Full Guidelines
Reproduced from the official EAU 2025 publication.
Recommendations
Recommendations
| Recommendation | Strength rating |
|---|---|
| Do not screen or treat asymptomatic bacteriuria in the following conditions: • women without risk factors; • patients with well-regulated diabetes mellitus; • post-menopausal women; • elderly institutionalised patients; • patients with dysfunctional and/or reconstructed lower urinary tracts; • patients with renal transplants; • patients prior to arthoplasty surgeries; • patients with recurrent urinary tract infections. | Strong |
| Do not screen or treat asymptomatic bacteriuria in patients prior to cardiovascular surgeries. | Weak |
| Screen for and treat asymptomatic bacteriuria prior to urological procedures breaching the mucosa. | Strong |
| Screen for and treat asymptomatic bacteriuria in pregnant women with standard short course treatment or single dose fosfomycin trometamol. | Weak |
Recommendations for the diagnostic evaluation of cystitis
| Recommendation | Strength rating |
|---|---|
| Diagnose cystitis in women who have no other risk factors for systemic urinary tract infections based on: • a focused history of lower urinary tract symptoms (dysuria, frequency and urgency); • the absence of vaginal discharge or irritation. | Strong |
| Use urine dipstick testing for diagnosis of acute cystitis. | Weak |
| Urine cultures should be done in the following situations: • suspected acute pyelonephritis; • symptoms that do not resolve or recur within four weeks after the completion of treatment; • women who present with atypical symptoms; • pregnant women. | Strong |
Recommendations for the management of cystitis
| Recommendation | Strength rating |
|---|---|
| Non-antibiotic management | |
| Advise female patients on the possibility of an antibiotic-sparing approach for the treatment and prevention of acute and recurrent cystitis. Patients should be fully informed on the level of evidence for the different approaches. | Strong |
| Use a combination of xyloglucan, hibiscus, and propolis, or Centaurii herba, Levistici radix, Rosmarini folium to reduce recurrent cystitis episodes and reduce antibiotic use. | Weak |
| Antimicrobial therapy | |
| Prescribe fosfomycin trometamol, pivmecillinam or nitrofurantoin as first-line treatment for cystitis in women. | Strong |
| Use non-antibiotic therapy options as an alternative to antibiotic treatment in non- geriatric patients. Shared decision-making with patients is essential. | Strong |
| Do not use aminopenicillins or fluoroquinolones to treat cystitis. | Strong |
Recommendations for the diagnostic evaluation and treatment of recurrent cystitis
| Recommendation | Strength rating |
|---|---|
| Diagnose recurrent cystitis by urine culture. | Strong |
| Do not perform an extensive routine workup (e.g cystoscopy, full abdominal ultrasound) in women younger than 40 years of age with recurrent cystitis and no risk factors. | Weak |
| Advise pre-menopausal women regarding increased fluid intake as it might reduce the risk of recurrent cystitis. | Weak |
| Use vaginal oestrogen replacement in post- menopausal women to prevent recurrent cystitis. | Strong |
| Use immunomodulatory prophylaxis to reduce recurrent cystitis in women in the context of well-regulated clinical trials. | Weak |
| Advise patients on the use of a local or oral probiotic containing strains of proven efficacy for vaginal flora regeneration to prevent cystitis. | Weak |
| Advise patients on the use of cranberry products, favouring juice, for symptom relief in acute cystitis and to prevent recurrence; however, patients should be informed that the quality of evidence underpinning this is low with contradictory findings. | Strong |
| Use D-mannose to reduce recurrent cystitis episodes, but patients should be informed of the overall weak and contradictory evidence of its effectiveness. | Weak |
