Smiths General Urology, Seventeenth Edition (LANGE Clinical Medicine)

Authors: Macfarlane, Michael T.

Title: Urology, 4th Edition

Copyright 2006 Lippincott Williams & Wilkins

> Table of Contents > Part Two - Selected Topics > Chapter 33 - Interstitial Cystitis

Chapter 33

Interstitial Cystitis

Interstitial cystitis (IC) is probably the least understood and most controversial of all urologic diseases. Even an agreed-on definition of the syndrome is not accepted; however, it is universally accepted that IC is a diagnosis of exclusion. The most commonly recognized symptoms are urgency, frequency, and suprapubic pain on bladder filling in the absence of any other reasonable causation. Hematuria has been reported in 20% to 30% of cases. It is an uncommon disease, primarily of women aged 30 to 70 years, with a 10:1 female-to-male preponderance. The etiology of IC remains obscure.

Diagnosis

The diagnosis of IC is one of exclusion based entirely on clinical and cystoscopic criteria.

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Workup

Workup should include urinalysis, urine culture, a careful voiding record, cystoscopy under anesthesia, bladder cytology or biopsy or both, intravenous urogram, and urodynamic studies. Carcinoma in situ and infection must be ruled out. Trial management with antimicrobials, anticholinergics, and antispasmodics is recommended. Relief of symptoms would exclude the diagnosis of IC.

Management

This disease rarely progresses and presents little threat to the patient's health. However, it can cause intolerable morbidity, at times making the patient's life unbearable. The uncertain etiology and diagnosis only worsen matters for these unfortunate patients when they are dealing with physicians. The goal of management is symptomatic relief. Both patient and physician must understand that no sure cure for IC exists. Patient education is important. Therapeutic options include the following:

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