Find information on thousands of medical conditions and prescription drugs.

Interstitial cystitis

Interstitial cystitis (commonly abbreviated to "IC") is a urinary bladder disease of unknown cause characterised by pelvic and intense bladder pain, urinary frequency (as often as every 10 minutes), pain with sexual intercourse, and often pain with urination. It is not unusual for patients to experience nocturia and pain with sexual intercourse. IC is also known as painful bladder syndrome (PBS), particularly outside of the USA. more...

ICF syndrome
Ichthyosis vulgaris
Imperforate anus
Inborn error of metabolism
Incontinentia pigmenti
Infant respiratory...
Infantile spinal muscular...
Infective endocarditis
Inflammatory breast cancer
Inguinal hernia
Interstitial cystitis
Iodine deficiency
Irritable bowel syndrome

IC affects men and women of all cultures, socioeconomics and ages. Previously believed to be a condition of post menopausal women, growing numbers of men and women are being diagnosed in their twenties and younger. IC is not a rare condition. Recent research suggests that IC prevalence ranges from 1 in 100,000 to 5.1 in 1,000 of the general population. New epidemiological data for the United States should be released in 2006.

It is not unusual for patients to have beeen misdiagnosed with a variety of other conditions, including: overactive bladder, urethritis, urethral syndrome, trigonitis, prostatitis and other generic terms used to describe frequency/urgency symptoms in the urinary tract.


The cause of interstitial cystitis is unknown, though several theories have been put forward (these include autoimmune, neurologic, allergic and genetic). Regardless of the origin, it is clear that IC patients struggle with a damaged mucin, aka the GAG layer, aka bladdering lining. When this protective coating is damaged (perhaps via a UTI, excessive consumption of coffees or sodas, traumatic injury, etc.), urinary chemicals can "leak" into surrounding tissues causing pain, inflammation and urinary symptoms. Oral medications like Elmiron and medications which are placed directly into the bladder via a catheter work to repair and hopefully rebuild this damaged/wounded lining, allowing for a reduction in symptoms.

Recent work by the University of Maryland indicates that genetics are a factor in, and may even (in some cases) be the cause of IC. Two genes, FZD8 and PAND, are associated with the syndrome. FZD8, at gene map locus 10p11.2, is assocated with an antiproliferative factor secreted by the bladders of IC patients which "profoundly inhibits bladder cell proliferation," thus causing the missing bladder lining. PAND, at gene map locus 13q22-q32, is associated with a constellation of disorders (a "pleiotropic syndrome") including IC and other bladder and kidney problems, thyroid diseases, serious headaches/migraines, panic disorder, and mitral valve prolapse.


It may well be that the symptoms of interstitial cystitis have multiple causes, and IC is actually several syndromes which will eventually be discerned. For example, patients with Hunner's Ulcers are believed to be the most advanced cases. They have larger "wounds" in the bladder that are much more difficult to treat. It is estimated that only 5 to 10% of patients have these ulcers. Far more patients may experience a very mild form of IC, inwhich they have no visible wounds in their bladder, yet struggle with symptoms of frequency, urgency and/or pain. Still other patients may have discomfort only in their urethra, while others struggle with pain in the entire pelvis. Some patients may experience pelvic floor tightness and dysfunction, while others have normal muscle tone.


[List your site here Free!]

Interstitial Cystitis: Urgency and Frequency Syndrome
From American Family Physician, 10/1/01 by Julius F. Metts

Interstitial cystitis is a chronic, severely debilitating disease of the urinary bladder. Excessive urgency and frequency of urination, suprapubic pain, dyspareunia, chronic pelvic pain and negative urine cultures are characteristic of interstitial cystitis. The course of the disease is usually marked by flare-ups and remissions. Other conditions that should be ruled out include bacterial cystitis, urethritis, neoplasia, vaginitis and vulvar vestibulitis. Interstitial cystitis is diagnosed by cystoscopy and hydrodistention of the bladder. Glomerulations or Hunner's ulcers found at cystoscopy are diagnostic. Oral treatments of interstitial cystitis include pentosan polysulfate, tricyclic antidepressants and antihistamines. Intravesicular therapies include hydrodistention, dimethyl sulfoxide and heparin, or a combination of agents. Referral to a support group should be offered to all patients with interstitial cystitis. (Am Fam Physician 2001;64:1199-206,1212-4.)