| Use methenamine hippurate to reduce recurrent cystitis episodes in women without abnormalities of the urinary tract. | Strong |
| Use endovesical instillations of hyaluronic acid or a combination of hyaluronic acid and chondroitin sulphate to prevent recurrent cystitis in patients where less invasive preventive approaches have been unsuccessful. Patients should be informed that further studies are needed to confirm the results of initial trials. | Weak |
| Use continuous or post-coital antimicrobial prophylaxis to prevent recurrent cystitis when non-antimicrobial interventions have failed. Counsel patients regarding possible side effects. | Strong |
| For patients with good compliance self- administered short-term antimicrobial therapy should be considered. | Strong |
Recommendations for the diagnostic evaluation and treatment of pyelonephritis
| Recommendation | Strength rating |
|---|---|
| Diagnostic evaluation | |
| Perform urinalysis (e.g., using a dipstick method), including the assessment of white and red blood cells and nitrite, for routine diagnosis. | Strong |
| Perform urine culture and antimicrobial susceptibility testing in patients with pyelonephritis. | Strong |
| Perform imaging of the urinary tract to exclude urgent urological disorders. | Strong |
| Treatment | |
| Treat patients with pyelonephritis not requiring hospitalisation with short course fluoroquinolones as first-line treatment. | Strong |
| Treat patients with pyelonephritis requiring hospitalisation with an intravenous antimicrobial regimen initially. | Strong |
| Switch patients initially treated with parenteral therapy, who improve clinically and can tolerate oral fluids, to oral antimicrobial therapy. | Strong |
| Do not use nitrofurantoin, oral fosfomycin, and pivmecillinam to treat pyelonephritis. | Strong |
Recommendations for the treatment of systemic UTIs
| Recommendation | Strength rating |
|---|---|
| Use the combination of: • amoxicillin plus an aminoglycoside; • a second-generation cephalosporin plus an aminoglycoside; • a third generation cephalosporin. | Strong |
| Only use ciprofloxacin provided: • the local resistance percentages are < 10%; • the patient has contraindications for third generation cephalosporins or aminoglycosides; • the patient has a hypersensitivity for beta-lactam antimicrobials. | Strong |
| Do not use ciprofloxacin and other fluoroquinolones for the empirical treatment of systemic UTI in patients from urology departments or when patients have used fluoroquinolones in the last six months. | Strong |
| Manage any urological abnormality and/or underlying complicating factors. | Strong |
Recommendations for diagnostic evaluation of CA-UTI
| Recommendation | Strength rating |
|---|---|
| Do not carry out routine urine culture in asymptomatic catheterised patients. | Strong |
| Do not use pyuria as sole indicator for catheter-associated UTI (CA-UTI). | Strong |
| Do not use the presence or absence of odorous or cloudy urine alone to differentiate catheter-associated asymptomatic bacteriuria from CA-UTI. | Strong |
Recommendations disease management and prevention of CA-UTI
| Recommendation | Strength rating |
|---|---|
| Treat symptomatic catheter-associated- UTI (CA-UTI) according to the recommendations for localised and systemic UTI. | Strong |
| Take a urine culture prior to initiating antimicrobial therapy in catheterised patients in whom the catheter has been removed. | Strong |
| Do not treat catheter-associated asymptomatic bacteriuria in general. | Strong |
| Treat catheter-associated asymptomatic bacteriuria prior to traumatic urinary tract interventions (e.g., transurethral resection of the prostate). | Strong |
| Replace or remove the indwelling catheter before starting antimicrobial therapy. | Strong |
| Do not apply topical antiseptics or antimicrobials to the catheter, urethra or meatus. | Strong |
