Urinalysis and Body Fluids Exam 1 Study Guide

Quality Assurance and Quality Control in the Urinalysis Laboratory

  • Quality Assurance (QA) Definition: Guaranteeing good patient care?

  • Quality Control (QC) Definition: Are your methods providing results as they should be?

  • Frequency of Quality Control Performance: Once per day of testing

  • Minimum Number of QC Levels: Two levels

  • Protocol for Out-of-Control QC:

    • Patient results cannot be reported if QC is out of range.

  • Qualitative vs. Quantitative Definitions:

    • Qualitative: Testing that determines the presence or absence of a substance (e.g., positive or negative).

    • Quantitative: Testing that determines the exact amount or concentration of a substance (e.g., 150mg/dm3150\,mg/dm^3).

Introduction to Urinalysis: Purpose, Composition, and Collection Methods

  • Value of Urinalysis in Patient Testing: Noninvasive means to evaluate kidney function, Easily collected, Inexpensive

  • Normal Components of Urine: Primarily water (95%95\%) and solutes (5%5\%) such as urea, creatinine, sodium, potassium, and chloride.

  • Sterility of Urine: Urine is generally considered sterile while in the bladder

  • Collection Methods and Types of Urine Samples:

    • Random Urine: Collected at any time. Used for routine screening. Most likely to be contaminated (least sterile).

    • Catheterized Urine: Collected via a sterile tube inserted into the bladder. Used for bacterial cultures and patients unable to void. This is one of the cleanest and most sterile collection methods.

    • First Morning Sample: It is highly concentrated

    • Midstream Clean-Catch: Patient cleans the area and catches the urine mid-stream to minimize contamination from skin flora.

  • Catheterized: May contain epithelial cells due to the trauma of the catheter insertion.

Urinalysis Preservation Methods and Effects of Delay

  • Testing Window: Urine should ideally be tested within 2hours2\,hours of collection if it is not preserved.

  • Effects of No Preservation (Time Delay):

    • Color: May darken due to the oxidation of metabolites.

    • Clarity: Decreases as bacteria multiply and crystals precipitate.

    • Odor: Becomes ammonia-like due to bacterial breakdown of urea.

    • pH: Increases (becomes more alkaline) as bacteria convert urea to ammonia.

    • Glucose: Decreases due to glycolysis by bacteria.

    • Bacteria: Population increases significantly due to multiplication.

  • Refrigeration of Urine:

    • Temperature: Required at 28C2-8\,^{\circ}C.

    • Value: Is that it’s simple

    • Disadvantage (Crystals): Refrigeration causes the precipitation of amorphous phosphates and urates, which can obscure microscopic examination.

  • Chemical Preservatives:

    • Advantages: Stabilize specific chemical analytes.

    • Disadvantages: Can cause drug and hormone interferences or interfere with chemical reagent strip reactions.

Physical Examination of Urine: Color and Appearance

  • Components of Physical Examination: Color, Clarity, Odor, Volume, Specific Gravity, and Osmolality.

  • Yellow Color Source: The pigment urochrome

  • Color as an Indicator of Hydration: Pale yellow indicates overhydration or dilute urine; dark yellow/amber indicates dehydration.

  • Pathological vs. Non-Pathological Colors:

    • Pink: Uroerythrin

    • Orange/Orange-Brown:

      • Non-Pathological: Old samples (oxidation) or Pyridium (Azo meds for UTI).

      • Pathological: Bilirubin (often accompanied by yellow foam).

    • Neon Yellow: Non-Pathological (B vitamins or asparagus).

    • Green:

      • Pathological: Pseudomonas infection.

    • Red:

      • Non-Pathological: Diet rich in beets.

      • Pathological: Presence of intact RBCs (hematuria) or hemoglobin (hemoglobinuria).

    • Port Red (Burgundy/Wine): Porphyrias

    • Brown-Black: Pathological (melanins due to melanoma).

    • Black: Pathological (homogentisic acid due to Alkaptonuria).

  • Foam Observations:

    • No foam: Normal.

    • White foam: Protein.

    • Orange foam: Bilirubin.

  • Follow-up Testing: Color observations must be referenced against Chemistry & Microscopy to verify pathological status.

Concentration and Concentration Instruments

  • Measures of Concentration: Concentration measures the amount of solute present in a given volume of solution. Common measures include:

    • Molarity (M): mols/L

    • Molality (m): mols/kg

  • Specific Gravity (SG):

    • Normal Range: Typically 1.0031.003 to 1.0351.035.

    • Non-Urine Readings: Values above 1.0401.040 usually indicate radiographic dyes (X-ray contrast).

    • Renal Failure: Often results in isosthenuria, where the SG is fixed at 1.0101.010.

  • Correction Formula for Refractometer: glucose and urine & add formua

    • The SG must be corrected for high levels of protein or glucose which contribute to the refractive index but not necessarily renal concentrating ability.

  • Osmometry and Colligative Properties:

    • Colligative Properties: Properties of a solution that depend on the number of solute particles, not their identity (e.g., freezing point depression).

    • Contributing Components: Sodium, chloride, and urea are the primary contributors to urine osmolality.

    • Normal Urine Osmometry: Ranges from 50mOsm/kg50\,mOsm/kg to 1200mOsm/kg1200\,mOsm/kg.

    • Abnormally High: Caused by dehydration or the presence of high-molecular-weight substances (e.g., glucose).

    • Abnormally Low: Caused by excessive fluid intake or conditions like Diabetes Insipidus where the kidneys cannot concentrate urine.