension, the walls of your pulmonary arteries may be thick and stiff, making them less able to expand to allow more blood through. Or, the pulmonary arteries may be blocked by a blood clot, which also hinders blood flow.
This makes it difficult for the right-hand side of the heart to pump blood through the arteries and means that this part of the heart has to work harder.
When the right-hand side of the heart keeps having to work harder, it can gradually become weaker. This makes it less efficient at pumping blood and can lead to heart failure.
For more information on why this condition happens, see Pulmonary hypertension – Causes.^^ Back to top
Symptoms of pulmonary hypertension include:
People with a particular type known as pulmonary arterial hypertension (PAH) may not experience any symptoms until their condition is already quite advanced.
Quality of life
Symptoms can become worse when you exercise, which may limit your ability to take part in physical activities. As your condition progresses, you may find it difficult to carry out even everyday activities.
When pulmonary hypertension begins to affect your everyday life, this can have a negative impact on your quality of life and can lead to depression.
Untreated pulmonary hypertension can lead to heart failure, which is when your heart is struggling to pump enough blood around your body. As well as shortness of breath and tiredness, heart failure can also cause:
Pulmonary hypertension is caused by changes to the pulmonary arteries, the vessels carrying blood from your heart to your lungs.
The walls of your pulmonary arteries can become stiff and thickened, or may be blocked by something such as a blood clot. This makes it harder for your heart to push blood through these arteries, which increases the pressure inside the vessels and results in pulmonary hypertension.
There can be many different reasons for the changes to your arteries. The World Health Organization (WHO) has classified pulmonary hypertension into five different types, depending on the underlying cause:
These are explained in more detail below.
Pulmonary arterial hypertension (PAH)
Pulmonary arterial hypertension (PAH) is caused by problems with the smaller branches of the pulmonary arteries. In PAH, these changes are usually the core medical problem, rather than a condition that has started somewhere else and then affected the pulmonary arteries.
Unlike the other types of pulmonary hypertension, PAH can therefore be treated directly, while in other cases the underlying cause is treated first.
PAH is further divided into specific subtypes, outlined below.
Idiopathic means the cause is unknown. If tests cannot find an underlying reason for your PAH, you may be diagnosed with idiopathic PAH. This is rare, affecting one or two people in every million each year.
Some cases of PAH can run in families. It is thought that a particular genetic mutation (a change in one of the genes you inherit from your parents) can cause PAH. In up to 10% of PAH cases there may be a family history of the condition.
PAH associated with other conditions
PAH can be associated conditions that affect your blood vessels, such as:
Other conditions or treatments associated with PAH include:
Sickle cell anaemia is an inherited disorder where your red blood cells are abnormal and die prematurely, leading to a shortage of red blood cells. The lack of red blood cells means that haemoglobin, a protein normally found in these cells, is released into the blood.
The haemoglobin seeks out and destroys nitric oxide. This is a substance produced by your body and used to widen blood vessels. Without nitric oxide, your blood vessels remain narrow, which increases the blood pressure within them and can cause pulmonary hypertension.
Persistent pulmonary hypertension of the newborn
This is a type of pulmonary hypertension estimated to affect two in every 1,000 newborn babies.
It has been linked to the mother taking non-steroidal anti-inflammatory drugs (NSAIDs) during the third trimester of the pregnancy (week 27 to the birth).
Conditions that may also be associated with persistent pulmonary hypertension of the newborn include:
Left heart disease
Pulmonary hypertension may sometimes be associated with diseases affecting the left side of your heart (which pumps blood around the body). The left side of the heart is made up of:
Because blood goes from the pulmonary arteries to the lungs and then to the left side of the heart, any problem with the left side of the heart could have a backwards effect on this circuit and affect the pulmonary arteries. This in turn could cause pulmonary hypertension.
For example, the mitral valve, which is located between the left atria and left ventricle, can become narrowed. If this happens there will be a build-up of blood trying to get through the valve, which will increase blood pressure in the left atria. This could in turn increase pressure in the blood vessels between the lungs and the heart, and then feed back and increase pressure in the pulmonary arteries, leading to pulmonary hypertension.
Up to 60% of people with a condition causing severe left ventricle dysfunction have pulmonary hypertension. Almost all people with a severe mitral valve condition, and nearly two thirds of those with a severe aortic valve condition, have pulmonary hypertension.
Lung disease and hypoxia
Pulmonary hypertension can also be associated with lung diseases or hypoxia (a shortage of oxygen in the body). This includes:
These types of conditions can restrict the amount of oxygen that is getting into the lungs, and therefore into the blood. A low level of oxygen in the blood causes the pulmonary arteries to constrict (become narrower). Because these vessels are narrower, the blood is squeezed into a smaller space, increasing the blood pressure and resulting in pulmonary hypertension.
