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Prostatitis treatments depend on the underlying cause. They can include:

  • Antibiotics. Taking antibiotics is the most commonly prescribed treatment for prostatitis. Your doctor will choose your medication based on the type of bacteria that might be causing your infection.

    If you have severe symptoms, you might need intravenous (IV) antibiotics. You'll likely need to take oral antibiotics for four to six weeks but might need longer treatment for chronic or recurring prostatitis.

  • Alpha blockers. These medications help relax the bladder neck and the muscle fibers where your prostate joins your bladder. This treatment might ease symptoms, such as painful urination.
  • Anti-inflammatory agents. Nonsteroidal anti-inflammatory drugs (NSAIDs) might make you more comfortable.

Acute bacterial prostatitis is an acute infection of the prostate gland that causes pelvic pain and urinary tract symptoms, such as dysuria, urinary frequency, and urinary retention, and may lead to systemic symptoms, such as fevers, chills, nausea, emesis, and malaise. Although the true incidence is unknown, acute bacterial prostatitis is estimated to comprise approximately 10% of all cases of prostatitis. Most acute bacterial prostatitis infections are community acquired, but some occur after transurethral manipulation procedures, such as urethral catheterization and cystoscopy, or after transrectal prostate biopsy. The physical examination should include abdominal, genital, and digital rectal examination to assess for a tender, enlarged, or boggy prostate. Diagnosis is predominantly made based on history and physical examination, but may be aided by urinalysis. Urine cultures should be obtained in all patients who are suspected of having acute bacterial prostatitis to determine the responsible bacteria and its antibiotic sensitivity pattern. Additional laboratory studies can be obtained based on risk factors and severity of illness. Radiography is typically unnecessary. Most patients can be treated as outpatients with oral antibiotics and supportive measures. Hospitalization and broad-spectrum intravenous antibiotics should be considered in patients who are systemically ill, unable to voluntarily urinate, unable to tolerate oral intake, or have risk factors for antibiotic resistance. Typical antibiotic regimens include ceftriaxone and doxycycline, ciprofloxacin, and piperacillin/tazobactam. The risk of nosocomial bacterial prostatitis can be reduced by using antibiotics, such as ciprofloxacin, before transrectal prostate biopsy.

Acute bacterial prostatitis is an acute infection of the prostate gland that causes urinary tract symptoms and pelvic pain in men.1 It is estimated to comprise up to 10% of all prostatitis diagnoses, and its incidence peaks in persons 20 to 40 years of age and in persons older than 70 years.2 Most cases can be diagnosed with a convincing history and physical examination.3 Although prostatitis-like symptoms have a combined prevalence of 8.2% in men, the incidence and prevalence of acute bacterial prostatitis are unknown.4

SORT: KEY RECOMMENDATIONS FOR PRACTICE

CLINICAL RECOMMENDATION EVIDENCE RATING REFERENCES COMMENTS

Prostatic massage should be avoided in patients suspected of having acute bacterial prostatitis.

C

11, 12, 20, 22

 

Expert consensus

Midstream urine culture should be used to guide antibiotic therapy for acute bacterial prostatitis.

C

3, 10, 11

Prospective cohort study, retrospective cohort study

Blood cultures are indicated in patients with a body temperature greater than 101.1°F (38.4°C), a possible hematogenous source of infection (e.g., endocarditis with Staphylococcus aureus), or complicated infections (e.g., sepsis), and in patients who are immunocompromised.

C

21

Prospective cohort study

Prostate-specific antigen testing is not indicated in the evaluation of acute bacterial prostatitis.

C

11, 12, 20

Prospective cohort study

Fevers that persist for longer than 36 hours should be evaluated with imaging to rule out prostatic abscess.

C

27

Expert opinion

Acute bacterial prostatitis occurring after a transrectal prostate biopsy should be treated with broad-spectrum antibiotics to cover fluoroquinolone-resistant bacteria and extended spectrum beta-lactamase–producing Escherichia coli.

C

15–18, 24

Multiple retrospective cohort studies and one prospective cohort study


Most cases of acute bacterial prostatitis are caused by ascending urethral infection or intraprostatic reflux and are facilitated by numerous risk factors (Table 1).4–10 These infections may occur from direct inoculation after transrectal prostate biopsy and transurethral manipulations (e.g., catheterization and cystoscopy).6–8 Occasionally, direct or lymphatic spread from the rectum or hematogenous spread via bacterial sepsis can cause acute bacterial prostatitis.11 Overall, community-acquired infections are three times more common than nosocomial infections.3

Table 1.

