Cover Page

Contents

Cover

Title Page

Copyright

Contributors

Preface to the First Edition

Section 1: Infections

Chapter 1: Infections of the urinary tract

Nomenclature

Epidemiology

Pathogenesis and basic science

Bladder infections

Kidney

Prostate

Testis and epididymis

Special infections

Multiple choice questions

References

Answers to multiple choice questions

Chapter 2: Antimicrobial prophylaxis for urologic procedures

Introduction

Risk factors for infection

Basic principles of antimicrobial prophylaxis

Procedure-specific recommendations

Special considerations

Multiple choice questions

References

Answers to multiple choice questions

Section 2: Urinary lithiasis

Chapter 3: Nephrolithiasis: etiology, stone composition, medical management, and prevention

Epidemiology

Stone formation

Stone composition

Medical evaluation

Medical management

Multiple choice questions

References

Answers to multiple choice questions

Chapter 4: Nephrolithiasis: evaluation and surgical treatment

Introduction

Evaluation

Surgical planning

Renal stone treatment

Ureteral stone treatment

Stone fragmentation techniques

Metabolic stone evaluation

Stones during pregnancy

Multiple choice questions

References

Answers to multiple choice questions

Section 3: Reproductive and sexual function

Chapter 5: Male infertility

Introduction

Physiology and pathophysiology of male reproduction

Seminal fluid, sperm characteristics

Etiology of male infertility

Management

Treatment

Conclusion

Multiple choice questions

References

Answers to multiple choice questions

Chapter 6: Erectile dysfunction and Peyronie’s disease

Erectile dysfunction

Peyronie's disease

Multiple choice questions

References

Answers to multiple choice questions

Section 4: Emergency urology

Chapter 7: Genitourinary trauma

Hematuria

Renal trauma

Ureteral trauma

Bladder injury

Urethral injury

Penile injury

Genital bites, burns, and skin loss

Multiple choice questions

References

Answers to multiple choice questions

Chapter 8: Testicular torsion and trauma

General evaluation

Epididymitis

Malignancy, erythema, and infectious orchitis

Testicular torsion: predisposing factors

Testicular torsion: types

Testicular torsion: presentation

Testicular torsion: surgical management

Torsion of the testicular appendices

Testicular trauma

Multiple choice questions

References

Answers to multiple choice questions

Chapter 9: Acute gross hematuria: etiology and management

Etiologies

Treatment of refractory hematuria

Multiple choice questions

References

Answers to multiple choice questions

Chapter 10: Priapism

Presentation and diagnosis

Treatment

Implantable penile prostheses

Multiple choice questions

References

Answers to multiple choice questions

Chapter 11: Urinary fistulae

Vesicovaginal fistulae

Ureterovaginal fistulae

Urethrovaginal fistulae

Uroenteric fistulae

Multiple choice questions

References

Answers to multiple choice questions

Chapter 12: Urethral stricture disease

Etiology and pathogenesis

Diagnosis

Conservative treatments and temporizing measures

Definitive management

Multiple choice questions

References

Answers to multiple choice questions

Section 5: Urine storage and emptying

Chapter 13: Neurourology

Normal micturition

Etiology of urinary incontinence

Neurologic conditions leading to lower urinary tract dysfunction

Management of neurogenic bladder disorders

Multiple choice questions

References

Answers to multiple choice questions

Chapter 14: Urogynecology

Classification of urinary incontinence

Pelvic floor anatomy and support

Pelvic organ prolapse

Urinary tract fistulae

Urethral diverticulum

Multiple choice questions

References

Answers to multiple choice questions

Chapter 15: Interstitial cystitis and chronic pelvic pain

Clinical presentation

Etiology

Diagnosis

Management

Multiple choice questions

References

Answers to multiple choice questions

Section 6: Oncology

Chapter 16: Prostate cancer screening and diagnosis

Introduction

Prostate-specific antigen

Multiple choice questions

References

Answers to multiple choice questions

Chapter 17: Prostate cancer: localized

Statistics and epidemiology

Prostate cancer screening

Other tools for screening

Prostate biopsy

Prostate cancer staging

Treatment for localized disease

Multiple choice questions

References

Answers to multiple choice questions

Chapter 18: Prostate cancer: treatment of metastatic disease

Introduction

Detection of metastatic disease

Hormone-naïve disease

Nonmetastatic castration-resistant disease

Chemotherapy for metastatic or hormone-refractory prostate cancer

Use of agents to decrease skeletal-related events

Palliative measures

Multiple choice questions

References

