Wagerlehner.qxp 8/10/08 4:07 pm Page 117
Advances in Urological Infections
assess inflammation/infection is the two-glass pre- and post-massage cases of suspected sexually transmitted pathogens, a therapeutic
test (PPMT). The PPMT has good concordance with the four-glass test regimen that covers both of these pathogens is mandatory.
for the initial evaluation.
27
The PPMT is therefore a reasonable
alternative when EPS cannot be obtained or when microbiological Antibiotic resistance in N. gonorrhoeae has increased dramatically over
assistance is not available, because EPS – due to its usually small the last few years. The World Health Organization (WHO) surveillance of
volume – has to be processed and plated immediately. antibiotic resistance in N. gonorrhoeae in the Western Pacific Region,
carried out in 2005, revealed up to 100% resistance to penicillins and
Antibiotic treatment is warranted only if CBP has been detected quinolones and up to 80% resistance to tetracyclines in some countries.
28
in a suitable localisation study; the treatment period is approximately four Penicillin- and fluoroquinolone-resistant strains have already reached
weeks. The agents of choice are the fluoroquinolones because western countries. The Centers for Disease Control and Prevention (CDC)
of their excellent pharmacokinetic properties within the prostate. has adapted to this resistance trend and now recommends ceftriaxone at
Prostatitis due to P. aeruginosa or enterococci often fails to respond to a rather low single intramuscular dose of 125mg for treatment of acute
treatment. Increasing fluoroquinolone resistance among enterobacteria urethritis and 250mg for the treatment of epididymitis as the first-line
also leads to increasing treatment failure. In the case of CBP due to agent for the treatment of acute urethritis and epididymitis caused by N.
fluoroquinolone-resistant strains, prolonged treatment with cotrimoxazole gonorrhoeae.
29
Additional treatment of non-gonococcal agents is also
for two to three months is recommended for susceptible pathogens. recommended; here, a tetracycline agent can be used.
29
Urethritis and Epididymitis Conclusion
The microbiological diagnosis of acute infectious urethritis and Antibiotic resistance is an increasing problem in all urological
acute epididymitis must be made as specifically as possible. A infections. Both uncomplicated and complicated, and especially
urethral Gram stain, urine culture and other studies, such as nosocomial, uropathogens may exhibit resistance to multiple antibiotics
amplification techniques, for the identification of N. gonorrhoeae and and pose problems for empirical therapy. In particular, N. gonorrhoeae
C. trachomatis should be obtained for all patients. with high resistance rates against various antibiotics has been seen
much more frequently in the last few years in sexually transmitted
In both infections antimicrobial agents should be chosen for initial diseases such as urethritis and epididymitis. In order to choose the right
empirical treatment based on the probability of the aetiological agent. antibiotic for empirical therapy it is necessary to consider the bacterial
Acute infectious urethritis is almost always a sexually transmitted disease spectrum and the local antibiotic susceptibility of the uropathogens. To
caused by N. gonorrhoeae and/or C. trachomatis. In acute epididymitis, combat the development of antibiotic resistance, a basic understanding
sexually transmitted pathogens and pathogens causing complicated UTIs of antibiotic action and resistance mechanisms is helpful. The rate of
are aetiological agents. Young sexually active men with acute antibiotic resistance will possibly continue to increase. Strategies to
epididymitis are at risk of C. trachomatis or N. gonorrhoeae, while older combat this trend, such as antibiotic policies, will need to be developed
men more frequently harbour pathogens seen in complicated UTIs. In and incorporated into urological praxis. ■
1. Bouza E, San Juan R, Munoz P, et al., A European perspective Europe and Brazil on clinical aspects and antimicrobial resistance (Suppl. 2):73–8.
on nosocomial urinary tract infections I. Report on the epidemiology in females with cystitis (ARESC): Implications for 20. Nicolle LE, Pivmecillinam in the treatment of urinary tract
microbiology workload, etiology and antimicrobial susceptibility empiric therapy, Eur Urol, 2008; in press. infections, J Antimicrob Chemother, 2000;46(Suppl. 1):35–9,
(ESGNI-003 study). European Study Group on Nosocomial 11. Gordon KA, Jones RN, Susceptibility patterns of orally discussion 63–5.
Infections, Clin Microbiol Infect, 2001;7(10):523–31. administered antimicrobials among urinary tract infection 21. Livermore DM, Woodford N, The beta-lactamase threat in
2. Foxman B, Epidemiology of urinary tract infections: incidence, pathogens from hospitalized patients in North America: Enterobacteriaceae, Pseudomonas and Acinetobacter, Trends
morbidity, and economic costs, Am J Med, 2002;113(Suppl 1A): comparison report to Europe and Latin America. Results from Microbiol, 2006;14(9):413–20.
