Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH) Overview
Learn About Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH)
Syndrome of inappropriate antidiuretic hormone secretion (SIADH) is a condition in which the body makes too much antidiuretic hormone (ADH). ADH is also called vasopressin. This hormone helps the kidneys regulate the amount of water your body loses through the urine. SIADH causes your body to retain too much water. This usually leads to a low blood sodium level (hyponatremia).
ADH is a substance produced naturally in an area of the brain called the hypothalamus. It is then released by the pituitary gland at the base of the brain.
SIADH; Inappropriate secretion of antidiuretic hormone; Syndrome of inappropriate ADH release; Syndrome of inappropriate antidiuresis
There are many reasons why your body may make too much ADH. Common situations when ADH is released into the blood when it should not be produced include:
- Medicines, such as certain seizure medicines, antidepressants, cancer medicines, opiates (less often), and heart, diabetes, and blood pressure medicines
- Surgery under general anesthesia
- Disorders of the brain, such as injury, infections, and stroke
- Brain surgery in the region of the hypothalamus
- Removal of a noncancerous (benign) pituitary tumor
- Tuberculosis
- Cancer (especially small cell cancer of the lung)
- Lung disease, such as pneumonia
- Substance use disorder
Rare causes include:
- Rare diseases of the hypothalamus or pituitary
- Leukemia and cancer of the small intestine, pancreas, and brain
- Behavioral health issues
With SIADH, the urine is very concentrated. Not enough water is excreted and there is too much water in the blood. This dilutes many substances in the blood such as sodium. A low blood sodium level is the most common cause of symptoms of too much ADH. It is also the most common clue that a person may have SIADH.
Often, there are no symptoms from a mildly low sodium level. More symptoms occur as the level gets lower.
When symptoms do occur, they may include any of the following:
- Nausea and vomiting
- Headache
- Problems with balance that may result in falls
- Mental changes, such as confusion, memory problems, strange behavior
- Seizures or coma, in severe cases
Treatment depends on the cause of the problem. For example, surgery is done to remove a tumor producing ADH. Or, if a medicine is the cause, its dosage may be changed or another medicine may be tried.
In all cases, the first step is to limit fluid intake. This helps prevent excess fluid from building up in the body. Your provider will tell you what your total daily fluid intake should be. The restriction is not just for water, but for almost all fluids (coffee, tea, juice, soda, etc.).
If you have severe symptoms, it is a medical emergency. This is usually treated with salt solution (3% saline) given through an IV into the veins (intravenous) in the hospital.
Medicines may be needed to block the effects of ADH on the kidneys so that excess water is excreted by the kidneys. These medicines may be given as pills or as injections given into the veins.
Medstar Medical Group Ii LLC
Joseph Verbalis is an Endocrinologist in Washington, Washington, D.c.. Dr. Verbalis is rated as an Elite provider by MediFind in the treatment of Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH). His top areas of expertise are Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH), Diabetes Insipidus (DI), Neurohypophyseal Diabetes Insipidus, Osteoporosis, and Vagotomy.
New York University
John Maesaka is a Nephrologist in Mineola, New York. Dr. Maesaka is rated as an Elite provider by MediFind in the treatment of Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH). His top areas of expertise are Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH), Low Sodium Level, Chronic Kidney Disease, and Osmotic Demyelination Syndrome.
Mirjam Crain-Christ practices in Basel, Switzerland. Crain-Christ is rated as an Elite expert by MediFind in the treatment of Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH). Their top areas of expertise are Diabetes Insipidus (DI), Neurohypophyseal Diabetes Insipidus, Low Sodium Level, Osmotic Diuresis, and Hormone Replacement Therapy (HRT).
The outcome depends on the condition that is causing the problem. Low blood sodium that occurs rapidly, in less than 48 hours (acute hyponatremia), is more dangerous than low blood sodium that develops slowly over time. When the blood sodium level falls slowly over days or weeks (chronic hyponatremia), the brain cells have time to adjust and the acute symptoms such as brain swelling don't occur.
Chronic hyponatremia is associated with nervous system problems such as poor balance and poor memory. Many causes of SIADH are reversible. Rapid correction of chronic hyponatremia can also cause dangerous complications (osmotic demyelination).
In severe cases, low blood sodium can lead to:
- Decreased consciousness, hallucinations or coma
- Brain herniation
- Death
When your body's sodium level drops too much, it can be a life-threatening emergency. Contact your provider right away if you have symptoms of this condition.
Summary: The purpose of this study is to confirm the safety of tolvaptan in patients with hyponatremia in syndrome of inappropriate antidiuretic hormone secretion (SIADH) in Japan
Summary: Hyponatremia is the most common electrolyte derangement occurring in hospitalized patients. It is usually classified as hypovolemic, euvolemic or hypervolemic. The most common aetiology of euvolemic hyponatremia is the syndrome of inappropriate antidiuresis (SIAD). Hypervolemic hyponatremia is common in patients with congestive heart failure (CHF) (10-27%) and liver cirrhosis (up to approximately ...
Published Date: April 24, 2025
Published By: Sandeep K. Dhaliwal, MD, board-certified in Diabetes, Endocrinology, and Metabolism, Springfield, VA. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.
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Soto-Rivera CL, Breault DT, Majzuob JA. Other abnormalities of arginine vasopressin metabolism and action. In: Kliegman RM, St. Geme JW, Blum NJ, et al, eds. Nelson Textbook of Pediatrics. 22nd ed. Philadelphia, PA: Elsevier; 2025:chap 597.
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Verbalis JG. Posterior pituitary. In: Goldman L, Cooney KA, eds. Goldman-Cecil Medicine. 27th ed. Philadelphia, PA: Elsevier; 2024:chap 206.