Towards New Strategies in Complicated Urinary Tract Infection C. van Nieuwkoop
Transcription
Towards New Strategies in Complicated Urinary Tract Infection C. van Nieuwkoop
Towards New Strategies in Complicated Urinary Tract Infection C. van Nieuwkoop Towards New Strategies in Complicated Urinary Tract Infection PROEFSCHRIFT Ter verkrijging van de graad van Doctor aan de Universiteit Leiden, op gezag van de Rector Magnificus Prof. Mr. P.F. van der Heijden, volgens besluit van het College voor Promoties te verdedigen op donderdag 17 februari 2011 klokke 16.15 uur door Cornelis van Nieuwkoop geboren te Gouda in 1972 Promotiecommissie Promotor: Prof. Dr. J.T. van Dissel Co-promotor: Dr. J.W. van’t Wout Overige leden: Prof. Dr. I.M. Hoepelman (Universiteit Utrecht) Prof. Dr. R.C.M. Pelger (Universiteit Leiden) Prof. Dr. J.M. Prins (Universiteit van Amsterdam) The clinical studies discussed in Part I of this Thesis, were financially supported by a grant of the Bronovo Research Foundation. financial support for the publication of this thesis by franje1 foundation, brahms biomarkers, astellas pharma bv, janssen-cilag bv, msd bv, viiv healthcare bv, roche nederland bv, boehringer-ingelheim bv, gilead sciences bv and abbott bv is gratefully acknowledged. isbn 978-90-9025932-1 printed by mostert & van onderen!, leiden, the netherlands graphic design jan kleingeld, leiden, the netherlands, www.hakijk.nl copyright © 2011 by c. van nieuwkoop, the netherlands Contents Introduction 7 Part I Clinical aspects of febrile urinary tract infection Chapter 1 Prospective cohort study of adults with acute pyelonephritis: safety of triage towards home based oral antimicrobial treatment. J Infect 2010;60:114-21. Chapter 2 Modified pneumonia severity index and CRB-65 identify low-risk patients with febrile urinary tract infection. 33 Submitted for publication. Chapter 3 Predicting the need for radiologic imaging in adults with febrile urinary tract infection. 47 Clin Infect Dis 2010; 51: 1266-72. Chapter 4 Procalcitonin reflects bacteremia and bacterial load in urosepsis syndrome: a prospective observational study. 61 Crit Care 2010; 14: R206. Chapter 5 Risk factors for bacteremia with uropathogen not cultured from urine in adults with febrile urinary tract infection. 79 Clin Infect Dis 2010;50:e69-72. Chapter 6 Fluoroquinolone resistant Escherichia coli in community-onset febrile urinary tract infection: risk factors and outcomes. 87 J Antimicrob Chemother 2010; epub ahead of print. Chapter 7 Treatment duration of febrile urinary tract infection (FUTIRST trial): a randomized placebo-controlled multicenter trial comparing short (7 days) antibiotic treatment with conventional treatment (14 days). 103 BMC Infect Dis 2009;9:131. 19 Part II Relation between pelvic floor dysfunction and urinary tract infection Chapter 8 Pelvic floor dysfunction is not a risk factor for febrile urinary tract infection in adults. BJU Int 2010; 105:1689-95. 119 Chapter 9.1 9.2 Pelvic floor dysfunction is not related with incidence or outcome of urinary tract infection. Submitted for publication. Part III Complicated cases of urinary tract infection Chapter 10 Intravesical gentamicin for recurrent urinary tract infection in patients with intermittent bladder catherization. 153 Int J Antimicrob Agents 2010; 36:485-95. Chapter 11 Gather ye buds: fungus formation of the bladder after cesarean section. 165 Am J Obstet Gynecol 2008;199:207.e1-2. Chapter 12 Chronic bacterial prostatitis and recurrent Enterococcus faecalis bacteremia successfully treated with moxifloxacin. J Infect 2008;56:155-56. 137 The role of pelvic floor dysfunction in adults with urinary tract infection. Urology 2010; 76: 1270-71. 