5S–13S. the SENTRY Antimicrobial Surveillance Program (2000), Diagn 22. Ena J, Arjona F, Martinez-Peinado C, et al., Epidemiology of
3. Maki DG, Tambyah PA, Engineering out the risk for infection Microbiol Infect Dis, 2003;45(4):295–301. urinary tract infections caused by extended-spectrum beta-
with urinary catheters, Emerg Infect Dis, 2001;7(2):342–7. 12. Kahlmeter G, Prevalence and antimicrobial susceptibility of lactamase-producing Escherichia coli, Urology, 2006;68(6):
4. Ruden H, Gastmeier P, Daschner FD, Schumacher M, pathogens in uncomplicated cystitis in Europe. The ECO.SENS 1169–74.
Nosocomial and community-acquired infections in Germany. study, Int J Antimicrob Agents, 2003;22(Suppl. 2):49–52. 23. Hammond ML, Ertapenem: a Group 1 carbapenem with distinct
Summary of the results of the First National Prevalence Study 13. McLuskey K, Cameron S, Hammerschmidt F, Hunter WN, antibacterial and pharmacological properties, J Antimicrob
(NIDEP), Infection, 1997;25(4):199–202. Structure and reactivity of hydroxypropylphosphonic acid Chemother, 2004;53(Suppl. 2):ii7–9.
5. Wagenlehner FM, Niemetz A, Dalhoff A, Naber KG, Spectrum epoxidase in fosfomycin biosynthesis by a cation- and flavin- 24. Meares EM, Stamey TA, Bacteriologic localization patterns
and antibiotic resistance of uropathogens from hospitalized dependent mechanism, Proc Natl Acad Sci U S A, 2005;102(40): in bacterial prostatitis and urethritis, Invest Urol, 1968;5(5):
patients with urinary tract infections: 1994–2000, Int J 14221–6. 492–518.
Antimicrob Agents, 2002;19(6):557–64. 14. Schito GC, Why fosfomycin trometamol as first line therapy 25. Krieger JN, McGonagle LA, Diagnostic considerations and
6. Elhanan G, Sarhat M, Raz R, Empiric antibiotic treatment and for uncomplicated UTI?, Int J Antimicrob Agents, 2003;22 interpretation of microbiological findings for evaluation of
the misuse of culture results and antibiotic sensitivities in (Suppl. 2):79–83. chronic prostatitis, J Clin Microbiol, 1989;27(10):2240–44.
patients with community-acquired bacteraemia due to urinary 15. Ungheri D, Albini E, Belluco G, In-vitro susceptibility of 26. Andreu A, Stapleton AE, Fennell C, et al., Urovirulence
tract infection, J Infect, 1997;35(3):283–8. quinolone-resistant clinical isolates of Escherichia coli to determinants in Escherichia coli strains causing prostatitis,
7. Schaeffer AJ, Prostatitis: US perspective, Int J Antimicrob Agents, fosfomycin trometamol, J Chemother, 2002;14(3):237–40. J Infect Dis, 1997;176(2):464–9.
1999;11(3-4):205–11, discussion 213–16. 16. Hof H, Antimicrobial therapy with nitroheterocyclic compounds, 27. Nickel JC, Shoskes D, Wang Y, et al., How does the pre-
8. Gupta K, Hooton TM, Stamm WE, Increasing antimicrobial for example, metronidazole and nitrofurantoin, Immun Infekt, massage and post-massage 2-glass test compare to the Meares-
resistance and the management of uncomplicated community- 1988;16(6):220–25. Stamey 4-glass test in men with chronic prostatitis/chronic pelvic
acquired urinary tract infections, Ann Intern Med, 2001;135(1): 17. Stein GE, Comparison of single-dose fosfomycin and a 7-day pain syndrome?, J Urol, 2006;176(1):119–24.
41–50. course of nitrofurantoin in female patients with uncomplicated 28. Surveillance of antibiotic resistance in Neisseria gonorrhoeae in
9. Talan DA, Stamm WE, Hooton TM, et al., Comparison of urinary tract infection, Clin Ther, 1999;21(11):1864–72. the WHO Western Pacific Region, 2005, Commun Dis Intell,
ciprofloxacin (7 days) and trimethoprim-sulfamethoxazole (14 18. Lancini G, Parenti F, Antibiotics, an integrated view, New York, 2006;30(4):430–33.
days) for acute uncomplicated pyelonephritis pyelonephritis in Heidelberg, Berlin: Springer-Verlag, 1982. 29. Department of Health and Human Services, Centers for Disease
women: a randomized trial, JAMA, 2000;283(12):1583–90. 19. Graninger W, Pivmecillinam—therapy of choice for lower urinary Control and Prevention. Available at: www.cdc.gov/std/
10. Naber KG, Schito GC, Botto H, et al., Surveillance study in tract infection, Int J Antimicrob Agent, 2003;22 Treatment/2006/epididymitis.htm
EUROPEAN UROLOGICAL REVIEW 117
Previous Page