Patients with irritative voiding symptoms and negative urine cultures frequently present a diagnostic challenge for primary care physicians. Interstitial cystitis is a severely debilitating disease of the urinary bladder. Symptoms of interstitial cystitis include excessive urgency and frequency of urination, suprapubic pain, dyspareunia and chronic pelvic pain.(1) Interstitial cystitis interferes with employment, social relationships and sexual activity. The course of the disease is usually marked by flare-ups and remissions. Interstitial cystitis is a chronic disease that persists throughout the patient's life. On clinical evaluation, patients with interstitial cystitis should have no other definable pathology, such as urinary infections, carcinoma, or radiation-induced or medication-induced cystitis (Parsons CL. Interstitial cystitis, new concepts in pathogenesis, diagnosis and management. Presentation at 3rd annual meeting of the American Urological Association, June 4, 1998, San Diego, Calif.).


Interstitial cystitis may affect as many as 700,000 women in the United States.(2) Data from the Nurses' Health Study suggest that the prevalence of interstitial cystitis among women is about 67 per 100,000 and 52 per 100,000.(3)

The nonulcer type of interstitial cystitis occurs in about 90 percent of patients. The more severe form of the disease (in about 10 percent of patients) involves Hunner's ulcers, which are lesions that involve all of the layers of the bladder wall and appear as brownish-red patches on the bladder mucosa.

Women make up 90 percent of patients with interstitial cystitis,1 while men comprise the remaining 10 percent. Children can also have interstitial cystitis.(3) Urinary frequency, sensory urgency and lower abdominal pain are common symptoms among children with the disease.

The onset of interstitial cystitis usually occurs between 30 and 70 years of age,(4) with a median age of 43.(5) The prevalence of the disease appears to be increasing among young and middle-aged women.(6)

Most patients consult at least five physicians, including psychiatrists, over a period of more than four years before interstitial cystitis is diagnosed. Symptomatic patients require considerably more medical care than their age-matched cohorts.(7)


While the exact cause of interstitial cystitis is not known, it is probably related to many factors, including autoimmune, allergic and infectious etiologies.2

According to one widely held theory, the symptoms of interstitial cystitis originate from a defect in the glycosaminoglycan component of the mucin layer that covers and protects the bladder urothelium(8) (Figure 1). A deficiency of this layer is thought to cause interstitial cystitis. Low rates of urinary glycosaminoglycan excretion have been found in patients with interstitial cystitis. The glycosaminoglycan hypothesis is the basis for treating interstitial cystitis with glycosaminoglycan "replacements," such as sodium pentosan polysulfate (an exogenous, oral glycosaminoglycan) and heparin or hyaluronic acid administered intravesically.(8,9) Irritating substances in the urine may leak through the urothelium, causing inflammation, tissue irritation and injury, mast cell degranulation and sensory nerve depolarization, which result in the urinary urgency, frequency and pain of interstitial cystitis.(5,6,10) Glycosaminoglycans are highly hydrophilic and protective. They maintain a stable layer of water between the urothelium and the bladder lumen, and prevent adhesion to and invasion of the urothelium by bacteria, microcrystals, ions, proteins and other substances in the urine.

Another working theory of interstitial cystitis etiology includes mast cell abnormalities. Mast cells are present in the bladder wall of many patients with interstitial cystitis. Increased numbers of submucosal mast cells are found in these patients.(11,12) Antigenic exposure of mast cells causes the release of pharmacologically active mediators (e.g., histamine, prostaglandins, leukotrienes and tryptases) that have a significant effect on smooth muscle, vascular epithelium and inflammation.


To date, no convincing evidence confirming a viral, bacterial or fungal cause of interstitial cystitis has been found.(13,14)

A psychologic etiology of interstitial cystitis has been mentioned, only to be condemned. Research has shown that definite objective abnormalities are present in patients with interstitial cystitis, including findings on bladder biopsy and cystoscopy. The chronic pain, frequency, urgency and sleep deprivation associated with interstitial cystitis may contribute to psychologic stress and secondary depression. Suicidal ideation is three to four times more common in patients with interstitial cystitis than in the general population.(15) More than one half of symptomatic patients with interstitial cystitis have depression. Chronic bladder and pelvic pain is usually moderate to severe.(1,8,16)

An unexplained association has been found between interstitial cystitis and other chronic disease or pain syndromes such as allergies, irritable bowel syndrome, skin sensitivity, vulvodynia, fibromyalgia, migraine, endometriosis and chronic fatigue syndrome.17 Dyspareunia is not uncommon in persons with interstitial cystitis and may be related to the mechanical effects of intercourse on the inflamed bladder. approach to diagnosis