| Do not use prophylactic antimicrobials to prevent CA-UTI. | Strong |
| Do not routinely use antibiotic prophylaxis to prevent clinical UTI after urethral catheter removal. | Weak |
| The duration of catheterisation should be minimal. | Strong |
| Use hydrophilic coated catheters to reduce CA-UTI. | Strong |
| Do not routinely use antibiotic prophylaxis to prevent clinical UTI after urethral catheter removal or in patients performing intermittent self-catheterisation. | Weak |
Recommendations for the diagnosis and treatment of urosepsis
| Recommendation | Strength rating |
|---|---|
| Perform the quickSOFA score to identify patients with potential sepsis. | Strong |
| Take a urine culture and two sets of blood cultures before starting antimicrobial treatment. | Strong |
| Administer parenteral high dose broad spectrum antimicrobials within the first hour after clinical assumption of sepsis. | Strong |
| Adapt initial empiric antimicrobial therapy on the basis of culture results. | Strong |
| Initiate source control including removal of foreign bodies, decompression of obstruction and drainage of abscesses in the urinary tract. | Strong |
| Provide immediate adequate life-support measures. | Strong |
Recommendations for the diagnostic evaluation and treatment of urethritis
| Recommendation | Strength rating |
|---|---|
| Perform a Gram stain of urethral discharge or a urethral smear to preliminarily diagnose gonococcal urethritis. | Strong |
| Perform a validated nucleic acid amplification test (NAAT) on a first-void urine sample or urethral smear prior to empirical treatment to diagnose chlamydial and gonococcal infections. | Strong |
| If possible, delay treatment until the results of the NAATs are available to guide treatment choice in patients with mild symptoms. | Strong |
| Perform a urethral swab culture, prior to initiation of treatment, in patients with a positive NAAT for gonorrhoea to assess the antimicrobial resistance profile of the infective strain. | Strong |
| Use a pathogen directed treatment based on local resistance data. | Strong |
| Sexual partners should be treated, while maintaining patient confidentiality. | Strong |
Recommendations for the diagnosis of bacterial prostatitis
| Recommendation | Strength rating |
|---|---|
| Do not perform prostatic massage in acute bacterial prostatitis (ABP). | Strong |
| Take a mid-stream urine dipstick to check nitrite and leukocytes in patients with clinical suspicion of ABP. | Weak |
| Take a mid-stream urine culture in patients with ABP symptoms to guide diagnosis and tailor antibiotic treatment. | Weak |
| Take a blood culture and a total blood count in patients presenting with ABP. | Weak |
| Perform accurate microbiological evaluation for atypical pathogens such as Chlamydia trachomatis or Mycoplasmata in patients with chronic bacterial prostatitis (CBP). | Weak |
| Perform the Meares and Stamey 2- or 4-glass test in patients with CBP. | Strong |
| Perform transrectal ultrasound in selected cases to rule out the presence of prostatic abscess. | Weak |
| Do not routinely perform microbiological analysis of the ejaculate alone to diagnose CBP. | Weak |
Recommendations for the management of bacterial prostatitis
| Recommendation | Strength rating |
|---|---|
| Acute bacterial prostatitis | |
| Treat acute bacterial prostatitis according to the recommendations for systemic UTI. | Strong |
| Chronic bacterial prostatitis (CBP) | |
| Prescribe a fluoroquinolone (e.g., ciprofloxacin, levofloxacin) as first-line treatment for CBP. | Strong |
| Prescribe a macrolide (e.g., azithromycin) or a tetracycline (e.g., doxycycline) if intracellular bacteria have been identified as the causative agent of CBP. | Strong |
| Prescribe metronidazole in patients with Trichomonas vaginalis CBP. | Strong |
Recommendations for the diagnosis and treatment of acute infective epididymitis
