eMedicine Specialties > Urology > Infections and Related Inflammatory Conditions

Prostatitis, Bacterial: Treatment & Medication

Author: Joe D Mobley III, MD, MPH, Chief Resident Physician, Department of Surgery, Division of Urology, University of Tennessee Graduate School of Medicine/University of Tennessee Medical Center
Coauthor(s): 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
Contributor Information and Disclosures

Updated: Oct 8, 2009

Treatment

Medical Care

The mainstay in the treatment of chronic bacterial prostatitis is the use of oral antimicrobial agents. The most effective medications are fluoroquinolones and TMP-SMZ.

All other oral agents are unlikely to eradicate the pathogenic bacteria successfully within the prostate because of suboptimal tissue penetration. Longer courses of antibiotic use provide better treatment outcomes. Relapse is not uncommon.

  • Relapsing urinary tract infections are due to poor penetration of most antimicrobial agents into the prostatic fluid and/or bacterial sequestration, which protects bacteria from antimicrobial exposure. Only small-molecular–sized, unionized, lipid-soluble drugs that are not firmly bound to plasma proteins are able to penetrate the epithelial membrane.
  • Antimicrobial agents that most effectively penetrate into the prostatic fluid, such as fluoroquinolones and TMP-SMZ, are good treatment choices for chronic bacterial prostatitis.
  • Treatment should be guided by urine culture results. Failure of an initial course of therapy (typically about 4 wk) should prompt longer courses of treatment. Best results have been observed with a 12-week course of therapy, although patient compliance may be difficult with longer durations of treatment.
  • High bactericidal activity has been demonstrated against the Enterobacteriaceae group of bacteria and P aeruginosa using fluoroquinolones, a class of antimicrobial agents that inhibits bacterial DNA replication and protein synthesis.
  • Fluoroquinolones are generally ineffective against the streptococci, including enterococcus, and anaerobes. Penicillin derivatives, while effective against gram-positive organisms, are generally ineffective in treating bacterial prostatitis because of poor prostate penetration.
  • While zinc supplements have been suggested as a medical therapy, clinical results have not been significant. A zinc-containing polypeptide called prostatic antibacterial factor (PAF) may be an important antimicrobial factor within the prostate.
  • Prostate fluid is also rich in spermine, which has activity against gram-positive bacteria. Other factors of potential importance in prostate fluid include magnesium, calcium, and lysozyme. Other local immune factors are also under investigation.
  • Barbalias et al (1998) suggested that the use of alpha-blockers in combination with fluoroquinolones would offer significantly superior symptom resolution and bacteriologic cure rates compared with fluoroquinolone treatment alone.6 Further study is necessary to define the benefit of the addition of alpha-blocker therapy.
  • Nonsteroidal anti-inflammatory agents and hot sitz baths are often used clinically for symptomatic relief. However, their benefit in bacteriologic eradication of organisms is not established. Frequent prostate massage was used extensively several decades ago and its use is still advocated by some in the treatment of difficult cases with persistent positive cultures despite appropriate antibiotic therapy.
  • Tetracycline, minocycline, and doxycycline have also been used. They are not considered first-line therapy but may be helpful if Pseudomonas infection is present. Paulson and White (1978) reported a 70% bacteriologic cure rate with 4 weeks of minocycline, but the study involved only 10 men, and 30% developed significant vestibular toxicity.7 More recent studies indicate a 35% bacteriologic cure rate with minocycline.
  • Penicillins are ineffective, with the exception of carbenicillin indanyl sodium at 500 mg/d. Carbenicillin may be effective for Enterobacteriaceae or Pseudomonas infections. Large-scale studies are not available.
  • Preliminary findings suggest that antinanobacterial therapy improves symptoms and decreases or eliminates prostatic calculi in patients with chronic bacterial prostatitis that is recalcitrant to standard therapy. Further investigation is needed.
  • A recent study in rats found that garlic was superior to placebo in terms of anti-inflammatory and antimicrobial effect. This study also demonstrated a statistically significant synergistic effect of ciprofloxacin plus garlic compared with ciprofloxacin alone. Studies in humans are needed to determine if these effects would translate into a clinical setting.8

Surgical Care

Prostatectomy is rarely indicated in the treatment of chronic bacterial prostatitis. When used, radical transurethral prostatectomy is suggested. This procedure may be more effective in men with prostatic calculi. Because most of the inflammation is located in the peripheral zone of the gland, an extensive resection of the gland is required to remove all infected and potentially infected tissue down to the level of the true prostatic capsule.

Only one series of 10 patients, most with prostatic calculi, has been reported, but all men were considered cured.9 This procedure is indicated, although only rarely, in men with well-documented bacterial infections in whom medical pharmacotherapy fails for one year.