Risk Factors for Acute Bacterial Prostatitis

Benign prostatic hypertrophy*

Genitourinary infections*

Epididymitis

Orchitis

Urethritis

Urinary tract infection

High-risk sexual behavior

History of sexually transmitted diseases*

Immunocompromised

Phimosis

Prostate manipulation*

Cystoscopy

Transrectal prostate biopsy

Transurethral surgery

Urethral catheterization

Urodynamic studies

Urethral stricture


*—Higher risk for infection.

Information from references 4 through 10.

Microbiology

Acute bacterial prostatitis is most frequently caused by Escherichia coli, followed by Pseudomonas aeruginosa, and Klebsiella, Enterococcus, Enterobacter, Proteus, and Serratia species.3,5,7,10 In sexually active men, Neisseria gonorrhoeae and Chlamydia trachomatis should be considered.12 Patients who are immunocompromised (e.g., persons with human immunodeficiency virus) are more likely to have uncommon causes for prostatitis, such as Salmonella, Candida, and Cryptococcus species (Table 2).3,7,10,12

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Table 2.

Pathogens in Acute Prostatitis

COMMON* UNCOMMON

Escherichia coli (> 50% of cases)

Chlamydia trachomatis

Pseudomonas aeruginosa

Fungi (Aspergillus, Candida, Cryptococcus, and Histoplasma species)

Klebsiella species

Mycobacterium tuberculosis

Enterococcus species

Mycoplasma genitalium

Enterobacter species

Neisseria gonorrhoeae

Proteus species

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Salmonella species

Serratia species

Staphylococcus species

Streptococcus species

Trichomonas vaginalis

Ureaplasma urealyticum


*—Listed in approximate order of frequency.

Information from references 3, 7, 10, and 12.

Infections that occur after transurethral manipulation are more likely to be caused by Pseudomonas species, which have higher rates of resistance to cephalosporins and carbapenems.7 Transrectal prostate biopsies can cause postoperative infections. Perioperative antibiotics have reduced the rates of postoperative prostatitis to between 0.67% and 2.10% of cases, but have increased the incidence of prostatitis caused by fluoroquinolone-resistant bacteria and extended spectrum beta-lactamase–producing E. coli.13–18

Clinical Presentation

Patients with acute bacterial prostatitis often present with acute onset of irritative (e.g., dysuria, urinary frequency, urinary urgency) or obstructive (e.g., hesitancy, incomplete voiding, straining to urinate, weak stream) voiding symptoms. Patients may report suprapubic, rectal, or perineal pain.6,9,11 Painful ejaculation, hematospermia, and painful defecation may be present as well.19 Systemic symptoms, such as fever, chills, nausea, emesis, and malaise, commonly occur, and their presence should prompt physicians to determine if patients meet clinical criteria for sepsis.

The physical examination should include an abdominal examination to detect a distended bladder and costovertebral angle tenderness, a genital examination, and a digital rectal examination. A digital rectal examination should be performed gently because vigorous prostatic massage can induce bacteremia, and subsequently, sepsis.9,11,20 In a patient with acute bacterial prostatitis, the prostate will often be tender, enlarged, or boggy. If there is concern for obstructed voiding, postvoid residual urine volumes should be measured using ultrasonography.

Several conditions present with similar symptoms and must be differentiated from acute bacterial prostatitis (Table 3).

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Table 3.

Differential Diagnosis of Acute Bacterial Prostatitis

DIAGNOSIS DISTINGUISHING CHARACTERISTICS

Benign prostatic hypertrophy

Obstructive voiding symptoms; enlarged, nontender prostate; negative urine culture

Chronic bacterial prostatitis

Recurring prostatitis symptoms for at least three months; positive urine culture with each episode

Chronic pelvic pain syndrome

WATER PENIS EXTENDER

Pain attributed to the prostate with no demonstrable evidence of infection

Cystitis

Irritative voiding symptoms; normal prostate examination

Diverticulitis

Left lower-quadrant abdominal pain; acute change in bowel habits; history of diverticulitis; tenderness to palpation localized to the left lower abdominal quadrant

Epididymitis

Irritative voiding symptoms; tenderness to palpation on affected epididymis

Orchitis

Swelling, pain, and/or tenderness to palpation in one or both testicles

Proctitis

Tenesmus; rectal bleeding; feeling of rectal fullness; passage of mucus through the rectum