Answers to multiple choice questions

Chapter 19: Benign prostatic hyperplasia

Introduction

Etiology

Pathophysiology

Epidemiology

Diagnosis

Treatment

Multiple choice questions

References

Answers to multiple choice questions

Chapter 20: Bladder cancer: superficial

Introduction

Grade, stage, and tumor biology

Diagnosis

Surgical management

Immunotherapy

Intravesical chemotherapy

Cystectomy for aggressive superficial and refractory high-grade disease

Surveillance

Multiple choice questions

References

Answers to multiple choice questions

Chapter 21: Invasive bladder cancer and urinary diversion

Introduction

Staging and histology

Surgical therapy

Neoadjuvant and adjuvant systemic chemotherapy

Bladder preservation protocols

Recurrence

Multiple choice questions

References

Answers to multiple choice questions

Chapter 22: Penile and urethral cancer

Epidemiology

Clinical presentation

Investigations

Staging and grading

Primary lesion

Inguinal lymph nodes

Palpable inguinal nodes

Surgical technique of inguinal node dissection

Pelvic lymph node dissection

Complications of lymph node dissection

Summary

Urethral cancer

Anatomy and pathology

Clinical presentation

Initial evaluation

Treatment

Summary

Multiple choice questions

References

Answers to multiple choice questions

Chapter 23: Ureteral and renal pelvic tumors

Introduction

Pathology

Epidemiology

Pathophysiology

Diagnosis

Management

Prognosis

Surveillance

Multiple choice questions

References

Answers to multiple choice questions

Chapter 24: Angiomyolipoma, oncocytoma, and retroperitoneal fibrosis

General considerations in the diagnosis and evaluation of benign renal masses

Angiomyolipoma

Oncocytoma

Retroperitoneal fibrosis

Multiple choice questions

References

Answers to multiple choice questions

Chapter 25: Malignant Renal parenchymal tumors

Epidemiology

Risk factors

Diagnosis and evaluation

Histology and tumor grade

Staging and prognosis

Treatment

Multiple choice questions

References

Answers to multiple choice questions

Chapter 26: Adrenal disorders

Introduction

Anatomy and normal physiology

Cushing's syndrome

Primary hyperaldosteronism (Conn's syndrome)

Pheochromocytoma

Adrenal insufficiency (Addison's disease)

Adrenal cortical carcinoma

Adenoma and other benign lesions

Adrenal metastases

Summary: the incidentaloma

Multiple choice questions

References

Answers to multiple choice questions

Chapter 27: Testicular tumors

Epidemiology

Biology and pathological classification

Diagnosis and staging

Treatment and prognosis of germ cell testicular tumors

Non-germ-cell testicular tumors

Extratesticular tumors

Multiple choice questions

References

Answers to multiple choice questions

Section 7: Congenital and acquired disease

Chapter 28: Obstructing congenital anomalies of the urinary tract

Ureteropelvic junction obstruction

Ureterocele

Megaureter

Posterior urethral valves

Multiple choice questions

References

Answers to multiple choice questions

Chapter 29: Developmental abnormalities of the genitalia: disorders of sexual differentiation, hypospadias, and cryptorchidism

Disorders of sexual differentiation

Hypospadias

Cryptorchidism

Multiple choice questions

References

Answers to multiple choice questions

Chapter 30: Pediatric urinary infections, vesicoureteral reflux, and voiding dysfunction

Pediatric urinary tract infections

Vesicoureteral reflux

Voiding dysfunction

Multiple choice questions

References

Answers to multiple choice questions

Chapter 31: Pediatric genitourinary oncology

Wilms' tumor (Nephroblastoma)

Other renal tumors

Neuroblastoma

Testicular tumors

Rhabdomyosarcoma

Multiple choice questions

References

Answers to multiple choice questions

Chapter 32: The exstrophy–epispadias complex

Classic bladder exstrophy

Epispadias

Cloacal exstrophy

Multiple choice questions

References

Answers to multiple choice questions

Chapter 33: Bladder augmentation, bladder neck reconstruction, and continent diversions in children

Bladder neck reconstruction

Patient evaluation

Techniques

Augmentation cystoplasty

Techniques

Complications

Continent diversions

Techniques

Conclusion

Multiple choice questions

References

Answers to multiple choice questions

Chapter 34: End-stage renal disease and transplantation

End-stage renal disease

Transplantation

Donor evaluation and selection

Surgical technique

Immunology and immunosuppression

Types of immunosuppression

Rejection

Multiple choice questions

References

Answers to multiple choice questions

Addendum

Uropharmacology

α-adrenergic receptor blockers (α-blockers)

5α-reductase inhibitors

Anticholinergics (muscarinic receptor antagonists)

Benzodiazepines

Botulinum Toxin

Phenazopyridine (Pyridium)

