Fluids and salt
Drinking more water and, if your doctor advises it, increasing salt helps raise blood volume.
When standing, the heart races and the body struggles to adapt: dizziness, palpitations, intense fatigue. POTS is one of the most common forms of dysautonomia.
The autonomic nervous system controls, without us thinking about it, heart rate, blood pressure, digestion and temperature. When it does not work properly, this is called dysautonomia.
Postural orthostatic tachycardia syndrome (POTS, Postural Orthostatic Tachycardia Syndrome, sometimes called STOP in French) is a form of dysautonomia: when moving from lying down to standing, the heart speeds up excessively and symptoms appear, which improve when lying down again.
It more often affects women, usually between 15 and 50, and sometimes appears after a viral infection, a pregnancy, surgery or a period of bed rest. Cases have also been described after COVID-19, as part of long COVID.
They vary from person to person and from day to day, and often ease when lying down.
Palpitations, a racing heart when getting up or staying upright.
Light-headedness, blurred vision, feeling faint, sometimes passing out.
Intense fatigue, exercise intolerance, long recovery time.
Difficulty concentrating and remembering, slowed thinking.
Headaches, nausea, digestive problems, breathlessness, tremors, legs turning purple when standing.
Heat, standing for a long time, large meals, dehydration, periods, alcohol, lack of sleep.
According to international criteria, POTS is diagnosed when:
The doctor carries out an active stand test (measurements lying down then standing) or a tilt-table test in hospital. They also look for other possible causes: dehydration, anaemia, thyroid problems, medication side effects, heart disease.
There is no single treatment: care combines several measures, tailored to each person by the doctor.
Drinking more water and, if your doctor advises it, increasing salt helps raise blood volume.
Compression stockings or tights, sometimes an abdominal binder, reduce blood pooling in the legs.
Getting up slowly, crossing your legs or tensing your calves when standing, eating smaller meals, avoiding heat.
Very gradual physical activity, first lying down or seated (recumbent bike, swimming never alone, rowing if your joints allow it), supervised if possible.
Depending on the case, a cardiologist or specialist may suggest treatment to slow the heart or support blood pressure.
POTS and other forms of dysautonomia are often reported in people with hypermobile EDS or a hypermobility spectrum disorder. Several studies find they are more common in these situations.
The reasons are still being studied: greater flexibility of the blood vessels, which would let blood pool in the legs, is one of the explanations suggested. POTS can also coexist with digestive problems or mast cell activation.
This page is based on the international reference consensus and on specialist resources.
The content of this page is provided for information only. It does not replace a consultation, a diagnosis or personalised advice from a healthcare professional.
SED Gastroparésie N’Cie enables patients, relatives and carers to talk to each other, share their experiences and not face the illness alone.