Prostate cancer

Presence of constitutional symptoms; presence of nodules on prostate examination

Evaluation

A convincing history and physical examination are typically sufficient to diagnose acute bacterial prostatitis. Physicians should obtain a urinalysis and midstream urine culture to support the clinical diagnosis before administering antibiotics.3,10,11

Blood cultures should be collected before initiating antibiotics in patients with a body temperature greater than 101.1°F (38.4°C), a possible hematogenous source of infection (e.g., endocarditis with Staphylococcus aureus), complicated infections (e.g., sepsis), or who are immunocompromised.11,21 Although blood and urine cultures can aid in diagnosis and management, up to 35% of urine cultures in patients with acute prostatitis will fail to grow an organism.3

In men younger than 35 years who are sexually active, and in men older than 35 years who engage in high-risk sexual behavior, a Gram stain of urethral swabs, a culture of urethral discharge, or a DNA amplification test should be obtained to evaluate for N. gonorrhoeae and C. trachomatis.11,22

Urine testing before and after prostatic massage (also known as the Meares-Stamey 2-glass or 4-glass test) is useful in diagnosing chronic prostate and pelvic disorders; however, such testing should not be performed in patients with suspected acute bacterial prostatitis because prostatic massage increases the risk of bacteremia, and subsequently, sepsis.

PROGNOSTIC FACTORS

A 2014 study of patients with acute bacterial prostatitis identified age older than 65 years, body temperature greater than 100.4°F (38°C), benign prostatic hypertrophy, urinary retention, and transurethral catheterization as factors associated with poor outcomes.23 These outcomes included septic shock, positive blood culture, and prostatic abscess.23 In patients with any of these factors, the physician should strongly consider ordering a complete blood count and a basic metabolic panel. In the same study, a white blood cell count greater than 18,000 per mm3 (18 × 109 per L) and a blood urea nitrogen level greater than 19 mg per dL (6.8 mmol per L) were independently associated with severe cases of acute bacterial prostatitis. Inflammatory markers, such as C-reactive protein and erythrocyte sedimentation rate, will likely be elevated, but these tests have minimal clinical or diagnostic utility.23

Prostate-specific antigen (PSA) levels are not indicated in the workup of acute bacterial prostatitis.11,12,20 Approximately 70% of men will have a spurious PSA elevation due to disruption of prostatic architecture caused by inflammation.19 Elevated PSA levels can persist for one to two months after treatment.11,12 If PSA levels remain elevated for more than two months, prostate cancer should be considered because 20% of persistent elevations are associated with malignancy.19

IMAGING

Imaging studies are usually unnecessary during the initial evaluation, but may help when the diagnosis remains unclear or when patients do not respond to adequate antibiotic therapy. Patients who remain febrile after 36 hours or whose symptoms do not improve with antibiotics should undergo transrectal ultrasonography to evaluate for prostatic abscess. Alternatively, noncontrast computed tomography (CT) or magnetic resonance imaging (MRI) of the pelvis could be considered. Prostate biopsy should not be performed to avoid inducing septicemia.

Management

Management of acute bacterial prostatitis should be based on severity of symptoms, risk factors, and local antibiotic resistance patterns (Figure 1). Most patients can be treated with outpatient antibiotics; fewer than one in six patients will require hospitalization.6  Admission criteria are listed in Table 4.

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Management of Acute Bacterial Prostatitis

Address correspondence to Timothy J. -

Figure 1.

Management of acute bacterial prostatitis. (CT = computed tomography; MRI = magnetic resonance imaging.)

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Table 4.

Admission Criteria for Acute Bacterial Prostatitis

Failed outpatient management

Inability to tolerate oral intake

Resistance risk factors

Recent fluoroquinolone use

Recent transurethral or transrectal prostatic manipulation

Systemically ill or septicemia

Urinary retention

Initial empiric antibiotic therapy should be based on the suspected mode of infection and the presumed infecting organism (Table 5).5,7–9,15–17,24,25 Antibiotics should be adjusted based on culture and sensitivity results, when available.10,15 Men younger than 35 years who are sexually active and men older than 35 years who engage in high-risk sexual behavior should be treated with regimens that cover N. gonorrhoeae and C. trachomatis.12 Patients with risk factors for antibiotic resistance require intravenous therapy with broad-spectrum regimens because of the high likelihood of complications.7,8,15,24

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Table 5.

