Practical Veterinary Urinalysis E-Book

Carolyn A. Sink

• Herausgeber: John Wiley & Sons
• Kategorie: Fachliteratur
• Sprache: Englisch

Seitenzahl: 197

Veröffentlichungsjahr: 2011

Beschreibung

Practical Veterinary Urinalysis is a comprehensive, clinically relevant resource for the veterinary laboratory. This bench-top guide covers sample handling guidelines, interpretation of dry chemical analysis, and recommendations for physical and microscopic evaluation. Emphasizing diagnostic techniques and result interpretation, Practical Veterinary Urinalysis is an ideal aid for anyone who performs and interprets urinalysis testing. Beginning with an overview of renal physiology and urine production, the main focus of the book is examination and analysis of urine samples, including physical properties, chemical analysis, and sediment examination. Additional chapters review diagnostic tests and considerations for proteinuria, advanced diagnostics, quality assurance and laboratory set-up. Practical Veterinary Urinalysis is an invaluable tool for achieving accurate and reliable laboratory results and is a useful addition to any veterinary library.

Leseprobe

Table of Contents

Cover

Title page

Copyright page

Dedication

Preface

Acknowledgments

Chapter 1 Functional Renal Physiology and Urine Production

Glomerular filtration

Tubular reabsorption and secretion

Collecting tubules

Renal function and measures of renal function

Laboratory assessment of renal function

Chapter 2 Specimen Procurement

Laboratory definitions for collection methods

Urine specimen containers

Specimen handling and preservation

Types of urine specimens

Chapter 3 Routine Urinalysis: Physical Properties

Solute concentration

Urine color

Chapter 4 Routine Urinalysis: Chemical Analysis

pH

Protein

Glucose

Ketone

Blood

Bilirubin

Urobilinogen

Nitrite

Leukocyte esterase

Specific gravity

Chapter 5 Routine Urinalysis: Microscopic Elements

Urine sediment preparation

Examination of urine sediment

Microscopic elements of urine sediment

Chapter 6 Proteinuria

Protein handling by the kidney

Significance of proteinuria

Laboratory diagnosis of proteinuria

Recommendations regarding diagnosis of proteinuria

Additional considerations for proteinuria

Chapter 7 Advanced Diagnostics

Detection of bacteriuria versus diagnosis of urinary tract infection

Urinary tract cytology

Fractional excretion

Urinary biomarkers

Chapter 8 Laboratory Quality Assurance

Physical requirements of the laboratory

Laboratory equipment

Reagents and supplies for the urinalysis laboratory

Laboratory waste

Quality control in the urinalysis laboratory

Procedure manuals

Index

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Library of Congress Cataloging-in-Publication Data

Sink, Carolyn A.

 Practical veterinary urinalysis / Carolyn Sink and Nicole Weinstein ; illustrations by Ashley Marlowe.

p. ; cm.

 Includes bibliographical references and index.

 ISBN 978-0-470-95824-7 (pbk. : alk. paper)

 ISBN 978-1-119-94602-1 (epub)

 ISBN 978-1-119-94601-4 (epdf)

 ISBN 978-1-119-94603-8 (mobi)

 I. Weinstein, Nicole. II. Title.

 [DNLM: 1. Urinalysis–veterinary–Laboratory Manuals. SF 773]

 LC classification not assigned

 636.089'66–dc23

2011035231

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Disclaimer

The publisher and the author make no representations or warranties with respect to the accuracy or completeness of the contents of this work and specifically disclaim all warranties, including without limitation warranties of fitness for a particular purpose. No warranty may be created or extended by sales or promotional materials. The advice and strategies contained herein may not be suitable for every situation. This work is sold with the understanding that the publisher is not engaged in rendering legal, accounting, or other professional services. If professional assistance is required, the services of a competent professional person should be sought. Neither the publisher nor the author shall be liable for damages arising herefrom. The fact that an organization or Website is referred to in this work as a citation and/or a potential source of further information does not mean that the author or the publisher endorses the information the organization or Website may provide or recommendations it may make. Further, readers should be aware that Internet Websites listed in this work may have changed or disappeared between when this work was written and when it is read.