| Recommendation | Strength rating |
|---|---|
| Obtain a mid-stream urine and a first voided urine for pathogen identification by culture and nucleic acid amplification test. | Strong |
| Initially prescribe a single antibiotic or a combination of two antibiotics active against Chlamydia trachomatis and Enterobacterales in young sexually active men; in older men without sexual risk factors only Enterobacterales have to be considered. | Strong |
| If gonorrhoeal infection is likely, give single dose ceftriaxone 500 mg intramuscularly or intravenously* in addition to a course of an antibiotic active against C. trachomatis. | Strong |
| Adjust antibiotic agent when pathogen has been identified and adjust duration according to clinical response. | Weak |
| Follow national policies on reporting and tracing/treatment of contacts for sexually transmitted infections. | Strong |
Recommendations for the management of Fournier’s Gangrene
| Recommendation | Strength rating |
|---|---|
| Start treatment for Fournier’s gangrene with broad-spectrum antibiotics on presentation, with subsequent refinement according to culture and clinical response. | Strong |
| Commence repeated surgical debridement for Fournier’s gangrene within 24 hours of presentation. | Strong |
| Do not use adjunctive treatments for Fournier’s gangrene except in the context of clinical trials. | Weak |
Recommendations for the treatment of anogenital warts
| Recommendation | Strength rating |
|---|---|
| Use self-administered imiquimd 5% cream applied to all external warts overnight three times each week for sixteen weeks for the treatment of anogenital warts. | Strong |
| Use self-administered sinecatechins 15% or 10% applied to all external warts three times daily until complete clearance, or for up to sixteen weeks for the treatment of anogenital warts. | Strong |
| Use self-administered podophyllotoxin 0.5% self-applied to lesions twice daily for three days, followed by four rest days, for up to four or five weeks for the treatment of anogenital warts. | Strong |
| Use cryotherapy or surgical treatment (excision, electrosurgery, electrocautery and laser therapy) to treat anogenital warts based on an informed discussion with the patient. | Strong |
| Recommendation male circumcision | |
| Discuss male circumcision with patients as an additional one-time preventative intervention for HPV-related diseases. | Strong |
| Recommendation therapeutic HPV vaccination | |
| Offer HPV vaccine to males after surgical removal of high-grade anal intraepithelial neoplasia. | Weak |
| Recommendations prophylactic HPV vaccination | |
| Offer early HPV vaccination to boys with the goal of establishing optimal vaccine- induced protection before the onset of sexual activity. | Strong |
| Apply diverse communication strategies in order to improve HPV vaccination knowledge in young adult males. | Strong |
Recommendations
| Recommendation | Strength rating |
|---|---|
| Obtain a comprehensive medical history, including history of previous sexual contacts from all patients presenting with genital ulcers potentially related to HSV. | Strong |
| Confirm the diagnosis with a clinical swab and type-specific virologic testing, such as PCR or culture, from the lesion. | Strong |
| Treat the first clinical episode of genital HSV infection. | Strong |
Recommendations for diagnosis and treatment of genitourinary tuberculosis
| Recommendation | Strength rating |
|---|---|
| Diagnosis | |
| Take a full medical history including history of previous tuberculosis infection (pulmonary and extrapulmonary) form all patients presenting with persistent non- specific genitourinary symptoms and no identifiable cause. | Strong |
| Perform smear microscopy on urine, semen, tissue specimens, discharged or prostatic massage fluid using Ziehl– Neelsen (ZN) or auramine staining in patients with suspected genitourinary tuberculosis (GUTB). | Weak |
