Recommendations and Conclusions
The American College of Obstetricians and Gynecologists (the College) and the American Urogynecologic Society (AUGS) make the following recommendations and conclusions:
- Urinalysis is a commonly performed test and microscopic hematuria is a common finding.
- Renal cancer and bladder cancer are more common in men than women.
- In low-risk, never-smoking women younger than 50 years without gross hematuria and with fewer than 25 red blood cells per high-power field, the risk of urinary tract malignancy is less than or equal to 0.5%.
- The College and AUGS encourage organizations producing future guidelines on the evaluation of microscopic hematuria to perform sex-specific analysis of the data and produce practical sex-specific recommendations.
- The College and AUGS recommend that asymptomatic, low-risk, never-smoking women aged 35–50 years undergo evaluation only if they have more than 25 red blood cells per high-power field.
Over the years, asymptomatic microscopic hematuria has been variably defined. Past guidelines required two microscopic urinalyses to establish a diagnosis of asymptomatic microscopic hematuria (1, 2). The 2012 American Urological Association guidelines on the evaluation and diagnosis of asymptomatic microscopic hematuria require only a single positive properly collected specimen with three or more red blood cells per high-power field with no obvious benign cause (3). Additionally, those guidelines have lowered the age threshold for evaluation from older than 40 years to 35 years. The recommended evaluation for all patients meeting the criteria for asymptomatic microscopic hematuria (after other causes have been ruled out) includes cystoscopy and upper tract imaging with multiphasic computed tomography (CT) urography, with and without intravenous contrast. It should be emphasized that “blood” on a dipstick urinalysis is not hematuria, and this finding indicates the need for a microscopic urinalysis to evaluate for red blood cells. In contrast to the American Urological Association recommendations, the U.S. Preventive Services Task Force in 2011 concluded the current evidence is insufficient to assess the balance of benefits and harms of screening for bladder cancer in asymptomatic adults (4).
The strength of the evidence behind the American Urological Association recommendations is Grade C (observational studies that are inconsistent, have small sample sizes, or have other problems that potentially confound interpretation of data) (3). In addition, the evidence primarily is based on data from male patients. However, whether the patient is a man or a woman influences the differential diagnosis of asymptomatic microscopic hematuria, and the risk of urinary tract malignancy (bladder, ureter, and kidney) is significantly less in women than in men. Therefore, female-specific data should be evaluated and female-specific recommendations should be made for the diagnostic evaluation of asymptomatic microscopic hematuria.
Urinalysis and the Prevalence of Microscopic Hematuria
Urinalysis is a commonly performed test and microscopic hematuria is a common finding. For example, in a large Kaiser Permanente database that spanned6 years, 3,742,348 urinalyses were performed on 2,705,696 women, and 552,119 (20%) of them had microscopic hematuria; however, this number includes some women with an identified cause of microscopic hematuria, such as urinary tract infection (5). In the American Urological Association systematic review of 80,000 women and men, the prevalence of asymptomatic microscopic hematuria ranged from 2.4% to 31.1% (3).
A voided midstream sample is the recommended method to collect a urine specimen from women. Based on the anatomic differences between men and women, this collection approach will result in more genital flora contamination in samples from women. Menstruation, urogenital tract atrophy, and pelvic organ prolapse are exclusively female conditions that can lead to urine contamination. Obesity also increases the risk of contamination. Although the hematuria guidelines panel noted nonlife-threatening diagnoses (eg, benign prostatic hypertrophy [12.9%] and urethral stricture [1.4%]) can be discovered during a microscopic hematuria evaluation (3), such conditions are not common to or relevant for women.
Prevalence of Urinary Tract Malignancies
Asymptomatic microscopic hematuria is an important clinical sign for urinary tract malignancy. Risk factors for urinary tract malignancy include being male, being older, being a past or current smoker, having gross hematuria, and having a history of pelvic irradiation. In 2017, there are estimated to be 3.3 times more new cases of bladder cancer in men than in women (60,490 versus 18,540) (6). Bladder cancer accounts for approximately 6% of cases of cancer in males and is the fourth most common cancer among men. In contrast, bladder cancer accounts for only 2% of cases of cancer in females and is not in the top 10 most common types of cancer among women. Similarly, there are estimated to be 1.7 times more new cases of renal cancer in men compared with women (40,610 versus 23,380). In terms of lethality, bladder cancer is the eighth most common cause of death in men, but is not in the top 10 for women. Men are 2.2 times more likely to die of urinary tract cancer than women (22,260 versus 9,930 estimated deaths) (6).
