You are in: eMedicine Specialties > Urology > Infections and Related Inflammatory Conditions Nonbacterial ProstatitisArticle Last Updated: Mar 18, 2008AUTHOR AND EDITOR INFORMATIONAuthor: Sunil K Ahuja, MD, Chief of Minimally Invasive Urology, Department of Urology, Staff Urologist, Santa Teresa Community Hospital Sunil K Ahuja is a member of the following medical societies: American Urological Association Editors: Peter Langenstroer, MD, Assistant Professor, Department of Surgery, Division of Urology, Medical College of Wisconsin; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; J Stuart Wolf, Jr, MD, FACS, David A Bloom Professor of Urology, Director, Division of Minimally Invasive Urology, Department of Urology, University of Michigan Medical Center; Edward David Kim, MD, FACS, Professor of Surgery, Division of Urology, University of Tennessee Graduate School of Medicine; Consulting Staff, University of Tennessee Medical Center Author and Editor Disclosure Synonyms and related keywords: nonbacterial prostatitis, chronic pelvic pain syndrome, CPPS, prostatodynia, abacterial prostatitis, noninflammatory chronic pelvic pain syndrome, noninflammatory CPPS, inflammatory chronic pelvic pain syndrome, inflammatory CPPS, asymptomatic inflammatory prostatitis, prostate pain, prostatitis symptom complex, chronic prostatitis symptom index, CPSI, irritative urologic symptoms, obstructive urologic symptoms INTRODUCTIONBackgroundNonbacterial prostatitis refers to a condition that affects patients who present with symptoms of prostatitis without a positive result after urine culture or expressed prostate secretion (EPS) culture. Bacterial causes and their presentations can be reviewed in Acute Bacterial Prostatitis and Prostatic Abscess, Chronic Bacterial Prostatitis, and Prostatitis, Bacterial. Prior to 1995, the diagnosis of prostatitis was based on the classification of Meares and Stamey, which classified prostatitis into 4 categories: acute bacterial prostatitis, chronic bacterial prostatitis, nonbacterial prostatitis, and prostatodynia. In 1995, the US National Institutes of Health (NIH) convened a workshop on prostatitis and developed a new classification scheme. The first 2 categories remained the same, ie, acute and chronic bacterial prostatitis. Nonbacterial prostatitis and prostatodynia were combined as category III, ie, chronic abacterial prostatitis/chronic pelvic pain syndrome (CPPS). Category III was further subdivided into IIIa, ie, inflammatory CPPS, and IIIb, ie, noninflammatory CPPS. Category IV encompasses asymptomatic inflammatory prostatitis. See Image 2 for a comparison of the old and new categories of prostatitis. Prostate specimens often reveal evidence of category IV prostatitis after a biopsy. However, patients with category IV prostatitis have no symptoms. Some physicians treat these patients with antibiotics in an effort to lower their prostate-specific antigen (PSA) level. The rationale for the new diagnostic classification was to promote additional research to find effective forms of treatment for a symptom complex that cannot always be attributed to a bacterial infection. PathophysiologyOf all men evaluated for prostatitis, only 5-10% actually have a true bacteriologic condition as evidenced by a positive urine culture. However, approximately 50% of these men actually receive antibiotics for treatment of the prostatitis symptom complex. Evidence suggests that despite negative culture findings, some patients with nonbacterial prostatitis in the traditional sense may have a bacterial infection. Recent studies found bacterial ribosomal ribonucleic acid (rRNA) by reverse transcriptase-polymerase chain reaction (RT-PCR) in the prostatic fluid of patients with prostatitis symptoms. In addition, some fastidious organisms that do not grow in standard culture media may be the cause of the symptom complex. Some of these organisms are Chlamydia trachomatous, Ureaplasma urealyticum, and Neisseria gonorrhoeae. Despite having nonbacterial prostatitis by the classic definition, these patients improve with an appropriate course of antibiotics. The pathophysiology of chronic abacterial prostatitis has not been fully elucidated, emphasizing the lack of understanding of this disease complex. However, chronic abacterial prostatitis may involve an etiology similar to that of chronic bacterial prostatitis. The peripheral zone of the prostate is composed of a system of ducts, which possess a poor drainage system that prevents the dependent drainage of secretions. As the prostate enlarges with increasing age, patients develop obstructive symptoms and urine refluxes into the prostatic ducts. Urine reflux may also occur in patients with urethral stricture disease, voiding dysfunction, or benign prostatic hyperplasia. Refluxing urine, even when it is sterile, may lead to chemical irritation and inflammation. Tubule fibrosis is initiated, and prostatic stones form and lead to intraductal obstruction and stagnation of intraductal secretions. This obstruction initiates an inflammatory response, and prostatitis symptoms develop. A fastidious organism may cause an infection by ascending up the urethra or through reflux of infected urine into the prostatic ducts. Additionally, many men with prostatitis are also more prone to having allergies. Thus, these men may also have autoimmune-mediated inflammation caused by a preceding true infection. FrequencyUnited StatesProstatitis symptoms are very common in men aged 35-50 years. These symptoms are the most common urologic problem in men younger than 50 years and the third most common urologic problem in older men. Recent studies using the NIH Chronic Prostatitis Symptom Index (NIH-CPSI) (see Image 1) found the prevalence of prostatitis symptoms to be approximately 10% in a population of men aged 20-74 years. The most common form of prostatitis (90%) is category III, ie, chronic abacterial prostatitis and CPPS. Mortality/Morbidity
Race
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Age
CLINICALHistoryPatients with abacterial prostatitis/CPPS (category III in the 1995 NIH prostatitis classification system) have the same symptom complex as those with chronic bacterial prostatitis. The chief symptom reported in patients with abacterial prostatitis/CPPS is pain.