| Perform acid-fact bacilli culture on three midstream first-void urine samples, on three consecutive days for M. tuberculosis isolation in patients with suspected GUTB. | Strong |
| Use a recommended PCR test system in addition to microbiological reference standard (MRS) in urine specimens as a diagnostic test in patients with signs and symptoms of GUTB. | Weak |
| Use imaging modalities in combination with culture and/or PCR to aid in the diagnosis of GUTB and to assess the location and extent of damage to the genitourinary system. | Weak |
| Treatment | |
| Use medical treatment as first-line treatment for GUTB. | Strong |
| Use a daily six-month regimen for treatment of newly diagnosed GUTB, this should include an intensive phase of two months with isoniazid, rifampicin, pyrazinamide and ethambutol. Followed by a continuation phase of four-months with isoniazid and rifampicin. | Strong |
| Treat multi-drug resistant TB with an individualised treatment regime including at least five effective tuberculosis medicines during the intensive phase, including pyrazinamide and four core second-line tuberculosis medicines. | Strong |
Recommendations for peri-procedural antibiotic prophylaxis
| Recommendation | Strength rating |
|---|---|
| Do not use antibiotic prophylaxis to reduce the rate of symptomatic urinary infection following: • urodynamics; • cystoscopy; • extracorporeal shockwave lithotripsy. | Strong |
| Use antibiotic prophylaxis to reduce the rate of symptomatic urinary infection following ureteroscopy. | Weak |
| Use single dose antibiotic prophylaxis to reduce the rate of clinical urinary infection following percutaneous nephrolithotomy. | Strong |
| Use antibiotic prophylaxis to reduce infectious complications in men undergoing transurethral resection of the prostate. | Strong |
| Use antibiotic prophylaxis to reduce infectious complications in high-risk patients undergoing transurethral resection of the bladder. | Weak |
| Perform prostate biopsy using the transperineal approach due to the lower risk of infectious complications and better antibiotic stewardship. | Strong |
| Use rectal cleansing with povidone-iodine in men prior to transrectal prostate biopsy. | Strong |
| Do not use fluoroquinolones for prostate biopsy in line with the European Commission final decision on EMEA/H/A-31/1452. | Strong |
| For antibiotic prophylaxis in transrectal biopsy*, and from an antimicrobial stewardship perspective, the following options are recommended**: • First option: Targeted prophylaxis based on rectal swab or stool culture. • Second option: Augmented prophylaxis (using two or more different classes of antibiotics). | Strong |
Classification & Evidence Tables
| LocalisedUTI(i.e.,cystitis) | SystemicUTI | |
|---|---|---|
| • Cytistis with typical signs/symptoms (e.g., frequency1, urgency2, suprapubic pain3) • No signs/symptoms of systemic infection • Applies to all sexes4 • Risk factors may be present and should be addressed | • UTI with signs/symptoms of systemic infection (e.g., fever5, chills6) • May also include typical local symptoms (e.g., for pyelonephritis7 or prostatitis8) • Risk factors may be present and should be addressed | |
| 1 2 3 4 | 5 6 7 8 |
| Localised UTI1 | Systemic UTI1,2 |
|---|---|
| Dysuria (pain, burning, stinging) | Fever or hypothermia |
| Urgency | Rigors, shaking chills |
| Frequency | Delirium |
| Incontinence | Hypotension |
| Urethral purulence | Tachycardia |
| Pressure or cramping in the lower abdomen | Costovertebral angle pain/ tenderness |
| Infants | Immunocompromised state | Male sex • Prostatic involvement |
|---|---|---|
| Geriatric or frail patients | Post void residual volume | |
| Anatomic or functional abnormalities of the urinary tract | Neurourological patients | Female sex • Pregnancy • Pelvic organ prolapse |
| Antibiotic use in the past | ||
