Nephrotic syndrome is a nonspecific disorder in which the kidneys are damaged, causing them to leak large amounts of protein

(proteinuria at least 3.5 grams per day per 1.73m body surface area) the urine. Kidneys affected by nephrotic syndrome have small pores in the podocytes, large enough to permit proteinuria (and subsequently hypoalbuminemia, because some of the proteinalbumin has gone from the blood to the urine) but not large enough to allow cells through (hence no hematuria). By contrast, in nephritic syndrome, RBCs pass through the pores, causing hematuria.
2 [2]

from the blood into

Presentation
It is characterized by proteinuria (>3.5g/day), hypoalbuminemia, hyperlipidemia and edema which is generalized & also known as anasarca or dropsy.Common among 2-6 years old boys. The edema begins in the face. Lipiduria (lipids in urine) can also occur, but is not essential for the diagnosis of nephrotic syndrome. Hyperlipidemia is caused by two factors:

Hypoproteinemia stimulates protein synthesis in the liver, resulting in the overproduction of lipoproteins. Lipid catabolism is decreased due to lower levels of lipoprotein lipase, the main enzyme involved in lipoprotein breakdown.

A few other characteristics seen in nephrotic syndrome are:

The most common sign is excess fluid in the body due to the serum hypoalbuminemia. Lower serum oncotic pressure causes fluid to accumulate in the interstitial tissues. Sodium and water retention aggravate the edema. This may take several forms:

Puffiness around the eyes, characteristically in the morning. Pitting edema over the legs. Fluid in the pleural cavity causing pleural effusion. More commonly associated with excess fluid is pulmonary edema.

Fluid in the peritoneal cavity causing ascites. Generalized edema throughout the body known as anasarca.

Most of the patients are normotensive but hypertension (rarely) may also occur. Anemia (iron resistant microcytic hypochromic type) maybe present due to transferrin loss. Dyspnea maybe present due to pleural effusion or due to diaphragmatic compression with ascites. Erythrocyte sedimentation rate is increased due to increased fibrinogen & other plasma contents. Some patients may notice foamy or frothy urine, due to a lowering of the surface tension by the severe proteinuria. Actual urinary complaints such as hematuria or oliguria are uncommon, though these are seen commonly in nephritic syndrome.

May have features of the underlying cause, such as the rash associated with systemic lupus erythematosus, or the neuropathyassociated with diabetes.

Examination

should

also

exclude

other

causes

of

gross

edemaespecially

the cardiovascular and hepatic system.

Investigations

The following are baseline, essential investigations:

24 hour bedside urinary total protein estimation.

2

Urine sample shows proteinuria (>3.5 g per 1.73 m per 24 hours). It is also examined for urinary casts, which are more a feature of active nephritis.

Comprehensive metabolic panel (CMP) shows hypoalbuminemia: albumin level 2.5 g/dL (normal=3.5-5 g/dL). Lipid profile. levels of cholesterol (hypercholesterolemia), specifically elevated LDL, usually with concomitantly

High

elevated VLDL is typical.

Electrolytes, urea and creatinine (EUCs): to evaluate renal function.

Further investigations are indicated if the cause is not clear:

Biopsy of kidney (in case of adult patients only). Auto-immune markers (ANA, ASOT, C3, cryoglobulins, serum electrophoresis). Ultrasound of the whole abdomen.

Classification and causes

Nephrotic syndrome has many causes and may either be the result of a disease limited to the kidney, called primary nephrotic syndrome, or a condition that affects the kidney and other parts of the body, called secondary nephrotic syndrome.

Etiologic classification
A broad classification of nephrotic syndrome based on etiology: Nephrotic syndrome Primary Secondary

Histologic classification
Nephrotic syndrome is often classified histologically: Nephrotic syndrome MCD FSGS MN MPGN

Primary causes
Primary causes of nephrotic syndrome are usually described by the histology, i.e. minimal change disease (MCD) like minimal change nephropathy which is the most common cause of nephrotic syndrome in children, focal segmental glomerulosclerosis (FSGS) andmembranous nephropathy (MN) like membranous glomerulonephritis which is the main cause of nephrotic syndrome in adult. They are considered to be "diagnoses of exclusion", i.e. they are diagnosed only after secondary causes have been excluded.

Secondary causes
Secondary causes of nephrotic syndrome have the same histologic patterns as the primary causes, though may exhibit some differences suggesting a secondary cause, such as inclusion bodies. They are usually described by the underlying cause.

