Introduction
Nephrotic syndrome is a kidney disorder marked by excessive protein loss in the urine, leading to various systemic complications. This condition often results from damage to the glomeruli—the kidney's filtering units—causing proteinuria, low blood protein levels, and fluid retention. Understanding the assessment, diagnosis, and management of nephrotic syndrome is essential for effective treatment and prevention of further kidney damage.
Assessment
Diagnosis
Medical Management
Nephrotic syndrome is diagnosed through a urine test detecting proteinuria, defined as daily protein excretion over 3.5 grams, mainly due to albumin loss.
Confirmation comes from a 24-hour urine collection showing normal excretion under 150 mg/day.
Next, urine protein electrophoresis and immunofixation tests categorize proteinuria and identify specific renal pathologies.
Additionally, urine microscopy may reveal WBCs, granular casts, or epithelial casts, indicating renal inflammation.
Blood tests typically show serum albumin under 3.5 g/dL and an elevated lipid profile.
Sometimes, a kidney biopsy provides histological evidence, confirming the diagnosis and underlying pathology.
Medical management includes loop diuretics like furosemide for edema, ACE inhibitors like enalapril to lower protein leakage and manage hypertension, and statins for hyperlipidemia.
Dietary management recommends a moderate protein intake and limits sodium to about 2 grams daily.