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Urinalysis: Microscopy

Roberts, James R. MD

doi: 10.1097/01.EEM.0000285238.19619.e6
InFocus

Part 2 in a Series

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Author Credentials and Financial Disclosure: James R. Roberts, MD, is the Chairman of the Department of Emergency Medicine and the Director of the Division of Toxicology at Mercy Health Systems, and a Professor of Emergency Medicine and Toxicology at the Drexel University College of Medicine, both in Philadelphia. Dr. Roberts has disclosed that he has no significant relationships with or financial interests in any commercial companies that pertain to this educational activity.

Learning Objectives: After reading this article, the physician should be able to:

Release Date: July 2007

Emergency physicians order routine urinalyses many times each shift. It's usually a straightforward issue, and most physicians think they are well versed in interpreting the results. You give it a quick glance and make a decision. The dipstick analysis, the microscopic exam, and other information gleaned from a UA make their way into decision-making for a variety of diagnostic, therapeutic, and disposition issues. Like most things learned in detail many years ago, the interpretation of the UA should be revisited on a regular basis.

I find myself thinking I know everything about a certain test only to find out that guidelines have changed, technology has advanced, and previously held dogma is now relegated to myth. With that in mind, I am reviewing the ins and outs of the urinalysis in emergency medicine. When one considers the complexity of the UA, it is obvious that this is not a simple test. The intricacies and subtleties are actually quite amazing. Last month's column discussed the vagaries of dipstick testing, and this discussion will review urine microscopy.

Urinalysis: A Comprehensive Review. Simerville J, et al, Amer Fam Phys 2005;71:1153

This article contains basic information on the microscopic urinalysis. Unlike the sometimes confusing dipstick, the microscopic UA is relatively straightforward. Overall, the microscopic UA is an indispensable part of the urinalysis when clinical information and the dipstick do not give all of the required answers. The primary task of the microscopic UA is to identify casts, cells, crystals, and bacteria.

The preparation of the sample is important to ensure reproducible results. The proper way to prepare a urine sample for microscopic analysis is to use 10–15 mls of freshly voided urine and centrifuge it at 1500 to 3000 rpm for five minutes. The supernatant is then decanted, and the sediment is resuspended in the remaining liquid. A single drop is then transferred to a glass slide, a cover slip is applied, and the urine is examined under low- and high-power magnification.

Cellular Elements: Generally men have fewer than 2 WBCs per HPF, and women and children normally have fewer than 5 WBCs per HPF. (These parameters often are used to define normal limits, but they are not universally agreed upon.) Finding large and irregularly shaped squamous epithelial cells with WBCs suggest contamination because these cells are not normally found in the urinary tract. The definition of hematuria by the American Urological Society is 3 or greater RBS per HPF in two or three urine sediment samples.

Casts: Casts in the sediment can localize disease to a specific portion of the GU tract. A cast is a coagulum of mucoprotein that traps contents in the tubule lumen or collecting ducts during periods of urinary concentration or urinary stasis. Casts contain hyaline, RBCs, leukocytes, or epithelial cells, or they can be granular, waxy, fatty, or broad. A specific type of cast can be associated with a specific pathologic condition. For example, RBC casts are nearly diagnostic of glomerulonephritis or vasculitis. WBC casts suggest some type of interstitial renal disease or pyelonephritis, but may be seen with a number of glomerular disorders.

Crystals: Healthy patients can excrete calcium oxalate crystals, uric acid crystals, or tripple phosphate crystals. The refractile characteristics of the crystals help the lab technician identify each crystal type. The tripple phosphate crystals, although normal, are often associated with alkaline urine (pH 9.0 and above), and may be associated with nephrolithiasis (staghorn calculus) or a proteus or other urea-splitting organism infection.

The use of the HIV-1 protease inhibitor indinavir can produce crystalluria, leading to urolithiasis and obstruction from stones comprised of these drug crystals. (It's an unusual piece of trivia, but the sagacious clinician who wants to be a star keeps this in the back of his mind when evaluating AIDS patients with the nsigns and symptoms of a kidney stone.)