PhysicalIn most cases, physical examination findings are nonspecific.
Causes
DIFFERENTIALSBladder Cancer Chronic Pelvic Pain Chronic Pelvic Pain Syndrome and Prostatodynia Mycoplasma Infections Nonbacterial Prostatitis Prostatitis, Bacterial Prostatitis, Tuberculous Urethral Strictures
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| Drug Name | Trimethoprim and sulfamethoxazole (Bactrim, Septra) |
|---|---|
| Description | Trimethoprim blocks dihydrofolate reductase, and sulfamethoxazole inhibits bacterial synthesis of dihydrofolic acid by competing with para-aminobenzoic acid (PABA). These are 2 sequential steps in bacterial biosynthesis of nucleic acids and proteins. May be taken in single- or double-strength form. In adults, most commonly taken in pill form, although a liquid suspension is available. |
| Adult Dose | 80 mg TMP/400 mg SMZ PO bid |
| Pediatric Dose | <2 months: Do not administer >2 months: Not established |
| Contraindications | Documented hypersensitivity, megaloblastic anemia due to folate deficiency |
| Interactions | May increase PT when used with warfarin (perform coagulation tests and adjust dose accordingly); coadministration with dapsone may increase blood levels of both drugs; coadministration of diuretics increases incidence of thrombocytopenia purpura in elderly persons; phenytoin levels may increase with coadministration; may potentiate effects of methotrexate in bone marrow depression; hypoglycemic response to sulfonylureas may increase with coadministration; may increase levels of zidovudine, PABA, methenamine, or cyclosporin. Rarely, Stevens-Johnson syndrome, a life-threatening fulminant epidermolysis, has been related to ongoing Septra therapy |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Discontinue at first appearance of skin rash or sign of adverse reaction; obtain CBC counts frequently; discontinue therapy if significant hematologic changes occur; goiter, diuresis, and hypoglycemia may occur with sulfonamides; prolonged IV infusions or high doses may cause bone marrow depression (if signs occur, give 5-15 mg/d leucovorin); caution in folate deficiency (eg, those with chronic alcoholism, who are elderly, who are receiving anticonvulsant therapy, or with malabsorption syndrome); hemolysis may occur in those with G-6-PD deficiency; patients with AIDS may not tolerate or respond to TMP-SMZ; caution in renal or hepatic impairment (perform urinalyses and renal function tests during therapy); give fluids to prevent crystalluria and stone formation; adverse effects include stomach upset, diarrhea, nausea, vomiting, and headache; photosensitivity may occur with prolonged exposure to sunlight or tanning equipment |
| Drug Name | Levofloxacin (Levaquin) |
|---|---|
| Description | Derivative of pyridine carboxylic acid with broad-spectrum bactericidal effect. Penetrates prostate well and is effective against N gonorrhoeae and C trachomatis. |
| Adult Dose | 250-500 mg PO qd |
| Pediatric Dose | <18 years: Not recommended >18 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | Antacids, iron salts, and zinc salts may reduce serum levels; administer antacids 2-4 h before or after taking fluoroquinolones; cimetidine may interfere with metabolism of fluoroquinolones; reduces therapeutic effects of phenytoin; probenecid may increase serum concentrations; may increase toxicity of theophylline, caffeine, cyclosporine, and digoxin (monitor digoxin levels); may increase effects of anticoagulants (monitor PT), NSAIDs, sucralfate, quinapril, or live vaccines |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | In prolonged therapy, perform periodic evaluations of organ system functions (eg, renal, hepatic, hematopoietic); adjust dose in renal function impairment; superinfections may occur with prolonged or repeated antibiotic therapy; adverse effects include stomach upset, loss of appetite, diarrhea, nausea, headache, dizziness, and drowsiness; less commonly observed are sleep problems, vaginal discomfort in women, vision problems, ringing in ears, muscle/tendon pain or tenderness, generalized weakness, mental or mood changes, unsteadiness, seizures, fainting, yellowing of the skin or eyes, and easy bruising or bleeding; photosensitivity may occur with prolonged exposure to sunlight or tanning equipment |
| Drug Name | Ciprofloxacin (Cipro) |
|---|---|
| Description | Fluoroquinolone with activity against pseudomonads, streptococci, MRSA, Staphylococcus epidermidis, and most gram-negative organisms but no activity against anaerobes. Inhibits bacterial DNA synthesis and, consequently, growth. Diffuses into prostatic fluid and is indicated for the treatment of chronic prostatitis. |