For refractory cases, other authorities have suggested that transurethral microwave therapy to ablate prostate tissue has shown some benefit.10 At this time, this intervention should be considered only in patients who have failed less-invasive therapies yet do not desire radical transurethral prostatectomy. Larger series would be helpful to define the benefit of this procedure.

Intraprostatic injection of antimicrobial agents is suggested to obtain high concentrations of antimicrobial agents in the prostatic parenchyma. Plomp et al (1980) noted a 66% bacteriologic cure rate with thiamphenicol in 29 men.11 Jiminez-Cruz et al (1988) noted a 59% cure rate with aminoglycoside injection in 51 men.12 Unfortunately, these studies have significant methodological flaws, so the conclusions cannot be considered definitive. This technique is rarely used.

Consultations

Consultation with a urologist may be appropriate for men with relapsing chronic bacterial prostatitis or when the diagnosis is unclear. A urologist may be able to properly perform the bacterial localization studies necessary to diagnose chronic bacterial prostatitis. In the author's experience, most primary care physicians are not comfortable or experienced with obtaining VB1, VB2, EPS, and VB3 specimens. Semen cultures or urine cultures collected before and following prostatic massage are simpler and represent effective alternatives to the 3-cup test.

Diet

Diet does not have an important role in treating chronic bacterial prostatitis. Some physicians have advocated the avoidance of spicy and caffeine-containing foods; however, no evidence has indicated any benefit in chronic bacterial prostatitis.

Activity

  • Activity changes do not have a prominent role in the treatment of chronic bacterial prostatitis, although the authors often advise patients to avoid bicycling or other activities that may put pressure on the perineal region.
  • The role of ejaculation in the treatment of chronic bacterial prostatitis is unknown. One theory is that frequent ejaculation may help clear prostatitic secretions, thereby allowing for quicker resolution.

Medication

The goals of pharmacotherapy are to treat the infection and to reduce morbidity.

Antibiotics

Empiric antimicrobial therapy must be comprehensive and should cover all likely pathogens in the context of the clinical setting. Fluoroquinolones are frequently used because they are able to concentrate in the prostate and are lipid soluble. Sulfonamides are also used because they are lipid-soluble.


Ciprofloxacin (Cipro)

Bactericidal antibiotic that inhibits bacterial DNA synthesis, and consequently growth, by inhibiting DNA-gyrase in susceptible organisms.

Adult

500 mg PO bid for 4 wk

Pediatric

<18 years: Not recommended
>18 years: Administer as in adults

Cimetidine may interfere with the metabolism of fluoroquinolones and reduce the therapeutic effects of phenytoin; probenecid may significantly increase ciprofloxacin serum concentrations; ciprofloxacin may increase theophylline and caffeine concentrations and prolong their duration of action; ciprofloxacin may also increase the nephrotoxic effects of cyclosporine; digoxin serum levels may be increased when used concurrently with ciprofloxacin, monitor digoxin levels; may increase the effects of anticoagulants (monitor prothrombin time)

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

May cause arthropathy in children from cartilage destruction; absorption is decreased in presence of divalent cations (Ca, Mg, Fe, Zn), avoid concurrent intake of milk, antacids, and multivitamins; phototoxicity, pseudomembranous colitis, and cataracts have been reported; adjust the dose in patients with impaired renal or liver function


Ofloxacin (Floxin)

Penetrates the prostate well and is effective against Neisseria gonorrhea and C trachomatis.

Adult

400 mg PO bid

Pediatric

<18 y: Not recommended
>18 y: Administer as in adults

Antacids, iron salts, and zinc salts may interfere with GI absorption of the fluoroquinolones, resulting in decreased serum levels; administer antacids 2-4 h before or after the fluoroquinolone; cimetidine may interfere with the metabolism of fluoroquinolones; ofloxacin may reduce the therapeutic effects of phenytoin; probenecid may reduce ofloxacin renal clearance by 50% and increase serum concentration by 50%; ofloxacin may increase theophylline and caffeine concentrations, prolonging their duration of action; may increase the nephrotoxic effect of cyclosporine; digoxin serum levels may be increased when used concurrently with ofloxacin (monitor digoxin levels); may increase the effects of anticoagulants (monitor prothrombin time)

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

May cause arthropathy in children from cartilage destruction; absorption is decreased in the presence of divalent cations (Ca, Mg, Fe, Zn), avoid concurrent intake of milk, antacids, and multivitamins; phototoxicity, pseudomembranous colitis, and cataracts have been described; adjust dose in patients with impaired renal or liver function, monitor patients


Levofloxacin (Levaquin)

Indicated for pseudomonal infections and those that are due to multidrug-resistant gram-negative organisms.