| Indwelling urinary catheters | Resistant organisms | |
| Stones | Obstruction | Recent instrumentation |
| Table 3: Suggested regimens for antimicrobial therapy in cystitis | |||
|---|---|---|---|
| Antimicrobial | Daily dose | Duration of therapy | Comments |
| First-line women | |||
| Fosfomycin trometamol | 3 g SD | 1 day | Recommended only in women with cystitis. |
| Nitrofurantoin macrocrystal | 50-100 mg four times a day | 5 days | |
| Nitrofurantoin monohydrate/ macrocrystals | 100 mg b.i.d | 5 days | |
| Nitrofurantoin macrocrystal prolonged release | 100 mg b.i.d | 5 days | |
| Pivmecillinam | 400 mg t.i.d | 3-5 days | |
| Alternatives | |||
| Cephalosporins (e.g., cefadroxil) | 500 mg b.i.d | 3 days | Or comparable |
| If the local resistance pattern for E. coli is < 20% | |||
| Trimethoprim | 200 mg b.i.d | 5 days | Not in the first trimenon of pregnancy |
| Trimethoprim- sulphamethoxazole | 160/800 mg b.i.d | 3 days | Not in the last trimenon of pregnancy |
| Treatment in men | |||
| Trimethoprim- sulphamethoxazole | 160/800 mg b.i.d | 7 days | Restricted to men, fluoroquinolones can also be prescribed in accordance with local susceptibility testing. |
| Table 4: Suggested regimens for empirical oral antimicrobial therapy in pyelonephritis | |||
|---|---|---|---|
| Antimicrobial | Daily dose | Duration of therapy | Comments |
| Ciprofloxacin | 500-750 mg b.i.d | 7 days | Fluoroquinolone resistance should be less than 10%. |
| Levofloxacin | Standard dosage: 500 mg oral q.d High dosage: 500 mg oral b.i.d | 5 days | |
| Trimethoprim sulphamethoxazol | 160/800 mg b.i.d | 14 days | If such agents are used empirically, an initial intravenous dose of a long- acting parenteral antimicrobial (e.g., ceftriaxone) should be administered. |
| Cefpodoxime | 200 mg b.i.d | 10 days | |
| Ceftibuten | 400 mg q.d | 10 days |
| Table 5: Suggested regimens for empirical parenteral antimicrobial therapy in pyelonephritis | ||
|---|---|---|
| Antimicrobials | Daily dose | Comments |
| First-line treatment | ||
| Ciprofloxacin | 400 mg b.i.d | |
| Levofloxacin | Standard dosage: 500 mg oral q.d High dosage: 500 mg oral b.i.d | |
| Cefotaxime | 2 g t.i.d | Not studied as monotherapy in acute pyelonephritis. |
| Ceftriaxone | Standard dosage: 2 g iv q.d High dosage: 2 g iv b.i.d | Lower dose studied, but higher dose recommended. |
|---|---|---|
| Second-line treatment | ||
| Cefepime | Standard dosage: 1 g iv t.i.d or 2 g iv b.i.d High dosage: 2 g iv t.i.d | Lower dose studied, but higher dose recommended. |
| Piperacillin/ tazobactam | Standard dosage: 4.5 g t.i.d High dosage: 4.5 g q.i.d prolonged infusion | |
| Gentamicin | 6-7 mg/kg q.d | Not studied as monotherapy in acute pyelonephritis. |
| Amikacin | 25-30 mg/kg q.d | |
| Last-line alternatives | ||
| Imipenem/ cilastatin | Standard dosage: 0.5 g iv q.i.d over 30 minutes High dosage: 1 g iv q.i.d over 30 minutes | Consider only in patients with early culture results indicating the presence of multi-drug resistant organisms. |
| Meropenem | 1 g t.i.d | |
| Ceftolozane/ tazobactam | 1.5 g t.i.d | |
| Ceftazidime/ avibactam | 2.5 g t.i.d | |
| Cefiderocol | 2 g t.i.d | |
| Meropenem- vaborbactam | 2 g t.i.d | |
| Plazomicin | 15mg/kg o.d |
| Table 6: Suggested regimens for antimicrobial therapy for urosepsis | ||
|---|---|---|
| Antimicrobials | Daily dose | Duration of therapy |
| Cefotaxime | 2 g t.i.d | 7-10 days Longer courses are appropriate in patients who have a slow clinical response |
| Ceftazidime | 1-2 g t.i.d | |
| Ceftriaxone | Standard dosage: 2 g q.d High dosage: 2 g iv b.i.d | |
| Cefepime | Standard dosage: 1 g iv t.i.d or 2 g iv bid High dosage: 2 g iv t.i.d | |
| Piperacillin/ tazobactam | Standard dosage: 4 g piperacillin + 0.5 g tazobactam x 4 iv 30-minute infusion or x 3 iv by extended 4-hour infusion High dosage: 4 g piperacillin + 0.5 g tazobactam x 4 iv by extended 3-hour infusion | |
