Alternative names
Glomerulonephritis - acute; Acute glomerulonephritis; Nephritis syndrome - acute
Definition
Acute nephritic syndrome is a group of disorders that cause inflammation of the internal kidney structures (specifically, the glomeruli).
Causes, incidence, and risk factors
Acute nephritic syndrome is often caused by an immune response triggered by an infection or other disease.
Casues seen more frequently in children and adolescents include the following:
Associated diseases seen more frequently in adults include:
Inflammation disrupts the functioning of the glomerulus, which is the part of the kidney that controls filtering and excretion. This inefficient functioning results in blood and protein appearing in the urine, and the accumulation of excess fluid in the body. Swelling results when protein is lost from the blood stream. (Protein maintains fluid within the blood vessels, and when it is lost the fluid collects in the tissues of the body).
Urine discoloration results from blood in the urine. This occurs because of loss of blood within the damaged glomeruli.
Acute nephritic syndrome may be associated with the development of high blood pressure, interstitial inflammation (inflammation of the spaces between the cells of the kidney tissue), and acute kidney failure.
Symptoms
Despite the diversity of diseases that cause acute nephritis below, they share many symptoms in common:
Late symptoms include the following:
Signs and tests
Your blood pressure may be elevated. There may be signs of fluid overload (more fluid in circulation than the heart can effectively pump), including abnormal heart and lung sounds. The jugular (neck) veins may be distended from increased pressure.
Generalized swelling is often present. When examining your abdomen, your health care provider may find signs of fluid overload and an enlarged liver. There may be signs of acute kidney failure in addition to the above symptoms.
Tests for the cause of the acute nephritic syndrome may include:
Treatment
The goal of treatment is to reduce glomerular inflammation. Hospitalization is required for diagnosis and treatment of many forms of acute nephritic syndrome. The cause must be identified and treated. This may include antibiotics or other medications or treatment.
Bedrest may be recommended. The diet may include restriction of salt, fluids, and potassium. Medications may include anti-hypertensive medications to control high blood pressure. Corticosteroids or other anti-inflammatory medications may be used to reduce inflammation.
Other treatment of acute kidney failure may be appropriate.
Support Groups
For information and support, see kidney disease support groups.
Expectations (prognosis)
The probable outcome is variable and depends on the disease responsible for the nephritis. When improvement occurs, symptoms associated with fluid retention (such as swelling and cough) and high blood pressure may resolve in a week or two, while urine tests take months to return to normal.
Children tend to do better than adults and usually recover completely. Only rarely do they develop complications or progress to chronic glomerulonephritis.
Adults do not recover quite as well or as rapidly as children. Although recurrence is unusual, at least one-third of adults whose acute nephritic syndrome recurs will eventually develop end-stage kidney disease.
Complications
Calling your health care provider
Call your health care provider if symptoms that are suggestive of acute nephritic syndrome develop.
Prevention
Many times the disorder cannot be prevented, although treatment of illness and infection may help to reduce the risk.