147 169 173 General Discussion Nederlandse samenvatting Dankwoord Curriculum Vitae List of publications Lijst van deelnemende centra Abbreviations 195 200 201 202 204 207 Introduction introduction Introduction Urinary tract infection (UTI) is the most common bacterial infection leading to substantial morbidity and considerable health care expenditures across all ages 1. Women, the elderly and persons with underlying illnesses, such as urologic abnormalities or diabetes mellitus, are at increased risk and many of these persons will develop an UTI at some point in their lives. Definitions UTI refers to an inflammation of the urinary tract in response to the presence of microbial pathogens. It encompasses a broad range of clinical syndromes associated with one common finding: a positive urine culture (bacteriuria). Based on clinical symptoms, UTI can be classified by the site of infection. Dysuria, frequency, urgency, suprapubic pain and/or hematuria all reflect the presence of bladder infection (cystitis or lower UTI); fever or chills, flank pain, nausea and vomiting reflect kidney infection (pyelonephritis of upper UTI) which is considered an ascending lower UTI. In men, fever or chills, myalgia, dysuria, pelvic or perineal pain may reflect infection of the prostate (prostatitis). For reasons of practicability and differences in clinical approach, UTIs are classified into ‘uncomplicated’ or ‘complicated’ 2, 3. The term ‘uncomplicated’ is usually restricted to non-pregnant women without underlying functional or anatomical abnormalities of the urinary tract but it remains controversial whether older, postmenopausal women, and women with underlying co-morbidities, like diabetes mellitus, also belong to this group 4. In adults the following international classification has been used: acute uncomplicated UTI (cystitis), acute uncomplicated pyelonephritis, complicated UTI (CUTI, cystitis), acute complicated pyelonephritis and in addition, for men there are several categories of prostatitis 2, 5-7. The term ‘asymptomatic bacteriuria’ is reserved for the presence of bacteriuria without accompanying symptoms of UTI. In the Netherlands, we use slightly adapted definitions for the terms ‘uncomplicated’ or ‘complicated’ UTI which indeed itself makes the terminology and classification of UTIs rather complex. Both the Dutch College of General Practitioners and the Dutch Study Group for Antibiotic Policy reserve the term ‘uncomplicated’ UTI for UTI in a non-pregnant immunocompetent woman with no anatomical or functional abnormality of the urinary tract who do not exhibit signs of tissue invasion or systemic infection (e.g. fever, chills, flank pain, nausea, vomiting) 8, 9. UTIs not meeting the criteria for ‘uncomplicated’ are all considered ‘complicated’. In this respect the term ‘complicated’ either implies the presence of a potentially complicating patient condition (e.g. abnormalities of the urinary tract, pregnancy or male sex) and/or the presence of extended disease as indicated by so-called signs of tissue invasion; in particular fever indicates that the infection is not restricted to the bladder mucosa but has spread locally or systemically (e.g. pyelonephritis and urosepsis). Pathogenesis The pathogenesis of UTI is complex and related to the interplay between a host and a pathogen invading the urinary tract. Several mainly local factors may influence the susceptibility of the host whereas pathogen factors comprise various virulence properties. Furthermore 9 figure 1 Pathogenesis of Urinary Tract infection (UTI) (adopted from 11 and 12 ). Factors enhancing susceptibility Factors enhancing exposure and transmission Factors enhancing bladder invasion Factors enhancing bacterial growth and/or affecting immune response Immunity Susceptible Host 10 Periurethral colonization (E. coli) Asymptomatic bacteriuria Symptomatic UTI Host response Bacterial virulence characteristics different behavioural and environmental factors determine the chance of periurethral uropathogen colonization that usually precedes the invasion of the urinary tract 10 (Figure 1). Several host factors have been identified as risk factors for UTI. Most factors in some way or another facilitate periurethral colonization or entry of uropathogens into the bladder. These include functional or anatomical abnormalities of the urinary tract, like pelvic floor dysfunction, benign prostatic hyperplasia and cystocele, and behavioural characteristics, such as sexual activity and bladder catherization 12, 13. Uropathogens possess diverse properties that may enable them to overcome the local host defense of the urinary tract. In particular such properties have been studied and characterized for Escherichia coli as the most common uropathogen. Several virulence factors of E. coli have been identified that contribute to its ability to adhere to, colonize or invade host cells and tissues in such a way