Bacteria: A variety of bacteria can be seen under high-powered magnification. While bacteriuria is usually associated with infection, specimens contaminated by vaginal flora can contain large amounts of bacteria. When five bacteria per HPF are seen, there are roughly 100,000 colony forming units per ml, the classic diagnostic criteria for true bacteriuria and compatible with UTI. Men rarely have enough contamination to demonstrate bacteria in the urine under the laboratory microscope.

Comment: I could find precious little rigorous data on the technique or interpretation subtleties of urine microscopy, and it seems that everyone just accepts the party line. When the lab receives a specimen, urine microscopy is not routine in most hospitals, but most labs have criteria for performing this test. Often microscopy is mandated by abnormal findings on the dipstick, but it can be ordered as a separate test.

I have always been puzzled, even occasionally flummoxed, by results from the laboratory that describe the microscopic findings in the sediment of the urinalysis. I am even more puzzled by the fact that a certain number of cells or elements have been attributed to various diseases. I just can't believe it's possible that every lab technician performs a urinalysis in exactly the same way. Just the fact that 5 or 15 mls of urine can be collected means that different volumes enter the centrifuge. Spinning down 5 mls versus spinning down 15 mls would seem to triple the amount of cellular elements in the sediment.

The act of “pouring off the supernatant” can lead to tremendous variability unless some standardization is used. It is my conclusion that this technique is not standardized. The amount of remaining fluid used to resuspend the sediment can affect the results under the high-powered field. Different fields under the microscope contained different numbers of cells when I was looking at urine sediment in medical school, allowing different fields to contain varying numbers of RBCs or WBCs. These variables could mean the difference between 5 or 10 cells per HPF, a 100 percent difference. If there are 100 versus 200 WBCs, it is of little consequence, but if 2 WBCs per HPF is considered normal, then 5 per HPF can suggest a different diagnosis if one uses standard criteria. To my mind, there is no difference between 3, 5, or 8 WBCs per HPF.

In my lab, the technician uses a plastic tube to collect urine for the centrifuge. About 10 mls are used, but the technician usually eyeballs it. Our technicians use a nifty device (the KOVA petter) to standardize a 1 ml volume of remaining supernatant, so at least in our lab that volume is a minimal variable. Fogazzi et al (Curr Opin Nephrol Hypertens 2003;12:625) report on the use of a new plastic 10 ml tube that has a 0.5 ml bottom ball to collect sediment. This has been termed the YX tube. After centrifugation, the bottom of the tube is opened to allow the first few drops of urine onto a glass slide, supposedly giving more reproducible counts in the microscopic field.

A few other variables seem to be ignored when reporting the microscopy results. Obviously, the specific gravity of urine would alter the number of cellular elements found under the microscope. The first part of the urine void can contain urethral contaminants, and the midstream sample is the one that is generally preferred. Of course, there are many other causes of pyuria that are not related to infection. I had mentioned previously that the presence of an obstructing stone by itself can produce pyuria, so WBCs in the UA do not always mean infection. TB is the classic cause of sterile pyuria, but some cancers also can cause it. Appendicitis and endocarditis often put WBCs and RBCs into the urine sediment.

While more than 5 WBCs per HPF seems to be a standard definition of abnormal pyuria, a more scientific definition is at least 8,000 WBCs per ml of uncentrifuged urine. While this often corresponds to 2 to 5 WBCs per HPF in the centrifuged sediments, the customary determination of pyuria using cells per HPF is not sufficiently accurate to be considered a gold standard. Laboratories and clinicians, however, often use this as a gold standard. The latest Fleisher et al edition of Pediatric Emergency Medicine states that for children (no age given), a normal urine sediment can contain five to 10 WBC per HPF. The Mandell et al text of infectious disease also uses greater than 10 WBC/HPF as being abnormal.

Hematuria has been defined as a presence of 3 or more RBCs per HPF in a spun urine sediment. If one field contains 2 RBCs and another contains 4, how is this interpreted? As with WBCs, the difference between 2 and 3 RBCs cannot possibly be clinically significant given the vagaries of the technique of sediment analysis.

Does This Woman Have an Acute Uncomplicated Urinary Tract Infection?. Bent S, et al, JAMA 2002;287(20):2701

JAMA frequently publishes articles in a format that helps clinicians evaluate every day clinical scenarios. I chose this article as an example of how one can diagnose uncomplicated UTI in women by correlating the clinical history and without laboratory investigation. The authors base their conclusion on a literature review of more than 400 studies, few of which had enough scientific rigor to be included.