The Evaluation of Microscopic Hematuria and the Detection of Urinary Tract Malignancy
Among the 10 studies that assessed bladder cancer rates by sex and were included in the 2012 microscopic hematuria guidelines, six studies found no cases of bladder cancer among female patients. The rate of female bladder cancer across these studies was 0–0.3% (7–16). In addition, a 2011 study of 100,000 women with hematuria that was not included in the 2012 American Urological Association guidelines (because it was published after the literature search) found that the rate of any urologic malignancy among women younger than 40 years with any degree of microscopic hematuria was 0.02%, and the rate among women older than 40 years was 0.4% (17). The identified risk factors for malignancy were having a history of gross hematuria, being male, being older than 50 years, and having a history of smoking. Table 1 lists the prevalence of urinary tract cancer by the degree of hematuria in women older than 40 years. The authors proposed using a cutoff of greater than 25 red blood cells per high-power field among women older than 40 years, noting this approach had a better sensitivity, specificity, and positive predictive value than the 2012 recommendations (17). In addition, a follow-up study of 3,573 women referred for urologic evaluation for asymptomatic hematuria, performed by Kaiser Permanente Southern California, found that being older than 60 years and having a history of smoking, gross hematuria, or both, were the strongest predictors of urologic cancer (5). Absent these risk factors, the rate of urologic cancer did not exceed 0.6% (Table 2). The risk scoring system suggests that women younger than 50 years have a very low rate of urinary tract cancer. Of note, in women without gross hematuria in the previous 6 months, microscopic hematuria was not significantly associated with the risk of urologic cancer (5). Of concern, several studies have failed to confirm the utility of asymptomatic microscopic hematuria as a screening tool for renal cancer. In one series that evaluated microscopic hematuria as a screening tool for renal cancer, the rate of renal cancer was only 0.33% (8, 18). Up to 60% of cases of renal cancer are diagnosed incidentally with imaging for unrelated symptoms (19).
Risk of Diagnostic Testing
Routine evaluation of all men and women older than 35 years with cystoscopy and CT urography has substantial cost and adverse event implications. In patients undergoing outpatient cystoscopy, 50% reported dysuria and 3% had a documented urinary tract infection (20). In addition, nephropathy from intravenous contrast has been calculated to be greater than 2% in the general population and greater than 20–30% in high-risk patients (21). Diagnostic CT scans involve much higher doses of radiation compared with plain-film radiography. It has been estimated that up to 2% of future malignancies may be iatrogenic secondary to CT radiation exposure, and the risk is greater when CT radiation exposure is administered to individuals younger than 40 years (22). The expected detection rate of cancer from a given test should exceed the potential risk of cancer that the test precipitates. Computed tomography scans for women younger than 40 years have the greatest risk and lowest yield in the evaluation of microscopic hematuria.
Implementation of the Evaluation of Microscopic Hematuria Recommendations
Because of the high prevalence of microscopic hematuria and the very low risk of urinary tract cancer, compliance with the recommendations among health care providers has been limited. For example, a survey of primary care physicians from two U.S. metropolitan areas reported that 64% of microscopic hematuria findings were not routinely referred for urologic evaluation (23). Another large primary care cohort study showed similar results and revealed that only 13.9% of patients with microscopic hematuria underwent imaging, 13.7% had cystoscopy, and only 5.7% received complete evaluation (24). Women had significantly lower evaluation rates (complete evaluation in only 3.8% of female patients), and this implies that health care providers already are using sex-specific risk factors to make clinical decisions about whom should be evaluated (24). At a large academic center, 35.6% of patients with microscopic hematuria underwent any imaging, 9% had cystoscopy, and 8.2% underwent both, further supporting these results (25). “Alarm fatigue” generated by the aggressive hematuria evaluation combined with the low rate of urologic cancer in this large segment of patients presenting with microscopic hematuria, as well as the potential for iatrogenic harm, warrant reconsideration of the guidelines.
Asymptomatic microscopic hematuria in women is common; however, it is less likely to be associated with urinary tract malignancy among women than men. For women, being older than 60 years, having a history of smoking, and having gross hematuria are the strongest predictors of urologic cancer. In low-risk, never-smoking women younger than 50 years without gross hematuria and with fewer than 25 red blood cells per high-power field, the risk of urinary tract malignancy is less than or equal to 0.5%. Furthermore, the evaluation may result in more harm than benefit and is unlikely to be cost effective. Thus, data support changing current hematuria recommendations in this low-risk group. The College and AUGS encourage organizations producing future guidelines on the evaluation of microscopic hematuria to perform sex-specific analysis of the data and produce practical sex-specific recommendations. In the meantime, the College and AUGS recommend that asymptomatic, low-risk, never-smoking women aged 35–50 years undergo evaluation only if they have more than 25 red blood cells per high-power field.
1. Grossfeld GD, Litwin MS, Wolf JS Jr, Hricak H, Shuler CL, Agerter DC, et al. Evaluation of asymptomatic microscopic hematuria in adults: the American Urological Association best practice policy–part II: patient evaluation, cytology, voided markers, imaging, cystoscopy, nephrology evaluation, and follow-up. Urology 2001;57:604–10.
2. Grossfeld GD, Litwin MS, Wolf JS, Hricak H, Shuler CL, Agerter DC, et al. Evaluation of asymptomatic microscopic hematuria in adults: the American Urological Association best practice policy–part I: definition, detection, prevalence, and etiology. Urology 2001;57:599–603.