Phosphodiesterase-5 inhibitors

Intracavernous injection

Testosterone

Index

Title Page

2013013055

Contributors


Ifeanyichukwu Anusionwu, MD

Resident, Urological Surgery

The James Buchanan Brady Urological Institute and Department of Urology

The Johns Hopkins School of Medicine

Baltimore, MD, USA


Mark W. Ball, MD

Resident, Urological Surgery

The James Buchanan Brady Urological Institute and Department of Urology

The Johns Hopkins School of Medicine

Baltimore, MD, USA


Trinity J. Bivalacqua MD, PhD

Associate Professor of Urology and Oncology

The James Buchanan Brady Urological Institute and Department of Urology

The Johns Hopkins School of Medicine

Baltimore, MD, USA


Arthur L. Burnett, MD, MBA

Patrick C. Walsh Professor of Urology

The James Buchanan Brady Urological Institute and Department of Urology

The Johns Hopkins School of Medicine

Baltimore, MD, USA


John B Eifler, MD

Resident, Urological Surgery

The James Buchanan Brady Urological Institute and Department of Urology

The Johns Hopkins School of Medicine

Baltimore, MD, USA


Nicholas C. Field, MD, MBA

Southern Alberta Institute of Urology

University of Calgary

Calgary, AB, Canada


Bishoy A. Gayed, MD

Chief Resident

University of Pittsburgh Medical Center

Pittsburgh, PA, USA


Angela D. Gupta, MD

Resident, Urological Surgery

The James Buchanan Brady Urological Institute and Department of Urology

The Johns Hopkins School of Medicine

Baltimore, MD, USA


Elias Hyams, MD

Instructor and Fellow

The James Buchanan Brady Urological Institute and Department of Urology

The Johns Hopkins School of Medicine

Baltimore, MD, USA


Matthew Eric Hyndman MD, PhD

Attending Physician

Rockyview General Hospital

Calgary, AB, Canada


Adam Kern, MD

Resident, Urological Surgery

The James Buchanan Brady Urological Institute and Department of Urology

The Johns Hopkins School of Medicine

Baltimore, MD, USA


Stacy Loeb, MD

Assistant Professor of Urology and Population Health

Department of Urology

New York University School of Medicine and Manhattan Veterans Affairs Medical Center

New York, NY, USA


Ahmed Magheli, MD, PhD

Attending Physician and Assistant Professor

Department of Urology

Charité Universitätsmedizin Berlin

Berlin, Germany


Markus Margreiter, MD, FEBU

Assistant Professor of Urology

Department of Urology

Medical University Vienna

Vienna, Austria


Eric Z Massanyi, MD

Pediatric Urology

The James Buchanan Brady Urological Institute and Department of Urology

The Johns Hopkins School of Medicine

Baltimore, MD, USA


Brian Matlaga, MD MPH

Associate Professor

The James Buchanan Brady Urological Institute and Department of Urology

The Johns Hopkins School of Medicine

Baltimore, MD, USA


Jeffrey K. Mullins, MD

Resident, Urological Surgery

The James Buchanan Brady Urological Institute and Department of Urology

The Johns Hopkins School of Medicine

Baltimore, MD, USA


Phillip M. Pierorazio, MD

Chief Resident, Urological Surgery

The James Buchanan Brady Urological Institute and Department of Urology

The Johns Hopkins School of Medicine

Baltimore, MD, USA


Ashley E Ross, MD, PhD

Assistant Professor Urology, Oncology and Pathology

The James Buchanan Brady Urological Institute and Department of Urology

The Johns Hopkins School of Medicine

Baltimore, MD, USA


Michelle Jo Semins, MD

Assistant Professor in Urology

University of Pittsburgh Medical Center

Pittsburgh, PA, USA


Varun Sharma MS, MCh (Urology)

Assistant Professor

Institute of Kidney Diseases and Research Centre

Institute of Transplantation Sciences (IKDRC - ITS)

Ahmedabad, Gujarat, India


Debasish Sundi MD

Resident

The James Buchanan Brady Urological Institute and Department of Urology

The Johns Hopkins School of Medicine

Baltimore, MD, USA


Kristina D. Suson, MD

Attending Physician, Pediatric Urology

Children's Hospital of Michigan

Detroit, MI, USA


Kenneth S Tseng, MD, MPH

Resident

The James Buchanan Brady Urological Institute and Department of Urology

The Johns Hopkins School of Medicine

Baltimore, MD, USA


Robert M. Turner II, MD

Resident

Department of Urology

University of Pittsburgh

Pittsburgh, PA, USA

Preface to the First Edition

Urology residency is challenging, both for the prodigious knowledge required to be a competent urologist and for the paucity of time available to acquire it. Our intention in writing the Handbook of Urology is to distill pertinent topics to the bare essentials that can be easily digested in one night of reading. Urology trainees selected the content of each chapter, drawing upon their experiences during training.

Each chapter is preceded by an abstract, a bulleted summary of key points, multiple choice questions and detailed answers, as well as key pitfalls and clinical vignettes. Important results from seminal clinical studies are included and should guide a more thorough review of the topic. As a result, I feel this book is an ideal reference for residents in urology and will also augment the in-service study material currently available.

I am indebted to the exceptional residents and fellows of the The James Buchanan Brady Urological Institute and Department of Urology of the The Johns Hopkins School of Medicine, whose insightfulness and industry were critical to the preparation of this resource.