This book is dedicated to veterinary students, clinical laboratory professionals, clinical veterinarians, and all those who continue to develop and improve the veterinary clinical laboratory.

Preface

Laboratory evaluation of urine provides a significant amount of information to the veterinarian, as a variety of disease states may produce abnormal findings. Routine laboratory tests used to assess urine are quick and inexpensive, as well as reliable, when performed by a well-trained laboratory professional. Practical Veterinary Urinalysis is intended to provide laboratory diagnosticians—veterinarians, medical technologists, veterinary technicians, and veterinary students—with a comprehensive study of all aspects of routine urinalysis, including chemical analysis and microscopy. Those tasked with performing routine urinalysis will find both consolidated and comprehensive information needed to produce timely and accurate results.

Practical Veterinary Urinalysis is designed to provide the reader with a concise, systematic overview of renal physiology and urine production. Both functional and physiological aspects of the urinary system are reviewed with disease processes highlighted. When appropriate, discussions are reinforced by images, tables, and drawings. Specimen collection and handling are reviewed with emphasis on differences in laboratory findings between three frequently used methods.

An in-depth discussion of urine physical properties, chemical analysis, and sediment analysis is covered in separate chapters. Summarized charts are provided as testing guides when appropriate. Within the microscopic analysis section, Practical Veterinary Urinalysis contains images of the wet prep along with cytology (Wright’s stain), and Gram stain if indicated.

Abnormal or suspicious results obtained by routine urinalysis may mandate additional or confirmatory tests. A chapter dedicated to advanced urine diagnostics presents newer test methodologies, and associated laboratory procedures are discussed.

Practical Veterinary Urinalysis also includes sections dedicated to laboratory setup, including physical and functional requirements along with instrument, reagent, and supply preferences. Quality assurance measures and quality goals are defined, assuring laboratorians that the results they produce are reliable.

Acknowledgments

We are grateful for the support and guidance of Drs. Rachel Cianciolo and Reema Patel, who provided invaluable insight and editorial commentary. We would also like to acknowledge veterinary students Rachel Baum and Alicyn Cross for their laboratory prowess in identifying interesting urine samples used in this book.

Carolyn Sink and Nicole Weinstein

Chapter 1

Functional Renal Physiology and Urine Production

Urinalysis can provide insight into hydration status, renal function or dysfunction, systemic disease, and toxic insults. Accurate interpretation of urinalysis results requires knowledge of renal physiology and urine formation.

Given the complexity of both, a brief overview is presented below; more detailed explanations can be found in a variety of references on which this chapter is based (Gregory 2003; Kaneko 2008; Schrier 2007; Stockham and Scott 2008; Watson 1998).

Descriptions of renal function and schematics of the kidney typically portray a single nephron, which is the functional unit of the kidney; each kidney contains hundreds of thousands of nephrons working in unison (Reece 1993). Each nephron requires:

(1) A blood supply

(2) A functional glomerulus, which filters a portion of the renal blood flow, to form an ultrafiltrate

(3) Renal tubules that function to reabsorb water, electrolytes, and other substances from the ultrafiltrate

(4) Collecting tubules and ducts, which further reabsorb or excrete water and solutes and thus determine final urine concentration.

Urine formation starts as an ultrafiltrate formed by glomerular filtration. The ultrafiltrate is then further altered by tubular reabsorption and secretion.