Adult

250-500 mg PO qd

Pediatric

<18 years: Not recommended
>18 years: Administer as in adults

Antacids, iron salts, and zinc salts may interfere with GI absorption of the fluoroquinolones, resulting in decreased serum levels; administer antacids 2-4 hours before or after the fluoroquinolone; cimetidine may interfere with the elimination of the fluoroquinolones; levofloxacin may reduce phenytoin serum levels, producing a decrease in therapeutic effects; probenecid may reduce levofloxacin renal clearance and significantly increase serum concentrations; total body clearance of caffeine is reduced, possibly resulting in increased pharmacologic effects; levofloxacin may increase the nephrotoxic effect of cyclosporine; digoxin serum levels may be increased when used concurrently with levofloxacin (monitor digoxin levels); levofloxacin may increase the effects of anticoagulants (monitor prothrombin time)

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

May cause arthropathy in children from cartilage destruction; absorption is decreased in the presence of divalent cations (Ca, Mg, Fe, Zn), avoid concurrent intake of milk, antacids, and multivitamins; phototoxicity, pseudomembranous colitis, and cataracts have been described; adjust dose in patients with impaired renal or liver function, monitor patients


Trimethoprim-sulfamethoxazole (TMP-SMZ, Bactrim)

Inhibits bacterial synthesis of dihydrofolic acid by competing with para -aminobenzoic acid. This results in the inhibition of bacterial growth.

Adult

1 double-strength tab (160 mg TMP/800 mg SMZ) PO bid for 4 wk

Pediatric

20 mg TMP/kg/d IV divided bid

May increase the prothrombin time with warfarin (monitor coagulation tests and adjust dose as necessary); increased serum levels of dapsone and TMP may occur when medications are administered concomitantly; in elderly patients, the incidence of thrombocytopenia purpura may increase when used concurrently with diuretics; the hepatic clearance of phenytoin may be decreased and its half-life prolonged when administered concurrently with TMP-SMZ; sulfonamides can displace methotrexate (MTX) from plasma protein-binding sites, increasing free MTX concentrations; this may potentiate MTX effects in bone marrow depression; the hypoglycemic response of sulfonylureas may be increased with the concurrent administration of both medications; may decrease the renal clearance of zidovudine, increasing zidovudine levels

Documented hypersensitivity; porphyria; megaloblastic anemia due to folate deficiency; age <2 mo

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 the drug upon the first appearance of skin rash or any sign of adverse reaction; obtain CBC counts frequently; if a significant reduction in the count of any formed blood element is noted, discontinue therapy; goiter production, diuresis, and hypoglycemia may occur in patients receiving sulfonamides; high IV doses or prolonged infusions may cause bone marrow depression manifested as thrombocytopenia, leukopenia, or megaloblastic anemia
Exercise caution in patients with possible folate deficiency, (eg, people with chronic alcoholism, elderly people, those receiving anticonvulsant therapy, people who have malabsorption syndrome); hemolysis may occur in individuals who are G-6-PD deficient; upon signs of bone marrow depression, administer leucovorin as needed to restore normal hematopoiesis (oral leucovorin, 5-15 mg/d has been recommended); because of their unique immune dysfunction, patients with AIDS may not tolerate or respond to TMP-SMZ; use with caution in patients diagnosed with renal or hepatic impairment; administer adequate fluid to prevent crystalluria and stone formation; perform urinalyses and renal function tests during therapy

More on Prostatitis, Bacterial

Overview: Prostatitis, Bacterial
Differential Diagnoses & Workup: Prostatitis, Bacterial
Treatment & Medication: Prostatitis, Bacterial
Follow-up: Prostatitis, Bacterial
Multimedia: Prostatitis, Bacterial
References
Further Reading

References

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  2. Wood HM, Shoskes DA. The role of nanobacteria in urologic disease. World J Urol. Feb 2006;24(1):51-4. [Medline].

  3. NIH Summary Statement. NIDDK Workshop on Chronic Prostatitis, Bethesda, Md. December 1995.

  4. Meares EM, Stamey TA. Bacteriologic localization patterns in bacterial prostatitis and urethritis. Invest Urol. Mar 1968;5(5):492-518. [Medline].

  5. Magri V, Wagenlehner FM, Montanari E, Marras E, Orlandi V, Restelli A, et al. Semen analysis in chronic bacterial prostatitis: diagnostic and therapeutic implications. Asian J Androl. Jul 2009;11(4):461-77. [Medline].

  6. Barbalias GA, Nikiforidis G, Liatsikos EN. Alpha-blockers for the treatment of chronic prostatitis in combination with antibiotics. J Urol. Mar 1998;159(3):883-7. [Medline].

  7. Paulson DF, White RD. Trimethoprium-sulfamethoxazole and minocycline- hydrochloride in the treatment of culture-proved bacterial prostatitis. J Urol. Aug 1978;120(2):184-5. [Medline].