3. Davis R, Jones JS, Barocas DA, Castle EP, Lang EK, Leveillee RJ, et al. Diagnosis, evaluation and follow-up of asymptomatic microhematuria (AMH) in adults: AUA guideline. Linthicum (MD): AUA;2012. Available at: http://www.jurology.com/article/S0022-5347(12)04958-0/pdf
. Retrieved December 21, 2016.
4. Moyer VA. Screening for bladder cancer: U.S. Preventive Services Task Force recommendation statement [published erratum appears in Ann Intern Med 2011;155:408]. Ann Intern Med 2011;155:246–51.
5. Lippmann QK, Slezak JM, Menefee SA, Ng CK, Whitcomb EL, Loo RK. Evaluation of microscopic hematuria and risk of urologic cancer in female patients. Am J Obstet Gynecol 2017;216:146.e1–7.
6. Siegel RL, Miller KD, Jemal A. Cancer statistics, 2017. CA Cancer J Clin 2017;67:7–30.
7. Murakami S, Igarashi T, Hara S, Shimazaki J. Strategies for asymptomatic microscopic hematuria: a prospective study of 1,034 patients. J Urol 1990;144:99–101.
8. Singh GS, Rigsby DC. Asymptomatic microscopic hematuria in women: case series and brief review. Int Urogynecol J Pelvic Floor Dysfunct 1999;10:361–4.
9. Bard RH. The significance of asymptomatic microhematuria in women and its economic implications. A ten-year study. Arch Intern Med 1988;148:2629–32.
10. Schmitz-Drager BJ, Tirsar LA, Schmitz-Drager C, Dorsam J, Mellan Z, Bismarck E, et al. Immunocytology in the assessment of patients with asymptomatic hematuria. World J Urol 2008;26:3–7.
11. Yamagata K, Yamagata Y, Kobayashi M, Koyama A. A long-term follow-up study of asymptomatic hematuria and/or proteinuria in adults. Clin Nephrol 1996;45:281–8.
12. Yamamoto M, Hibi H, Miyake K. Etiology of asymptomatic microscopic hematuria in adults. Hinyokika Kiyo 1993;39:413–7.
13. Yasumasu T, Koikawa Y, Uozumi J, Ueda T, Kumazawa J. Clinical study of asymptomatic microscopic haematuria. Int Urol Nephrol 1994;26:1–6.
14. Hiatt RA, Ordonez JD. Dipstick urinalysis screening, asymptomatic microhematuria, and subsequent urological cancers in a population-based sample [published erratum appears in Cancer Epidemiol Biomarkers Prev 1994;3:523]. Cancer Epidemiol Biomarkers Prev 1994;3:439–43.
15. Howard RS, Golin AL. Long-term followup of asymptomatic microhematuria. J Urol 1991;145:335–6.
16. Schmitz-Drager BJ, Beiche B, Tirsar LA, Schmitz-Drager C, Bismarck E, Ebert T. Immunocytology in the assessment of patients with asymptomatic microhaematuria. Eur Urol 2007;51:1582–8; discussion 1588.
17. Jung H, Gleason JM, Loo RK, Patel HS, Slezak JM, Jacobsen SJ. Association of hematuria on microscopic urinalysis and risk of urinary tract cancer. J Urol 2011;185:1698–703.
18. Wolf JS Jr. Evaluation and management of solid and cystic renal masses. J Urol 1998;159:1120–33.
19. Luciani LG, Cestari R, Tallarigo C. Incidental renal cell carcinoma-age and stage characterization and clinical implications: study of 1092 patients (1982–1997). Urology 2000;56:58–62.
20. Burke DM, Shackley DC, O’Reilly PH. The community-based morbidity of flexible cystoscopy. BJU Int 2002;89:347–9.
21. Golshahi J, Nasri H, Gharipour M. Contrast-induced nephropathy; a literature review. J Nephropathol 2014;3:51–6.
22. Brenner DJ, Hall EJ. Computed tomography—an increasing source of radiation exposure. N Engl J Med 2007;357:2277–84.
23. Nieder AM, Lotan Y, Nuss GR, Langston JP, Vyas S, Manoharan M, et al. Are patients with hematuria appropriately referred to Urology? A multi-institutional questionnaire based survey. Urol Oncol 2010;28:500–3.
24. Friedlander DF, Resnick MJ, You C, Bassett J, Yarlagadda V, Penson DF, et al. Variation in the intensity of hematuria evaluation: a target for primary care quality improvement. Am J Med 2014;127:633,640.e11.
© 2017 by The American College of Obstetricians and Gynecologists. Published by Wolters Kluwer Health, Inc. All rights reserved.
25. Buteau A, Seideman CA, Svatek RS, Youssef RF, Chakrabarti G, Reed G, et al. What is evaluation of hematuria by primary care physicians? Use of electronic medical records to assess practice patterns with intermediate follow-up. Urol Oncol 2014;32:128–34.