Finally, I am grateful for the mentorship and expertise of my co-editors, J. Kellogg Parsons, MD, and Misop Han, MD, without whom this book would not be possible.

John B. Eifler, M.D.
Department of Urologic Surgery
Vanderbilt University Medical Center
Nashville, TN
USA

Section 1 Infections

1

Infections of the urinary tract

Mark W. Ball

The James Buchanan Brady Urological Institute and Department of Urology, The Johns Hopkins School of Medicine, Baltimore, MD, USA


KEY POINTS


CASE STUDY
A previously healthy 27-year-old woman presents to the Emergency Department with fever to 39°C, tachycardia to 150 bpm, respirations of 25 breaths per minute, and a leukocytosis to 13,000 WBC. Urinalysis is significant for large leukocyte esterase, positive nitrite, and bacteria are too numerous to count. CT of the abdomen and pelvis reveals a 6-mm left mid-ureteral stone with ipsilateral hydronephrosis and perinephric fat stranding. The patient is taken emergently to the operating room for left-sided ureteral stent placement. Upon cannulating the ureter, purulent urine drains from the ureteral orifice. Postoperatively, the patient has a profound systemic inflammatory response syndrome (SIRS), requiring several days of mechanical ventilation, vasoactive infusions, and broad-spectrum antibiotics. She eventually makes a full recovery.

Nomenclature

Urinary tract infection (UTI) refers to bacterial invasion of the urothelium causing an inflammatory response. When the site of infection is known, it is more informative to name the site of infection; in other words, cystitis should be used for bladder infection and pyelonephritis for kidney injection, rather than using the generic UTI. Bacteriuria, on the other hand, refers to the presence of bacteria in the urine, which may be either asymptomatic or associated with infection. Pyuria refers to the presence of white blood cells (WBCs) in the urine, which can occur in the setting of either infection or other inflammatory states (nephrolithiasis, malignancy, or foreign body).

Epidemiology

UTI is the most common bacterial infection, responsible for at least 7 million office visits and 100,000 hospitalizations per year. Most infections are diagnosed based on clinical symptoms and a suggestive urinalysis (UA). This algorithm, however, misses 20% of patients who will have positive urine cultures and causes unnecessary treatment of 50% of patients who will not go on to have a positive urine culture. The bacteria that most often cause UTIs are enteric in origin, with Escherichia coli being the most common [1].

Pathogenesis and basic science

Infection of the urinary tract occurs as a complex interaction of both bacterial virulence factors and impaired host defense. Routes of entry into the genitourinary (GU) tract are (in order of frequency) ascending infection via the urethra, direct hematogenous spread, and lymphatic spread.

Bacterial virulence factors increase the infectivity of a bacterial inoculum. The ability of bacteria to adhere to vaginal and urothelial epithelial cells is necessary for an infection to develop. Type 1 pili are expressed by E. coli and adhere to uroplakins on umbrella cells of the bladder epithelium. Studies have shown that inoculation of the urinary tract with type 1 piliated organisms results in increased colonization with those organisms. P pili are bacterial adhesins that bind glycolipid receptors in the kidney. The P stands for pyelonephritis, designated because of the high percentage of pyelonephrogenic E. coli that express these pili. Bacteria may downregulate the expression of pili once infection is established since pili increase phagocytosis of the organisms. The ability of bacteria to regulate the expression of their pili is known as phase variation.

Host defense factors decrease the likelihood of infection. Colonization of the vaginal introitus, urethra, and periurethral skin by non-uropathogenic bacteria provide a mechanical barrier to colonization. Normal voiding also washes away colonizing uropathogenic bacteria. There is genetic variation in the receptivity of epithelial cells to bacterial adhesion. There may be an association between adherence and a protective effect of the HLA-A3 allele. Complicating factors that increase infection risk are due to obstruction, anatomic abnormality, and epithelial cell receptivity. Obstruction or urinary stasis can increase host susceptibility to UTIs. Calculus disease, vesicoureteral reflux, benign prostatic hypertrophy, and neurogenic bladder all increase the susceptibility of the host to UTIs [1].

Interpreting the urinalysis

While urine culture is the gold standard for diagnosing UTIs, it is a test that takes 1–2 days to provide results and potentially longer for antibacterial sensitivity analysis. UA is more expeditious and can support the diagnosis made by history and physical. A UA often consists of two parts: a dipped UA and a microscopic UA. The dipped component tests for pH and the presence of leukocyte esterase (LE), nitrates, and blood. The microscopic component identifies red and white blood cells, red and white blood cells casts, granular casts, bacteria, and yeast.

A UA suggestive of infection typically has positive LE, pyuria, microscopic hematuria, and bacteria. Nitrite is present with gram-negative infection. The presence of epithelial cells can indicate contamination with vaginal flora and should prompt repeat midstream collected urine after adequate cleaning [1].