Glomerular Filtration

The glomerulus is a collection of twisted capillaries that receive blood from the afferent arteriole of the renal blood supply and exit the kidney via the efferent arteriole (Figure 1.1). The high pressure within this system results in passage of fluids and small substances out of the capillaries into a space around the glomerulus, known as Bowman’s capsule, which together form a renal corpuscle. Glomerular filtration is driven by both blood volume and pressure and is considered a primarily passive process. Ultrafiltrate is the product of glomerular filtration of blood following its passage through a glomerular filtration barrier, the glomerular capillary wall (GCW). The GCW prevents entry of red and white blood cells, platelets, and larger proteins into the ultrafiltrate. The exact composition and function of the GCW is the subject of intense research and debate currently in the human literature. Additional information is presented about glomerular filtration and the GCW in Chapter 6, “Proteinuria.”

Figure 1.1 Glomerulus.

Concentrations of urea, creatinine, amino acids, glucose, bicarbonate, and electrolytes are similar between the ultrafiltrate and plasma. Specific gravity (SG) which ranges from 1.008 to 1.012 and osmolality (300 mOsm/kg with a range of 280–310 mOsm/kg) will also be similar between the two (Watson 1998). Note the SG range of 1.008–1.012 is identical to the range described for isosthenuria. For additional information regarding interpretation of urine specific gravity (USG), see Chapter 3. Knowledge of this range is relevant for the diagnosis of renal failure as well as the interpretation of urine with an SG of less than 1.008. Chapter 3, “Routine Urinalysis: Physical Properties,” discusses USG in greater detail.

Renal blood flow ultimately determines the glomerular filtration rate (GFR) or rate of blood flow within the glomerulus. GFR can be affected by numerous factors such as a patient’s blood volume, cardiac output, and total number of functional glomeruli (Stockham and Scott 2008). GFR and direct and indirect measures of GFR can therefore be influenced by renal disease as well as nonrenal factors such as dehydration, severe blood loss, hypotension, diuretic use, fluid therapy, and hypoalbuminemia to name a few.

Ultrafiltrate exiting Bowman’s capsule enters into the proximal convoluted tubule (PCT).

Tubular Reabsorption and Secretion

Tubular reabsorption and secretion employ both passive and active mechanisms to ultimately form urine, conserve water and necessary solutes, and excrete waste products. The renal tubules are divided into the PCT, ascending and descending loops of Henle, distal convoluted tubule, and the collecting duct. Each segment serves to reabsorb and/or secrete water and various solutes (Figure 1.2). Reabsorption serves to prevent water and solutes from being excreted into the tubular fluid while secretion results in loss of either into the tubular fluid. Water and solutes remaining in the tubular fluid are excreted as urine.

Figure 1.2 Solute and water handling in the renal tubule.

Source: Gregory (2003); Kaneko (2008); Stockham and Scott (2008).

Proximal Convoluted Tubule

The majority of water and solutes are reabsorbed in the PCT. Sodium is actively reabsorbed in the PCT via several mechanisms and water follows passively. In addition to sodium reabsorption, conservation of amino acids, glucose, phosphate, chloride, potassium, and bicarbonate occurs in the PCT. Fluid in the PCT displays only mild increases in SG and osmolality relative to the ultrafiltrate. Ultimately, water conservation reduces the volume of tubular fluid by 70% (Kaneko 2008; Stockham and Scott 2008; Watson 1998).

Loop of Henle

The loop of Henle includes a descending loop and ascending loop that serve to reabsorb more water and electrolytes through both passive and active mechanisms. The renal medullary interstitium, which is the tissue and fluid surrounding the tubules, and peritubular capillaries are integral parts of the conservation of water and electrolytes.

The descending loop of Henle is permeable to water but is impermeable to electrolytes. As the loop descends into the renal medulla, which is maintained at a higher osmolality due to higher concentrations of both sodium and urea, the water will exit the loop in an attempt to equilibrate with the surrounding interstitium, thus serving to conserve water. As water exits the tubular fluid, the osmolality and SG greatly increase as the tubular fluid prepares to enter the ascending loop.