that it leads to the pathologic changes that are clinically recognized as symptoms of UTI. Examples of such virulence factors are adhesions, siderophores, toxins, polysaccharides and proteases 14, 15. Finally, the host immune response plays an important role in keeping the urinary tract to be sterile. Alterations in the host defense mechanisms may thus contribute to the susceptibility to UTI. The innate immune system of the urinary tract is diverse and includes many components like toll-like receptors, chemokines, antimicrobial peptides and interleukins 16, 17. Recently it has been shown that variations in this innate immune system may have a genetic basis which provides evidence of an inherited host susceptibility to UTI 18-20. Management The clinical approach of an acute uncomplicated UTI is straightforward and consists of a short course of oral antimicrobials on an outpatient basis. There is no need for additional microbiological tests or radiologic imaging of the urinary tract. In contrast, there is less conformity on the clinical approach for CUTI and acute (un)complicated pyelonephritis, reflecting the fact introduction that these conditions represent a broad spectrum of clinical syndromes. In particular this holds for pyelonephritis for which different definitions have been used in clinical trials 21. As fever in UTI is considered to be the most sensitive sign of pyelonephritis, it makes sense to classify UTI patients according to the presence or absence of fever 8, 9, 21, 22. From a clinical point of view, fever in UTI only indicates tissue inflammation of the urinary tract and the ensuing host response 8, 9. From a scientific point of view, it is of interest to know whether this involves the kidney, bladder, prostate, lymph nodes of the pelvis, blood circulation or a combination of those, but an exact anatomical distinction on clinical grounds can often not be made. To date, many practical issues of febrile UTI have not yet been fully addressed. Thus, facing a patient with febrile UTI, the attending physician is lacking clear evidence-based guidelines, and questions upon its management decisions remain. Does this patient need to be referred to the hospital and subsequently to be hospitalized? What is the risk of complications for this individual patient? What is the optimal empiric antibiotic therapy? What is the risk of antibiotic resistance of the causative uropathogen in this patient? What is the optimal duration of therapy and how should it be administered? Are blood cultures indicated and what is the clinical relevance of detecting bacteremia? Is there a need for radiologic survey to detect potential underlying abnormalities of the urinary tract? Are laboratory biomarkers of any value in answering these questions? To address these questions we set up a prospective observational multicenter cohort study including consecutive adults presenting with febrile UTI either at primary care or at regional emergency departments (Figure 2). The aim of this study was to assess clinical predictors for the different clinical and microbiological outcomes. Patients with febrile UTI usually present with a mild illness in primary care but may rapidly develop a life-threatening condition, progressing into septic shock and multiple organ failure. The overall mortality of patients with febrile UTI admitted to hospital amounts to about 7-8% 23, 24. Given the spectrum of clinical presentation, disease severity and outcome, the clinically well-recognizable syndrome of febrile UTI is a good candidate for the development of a clinical scoring system of disease severity. It is also suitable to characterize new biomarkers of disease that figure 1 Participating sites of prospective observational study on adults with febrile urinary tract infection. Hoofddorp the Netherlands Leiden the Hague Leiderdorp Gouda Hospital Primary Health Care Center 11 12 will allow not only a timely diagnosis of UTI and the etiologic microbial agent (and/or antibiotic resistance), but also allow early identification of those patients who will progress into more severe stages of the host inflammatory response, e.g., sepsis and septic shock with multiple organ failure. For patients with pneumonia, the risk of complications contributing to an adverse outcome, i.e., death, can reliably