What Is Postural Orthostatic Tachycardia Syndrome (POTS)? Symptoms, Causes, Diagnosis, Treatment, and Prevention | Healthcarthub

Postural orthostatic tachycardia syndrome, or POTS, is a condition in which your heart starts to race when you stand up. Specifically, adults with POTS will experience a heart rate that is faster by at least 30 beats per minute in the first 10 minutes after standing.

POTS is a problem of the autonomic nervous system’s control of blood flow (or circulation). Normally, when you stand up, gravity pulls more blood into your lower body; but to make sure that enough blood is still flowing to the brain, the body releases the hormones epinephrine and norepinephrine, which help tighten the blood vessels and increase your heart rate.

In people with POTS, however, the blood vessels aren’t always able to tighten adequately, which causes more blood to settle in the lower half the body and less blood to reach your brain. When this happens, the heart beats faster in an attempt to shuttle enough blood to the brain to prevent you from losing consciousness.right up arrow

Signs and Symptoms of POTS

While the main symptom of POTS is an increased heart rate upon standing up, there are many other symptoms that have been linked to the condition, including:

Lightheadedness or dizziness
Brain fog
Fatigue or exhaustion
Blurry vision
Heart palpitations
Head and neck discomfort
Chest pain
Shortness of breath
Coldness or pain in the extremities

A decrease in blood plasma volume, due to blood pooling in the abdomen and legs
Some people with POTS can experience a drop in blood pressure (hypotension) after standing, whereas others can have an increase in blood pressure (hypertension).right up arrow

Causes and Risk Factors of POTS

Not much is known about what causes POTS. Episodes of the condition can occur after major life events such as pregnancies, major surgeries, trauma, or viral illnesses. POTS may also occur before menstruation.right up arrowOther health problems that are linked to POTS include impaired nerve function, poor blood circulation, and blood pressure abnormalities. In some people, POTS may be influenced by genes. For example, variations in the genes NOS3 and ADRB2 may be linked to an increased risk of developing POTS.right up arrow

How Is POTS Diagnosed?

A POTS diagnosis can be challenging because of the numerous symptoms involved and the fact that symptoms can differ for each patient.right up arrow

In addition to a physical exam, POTS is diagnosed with electrocardiogram (ECG) monitoring and in some cases with a tilt table test. A person will lie flat on a table, which is then raised to an upright position. As you’re lifted up, doctors will measure your heart rate and blood pressure.

Other tests for POTS include blood and urine tests (to detect what might be causing the condition), and the quantitative sudomotor axon reflex test (QSART), which measures how well certain nerves are responding.right up arrowSometimes, people with POTS can be misdiagnosed with anxiety. The orthostatic symptoms of POTS — lightheadedness, dizziness, tremulousness, palpitation, chest pain, fatigue, nausea, headache, and shortness of breath — overlap with common symptoms of anxiety, according to a review of studies published in December 2018 in the journal Autonomic Neuroscience. Study authors note that it’s important to consider that people with POTS may also have an anxiety disorder.right up arrow But POTS is not caused by anxiety.right up arrow

Prognosis of POTS

Many people with POTS have mild symptoms, and therefore the long-term outlook is good. Medication, along with dietary and exercise changes, can help ease the symptoms of POTS — improving a patient’s condition and quality of life. With time, some people may no longer experience any symptoms.

But prognosis varies, and some people may have more severe symptoms, which can interfere with their daily lives and worsen over time.right up arrow

Duration of POTS

For some people, the symptoms of POTS may diminish — or disappear altogether — over time. This doesn’t mean, though, that whatever is causing POTS is also gone. Sometimes the symptoms of POTS reappear unexpectedly.right up arrow

Treatment and Medication Options for POTS

POTS can usually be treated by your primary care physician. More severe cases may need to be treated in part by a specialist, including a neurologist or cardiologist.right up arrow

Medication Options

There’s no one medication that can directly treat POTS. Rather, doctors will prescribe certain medications to treat symptoms. Some of these medications include:

Fludrocortisone, which helps the kidneys retain sodium
Beta-blockers, which can decrease the increase in heart rate
Midodrine, which causes the blood vessels to constrict
Pyridostigmine, which affects parasympathetic nervous syste m activity right up arrow

Your doctor may also prescribe medical compression stockings, which help push the blood upward in your legs. Additionally, your doctor might suggest you buy an at-home blood pressure monitor so you can check your blood pressure and heart rate.right up arrow

Alternative and Complementary Therapies

One way to treat POTS is by changing your diet. Experts recommend drinking about 2 to 2.5 liters of fluid each day and increasing your sodium intakeright up arrow (the usual recommended daily intake for adults is less than 2,300 mg).right up arrow This helps expand blood volume, which then helps keep blood flowing to the heart and brain. Your doctor may recommend you take salt tablets to increase your salt consumption.

Certain foods or drinks can make POTS symptoms worse. Alcohol tends to exacerbate symptoms. Caffeine can increase nervousness and lightheadedness in some people, while helping to constrict blood vessels in other people. It’s a good idea to work with your doctor to find the dietary modifications that may be right for you.right up arrow

Exercise can sometimes exacerbate the symptoms of POTS, so you may need to work with a physical therapist to learn what types of physical activity you can do. If you have difficulty remaining standing, for instance, you may want to try a mode of exercise you can do in a horizontal or reclined position, such as rowing or swimming.right up arrow

Prevention of POTS

If an underlying cause of POTS can be identified and treated or managed, you may be able to resolve symptoms of POTS.right up arrow

And it may be possible to prevent episodes of POTS by wearing compression stockings, changing your diet, or taking certain medications.right up arrow

Complications of POTS

People with POTS can be at risk for falls, especially from fainting. Others, who have a more severe form of the condition, can experience a diminished quality of life. But POTS is not a life-threatening condition.right up arrow

Research and Statistics: How Many People Have POTS?

An estimated one to three million Americans have POTS, according to Dysautonomia International. About 1 in 100 teenagers may have POTS.right up arrow

While people of all ages, sexes, or races can develop POTS, the condition is more common in young women — particularly those younger than 35 — than men. (For each man who has POTS, five women will have it.) The condition commonly occurs after pregnancy, surgery, trauma, and sepsis.right up arrow

Related Conditions and Causes of POTS

POTS is one type of dysautonomia, a term that refers to multiple conditions that affect the nervous system, which regulates functions such as heart rate, blood pressure, digestion, body temperature, and more.

More than 70 million people have some type of dysautonomia, including POTS. Other forms of dysautonomia include neurocardiogenic syncope (NCS), or fainting spells. Another is inappropriate sinus tachycardia (IST), in which the heart beats unexpectedly quickly while a person is at rest or only slightly active.

According to Johns Hopkins Medicine, most adolescents and young adults with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) have POTS or related forms of orthostatic intolerance.

And fibromyalgia patients, people with gastrointestinal motility disorders (such as irritable bowel syndrome), excessive sweating (hyperhidrosis), and a number of other conditions can also develop

Dysautonomia International

Dysautonomia International is a nonprofit organization dedicated to improving the lives of people with autonomic nervous system disorders, including POTS. They do advocacy work, spread awareness, and raise money to fund research opportunities. On their site you can also find information about POTS, both for patients and for family and friends.

Dysautonomia Information Network

This volunteer-run nonprofit provides information on dysautonomia disorders and offers a moderated online forum where you can connect with others and discuss issues related to POTS.

Genetic and Rare Diseases Information Center (GARD)

In addition to an overview of the symptoms, diagnosis, and treatment of POTS, GARD provides links to current clinical trials as well as a list of helpful organizations for people with the condition. It’s run by the National Institutes of Health.