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  • App C Hemocue Qc Log Dch-1488 0811.doc - Michigan

Get App C Hemocue Qc Log Dch-1488 0811.doc - Michigan

WIC HemoCue QC Log Analyzer Type : Hemocue 201+ Control Manufacturer: Site: QC Data (reagent specifics): This area must be completed during the first clinic of each week. If a bottle is opened with.

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How to fill out the App C HemoCue QC Log DCH-1488 0811.doc - Michigan online

This guide provides step-by-step instructions for filling out the App C HemoCue QC Log DCH-1488 0811.doc online. Understanding each component of this form is essential for ensuring accurate quality control in your facility.

Follow the steps to successfully complete the QC log

  1. Press the ‘Get Form’ button to access the form and open it in your browser.
  2. In the 'Control Manufacturer' field, enter the name of the manufacturer for your HemoCue control.
  3. Fill in the 'Site' section with the appropriate location where the quality control is being performed.
  4. Complete the 'QC Data' section during the first clinic of each week, entering details for the reagent specifics.
  5. If a new lot number is in use due to a newly opened bottle, make sure to document it by completing a new sheet as well.
  6. Refer to the package insert to fill out the 'Close vial expiration date' and 'Open vial expiration date', as well as the 'Expected Range' for both low and high controls.
  7. In the 'Cuvette' field, enter any necessary data, and ensure that the 'Date' field reflects the current date of completion.
  8. Indicate the weekly cleaning date in the specified field to maintain compliance.
  9. Fill in the 'Q.C. Results' for both low and high controls, marking 'Pass/Fail' for daily and weekly assessments.
  10. Initial your entries to confirm accuracy and completeness.
  11. Document any corrective actions that may be necessary, utilizing the reverse side of the log as needed.
  12. Ensure that the Site Coordinator reviews the log, making a note of the review date.
  13. Finally, save your changes, download, print, or share the completed form as required.

Complete your documentation effectively by filling out the form online today.

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HemoCue thus underestimates the Hb concentration by 2-5% and exhibits a 8-10 times higher variability with only 86.4% of HbHC being within +/- 10% of HbCOOX.

Results. Capillary blood measured by the Hemocue 301 has a bias of 0.36 ± 0.93 g/dL respect to the automated Hb. More than 50% of women with normal ferritin values were classified as anemics ing to the HemoCue 301.

Adult males 130 – 170 g/L Adult females 120 – 150 g/L Infants, after neonatal period 110 – 140 g/L Children, two years to teenage: gradual increase to adult normal. If the haemoglobin results do not reflect the patient's clinical symptoms, or seem unusually high or low, perform a control test.

The HemoCue point-of-care testing systems can test glucose, hemoglobin and white blood cell count. The systems give immediate results with laboratory quality and are unaffected by interference factors commonly associated with critically ill patients.

HemoCue point-of-care systems are available to test blood glucose, HbA1c, urine albumin, Hb and white blood cells with five part differential counts. The systems give immediate results with laboratory accuracy.

HemoCue Hb 201+ SystemSpecifications Testing Sample Material Capillary, venous or arterial whole blood Sample Volume ~10 µL Measuring Time within 60 seconds Measurement Range 0–25.6 g/dL (0–256 g/L, 0–15.9 mmol/L)16 more rows

The HemoCue system utilizes the principle of oxidation of haemoglobin to hemiglobin by sodium nitrite and the subsequent conversion of hemiglobin to hemiglobinazide by sodium azide. The reagents for these reactions are contained within a small disposable microcuvette of approximately 10 microliters in volume.

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