Antibiotic Regimens for Acute Bacterial Prostatitis

GROUP PRIMARY REGIMEN ALTERNATIVE REGIMEN CONSIDERATIONS

A

Single dose of ceftriaxone (Rocephin), 250 mg intramuscularly, or single dose of cefixime (Suprax), 400 mg orally

Regimen covers Neisseria gonorrhoeae and Chlamydia trachomatis infections in addition to other common bacterial pathogens

then

Doxycycline, 100 mg orally twice daily for 10 days

B

Ciprofloxacin, 500 mg orally twice daily for 10 to 14 days

Trimethoprim/sulfamethoxazole, 160/800 mg orally twice daily for 10 to 14 days

Extend treatment for 2 weeks if patient remains symptomatic

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or

Levofloxacin (Levaquin), 500 to 750 mg orally daily for 10 to 14 days

C

Ciprofloxacin, 400 mg IV every 12 hours

Ceftriaxone, 1 to 2 g IV every 24 hours

Continue treatment until patient is afebrile, then transition to oral regimen (group B) for an additional 2 to 4 weeks

or

plus

Levofloxacin, 500 to 750 mg IV every 24 hours

Levofloxacin, 500 to 750 mg IV every 24 hours

or

Piperacillin/tazobactam (Zosyn), 3.375 g IV every 6 hours

D

Piperacillin/tazobactam, 3.375 g IV every 6 hours plus aminoglycosides*

Fluoroquinolone (group C)

Continue treatment until patient is afebrile, then transition to oral regimen (group B) for an additional 2 to 4 weeks

plus

or

Aminoglycosides*

Cefotaxime (Claforan), 2 g IV every 4 hours plus aminoglycosides*

or

or

Ertapenem (Invanz), 1 g IV every 24 hours

Ceftazidime (Fortaz), 2 g IV every 8 hours plus aminoglycosides*

or

Imipenem/cilastatin (Primaxin), 500 mg IV every 6 hours

or

Meropenem (Merrem IV), 500 mg IV every 8 hours

E

Transrectal manipulation—fluoroquinolone resistance and extended spectrum beta-lactamase–producing Escherichia coli

Continue treatment until patient is afebrile, then transition to oral regimen (group B) for an additional 2 to 4 weeks

Carbapenems can be used if patient is unstable

Piperacillin/tazobactam, 3.375 g IV every 6 hours plus aminoglycosides*

Ertapenem, 1 g IV every 24 hours

If patient is stable, follow primary regimen while awaiting culture results

or

Imipenem/cilastatin, 500 mg IV every 6 hours

Transurethral manipulation—Pseudomonas species

Piperacillin/tazobactam, 3.375 g IV every 6 hours†

Fluoroquinolone (group C)†

or

or

Ceftazidime, 2 g IV every 8 hours†

Imipenem/cilastatin, 500 mg IV every 6 hours

or

or

Cefipime, 2 g IV every 12 hours†

Meropenem, 500 mg IV every 8 hours

Fluoroquinolone exposure—fluoroquinolone resistance

Piperacillin/tazobactam, 3.375 g IV every 6 hours†

Ceftriaxone, 1 g IV every 24 hours†

or

or

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Ceftazidime, 2 g IV every 8 hours†

Ertapenem, 1 g IV every 24 hours

or

Cefepime, 2 g IV every 12 hours†


IV = intravenously.

*—Dosing instructions: gentamicin, 7 mg per kg IV every 24 hours, peak 16 to 24 mcg per mL, trough less than 1 mcg per mL; amikacin, 15 mg per kg IV every 24 hours, peak 56 to 64 mcg per mL, trough less than 1 mcg per mL.

†—Aminoglycosides should be added to regimen if patient is clinically unstable.

Information from references 5, 7 through 9, 15 through 17, 24, and 25.

