, Score: 0%, must retake test. Scroll down for missed test question numbers

       Quidel QuickVue Influenza A+B
         POCT Competency Record

Name:  

Date:

Emp ID:

Clinic / Unit:
TSM Name:

Preceptor(s):

CERT EXPIRES

POC Test: Quidel QuickVue Influenza A+B 

AFTER TAKING ONLINE TEST AND READING THE POLICY, EMPLOYEE PERFORMS A TEST AND  MARKS RESULTS BELOW.  THE PRECEPTOR OR TSM GRADES RESULTS FOR ACCURACY.

1. Reads entire Policy/Procedure
2. Completes and passes written test (Passing criteria is 100%)
3. Return demonstration

TEST SCORE: 0
Test taken on:
5/26/2013

 CRITICAL POINTS FROM POLICY AND PROCEDURE

OPERATOR INITIALS

a. Specimen:
Acceptable specimens for the QuickVue Influenza A+B Test are: a nasal swab, nasal wash, or nasal aspirate.
Specimens should be tested as soon as possible after collection.
Specimens may be stored refrigerated (2-8°C), or at room temperature (15-30°C) in a clean dry closed container for up to eight (8) hours prior to testing. DO NOT use any kind of transport media to store or transport samples.

Unacceptable specimens: Specimens taken from other sites i.e. saliva, sputum, urine. Samples collected with swabs not provided by Quidel test kit

 

b. Patient Testing:
1. Dispense one reagent tube of Extraction Reagent Solution into an Extraction Tube and gently swirl to dissolve contents.
2. Place patient nasal swab into extraction tube. Swabs MUST stay in the extraction solution for 1 minute prior to removal.
3. Roll swab at least three times while pressing the head against the bottom and side of the extraction tube. Roll the swab head against the inside of the Extraction Tube as you remove it. 4. Dispose of the swab in accordance with your biohazard waste disposal protocol.
5. Place the test strip into the extraction tube with the arrows on the test strip pointing down. Do not handle or move the test strip until the test is complete and ready for reading.

6. After ten minutes has elapsed, hold the test strip with the arrows pointed down to interpret test results.

 

 c. Interpretation of Results:
Postiive Result:
At 10 minutes, ANY shade of pink-to-red Test line forms AND appearance of a blue procedural Control Line indiciates a positive result for the presence of viral antigen

Negative Result: At 10 minutes, the appearance of ONLY the blue procedural Control Line indicated the sample is negative for viral antigen.
A negative result should be reported as a presumptive negative for the presence of influenza antigen and a second nasal swab should be submitted to the MICRO lab for viral culture
 

Invalid Result: If at 10 minutes, the blue procedural Control Line does not appear, even if any shade of pink-to-red Test line appears, the result is considered invalid. If at  10 minutes the background color does not clear and it interferes with the reading of the test, the result is considered invalid. If the test is invalid, a new test should be performed with a new patient sample and a new test strip.

 

c. Quality Control:
Document appearance of onboard Control Line on first sample on day of patient testing. Also 2 Liquid Controls must be documented when a new Lot Number of kits is opened.

 

d. Reagent Storage:
Store test kit at room temperature (15-30°C) and kept away from direct sunlight. Do NOT freeze and Do NOT use kits beyond the expiration date printed on the outside of the box.

 

 

Sample: _________________     Result: ________________      Pass: _____Yes _____No 

VALIDATOR:

___________

                          

Please Print this page and bring to check offs. Passing Score is 100%
This application requires INTERNET EXPLORER. Application will not work properly with NETSCAPE.
 

To Online Tests  

 To POC HOME


If experiencing problems with this application, please contact David Shumate at (409) 747-2497 
Online Test Program maintained by Pathology Clinical Services POC at the University of Texas Medical Branch
This application requires INTERNET EXPLORER. Application will not work properly with NETSCAPE.