| Adult Dose | 250-500 mg PO bid |
| Pediatric Dose | <18 years: Not recommended >18 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | Antacids, iron salts, and zinc salts may reduce serum levels; administer antacids 2-4 h before or after taking fluoroquinolones; cimetidine may interfere with metabolism of fluoroquinolones; reduces therapeutic effects of phenytoin; probenecid may increase serum concentrations; may increase toxicity of theophylline, caffeine, cyclosporine, and digoxin (monitor digoxin levels); may increase effects of anticoagulants (monitor PT), cyclosporin, live vaccines, probenecid, sucralfate, quinapril, and didanosine; may increase or prolong effects of caffeine |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | In prolonged therapy, perform periodic evaluations of organ system functions (eg, renal, hepatic, hematopoietic); adjust dose in renal function impairment; superinfections may occur with prolonged or repeated antibiotic therapy; adverse effects include stomach upset, loss of appetite, diarrhea, nausea, headache, or dizziness; less commonly observed are tendonitis, visual changes, restlessness, ringing in ears, or mental changes; photosensitivity may occur with prolonged exposure to sunlight or tanning equipment |
Selective alpha-1 receptor blockers relax smooth muscle in the prostate and bladder neck. Found to improve symptoms of prostatic obstruction. First choice in therapy for benign prostatic hyperplasia and can be very effective in patients with prostatitis symptoms by improving urine flow and decreasing irritative symptoms.
| Drug Name | Doxazosin (Cardura) |
|---|---|
| Description | Inhibits postsynaptic alpha-adrenergic receptors, resulting in vasodilation of veins and arterioles and decrease in total peripheral resistance and blood pressure. Has antihypertensive effects and is recommended to be given hs to prevent patient injury if syncopal episode occurs. If added to the regimen of antihypertensive medicines a patient is already taking, monitor patient's blood pressure while in titration phase. Usually started as a titration up to the effective dose. Available in a starter pack containing 1-, 2-, 4-, and 8-mg tabs. Usual effective dose is 4 or 8 mg. |
| Adult Dose | 1 mg hs for 7-14 d, titrate up to 2 mg for next 7-14 d, then up to 4 mg; reassess symptoms and maintain 4-mg dose or increase to 8 mg |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity |
| Interactions | Effects decrease with coadministration of NSAIDs; effects increase with coadministration of diuretics and antihypertensive medications |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Caution in renal impairment; may cause marked hypotension following first dose (rise slowly after lying or sitting to avoid dizziness); common adverse effects include dizziness, drowsiness, lightheadedness, headache, constipation, loss of appetite, dry mouth, fatigue, nasal congestion, blurred vision, dry eyes, or insomnia; rarely, priapism occurs; avoid alcohol or activity that may cause patient to become overheated (may increase dizziness and sedating effects) |
| Drug Name | Terazosin (Hytrin) |
|---|---|
| Description | Decreases arterial tone by allowing peripheral postsynaptic blockade. Has minimal alpha-2 effect. Antihypertensive agent and is recommended to be given hs to prevent patient injury if syncopal episode occurs. If given to a patient already on antihypertensive agents, monitor blood pressure routinely while in titration phase. Usually is titrated up to the effective dose. Available as a starter pack that has doses of 1, 2, 5, and 10 mg. Available in capsule form and cannot be broken in half easily; therefore, each specific dose must be prescribed. |
| Adult Dose | 1 mg PO for 1-2 wk, then 2 mg for PO 1-2 wk, then advanced to 5 mg; reevaluate; may need to advance to 10 mg |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; hypotension |
| Interactions | Effects decrease with coadministration of NSAIDs; effects increase with coadministration of diuretics and antihypertensive medications; decongestants can counteract antihypertensive effects |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Patients should be cautioned to rise slowly after sitting or lying to avoid dizziness or syncope; caution in renal impairment; may cause marked hypotension following first dose and with coadministration with beta-blockers; alcohol intake and overexertion should also be avoided to prevent dizziness and drowsiness; adverse effects include dizziness, drowsiness, headache, constipation, fatigue, nasal congestion, and dry eyes |
Inhibit action of cyclooxygenase, which results in decrease of prostaglandin synthesis.