| Ceftolozane/ tazobactam | 1.5 g t.i.d | |
| Ceftazidime/ avibactam | 2.5 g t.i.d | |
| Gentamicin* | 6-7 mg/kg q.d | |
| Amikacin* | 25 - 30 mg/kg q.d | |
| Ertapenem | 1 g q.d | |
| Imipenem/ cilastatin | 0.5 g q.i.d | |
| Meropenem | Standard dosage: 1 g t.i.d High dosage: 2 g iv t.i.d |
| Table 7: Suggested regimens for antimicrobial therapy for urethritis | |||
|---|---|---|---|
| Suspected | Antimicrobial | Dosage & Duration of therapy | Alternative regimens |
| Gonococcal infection | Ceftriaxone Doxycycline | 1-2 g i.m. or i.v.*, SD 100 mg b.i.d, p.o., 7 days | In case of doxycycline allergy, in combination with ceftriaxone: Azithromycin 4-day regimen: Day 1: 1 g; Days 2–4: 500 mg p.o. |
| Non- Gonococcal infection | Doxycycline | 100 mg b.i.d, p.o., 7 days | Azithromycin 4-day regimen: Day 1: 1 g; Days 2–4: 500 mg p.o. |
| Table 8: Regimens for antimicrobial therapy for urethritis with causing pathogen detected | |||
|---|---|---|---|
| Pathogen | Antimicrobial | Dosage & Duration of therapy | Alternative regimens |
| Neisseria gonorrhoeae | Ceftriaxone Doxycycline | 1-2 g i.m. or i.v.*, SD 100 mg b.i.d, p.o., 7 days | • Azithromycin 1 g p.o., SD, if M. genitalium has been excluded • Azithromycin 4-day regimen: Day 1 1 g; Days 2–4: 500 mg p.o. if M. genitalium cannot be ruled out • Cefixime 400 mg p.o., SD plus Azithromycin 1 g p.o., SD • Gentamicin 240 mg i.m SD plus Azithromycin 2 g p.o., SD • Gemifloxacin 320 mg p.o. SD plus Azithromycin 2 g p.o. SD • Spectinomycin 2 g i.m. SD • Fosfomycin trometamol 3 g p.o. on days 1, 3 and 5 In case of doxycycline allergy, in combination with ceftriaxone: Azithromycin 4-day regimen: Day 1: 1 g; Days 2–4: 500 mg orally |
| Chlamydia trachomatis | Doxycycline | 100 mg b.i.d, p.o., for 7 days | • Azithromycin 1 g p.o., SD, if M. genitalium has been excluded • Azithromycin 4-day regimen: Day 1 1 g; Days 2–4: 500 mg orally if M. genitalium cannot be ruled out • Levofloxacin 500 mg p.o. q.d. 7 days • Ofloxacin 200 mg p.o. b.i.d., 7 days |
|---|---|---|---|
| Mycoplasma genitalium | Azithromycin | 4-day regimen: Day 1 1 g; Days 2–4: 500 mg p.o. | In case of macrolide resistance: • Moxifloxacin 400 mg q.d., p.o., 7 days |
| Ureaplasma urealyticum | Doxycycline | 100 mg b.i.d, p.o., 7 days | Azithromycin 1 g p.o., SD |
| Trichomonas vaginalis | Metronidazole | 1.5-2 g p.o., SD | Tinidazole 2 g p.o., SD |
| Table 9: Suggested regimens for antimicrobial therapy for chronic bacterial prostatitis | |||
|---|---|---|---|
| Antimicrobial | Daily dose | Duration of therapy | Comments |
| Floroquinolone | Optimal oral daily dose | 4-6 weeks | |
| Doxycycline | 100 mg b.i.d | 10 days | Only for C. trachomatis or mycoplasma infections |
| Azithromycin | 500 mg once daily | 3 weeks | Only for C. trachomatis infections |
| Metronidazole | 500 mg t.i.d. | 14 days | Only for T. vaginalis infections |
| Suspected acute epididymitis | ||||
|---|---|---|---|---|
| Pain, swelling, elevated temperature of epididymis | Severe unilateral pain, sudden onset, swelling | |||
| Clinical diagnosis: acute epididymitis | Suspected testicular torsion | |||
| Urgent surgical exploration |
| Sexuallayactive men |
|---|
| Nourethral discharge, lowprobability of gonorrhea |
| levofloxacin OR doxycycline + trimethoprimsulfa methoxazol (C. trachomatis, Enterobacterales) |
| Table 10: Suggested regimens for antimicrobial therapy for Fournier’s Gangrene of mixed microbiological aetiology | |
|---|---|
| Antimicrobial | Dosage |
| Piperacillin-tazobactam plus Vancomycin | 4.5 g q.i.d or t.i.d iv 15 mg/kg b.i.d |
| Imipenem-cilastatin | Standard dosage: 0.5 g iv q.i.d over 30 minutes High dosage: 1 g iv q.i.d over 30 minutes |
| Meropenem | 1 g t.i.d iv |
| Ertapenem | 1 g o.d |
| Gentamicin | 6-7 mg/kg iv q.d |
| Cefotaxime plus metronidazole or clindamycin | 2 g q.i.d iv 500 mg q.i.d iv 600-900 mg t.i.d iv |
|---|---|