The ascending loop of Henle is opposite to the descending loop and is permeable to urea and electrolytes (mostly sodium, chloride, and potassium) but impermeable to water. Tubular fluid ascends the loop of Henle and becomes increasingly more dilute as sodium and chloride are first passively and then actively reabsorbed into the medullary interstitium. Medullary interstitial hypertonicity results from the increase in sodium concentration.

Blood vessels, specifically peritubular capillaries that parallel the loop of Henle, are termed the “vasa recta.” Blood in the vasa recta flows in the opposite direction to the fluid in the loop of Henle. The loop of Henle, together with the vasa recta and interstitium, comprise a countercurrent system. The process of countercurrent multiplication is essential in maintaining a concentration gradient within the medullary interstitium as both the descending loop of Henle and collecting ducts require a hypertonic medullary interstitium for water reabsorption. Therefore, the hypertonicity of the medullary interstitium is a product of the descending loop of Henle as described above. A basic understanding of this gradient aids in interpreting extrarenal influences on urine concentration and will be discussed below (Gregory 2003; Kaneko 2008; Schrier 2007; Stockham and Scott 2008; Watson 1998).

Distal (Convoluted) Tubule

The epithelial cells of the distal tubule demonstrate minimal permeability to water. Sodium and chloride, however, can be reabsorbed from the tubular fluid in this segment primarily under the influence of aldosterone, antidiuretic hormone (ADH), and other substances.

Collecting Tubules

Although the majority of water and solute reabsorption occurs in the PCT and loop of Henle, the collecting tubules determine the final urine volume and USG. The collecting tubule is impermeable to water except in the presence of ADH, which results in reabsorption of water. ADH levels ultimately determine whether urine will be dilute or concentrated. High concentrations of urea, sodium, or chloride in the medullary interstitium facilitate ADH reabsorption of water, again reinforcing the necessity of a hypertonic renal medullary interstitium. In the absence of ADH, dilute urine is produced.

Renal function and measures of Renal Function

In the normal state, the goal of the kidneys is to conserve water, glucose, amino acids, sodium, chloride, bicarbonate, calcium, magnesium, and most proteins, and to excrete urea, creatinine, phosphate, potassium, hydrogen ions, ammonium, ketones, bilirubin, hemoglobin, and myoglobin (Stockham and Scott 2008). Additional roles of the kidneys include, but are not limited to, erythropoietin synthesis to stimulate red blood cell development, acid–base regulation, renin secretion, calcium and phosphorous homeostasis, and blood pressure regulation. Urea nitrogen (UN) and creatinine are both waste products of metabolism and are filtered and excreted by the kidneys into the urine.

Urea Production and Excretion

The liver converts ammonia, which is a product of intestinal protein catabolism, into urea. Urea, following release by the liver into the blood, is freely filtered by the glomerulus and enters the ultrafiltrate. Urea follows water into and out of the renal tubules. The amount of urea excreted in the urine varies from 40% to 70% of the ultrafiltrate and is mostly determined by flow rate within the tubules (Schrier 2007). At higher urine flow rates (i.e. increased water or fluid intake), less urea is reabsorbed and so more is excreted in the urine. Decreased urine flow rate (i.e. dehydration) results in a greater amount of urea reabsorption and so less is excreted into the urine.

Creatinine Excretion

Creatinine is produced at a constant rate from normal muscle metabolism where creatine in muscle is converted to creatinine (Gregory 2003; Kaneko 2008; Stockham and Scott 2008). Creatine concentrations are influenced by an animal’s muscle mass and underlying disease states. Similar to urea, creatinine is freely filtered by the glomerulus, meaning it passes through the glomerular filtration barrier and enters into the tubular fluid. In contrast to urea, creatinine is not reabsorbed by the renal tubules. A small amount of creatinine, however, is excreted by the proximal tubule in male dogs.