Bladder infections

Cystitis

Cystitis, or infection of the bladder, may be classified as uncomplicated or complicated. Factors that make cystitis complicated are infections in a male, the elderly, children, diabetics, the immunosuppressed, in the presence of anatomic abnormality, during pregnancy, after recent instrumentation, in the presence of a urinary catheter, and after recent antimicrobials or hospitalization. The typical presentation of cystitis includes symptoms of dysuria, frequency, urgency, ±suprapubic pain, and ±hematuria. Notably, constitutional symptoms including fever and chills are usually absent. This history is crucial in making diagnosis since as many as 50–90% of patients presenting with these symptoms will have cystitis. The diagnosis is supported by urinalysis findings of pyuria, bacteriuria, and the presence of nitrite and LE [1].

Treatment of uncomplicated UTI is dependent on availability, allergy, and local resistance patterns. The Infectious Diseases Society of America (IDSA) guidelines recommend the following agents as first line: Nitrofurantoin macrocrystals 100 mg bid × 5 days, trimethoprim–sulfamethoxazole 160/800 mg bid × 3 days, or fosfomycin 3 g single dose. Second-line agents include fluoroquinolones or beta-lactams. Knowledge of institutional and community antibiograms should influence prescriber patterns [2].

Cystitis is considered complicated when it occurs in a compromised urinary tract. Treatment regimens are generally the same as for complicated UTI, but the duration is 7–14 days. Nitrofurantoin should not be used in complicated UTI as it has poor tissue penetration. Additionally, modifiable factors such as removal of foreign bodies including stones and indwelling urinary catheters should be considered if clinically indicated. Indwelling catheters in place for over 2 weeks associated with UTI should be changed [3, 4].

Asymptomatic bacteriuria

Asymptomatic bacteriuria is defined as bacteria in the urine in the absence of clinical signs of infection. It is more common in women than men, but increases in prevalence in both sexes with age. Patients with indwelling catheters, bladder reconstruction using bowel, and patients with neurogenic bladders almost always have bacteriuria. Asymptomatic bacteriuria should not be screened for nor treated with a few important exceptions. Pregnant women and patients undergoing urologic procedures should be screened and treated [5].

Recurrent UTI

Unresolved UTI refers to an infection that has not responded to antimicrobial therapy. This commonly occurs because of resistant bacteria or can occur in the case of other unrealized complicating factors (see section Cystitis).

Recurrent UTI is an infection that occurs after resolution of a previous infection. These infections may represent either reinfection or bacterial persistence. Reinfection designates a new event in which the same or different organism enters the urinary tract, or bacterial persistence. Persistence, on the other hand, is when the same bacteria reappear from a nidus such as infected stone or hardware. Reinfection is responsible for 80% of recurrent UTIs [1].

Pyocystis

Pyocystis is a condition in which purulent material is retained in the bladder. Typically, the bladder is defunctionalized as a result of urinary diversion or hemodialysis. Presenting symptoms include purulent discharge, fever, or suprapubic pain. Treatment begins with placing a catheter to drain the purulent material and antibiotics. Oral antibiotics may be used in nonseptic patients, while intravenous (IV) antibiotics should be chosen in ill patients. Additionally, intravesical instillation of an antibiotic or antiseptic may be considered as well as periodic self-catheterization and saline irrigation. Refractory cases warrant more aggressive management—including cystectomy, bladder sclerosis, or surgically created fistula (vaginal or perineal vesicostomy) [1].

Emphysematous cystitis

Emphysematous cystitis is a rare type of cystitis in which gas is found within the wall of the urinary bladder. It is caused by infection with gas-forming bacteria and most often presents in diabetics and elderly patients. Symptoms are essentially the same as in typical cystitis, and treatment consists of culture-specific antibiotics. This condition must be distinguished from air within the lumen of bladder, which is much more common, and often caused by urinary tract instrumentation, indwelling Foley catheter, or by colovesical or enterovesical fistula [1].

Kidney

Acute pyelonephritis

Diagnosis and workup

Acute pyelonephritis is a renal parenchymal infection that is usually caused by ascending infection from the bladder. Escherichia coli is the most common organism. The classic presentation is acute onset of fever, chills, and flank pain; however, presentation is variable and there is no sine qua non to make the diagnosis. Abdominal pain, nausea or vomiting often accompanies the condition. Physical examination often reveals costovertebral angle tenderness. Laboratory tests often reveal an elevated serum WBC count, while UA findings are similar to those found in acute cystitis. Figure 1.1 shows classic radiographic signs of acute pyelonephritis, including enlarged kidney, wedge-shaped areas of low attenuation giving a “moth-bitten appearance,” and asymmetrical nephrogram [1].

Figure 1.1 CT of pyelonephritis. Contrast CT of the abdomen and pelvis demonstrating enlarged right kidney with wedge-shaped areas of low attenuation, giving a “moth-bitten appearance” consistent with pyelonephritis. Right ureteral stent in place.