| Cefotaxime plus fosfomycine plus metronidazole | 2 g q.i.d iv 5 g t.i.d iv 500 mg q.i.d iv |
| Table 11: Treatment regimens for genital HSV infection | |
|---|---|
| Antimicrobials | Dosage |
| Recommended therapy and dose for first clinical episode HSV | |
| ACICLOVIR | 400 mg orally t.i.d for 10 days OR 200 mg orally five times daily for 10 days. |
| VALACICLOVIR | 500 mg orally b.i.d for 10 days. |
| Recommended therapy and dose for recurrent genital HSV | |
| ACICLOVIR | 400 mg orally t.i.d for 5 days OR 800 mg b.i.d for 5 days OR 800 mg t.i.d for 2 days. |
| VALACICLOVIR | 500 mg orally b.i.d for 3 days. |
| Table 12: Treatment regimens for newly diagnosed GUTB and MDR-TB | |
|---|---|
| Antimicrobials | Dosage |
| Six month regimen for treatment of newly diagnosed GUTB | |
| Intensive two month phase | |
| Isoniazid | 5 mg/kg q.d; max daily dosage 300 mg |
| Rifampicin | 10 mg/kg q.d; max daily dosage 600 mg |
| Pyrazinamide | 25 mg/kg q.d; max daily dosage 2000 mg |
| Ethambutol | 15–20 mg/kg q.d; max daily dosage ranging from 800 mg to 1600 mg depending on body weight |
| Continuation four month phase | |
| Isoniazid | 5 mg/kg q.d; max daily dosage 300 mg |
| Rifampicin | 10 mg/kg q.d; max daily dosage 600 mg |
| Treatment regimen for multi-drug resistant TB | |
|---|---|
| Treat multi-drug resistant TB with an individualised treatment regime including at least five effective tuberculosis medicines during the intensive phase, including pyrazinamide and four core second-line tuberculosis medicines*. | |
| Group A Fluoroquinolones | Levofloxacin, Moxifloxacin and Gatifloxacin |
| Group B Second-line injectables | Amikacin, Capreomycin, Kanamycin and Streptomycin** |
| Group C Other second- line agents | Ethionamide/ Prothionamide, Cycloserine/ Terizidone, Linezolid and Clofazimine |
| Group D Add-on agents (not part of the core MDR-TB regime) | D1: Pyrazinamide, Ethambutol, and high-dose isoniazid D2: Bedaquiline and Delamamid D3: p-aminosalicylic acid, Imipenem-cilastatin, Meropenem, Amoxicillin-clavulanate and Thioacetazone*** |
| Table 13: Suggested regimens for antimicrobial prophylaxis prior to urological procedures | ||
|---|---|---|
| Procedure | Prophylaxis recommended | Antimicrobial |
| Urodynamics | No | N/A |
| Cystoscopy | No | |
| Extracorporeal shockwave lithotripsy | No |
| Ureteroscopy | Yes | Trimethoprim Trimethoprim- sulphamethoxazole Cephalosporin group 2 or 3 Aminopenicillin plus a beta- lactamase inhibitor |
|---|---|---|
| Percutaneous nephrolithotomy | Yes (single dose) | |
| Transurethral resection of the prostate | Yes | |
| Transurethral resection of the bladder | Yes in patients who have a high risk of suffering post-operative sepsis. | |
| Transrectal prostate biopsy | Yes | 1. Targeted prophylaxis - based on rectal swab or stool culture. 2. Augmented prophylaxis - two or more different classes of antibiotics*. 3. Alternative antibiotics • fosfomycin trometamol** (e.g., 3 g before and 3 g 24-48 hrs after biopsy) • cephalosporin (e.g., ceftriaxone 1 g i.m.; cefixime 400 mg p.o. for 3 days starting 24 hrs before biopsy) • aminoglycoside (e.g., gentamicin 6-7 mg/kg iv q.d.; amikacin 25-30 mg/kg iv q.d.) |
| 1. Targeted prophylaxis1,7:based on rectal swab or stool cultures 2. Augmented prophylaxis1,2,4: two or more different classes of antibiotics 3. Alternative antibiotics5 ( ): •fosfomycintrometamol (e.g., 3 g before and 3 g 24-48 hrs after biopsy)* •cephalosporin (e.g., ceftriaxone 1 g i.m.; cefixime 400 mg p.o. for 3 days starting 24 hrs before biopsy) •aminoglycoside (e.g., gentamicin 3mg/kg i.v.; amikacin 15mg/kg i.m.) | Duration of antibiotic prophylaxis ≥24 hrs ( ) 1. Targeted prophylaxis6,7 ( ): based on rectal swab or stool cultures 2. Augmented prophylaxis2,4,6,8( ): •Fluoroquinolone plus aminoglycoside •Fluoroquinolone plus cephalosporin 3. Fluoroquinolone prophylaxis 5 ( ; ) |
|---|