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Clinical Briefing: Interdisciplinary Management of Glomerulonephritis

November/December 2007

At Penn's Renal-Electrolyte and Hypertension Division, the effective clinical management of glomerular disease is directed at abating the acute manifestations of kidney disease, protecting kidney function, and managing symptoms of renal and nonrenal disease.

These objectives are achieved through the interdisciplinary collaboration of nephrologists, immunologists, pathologists, rheumatologists, and others. The coordination of care between these various specialties ensures that the intricacies of management, which are so profoundly affected by the patient's clinical characteristics and comorbidities, are effectively addressed.

Kidney biopsy showing a glomerulus with diffuse cellular proliferation occluding the capillary loops. Original magnification X25.

Penn's multidisciplinary approach also allows its physicians to orchestrate the intricate balance between immunosuppressive and cytotoxic drug therapy, antihypertensive medications, and other therapies used to treat the disease and its effects, and when appropriate, provide for optimally timed renal replacement therapy, whether in-center hemodialysis, home dialysis, or transplantation.

Case Study
Ms. K, a 23-year-old woman, was referred with 6 weeks of lower extremity edema, facial rash and arthralgias. She had a BP of 160/95 mmHg. A urinalysis had 3+ protein and 1+ blood; dysmorphic RBCs and granular and rare RBC casts were evident. A 24-hour urine collection had 2.1 g of protein. Ms K's Hgb level was 9.9 g/dl; platelet count was 110,000; serum creatinine (Cr) was 1.8 mg/dl.

Additional workup revealed positive ANA, elevated anti-dsDNA Ab and hypocomplementemia. A percutaneous renal biopsy demonstrated diffuse proliferative glomerulonephritis. A repeat Cr was 2.7 mg/dl. Ms. K was diagnosed with SLE and stage IV (WHO) lupus nephritis.

“Acute glomerulonephritis is generally marked by a significant decline in kidney function, and is often associated with serious systemic complications affecting multiple organs. To ensure effective management, it is essential that the clinical environment include the ability to undertake prompt institution of a coordinated, systemic approach to diagnosis and treatment that encompasses the capacity to shift medications and treatment direction when necessary and the ability to manage multi-system disease manifestations when they develop.”

Jeffrey S. Berns, MD
Associate Chief for Clinical Affairs;
Director, Renal Fellowship Program

Treatment with intravenous methylprednisolone followed by oral prednisone and intravenous cyclophosphamide brought rapid improvement of her symptoms. Alendronate with calcium supplementation was introduced as part of a comprehensive treatment plan coordinated with the Division of Rheumatology.

At six months, Ms. K began mycophenolate mofetil (1.5 gm b.i.d.); cyclophosphamide was discontinued. Her urine protein at this time was <200 mg/24 h, her Cr was 0.9 mg/dl and her serum complement levels had nearly normalized.

Five months later, however, Ms. K reported an increase in arthralgias. Her proteinuria had increased to 1.4 gm/24 h, her Cr was increased to 1.7 mg/dl, and her C3 and C4 complement levels were again low, with an increase in anti-dsDNA Ab titer. After discussions with Ms. K and her rheumatologists, treatment with the anti-CD20 antibody rituximab (375 mg/m2 weekly) was initiated.

Ms. K reported no active symptoms of lupus after three once-weekly doses. Over the next few months her Cr declined to 0.6 mg/dl, and her proteinuria fell to <100 mg/24 h. She has remained stable without recurrence of her lupus manifestations.

Our Team of Faculty
The faculty of the Penn Renal-Electrolyte and Hypertension Division offers diagnostic evaluation and clinical management for patients with acute or chronic kidney diseases, renal failure, acute glomerulonephritis, complex hypertension, diabetic nephropathy, nephrotic syndrome, amyloidosis, electrolyte and acid-based disturbances, genetic kidney diseases, hematuria, proteinuria, and kidney stones. Patient care is provided in a setting with access to a full array of multidisciplinary state-of-the-art clinical and diagnostic services.

 


Referring Physicians: To speak with a Penn physician or refer a patient, contact PennHealth through the secure online referral form or by calling
1-800-789-PENN (7366).

   
   

 

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