be estimated by means of a set of clinical criteria. If the estimated risk for complications is low, a patient may be treated at home with oral antibiotics; in high risk patients hospital admission is advised. For UTI, being the second most frequent cause of fever in adults presenting at emergency departments after pneumonia 25-27, a set of clinical criteria have not been established. Thus, the general practitioner and emergency room specialist will decide to refer and hospitalize a patient or not guided by the perception of the patient’s illness 8. In this study, besides deriving and validating a clinical scoring system of disease severity, we aimed to survey for diseaserelated biomarkers of both human host response and microbial agent, in blood and urine samples of clinically and microbiologically well characterized individuals with fever due to UTI. To obtain these data, the participating patients were thoroughly followed clinically including the monitoring of blood and urine samples over time (Table 1). In this thesis part of the results of this study are discussed with a focus on clinical predictors. The analysis of the stored blood and urine samples is currently in progress and the results of that will appear later. The aim of these more laboratory derived studies will be on microbiological, diagnostic, prognostic, pathophysiologic, immunogenetic and immunologic aspects of febrile UTI. This will include the proteomic analysis of urine samples of which the methodology has recently been described 28. Furthermore a genomic analysis of stored DNA of the participating patients will be done to further elucidate aspects of genetic host susceptibility, responses of the innate immune system of the urinary tract as measured in human urine during febrile UTI and the evaluation of antimicrobial resistance mechanisms by using stored uropathogens. Table 1. Flowchart of assessments in patients with febrile urinary tract infection. Evaluation 0 Enrolment x Demography x Clinical data Adverse events Days after enrolment 3-4 24-32 84-92 x x x x x x x x x x x Survival Blood culture x Urine culture x x Plasma sample x x x Urine sample x x x Contact – in person x x x Contact – by phone x introduction Outline of the Thesis The focus of this thesis in on different clinical aspects of febrile UTI, examined in a large prospective observational multicenter cohort study, and on clinical observations in individuals with very complicated UTIs. Part I addresses different aspects of unresolved issues in the clinical management of febrile UTI. Chapter 1 evaluates the safety of triage towards home based oral antimicrobial treatment of febrile UTI or acute pyelonephritis, as guided by the Dutch College of General Practitioners guideline on management of UTIs 8, 29. In addition this study discusses the adherence to this guideline and risk factors for adverse outcome. The study in Chapter 2 evaluated the predictive value of clinical severity assessments used in community-acquired pneumonia in predicting clinical outcome of adults with febrile UTI. The aim of this study was to differentiate patients into low and high risk febrile UTI that may be helpful in guiding physicians to decide upon hospitalization. Chapter 3 focuses on adults with febrile UTI presenting at emergency departments. The majority of such patients are specifically referred by their general practitioner and thus they do have a higher risk for complications or underlying conditions 25, 29. In this respect radiologic imaging of the urinary tract will frequently be performed. This study presents a clinical prediction rule predicting outcome of radiologic imaging. The studies presented in Chapter 4 and Chapter 5 both focus on the presence of bacteremia in adults with febrile UTI. Chapter 4 displays risk factors for bacteremia and the predictive diagnostic value of the biomarker procalcitonine. Chapter 5 describes the diagnostic value of blood cultures over urine cultures 30. As antimicrobial resistance is emerging, the aim of the case-control study in Chapter 6 was to assess risk factors of E. coli resistance to fluoroquinolones 31. This included not only host-related risk factors but also potential environmental risk factors as contact with animals and health care workers. Chapter 7 describes a protocol of a