Employee Information  Agency staff, please use your assigned 4 digit ID. Core staff must use UTMB employee ID
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Workplace  Using the appropriate selection box below, please select your area of workplace. Note: TDC, Agency, and Medical Students may be selected using the Hospital Service selection box.
 
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I have read the UA Dip Policy and Procedure  Yes

Click on START TEST to begin

Test Date:     

      

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

1. The pH pad is read as a negative or positive result.

TRUE
FALSE
 


                                                                                            

 

 

 

 

 

2. It is Monday morning and you work at a local Geriatrics Clinic; your patient's sibling hands you her mother's urine specimen for testing as requested by MD. While in the process of dipping the urine specimen, the LVN asks you for Ms. Field's BP reading. You lay the urine-dipped strip on counter to look up Ms. Field's BP reading in EPIC. When you come back the strip is almost dry, you proceed to:

Record the UA strip results, and document/ report to physician.
Re-dip urine and read results at one minute, but no later than 2 minutes.

                                                                                            

3. Joint Commission oversees POC testing compliance at UTMB. How often are urine strips QC'd?

1X a week for every opened bottle and when a new vial is opened
2X a week for every opened bottle and when a new vial is opened
3X a week for every opened bottle and when a new vial is opened
1X a month for every opened bottle and when a new vial is opened

                                                                                       

 

 

 

 

 

 

4. Laura Mills is a 39 y/o pregnant female who came into the ER. Upon dipping her urine you notice a speckled pattern on the blood reagent pad. The most likely explanation for this phenomenon is:

The reagent on the pad is no longer reactive. More than likely due to expired, non-functional strips.

Intact rbc's are present in the sample (as opposed to free hemoglobin released from rbc lysis which gives a homogenous pattern)

The blood reagent pad is contaminated

                                                                                            

5. When dipping a urine specimen, what is the reasoning behind blotting off excess urine off the strip?

The reagent pads on the strip need just the right amount of urine to react properly and produce accurate results.

The 'run-off' phenomenon which may lead to erroneous results is avoided as each reagent pad or reacting area holds a different active ingredient.

The acidity effects of the urine on the reagent pads are minimized.

  It avoids having to read the strip at a longer read time.

                                                                                            

6. Sensitivity of the bilirubin reacting area may not be sufficient to detect small amounts of bilirubin in the urine.

TRUE
FALSE

                                                                                            

7. A positive PROTEIN result most likely indicates the presence of albumin; however, other proteins such as globulins, Bence Jones (immunoglobin's light chains) can give a positive result.

TRUE
FALSE

                                                                                            

8. When Urine Control Solutions are stored at refrigerator temperatures (2-4 celsius), the control material is good until the expiration date on dropper vial.  However, if room temperature option is chosen, controls are only good for 1 MONTH.

TRUE
FALSE

                                                                                            

9. Unlike the URINE CLINITEST TABLETS which detect multiple sugars in addition to glucose (i.e. lactose, galactose, fructose) in urine and stool specimens, the glucose reagent pad on the chemstrip ONLY DETECTS GLUCOSE.

TRUE
FALSE

                                                                                            

10. The following are good QUALITY CONTROL practice:

Verifying function & stability of STRIPS using UA CONTROL SOLUTIONS
Checking expiration dates of UA CONTROL SOLUTIONS prior to using
Writing 'Open Dates' on both CONTROL SOLUTIONS, STRIPS, or any other kits used for patient assessment.
Verifying LOT NUMBER of UA CONTROL solutions match those on the QC LOG / SHEET
ALL OF THE ABOVE