Evidence-Based Medicine

Acute Bacterial Prostatitis

Acute Bacterial Prostatitis

Background

  • Acute bacterial prostatitis is a bacterial infection of the prostate gland typically causing acute pelvic pain and urinary tract symptoms.
  • Up to 16% of men have prostatitis during their lifetime and of those up to 10% are diagnosed with acute bacterial prostatitis.
  • Most cases of acute bacterial prostatitis are due to uropathogens, most commonly Escherichia coli.
  • In nosocomial-acquired infections, organisms such as Pseudomonas aeruginosa and enterococci are also common.
  • Risk factors include urinary tract manipulation such as catheterization, cystoscopy, prostate biopsy, prostate surgery, anatomic abnormalities such as benign prostatic hypertrophy, high-risk sexual behaviors, and immunocompromise.

Evaluation

  • Diagnosis of bacterial prostatitis is made clinically based on acute onset of:
    • irritative urinary tract symptoms such as dysuria, frequency, and urgency.
    • obstructive urinary tract symptoms such as straining, hesitancy, weak stream, incomplete voiding, or urinary retention.
    • fever and other signs of systemic illness.
    • suprapubic, perineal, rectal, and/or genital pain.
    • tender and enlarged prostate on digital rectal exam (do not perform prostate massage).
  • Obtain midstream urine for urinalysis and urine culture.
    • Urinalysis may support an early diagnosis and culture should identify a bacterial cause and guide any change in the antibiotic choice.
    • Consider a urine Gram stain to guide the initial therapy while awaiting the culture results.
  • Consider a complete blood count and a blood culture if the patient has systemic symptoms or bacteremia is suspected (Weak recommendation).
  • The Prostatic-specific antigen (PSA) should not be performed in the acute setting. It will likely be elevated and is not a recommended test for the diagnosis of prostatitis.
  • Imaging is typically reserved for when an abscess is suspected (poor response to antibiotic therapy) or when signs of urinary retention are present.

Management

  • If the patient is unable to urinate and is in urinary retention, indwelling, intermittent, or suprapubic catheterization may be necessary.
  • Empiric choice of antibiotic is based on the ability of an antibiotic to penetrate the prostate, the suspected pathogen, and the local antibiotic resistance patterns.
    • For uncomplicated cases, common options include either of:
      • a fluoroquinolone, if local resistance is known to be < 10% (for example, ciprofloxacin 500 mg orally twice daily or levofloxacin 500 mg orally once daily)
      • co-trimoxazole (trimethoprim/sulfamethoxazole) 160 mg/800 mg orally twice daily
    • For patients at risk for sexually transmitted infection, combination therapy with coverage for Neisseria gonorrhoeae and Chlamydia trachomatis is appropriate. (See Gonococcal Urethritis and Chlamydia Genital Infection for additional information.)
    • For hospitalized patients:
      • For patients who do not have risk factors for antibiotic resistance and are not severely ill, options include::
        • ceftriaxone 1-2 g IV every 24 hours plus levofloxacin 500-750 mg IV every 24 hours
        • piperacillin/tazobactam 3.375 g IV every 6 hours
        • a fluoroquinolone (for example, ciprofloxacin 400 mg IV every 12 hours or levofloxacin 500-750 mg IV every 24 hours); however, the European Association of Urology (EAU) recommends against fluoroquinolone monotherapy in hospitalized patients with acute prostatitis
      • For patients who do not have risk factors for antibiotic resistance and are severely ill:
        • Preferred regimens include any of:
          • piperacillin/tazobactam 3.375 g IV every 6 hours plus aminoglycosides
          • cefotaxime 2 g IV every 4 hours plus aminoglycosides
          • ceftazidime 2 g IV every 8 hours plus aminoglycosides
        • Alternative regimens include a fluoroquinolone plus an aminoglycosides or a carbapenem.
      • For patients of any severity with risk factors for antibiotic resistance:
        • For patients with prior fluoroquinolone use or known fluoroquinolone resistance rates > 10%:
          • Preferred regimens include piperacillin/tazobactam 3.375 g IV every 6 hours, ceftazidime 2 g IV every 8 hours, or cefepime 2 g IV every 12 hours, with the addition of an aminoglycoside if the patient is clinically unstable.
          • Alternative regimens include ceftriaxone 1 g IV every 24 hours (plus an aminoglycosides if the patient is clinically unstable) or ertapenem 1 g IV every 24 hours.
        • For patients with transurethral or transrectal manipulation and risk of:
          • extended spectrum beta-lactamase-producing Escherichia coli, see Extended Spectrum Beta-Lactamases (ESBLs) for details on empiric antibiotic options.
          • Pseudomonas species infection:
            • preferred regimens include piperacillin/tazobactam 3.375 g IV every 6 hours, ceftazidime 2 g IV every 8 hours, or cefepime 2 g IV every 12 hours, with the addition of an aminoglycoside if the patient is clinically unstable
            • alternative regimens include imipenem/cilastatin 500 mg IV every 6 hours or meropenem 500 mg IV every 8 hours
          • fluoroquinolone resistance, see above for preferred regimens.
    • Consider the addition of vancomycin or ampicillin if the patient's history or urine Gram stain (gram-positive) suggests enterococci.
    • Empiric coverage for methicillin-resistant Staphylococcus aureus or vancomycin-resistant enterococci may be appropriate based on the patient's history or prior microbiologic data.
    • Adjust antibiotics based on culture results.
  • Antibiotics are usually given for 10-14 days, but 4-6 weeks may be needed based on the response to treatment and the severity of disease.
  • For patients having IV therapy, transition to an oral antibiotic regimen after clinical improvement and continue therapy to complete 2-6 weeks.
  • Supportive care may include nonsteroidal anti-inflammatory drugs (NSAIDs) for pain and alpha-1 blockers (such as tamsulosin) for lower urinary tract symptoms, but no evidence specific to use in prostatitis.
  • Consider an evaluation for a prostatic abscess or an anatomic abnormality for persistent symptoms or recurrence.

Published: 25-06-2023 Updeted: 25-06-2023

References

  1. Coker TJ, Dierfeldt DM. Acute Bacterial Prostatitis: Diagnosis and Management. Am Fam Physician. 2016 Jan 15;93(2):114-20
  2. Brede CM, Shoskes DA. The etiology and management of acute prostatitis. Nat Rev Urol. 2011 Apr;8(4):207-212
  3. Bonkat G, Bartoletti RR, Bruyère F, et al; European Association of Urology. Guidelines on urological infections. EAU 2023 (PDF)
  4. Wagenlehner FM, Pilatz A, Bschleipfer T, et al. Bacterial prostatitis. World J Urol. 2013 Aug;31(4):711-6
  5. Lipsky BA, Byren I, Hoey CT. Treatment of bacterial prostatitis. Clin Infect Dis. 2010 Jun 15;50(12):1641-52, commentary can be found in Clin Infect Dis 2011 Dec;53(12):1306

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