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Treatment

Treatment is dependent upon the severity of illness and comorbidities. Patients who are nonseptic and can tolerate oral antibiotics may be treated empirically with a fluoroquinolone as an outpatient after urine culture is obtained. Most patients will improve within 72 hours of antimicrobial initiation. Failure to improve warrants more aggressive therapy with hospitalization and broad spectrum antibiotics initiated if culture data are not available. Additionally, radiologic investigation is indicated to rule out obstruction or development of an abscess. Abscesses may require drainage, and obstruction should be relieved with a ureteral stent or percutaneous nephrostomy tube.

In septic patients, blood and urine cultures should be obtained and intravenous antibiotics should be initiated. Common regimens include third-generation cephalosporins (e.g., ceftriaxone), fluoroquinolones (e.g., levofloxacin or ciprofloxacin), or ampicillin plus gentamicin. Early radiologic investigation is warranted in these patients as well [1, 2].

Chronic pyelonephritis

Chronic pyelonephritis is an often asymptomatic condition caused by multiple bouts of acute pyelonephritis. It can result in renal insufficiency. The diagnosis is made with imaging, which demonstrates atrophic, scarred, and pitted kidneys. Management is to treat active infection and prevent future infections. The condition is rare in patients without underlying urinary tract disease but may occur in vesicoureteral reflux and other abnormalities [1].

Emphysematous pyelonephritis

Emphysematous pyelonephritis is an acute, necrotizing infection of the renal parenchyma resulting from infection with gas-producing organisms. It is more common in diabetic patients and in the presence of obstruction. Diagnosis is made by cross-sectional imaging, demonstrating air in the renal parenchyma. Treatment consists of IV antibiotics, relief of any obstruction, supportive care, and often nephrectomy. Despite aggressive treatment, the mortality rate is over 50% [1].

Renal abscess

Renal abscess (or renal carbuncle) is a collection of purulent material within and confined to the parenchyma. Gram-negative organisms from ascending infection are the most common causative organisms. Hematogenous spread can also occur and gram-positive organisms are often isolated in this mechanism. Risk factors include diabetes mellitus and recurrent UTIs. Presentation begins identical to pyelonephritis, but it does not respond to typical antimicrobial therapy. Failure to respond after 72 hours of therapy warrants imaging to rule out an abscess [1].

Treatment is directed by abscess size. Lesions of any size require parenteral antibiotics. Abscesses less than 3 cm may be observed in the patients that are not immunocompromised or severely ill. Abscesses, 3–5 cm, along with small abscesses that fail conservative therapy necessitate percutaneous drainage. Abscess greater than 5 cm and others failing percutaneous drainage may require surgical drainage [6].

Perinephric abscess

Perinephric abscess is a collection of purulence outside the kidney parenchyma but inside Gerota's fascia. Gram-negative organisms are usually causative, with E. coli being the most common. Clinical presentation, diagnosis, and treatment are similar to parenchymal infection. Up to 50% of blood cultures will be positive.

Treatment of perinephric abscess almost always requires drainage. Percutaneous drainage should be considered first line for smaller lesions. Larger abscess or those associated with a nonfunctioning kidney may require nephrectomy [1].

Infected hydronephrosis

Infected hydronephrosis is an infection in an obstructed, hydronephrotic kidney. It is a urologic emergency. Patients are typically very ill, often in urosepsis, with flank pain. It can lead to pyonephrosis or suppurative damage to renal parenchyma. Treatment consists of broad spectrum antibiotics and emergent drainage with either retrograde ureteral stent or percutaneous nephrostomy tube. In decompensating patients, percutaneous nephrostomy is preferred given that it may be performed under less sedation, and to avoid high pressure from irrigation on the collecting system. Drainage should be followed by 10–14 day course of culture-specific antibiotics [1, 7].

Xanthogranulomatous pyelonephritis

Xanthogranulomatous pyelonephritis (XGP) is a chronic, destructive renal infection. It is often associated with unilateral obstructing calculi. The end result is an enlarged, nonfunctioning kidney. The differential diagnosis includes renal cell carcinoma; consequently, this entity must be ruled out. The pathognomonic feature at the cellular level is the presence of lipid-laden macrophages. Treatment often requires nephrectomy [1].

Prostate

Prostatitis

The most common urologic diagnosis in men younger than 50 years is prostatitis and is most prevalent in men between aged 20 and 49 years. Enterobacteriaceae and Enterococci are the two most common pathogens. The NIH classifies prostatitis into four categories.

Category I: Acute bacterial prostatitis

Patients with acute bacterial prostatitis present with lower urinary tract symptoms, including dysuria, frequency and urgency, and often obstruction. It typically is associated with a profound systemic inflammatory response, including fever, chills, and malaise. Systemic symptoms include fever, chills, or perineal pain. Digital rectal examination demonstrates a swollen, exquisitely tender prostate.