The duration of antibiotic therapy for mild infections is typically 10 to 14 days (with a two-week extension if the patient remains symptomatic), or four weeks for severe infections.9,26 Febrile patients should generally become afebrile within 36 hours of starting antibiotic therapy.27 Otherwise, imaging with transrectal ultrasonography, CT, or MRI is required to rule out prostatic abscess.27 After severe infections improve and the patient is afebrile, antibiotics should be transitioned to oral form and continued for another two to four weeks.5,28 Repeat urine cultures should be obtained one week after cessation of antibiotics to ensure bacterial clearance.12

Supportive measures include providing antipyretics, hydrating fluids, and pain control. Acute urinary retention occurs in approximately one in 10 patients with acute bacterial prostatitis. Relieving urinary obstruction is an important treatment consideration in clearing the infection and providing pain relief.6 However, the best approach to this intervention has not been determined. Cystostomy provides good relief and may prevent chronic infection, but urethral catheterization is an easier option for relieving obstruction.29

Complications

Prostatic abscesses occur in 2.7% of patients with acute bacterial prostatitis and require urology consultation for drainage.6 Risk factors for prostatic abscess include long-term urinary catheterization, recent urethral manipulation, and an immunocompromised state.

Approximately 13% of patients with acute bacterial prostatitis experience recurrence necessitating a longer course of antibiotics.6 Patients with persistent or recurrent symptoms should have a repeat urine culture to evaluate for repeat bacterial prostatitis and be treated based on culture results. After three months of persistent or recurrent symptoms, patients should be evaluated and treated based on chronic prostate syndrome guidelines.1 Approximately one in nine patients with acute bacterial prostatitis will develop chronic bacterial prostatitis or chronic pelvic pain syndrome.29

Prevention

Although there are no known strategies for preventing community-acquired acute bacterial prostatitis, nosocomial infections can be reduced by avoiding unnecessary manipulation of the prostate, such as transrectal biopsy or urethral catheterization. Administering antibiotics before transrectal prostate biopsies reduces postoperative complications such as urinary tract infections, acute prostatitis, bacteriuria, and bacteremia; new approaches to prevention are needed to reduce fluoroquinolone resistance and extended spectrum beta-lactamase–producing E. coli infections.13,14 A 500-mg oral dose of ciprofloxacin 12 hours before transrectal prostate biopsy with a repeat dose at the time of biopsy is the typical prophylactic regimen.25 Preoperative enemas do not reduce infection rates.24 In patients who are at increased risk of harboring fluoroquinolone-resistant bacteria, preoperative stool cultures may allow for tailoring of antibiotics at the time of the procedure.17,30

Data Sources: A PubMed search was completed in Clinical Queries using the keywords acute prostatitis, title words acute prostatitis, and prostatitis [MeSH] AND acute. The search included meta-analyses, randomized controlled trials, clinical trials, and reviews. Also searched were the Agency for Healthcare Research and Quality evidence reports, Cochrane Database of Systematic Reviews, National Guideline Clearing-house, Essential Evidence Plus, and UpToDate. Search Dates: November 19, 2014, and October 20, 2015.

The opinions and assertions contained herein are the private views of the authors and are not to be construed as official or as reflecting the views of the U.S. Air Force Medical Department or the U.S. Air Force at large.

The Authors

show all author info

TIMOTHY J. COKER, MD, FAAFP, is associate program director at the Ehrling Bergquist Family Medicine Residency Program, Offutt Air Force Base, Neb. He is also an assistant professor at the Uniformed Services University of the Health Sciences, Bethesda, Md....

DANIEL M. DIERFELDT, DO, is an assistant professor at the Uniformed Services University of the Health Sciences. He is also an attending physician at the Offutt Family Medicine Residency, Offutt Air Force Base, Neb.

Address correspondence to Timothy J. Coker, MD, Ehrling Bergquist Family Medicine Residency Program, 2501 Capehart Rd., Offutt Air Force Base, NE 68113 (e-mail: t.j.coker@hotmail.com). Reprints are not available from the authors.

Author disclosure: No relevant financial affiliations.

REFERENCES

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1. Krieger JN, Nyberg L Jr, Nickel JC. NIH consensus definition and classification of prostatitis. JAMA. 1999;282(3):236–237....

2. Roberts RO, Lieber MM, Rhodes T, Girman CJ, Bostwick DG, Jacobsen SJ. Prevalence of a physician-assigned diagnosis of prostatitis: The Olmsted County study of urinary symptoms and health status among men. Urology. 1998;51(4):578–584.

3. Etienne M, Chavanet P, Sibert L, et al. Acute bacterial prostatitis: heterogeneity in diagnostic criteria and management. Retrospective multicentric analysis of 371 patients diagnosed with acute prostatitis. BMC Infect Dis. 2008;8:12.

4. Krieger JN, Lee SW, Jeon J, Cheah PY, Liong ML, Riley DE. Epidemiology of prostatitis. Int J Antimicrob Agents. 2008;31(suppl 1):S85–S90.

