Postural tachycardia syndrome (PoTS) is an abnormal increase in heart rate that occurs after sitting up or standing. It typically causes dizziness, fainting and other symptoms.

It's sometimes known as postural orthostatic tachycardia syndrome.

PoTS affects many different people, but is most common in girls and women aged 15 to 50.

Some people have mild symptoms, while others find the condition affects their quality of life. PoTS often improves gradually over time, and there are a number of self-care measures and medications that can help.

This page covers:

What happens in PoTS

Symptoms

When to get medical advice

Tests and diagnosis

Treatments

Causes

Links to more information

What happens in PoTS

Normally when you sit up or stand, gravity pulls some of your blood down to your belly area, hands and feet.

In response, your blood vessels quickly narrow and your heart rate increases slightly to maintain blood flow to the heart and brain, and prevent blood pressure dropping.

This is all done without needing to think about it by the autonomic nervous system – the nervous system in charge of automatic body functions.

In PoTS, the autonomic nervous system doesn't work properly. There's a drop in blood supply to the heart and brain when you become upright and the heart races to compensate for this.

Symptoms of PoTS

You can develop PoTS suddenly, or it can come on gradually over time.

It causes a range of symptoms that occur within a few minutes of sitting up or standing. Lying down may relieve some of the symptoms.

Typical symptoms of PoTS include:

Some people notice that things such as feeling hot, eating, strenuous exercise and being on their period make their symptoms worse.

When to get medical advice

See your GP if you think you have PoTS.

The symptoms can have a number of causes, such as medication or low blood pressure, so it's a good idea to get a proper diagnosis. Sometimes it can be misdiagnosed as anxiety or panic attacks.

Some doctors may not be aware of PoTS, so it may help to print out this page and take it with you to the consultation. Your GP will probably need to refer you to a specialist for tests (see below).

PoTS UK has a list of doctors with an interest in PoTS that you can use to find a specialist near you. You can't usually self-refer to these doctors, but you could discuss a referral with your GP.

Tests for PoTS

A diagnosis of PoTS is made if your heart rate increases by 30 beats per minute (bpm) or more (40bpm in those aged 12-19) after 10 minutes of standing, or if it increases to more than 120bpm.

You may have a range of tests to confirm a diagnosis and rule out other conditions, including:

  • the tilt table test – your heart rate and blood pressure are measured while lying on a bed, and the bed is then tilted into a more upright position while further measurements are taken
  • the active stand test – your heart rate and blood pressure are measured after lying down, immediately upon standing, and after 2, 5 and 10 minutes
  • an electrocardiogram (ECG) – a test of your heart's electrical activity
  • an echocardiogram – an ultrasound scan of your heart
  • 24-hour ambulatory blood pressure and heart rate monitoring – small devices attached to your belt take regular readings while you're doing normal activities
  • blood tests – to test your kidney, liver and thyroid function, and measure blood count and your calcium and glucose levels

Treatments for PoTS

Self-care measures can sometimes help reduce the symptoms of PoTS. If these don't work, you may need to take medication.

Treating an episode

If you suddenly feel faint or dizzy, you can try countering the fall in blood flow by:

  • lying down and, if you can, raising your legs
  • crossing your legs in front of each other while standing, rocking up and down on your toes, clenching your buttocks and tummy muscles and/or clenching your fists if you're unable to lie down

Reducing your symptoms

You may be able to reduce your symptoms in the long-term by following this advice:

  • drink plenty of fluids until your urine is pale yellow
  • keep active, but pace yourself and choose your exercise wisely – swimming, rowing, lower limb resistance training, walking, jogging and pilates can help you keep fit and build muscle (strong calf muscles should help pump blood back to your heart)
  • elevate the head end of your bed, so you're not sleeping fully horizontal
  • try wearing support tights or other forms of compression clothing, to improve blood flow in your legs 
  • avoid long periods of standing
  • come up from lying slowly – sit for a while before standing
  • avoid drinking lots of caffeine or alcohol
  • include more salt in your diet – this isn't advisable if you have high blood pressure or kidney or heart disease though, so ask your specialist first

The PoTS UK website has more general advice about reducing your symptoms and the charity STARS has information about managing your symptoms.

Medication

There's currently no medication licensed for the treatment of PoTS, but your specialist might suggest trying a medication "off label", such as:

If a medicine is used "off label", it means it hasn't undergone clinical trials for this use, but many experts believe it's likely to be effective and your doctor will discuss the possible benefits and risks with you.

Causes of PoTS

In many cases, the cause of the problem with the nervous system in people with PoTS is unknown.

Teenagers will sometimes develop PoTS and find it gradually disappears a few years later. Sometimes it can develop suddenly after a viral illness or traumatic event, or during or after pregnancy.

Some of the other known causes are:

PoTS also occurs quite commonly alongside chronic fatigue syndrome (CFS).

More information and advice

The following organisations can provide more information, support and advice for people with PoTS.

POTS UK

Syncope Trust And Reflex anoxic Seizures (STARS)

Information about you

If you or your child has PoTS, your clinical team may pass information about you/your child on to the National Congenital Anomaly and Rare Diseases Registration Service (NCARDRS).

This helps scientists look for better ways to prevent and treat this condition. You can opt out of the register at any time.

Find out more about the register.

Page last reviewed: 09/08/2016

Next review due: 09/08/2019