The executive summary is that women who present with one or more symptoms of UTI (dysuria, frequency, urgency, hematuria, suprapubic or back pain) have a 50 percent to 90 percent chance of having a UTI on the basis of history alone. Further history, examination, dipstick analysis, or microscopy adds little additional statistical value in ruling out the diagnosis when these symptoms are present. Of course, other risk factors should be considered, such as sexual activity, immune status, prior UTI, and the patient's own past experience to swing the pendulum toward or away from the diagnosis of an uncomplicated UTI. The presence of vaginal discharge leads the diagnosis away from UTI, but the absence of a discharge is a strong indication that symptoms alone define an uncomplicated UTI.

The authors conclude that empirical antibiotic treatment without dipstick analysis, microscopy, or urine culture is an appropriate algorithm in women who have one or more symptoms of a UTI. Note that this defines an uncomplicated UTI, such as cystitis. Importantly, according to these authors, a microscopic urinalysis is not even considered in the algorithm, and the urine dipstick is not required if one or more elements of the history are positive. Women with dysuria, frequency, urgency, and hematuria without back pain and without vaginal discharge have a 96 percent probability of having an uncomplicated UTI. This algorithm negates the use of urine culture or urine dipstick analysis for such individuals.

Bottom line: A urine collection for at least dipstick analysis seems to be a general standard of care in men and women who present with urinary tract symptoms or undiagnosed abdominal or vaginal complaints. There also appears to be a consensus that urine microscopy and culture are not required unless the patient has an abnormal dipstick analysis or some reason to have an unusual or bizarre condition (weight loss, HIV, unusual family history, atypical presentation, etc.). It seems rather silly to diagnose UTI if the WBC count is 6 WBCs per HPF, and rule it out if the microscopy demonstrates only 2 WBCs per HPF. Likewise, for hematuria, basing your ED plan on a microscopy that has one or two extra cells or that lacks one or two cells per HPF seems rather unscientific. We have all seen the appendicitis that causes pyuria, the aortic dissection that causes hematuria, and the uncomplicated kidney stone that causes both.

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URINALYSIS MICROSCOPY

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This microscopic report by itself defines pyuria and hematuria by some criteria. It essentially cannot be rigorously interpreted, and must be correlated with the clinical scenario. Likely it does not define a UTI in a patient with only vague abdominal pain (or perhaps it does if there is ureteral obstruction by a calculus). Such a urinalysis can be seen with appendicitis, endocarditis, tumor, and a plethora of other conditions. Of course, it can merely represent a contaminated sample.

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PRESUMPTIVE DIAGNOSIS OF URINARY TRACT INFECTION

“A clean-catch midstream urine specimen is centrifuged for 5 minutes at 2000 rpm, and then the sediment is examined under high power. Each leukocyte seen represents about 5 to 10 cells/mm3 of urine; 10 to 50 white cells/mm3 are considered the upper limit of normal. With this criterion, 5 to 10 leukocytes per high power field in the sediment from a clean-catch midstream urine specimen is the upper limit of normal, as they represent 50 to 100 cells mm3. It should be emphasized that the finding of pyuria is nonspecific, and patients with and without pyuria may or may not have infection.”

Source: Mandell GL, et al (2000). Mandell's Principles and Practice of Infectious Diseases. (5th edition.) Philadelphia: Churchill Livingston.

The exact number of WBCs per HPF that represent significant pyuria varies among sources in the literature and from lab to lab. More commonly quoted upper limits are 0–3 WBC/HPF for men and 0–5 WBC/HPF for women. This prestigious source uses 5–10 WBC/HPF as being normal.

This urine sample had positive nitrites and leukocyte esterase on the dipstick and was by protocol subjected to routine analysis of the sediment. These pictures demonstrate how technician dependent the preparation of the sediment is, with great potential for varying results.

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Reader Feedback

Readers are invited to ask specific questions and offer personal experiences, comments, or observations on InFocus topics. Literature references are appreciated. Pertinent responses will be published in a future issue. Please send comments to emn@lww.com. Dr. Roberts requests feedback on this month's column, especially personal experiences with successes, failures, and technique.

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