5. Yoon BI, Kim S, Han DS, et al. Acute bacterial prostatitis: how to prevent and manage chronic infection? J Infect Chemother. 2012;18(4):444–450.

Hydromax water pump has gained popularity among users all over the world.

6. Millán-Rodríguez F, Palou J, Bujons-Tur A, et al. Acute bacterial prostatitis: two different sub-categories according to a previous manipulation of the lower urinary tract. World J Urol. 2006;24(1):45–50.

7. Kim SH, Ha US, Yoon BI, et al. Microbiological and clinical characteristics in acute bacterial prostatitis according to lower urinary tract manipulation procedure. J Infect Chemother. 2014;20(1):38–42.

8. Ha US, Kim ME, Kim CS, et al. Acute bacterial prostatitis in Korea: clinical outcome, including symptoms, management, microbiology and course of disease. Int J Antimicrob Agents. 2008;31(suppl 1):S96–S101.

9. Lipsky BA, Byren I, Hoey CT. Treatment of bacterial prostatitis. Clin Infect Dis. 2010;50(12):1641–1652.

10. Nagy V, Kubej D. Acute bacterial prostatitis in humans: current microbiological spectrum, sensitivity to antibiotics and clinical findings. Urol Int. 2012;89(4):445–450.

11. Ramakrishnan K, Salinas RC. Prostatitis: acute and chronic. Prim Care. 2010;37(3):547–563, viii–ix.

12. Brede CM, Shoskes DA. The etiology and management of acute prostatitis. Nat Rev Urol. 2011;8(4):207–212.

13. Zani EL, Clark OA, Rodrigues Netto N Jr. Antibiotic prophylaxis for transrectal prostate biopsy. Cochrane Database Syst Rev. 2011;(5):CD006576.

14. Campeggi A, Ouzaid I, Xylinas E, et al. Acute bacterial prostatitis after transrectal ultrasound-guided prostate biopsy: epidemiological, bacteria and treatment patterns from a 4-year prospective study. Int J Urol. 2014;21(2):152–155.

15. Özden E, Bostanci Y, Yakupoglu KY, et al. Incidence of acute prostatitis caused by extended-spectrum beta-lactamase-producing Escherichia coli after transrectal prostate biopsy. Urology. 2009;74(1):119–123.

16. Ekici S, Cengiz M, Turan G, Aliş EE. Fluoroquinolone-resistant acute prostatitis requiring hospitalization after transrectal prostate biopsy: effect of previous fluoroquinolone use as prophylaxis or long-term treatment. Int Urol Nephrol. 2012;44(1):19–27.

17. Minamida S, Satoh T, Tabata K, et al. Prevalence of fluoroquinolone-resistant Escherichia coli before and incidence of acute bacterial prostatitis after prostate biopsy. Urology. 2011;78(6):1235–1239.

18. Song W, Choo SH, Sung HH, et al. Incidence and management of extended-spectrum beta-lactamase and quinolone-resistant Escherichia coli infections after prostate biopsy. Urology. 2014;84(5):1001–1007.

19. Ludwig M. Diagnosis and therapy of acute prostatitis, epididymitis and orchitis. Andrologia. 2008;40(2):76–80.

20. Touma NJ, Nickel JC. Prostatitis and chronic pelvic pain syndrome in men. Med Clin North Am. 2011;95(1):75–86.

21. Etienne M, Pestel-Caron M, Chapuzet C, Bourgeois I, Chavanet P, Caron F. Should blood cultures be performed for patients with acute prostatitis? J Clin Microbiol. 2010;48(5):1935–1938.

22. Sharp VJ, Takacs EB, Powell CR. Prostatitis: diagnosis and treatment. Am Fam Physician. 2010;82(4):397–406.

23. Yazawa S, Nagata H, Kanao K, et al. Novel algorithm for predicting severe cases of acute bacterial prostatitis. J Urol. 2013;189(4S):e475–e476.

24. Mosharafa AA, Torky MH, El Said WM, Meshref A. Rising incidence of acute prostatitis following prostate biopsy: fluoroquinolone resistance and exposure is a significant risk factor. Urology. 2011;78(3):511–514.

25. Acute prostatitis. In: Gilbert DN, Chambers HF, Eliopoulos GM, Saag MS, eds. The Sanford Guide to Antimicrobial Therapy. 44th ed. Sperryville, Va.: Antimicrobial Therapy; 2014:27.