randomized placebo-controlled non-inferiority multicenter trial on treatment duration of febrile UTI 32. This study is currently enrolling patients and the results will await another year. Included is an evidence-based review of trials examining treatment duration of febrile UTI or acute pyelonephritis. Part II evaluates the relation between UTI and pelvic floor dysfunction; that is a general term for functional clinical problems affecting the urinary, rectal and/or sexual function and considered to be a risk factor for UTI 12, 33-35. Chapter 8 and Chapter 9 describe the results of two case-control studies evaluating risk factors for febrile UTI and pelvic floor dysfunction. In particular, the relation between pelvic floor dysfunction and incidence and outcome of febrile UTI has been addressed. 13 Part III discusses complicated clinical cases of UTI requiring unconventional methods of treatment. In Chapter 10, two patients with a neurogenic bladder are described who have practiced intermittent bladder catherization and developed recurrent UTI with a multiresistent E. coli. Antibiotic treatment options were very limited and finally they were treated with gentamicin intravesically. In addition, the results of a systematic review on intravesical treatment with aminoglycosides are presented. Chapter 11 describes a patient who participated in the observational study and had extensive fungal disease of the bladder 36. Embolization of uterine artery after complicated cesarean section may have contributed to this kind of complicated UTI. Finally, Chapter 12 describes a renal transplant patient who suffered recurrent bacteremic Enterococcus faecalis UTI in the context of chronic bacterial prostatitis. Antibiotic agents to treat E. faecalis do poorly penetrate the prostate; thus limiting the treatment options for such a complicated UTI 37-39. 14 References 1. Foxman B. Epidemiology of urinary tract infections: incidence, morbidity, and economic costs. Am J Med 2002; 113 Suppl 1A:5S-13S. 2. Rubin RH, Shapiro ED, Andriole VT, Davis RJ, Stamm WE. Evaluation of new anti-infective drugs for the treatment of urinary tract infection. Infectious Diseases Society of America and the Food and Drug Administration. Clin Infect Dis 1992; 15 Suppl 1:S216-S227. 3. Neal DE Jr. Complicated Urinary Tract Infections. Urol Clin North Am 2008; 35(1):13-22. 4. Naber KG. Experience with the new guidelines on evaluation of new anti-infective drugs for the treatment of urinary tract infections. Int J Antimicrob Agents 1999; 11(3-4):189-196. 5. Schaeffer AJ. Clinical practice. Chronic prostatitis and the chronic pelvic pain syndrome. N Engl J Med 2006; 355(16):1690-1698. 6. Hooton TM. The current management strategies for community-acquired urinary tract infection. Infect Dis Clin North Am 2003; 17(2):303-332. 7. Warren JW, Abrutyn E, Hebel JR, Johnson JR, Schaeffer AJ, Stamm WE. Guidelines for antimicrobial treatment of uncomplicated acute bacterial cystitis and acute pyelonephritis in women. Infectious Diseases Society of America (IDSA). Clin Infect Dis 1999; 29(4):745-758. 8. van Haaren KAM, Visser HS, van Vliet S et al. NHG-Standaard Urineweginfecties: tweede herziening [Guideline of the Dutch College of General Practitioners on urinary tract infections: second revision]. Huisarts Wet 2005; 48:341-352. 9. Geerlings SE, van den Broek PJ, van Haarst EP et al. [Optimisation of the antibiotic policy in the Netherlands. X. The SWAB guideline for antimicrobial treatment of complicated urinary tract infections]. Ned Tijdschr Geneeskd 2006; 150(43):2370-2376. introduction 10. Czaja CA, Stamm WE, Stapleton AE et al. Prospective cohort study of microbial and inflammatory events immedi- ately preceding Escherichia coli recurrent urinary tract infection in women. J Infect Dis 2009; 200(4):528-536. 11. Foxman B, Brown P. Epidemiology of urinary tract infections: transmission and risk factors, incidence, and costs. Infect Dis Clin North Am 2003; 17(2):227-241. 12. Finer G, Landau D. Pathogenesis of urinary tract infections with normal female anatomy. Lancet Infect Dis 2004; 4(10):631-635. 13. Hooton TM. Pathogenesis of urinary tract infections: an update. J Antimicrob Chemother 2000; 46 Suppl A:1-7. 