Interstitial cystitis is often underdiagnosed or improperly diagnosed. A presumptive diagnosis may be made by looking for appropriate clinical criteria. The National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) developed inclusion and exclusion criteria for patients who are being considered for interstitial cystitis research (Table 1).(18) While the NIDDK criteria are useful for research, they are too restrictive to be used by physicians in diagnosing interstitial cystitis. Inclusion criteria would involve bladder pain, urinary urgency and frequency, bladder capacity of less than 350 mL and cystoscopic evidence of Hunner's ulcers. Strict application of the NIDDK criteria would have misdiagnosed more that 60 percent of patients who were diagnosed by researchers as definitely having or likely to have interstitial cystitis.(6)

The most typical symptom of interstitial cystitis is pelvic pain. The pain is relieved by voiding small amounts of urine from the bladder, but soon recurs as the bladder fills. Another common symptom is an uncomfortable, constant urge to void that does not go away even after the patient has voided. Incontinence is not typical of interstitial cystitis and, if present, requires that other diagnoses be diligently sought. Dyspareunia (on deep penetration) is not uncommon in patients with interstitial cystitis.

The symptoms of interstitial cystitis typically worsen in the week before menstruation in contrast to the symptoms of endometriosis, which are worse during menses. Sometimes the symptoms of interstitial cystitis are exacerbated after patients consume certain foods, especially coffee, alcohol, carbonated drinks, citrus fruits, tomatoes and chocolate.(19) Conditions that must be excluded to diagnose interstitial cystitis include bacteriuria, Chlamydia trachomatis infection, prostatitis, herpes simplex virus infection, neoplasia, neuropathic bladder dysfunction and gynecologic diseases such as vaginitis, urethral diverticulum, vulvar vestibulitis and endometriosis.

Urinary frequency in patients with interstitial cystitis averages 16 times per day but can be as much as 40 times per day. Nonbacteriuric patients with pyuria should be tested or empirically treated for Chlamydia infection.(20)

A careful pelvic examination is needed to rule out vaginitis, vulvar lesions and urethral diverticula. Pelvic examination in women often reveals tenderness of the bladder base. Patients should be asked to keep a 24-hour log of voiding activity for frequency of urination and voiding patterns. The patient may be accustomed to an abnormal pattern. Findings on urinalysis may be entirely normal or may show microscopic hematuria or pyuria. Urine culture results are usually sterile. However, patients with interstitial cystitis may also have a concurrent bladder infection. Urine cytology may be helpful in ruling out transitional cell carcinoma of the bladder.(21) If indicated, tuberculosis may be ruled out with urine testing for acid-fast bacillus, or bladder biopsy.

Urodynamic studies are not specifically diagnostic of interstitial cystitis. Radiographic studies, such as intravenous pyelography or voiding cystourethrography, are seldom indicated in the evaluation of patients with suspected interstitial cystitis.(6)

After the above evaluations are completed, confirmation of the diagnosis of interstitial cystitis depends on cystoscopic findings. Hydrodistention of the bladder is often performed during cystoscopy under general anesthesia. Hydrodistention consists of filling the bladder with saline solution or sterile water beyond its normal capacity. On distention, pinpoint hemorrhages or fissures with bleeding, called glomerulations, may appear(6,21) (Figure 2). Glomerulations may be seen in various types of bladder conditions and may also be seen in asymptomatic women.(22)

Hunner's ulcers (Figure 3) and severe reductions in bladder capacity are found infrequently because most patients have the nonulcer variety of interstitial cystitis. Reductions in bladder capacity are manifested by scarring of the bladder wall (Figures 4a and 4b). Following bladder hydrodistention, terminal blood tinge of the draining distention fluids occurs in about 90 percent of patients. Biopsies are indicated in patients with suspected interstitial cystitis to exclude specific bladder pathology such as carcinoma, dysplasia or tuberculosis; to confirm bladder wall inflammation; and to identify subgroups of patients, such as those with excessive mast cells or eosinophils.(11) Generally, cystoscopy and bladder biopsy are performed in ambulatory surgery settings.(6) The hydrodistention performed at the time of cystoscopy may be therapeutic.(6) This relief may last from several weeks to months. Figure 5 depicts the diagnosis of interstitial cystitis.