| Drug Name | Ibuprofen (Motrin, Advil, Ibuprin) |
|---|---|
| Description | DOC for patients with mild to moderate pain. Inhibits inflammatory reactions and pain by decreasing prostaglandin synthesis. Also has anti-inflammatory and antipyretic properties. Available in 200-, 400-, 600-, and 800-mg doses. |
| Adult Dose | OTC: 400 mg PO tid Prostatitis: 600-800 mg PO tid |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; peptic ulcer disease, recent GI bleeding or perforation, renal insufficiency, or high risk of bleeding |
| Interactions | Coadministration with aspirin increases risk of inducing serious NSAID-related adverse effects; probenecid may increase concentrations and, possibly, toxicity of NSAIDs; may decrease effect of hydralazine, captopril, and beta-blockers; may decrease diuretic effects of furosemide and thiazides; monitor PT closely (instruct patients to watch for signs of bleeding); may increase risk of methotrexate toxicity; phenytoin levels may be increased when administered concurrently with lithium, cyclosporin, or digoxin |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus |
| Precautions | Caution in congestive heart failure, hypertension, and decreased renal and hepatic function; caution in anticoagulation abnormalities or during anticoagulant therapy; alcohol may increase risk of GI bleed; adverse effects include stomach upset, dizziness, drowsiness, and blurred vision; rarely, ringing in ears, hearing loss, or photosensitivity may occur |
Work on limbic system, thalamus, and hypothalamus, inducing a calming effect and relieving anxiety and skeletal muscle spasm.
| Drug Name | Diazepam (Valium) |
|---|---|
| Description | Depresses all levels of CNS (eg, limbic, reticular formation), possibly by increasing activity of GABA. Available as 2-, 5-, and 10-mg doses. |
| Adult Dose | 2-5 mg PO tid/qid for muscle relaxation; increase to 10 mg prn |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity, narrow-angle glaucoma |
| Interactions | Increases toxicity of benzodiazepines in CNS with coadministration of phenothiazines, barbiturates, alcohol, MAOIs, kava, and cimetidine |
| Pregnancy | D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus |
| Precautions | Use of alcohol or other sedatives in conjunction can lead to excessive drowsiness; caution with other CNS depressants, low albumin levels, or hepatic disease (may increase toxicity); smoking can decrease effectiveness; long-term use can lead to dependance; elderly persons may be more sensitive to effects; adverse effects include drowsiness, dizziness, stomach upset, blurred vision, headache, confusion, depression, impaired coordination, change in heart rate, trembling, weakness, memory loss, fatigue, and nightmares |
For symptomatic relief of pain, burning, urgency, and frequency associated with prostatitis.
| Drug Name | Pentosan polysulfate sodium (Elmiron) |
|---|---|
| Description | Heparinlike derivative of macromolecular carbohydrate that resembles glycosaminoglycans. Has anticoagulant and fibrinolytic properties. Mechanism of action is unknown but may act to prevent irritative or noxious stimuli in the bladder by inhibiting mucosal cell wall permeability. |
| Adult Dose | 100 mg PO tid |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity |
| Interactions | May increase risk of spontaneous bleeding in patients concurrently taking NSAIDs, ASA, heparin, or Coumadin |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Adverse effects include stomach upset, nausea, headache, dizziness, or diarrhea |
| Drug Name | Dimethyl sulfoxide (Rimso-50) |
|---|---|
| Description | Converted to dimethyl sulfone and dimethyl sulfide in vivo. Used intravesically to treat symptoms of interstitial cystitis. When administered intravesically, patients often complain of garliclike taste. |
| Adult Dose | 50 mL of 50% solution instilled into bladder |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Perform liver and renal function tests and CBC counts before initiating therapy and every 6 mo thereafter |
Tamsulosin is an antagonist of the alpha-1a receptor found in smooth muscle of prostate and bladder neck. Effective for relieving symptoms of prostatic enlargement.