14. Johnson JR. Microbial virulence determinants and the pathogenesis of urinary tract infection. Infect Dis Clin North Am 2003; 17(2):261-78,viii. 15. Johnson JR. Virulence factors in Escherichia coli urinary tract infection. Clin Microbiol Rev 1991; 4(1):80-128. 16. Weichhart T, Haidinger M, Horl WH, Saemann MD. Current concepts of molecular defence mechanisms operative during urinary tract infection. Eur J Clin Invest 2008; 38 Suppl 2:29-38. 17. Chromek M, Brauner A. Antimicrobial mechanisms of the urinary tract. J Mol Med 2008; 86(1):37-47. 18. Lundstedt AC, McCarthy S, Gustafsson MC et al. A genetic basis of susceptibility to acute pyelonephritis. PLoS ONE 2007; 2(9):e825. 19. Hawn TR, Scholes D, Wang H et al. Genetic variation of the human urinary tract innate immune response and asymptomatic bacteriuria in women. PLoS ONE 2009; 4(12):e8300. 20. Hawn TR, Scholes D, Li SS et al. Toll-like receptor polymorphisms and susceptibility to urinary tract infections in adult women. PLoS ONE 2009; 4(6):e5990. 21. Piccoli GB, Consiglio V, Colla L et al. Antibiotic treatment for acute ‘uncomplicated’ or ‘primary’ pyelonephritis: a systematic, ‘semantic revision’. Int J Antimicrob Agents 2006; 28 Suppl 1:S49-S63. 22. Pinson AG, Philbrick JT, Lindbeck GH, Schorling JB. Fever in the clinical diagnosis of acute pyelonephritis. Am J Emerg Med 1997; 15(2):148-151. 23. Foxman B, Klemstine KL, Brown PD. Acute pyelonephritis in US hospitals in 1997: hospitalization and in-hospital mortality. Ann Epidemiol 2003; 13(2):144-150. 24. Efstathiou SP, Pefanis AV, Tsioulos DI et al. Acute pyelonephritis in adults: prediction of mortality and failure of treatment. Arch Intern Med 2003; 163(10):1206-1212. 25. Hoogendoorn M, van ’t Wout JW, Schijf V, van Dissel JT. [Predictive value of chills in patients presenting with fever to urgent care department]. Ned Tijdschr Geneeskd 2002;146(3):116-120. 26. van Dissel JT, van Langevelde P, Westendorp RG, Kwappenberg K, Frolich M. Anti-inflammatory cytokine profile and mortality in febrile patients. Lancet 1998; 351(9107):950-953. 27. van Dissel JT, Numan SC, van’t Wout JW. Chills in ‘early sepsis’: good for you? J Intern Med 2005; 257(5):469-472. 28. Ramautar R, Mayboroda OA, Derks RJ et al. Capillary electrophoresis-time of flight-mass spectrometry using noncovalently bilayer-coated capillaries for the analysis of amino acids in human urine. Electrophoresis 2008; 29(12):2714-2722. 29. van Nieuwkoop C, van’t Wout JW, Spelt IC et al. Prospective cohort study of acute pyelonephritis in adults: Safety of triage towards home based oral antimicrobial treatment. J Infect 2010; 60(2):114-121. 30. van Nieuwkoop C, Bonten TN, van ’t Wout JW et al. Risk factors for bacteremia with uropathogen not cultured from urine in adults with febrile urinary tract infection. Clin Infect Dis 2010; 50(11):e69-e72. 15 31. Degener JE, de Neeling AJ. Consumption of antimicrobial agents and antimicrobial resistance among medically important bacteria in the Netherlands. Nethmap 2009. 32. van Nieuwkoop C, van’t Wout JW, Assendelft WJ et al. Treatment duration of febrile urinary tract infection (FUTIRST trial): a randomized placebo-controlled multicenter trial comparing short (7 days) antibiotic treatment with conventional treatment (14 days). BMC Infect Dis 2009;19;9:131. 33. Carlson KV, Rome S, Nitti VW. Dysfunctional voiding in women. J Urol 2001; 165(1):143-147. 34. Minardi D, Parri G, d’Anzeo G, Fabiani A, El AZ, Muzzonigro G. Perineal ultrasound evaluation of dysfunctional voiding in women with recurrent urinary tract infections. J Urol 2008; 179(3):947-951. 35. van Nieuwkoop C, Voorham-van der Zalm PJ, van Laar AM et al. Pelvic floor dysfunction is not a risk factor for febrile urinary tract infection in adults. BJU Int 2010; 105(12):1689-1695. 36. van Nieuwkoop C, Tijsterman JD, van Dissel JT. Gather ye buds: fungus formation of the bladder after complicated cesarean section. Am J Obstet Gynecol 2008; 199(2):207-2. 37. Barza M. Anatomical barriers for antimicrobial agents. Eur J Clin Microbiol Infect Dis 1993; 12 Suppl 1: S31-S35. 16 38. Lipsky BA, Byren I, Hoey CT. Treatment of bacterial prostatitis. Clin Infect Dis 2010; 50(12):1641-1652. 39. van Nieuwkoop C, Visser LG, Groeneveld JH, Kuijper EJ. Chronic bacterial prostatitis and relapsing Enterococcus faecalis bacteremia successfully treated with moxifloxacin. J Infect 2008; 56(2):155-156.