Although treatment is usually nonspecific and empiric, relief of the symptoms of interstitial cystitis should be the goal6 (Table 2(20)). Support, understanding and reassurance should be provided by caregivers and family. The patient should be told that interstitial cystitis is not a malignancy or a harbinger of systemic disease.23 Treatment, especially in young patients with nonulcer interstitial cystitis, should involve the least invasive therapy that provides reasonable symptomatic improvement. Patients should be counseled that treatment is meant to alleviate symptoms, that there is not yet a specific cure and that the disease is chronic in nature. The rationale for each treatment option and the possible necessity of changing medications and using combination treatments should be emphasized.

Acidic foods, caffeine, alcohol, artificial sweeteners and chocolate may aggravate the symptoms of interstitial cystitis in some patients and should be avoided.(16)


First-line oral treatments for interstitial cystitis include tricyclic antidepressants, antihistamines and pentosan polysulfate (Elmiron). No placebo-controlled studies with tricyclic antidepressants have been performed, but these medications have been found to be beneficial in several open-label studies.(24) Tricyclic antidepressants block pain arousal and are widely used in pain clinics for their pain blocking effects. Other medications that may reduce the symptoms of interstitial cystitis include sedatives (for improved sleep) and medications that inhibit nociception. Some of the most commonly used tricyclics are amitriptyline (Elavil), doxepin (Sinequan) and imipramine (Tofranil), administered in dosages of 25 to 75 mg at bedtime. These agents may be started at very low dosages and gradually titrated up until symptom relief is obtained or until side effects become bothersome. Use of hydroxyzine (Atarax), an antihistamine, is based on the hypothesis that histamine released by mast cell degranulation may be responsible for symptoms of interstitial cystitis. Hydroxyzine (in a dosage of 25 to 75 mg at bedtime) and the H2-receptor antagonist cimetidine (Tagamet), in a dosage of 300 mg twice daily, were both effective in open-label studies.(25,26)

Pentosan polysulfate is the only oral therapy for the treatment of interstitial cystitis symptoms that has been studied in placebo-controlled trials.(9,25,27,28) Pentosan polysulfate is a highly sulfated, semisynthetic glucosaminoglycan with chemical and structural similarities to naturally occurring glucosaminoglycans. The medication is well tolerated and has a favorable side effect profile. In one study, bladder pain was relieved by at least 50 percent in 38 percent of patients taking pentosan polysulfate compared with 18 percent improvement in patients treated with placebo.(29)

It may take three to six months for patients to respond to pentosan polysulfate.(29) The usual dosage is 100 mg orally three times per day. Adverse reactions to pentosan polysulfate include diarrhea, dyspepsia, reversible alopecia, headache, rash, dizziness, abdominal pain and uncommon liver function abnormalities (1 to 4 percent).

Although no research has been done, some experts in the treatment of interstitial cystitis combine two of the above oral medications for an enhanced treatment response. Some patients feel better after taking aspirin or a nonsteroidal anti-inflammatory drug, probably because mast cell degranulation releases prostaglandins and leukotrienes.(11) Other drugs that may be used to treat interstitial cystitis are anticholinergics, bladder analgesics such as phenazopyridine (Pyridium) or oxybutynin chloride (Ditropan), calcium channel blockers such as nifedipine (Procardia), or gabapentin (Neurontin). No studies have been done to show the efficacy of these medications.


Intravesicular pharmacotherapy provides high local drug concentrations in the bladder, avoids systemic side effects and eliminates the problem of low levels of urinary excretion with orally administered agents.(11) The most commonly used and only intravesical agent labeled by the U.S. Food and Drug Administration for the treatment of interstitial cystitis is dimethyl sulfoxide (Rimso-50). A controlled study of patients with interstitial cystitis showed that dimethyl sulfoxide was superior to placebo, with 53 percent of patients in the treatment group having significant improvement of symptoms.(30) Although dimethyl sulfoxide is an anti-inflammatory agent, it seems to have some analgesic and muscle relaxant properties as well.

Instillations of dimethyl sulfoxide are usually given every one to two weeks for a total of four to eight treatments. Following the initial course of treatment, some patients achieve long-term remission, but most relapse eventually. Additional treatment schedules for those who relapse vary but usually consist of instillation every four to six weeks.(6) The technique does not require anesthesia, hospitalization or the use of an operating room. Patients who are suitably motivated and trained can be taught the technique of intermittent self-catheterization and instillation of dimethyl sulfoxide, allowing for self-treatment when symptoms occur. Sometimes dimethyl sulfoxide is combined with heparin, steroids, bicarbonate and a local anesthetic for intravesical administration.(6)