26. Ulleryd P, Sandberg T. Ciprofloxacin for 2 or 4 weeks in the treatment of febrile urinary tract infection in men: a randomized trial with a 1 year follow-up. Scand J Infect Dis. 2003;35(1):34–39.

27. Nickel JC. Recommendations for the evaluation of patients with prostatitis. World J Urol. 2003;21(2):75–81.

28. Prostatitis and chronic pelvic pain syndrome. In: Grabe M, Bjerklund-Johansen TE, Botto H, et al. Guidelines on Urological Infections. Arnhem, The Netherlands: European Association of Urology (EAU); 2011:65–73.

29. Yoon BI, Han DS, Ha US, et al. Clinical courses following acute bacterial prostatitis. Prostate Int. 2013;1(2):89–93.

30. Shakil J, Piracha N, Prasad N, et al. Use of outpatient parenteral antimicrobial therapy for transrectal ultrasound-guided prostate biopsy prophylaxis in the setting of community-associated multidrug-resistant Escherichia coli rectal colonization. Urology. 2014;83(4):710–713.



Address correspondence to Timothy J. -



Address correspondence to Timothy J. -

Address correspondence to Timothy J. -

Address correspondence to Timothy J. -

BATHMATE REVIEW AND PENIS PUMP

BATHMATE SIZE GUIDE

VIBRATING COCK EXTENDER

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WHAT IS BATHMATE

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HYDROMAX-7

Can I ask a question? How much water should be in the hydropump during a procedure? My flask is almost full. What affects the amount of water? How many times a set do I need to press on the vacuum? The thing is that I got a full pump of water and began to vacuum. I felt like my penis filled with blood, and then it weakens. Do I need to increase the pressure again? Thanks.

Paul Already bought
05/08/2020
Admin

The pump should be completely full of water. Yes, of course, you need to increase the pressure. It weakens because your penis expands. Compress the corrugation, and the pressure will increase.

HYDROMAX - X30

Hello! I’ve been using a pump for seven months. I have hydromax-30. When I first started, my penis was 16 cm, according to the scale. Now it’s 17.5, but it gets to 18 sometimes. I noticed about 0.5 cm of growth every two weeks. For the last month, it has stopped growing. 1. Could it be possible that I’ve reached my limit? Or maybe I pressed the corrugation too hard? Does it matter if I press the pump 3 or 6 times? 2. Or maybe I simply need the larger size, like the 40th model?

Fred Already bought
24/07/2020
Admin

Good day! We recommend that you add jelqing exercises to your training sessions. If there aren’t any traumas, swelling, and erecting is great during sex, then you’re doing everything correctly. Add the jelqing exercises, and you will see the additional changes. You shouldn’t change the pump yet. The decrease in growth is normal. The body’s resources are restricted, but we are sure that you haven’t used yours up yet. It’s normal to get used to the loads. Thanks for your message. Right us back when you have any questions.

HYDROMAX-3

Hello, after using the Bathmate, my skin expands a lot under the bridle. It’s swelling up a lot more than the penis itself. Is it normal? It seems so swollen!

Mike Already bought
21/03/2020
Admin

Reduce the number of sets or vacuum pressure to avoid such swelling. If you’re overusing the pump, take a few days of rest and when you begin again, take shorter sessions.

HYDROMAX-9

Hi guys! Does anyone have two pump versions, the regular one, and the xtreme? Is there any difference between them? Also, my penis doesn’t want to grow much in length. I only added 2 cm, but my diameter has increased a lot. Condoms roll back tighter, plus the insert by the end of the session is a little tight. According to the manufacturer's recommendations, I must get the x7. Right now, with a maximum pressing, its 17.5 cm, but it’s a bit too tight. Is it time to get the x9?