Laboratory Assessment of Renal Function

Urea and creatinine concentrations are the most commonly utilized tests to evaluate renal function. Urea concentration, typically measured in serum or plasma, is reported as UN or blood urea nitrogen (BUN). The amount of urea in whole blood, serum, or plasma is identical because urea rapidly equilibrates between compartments. Because of the variability in the amount of urea presented to the kidney and the potential for tubular reabsorption of urea, both nonrenal and renal factors influence BUN. Creatinine is a more accurate measure of GFR given its constant rate of formation and lack of tubular reabsorption (Kaneko 2008; Stockham and Scott 2008).

Azotemia

An increase in BUN and creatinine is termed azotemia. Azotemia can be prerenal, renal, or postrenal in origin although causes may be multifactorial. Prerenal azotemia results from decreased renal blood flow. Examples of prerenal azotemia include hypovolemia due to dehydration or hemorrhage, shock, decreased cardiac output, hypotension, and so on. Concentrated urine (USG > 1.030 in dogs and >1.035 in cats) is an expected finding with prerenal azotemia. Renal azotemia can be due to acute or chronic renal failure as a result of greater than 75% loss of functioning glomeruli. Renal azotemia results in inadequately concentrated urine (USG < 1.030 in dogs and <1.035 in cats); isosthenuria (USG 1.008–1.012) in the face of azotemia is indicative of renal disease. Postrenal azotemia is caused by obstructed urine flow from urethral or ureteral obstruction (i.e. urinary calculi), bladder rupture, neoplasia, neurologic disease, or congenital abnormalities. The USG can vary with postrenal azotemia. BUN and creatinine concentrations tend to parallel one another in renal and postrenal causes of azotemia. Increases in BUN without a concomitant increase in creatinine or a disproportionally higher increase in BUN relative to the increase in creatinine can be seen in certain prerenal conditions, that is, increased protein catabolism and dehydration. As described earlier, diminished renal tubular flow rate and the presence of ADH both increase urea reabsorption by the renal tubules and can elevate BUN. Increased protein catabolism, especially in animals fed a high-protein diet or with small intestinal bleeding, can result in elevated BUN (Table 1.1).

Table 1.1 Pre-renal causes of an increased BUN

Source: Gregory (2003); Stockham and Scott (2008)

Increased protein catabolismFever Starvation Corticosteriods High protein diet Prolonged exercise Small intestinal hemorrhageDecreased excretion due to decreased renal blood flow*Shock Hypotension Decreased cardiac output (e.g., heart failure) Hypovolemia (dehydration, hemorrhage, hypoadrenocorticism)

* May also cause increase in serum creatinine concentration.

Decreased BUN can hinder renal concentrating ability. Urea contributes approximately half of the hypertonicity of the renal medullary interstitial fluid, which facilitates water reabsorption from the tubular fluid. Decreased BUN can result from hepatic failure or shunting of hepatic blood flow away from the liver (i.e. portosystemic shunt) so that ammonia cannot be converted into urea. Increased renal excretion of urea can also decrease BUN such as with excess glucose in the renal tubular fluid (i.e. diabetes mellitus) or very high renal tubular flow rates. Low BUN can then result in a lower than expected USG even in a dehydrated patient. BUN value should be considered when interpreting USG. Similarly, low plasma concentrations of sodium and chloride, termed hyponatremia and hypochloremia, respectively, can also diminish renal concentrating function due to a less hypertonic renal medullary interstitium.

Although routine, BUN and creatinine are relatively insensitive measures of renal function. Renal azotemia does not develop until after 75% or greater functional nephrons are lost or damaged. In renal failure, the diseased kidneys cannot adequately excrete urea or creatinine. Postrenal causes of azotemia also result in an inability to excrete urea and creatinine from the body. Determination of prerenal, renal, and postrenal causes of azotemia utilize USG as well as historical, physical exam, and other clinicopathological data.