Pulmonary hypertension may sometimes be caused by a foreign object, usually a blood clot, blocking or obstructing a vein.
When a blood clot blocks one of the blood vessels supplying your lungs, this is called a pulmonary embolism. After a pulmonary embolism, up to two in 100 people may have pulmonary hypertension.
Other, less common causes of pulmonary hypertension include:
It can be difficult to diagnose pulmonary hypertension because the symptoms are similar to other conditions affecting the heart or lungs. This means there can be a delay of up to three years before you are correctly diagnosed.
However, as pulmonary hypertension can be a serious condition, it is important that you see your GP if you experiencing any symptoms. Your GP will ask about:
Several tests may be used to either diagnose pulmonary hypertension or identify an underlying condition that may be causing it. These may be carried out by your GP, or you may be referred to a hospital to have the tests done there.
An echocardiogram is a type of ultrasound scan that can be used to see how well your heart is working. An ultrasound is a procedure that uses high-frequency sound waves to create an image of part of the inside of your body, such as your heart. This can be used to estimate the pressure in your pulmonary arteries.
An electrocardiogram (ECG) is a test that records the rhythm and electrical activity of your heart. Small stickers called electrodes are stuck to your arms, legs and chest and connected with wires to an ECG machine.
Every time your heart beats, it produces tiny electrical signals. The ECG machine traces these signals onto paper.
An X-ray is an imaging technique that uses high-energy radiation to show up abnormalities in bones and certain body tissue.
A chest X-ray can be used to look for other causes of your symptoms; for example, scarring in your lungs can also cause shortness of breath. A chest X-ray can also check if your heart is larger than normal (pulmonary hypertension makes the right-hand side of your heart work harder, causing it to become enlarged).
Lung function tests
Lung function tests, also called breathing tests, assess how well your lungs work. These tests measure how quickly you can move air in and out of your lungs, how much air they can hold and how well they transfer oxygen into and remove carbon dioxide from your blood.
The tests require you to breathe in and out of a lung function machine and the information collected will help to diagnose different lung diseases.
Exercise tests involve carrying out some form of exercise while checking your symptoms. For example, you may need to walk for six minutes, either on a treadmill or up and down a corridor, while your heart rate and blood pressure are monitored. This can be useful in determining any underlying causes for your symptoms.
Ventilation (perfusion) scan
A ventilation scan measures the amount of air and the blood flow in your lungs. This can be used to look for blood clots in your vessels that may be causing pulmonary hypertension.
A sample of blood may be taken and tested to rule out other conditions.
Confirming the diagnosis
The tests above may all suggest pulmonary hypertension, but the diagnosis is only confirmed by measuring the blood pressure in:
Your blood pressure is measured in a procedure called right-heart catheterisation.
In right-heart catheterisation, a thin flexible tube called a catheter is inserted into a vein in your neck, arm or groin. This catheter is fed through into the right side of your heart and into your pulmonary arteries. As well as measuring the blood pressure, the catheter can be used to measure the:
If the pressure in your pulmonary arteries is above a certain level, you will be diagnosed with pulmonary hypertension.
If the above diagnostic tests reveal an underlying cause, you will be diagnosed with a particular type of pulmonary hypertension (see Pulmonary hypertension – Causes). If no cause is found, you will be diagnosed with idiopathic pulmonary arterial hypertension.
Classifying pulmonary hypertension
As part of your diagnosis, your condition will be classified depending on how severe it is. This will help the healthcare professionals find the best treatment for you.
Pulmonary hypertension is classified into four types depending on how your symptoms affect you:
If your pulmonary hypertension caused by an underlying condition (see Pulmonary hypertension – Causes), your treatment will focus on tackling it. If the cause is treated early, it may be possible to prevent permanent damage to your pulmonary arteries (the blood vessels supplying your lungs).
If you have pulmonary arterial hypertension (PAH), you will be referred for treatment at a centre that specialises in PAH. There are seven such centres across England and one in Scotland:
A number of different medicines can be used to treat PAH and other types of pulmonary hypertension. You will usually be started on conventional therapy or background therapy, and your treatment will then be changed or increased as necessary. Further treatment is called targeted therapy.
Background therapy includes:
These are explained in more detail below.
PAH can increase your risk of venous thromboembolism, which is when a blood clot forms in a vein and then breaks free. The clot can become trapped in a blood vessel, blocking the vessel and the blood supply. If this blocks one of the blood vessels supplying your lungs, this is called a pulmonary embolism.
Anticoagulant medicines reduce the ability of the blood to clot. Taking anticoagulants, such as warfarin, may therefore reduce your risk of venous thromboembolism.