Arthur Already bought
21/03/2020
HYDROMAX-7

I want to share my experience, and maybe it will be useful for somebody. The essence of active growth is overcoming. If your penis is 17 cm today, you need to reach 17.2 in the bathtub and don’t leave the tub until you get that! Then you fixate this result for 1-2 weeks. Don’t exit your bathroom until you get that 17.2. Then you will start noticing that 17.2 is getting too easy. You’re reaching this number in a first set. Next time do it until you’re 17.3-17.4 cm. That is how we grow. Also, check your hormones. If your testosterone is low, you can start taking Omnadren or Sustanon. They are substitutes for testosterone. Next, check your pump. If you can afford it, get the Xtreme. If you can’t, do the following: pump with a Hydromax to the edge (this advice isn’t for the beginners), then while you’re in the bathtub, push your pelvis forward. Your penis will lengthen a bit, press on the Hydromax, and you will be able to let some more water out of it, fixating this penis length. Pull your pelvis backward (to a normal position), and you will feel true vacuum! )) You can tilt the pump and stretch the ligament. Tilt ahead of you. Pull the pump away from yourself. Anyway, it’s a fight for the extra millimeters. It’s training. You don’t just put on the pump, yawn, and you’re done. Yes, it will still grow if you’re in a passive mode, but mine grew for 2 cm, and then the growing stopped! I started coming up with ideas, and the ice started moving! Good luck to you all!

Alex Already bought
20/03/2020
Admin

Alex, thank you for your advice! You’re a true professional!

HYDROMAX-7

How many times a week, and for how long should I use the pump?

Max
19/03/2020
Admin

Hello! Intensive training: 15 minutes a day, 3 sets at 5 minutes each, 5 days a week, during a 6 week period. The result may be up to 30% of volume and length as a whole. It depends on the individual specialties of the body. Maintaining training: 2-3 times a week with three sets at 5 minutes each. With regular training, you will get 2-3 cm of growth within a year. This result is permanent.

HYDROMAX-7

I decided to leave feedback about the hydropumps because I see that users aren’t very active at posting reviews. Maybe someone will reply with their experience and techniques in the use of hydropumps. So, I have two pumps: Hydromax 7 and Xtreme 9. In February, I purchased the Hydromax, and one week later, I knew that it was getting too small in diameter. I guess I underestimated my measurements. I like the result, so I decided to get a larger and more powerful pump. Now I only pump with the Xtreme 9. In a matter of six months, I have the following results: 1. I added 2.5 cm to my length right after I started using the pump. 2. If I stop using the pump for 2-3 days, I keep about 1.5 cm that was added. I am hoping that it will continue to grow as it does now. I understand that at some point, the growing process will slow down, but I sure don’t want to slow down. Theoretically, I saw some very big enlargements by pumps over the internet, so I am hoping that in a year or two, I will be getting the xtreme 11.

Omar Already bought
13/02/2020
HYDROMAX-9

I purchased a pump to solve my manhood problems. I’m warning you - it’s going to be a long story. I have prostates for over 1.5 years now. I caught a cold once and started peeing a lot. My urination flow got weak, and the bladder wouldn’t get empty. I had to strain myself, but it still felt like I didn’t finish urinating. Plus, in about 3-4 months, I started experiencing slight pain during urination, and my erection got weaker. I am only 31 years old, you guys! I went to see the urologist twice. He didn’t find any viruses or infections. It’s just those darn consequences of a cold (by the way, take good care of yourself and train your body to cold temperatures). Pills, suppositories (Prostatilen, Polioksidoniy), and sessions with a magnet didn’t help. When I came in for the second time, the doctor prescribed the same thing, and I knew that it wasn’t going to help me. By the way, my doctor didn’t recommend a pump. I did some research over the internet and read that hydropump is the best device for treating male problems and other issues. Also, I learned that it increases the size and volume of the penis. I wouldn’t say I needed that, but why not? ) Anyway, I was researching for a long time, and then I found a post about a hydropump. It wasn’t an advertisement but an actual post, describing which hydropump is better. They said that Hydromax hydropump was the best. I found this website – they are the official suppliers. It took me a while to find them. Anyway, I don’t think it’s too expensive (there are many options on the website), plus this hydropump lasts for many years. It recovers my health, that’s all I have to say. RESULTS: It’s been 6 days since I started using it (I use it every day). I noticed the effect after the first session! It felt as if stagnation started to go away. I stopped running to the restroom so often, my urination flow became stronger, and I began to empty my bladder. And the pain is gone! The results are unreal! I mean, I’ve been suffering for 1.5 years, and I just started using the pump! I understand that results will get even better the more I use it! Plus, my penis will get more substantial, and my overall male health will improve! Anyway, thanks for reading till the end! I am so grateful to this company and especially Mary, who were so kind in providing detailed consultation I needed! You guys are fantastic!

David Already bought
08/02/2020
Admin

Hello, David! Thank you so much for such a detailed review! We always rejoice when our product helps in solving people’s problems! We wish you excellent health and full recovery!

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