Osmolality

Osmolality is the concentration of solutes in a solution (Kaneko 2008; Stockham and Scott 2008; Watson 1998). The largest contributors to plasma osmolality are sodium, urea, and glucose (Stockham and Scott 2008). Plasma osmolality is sensed by receptors in the hypothalamus. Plasma osmolality and osmolality within the renal tubular fluid and medullary interstitium, as described above, impact urine formation. Increased plasma osmolality results in ADH release, which stimulates the collecting tubules and ducts to reabsorb water. The opposite is true of decreased osmolality. With low plasma osmolality, ADH is not secreted and more water is excreted into the urine.

In conclusion, renal physiology is a complex and elaborate process. This chapter provides only a brief summary of basic renal function so as to facilitate understanding of the physiologic processes that impact and determine urine formation and to maximize interpretation of urinalysis.

References

Gregory CR. 2003. Urinary system. In Duncan & Prasse’s Veterinary Laboratory Medicine Clinical Pathology, 4th ed. Latimer KS, Mahaffe EA, Prasse KW, eds., pp. 231–59. Ames, IA: Iowa State Press.

Kaneko JJ. 2008. Kidney function and damage. In Clinical Biochemistry of Domestic Animals, 6th ed. Kaneko JJ, Harvey JW, Bruss ML, eds., pp. 485–528. Burlington, VT: Elsevier Inc.

Reece WO. 1993. The kidneys. In Dukes’ Physiology of Domestic Animals, 11th ed. Swenson MJ, Reece WO, eds., pp. 573–603. Ithaca, NY: Cornell University Press.

Schrier RW. 2007. Laboratory evaluation of kidney function. In Diseases of the Kidney and Urinary Tract, vol. 1, 8th ed. Schrier RW, ed., pp. 299–366. Philadelphia: Lippincott Williams & Wilkins.

Stockham SL, Scott MA. 2008. Urinary system. In Fundamentals of Veterinary Clinical Pathology, 2nd ed. Stockham SL, Scott MA, eds., pp. 415–94. Ames, IA: Blackwell Publishing.

Watson ADJ. 1998. Urine specific gravity in practice. Australian Veterinary Journal 76(6): 392–8.

Chapter 2

Specimen Procurement

Urinalysis test results are influenced by many preanalytical variables, the majority of which can be controlled during urine specimen collection. This chapter reviews common methods of urine collection, appropriate use of urine specimen containers and urine preservation techniques, and the potential impact of each on urinalysis results. Minimizing these preanalytical variables will allow for the most consistent and reliable urinalysis results.

Laboratory Definitions for Collection Methods

An overview of collection methods may be found in Table 2.1.

Table 2.1 Advantages and disadvantages of urine collection methods

Method of CollectionProConFree-catchNo risk to the patient Easy to perform Can be used to localize lesionUnsuitable for bacterial culture Contaminants common Subject to patient’s need to urinateManual expressionNoneRisk of bladder injury Possible reflux of urine into kidneys, prostate Difficult to impossible in awake patientsCatheterizationLower risk of contamination Relatively safe for the patientTechnical skill required Often requires sedation Challenging in a patient with obstructionCystocentesisBest sample for bacterial culture Can be performed in awake patient Relatively safeTechnical skill required Blood contamination in sample Increased risk to patient for hemorrhage, bladder rupture Avoid in patient with coagulopathy

Voided or “Free Catch”

Natural micturition is the least invasive method of collecting urine (Wamsley and Alleman 2007). Ideally, urine is collected midstream as first-stream urine is more likely to contain bacteria, cells, and other debris from the vulva, urethra, or prepuce. To further minimize contamination, the patient’s urogenital area can be cleansed prior to specimen collection and a sterile container can be used to catch the urine. Free-catch samples are most at risk for contamination by the genital tract, skin, or hair, which can result in a false-positive urine bacterial culture (Osborne and Stevens 1999). If the only urine sample available for culture is a free-catch sample, quantitative analysis should be performed (Reine and Langston 2005).