Treatment should be tailored to cultures. Fluoroquinolones may be empirically started with duration of 4–6 weeks. Bladder obstruction has classically been treated with a suprapubic cystostomy tube, since indwelling Foley catheters are through to cause further obstruction of urethral ducts. However, straight catheterization to relive the initial obstruction is an appropriate first step [8].

Category II: Chronic bacterial prostatitis

The hallmark of chronic bacterial prostatitis is a history of recurrent UTIs. The traditional classification of chronic prostatitis relied on the Meares–Stamey four-glass test. This technique consists of collecting four samples of urine to distinguish urethral, bladder, and prostate infection. The voided bladder 1 (VB1) specimen is the first 10 mL of urine, representing the ureteral specimen. Voided bladder 2 (VB2) is a midstream specimen, representing the bladder specimen. Next, the prostate is massage, and the expressed prostatic secretions (EPSs) are collected. Finally, voided bladder 3 (VB3) is the first 10 mL of urine after massage. Each specimen is analyzed for leukocytes and microbes, as well as sent for culture. Alternatively, a two-cup test has been proposed that consists of collecting urine before and after massage. Chronic bacterial prostatitis will have both WBCs and positive cultures in both the EPS and VB3 specimens [8].

Category III: Chronic pelvic pain syndrome

Patients with chronic pelvic pain syndrome (CPPS) present with pain lasting greater than 3 months. The pain is most often in the perineum. Men often complain of pain associated with ejaculation. This category is subdivided into inflammatory (IIIa) and noninflammatory (IIIB) CPPS. This is distinguished by the four-glass test that demonstrates WBCs in the EPS and VB3 in category IIIA, and no WBC in IIIB. Cultures are negative for both. More information about chronic pelvic pain can be found in Chapter 15 [8].

Category IV: Asymptomatic inflammatory prostatitis

This classification is reserved for asymptomatic patients who are found to have inflammation incidentally during prostate biopsy or fertility workup. Treatment is not warranted unless treating an elevated prostate-specific antigen (PSA) with a trial of antimicrobials [8].

Prostate abscess

Prostate abscesses typically evolve from cases of acute bacterial prostatitis. An abscess should be suspected when a patient with acute prostatitis fails to respond to antimicrobial therapy. The diagnosis is confirmed with transrectal ultrasound or computed tomography (CT). Treatment involves drainage of the abscess by one of several methods. Classically, transurethral incision has been used for most prostatic abscess, though transperineal incision and drainage may be required for abscesses that extend beyond the prostatic capsule. Percutaneous drainage may also be employed to drain a prostatic abscess and may offer a less morbid approach [8].

Testis and epididymis

Orchitis often presents with associated epididymitis, or epididymo-orchitis. The presence of orchitis alone suggests viral infection, such as mumps orchitis. More commonly, the combined epididymo-orchitis usually occurs via retrograde spread of bacteria through the ejaculatory ducts and vas deferens into the epididymis. The original source is often the bladder, urethra, or prostate. In prepubescent patients, a chemical etiology is more common than an infectious etiology and is related to the reflux of urine up the genital tract in dysfunctional voiders. In adults younger than 35 years, the most common cause of epididymitis is sexually transmitted infection, most common Neisseria gonorrhoeae and Chlamydia trachomatis. In men older than 35 years, the source is often coliform bacteria that have colonized the bladder or prostate, with E. coli being the most common.

Clinical presentation reveals tender epididymis and testis. The spermatic cord is often tender as well. Radiographic presentation with ultrasound demonstrates increased vascularity in the epididymis, testis, or both. Ultrasound should be obtained when the diagnosis is unclear to rule out torsion, which has decreased or no flow, as well as malignancy. Untreated epididymitis sometimes progresses to a paratesticular abscess or pyocele. Figure 1.2 demonstrates the appearance of pyocele on ultrasound. This requires open incision and drainage [8].

Figure 1.2 Ultrasound of pyocele. Scrotal ultrasound demonstrating heterogenous collection adjacent to testis found to be pus upon scrotal exploration.

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Treatment

Treatment of isolated orchitis is mainly supportive—scrotal support, bed rest, antipyretics. Antimicrobials may be used when a bacterial origin is presumed with fluoroquinolones being the agent of choice. There is no antiviral regimen for mumps orchitis. Treatment of epididymitis is dependent on age. The Center for Disease Control and Preventions guidelines recommend ceftriaxone and doxycycline for men younger than 35 years and levofloxacin or ofloxacin for men older than 35 years. The antibiotic course is typically 10 days but may be longer if concomitant prostatitis is suspected [8].

