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Accu-Chek Inform � System

General Information

  • The Inform meter is ready for use when it has been charged on the base unit.
  • Meter should be docked in the base unit when not in use.
  • Accu-Chek Inform meters use a rechargeable battery. 
  • You must have an order written by a physician for glucose testing. 
  • Operator ID is your license number.
  • Patient ID is the 12 digit medical record number.
  • Labels are not to be used for patient identification.
  • Patient armband is the only method for positive patient identification.
  • Patient ID can be scanned or entered into the meter.
  • Meters are configured according to Sinai�s policies and procedures.
  • The Accu-Chek meter will not allow patient testing when controls have not been run (QC lock-out).
  • Two levels of controls, high and low once a day.
  • Controls are good for 3 months after opened or the expiration date on the label. When a new bottle of controls is opened it should be labeled with the date opened and the 3 month expiration date.
  • Inform meter will store up to 4,000 results.
  • Strips are good until the expiration date written on the bottle.
  • When a strip is removed it should be closed immediately. Moisture from the air can make the strip give inaccurate results if the bottle is left open. If you find a bottle left opened, discard and use a new bottle.
  • Insulin is not to be stored in the glucose accessory box.
  • The accessory box contains a troubleshooting guide for the Accu-Chek Inform system. 
  • Range of the meter is from 10mg/dL to 600mg/dL.
  • All of the yellow area on the test strip should be covered either with control or blood when performing test.  You have up to 15 seconds to add additional blood or control if area is not filled completely.
  • Gloves must be worn when performing QC or patient test and then discarded in biohazard container.
  • Finger stick is always performed on the side of the finger and not in the middle because of nerve endings.
  • Capillary, whole blood samples can be used when testing with the inform system.
  • If results do not coincide with clinical symptoms, repeat test or send sample to main laboratory. 
  • Critical Values for Adults: Obtain a specimen and send to the laboratory if the glucose is: 
    50 mg/dL  or 400mg/dL
    (Only exception is the patient who is on an insulin drip and on a tight glucose protocol.)
  • Comments: One of the following comments may be added to a result.
    • Sent specimen to lab
    • Repeat Test
    • Wrong QC Level
    • Operator Error
    • Cleaned Meter
    • GTC Protocol (for those units that have a patient on an insulin drip on tight glucose control)

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