  8. Sohn DW, Han CH, Jung YS, Kim SI, Kim SW, Cho YH. Anti-inflammatory and antimicrobial effects of garlic and synergistic effect between garlic and ciprofloxacin in a chronic bacterial prostatitis rat model. Int J Antimicrob Agents. Sep 2009;34(3):215-9. [Medline].

  9. Meares ET. Chronic bacterial prostatitis: role of transurethral prostatectomy (TURP) in therapy. In: Schmiedt E, Alken JE, Bauer HW, eds. Therapy of prostatitis. Munich, Germany: Zuckerschwerdt Verlag; 1986:193-197.

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  11. Plomp TA, Baert L, Maes RA. Treatment of recurrent chronic bacterial prostatitis by local injection of thiamphenicol into prostate. Urology. Jun 1980;15(6):542-7. [Medline].

  12. Jiménez-Cruz JF, Tormo FB, Gómez JG. Treatment of chronic prostatitis: intraprostatic antibiotic injections under echography control. J Urol. May 1988;139(5):967-70. [Medline].

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  29. Shoskes DA, Thomas KD, Gomez E. Anti-nanobacterial therapy for men with chronic prostatitis/chronic pelvic pain syndrome and prostatic stones: preliminary experience. J Urol. Feb 2005;173(2):474-7. [Medline].

  30. Stamey TA, Meares EM Jr, Winningham DG. Chronic bacterial prostatitis and the diffusion of drugs into prostatic fluid. J Urol. Feb 1970;103(2):187-94. [Medline].

  31. Wagenlehner FM, Naber KG. Fluoroquinolone antimicrobial agents in the treatment of prostatitis and recurrent urinary tract infections in men. Curr Urol Rep. Aug 2004;5(4):309-16. [Medline].

  32. Wiygul RD. Prostatitis: epidemiology of inflammation. Curr Urol Rep. Jul 2005;6(4):282-9. [Medline].

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Further Reading

For additional information, see Medscape’s Prostatitis Resource Center.

Keywords

chronic urinary tract infections, UTI, acute bacterial prostatitis, chronic bacterial prostatitis, chronic abacterial prostatitis, asymptomatic inflammatory prostatitis, nonbacterial prostatitis, chronic pelvic pain syndrome, CPPS, prostatodynia, asymptomatic bacteriuria, dysuria, ascending urethral infection, gonococcal prostatitis, intraprostatic urinary reflux

Contributor Information and Disclosures

Author

Joe D Mobley III, MD, MPH, Chief Resident Physician, Department of Surgery, Division of Urology, University of Tennessee Graduate School of Medicine/University of Tennessee Medical Center
Joe D Mobley III, MD, MPH is a member of the following medical societies: American College of Surgeons, American Medical Association, American Urological Association, Endourological Society, and Tennessee Medical Association
Disclosure: Nothing to disclose.

Coauthor(s)

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
Edward David Kim, MD, FACS is a member of the following medical societies: American College of Surgeons, American Society for Reproductive Medicine, American Society of Andrology, American Urological Association, and Tennessee Medical Association
Disclosure: Lilly Consulting fee Consulting; Astellas Consulting fee Speaking and teaching; Indevus Consulting fee Speaking and teaching

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

Managing Editor

Shlomo Raz, MD, Professor, Department of Surgery, Division of Urology, University of California at Los Angeles School of Medicine
Shlomo Raz, MD is a member of the following medical societies: American College of Surgeons, American Medical Association, American Urological Association, and California Medical Association
Disclosure: Nothing to disclose.

CME Editor

J Stuart Wolf Jr, MD, FACS, David A Bloom Professor of Urology, Director of Division of Minimally Invasive Urology, Department of Urology, University of Michigan
J Stuart Wolf Jr, MD, FACS is a member of the following medical societies: American College of Surgeons, American Urological Association, Catholic Medical Association, Endourological Society, Society for Urology and Engineering, Society of Laparoendoscopic Surgeons, Society of University Urologists, and Society of Urologic Oncology
Disclosure: Terumo Corporation Consulting fee Consulting; Gyrus-ACMI Honoraria Speaking and teaching

Chief Editor

Bradley Fields Schwartz, DO, FACS, Professor of Urology, Director, Center for Laparoscopy and Endourology, Department of Surgery, Southern Illinois University School of Medicine
Bradley Fields Schwartz, DO, FACS is a member of the following medical societies: American College of Surgeons, American Urological Association, Association of Military Osteopathic Physicians and Surgeons, Endourological Society, Society of Laparoendoscopic Surgeons, and Society of University Urologists
Disclosure: Nothing to disclose.

 
 
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