Special infections

Genitourinary tuberculosis

While tuberculosis (TB) is most commonly a pulmonary process, 10% of cases occur in extrapulmonary sites. Of these, 30–40% of extrapulmonary TB occurs in the GU tract. Seeding of the GU tract occurs via hematogenous spread from the alveoli to hilar lymph nodes to the blood stream. The primary landing site is the kidney due to its high vascularity. Downstream infection of the bladder and urethra can occur. The epididymis may also be seeded due to hematogenous spread [9].

Fournier gangrene

Fournier Gangrene is necrotizing fasciitis of the perineum. It is a rapidly progressive, potentially life-threatening infection that is usually polymicrobial, consisting of gram-positive, gram-negative, and anaerobic bacteria. Because of the high morbidity and mortality (16–40%) associated with the infection, it must be ruled out in every case of soft tissue infection of the genitalia. Diabetes mellitus, peripheral vascular disease, alcoholism, and malnutrition are risk factors. Examination may demonstrate cellulitis, blisters, or frankly necrotic areas. Pain out of proportions to visible infection may indicate more extensive underlying infection. Treatment includes broad-spectrum parenteral antibiotics and extensive surgical debridement [1, 9].

Antimicrobial therapy

The goal of antimicrobial therapy is to eliminate microbial growth in the urinary tract. Table 1.1 lists the most common antibiotics used to treat infections of the urinary tract, along with the mechanism of action, spectrum, and common adverse reactions of each drug. Institutional antibiograms and regional resistance patterns should guide antimicrobial therapy [1].

Table 1.1 Common antimicrobials

table

table


WHAT TO AVOID


KEY WEB LINKS
Johns Hopkins Antibiotic Guide
http://www.hopkinsguides.com/hopkins/ub/index/Johns_Hopkins_ABX_Guide/All_Topics/A
Infectious Disease Society of America Practice Guidelines
http://www.idsociety.org/IDSA_Practice_Guidelines/
American Urological Association Clinical Guidelines
http://www.auanet.org/content/clinical-practice-guidelines

Multiple choice questions

1 Which of the following antimicrobials is not appropriate in the treatment of pyelonephritis?
a Ciprofloxacin
b Nitrofurantoin
c Ceftriaxone
d Trimethoprim/Sulfamethoxazole
2 Which of the following is the mechanism of action of levofloxacin?
a Inhibition of cell wall synthesis
b Inhibition of DNA gyrase
c Inhibition of protein synthesis
d Inhibition of folic acid synthesis

References

1 Schaeffer AJ, Schaeffer EM. Infections of the urinary tract. In: Wein AJ, Kavoussi LR, Novick AC, Partin AW, Peters CA, editors. Campbell-Walsh Urology. 10th ed. Philadelphia, PA: Saunders; 2011.

2 Gupta K, Hooton TM, Naber KG, et al. International clinical practice guidelines for the treatment of acute uncomplicated cystitis and pyelonephritis in women: A 2010 update by the Infectious Diseases Society of America and the European Society for Microbiology and Infectious Diseases. Clin Infect Dis 2011;52(5):e103–e120.

3 Hooton TM, Bradley SF, Cardenas DD, et al. Diagnosis, prevention, and treatment of catheter-associated urinary tract infection in adults: 2009 International Clinical Practice Guidelines from the Infectious Diseases Society of America. Clin Infect Dis 2010;50(5):625–663.

4 Johns Hopkins Antibiotic Handbook, 2012–2013. Johns Hopkins Hospital Antimicrobial Stewardship Program.

5 Nicolle LE, Bradley S, Colgan R, et al. Infectious Diseases Society of America guidelines for the diagnosis and treatment of asymptomatic bacteriuria in adults. Clin Infect Dis 2005;40(5):643–654.

6 Lee SH, Jung HJ, Mah SY, Chung BH. Renal abscesses measuring 5 cm or less: outcome of medical treatment without therapeutic drainage. Yonsei Med J 2010;51(4):569–573.

7 Mokhmalji H, Braun PM, Martinez Portillo FJ, Siegsmund M, Alken P, Köhrmann KU. Percutaneous nephrostomy versus ureteral stents for diversion of hydronephrosis caused by stones: a prospective, randomized clinical trial. J Urol 2001;165(4):1088–1092.

8 Nickel J. Prostatitis and related conditions, orchitis, and epididymitis. In: Wein AJ, editor. Campbell-Walsh Urology. 10th ed. Philadelphia, PA: Saunders; 2011.

9 Ghoneim I, Rabets J, Mawhorter S. Tuberculosis and other opportunistic infections of the genitourinary system. In: Wein A, Kavoussi L, Novick A, Partin A, Peters C, editors. Campbell-Walsh Urology. 10th ed. Philadelphia, PA: Saunders; 2011.

Answers to multiple choice questions

1 Nitrofurantoin is not appropriate for the treatment of pyelonephritis. The drug does not reach adequate tissue levels to irradiate parenchymal infection.
2 Fluoroquinolones inhibit the enzyme DNA gyrase, blocking the unzipping of double stranded DNA required for DNA replication.