In an open-label study, 56 percent of patients with interstitial cystitis experienced relief from symptoms using heparin intravesically, in a dosage of 10,000 U three times a week.(31) In another study, monthly heparin instillation prolonged the response to dimethyl sulfoxide.(32) Instillation of hyaluronic acid, in a dosage of 40 mg weekly, provided complete symptom relief in 25 percent of patients and partial relief in 46 percent.(33)

In a controlled study using six weekly instillations of bacillus Calmette-Guerin, 60 percent of patients with interstitial cystitis had symptom reduction compared with 27 percent of patients receiving placebo.34


Transcutaneous electrical nerve stimulation resulted in improvement or remission in 54 percent of patients with classic interstitial cystitis (i.e., Hunner's ulcers) and in 26 percent of patients with nonulcer interstitial cystitis.35 Many patients with interstitial cystitis have spasms of the pelvic floor muscles that contribute to symptoms of pelvic pain, urgency and frequency. Physical therapy with biofeedback for pelvic floor relaxation may be helpful in such patients.

Support groups of persons who have the same disorder may be especially helpful. Physician support and attention to associated psychosocial problems can greatly improve the patient's response to treatment.

Figures 2 and 3 were supplied by Baker Norton Pharmaceuticals, Inc., Medical Affairs Dept., Miami, Fla. Figures 4a and 4b were supplied by Victoria Handa, M.D., Dept. of Obstetrics and Gynecology, University of California, Davis, School of Medicine.

The author thanks Dennice Caldwell, University of California, Davis, Student Health Medical Staff Office, for assistance in preparing the manuscript.

The authors indicate that they do not have any conflicts of interest. Sources of funding: none reported.

JULIUS F. METTS, M.D., is assistant clinical professor in family practice at the University of California, Davis, School of Medicine, and associate physician at Cowell Student Health Center, also in Davis. He received his medical degree from East Carolina University School of Medicine, Greenville, N.C., and completed a residency in family practice at San Bernardino County Medical Center, San Bernardino, Calif.

Address correspondence to Julius F. Metts, M.D., University of California, Davis, Cowell Student Health Center, 1 Shields Ave., Davis, CA 95616. Reprints are not available from the author.


(1.) Parsons CL, Parsons JK. Interstitial cystitis. In: Raz S, ed. Female urology. 2d ed. Philadelphia: Saunders, 1996:Chapter 15.

(2.) Ratner V, Taylor N, Wein AJ, Hanno PJ. Re: Epidemiology of interstitial cystitis: a population based study [Letter]. J Urol 1999:162:500.

(3.) Curhan GC, Speizer FE, Hunter DJ, Curhan SG, Stampfer MJ. Epidemiology of interstitial cystitis: a population based study. J Urol 1999;161:549-52.

(4.) Jensen H, Nielsen K, Frimodt-Moller C. Interstitial cystitis: review of the literature. Urol Int 1989; 44:189-93.

(5.) Jones CA, Nyberg L. Epidemiology of interstitial cystitis. Urology 1997;49(suppl 5A):2-9.

(6.) Hanno PM, Landis JR, Matthews-Cook Y, Kusek J, Nyberg L. The diagnosis of interstitial cystitis revisited: lessons learned from the National Institutes of Health Interstitial Cystitis Database study. J Urol 1999;161:553-7.

(7.) Held PJ. Epidemiology of interstitial cystitis: 2. In: Hanno PM, et al., eds. Interstitial cystitis. New York: Springer-Verlag, 1990:Chapter 4.

(8.) Ruggieri MR, Chelsky MJ, Rosen SI, Shickley TJ, Hanno PM. Current findings and future research avenues in the study of interstitial cystitis. Urol Clin North Am 1994;21:163-76.

(9.) Mulholland SG, Hanno P, Parsons CL, Sant GR, Staskin DR. Pentosan polysulfate sodium for therapy of interstitial cystitis. A double-blind placebo-controlled clinical study. Urology 1990;35:552-8.

(10.) Parsons CL. The therapeutic role of sulfated polysaccharides in the urinary bladder. Urol Clin North Am 1994;21:93-100.

(11.) Sant GR. Interstitial cystitis: pathophysiology, clinical evaluation and treatment. In: Rous SN, ed. Urology annual. Vol. 3. Norwalk, Conn.: Appleton & Lange, 1989:177-96.

(12.) Hofmeister MA, He F, Ratliff TL, Mahoney T, Becich MJ. Mast cells and nerve fibers in interstitial cystitis (IC): an algorithm for histologic diagnosis via quantitative image analysis and morphometry (QIAM). Urology 1997;49(suppl 5A):41-7.