| Drug Name | Tamsulosin (Flomax) |
|---|---|
| Description | Antagonist of alpha-1a receptor found in prostate and bladder neck. Because it is more selective than alpha-blockers (terazosin and doxazosin), does not require dose titration (has minimal, if any, effect on blood pressure). |
| Adult Dose | 0.4-0.8 mg PO qd |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity |
| Interactions | Excretion may be impaired when used in conjunction with cimetidine; has inconclusive reaction in patients using warfarin; use caution when administering |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Evaluate for prostate cancer because this may also cause prostatic obstructive symptoms |
Reduce uric acid levels. Has no analgesic or anti-inflammatory activity.
| Drug Name | Allopurinol (Zyloprim) |
|---|---|
| Description | Inhibits xanthine oxidase, the enzyme that synthesizes uric acid from hypoxanthine. Reduces synthesis of uric acid without disrupting biosynthesis of vital purines. |
| Adult Dose | 220-300 mg PO qd/bid |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity |
| Interactions | Alcohol decreases effects; increases incidence of skin rash when used concurrently with ampicillin and amoxicillin; large amounts of vitamin C acidify urine and may cause kidney stone formation; inhibits metabolism of azathioprine and mercaptopurine |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Reduce dose in renal insufficiency; monitor liver function and perform CBC counts before initiating therapy and periodically thereafter; caution in pregnancy or breastfeeding; adverse effects include drowsiness, stomach upset, nausea, diarrhea, vomiting, and headache |
Pollen (male flower microspore) enables plant reproduction. Produced in anthers of the flower. May have effects on inflammatory response.
| Drug Name | Cernitin pollen extract (Cernilton, Cervital) |
|---|---|
| Description | May have anti-inflammatory activity. |
| Adult Dose | 1 tab PO tid for 6 mo for symptom improvement |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Rare reports of stomach upset and skin rash |
Helpful in relieving discomfort associated with tonically contracted muscles.
| Drug Name | Methocarbamol (Robaxin) |
|---|---|
| Description | Reduces nerve impulse transmission from spinal cord to skeletal muscle |
| Adult Dose | 1.5 g PO qid for 2-3 d; then decrease to 4-4.5 g/d in 3-6 divided doses |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; renal impairment |
| Interactions | Increases toxicity of CNS depressants |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Caution in history of seizures |
| Drug Name | Cyclobenzaprine (Flexeril) |
|---|---|
| Description | Skeletal muscle relaxant that acts centrally and reduces motor activity of tonic somatic origins, influencing both alpha and gamma motor neurons. Structurally related to tricyclic antidepressants and thus carries some same liabilities. |
| Adult Dose | 20-40 mg/d PO divided bid/qid; not to exceed 60 mg/d |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; MAOIs within 14 d |
| Interactions | Coadministration with MAOIs and tricyclic antidepressants may increase toxicity; may have additive effect when used concurrently with anticholinergics; effects of alcohol, CNS depressants, and barbiturates may be enhanced |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Caution in angle-closure glaucoma and urinary hesitancy |
Used for treatment of overactive bladder to prevent associated symptoms of urinary frequency, urgency, and incontinence.
| Drug Name | Tolterodine tartrate (Detrol) |
|---|---|
| Description | Competitive muscarinic receptor antagonist for overactive bladder. Differs from other anticholinergic types in that it has selectivity for urinary bladder over salivary glands. Exhibits high specificity for muscarinic receptors and has minimal activity or affinity for other neurotransmitter receptors and other potential targets, such as calcium channels. |
| Adult Dose | 2 mg PO bid; reduce to 1 mg bid if patient does not tolerate medication well |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; urinary retention, gastric retention, or uncontrolled narrow-angle glaucoma |
| Interactions | Patients being treated with macrolide antibiotics or antifungal agents should not receive doses of tolterodine higher than 1 mg bid |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Do not give doses > 1 mg bid to patients with significantly reduced hepatic function; caution in renal impairment |
For additional information, see Medscape’s Prostatitis Resource Center
| Media file 1: Nonbacterial prostatitis. National Institutes of Health Chronic Prostatitis Symptom Index. | |
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| Media file 2: Nonbacterial prostatitis. Comparison of new and old prostatitis classifications. | |
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| Media file 3: Treatment algorithm for nonbacterial prostatitis. | |
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Nonbacterial Prostatitis excerpt
Article Last Updated: Mar 18, 2008