Secondary causes by histologic pattern:

Hepatitis B & Hepatitis C Sjgren's syndrome Systemic lupus erythematosus(SLE) Diabetes mellitus Sarcoidosis Amyloidosis Drugs (such as corticosteroids, gold, intravenous heroin) Malignancy (cancer) Bacterial infections, e.g. leprosy & syphilis Protozoal infections, e.g. malaria

Focal segmental glomerulosclerosis (FSGS) Hypertensive nephrosclerosis

Human immunodeficiency virus (HIV)*Obesity Kidney loss

Minimal change disease (MCD) Drugs, especially NSAIDs in the elderly

Malignancy, especially Hodgkin's lymphoma Leukemia

Allergy

Bee sting

Differential diagnosis of gross edema

When someone presents with generalized edema, the following causes should be excluded:

1. Heart failure: The patient is older, with a history of heart disease. Jugular venous pressure is elevated on examination, might hear heart murmurs. An echocardiogram is the gold standard investigation. 2. Liver failure: History suggestive of hepatitis/ cirrhosis: alcoholism, IV drug use, some hereditary causes. Signs of liver disease are seen: jaundice (yellow skin and eyes), dilated veins over umbilicus (caput medusae), scratch marks (due to widespread itching, known as pruritus), enlarged spleen, spider angiomata, encephalopathy, bruising, nodular liver. 3. Acute fluid overload in someone with kidney failure: These people are known to have kidney failure, and have either drunk too much or missed their dialysis. 4. Metastatic cancer: when cancer spreads to the lungs or abdomen it causes effusions and fluid accumulation due to obstruction of lymphatics and veins, as well as serous exudation.

Diagnosis

The gold standard in diagnosis of nephrotic syndrome is 24 hour urine protein measurement. Aiding in diagnosis are blood tests and sometimes imaging of the kidneys (for structure and presence of two kidneys), and/or a biopsy of the kidneys.

Treatment

Treatment includes:

General measures (supportive)

Monitoring and maintaining euvolemia (the correct amount of fluid in the body):

Monitoring urine output, BP regularly. Fluid restrict to 1 L. Diuretics (IV furosemide).

Monitoring kidney function:

do EUCs daily and calculating GFR.

Treat hyperlipidemia to prevent further atherosclerosis.

Prevent and treat any complications [see below]

Albumin infusions are generally not used because their effect lasts only transiently.
[5]

Prophylactic anticoagulation may be appropriate in some circumstances.

Specific treatment of underlying cause

Immunosuppression for the glomerulonephritides (corticosteroids , ciclosporin).
2 [6]

Standard ISKDC regime for first episode: prednisolone -60 mg/m /day in 3 divided doses for 4 weeks followed by 40 mg/m /day in a single dose on every alternate day for 4 weeks.
2

Relapses by prednisolone 2 mg/kg/day till urine becomes negative for protein. Then, 1.5 mg/kg/day for 4 weeks.

Frequent relapses treated by: cyclophosphamide or nitrogen mustard or ciclosporin or levamisole.

Achieving better blood glucose level control if the patient is diabetic.

Blood pressure control. ACE inhibitors are the drug of choice. Independent of their blood pressure lowering effect, they have been shown to decrease protein loss.

Dietary recommendations
Reduce sodium intake to 10002000 mg daily. Foods high in sodium include salt used in cooking and at the table, seasoning blends (garlic salt, Adobo, season salt, etc.) canned soups, canned vegetables containing salt, luncheon meats including turkey, ham, bologna, and salami, prepared foods, fast foods, soy sauce, ketchup, and salad dressings. On food labels, compare milligrams of sodium to calories per serving. Sodium should be less than or equal to calories per serving.

Eat a moderate amount of high protein animal food: 3-5 oz per meal (preferably lean cuts of meat, fish, and poultry) Avoid saturated fats such as butter, cheese, fried foods, fatty cuts of red meat, egg yolks, and poultry skin. Increase unsaturated fat intake, including olive oil, canola oil, peanut butter, avocadoes, fish and nuts. Eat low-fat desserts. Increase intake of fruits and vegetables. No potassium or phosphorus restriction necessary. Monitor fluid intake, which includes all fluids and foods that are liquid at room temperature. Fluid management in nephrotic syndrome is tenuous, especially during an acute flare.

Complications

Venous thrombosis: due to leak of anti-thrombin 3, which helps prevent thrombosis. This often occurs in the renal veins. Treatment is with oral anticoagulants (not heparin as heparin acts via anti-thrombin 3 which is lost in the proteinuria so it will be ineffective.)

Infection:

due

to

leakage

of

immunoglobulins,

encapsulated

bacteria

such

as Haemophilus

influenzae and Streptococcus pneumoniae can cause infection.

Acute renal failure is due to hypovolemia. Despite the excess of fluid in the tissues, there is less fluid in the vasculature. Decreased blood flow to the kidneys causes them to shutdown. Thus it is a tricky task to get rid of excess fluid in the body while maintaining circulatory euvolemia.

Pulmonary edema: again due to fluid leak, sometimes it leaks into lungs causing hypoxia and dyspnoea.

Growth retardation: does not occur in MCNS.It occurs in cases of relapses or resistance to therapy. Causes of growth retardation are protein deficiency from the loss of protein in urine, anorexia (reduced protein intake), and steroid therapy (catabolism).

Vitamin D deficiency can occur. Thyroxine is reduced due to decreased thyroid binding globulin.

Microcytic hypochromic anaemia is typical. It is iron-therapy resistant.

Hypocalcemia can occur as a result of nephrotic syndrome. It may be significant enough to cause tetany.

Cushing Syndrome

Prognosis
The prognosis depends on the cause of nephrotic syndrome. It is usually good in children, because minimal change disease responds very well to steroids and does not cause chronic renal failure. However other causes such as focal segmental glomerulosclerosisfrequently lead to end stage renal disease. Factors associated with a poorer prognosis in these cases include level of proteinuria, blood pressure control and kidney function (GFR)