Hematuria PDF
Hematuria PDF
Hematuria PDF
Variant 2: Microhematuria. Patients with risk factors, without any of the following: history of recent
vigorous exercise, or presence of infection or viral illness, or present or recent menstruation,
or renal parenchymal disease. Initial imaging.
Expert Panel on Urological Imaging: Darcy J. Wolfman, MD a; Jamie Marko, MD, MSb; Paul Nikolaidis, MDc;
Gaurav Khatri, MDd; Vikram S. Dogra, MDe; Dhakshinamoorthy Ganeshan, MBBSf; Stanley Goldfarb, MDg;
John L. Gore, MD, MSh; Rajan T. Gupta, MDi; Marta E. Heilbrun, MD, MSj; Andrej Lyshchik, MD, PhDk;
Andrei S. Purysko, MDl; Stephen J. Savage, MDm; Andrew D. Smith, MD, PhDn; Zhen J. Wang, MDo;
Jade J. Wong-You-Cheong, MDp; Don C. Yoo, MDq; Mark E. Lockhart, MD, MPH.r
Summary of Literature Review
Introduction/Background
Hematuria has a prevalence rate of 2% to 31% in the population [1] and is therefore a common reason patients are
referred for imaging of the urinary tract. This document summarizes the initial imaging approach for these patients.
Follow-up of normal or abnormal initial imaging findings is beyond the scope of this document. All patients
diagnosed with microhematuria should undergo a thorough history, physical examination, urinalysis, and serologic
testing prior to any initial imaging. Further, many patients should undergo cystoscopy in addition to any imaging
evaluation [2]. For children with hematuria, see the ACR Appropriateness Criteria® topic on “Hematuria-Child”
[3].
Hematuria is characterized as either microhematuria or gross hematuria. Microhematuria is defined by the American
Urological Association as 3 or more red blood cells per high power field on microscopic evaluation of urinary
sediment from “one properly collected, noncontaminated urinalysis with no evidence of infection for which a
combination of microscopic urinalysis and dipstick excludes other abnormalities such as pyuria, bacteriuria, and
contaminants” [4]. Gross hematuria is defined as hematuria visible to the physician or patient.
Causes of hematuria can arise from anywhere along the urinary tract and are generally divided into nephrogenic
and urogenic causes. Renal parenchymal disease is the most common benign nephrogenic cause of hematuria [1].
Common benign urogenic causes of hematuria include urolithiasis, infection, and benign prostatic hypertrophy [1].
Malignant causes can occur anywhere in the urinary tract and are the main entity that must be excluded during the
imaging evaluation of hematuria.
The most common factors associated with development of a urinary malignancy include gross hematuria, male
gender, age >35 years, smoking, occupational exposure to chemicals, analgesic abuse, history of urologic disease,
irritative voiding symptoms, history of pelvic irradiation, chronic urinary tract infection, exposure to known
carcinogenic agents or chemotherapy, and chronic indwelling foreign body [1,2].
Gross hematuria has a high association with malignancy of up to 30% to 40%, and therefore all patients with gross
hematuria should have a full urologic workup [1]. Conversely, patients with microhematuria have a low risk of
malignancy ranging from 2.6% to 4%, and, in most patients with asymptomatic microhematuria, a cause is never
found [1,2].
Patients without risk factors and with an identified benign cause of microhematuria including vigorous exercise,
infection, trauma, menstruation, or recent urologic procedure are unlikely to gain any benefit from a complete
imaging workup of microhematuria [1,2,5,6]. Patients with suspected urinary tract infection as a cause of
microhematuria should have urine cultures performed, preferably before antibiotic therapy, to confirm an infection
[1,2]. Patients with a suspected cause of microhematuria, including interstitial cystitis or benign prostatic
hyperplasia, should have the appropriate clinical workup before undertaking imaging, including a pelvic
examination in women, a rectal examination in men, and cystoscopy [1,2,6]. Interstitial cystitis, in particular, should
a
Johns Hopkins University School of Medicine, Washington, District of Columbia. bNational Institutes of Health Clinical Center, Bethesda, Maryland. cPanel
Chair, Northwestern University, Chicago, Illinois. dPanel Vice-Chair, UT Southwestern Medical Center, Dallas, Texas. eUniversity of Rochester Medical
Center, Rochester, New York. fThe University of Texas MD Anderson Cancer Center, Houston, Texas. gUniversity of Pennsylvania School of Medicine,
Philadelphia, Pennsylvania, American Society of Nephrology. hUniversity of Washington, Seattle, Washington, American Urological Association. iDuke
University Medical Center, Durham, North Carolina. jEmory University School of Medicine, Atlanta, Georgia. kThomas Jefferson University Hospital,
Philadelphia, Pennsylvania. lCleveland Clinic, Cleveland, Ohio. mMedical University of South Carolina, Charleston, South Carolina, American Urological
Association. nUniversity of Alabama at Birmingham Medical Center, Birmingham, Alabama. oUniversity of California San Francisco School of Medicine, San
Francisco, California. pUniversity of Maryland School of Medicine, Baltimore, Maryland. qRhode Island Hospital/The Warren Alpert Medical School of Brown
University, Providence, Rhode Island. rSpecialty Chair, University of Alabama at Birmingham, Birmingham, Alabama.
The American College of Radiology seeks and encourages collaboration with other organizations on the development of the ACR Appropriateness
Criteria through society representation on expert panels. Participation by representatives from collaborating societies on the expert panel does not necessarily
imply individual or society endorsement of the final document.
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