(13.) Duncan JL, Schaeffer AJ. Do infectious agents cause interstitial cystitis? Urology 1997;49(5A):48-51.

(14.) Keay S, Schwalbe RS, Trifillis AL, Lovchik JC, Jacobs S, Warren JW. A prospective study of microorganisms in urine and bladder biopsies from interstitial cystitis patients and controls. Urology 1995;45: 223-9.

(15.) Krishnan R, Marson L, Khoury JM. Interstitial cystitis. In: Pfizer Pharmaceuticals mediguide to urology. New York: Lawrence DellaCorte, 1996;9:1-6.

(16.) Koziol JA. Epidemiology of interstitial cystitis. Urol Clin North Am 1994;21:7-20.

(17.) Alagiri M, Chottiner S, Ratner V, Slade D, Hanno PM. Interstitial cystitis: unexplained associations with other chronic disease and pain syndromes. Urology 1997;49(5A):52-7.

(18.) National Institute of Diabetes and Digestive and Kidney Diseases. Interstitial cystitis. Rockville, Md.: U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health; 1994. NIH publication no. 94-3220.

(19.) Erickson DR, Davies MF. Interstitial cystitis. Int Urogynecol J Pelvic Floor Dysfunct 1998;9:174-83.

(20.) Sant GR, Meares EM. Interstitial cystitis: pathogenesis, diagnosis, and treatment. Infections in Urology Jan/Feb 1990:24-30.

(21.) Mobley DF, Baum N. Interstitial cystitis. When urgency and frequency mean more than routine inflammation. Postgrad Med 1996;99:201-4,207-8,214.

(22.) Waxman JA, Sulak PJ, Kuehl TJ. Cystoscopic findings consistent with interstitial cystitis in normal women undergoing tubal ligation. J Urol 1998;160:1663-7.

(23.) Sant GR. Intravesical 50% dimethyl sulfoxide (Rimso-50) in treatment of interstitial cystitis. Urology 1987;29(suppl 4):17-21.

(24.) Hanno PM. Amitriptyline in the treatment of interstitial cystitis. Urol Clin North Am 1994;21:89-91.

(25.) Theoharides TC, Sant GR. Hydroxyzine therapy for interstitial cystitis. Urology 1997;49(5A suppl):108-10.

(26.) Seshadri P, Emerson L, Morales A. Cimetidine in the treatment of interstitial cystitis. Urology 1994;44: 614-6.

(27.) Parsons CL, Schmidt JD, Pollen JJ. Successful treatment of interstitial cystitis with sodium pentosanpolysulfate. J Urol 1983;130:51-3.

(28.) Bade JJ, Laseur M, Nieuwenburg A, van der Weele LT, Mensink HJ. A placebo-controlled study of intravesical pentosanpolysulphate for the treatment of interstitial cystitis. Br J Urol 1997;79:168-71.

(29.) Parsons CL, Benson G, Childs SJ, Hanno P, Sant GR, Webster G. A quantitatively controlled method to study prospectively interstitial cystitis and demonstrate the efficacy of pentosanpolysulfate. J Urol 1993;150:845-8.

(30.) Perez-Marrero R, Emerson LE, Feltis JT. A controlled study of dimethyl sulfoxide in interstitial cystitis. J Urol 1988;140:36-9.

(31.) Parsons CL, Housley T, Schmidt JD, Lebow D. Treatment of interstitial cystitis with intravesical heparin. Br J Urol 1994;73:504-7.

(32.) Perez-Marrero R, Emerson LE, Maharajh DO, Juma S. Prolongation of response to DMSO by heparin maintenance. Urology 1993;41:64-6.

(33.) Morales A, Emerson L, Nickel JC, Lundie M. Intravesical hyaluronic acid in the treatment of refractory interstitial cystitis. J Urol 1996;156:45-8.

(34.) Peters K, Diokno A, Steinert B, Yuhico M, Mitchell B, Krohta S, et al. The efficacy of intravesical Tice strain bacillus Calmette-Guerin in the treatment of interstitial cystitis: a double-blind, prospective, placebo controlled trial. J Urol 1997; 157:2090-4.

(35.) Fall M, Lindstrom S. Transcutaneous electrical nerve stimulation in classic and nonulcer interstitial cystitis. Urol Clin North Am 1994;21:131-9.

COPYRIGHT 2001 American Academy of Family Physicians
COPYRIGHT 2001 Gale Group

Return to Interstitial cystitis
Home Contact Resources Exchange Links ebay