These medicines can cause side effects, such as increased bleeding, so you will be carefully monitored while taking them.
See the topic about Anticoagulant medicines.
Diuretic medicines are used to remove excess fluid from the body by increasing the production and flow of urine. Diuretics may be used in pulmonary hypertension to treat any fluid retention and swelling (oedema). This can occur if pulmonary hypertension starts to cause heart failure (when your heart struggles to pump blood around your body).
Possible diuretics that may be used include:
Diuretics can cause some side effects, such as:
Diuretics can also disrupt your levels of electrolytes (minerals in your blood, such as potassium) and affect your kidney function. Because of this, your kidneys and blood will be monitored while you are taking diuretics.
If you have low oxygen levels in your blood, you may need to be treated with oxygen. This involves inhaling air that has a higher amount of oxygen in it than normal. This increases the amount of oxygen in your blood and should improve your symptoms.
If your pulmonary hypertension leads to heart failure, you may be treated with digoxin. This increases the strength of your heart muscle contractions and can slow down your heart rate.
Calcium channel blockers
Calcium channel blockers are medicines normally used to treat high blood pressure (hypertension). They work by relaxing the muscles that make up the walls of your arteries. This widens your arteries and reduces your blood pressure.
Possible calcium channel blockers include:
Calcium channel blockers may work for people with idiopathic PAH (PAH with no known cause), but the effect in other types of PAH is less clear.
You will need a vasoreactivity test to find out if calcium channel blockers will be suitable for you. This involves taking some of the medication and then checking the blood pressure in your pulmonary arteries to see if it has fallen. If it has, you may be prescribed calcium channel blockers.
If calcium channel blockers were not suitable for you, or if they are no longer effective, further treatments can be tried. These are called targeted therapies and include the following medicines:
These are explained in more detail below.
Bosentan tablets may be taken to improve your symptoms and your ability to exercise. You usually take two tablets twice a day (in the morning and evening), although the dose can vary.
You may spend a day in hospital starting treatment and should then be able to return home and carry on taking the medicine. If after 8-16 weeks your condition has not improved or has got worse, you may be given additional treatment as well as or instead of bosentan.
Bosentan can increase the levels of some enzymes in the liver, which can lead to liver damage. Enzymes are proteins that speed up and control chemical reactions in the body, such as digestion. Because of this, your liver will need to be monitored once a month for as long as you are taking bosentan.
Bosentan will not be suitable for you if you:
Women who could get pregnant must use contraception if they are taking bosentan. Bosentan can interact with hormonal contraception, such as the combined contraceptive pill, so it is better to use an alternative method, such as condoms.
Sildenafil tablets are usually taken three times a day to improve your ability to exercise.
You may spend a day in hospital starting treatment and should then be able to return home and carry on taking the medicine. How long you can take sildenafil for will depend on your condition. If at any time your condition gets worse, you may be given additional treatment as well as or instead of sildenafil.
Sildenafil may not be suitable for you if you:
Iloprost is inhaled through a nebuliser. This is a device that turns the liquid medicine into a mist that you breathe into your lungs. You may need to take iloprost around six to nine times a day. Each dose can take up to 10 minutes to inhale.
You will need to stay in hospital for up to three days to be trained in using the nebuliser and to monitor your response. After this time, you should be able to return home and keep taking the medicine yourself.
How long you need to take iloprost for will depend on your condition. You may need to continue taking it, possibly alongside other treatments, until your condition worsens and you need epoprostenol (see below).
Iloprost may not be suitable if:
Epoprostenol (full name epoprostenol sodium) may be used if you do not respond to other treatments. Epoprostenol needs to be given through an intravenous infusion, which means a constant drip of medicine goes through a narrow tube into a vein in your arm.
Treatment with epoprostenol will begin in hospital. It may take one or two weeks to find the correct dose for you. After this time it is possible, with special training and equipment, for you or your carer to learn how to take this medicine yourself at home.
Once you have started taking epoprostenol you may not be able to stop. Coming off epoprostenol can cause your pulmonary hypertension to rapidly return, so you may need to take epoprostenol for the rest of your life. This is why epoprostenol is considered last, after other treatments have not worked or your condition has got worse.
Epoprostenol may not be suitable for you if you have heart failure caused by a problem with the left side of your heart, or if you have or develop pulmonary oedema (fluid on the lungs).
For severe pulmonary hypertension, a heart-lung transplant may be a treatment option. This involves transplanting the healthy heart and lungs from a donor into you. However, because of a shortage of donors, these are rarely carried out. There are probably fewer than 10 heart-lung transplants a year in the UK.
See the topic about Heart-lung transplants.^^ Back to top
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