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Step 1: Understand the rules for safe specimen processing
· The lab technician must adhere to the standard precautions to maintain the viability of the specimen.
· The tube with plasma must be placed in an upright position. The position allows the blood to clot for at least half an hour.
· For Plasma, centrifuge the specimen upon drawing it.
· Maintain the ideal temperatures to conserve its integrity.
· The universal precautions of infection prevention must be followed succinctly
· Where blood fluids are anticipated, the worker must wear the protective gears
· A recap of sharp objects is not allowed. They must be disposed of in a sharps container
· A stable collecting rack should be available to collect all the well-labeled tubes (with blood specimens) in their respective bar codes
Tubes for Blood specimen collection
Step 2: Immediate processing and Operating the Centrifuge process
· Allow the specimen tubes to remain at room temperatures for at least half an hour until blood clotting occurs. Setting a timer for this can be quite efficient (Specimen tubes A and B).
· Do quick centrifugation to separate all the layers of the blood
· Specimen Tubes C and D can be centrifuged within 15 minutes of collection for at least 10 minutes at four degrees Celsius to maintain integrity. A concise record of the time at the start of spinning works well.
· The centrifuge should come to a halt before opening the specimen lid
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Figure 1: The samples after centrifuge process
Step 3: Processing the Plasma
· Begins within 15 minutes after venipuncture
· The blood sample must be mixed with the anticoagulant such as EDTA, heparin or sodium citrate to counteract any probability of coagulation (Estridge, Anna and Norma 12)
· Do not alter and disturb the white blood cells layer. The layer is a buffy coat and is evident as a thin layer between the lower pack of red blood cells and the upper plasma layer
· Do clear labeling indicating that the specimen has undergone centrifuging
· After aspirating the plasma, discard the rest in the biohazard waste container
· In case the sample is supposed to be shipped, freezing at -80 degrees Celsius is mandatory.
· Pipette the plasma to the transport tube, clearly indicating the volume, and labeled as per the client details.
· If the D Vacutainer® Plasma Preparation Tube was used in plasma preparation, then there is no need of transferring to the transporter tube again.
·
Figure 2: Plasma processing
Step 4: Processing of the serum
· The separation of serum should start at least within 30 minutes after venipuncture.
· The specimen tubes should be spun at room temperature for at least ten minutes.
· Remove the stoppers when the centrifuge comes to a close stop
· Withdraw the serum using a pipet
· Discard the remaining content in a biohazard container
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· Figure 3: separating the Serum Figure 3:
Step 5: Blood smear preparation
· The procedure allows the technologist to view the actual physical appearance of the blood cells and their morphology (Ernst, 395)
· Handle the glass slide by the edges
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· Introduce a small drop of blood on one of the clean glass. Repeat and introduce a second drop on the second slide (at least 1-2mm in diameter).
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· Spread the drop at an angle of 45 degrees. Blood should spread to the edges of the spreader slide.
· Let the sample films to dry without blowing or applying fixatives
Blood Smear preparation summary
Works cited
Ernst, Dennis J. Applied Phlebotomy. Baltimore, MD: Lippincott Williams & Wilkins, 2005. Print.
Estridge, Barbara H, Anna P. Reynolds, and Norma J. Walters. Basic Medical Laboratory Techniques. Spain: Delmar, 2000. Print.