background image

 

 

 
 

 

 
 
 

HOSPITAL 

 

GUIDELINES OF PRACTICE

 

 

NUMBER:

  HP 300-121 

Page 1 of 5 

 

EFFECTIVE DATE:

 

 

June 12, 1991 

 

TITLE:

 

ACCU-CHECK INFORM II BLOOD GLUCOSE MONITORING SYSTEM 

PRINCIPLE 

The ACCU-CHEK Inform II system quantitatively measures glucose in whole blood.  The enzyme on the 
test  strip,  mutant  variant  of  quinoprotein  glucose  dehydrogenase  from  Acinetobacter  calcoaceticus, 
recombinant in E. coli, converts the glucose in the blood sample to gluconolactone.  This reaction creates 
a  harmless  electrical  DC  current  that  the  meter  interprets  for  a  glucose  result.    The  sample  and 
environmental conditions are also evaluated using a small AC signal. 

The system is calibrated with venous blood containing various glucose concentrations and is calibrated to 
deliver plasma-like results.  The reference values are obtained using a validated test method.   This test 
method is referenced to the hexokinase method and is traceable to an NIST standard. 

SPECIMEN 

Proper blood sample collection is an essential and integral part of bedside blood glucose testing.

 

Acceptable Samples 

1.  The  following  fresh  whole  blood  sample  types  may  be  used  (all  line  draws  must  be  used  within  30 

minutes of collection): 

a.  Venous whole blood 
b.  Arterial whole blood 
c.  Capillary (non-neonate finger stick and neonate heel stick) whole blood (test immediately)  

2.  The following anticoagulants are acceptable (do not use any other anticoagulants for meter testing): 

a.  Lithium or Sodium Heparin; EDTA 

3.  Refer to 

Mosby’s Nursing Skills

 for detailed instructions on how to perform a finger or heel stick. 

MATERIALS 

 

Accu-Chek Inform II meter 

 

Accu-Check Inform II glucose strips 

 

Accu-Chek Inform II Quality Control solutions 

 

Accu-Chek Inform II Linearity Kit 

 

Accu-Check Inform II base unit 

 

Lancet devices 

 

Gloves 

 

Sharps container 

  Alcohol wipe 

REAGENT STORAGE, HANDLING, AND STABILITY 

Meters,  system  components  and  reagents  are  stored,  maintained  and  handled  according  to 
manufacturer’s  instructions  and  in  compliance  with  all  established  safety  and  infection  control  policies 
and regulatory guidelines. 

Test Strip Storage and Handling 

 

Use the test strips at temperatures between 61-95°F (16-35°C) and between 10-80% relative humidity. 

 

Store the test strips at temperatures between 36-86°F (2-30°C).  Do not freeze. 

 

Store unused test strips in the original container with the cap closed.  Do not remove test strips from the 
test strip container and put them into another container such as a plastic bag or pocket, etc., (to protect 
from humidity). 

 

Use the test strip immediately after removing it from the container. 

 

Discard the test strips that are past the expiration date printed on the test strip container.  If the expiration 
date is missing or illegible, do not use the test strips. 

 

Do not apply blood or control solution to the test strip before inserting it into the meter.  If a result appears 
before applying

 

blood or control solution, do not act on that result. 

 

APPROVED BY/TITLE: 

 

 

DATE REVIEWED: 

 

DATE REVISED:

  06/26/13 

Summary of Contents for Inform II Competency

Page 1: ...NORTHERN ARIZONA HEALTHCARE ACCU CHEK Inform II Competency 2013 Sponsored by the Education Department...

Page 2: ...your clinicals 2 Complete the Post Test and use the Answer Sheet provided to record your responses to the Post Test Print out the answer sheet and sign the statement showing that you have read the Gui...

Page 3: ...erstick and neonate heelstick whole blood b The following anticoagulants are acceptable do not use any other anticoagulants for meter testing i Lithium or Sodium Heparin EDTA c Sufficient sample size...

Page 4: ...oratory DO NOT attempt to perform tests under another operator s ID c From the Main Menu touch Control Test d Select the level of control that you wish to test e Confirm that the meter is coded calibr...

Page 5: ...Patient Testing a Wash hands and don personal protective equipment gloves gowns etc as required by infection control and isolation policies and procedures b Assemble the finger stick equipment the me...

Page 6: ...ent is complete when the result is displayed on the screen Depending upon how high or low the result is it may appear in a numeric or non numeric format See Interpretation of Results section below for...

Page 7: ...ent result obtained by the ACCU CHEK Inform ll does not appear to fit the clinical picture repeat the QC and patient specimen A You must use the comment Repeat will not post on the repeat test The pat...

Page 8: ...nd results as soon as a wireless connection is established The meter will connect to Cerner every 10 minutes and transfer new data when a wireless connection is available even if the meter is powered...

Page 9: ...elson MT ASCP 7 12 Karen McMullin Director 7 12 4 13 Approved by Title Date Susanne Maiden CNO VP 6 13 Committee Approval Date Policy Procedure 10 06 5 18 07 Nursing Practice 8 25 10 GOP 9 21 10 7 17...

Page 10: ...anticoagulants for meter testing a Lithium or Sodium Heparin EDTA 3 Refer to Mosby s Nursing Skills for detailed instructions on how to perform a finger or heel stick MATERIALS Accu Chek Inform II met...

Page 11: ...ated to the same test strip code that is printed on the test strip vial by scanning the test strip vial s barcode Contact the laboratory if unable to confirm the correct test strip code 6 The meter wi...

Page 12: ...ID by means of scanning the barcode on your identification badge NOTE If the operator ID you enter is not accepted attempt to re enter it If it is still rejected contact your supervisor or Point of Ca...

Page 13: ...ensuring proper sample application or refer to the test strip package insert Guidance for Interpreting On Screen Message and Error Codes All error messages displayed by the system have a letter ident...

Page 14: ...0 mg dL and for newborns 30 mg dL and 300 mg dL Patient test results that exceed critical limits must be called to the patient s provider and then documented in the patient electronic medical records...

Page 15: ...If it is not the correct amount it will give an error code a True b False 3 After applying the sample to the test strip and the measurement begins an error message occur this means a The sample is in...

Page 16: ...e more times to be sure d None of the above 9 What is true of test strip handling a Test strips do not have an expiration date b Remove the test strip from the vial and immediately recap the vial c Un...

Page 17: ...rop of blood to the front edge of the Accu chek Inform ll test strip a True b False 14 Only capillary whole blood samples should be used when testing the Accu chek Inform ll meter and the Accu chek In...

Page 18: ...d 7 a b c d 8 a b c d 9 a b c d 10 a b 11 a b c d e 12 a b c d e 13 a b 14 a b Instructor s Name ___________________________________________________ The undersigned certifies as follows I have read t...

Page 19: ...onfirmation 30 or 500 mg dL 6 months to Adult 30 or 500mg dL 0 6months States emergency ID when patient is unidentified 0911911 Verbalizes how to enter a custom comment patient s name 5 Cleaning State...

Page 20: ...ral laboratory for confirmation 30 or 500 mg States emergency ID when patient is unidentified 0911911 Verbalizes how to enter a custom comment patient s name 5 Cleaning States proper infection control...

Reviews: